Genomics Really Gets Personal: How Exome and Whole Genome Sequencing Challenge the Ethical Framework of Human Genetics ResearchTABOR, Holly K; BERKMAN, Benjamin E; CHANDROS HULL, Sara et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 2916-2924, issn 1552-4825, 9 p.Article

Priorities for autism spectrum disorder risk communication and ethicsYUDELL, Michael; TABOR, Holly K; DAWSON, Geraldine et al.Autism (London). 2013, Vol 17, Num 6, pp 701-722, issn 1362-3613, 22 p.Article

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effectsMCGOWAN, Kelly A; LI, Jun Z; ATTARDI, Laura D et al.Nature genetics. 2008, Vol 40, Num 8, pp 963-970, issn 1061-4036, 8 p.Article

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndromeNG, Sarah B; BIGHAM, Abigail W; LEE, Choli et al.Nature genetics. 2010, Vol 42, Num 9, pp 790-793, issn 1061-4036, 4 p.Article

Spectrum of MLL2 [ALR] Mutations in 110 Cases of Kabuki SyndromeHANNIBAL, Mark C; BUCKINGHAM, Kati J; COOK, Joseph et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 7, pp 1511-1516, issn 1552-4825, 6 p.Article

A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery diseaseASSIMES, Themistocles L; KNOWLES, Joshua W; SIDNEY, Steve et al.Atherosclerosis. 2008, Vol 198, Num 1, pp 136-144, issn 0021-9150, 9 p.Article

Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery diseaseASSIMES, Themistocles L; KNOWLES, Joshua W; TABIBIAZAR, Raymond et al.Human genetics. 2008, Vol 123, Num 4, pp 399-408, issn 0340-6717, 10 p.Article

Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosisEMOND, Mary J; LOUIE, Tin; BARNES, Kathleen C et al.Nature genetics. 2012, Vol 44, Num 8, pp 886-889, issn 1061-4036, 4 p.Article

Informed Consent for Whole Genome Sequencing: A Qualitative Analysis of Participant Expectations and Perceptions of Risks, Benefits, and HarmsTABOR, Holly K; STOCK, Jacquie; BRAZG, Tracy et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 6, pp 1310-1319, issn 1552-4825, 10 p.Article

Exome sequencing as a tool for Mendelian disease gene discoveryBAMSHAD, Michael J; NG, Sarah B; BIGHAM, Abigail W et al.Nature reviews. Genetics (Print). 2011, Vol 12, Num 11, pp 745-755, issn 1471-0056, 11 p.Article

Exome sequencing identifies the cause of a mendelian disorderNG, Sarah B; BUCKINGHAM, Kati J; SHENDURE, Jay et al.Nature genetics. 2010, Vol 42, Num 1, pp 30-35, issn 1061-4036, 6 p.Article

Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary diseaseHLATKY, Mark A; QUERTERMOUS, Thomas; TIBSHIRANI, Robert J et al.The American heart journal. 2007, Vol 154, Num 6, pp 1035-1042, issn 0002-8703, 8 p.Article

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex familiesJUN LI; TABOR, Holly K; NGUYEN, Loan et al.American journal of medical genetics. 2002, Vol 114, Num 1, pp 24-30, issn 0148-7299Article

Older women with diabetes have an increased risk of fracture : A prospective StudySCHWARTZ, Ann V; SELLMEYER, Deborah E; ENSRUD, Kristine E et al.The Journal of clinical endocrinology and metabolism. 2001, Vol 86, Num 1, pp 32-38, issn 0021-972XArticle