Showing 181 - 195 of 593 results
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Guo S, Diep D, Plongthongkum N, Fung HL, Zhang K, Zhang K. (2017 Apr). Identification of methylation haplotype blocks aids in deconvolution of heterogeneous tissue samples and tumor tissue-of-origin mapping from plasma DNA. Nat. Genet.. 49(4):635-642.
PubMed ID: 28263317
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Grassmann F, Kiel C, Zimmermann ME, Gorski M, Grassmann V, Stark K,...Weber BH [including International AMD Genomics Consortium (IAMDGC).] (2017 March 27). Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits. Genome Med. 9(1):29.
PubMed ID: 28347358
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Sanderson SC, Brothers KB, Mercaldo ND, Clayton EW, Antommaria AH, Aufox SA,...Holm IA [including Brilliant MH, Kitchner TE, McManus VD.] (2017 March 2). Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US. Am J Hum Genet. 100(3):414-427.
PubMed ID: 28190457
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Almoguera B, Vazquez L, Mentch F, Connolly J, Pacheco JA, Sundaresan AS,...Hakonarson H [including Peissig PL, Linneman JG, Brilliant M.] (2017 February 15). Identification of Four Novel Loci in Asthma in European American and African American Populations. Am J Respir Crit Care Med. 195(4):456-463.
PubMed ID: 27611488
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Pasquale LR, Aschard H, Kang JH, Bailey JN, Lindström S, Chasman DI,...Wiggs JL [including Brilliant MH.] (2017 February). Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample. Menopause. 24(2):150-156.
PubMed ID: 27760082
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Schmidt AF, Swerdlow DI, Holmes MV, Patel RS, Fairhurst-Hunter Z, Lyall DM,...Sattar N [including Brilliant M, Kitchner T.] (2017 February). PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study. Lancet Diabetes Endocrinol. 5(2):97-105.
PubMed ID: 27908689
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Marouli E, Graff M, Medina-Gomez, [...], Brilliant MH, Peissig PL, et al. (2017 February). Rare and low-frequency coding variants alter human adult height. NATURE. 542(7640):186-90.
PubMed ID: 28146470
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Geng X, Pu W, Tan Y, Lu Z, Wang A, Tan L,...Chen X [including Guo S.] (2017 Jan 24). Quantitative assessment of the diagnostic role of FHIT promoter methylation in non-small cell lung cancer. Oncotarget. 8(4):6845-6856.
PubMed ID: 28036263
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Jones GT, Tromp G, Kuivaniemi H, Gretarsdottir S, Baas AF, Giusti B,...Bown MJ [including Ye Z, Peissig PL.] (2017 January 20). Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci. Circ Res. 120(2):341-353.
PubMed ID: 27899403
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Teixeira PL, Wei WQ, Cronin RM, Mo H, VanHouten JP, Carroll RJ,...Denny JC [including LaRose E, Dart RA, Nikolai AM, Peissig PL.] Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals. J Am Med Inform Assoc. 2017 January; 2017 Jan(24(1)):162-171. doi: 10.1093/JAMIA/OCW071. PMCID: PMC5201185.
PubMed ID: 27497800
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Dumitrescu L, Ritchie MD, Denny JC, El Rouby NM, McDonough CW, Bradford Y,...Crawford DC [including Peissig P.] (2017). Genome-wide study of resistant hypertension identified from electronic health records. PLoS One. 12(2):e0171745.
PubMed ID: 28222112
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Pu W, Wang C, Chen S, Zhao D, Zhou Y, Ma Y,...Wang M [including Guo S.] (2017). Targeted bisulfite sequencing identified a panel of DNA methylation-based biomarkers for esophageal squamous cell carcinoma (ESCC). Clin Epigenetics. 9 :129.
PubMed ID: 29270239
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Guo S, Wang R, Jiang T, Bai F, Ding Q, Ma Y,...Tan L. (2017). Alterations and diagnosis potential of serum lipid profiles in rheumatoid arthritis patients. Int J Clin Exp Pathol.. :3503-3509.
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Fan L, Chen L, Ni X, Guo S, Zhou Y, Wang C,...Wang M. (2017). Genetic variant of miR-4293 rs12220909 is associated with susceptibility to non-small cell lung cancer in a Chinese Han population. PLoS ONE. 12(4):e0175666.
PubMed ID: 28410417
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Maadooliat M, Bansal NK, Upadhya J, Farazi MR, Li X, He MM,...Schrodi SJ [including Hebbring SJ, Ye Z.] (2016 December 12). The Decay of Disease Association with Declining Linkage Disequilibrium: A Fine Mapping Theorem. Front Genet. 7 :217.
PubMed ID: 28018425
