J Genet Couns
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Publication Venue For
- Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples. 2021
- Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice.. 30:439-447. 2021
- Men with an FMR1 premutation and their health education needs. 2021
- Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing.. 28:1107-1118. 2019
- A toolkit for genetics providers in follow-up of patients with non-diagnostic exome sequencing.. 28:213-228. 2019
- Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era.. 28:194-201. 2019
- INTRODUCTION TO EXPLORING THE EXOME SPECIAL ISSUE.. 28:181. 2019
- Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network.. 27:1087-1101. 2018
- Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?. 27:935-946. 2018
- Comparison of Telephone and Televideo Modes for Delivery of Genetic Counseling: a Randomized Trial.. 27:339-348. 2018
- Adherence to Recommended Risk Management among Unaffected Women with a BRCA Mutation.. 26:79-92. 2017
- Impact of Genetic Testing and Family Health History Based Risk Counseling on Behavior Change and Cognitive Precursors for Type 2 Diabetes.. 26:133-140. 2017
- Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.. 25:1019-1031. 2016
- Clinical and Counseling Experiences of Early Adopters of Whole Exome Sequencing.. 25:337-343. 2016
- Attitudes and Knowledge of Maternal-Fetal Medicine Fellows Regarding Noninvasive Prenatal Testing.. 25:73-78. 2016
- Communication of Psychiatric Risk in 22q11.2 Deletion Syndrome: A Pilot Project.. 25:6-17. 2016
- Randomized Trial of Telegenetics vs. In-Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance.. 24:961-970. 2015
- Parental Communication and Experiences and Knowledge of Adolescent Siblings of Children with 22q11.2 Deletion Syndrome.. 24:752-759. 2015
- Information-seeking and sharing behavior following genomic testing for diabetes risk.. 24:58-66. 2015
- Use of a patient-entered family health history tool with decision support in primary care: impact of identification of increased risk patients on genetic counseling attendance.. 24:179-188. 2015
- Genomic counseling: next generation counseling.. 23:689-692. 2014
- Public trust in genomic risk assessment for type 2 diabetes mellitus.. 23:401-408. 2014
- Promoting public awareness and engagement in genome sciences.. 22:508-516. 2013
- Assessment of parental disclosure of a 22q11.2 deletion syndrome diagnosis and implications for clinicians.. 21:835-844. 2012
- Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors.. 21:752-760. 2012
- Celebrating the 20th anniversary of the Journal of Genetic Counseling.. 21:1-2. 2012
- Influence of genetic risk information on parental role identity in adolescent girls and young women from families with fragile X syndrome.. 21:59-71. 2012
- Communication of genetic risk information to daughters in families with fragile X syndrome: the parent's perspective.. 20:58-69. 2011
- Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.. 19:535-544. 2010
- Considerations for the impact of personal genome information: a study of genomic profiling among genetics and genomics professionals.. 19:387-401. 2010
- Cancer genetics service interest in women with a limited family history of breast cancer.. 18:339-349. 2009
- Genetic risk communication: experiences of adolescent girls and young women from families with fragile X syndrome.. 18:313-325. 2009