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  • Lock, Eric F., Karen L. Soldano, Melanie E. Garrett, Heidi Cope, Christina A. Markunas, Herbert Fuchs, Gerald Grant, David B. Dunson, Simon G. Gregory, and Allison E. Ashley-Koch. “Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation.” BMC Genomics 16, no. 1 (January 22, 2015): 11. https://doi.org/10.1186/s12864-014-1211-8.
  • Riley, Ronald T., Jency L. Showker, Christine M. Lee, Cody E. Zipperer, Trevor R. Mitchell, Kenneth A. Voss, Nicholas C. Zitomer, et al. “A blood spot method for detecting fumonisin-induced changes in putative sphingolipid biomarkers in LM/Bc mice and humans.” Food Addit Contam Part A Chem Anal Control Expo Risk Assess 32, no. 6 (2015): 934–49. https://doi.org/10.1080/19440049.2015.1027746.
  • Li, Jing, Simon G. Gregory, Mariano A. Garcia-Blanco, and Andrew J. Armstrong. “Using circulating tumor cells to inform on prostate cancer biology and clinical utility.” Crit Rev Clin Lab Sci 52, no. 4 (2015): 191–210. https://doi.org/10.3109/10408363.2015.1023430.
  • Torres, O., J. Matute, J. Gelineau-Van Waes, J. R. Maddox, S. G. Gregory, A. E. Ashley-Koch, J. L. Showker, K. A. Voss, and R. T. Riley. “Human health implications from co-exposure to aflatoxins and fumonisins in maize-based foods in Latin America: Guatemala as a case study.” World Mycotoxin Journal 8, no. 2 (January 1, 2015): 143–59. https://doi.org/10.3920/WMJ2014.1736.
  • Krupp, Deidre R., Karen L. Soldano, Melanie E. Garrett, Heidi Cope, Allison E. Ashley-Koch, and Simon G. Gregory. “Missing genetic risk in neural tube defects: can exome sequencing yield an insight?” Birth Defects Res A Clin Mol Teratol 100, no. 8 (August 2014): 642–46. https://doi.org/10.1002/bdra.23276.
  • Markunas, Christina A., Eric Lock, Karen Soldano, Heidi Cope, Chien-Kuang C. Ding, David S. Enterline, Gerald Grant, Herbert Fuchs, Allison E. Ashley-Koch, and Simon G. Gregory. “Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics.” BMC Med Genomics 7 (June 25, 2014): 39. https://doi.org/10.1186/1755-8794-7-39.
  • Li, Yi-Ju, Mollie A. Minear, Xuejun Qin, Jacqueline Rimmler, Michael A. Hauser, R Rand Allingham, Robert P. Igo, et al. “Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.” Invest Ophthalmol Vis Sci 55, no. 7 (June 10, 2014): 4577–84. https://doi.org/10.1167/iovs.13-13517.
  • Li, Jing, Joshua Beaver, Rhonda Lynn Bitting, Simon Gregory, and Andrew J. Armstrong. “Genomic analysis of circulating tumor cells (CTCs) from men with metastatic castration resistant prostate cancer (mCRPC) in the context of enzalutamide therapy.” In Journal of Clinical Oncology, 32:e16059–e16059. American Society of Clinical Oncology (ASCO), 2014. https://doi.org/10.1200/jco.2014.32.15_suppl.e16059.
  • Torres, Olga, Jorge Matute, Janee Gelineau-van Waes, Joyce R. Maddox, Simon G. Gregory, Allison E. Ashley-Koch, Jency L. Showker, Nicholas C. Zitomer, Kenneth A. Voss, and Ronald T. Riley. “Urinary fumonisin B1 and estimated fumonisin intake in women from high- and low-exposure communities in Guatemala.” Mol Nutr Food Res 58, no. 5 (May 2014): 973–83. https://doi.org/10.1002/mnfr.201300481.
  • Miranda, Marie Lynn, Rebecca Anthopolos, and Simon G. Gregory. “Association of autism with induced or augmented childbirth.” Am J Obstet Gynecol 210, no. 5 (May 2014): 492–93. https://doi.org/10.1016/j.ajog.2013.12.038.
  • McGarrah, Robert, Damian M. Craig, Carol Haynes, Elizabeth Hauser, Christopher B. Newgard, Simon G. Gregory, William Kraus, and Svati Shah. “OMICS PROFILING HIGHLIGHTS ENDOPLASMIC RETICULUM-ASSOCIATED DEGRADATION AND UBIQUITIN PROTEASOME PATHWAYS IN INSULIN RESISTANCE AND GLYCEMIC CONTROL.” Journal of the American College of Cardiology 63, no. 12 (April 2014): A1600–A1600. https://doi.org/10.1016/s0735-1097(14)61603-x.
  • Gregory, Simon G. “Genetic predisposition of behavioral response.” Proc Natl Acad Sci U S A 111, no. 5 (February 4, 2014): 1672–73. https://doi.org/10.1073/pnas.1323421111.
  • Miranda, Marie Lynn, Rebecca Anthopolos, and Simon G. Gregory. “Induction or augmentation of labor and autism--reply.” JAMA Pediatr 168, no. 2 (February 2014): 191–92. https://doi.org/10.1001/jamapediatrics.2013.4792.
  • Armstrong, Andrew J., Jing Li, Joshua Beaver, Rhonda Lynn Bitting, and Simon Gregory. “Genomic analysis of circulating tumor cells (CTCs) from men with metastatic castration resistant prostate cancer (mCRPC) in the context of enzalutamide therapy.” In Journal of Clinical Oncology, 32:65–65. American Society of Clinical Oncology (ASCO), 2014. https://doi.org/10.1200/jco.2014.32.4_suppl.65.
  • Markunas, Christina A., David S. Enterline, Kaitlyn Dunlap, Karen Soldano, Heidi Cope, Jeffrey Stajich, Gerald Grant, Herbert Fuchs, Simon G. Gregory, and Allison E. Ashley-Koch. “Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation.” Ann Hum Genet 78, no. 1 (January 2014): 1–12. https://doi.org/10.1111/ahg.12041.
  • Gregory, S. G. “The epigenetics of Autism-Running beyond the bases.” In Frontiers in Autism Research New Horizons for Diagnosis and Treatment, 303–33, 2014. https://doi.org/10.1142/9789814602167_0013.
  • Shah, Svati H., Lydia C. Kwee, Elizabeth A. Grass, William E. Kraus, and Simon G. Gregory. “DNA Methylation Profiling Identifies Novel Epigenetic Markers of Cardiovascular Events.” In CIRCULATION, Vol. 130, 2014.
  • Gregory, Simon G., Rebecca Anthopolos, Claire E. Osgood, Chad A. Grotegut, and Marie Lynn Miranda. “Association of Autism With Induced or Augmented Childbirth in North Carolina Birth Record (1990–1998) and Education Research (1997–2007) Databases.” Obstetrical & Gynecological Survey 69, no. 1 (January 2014): 7–9. https://doi.org/10.1097/01.ogx.0000442814.50107.fa.
  • Connelly, Jessica J., Olga A. Cherepanova, Jennifer F. Doss, Themistoclis Karaoli, Travis S. Lillard, Christina A. Markunas, Sarah Nelson, et al. “Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis.” Hum Mol Genet 22, no. 25 (December 20, 2013): 5107–20. https://doi.org/10.1093/hmg/ddt365.
  • Ward-Caviness, Cavin, Carol Haynes, Colette Blach, Elaine Dowdy, Simon G. Gregory, Svati H. Shah, Benjamin D. Horne, William E. Kraus, and Elizabeth R. Hauser. “Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.” Hum Genet 132, no. 12 (December 2013): 1371–82. https://doi.org/10.1007/s00439-013-1339-7.
  • Shah, Svati H., Lydia Kwee, Nathan Stitziel, Elizabeth R. Hauser, Carol Haynes, Sekar Kathiresan, Simon G. Gregory, and William E. Kraus. “Rare Variants Identified With Whole Exome Chip Genotyping Are Associated With Insulin Resistance and Glycemic Control.” In CIRCULATION, Vol. 128. LIPPINCOTT WILLIAMS & WILKINS, 2013.
  • Gregory, Simon G., Rebecca Anthopolos, Claire E. Osgood, Chad A. Grotegut, and Marie Lynn Miranda. “Association of autism with induced or augmented childbirth in North Carolina Birth Record (1990-1998) and Education Research (1997-2007) databases.” JAMA Pediatr 167, no. 10 (October 2013): 959–66. https://doi.org/10.1001/jamapediatrics.2013.2904.
  • Soldano, Karen L., Melanie E. Garrett, Heidi L. Cope, J Michael Rusnak, Nathen J. Ellis, Kaitlyn L. Dunlap, Marcy C. Speer, Simon G. Gregory, and Allison E. Ashley-Koch. “Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype.” Birth Defects Res B Dev Reprod Toxicol 98, no. 5 (October 2013): 365–73. https://doi.org/10.1002/bdrb.21079.
  • Zeng, Yi, Lingguo Cheng, Ling Zhao, Qihua Tan, Qiushi Feng, Huashuai Chen, Ke Shen, et al. “Interactions between social/ behavioral factors and ADRB2 genotypes may be associated with health at advanced ages in China.” BMC Geriatr 13 (September 9, 2013): 91. https://doi.org/10.1186/1471-2318-13-91.
  • Cope, Heidi, Kelly McMahon, Elizabeth Heise, Sonja Eubanks, Melanie Garrett, Simon Gregory, and Allison Ashley-Koch. “Outcome and life satisfaction of adults with myelomeningocele.” Disabil Health J 6, no. 3 (July 2013): 236–43. https://doi.org/10.1016/j.dhjo.2012.12.003.
  • Sikich, Linmarie, Cheryl Alderman, Lindsey Hazzard, Terrence C. Bethea, Simon Gregory, and Jacqueline Johnson. “Pilot Study of Sustained Oxytocin Treatment in Children and Adolescents with Autistic Disorder.” In BIOLOGICAL PSYCHIATRY, 73:145S-145S. ELSEVIER SCIENCE INC, 2013.
  • Kraus, William E., Sheng Feng, Elizabeth R. Hauser, Simon G. Gregory, Carol Haynes, Z. E. Dowdy, Damian M. Craig, and Svati H. Shah. “Association of Gene Expression Signatures with Small Molecule Metabolic Intermediates that Predict Cardiovascular Mortality in CATHGEN.” In CIRCULATION, Vol. 127. LIPPINCOTT WILLIAMS & WILKINS, 2013.
  • Markunas, C. A., A. E. Ashley-Koch, and S. G. Gregory. “Genetics of the Chiari i and II malformations.” In Chiari Malformations, 9781461463696:93–101, 2013. https://doi.org/10.1007/978-1-4614-6369-6_7.
  • Markunas, Christina A., Karen Soldano, Kaitlyn Dunlap, Heidi Cope, Edgar Asiimwe, Jeffrey Stajich, David Enterline, et al. “Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.” PLoS One 8, no. 4 (2013): e61521. https://doi.org/10.1371/journal.pone.0061521.
  • Evsyukova, Irina, Shelton S. Bradrick, Simon G. Gregory, and Mariano A. Garcia-Blanco. “Cleavage and polyadenylation specificity factor 1 (CPSF1) regulates alternative splicing of interleukin 7 receptor (IL7R) exon 6.” RNA 19, no. 1 (January 2013): 103–15. https://doi.org/10.1261/rna.035410.112.
  • Minear, Mollie A., Yi-Ju Li, Jacqueline Rimmler, Elmer Balajonda, Shera Watson, R Rand Allingham, Michael A. Hauser, Gordon K. Klintworth, Natalie A. Afshari, and Simon G. Gregory. “Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.” Mol Vis 19 (2013): 2508–16.
  • Nolan, Daniel, William E. Kraus, Elizabeth Hauser, Yi-Ju Li, Dana K. Thompson, Jessica Johnson, Hsiang-Cheng Chen, et al. “Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family.” PLoS One 8, no. 8 (2013): e71779. https://doi.org/10.1371/journal.pone.0071779.
  • Ward-Caviness, Cavin, Lucas Neas, Carol Haynes, Colette Blach, Elizabeth Burns, Karen LaRocque-Abramson, Elaine Dowdy, et al. “Genetic Variants in the Bone Morphogenic Protein (BMP) Family of Genes Interact with Mobile Source Air Pollution to Increase Risk of Peripheral Arterial Disease.” CIRCULATION 126, no. 21 (November 20, 2012).
  • Shah, Svati H., Sheng Feng, Elizabeth Grass, Carol Haynes, Megan Chryst-Ladd, Damian Craig, Elizabeth R. Hauser, Christopher B. Newgard, William E. Kraus, and Simon G. Gregory. “Integration of Whole Genome Methylation with Metabolomics Identifies Novel Cardiovascular Disease Genes.” CIRCULATION 126, no. 21 (November 20, 2012).
  • Krupp, Deidre R., Pu-Ting Xu, Sophie Thomas, Andrew Dellinger, Heather C. Etchevers, Michel Vekemans, John R. Gilbert, et al. “Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).” Birth Defects Res A Clin Mol Teratol 94, no. 9 (September 2012): 683–92. https://doi.org/10.1002/bdra.23040.
  • Riley, Ronald T., Olga Torres, Jency L. Showker, Nicholas C. Zitomer, Jorge Matute, Kenneth A. Voss, Janee Gelineau-van Waes, Joyce R. Maddox, Simon G. Gregory, and Allison E. Ashley-Koch. “The kinetics of urinary fumonisin B1 excretion in humans consuming maize-based diets.” Mol Nutr Food Res 56, no. 9 (September 2012): 1445–55. https://doi.org/10.1002/mnfr.201200166.
  • Markunas, Christina A., R Shane Tubbs, Roham Moftakhar, Allison E. Ashley-Koch, Simon G. Gregory, W Jerry Oakes, Marcy C. Speer, and Bermans J. Iskandar. “Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.” J Neurosurg Pediatr 9, no. 4 (April 2012): 372–78. https://doi.org/10.3171/2011.12.PEDS11113.
  • Nolan, Daniel K., Beth Sutton, Carol Haynes, Jessica Johnson, Jacqueline Sebek, Elaine Dowdy, David Crosslin, et al. “Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5.” BMC Genet 13 (February 27, 2012): 12. https://doi.org/10.1186/1471-2156-13-12.
  • Lin, Ningjing, Chunhui Di, Kathy Bortoff, Jinrong Fu, Peter Truszkowski, Patrick Killela, Chris Duncan, et al. “Deletion or epigenetic silencing of AJAP1 on 1p36 in glioblastoma.” Mol Cancer Res 10, no. 2 (February 2012): 208–17. https://doi.org/10.1158/1541-7786.MCR-10-0109.
  • Feng, Jie, Jianyi Zhang, Ming Liu, Gang Wan, Keyan Qi, Chenguang Zheng, Zeping Lv, et al. “Association of mtDNA haplogroup F with healthy longevity in the female Chuang population, China.” Exp Gerontol 46, no. 12 (December 2011): 987–93. https://doi.org/10.1016/j.exger.2011.09.001.
  • Shah, Asad A., Damian M. Craig, Carol Haynes, Jacqueline K. Sebek, Elizabeth Grass, Karen Abramson, Peter K. Smith, et al. “Genome-Wide Association Identifies Genetic Variants Associated With Vein Graft Stenosis After Coronary Artery Bypass Grafting.” In CIRCULATION, Vol. 124. LIPPINCOTT WILLIAMS & WILKINS, 2011.
  • Gregory, S. G. “Genomic Rearrangements in Autism: The Contribution of Copy Number Loss and Gain to the Etiology of Autism Spectrum Disorders.,” 52:S17–S17. WILEY-BLACKWELL, 2011.
  • Hara, Makoto R., Jeffrey J. Kovacs, Erin J. Whalen, Sudarshan Rajagopal, Ryan T. Strachan, Wayne Grant, Aaron J. Towers, et al. “A stress response pathway regulates DNA damage through β2-adrenoreceptors and β-arrestin-1.” Nature 477, no. 7364 (August 21, 2011): 349–53. https://doi.org/10.1038/nature10368.
  • Minear, Mollie A., David R. Crosslin, Beth S. Sutton, Jessica J. Connelly, Sarah C. Nelson, Shera Gadson-Watson, Tianyuan Wang, et al. “Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.” Hum Genet 129, no. 6 (June 2011): 641–54. https://doi.org/10.1007/s00439-011-0959-z.
  • Li, Yi-Ju, Mollie A. Minear, Jacqueline Rimmler, Bei Zhao, Elmer Balajonda, Michael A. Hauser, R Rand Allingham, et al. “Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.” PLoS One 6, no. 4 (April 20, 2011): e18044. https://doi.org/10.1371/journal.pone.0018044.
  • Sun, Albert Y., Jason I. Koontz, Svati H. Shah, Jonathan P. Piccini, Kent R. Nilsson, Damian Craig, Carol Haynes, Simon G. Gregory, Patrick M. Hranitzky, and Geoffrey S. Pitt. “The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fraction.” Circ Cardiovasc Genet 4, no. 2 (April 2011): 163–68. https://doi.org/10.1161/CIRCGENETICS.110.958652.
  • Jin, Genglin, Stephen Cook, Bo Cui, William C. Chen, Stephen T. Keir, Patrick Killela, Chunhui Di, et al. “HDMX regulates p53 activity and confers chemoresistance to 3-bis(2-chloroethyl)-1-nitrosourea.” Neuro Oncol 12, no. 9 (September 2010): 956–66. https://doi.org/10.1093/neuonc/noq045.
  • Duncan, Christopher G., Patrick J. Killela, Cathy A. Payne, Benjamin Lampson, William C. Chen, Jeff Liu, David Solomon, et al. “Integrated genomic analyses identify ERRFI1 and TACC3 as glioblastoma-targeted genes.” Oncotarget 1, no. 4 (August 2010): 265–77. https://doi.org/10.18632/oncotarget.137.
  • Zhang, Lisheng, Jessica J. Connelly, Karsten Peppel, Leigh Brian, Svati H. Shah, Sarah Nelson, David R. Crosslin, et al. “Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.” Hum Mol Genet 19, no. 14 (July 15, 2010): 2754–66. https://doi.org/10.1093/hmg/ddq172.
  • Vogazianou, Artemis P., Raymond Chan, L Magnus Bäcklund, Danita M. Pearson, Lu Liu, Cordelia F. Langford, Simon G. Gregory, V Peter Collins, and Koichi Ichimura. “Distinct patterns of 1p and 19q alterations identify subtypes of human gliomas that have different prognoses.” Neuro Oncol 12, no. 7 (July 2010): 664–78. https://doi.org/10.1093/neuonc/nop075.
  • Fraser, Heather I., Calliope A. Dendrou, Barry Healy, Daniel B. Rainbow, Sarah Howlett, Luc J. Smink, Simon Gregory, et al. “Nonobese diabetic congenic strain analysis of autoimmune diabetes reveals genetic complexity of the Idd18 locus and identifies Vav3 as a candidate gene.” J Immunol 184, no. 9 (May 1, 2010): 5075–84. https://doi.org/10.4049/jimmunol.0903734.
  • Minear, M. A., N. A. Afshari, E. Balajonda, B. Zhao, J. Rimmler, Y. -. J. Li, G. K. Klintworth, and S. G. Gregory. “Analysis of SLC4A11 and COL8A2 Mutations in Fuchs Endothelial Corneal Dystrophy (FECD).” In INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, Vol. 51. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2010.
  • Chen, Hsiang-Cheng, Virginia Byers Kraus, Yi-Ju Li, Sarah Nelson, Carol Haynes, Jessica Johnson, Thomas Stabler, et al. “Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family.” Arthritis Rheum 62, no. 3 (March 2010): 781–90. https://doi.org/10.1002/art.27288.
  • Riazuddin, S Amer, Norann A. Zaghloul, Amr Al-Saif, Lisa Davey, Bill H. Diplas, Danielle N. Meadows, Allen O. Eghrari, et al. “Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9p.” Am J Hum Genet 86, no. 1 (January 2010): 45–53. https://doi.org/10.1016/j.ajhg.2009.12.001.
  • Evsyukova, Irina, Jason A. Somarelli, Simon G. Gregory, and Mariano A. Garcia-Blanco. “Alternative splicing in multiple sclerosis and other autoimmune diseases.” RNA Biol 7, no. 4 (2010): 462–73. https://doi.org/10.4161/rna.7.4.12301.
  • Gregory, Simon G., Jessica J. Connelly, Aaron J. Towers, Jessica Johnson, Dhani Biscocho, Christina A. Markunas, Carla Lintas, et al. “Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.” BMC Med 7 (October 22, 2009): 62. https://doi.org/10.1186/1741-7015-7-62.
  • McCauley, J. L., R. L. Zuvich, Y. Bradford, S. J. Kenealy, N. Schnetz-Boutaud, S. G. Gregory, S. L. Hauser, et al. “Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.” Genes Immun 10, no. 7 (October 2009): 624–30. https://doi.org/10.1038/gene.2009.53.
  • Wang, Tianyuan, Terrence S. Furey, Jessica J. Connelly, Shihao Ji, Sarah Nelson, Steffen Heber, Simon G. Gregory, and Elizabeth R. Hauser. “A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease.” Hum Genomics 3, no. 3 (April 2009): 221–35. https://doi.org/10.1186/1479-7364-3-3-221.
  • Afshari, Natalie A., Yi-Ju Li, Margaret A. Pericak-Vance, Simon Gregory, and Gordon K. Klintworth. “Genome-wide linkage scan in fuchs endothelial corneal dystrophy.” Invest Ophthalmol Vis Sci 50, no. 3 (March 2009): 1093–97. https://doi.org/10.1167/iovs.08-1839.
  • Crosslin, David R., Svati H. Shah, Sarah C. Nelson, Carol S. Haynes, Jessica J. Connelly, Shera Gadson, Pascal J. Goldschmidt-Clermont, et al. “Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.” Hum Genet 125, no. 2 (March 2009): 217–29. https://doi.org/10.1007/s00439-008-0619-0.
  • Shah, Svati H., Neil J. Freedman, Lisheng Zhang, David R. Crosslin, David H. Stone, Carol Haynes, Jessica Johnson, et al. “Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis.” PLoS Genet 5, no. 1 (January 2009): e1000318. https://doi.org/10.1371/journal.pgen.1000318.
  • Maier, Lisa M., Christopher E. Lowe, Jason Cooper, Kate Downes, David E. Anderson, Christopher Severson, Pamela M. Clark, et al. “IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production.” PLoS Genet 5, no. 1 (January 2009): e1000322. https://doi.org/10.1371/journal.pgen.1000322.
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  • Shah, Svati H., Elizabeth R. Hauser, David Crosslin, Liyong Wang, Carol Haynes, Jessica Connelly, Sarah Nelson, et al. “ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention.” Atherosclerosis 201, no. 1 (November 2008): 148–54. https://doi.org/10.1016/j.atherosclerosis.2008.01.011.
  • Goswami, Robi, Beth S. Sutton, Cynthia Rouf, Sarah Nelson, Carol Haynes, Jessica Johnson, Pascal Goldschmidt-Clermont, et al. “Biliverdin Reductase Genetic Polymorphisms are Associated with Early-Onset Coronary Artery Disease In Two Datasets.” CIRCULATION 118, no. 18 (October 28, 2008): S389–90.
  • Deak, Kristen L., Deborah G. Siegel, Timothy M. George, Simon Gregory, Allison Ashley-Koch, Marcy C. Speer, and NTD Collaborative Group. “Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects.” Birth Defects Res A Clin Mol Teratol 82, no. 10 (October 2008): 662–69. https://doi.org/10.1002/bdra.20511.
  • Wang, L., E. R. Hauser, S. H. Shah, D. Seo, P. Sivashanmugam, S. T. Exum, S. G. Gregory, et al. “Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.” Ann Hum Genet 72, no. Pt 4 (July 2008): 443–53. https://doi.org/10.1111/j.1469-1809.2008.00433.x.
  • Stamm, Demetra S., Deborah G. Siegel, Lorraine Mehltretter, Jessica J. Connelly, Alison Trott, Nathen Ellis, Victoria Zismann, et al. “Refinement of 2q and 7p loci in a large multiplex NTD family.” Birth Defects Res A Clin Mol Teratol 82, no. 6 (June 2008): 441–52. https://doi.org/10.1002/bdra.20462.
  • Kennerly, Erin, Anne Ballmann, Stanton Martin, Russ Wolfinger, Simon Gregory, Michael Stoskopf, and Greg Gibson. “A gene expression signature of confinement in peripheral blood of red wolves (Canis rufus).” Mol Ecol 17, no. 11 (June 2008): 2782–91. https://doi.org/10.1111/j.1365-294X.2008.03775.x.
  • Sutton, Beth S., David R. Crosslin, Svati H. Shah, Sarah C. Nelson, Anthony Bassil, A Brent Hale, Carol Haynes, et al. “Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.” Hum Mol Genet 17, no. 9 (May 1, 2008): 1318–28. https://doi.org/10.1093/hmg/ddn020.
  • Connelly, Jessica J., Svati H. Shah, Jennifer F. Doss, Shera Gadson, Sarah Nelson, David R. Crosslin, A Brent Hale, et al. “Genetic and functional association of FAM5C with myocardial infarction.” BMC Med Genet 9 (April 22, 2008): 33. https://doi.org/10.1186/1471-2350-9-33.
  • Ichimura, K., A. P. Vogazianou, L. Liu, D. M. Pearson, L. M. Bäcklund, K. Plant, K. Baird, C. F. Langford, S. G. Gregory, and V. P. Collins. “1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomas.” Oncogene 27, no. 14 (March 27, 2008): 2097–2108. https://doi.org/10.1038/sj.onc.1210848.
  • Wang, Liyong, Elizabeth R. Hauser, David Crosslin, Sarah Nelson, A. B. Hale, Simon G. Gregory, Svati H. Shah, William E. Kraus, Pascal J. Goldschmidt-Clermont, and Jeffery M. Vance. “Genomic convergence identified CAPG and VAMP8 as candidate genes for CAD.” In CIRCULATION, 116:807–807. LIPPINCOTT WILLIAMS & WILKINS, 2007.
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