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Subject Areas on Research
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30-Year Review of Pediatric- and Adult-Onset CVID: Clinical Correlates and Prognostic Indicators.
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A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets.
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A Phase 2 Study of AMO-02 (Tideglusib) in Congenital and Childhood-Onset Myotonic Dystrophy Type 1 (DM1).
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A TOMM40 variable-length polymorphism predicts the age of late-onset Alzheimer's disease.
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A bivariate survival model with compound Poisson frailty.
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A common biological basis of obesity and nicotine addiction.
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A common variant on chromosome 9p21 affects the risk of myocardial infarction.
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A dynamic cascade model of the development of substance-use onset.
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A genome-wide association study of myasthenia gravis.
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A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.
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A large kindred of early-onset osteoarthritis of the knee and hip: excluding the link to COL2A1 gene.
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A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14.
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A longitudinal study of differences in late- and early-onset geriatric depression: depressive symptoms and psychosocial, cognitive, and neurological functioning.
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A mouse model of adult-onset anaemia due to erythropoietin deficiency.
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A multinational study on motor function in early-onset FSHD.
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A mutation in cartilage oligomeric matrix protein (COMP) causes early-onset osteoarthritis in a large kindred study.
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A novel human disease with abnormal prion protein sensitive to protease.
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A pooled analysis of individual patient data from National Clinical Trials Network clinical trials of concurrent chemoradiotherapy for limited-stage small cell lung cancer in elderly patients versus younger patients.
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A randomized study of alglucosidase alfa in late-onset Pompe's disease.
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A reevaluation of the duration of survival after the onset of dementia.
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A report on older-age bipolar disorder from the International Society for Bipolar Disorders Task Force.
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A second locus for familial high myopia maps to chromosome 12q.
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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
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A twin study of late-onset depression and apolipoprotein E epsilon 4 as risk factors for Alzheimer's disease.
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A variable age of onset segregation model for linkage analysis, with correction for ascertainment, applied to glioma.
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A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
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ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.
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ADHD and smoking: from genes to brain to behavior.
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ALSUntangled 41: "Eric Is Winning".
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APOE and AD concordance in twin pairs as predictors of AD in first-degree relatives.
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APOE genotype predicts when--not whether--one is predisposed to develop Alzheimer disease.
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APOE: The New Frontier in the Development of a Therapeutic Target towards Precision Medicine in Late-Onset Alzheimer's.
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Abdominal obesity, liver fat, and muscle composition in survivors of childhood acute lymphoblastic leukemia.
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Abuse liability of medications used to treat attention-deficit/hyperactivity disorder (ADHD).
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Academic achievement, close up work parameters, and myopia in Singapore military conscripts.
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Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles.
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Adjustment of caregivers of pediatric patients with brain tumors: a cross-sectional analysis.
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Adolescent-onset nicotine self-administration modeled in female rats.
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Adult-onset eccrine angiomatous hamartoma: report of a rare entity with unusual histological features.
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Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American families.
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Age at diagnosis and multiple primary cancers of the breast and ovary.
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Age at menarche, time to regular cycling, and breast cancer (North Carolina, United States).
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Age at onset in two common neurodegenerative diseases is genetically controlled.
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Age of onset for binge eating: Are there different pathways to binge eating?
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Age of onset in chronic major depression: relation to demographic and clinical variables, family history, and treatment response.
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Age of onset of myopia predicts risk of high myopia in later childhood in myopic Singapore children.
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Aging-related diagnostic variations: need for diagnostic criteria appropriate for elderly psychiatric patients.
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Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis.
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Allelic differences in the brain-derived neurotrophic factor Val66Met polymorphism in late-life depression.
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Alzheimer's Disease Risk Polymorphisms Regulate Gene Expression in the ZCWPW1 and the CELF1 Loci.
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Alzheimer's disease and apolipoprotein E-4 allele in an Amish population.
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Amygdala volume in late-life depression: relationship with age of onset.
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An exploration of genetic association tests for disease risk and age at onset.
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An immune tolerance approach using transient low-dose methotrexate in the ERT-naïve setting of patients treated with a therapeutic protein: experience in infantile-onset Pompe disease.
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An miR-502-binding site single-nucleotide polymorphism in the 3'-untranslated region of the SET8 gene is associated with early age of breast cancer onset.
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Analysis of association at single nucleotide polymorphisms in the APOE region.
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Anatomic location and laterality of MRI signal hyperintensities in late-life depression.
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Anhedonia in Japanese patients with Parkinson's disease: analysis using the Snaith-Hamilton Pleasure Scale.
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Antibodies in sera of patients with late-onset myasthenia gravis recognize the PEVK domain of titin.
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Anxiety Disorders in Late Life.
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Apolipoprotein E and Alzheimer's disease.
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Apolipoprotein E controls the risk and age at onset of Parkinson disease.
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Apolipoprotein E epsilon 4.
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Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease.
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Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis.
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Apolipoprotein E, survival in Alzheimer's disease patients, and the competing risks of death and Alzheimer's disease.
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Appetite loss and neurocognitive deficits in late-life depression.
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Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study.
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Are Patients with Childhood Onset of Insomnia and Depression More Difficult to Treat Than Are Those with Adult Onsets of These Disorders? A Report from the TRIAD Study.
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Are depressed outpatients with and without a family history of substance use disorder different? A baseline analysis of the STAR*D cohort.
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Are quit attempts among U.S. female nurses who smoke different from female smokers in the general population? An analysis of the 2006/2007 tobacco use supplement to the current population survey.
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Arteriosclerotic depression.
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Assessing Acute Secondary Treatment Outcomes in Early-Onset Obsessive-Compulsive Disorder.
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Association between smoking and attention-deficit/hyperactivity disorder symptoms in a population-based sample of young adults.
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Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease.
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Association of AGTR1 with 18-month treatment outcome in late-life depression.
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Association of MDMA/ecstasy and other substance use with self-reported sexually transmitted diseases among college-aged adults: a national study.
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Association of circadian genes with diurnal blood pressure changes and non-dipper essential hypertension: a genetic association with young-onset hypertension.
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Association of five-factor model personality domains and facets with presence, onset, and treatment outcomes of major depression in older adults.
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Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis.
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Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease.
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Association test for X-linked QTL in family-based designs.
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Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A).
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Autoimmune myasthenia gravis: emerging clinical and biological heterogeneity.
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Autopsy findings in late-onset Pompe disease: a case report and systematic review of the literature.
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Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.
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Axis I psychiatric comorbidity and its relationship to historical illness variables in 288 patients with bipolar disorder.
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BPT for Early-Onset Behavior Disorders: Examining the Link Between Treatment Components and Trajectories of Child Internalizing Symptoms.
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BRCA1 mutations in primary breast and ovarian carcinomas.
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Bariatric Surgery: A Potential Treatment for Type 2 Diabetes in Youth.
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Bayesian model selection and averaging in additive and proportional hazards models.
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Bayesian modeling of incidence and progression of disease from cross-sectional data.
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Behavioral and emotional disturbances in the offspring of depressed parents with anger attacks.
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Benchmarking the Cost-Effectiveness of Interventions Delaying Diabetes: A Simulation Study Based on NAVIGATOR Data.
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Benzoate treatment and the glycine index in nonketotic hyperglycinaemia.
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Bimodal age distribution at diagnosis in breast cancer persists across molecular and genomic classifications.
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Blau syndrome and related genetic disorders causing childhood arthritis.
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Blood Lead, Bone Turnover, and Survival in Amyotrophic Lateral Sclerosis.
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Body mass index and risk, age of onset, and survival in patients with pancreatic cancer.
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Brain-stem auditory and visual evoked potentials in children with Krabbe disease.
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Breast cancer and dietary factors in Taiwanese women.
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Breast cancer deaths averted over 3 decades.
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Burden of disease in adult patients with hypophosphatasia: Results from two patient-reported surveys.
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CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group.
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Can We RISE to the Challenge of Youth-Onset Type 2 Diabetes?
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Cancer risk in childhood-onset systemic lupus.
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Cardiovascular Risk of Isolated Systolic or Diastolic Hypertension in Young Adults.
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Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy.
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Carotid web: an occult mechanism of embolic stroke.
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Case reports of heart failure after therapy with a tumor necrosis factor antagonist.
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Caudate volume measurement in older adults with bipolar disorder.
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Challenges in the phenotypic characterisation of patients in genetic studies of coronary artery disease.
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Changes in Aβ biomarkers and associations with APOE genotype in 2 longitudinal cohorts.
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Characteristics, management, and outcomes of patients with hepatocellular carcinoma in Africa: a multicountry observational study from the Africa Liver Cancer Consortium.
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Child, Parent, and Peer Predictors of Early-Onset Substance Use: A Multi-Site Longitudinal Study
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Child-, adolescent- and young adult-onset depressions: differential risk factors in development?
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Childhood gastroesophageal reflux symptoms in adult patients.
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Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium.
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Childhood trauma is associated with depressive symptoms in Mexico City women.
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Children in South Asia have higher body mass-adjusted blood pressure levels than white children in the United States: a comparative study.
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Chorea-acanthocytosis: genetic linkage to chromosome 9q21.
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Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.
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Chromosome 8q24 markers: risk of early-onset and familial prostate cancer.
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Classification of child and adolescent eating disturbances. Workgroup for Classification of Eating Disorders in Children and Adolescents (WCEDCA).
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Clinical Characteristics and Factors Associated With Disability and Impaired Quality of Life in Children With Juvenile Systemic Sclerosis: Results From the Childhood Arthritis and Rheumatology Research Alliance Legacy Registry.
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Clinical and Molecular Disease Spectrum and Outcomes in Patients with Infantile-Onset Pompe Disease.
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Clinical and electrographic manifestations of lesional neocortical temporal lobe epilepsy.
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Clinical and molecular predictors of disease severity and survival in chronic lymphocytic leukemia.
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Clinical and neuropsychological differences between patients with earlier and later onset of Alzheimer's disease: A CERAD analysis, Part XII.
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Clinical and pathological features of ovarian cancer in women with germ-line mutations of BRCA1.
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Clinical and phenomenological comparisons of late-onset and early-onset depression.
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Clinical and radiological characteristics of early versus late mild cognitive impairment in patients with comorbid depressive disorder.
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Clinical and treatment response characteristics of late-life depression associated with vascular disease: a pooled analysis of two multicenter trials with sertraline.
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Clinical aspects of ALS in Gulf War veterans.
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Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis.
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Clinical characteristics of African-American men with hereditary prostate cancer: the AAHPC Study.
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Clinical characteristics of magnetic resonance imaging-defined subcortical ischemic depression.
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Clinical course and flow cytometric analysis of paroxysmal nocturnal hemoglobinuria in the United States and Japan.
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Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred.
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Cognitive and academic outcomes in long-term survivors of infantile-onset Pompe disease: A longitudinal follow-up.
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Cognitive functioning throughout the treatment history of clinical late-life depression.
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Cognitive improvement following treatment in late-life depression: relationship to vascular risk and age of onset.
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Cognitive performance and informant reports in the diagnosis of cognitive impairment and dementia in African Americans and whites.
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Combined effects of E2F1 and E2F2 polymorphisms on risk and early onset of squamous cell carcinoma of the head and neck.
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Combined immunodeficiency in the United States and Kuwait: Comparison of patients' characteristics and molecular diagnosis.
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Coming closer to describing the variable onset patterns in autism.
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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
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Common variants in the periostin gene influence development of atherosclerosis in young persons.
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Comorbidity.
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Comparative phenotypic and CARD15 mutational analysis among African American, Hispanic, and White children with Crohn's disease.
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Comparison of brain structural variables, neuropsychological factors, and treatment outcome in early-onset versus late-onset late-life depression.
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Comparison of quality of life measures in a depressed population.
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Comparison of short bowel syndrome acquired early in life and during adolescence.
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Complete genomic screen in Parkinson disease: evidence for multiple genes.
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Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12.
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Complete genomic screen in late-onset familial Alzheimer's disease.
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Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer disease.
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Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.
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Concurrent use of methamphetamine, MDMA, LSD, ketamine, GHB, and flunitrazepam among American youths.
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Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation.
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Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13.
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Consensus statement on generalized anxiety disorder from the International Consensus Group on Depression and Anxiety.
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Controlled comparison of electrophysiological sleep in families of probands with unipolar depression.
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Correspondence re: E. Hawk, et al., Male pattern baldness and clinical prostate cancer in the epidemiologic follow-up of the First National Health and Nutrition Examination Survey. Cancer Epidemiol.Biomark. Prev., 9: 523-527, 2000.
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Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium.
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Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus.
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Cox regression model with randomly censored covariates.
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Cumulative prevalence of psychiatric disorders by young adulthood: a prospective cohort analysis from the Great Smoky Mountains Study.
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Current concepts in pediatric temporomandibular joint disorders: Part 1. Etiology, epidemiology, and classification.
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Cyclin D1 polymorphism and increased risk of colorectal cancer at young age.
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DNMT3b polymorphism and hereditary nonpolyposis colorectal cancer age of onset.
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De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia.
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Death from supine asphyxia in late onset pompe disease: Two patients.
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Decreasing age at prostate cancer diagnosis over successive generations in prostate cancer families.
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Default mode network connectivity in children with a history of preschool onset depression.
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Deficiency of Adenosine Deaminase 2 in Adults and Children: Experience From India.
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Delayed onset of Alzheimer's disease with nonsteroidal anti-inflammatory and histamine H2 blocking drugs.
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Delays to Care in Pediatric Lupus Patients: Data From the Childhood Arthritis and Rheumatology Research Alliance Legacy Registry.
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Delta sleep EEG in depressed adolescent females and healthy controls.
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Depression and generalized anxiety disorder: cumulative and sequential comorbidity in a birth cohort followed prospectively to age 32 years.
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Design of the Genetics of Early Onset Cardiovascular Disease (GENECARD) study.
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Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.
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Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing.
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Diagnosis, grading and management of toxicities from immunotherapies in children, adolescents and young adults with cancer.
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Diagnostic and treatment challenges of neuronopathic Gaucher disease: two cases with an intermediate phenotype.
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Diagnostic criteria for late-onset (childhood and adult) Pompe disease.
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Disability in geriatric depression.
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Disrupted amygdala reactivity in depressed 4- to 6-year-old children.
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Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking.
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Do acetylcholine receptor and striated muscle antibodies predict the presence of thymoma in patients with myasthenia gravis?
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Does early-onset chronic or recurrent major depression impact outcomes with antidepressant medications? A CO-MED trial report.
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Double-blind comparison of sertraline, imipramine, and placebo in the treatment of dysthymia: psychosocial outcomes.
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Ductal carcinoma in situ in BRCA mutation carriers.
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Duration of empirical antibiotic therapy for infants suspected of early-onset sepsis.
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EBV-positive diffuse large B-cell lymphoma of the elderly: 2016 update on diagnosis, risk-stratification, and management.
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EMK: a novel program for family-based allelic and genotypic association tests on quantitative traits.
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Early atherosclerosis is associated with retinal microvascular changes in adolescents with type 1 diabetes.
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Early onset baldness and prostate cancer risk.
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Early onset neonatal sepsis: the burden of group B Streptococcal and E. coli disease continues.
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Early onset prostate cancer has a significant genetic component.
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Early onset prostate cancer: predictors of clinical grade.
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Early-but Not Late-Onset Hypertension Is Related to Midlife Cognitive Function.
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Early-onset obesity and the unwanted promise of thrombosis.
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Early-onset stroke and vasculopathy associated with mutations in ADA2.
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Editorial Perspective: Delayed circadian rhythm phase: a cause of late-onset attention-deficit/hyperactivity disorder among adolescents?
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Effect of Sociodemographic Factors on Uptake of a Patient-Facing Information Technology Family Health History Risk Assessment Platform.
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Effect of age at onset on the course of major depressive disorder.
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Effect of extended-release niacin on new-onset diabetes among hyperlipidemic patients treated with ezetimibe/simvastatin in a randomized controlled trial.
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Effectiveness of second-generation antipsychotics in patients with treatment-resistant schizophrenia: a review and meta-analysis of randomized trials.
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Effects of MDM2 promoter polymorphisms and p53 codon 72 polymorphism on risk and age at onset of squamous cell carcinoma of the head and neck.
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Effects of alcohol consumption on disability among the near elderly: a longitudinal analysis.
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Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.
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Efficacy, safety profile, and immunogenicity of alglucosidase alfa produced at the 4,000-liter scale in US children and adolescents with Pompe disease: ADVANCE, a phase IV, open-label, prospective study.
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Electroencephalographic changes in pyridoxine-dependant epilepsy: new observations.
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Enhancing recovery in coronary heart disease (ENRICHD): baseline characteristics.
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Epileptic and electroencephalographic manifestations of guanidinoacetate-methyltransferase deficiency.
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Ethnic issues in the epidemiology of childhood obesity.
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Evaluation and treatment of dystonia.
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Evaluation of underlying mechanisms in the link between childhood ADHD symptoms and risk for early initiation of substance use.
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Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS.
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Exercise has a disproportionate role in the pathogenesis of arrhythmogenic right ventricular dysplasia/cardiomyopathy in patients without desmosomal mutations.
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Exogenous hormone use, reproductive factors, and risk of intracranial meningioma in females.
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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
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Expanding the phenotype of late-onset Pompe disease: tongue weakness: a new clinical observation.
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Facioscapulohumeral muscular dystrophy can be a cause of isolated childhood cognitive dysfunction.
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Factors Associated with Recurrence Rates and Long-Term Survival in Women Diagnosed with Breast Cancer Ages 40 and Younger.
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Factors associated with health-related quality of life among outpatients with major depressive disorder: a STAR*D report.
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Factors associated with survival in the National Registry of Veterans with ALS.
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Factors that differentiate early vs. later onset of major depression disorder.
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Familial influence and childhood trauma in female alcoholism.
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Familial leukoencephalopathy in bipolar disorder.
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Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.
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Family history of atrial fibrillation is associated with earlier-onset and more symptomatic atrial fibrillation: Results from the Outcomes Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF) registry.
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Family history of completed suicide and characteristics of major depressive disorder: a STAR*D (sequenced treatment alternatives to relieve depression) study.
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Family history of mood disorder and characteristics of major depressive disorder: a STAR*D (sequenced treatment alternatives to relieve depression) study.
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Family physician preferences and knowledge gaps regarding the care of adolescent and young adult survivors of childhood cancer.
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Family-based association tests for rare variants with censored traits.
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Family-based case-control study of cigarette smoking and Parkinson disease.
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Fast Algorithms for Conducting Large-Scale GWAS of Age-at-Onset Traits Using Cox Mixed-Effects Models.
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Fasting Glucose Variability in Young Adulthood and Cognitive Function in Middle Age: The Coronary Artery Risk Development in Young Adults (CARDIA) Study.
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Female and male antisocial trajectories: from childhood origins to adult outcomes.
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Fertility treatment is associated with multiple meningiomas and younger age at diagnosis.
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Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity.
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Fine-mapping the putative chromosome 17q21-22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis.
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Fluvoxamine treatment of social phobia (social anxiety disorder): a double-blind, placebo-controlled study.
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Folate metabolism genes, dietary folate and response to antidepressant medications in late-life depression.
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Food group intake and brain lesions in late-life vascular depression.
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Functional brain activation to emotionally valenced faces in school-aged children with a history of preschool-onset major depression.
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Functional connectivity of the amygdala in early-childhood-onset depression.
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Functional evidence implicating a novel TOR1A mutation in idiopathic, late-onset focal dystonia.
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Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients.
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GATA2 is associated with familial early-onset coronary artery disease.
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Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.
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Generalized anxiety disorder: nature and course.
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Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutations.
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Genetic association tests based on ranks (GATOR) for quantitative traits with and without censoring.
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Genetic complexity and Parkinson's disease. Deane Laboratory Parkinson Disease Research Group.
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Genetic diagnosis in Lafora disease: genotype-phenotype correlations and diagnostic pitfalls.
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Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma.
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Genetic sharing and heritability of paediatric age of onset autoimmune diseases.
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Genetic susceptibility for lung cancer: interactions with gender and smoking history and impact on early detection policies.
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Genetic variation at a single locus and age of onset for Alzheimer's disease.
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Genetics of Alzheimer's disease.
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Genetics of parkin-linked disease.
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Genetics of pediatric epilepsy.
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Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan.
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Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci.
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Genome-wide scan for adult onset primary open angle glaucoma.
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Genome-wide scan for prostate cancer susceptibility genes using families from the University of Michigan prostate cancer genetics project finds evidence for linkage on chromosome 17 near BRCA1.
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Genomewide search for type 2 diabetes susceptibility genes in four American populations.
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Genomics of human health and aging.
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Genotype-phenotype correlation in two frequent mutations and mutation update in type III glycogen storage disease.
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Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India.
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Germline PTEN mutations as a cause of early-onset endometrial cancer.
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Germline genetic variants in men with prostate cancer and one or more additional cancers.
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Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors.
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Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.
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Growing up with a chronic illness: social success, educational/vocational distress.
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HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.
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HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.
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HLA-Mismatched Microtransplant in Older Patients Newly Diagnosed With Acute Myeloid Leukemia: Results From the Microtransplantation Interest Group.
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HNF-4alpha: from MODY to late-onset type 2 diabetes.
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Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome.
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Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
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Heterogeneity of the Predictive Polygenic Risk Scores for Coronary Heart Disease Age-at-Onset in Three Different Coronary Heart Disease Family-Based Ascertainments.
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Hierarchy of risk of childhood-onset rheumatoid arthritis conferred by HLA-DRB1 alleles encoding the shared epitope.
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High heritability of metabolomic profiles in families burdened with premature cardiovascular disease.
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Hippocampus shape analysis and late-life depression.
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How common is misdiagnosis in late-onset Pompe disease?
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Human epidermal growth factor receptor-2 and estrogen receptor expression, a demonstration project using the residual tissue repository of the Surveillance, Epidemiology, and End Results (SEER) program.
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ISPAD Clinical Practice Consensus Guidelines 2018: Microvascular and macrovascular complications in children and adolescents.
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Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia.
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Identification of a novel locus on 2q for autosomal dominant high-grade myopia.
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Identification of novel genes in late-onset Alzheimer's disease.
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Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.
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Identifying risk factors for first-episode neck pain: A systematic review.
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Imaging and genetics advances in understanding geriatric depression.
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Imaging frontostriatal function in ultra-high-risk, early, and chronic schizophrenia during executive processing.
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Impact of Early-Onset Sepsis and Antibiotic Use on Death or Survival with Neurodevelopmental Impairment at 2 Years of Age among Extremely Preterm Infants.
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Impact of Risk-Adapted Therapy for Pediatric Hodgkin Lymphoma on Risk of Long-Term Morbidity: A Report From the Childhood Cancer Survivor Study.
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Impact of age at diagnosis on racial disparities in endometrial cancer patients.
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Impact of early and late age-related macular degeneration on vision-specific functioning.
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Impact of early personal-history characteristics on the Pace of Aging: implications for clinical trials of therapies to slow aging and extend healthspan.
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Implications of early versus late onset of attention-deficit/hyperactivity disorder symptoms.
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Implications of extending the ADHD age-of-onset criterion to age 12: results from a prospectively studied birth cohort.
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Incidence and survival rates for young blacks with nasopharyngeal carcinoma in the United States.
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Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers.
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Infantile Pompe disease on ERT: update on clinical presentation, musculoskeletal management, and exercise considerations.
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Infections in Infants with SCID: Isolation, Infection Screening, and Prophylaxis in PIDTC Centers.
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Influence of serotonin transporter promoter region polymorphisms on hippocampal volumes in late-life depression.
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Influence of the susceptibility genes apolipoprotein E-epsilon 4 and apolipoprotein E-epsilon 2 on the rate of disease expressivity of late-onset Alzheimer's disease.
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Injection drug use among stimulant users in a national sample.
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Insulin resistance and risk factors for cardiovascular disease in young adult survivors of childhood acute lymphoblastic leukemia.
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Intellectual, neurocognitive, and academic achievement in abstinent adolescents with cannabis use disorder.
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International Consensus for the Dosing of Corticosteroids in Childhood-Onset Systemic Lupus Erythematosus With Proliferative Lupus Nephritis.
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Intima-media thickness and age of first depressive episode.
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Intracerebral adeno-associated virus gene delivery of apolipoprotein E2 markedly reduces brain amyloid pathology in Alzheimer's disease mouse models.
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Inverse association of general joint hypermobility with hand and knee osteoarthritis and serum cartilage oligomeric matrix protein levels.
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Investigation of Notch3 as a candidate gene for bipolar disorder using brain hyperintensities as an endophenotype.
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Is aspirin intake associated with early age-related macular degeneration? The Singapore Indian Eye Study.
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Is there a link between passive smoke exposure and early-onset myopia in preschool Asian children?
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Juvenile Spondyloarthritis in the Childhood Arthritis and Rheumatology Research Alliance Registry: High Biologic Use, Low Prevalence of HLA-B27, and Equal Sex Representation in Sacroiliitis.
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Kinetics of visual field loss in Usher syndrome Type II.
-
Krabbe disease: neurophysiologic studies and MRI correlations.
-
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis.
-
Late onset N-acetylglutamate synthase deficiency caused by hypomorphic alleles.
-
Late onset Pompe Disease in India - Beyond the Caucasian phenotype.
-
Late-Onset ADHD Reconsidered With Comprehensive Repeated Assessments Between Ages 10 and 25.
-
Late-life onset bipolar disorder presenting as a case of pseudo-dementia: a case discussion and review of literature.
-
Late-onset adenosine deaminase deficiency presenting with Heck's disease.
-
Leiomyosarcoma in childhood and adolescence.
-
Lifetime perturbations of bipolar disorder.
-
Limited family structure and breast cancer risk.
-
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.
-
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity.
-
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.
-
Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.
-
Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype.
-
Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
-
Long-Term Blood Pressure Variability, New-Onset Diabetes Mellitus, and New-Onset Chronic Kidney Disease in the Japanese General Population.
-
Long-term health-related outcomes in survivors of childhood cancer treated with HSCT versus conventional therapy: a report from the Bone Marrow Transplant Survivor Study (BMTSS) and Childhood Cancer Survivor Study (CCSS).
-
Long-term seizure control outcomes after resection of gangliogliomas.
-
Longitudinal Cognitive Outcomes of Clinical Phenotypes of Late-Life Depression.
-
Longitudinal follow-up of late-onset Alzheimer disease families.
-
Lyme disease serology in amyotrophic lateral sclerosis.
-
MRI signal hyperintensities in geriatric depression.
-
MRI subcortical hyperintensities in old and very old depressed outpatients: the important role of age in late-life depression.
-
MRI-defined vascular depression.
-
Magnetic resonance imaging correlates of depression in early- and late-onset Alzheimer's disease.
-
Magnetic resonance imaging signal hypointensity and iron content of putamen nuclei in elderly depressed patients.
-
Major depressive disorder in youths with IDDM. A controlled prospective study of course and outcome.
-
Management patterns of childhood-onset nephrotic syndrome.
-
Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study.
-
Medial orbital frontal lesions in late-onset depression.
-
Medical comorbidity in late-life depression.
-
Melancholia in later life: late and early onset differences in presentation, course, and dementia risk.
-
Mental health antecedents of early midlife insomnia: evidence from a four-decade longitudinal study.
-
Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class.
-
Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomes.
-
Metabolic profiling of patients with schizophrenia.
-
Mice deficient for the secreted glycoprotein SPARC/osteonectin/BM40 develop normally but show severe age-onset cataract formation and disruption of the lens.
-
Microphthalmia-associated transcription factor (MITF) locus lacks linkage to human vitiligo or osteopetrosis: an evaluation.
-
Midlife activity predicts risk of dementia in older male twin pairs.
-
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.
-
Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorder.
-
Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene X environment interaction.
-
Molecular analysis and protein processing in late-onset Pompe disease patients with low levels of acid α-glucosidase activity.
-
Morphological, biochemical, and genetic support for an apolipoprotein E effect on microtubular metabolism.
-
MuSK-antibody positive myasthenia gravis: questions from the clinic.
-
Multifocal motor neuropathy: 30 years from onset to diagnosis.
-
Myasthenia gravis in the tenth decade.
-
NOS2A and the modulating effect of cigarette smoking in Parkinson's disease.
-
Neural correlates associated with cognitive decline in late-life depression.
-
Neurodevelopmental outcomes following neonatal late-onset sepsis and blood culture-negative conditions.
-
Neurodevelopmental outcomes of umbilical cord blood transplantation in metachromatic leukodystrophy.
-
Neuroimaging in late-life depression.
-
Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684.
-
Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis.
-
Neuropsychological status of subjects at high risk for a first episode of psychosis.
-
New onset and remission of suicidal ideation among a depressed adult sample.
-
New onset focal weakness in children with Down syndrome.
-
No association between OPA1 polymorphisms and primary open-angle glaucoma in three different populations.
-
No association between the HLA-A2 allele and Alzheimer disease.
-
No association of alpha1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients.
-
No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease.
-
No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease.
-
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.
-
Novel approaches to quantify CNS involvement in children with Pompe disease.
-
Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C-encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window current.
-
Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy.
-
Obesity and age of first non-ST-segment elevation myocardial infarction.
-
Occurrence of amyotrophic lateral sclerosis among Gulf War veterans.
-
Ocular motility in North Carolina autosomal dominant ataxia.
-
Open-label extension study following the Late-Onset Treatment Study (LOTS) of alglucosidase alfa.
-
Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.
-
Origins of depression in later life.
-
Outcomes in two Japanese adenosine deaminase-deficiency patients treated by stem cell gene therapy with no cytoreductive conditioning.
-
PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease.
-
Paediatric rheumatic disease: lessons from SLE: children are not little adults.
-
Pain coping and the pain experience in children with juvenile chronic arthritis.
-
Patent foramen ovale in adults with sickle cell disease and stroke.
-
Pathologic changes in highly myopic eyes of young males in Singapore.
-
Pathways to PTSD, part II: Sexually abused children.
-
Pediatric Bipolar Disorder: Onset, Risk Factors, and Protective Factors.
-
Pediatric deep venous thrombosis.
-
Pediatric spinal deformities.
-
Perinatal factors associated with clinical presentation of osteosarcoma in children and adolescents.
-
Personality--life event congruence effects in late-life depression.
-
Phenol sulfotransferases: hormonal regulation, polymorphism, and age of onset of breast cancer.
-
Phenotypic analysis of 303 multiplex families with common epilepsies.
-
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.
-
Physical and Family History Variables Associated With Neurological and Cognitive Development in Sturge-Weber Syndrome.
-
Physical therapy and chiropractic use among childhood cancer survivors with chronic disease: impact on health-related quality of life.
-
Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms.
-
Polymorphisms in hMLH1 and risk of early-onset lung cancer in a southeast Chinese population.
-
Polymorphisms in the SULF1 gene are associated with early age of onset and survival of ovarian cancer.
-
Polymorphisms of p21 and p27 jointly contribute to an earlier age at diagnosis of pancreatic cancer.
-
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.
-
Pompe disease: design, methodology, and early findings from the Pompe Registry.
-
Possible bipolar nature of irritability in major depressive disorder.
-
Preadult onset vs. adult onset of major depressive disorder: a replication study.
-
Precision, reliability and accuracy in the dating of symptom onsets in child and adolescent psychopathology.
-
Prediction of differential adult health burden by conduct problem subtypes in males.
-
Prediction of disease relapse in a cohort of paediatric patients with localized scleroderma.
-
Predictive value of family history on severity of illness: the case for depression, anxiety, alcohol dependence, and drug dependence.
-
Predictors of Outcome in Ulcerative Colitis.
-
Predictors of antipsychotic treatment response in patients with first-episode schizophrenia, schizoaffective and schizophreniform disorders.
-
Predictors of recurrence in remitted late-life depression.
-
Predictors of treatment response in patients with posttraumatic stress disorder.
-
Preliminary criteria for global flares in childhood-onset systemic lupus erythematosus.
-
Preschool psychopathology: lessons for the lifespan.
-
Presenilin-1 polymorphism and Alzheimer's disease.
-
Presenilin-1 polymorphism and Alzheimer's disease.
-
Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patients.
-
Prevalence of mutations in TIGR/Myocilin in patients with adult and juvenile primary open-angle glaucoma.
-
Prevalence of radiological and clinical cerebrovascular disease in idiopathic Parkinson's disease.
-
Prevalence, correlates, and course of minor depression and major depression in the National Comorbidity Survey.
-
Principles of pediatric lupus nephritis in a prospective contemporary multi-center cohort.
-
Probable exclusion of GLC1A as a candidate glaucoma gene in a family with middle-age-onset primary open-angle glaucoma.
-
Probing the role of PPARγ in the regulation of late-onset Alzheimer's disease-associated genes.
-
Prognostic factors in early-onset epithelial ovarian cancer: a population-based study.
-
Progression of cognitive, functional, and neuropsychiatric symptom domains in a population cohort with Alzheimer dementia: the Cache County Dementia Progression study.
-
Prominent reduction in pyramidal neurons density in the orbitofrontal cortex of elderly depressed patients.
-
Prospective developmental subtypes of alcohol dependence from age 18 to 32 years: implications for nosology, etiology, and intervention.
-
Prostate cancer in young men: an important clinical entity.
-
Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study.
-
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease.
-
Quantifying the Dynamics of Field Cancerization in Tobacco-Related Head and Neck Cancer: A Multiscale Modeling Approach.
-
Quantitative assessment of early diabetic retinopathy using fractal analysis.
-
Quantitative assessment of lingual strength in late-onset Pompe disease.
-
Racial differences in herpes zoster and age at onset of varicella.
-
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.
-
Reduction in Late Mortality among 5-Year Survivors of Childhood Cancer.
-
Refractory calculation-induced idiopathic generalized epilepsy: a case report and review of the literature.
-
Relational aggression in children with preschool-onset psychiatric disorders.
-
Relationship Between Binocular Summation and Stereoacuity After Strabismus Surgery.
-
Relationship of cognitive reserve and APOE status to the emergence of clinical symptoms in preclinical Alzheimer's disease.
-
Relative effectiveness of reappraisal and distraction in regulating emotion in late-life depression.
-
Religious service attendance and major depression: a case of reverse causality?
-
Reproductive health needs of adolescent and young adult women with pediatric rheumatic diseases.
-
Research review: DSM-V conduct disorder: research needs for an evidence base.
-
Residency training in transition of youth with childhood-onset chronic disease.
-
Respiratory muscle training (RMT) in late-onset Pompe disease (LOPD): Effects of training and detraining.
-
Response inhibition predicts poor antidepressant treatment response in very old depressed patients.
-
Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases.
-
Risk Factors for Early-Onset Colorectal Cancer.
-
Risk factors and prevention of late-onset sepsis in premature infants.
-
Risk of Alzheimer disease with the epsilon4 allele for apolipoprotein E in a population-based study of men aged 62-73 years.
-
Risk of Prostate Cancer Associated With Familial and Hereditary Cancer Syndromes.
-
Risk of dementia among relatives of Alzheimer's disease patients in the MIRAGE study: What is in store for the oldest old?
-
Risk of second primary tumors in men diagnosed with prostate cancer: a population-based cohort study.
-
SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease.
-
Safety and efficacy of alternative alglucosidase alfa regimens in Pompe disease.
-
Screening for Pompe disease using a rapid dried blood spot method: experience of a clinical diagnostic laboratory.
-
Self-reported Age of Hypertension Onset and Hypertension-Mediated Organ Damage in Middle-Aged Individuals.
-
Seven novel mutations in the adenosine deaminase (ADA) gene in patients with severe and delayed onset combined immunodeficiency: G74C, V129M, G140E, R149W, Q199P, 462delG, and E337del. Mutations in brief no. 142. Online.
-
Severe Cardiac Involvement Is Rare in Patients with Late-Onset Pompe Disease and the Common c.-32-13T>G Variant: Implications for Newborn Screening.
-
Severe disease presentation and poor outcomes among pediatric systemic lupus erythematosus patients in South Africa.
-
Severe stress and adjustment disorder diagnoses in the population of Denmark.
-
Sex differences in cardiovascular risk factors before and after the development of type 2 diabetes and risk for incident cardiovascular disease.
-
Sex-Related Disparities in Cardiovascular Health Care Among Patients With Premature Atherosclerotic Cardiovascular Disease.
-
Signs and symptoms of first-onset TMD and sociodemographic predictors of its development: the OPPERA prospective cohort study.
-
Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.
-
Sluggish cognitive tempo (SCT) in an adult outpatient sample seeking an attention-deficit/hyperactivity disorder assessment: Age of onset and assessment method impact on SCT rates.
-
Smoking Paradox in Patients Hospitalized With Coronary Artery Disease or Acute Ischemic Stroke: Findings From Get With The Guidelines.
-
Social information-processing patterns partially mediate the effect of early physical abuse on later conduct problems.
-
Social support in elderly patients with bipolar disorder.
-
Somatic mutations in the transcriptional corepressor gene BCORL1 in adult acute myelogenous leukemia.
-
Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome.
-
Spontaneous Resolution and Timing of Intervention in Congenital Nasolacrimal Duct Obstruction.
-
Strategies for dissecting genetic-environmental interactions in neurodegenerative disorders.
-
Structural brain changes as biomarkers and outcome predictors in patients with late-life depression: a cross-sectional and prospective study.
-
Studying health histories of cancer: a new model connecting cancer incidence and survival.
-
Substance abuse, treatment needs and access among female sex workers and non-sex workers in Pretoria, South Africa.
-
Substance use disorders among inhalant users: results from the National Epidemiologic Survey on alcohol and related conditions.
-
Summary of findings from the OPPERA prospective cohort study of incidence of first-onset temporomandibular disorder: implications and future directions.
-
Support for the vascular depression hypothesis in late-life depression: results of a 2-site, prospective, antidepressant treatment trial.
-
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.
-
TOMM40 and APOE: Requirements for replication studies of association with age of disease onset and enrichment of a clinical trial.
-
Temporal patterns in the risk of chronic health conditions in survivors of childhood cancer diagnosed 1970-99: a report from the Childhood Cancer Survivor Study cohort.
-
Temporoparietal hypometabolism in frontotemporal lobar degeneration and associated imaging diagnostic errors.
-
The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part VI. Family history assessment: a multicenter study of first-degree relatives of Alzheimer's disease probands and nondemented spouse controls.
-
The Duke myasthenia gravis clinic registry: I. Description and demographics.
-
The HOXB13 variant X285K is associated with clinical significance and early age at diagnosis in African American prostate cancer patients.
-
The Localized Scleroderma Cutaneous Assessment Tool: responsiveness to change in a pediatric clinical population.
-
The Systemic Juvenile Idiopathic Arthritis Cohort of the Childhood Arthritis and Rheumatology Research Alliance Registry: 2010-2013.
-
The age at onset of attention deficit hyperactivity disorder.
-
The association of strabismus, amblyopia, and refractive errors in spasmus nutans.
-
The brain-derived neurotrophic factor VAL66MET polymorphism and cerebral white matter hyperintensities in late-life depression.
-
The cis-regulatory effect of an Alzheimer's disease-associated poly-T locus on expression of TOMM40 and apolipoprotein E genes.
-
The distinction between juvenile and adult-onset primary open-angle glaucoma.
-
The effects of the TOMM40 poly-T alleles on Alzheimer's disease phenotypes.
-
The emerging phenotype of late-onset Pompe disease: A systematic literature review.
-
The epidemiology of social phobia: findings from the Duke Epidemiological Catchment Area Study.
-
The genetic attributable risk of breast and ovarian cancer.
-
The high prevalence of substance use disorders among recent MDMA users compared with other drug users: Implications for intervention.
-
The impact of age on thyroid cancer staging.
-
The impact of antibodies in late-onset Pompe disease: a case series and literature review.
-
The influence of neighborhood disadvantage and perceived disapproval on early substance use initiation.
-
The mutational landscape of early- and typical-onset oral tongue squamous cell carcinoma.
-
The neuregulin 1 promoter polymorphism rs6994992 is not associated with chronic schizophrenia or neurocognition.
-
The polymorphic exon 1 androgen receptor CAG repeat in men with a potential inherited predisposition to prostate cancer.
-
The prevalence and 3-year incidence of dementia in older Black and White community residents.
-
The prevalence, onset, and clinical significance of antiphospholipid antibodies prior to diagnosis of systemic lupus erythematosus.
-
The relation of prophylactic inoculations to the onset of poliomyelitis. 1950.
-
The stability of psychopathy across adolescence.
-
The ubiquilin 1 gene and Alzheimer's disease.
-
The undertreatment of dysthymia.
-
The value of muscle biopsies in Pompe disease: identifying lipofuscin inclusions in juvenile- and adult-onset patients.
-
Thought suppression and treatment outcome in late-life depression.
-
Thymectomy may not be associated with clinical improvement in MuSK myasthenia gravis.
-
Tibiofibular synostosis stress fracture: a case report.
-
Time to diagnosis in the National Registry of Veterans with Amyotrophic Lateral Sclerosis.
-
Time trends of incidence of age-associated diseases in the US elderly population: Medicare-based analysis.
-
Timing of diagnosis of patients with Pompe disease: data from the Pompe registry.
-
Tobacco smoke exposure and respiratory morbidity in young children.
-
Trade-off in the effect of the APOE gene on the ages at onset of cardiocascular disease and cancer across ages, gender, and human generations.
-
Trade-off in the effects of the apolipoprotein E polymorphism on the ages at onset of CVD and cancer influences human lifespan.
-
Transancestral mapping and genetic load in systemic lupus erythematosus.
-
Treatment outcomes for older depressed patients with earlier versus late onset of first depressive episode: a Sequenced Treatment Alternatives to Relieve Depression (STAR*D) report.
-
Trends in cannabis use prior to first presentation with schizophrenia, in South-East London between 1965 and 1999.
-
Trends in risk profiles for and mortality associated with invasive aspergillosis among liver transplant recipients.
-
Twenty-five year follow-up of childhood Wilms tumor: a report from the Childhood Cancer Survivor Study.
-
Twin pairs discordant for neuropathologically confirmed Lewy body dementia.
-
Two Sides of the Same Coin: Pediatric-Onset and Adult-Onset Common Variable Immune Deficiency.
-
Unraveling a multifactorial late-onset disease: from genetic susceptibility to disease mechanisms for age-related macular degeneration.
-
Unusually high rate of young-onset pancreatic cancer in the East Nile Delta region of Egypt.
-
Urea cycle disorders: clinical presentation outside the newborn period.
-
Use of decrease in apparent diffusion coefficient values to predict infarct age.
-
Use of the complete blood cell count in early-onset neonatal sepsis.
-
Use of the complete blood cell count in late-onset neonatal sepsis.
-
Validation of the Davidson Trauma Scale in a sample of survivors of childhood sexual abuse.
-
Validation of the phenomenon of autistic regression using home videotapes.
-
Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking.
-
Vascular nutritional correlates of late-life depression.
-
Very late onset infections in the neonatal intensive care unit.
-
Very low birth weight neonates who survive early-onset sepsis do not have an increased risk of developing late-onset sepsis.
-
Very low birth weight preterm infants with early onset neonatal sepsis: the predominance of gram-negative infections continues in the National Institute of Child Health and Human Development Neonatal Research Network, 2002-2003.
-
Visual event-related potential changes at two different tasks in nondemented Parkinson's disease.
-
White matter lesion volumes and caudate volumes in late-life depression.
-
Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice-site and Charcot-Marie-Tooth phenotype with early onset symptoms.
-
Whole-body magnetic resonance imaging in late-onset Pompe disease: Clinical utility and correlation with functional measures.
-
Worldwide trends in diabetes since 1980: a pooled analysis of 751 population-based studies with 4.4 million participants.
-
X-linked high myopia associated with cone dysfunction.
-
Young adult weight trajectories through midlife by body mass category.
-
Youth employment, income, and smoking initiation: results from Korean panel data.
-
[Analysis of genetic heterogeneity of bronchial asthma in relation with the age at the onset of disease]
-
[Comparison and analysis of clinicopathology of lung cancer between 1980s and 1990s in the Shenyang area (1,224 cases)].
-
[Population risk of bronchial asthma occurrence in Moscow]
-
Keywords of People
-
Berchuck, Andrew,
James M. Ingram Distinguished Professor of Gynecologic Oncology,
Obstetrics and Gynecology, Gynecologic Oncology
-
Cohen-Wolkowiez, Michael,
Professor of Pediatrics,
Pediatrics, Infectious Diseases
-
Dodge, Kenneth A.,
William McDougall Distinguished Professor of Public Policy Studies,
Duke Science & Society
-
Grambow, Steven C.,
Associate Professor of Biostatistics & Bioinformatics,
Biostatistics & Bioinformatics
-
Hogan, Brigid L. M.,
Research Professor of Cell Biology,
Cell Biology
-
Li, Yi-Ju,
Professor of Biostatistics & Bioinformatics,
Biostatistics & Bioinformatics
-
Liu, Yutao,
Adjunct Assistant Professor in the Department of Medicine,
Medicine, Medical Genetics
-
Schanberg, Laura Eve,
Professor of Pediatrics,
Pediatrics, Rheumatology
-
Wu, Li-Tzy,
Professor in Psychiatry and Behavioral Sciences,
Medicine, General Internal Medicine