DeWan AT - Search Results

1

A genome scan for renal function among hypertensives: the HyperGEN study.

DeWan AT, Arnett DK, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt J. DeWan AT, et al. Am J Hum Genet. 2001 Jan;68(1):136-144. doi: 10.1086/316927. Epub 2000 Dec 12. Am J Hum Genet. 2001. PMID: 11115379 Free PMC article.

2

Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN).

Oetting WS, Armstrong CM, Holleschau AM, DeWan AT, Summers GC. Oetting WS, et al. Among authors: dewan at. Ophthalmic Genet. 2000 Dec;21(4):227-33. Ophthalmic Genet. 2000. PMID: 11135493

3

Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysis.

Young TL, Atwood LD, Ronan SM, Dewan AT, Alvear AB, Peterson J, Holleschau A, King RA. Young TL, et al. Among authors: dewan at. Ophthalmic Genet. 2001 Jun;22(2):69-75. doi: 10.1076/opge.22.2.69.2233. Ophthalmic Genet. 2001. PMID: 11449316

4

Linkage of left ventricular contractility to chromosome 11 in humans: The HyperGEN Study.

Arnett DK, Devereux RB, Kitzman D, Oberman A, Hopkins P, Atwood L, Dewan A, Rao DC; Hypertension Genetic Epidemiology Network Study Group. Arnett DK, et al. Hypertension. 2001 Oct;38(4):767-72. doi: 10.1161/hy1001.092650. Hypertension. 2001. PMID: 11641284

5

Refined mapping of suggestive linkage to renal function in African Americans: the HyperGEN study.

DeWan AT, Arnett DK, Miller MB, Peacock JM, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt JH. DeWan AT, et al. Am J Hum Genet. 2002 Jul;71(1):204-5. doi: 10.1086/340730. Am J Hum Genet. 2002. PMID: 12068377 Free PMC article. No abstract available.

6

X-linked high myopia associated with cone dysfunction.

Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, Motulsky AG, King RA. Young TL, et al. Among authors: dewan at. Arch Ophthalmol. 2004 Jun;122(6):897-908. doi: 10.1001/archopht.122.6.897. Arch Ophthalmol. 2004. PMID: 15197065

7

Confronting the missing epistasis problem: on the reproducibility of gene-gene interactions.

Murk W, Bracken MB, DeWan AT. Murk W, et al. Among authors: dewan at. Hum Genet. 2015 Aug;134(8):837-49. doi: 10.1007/s00439-015-1564-3. Epub 2015 May 22. Hum Genet. 2015. PMID: 25998948

8

Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans.

Salinas YD, Wang L, DeWan AT. Salinas YD, et al. Among authors: dewan at. BMC Genet. 2016 Jun 13;17(1):78. doi: 10.1186/s12863-016-0387-0. BMC Genet. 2016. PMID: 27296613 Free PMC article.

9

A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish population.

Streicher SA, Klein AP, Olson SH, Kurtz RC, Amundadottir LT, DeWan AT, Zhao H, Risch HA. Streicher SA, et al. Among authors: dewan at. Hum Genet. 2021 Feb;140(2):309-319. doi: 10.1007/s00439-020-02205-8. Epub 2020 Jul 15. Hum Genet. 2021. PMID: 32671597 Free PMC article.

10

Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).

Zhu M, Yang T, Wei S, DeWan AT, Morell RJ, Elfenbein JL, Fisher RA, Leal SM, Smith RJ, Friderici KH. Zhu M, et al. Among authors: dewan at. Am J Hum Genet. 2003 Nov;73(5):1082-91. doi: 10.1086/379286. Epub 2003 Sep 16. Am J Hum Genet. 2003. PMID: 13680526 Free PMC article.

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