Oetting WS - Search Results

1

Getting ready for the Human Phenome Project: the 2012 forum of the Human Variome Project.

Oetting WS, Robinson PN, Greenblatt MS, Cotton RG, Beck T, Carey JC, Doelken SC, Girdea M, Groza T, Hamilton CM, Hamosh A, Kerner B, MacArthur JA, Maglott DR, Mons B, Rehm HL, Schofield PN, Searle BA, Smedley D, Smith CL, Bernstein IT, Zankl A, Zhao EY. Oetting WS, et al. Hum Mutat. 2013 Apr;34(4):661-6. doi: 10.1002/humu.22293. Hum Mutat. 2013. PMID: 23401191 Free PMC article.

2

Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene.

Oetting WS, King RA. Oetting WS, et al. Hum Mutat. 1993;2(1):1-6. doi: 10.1002/humu.1380020102. Hum Mutat. 1993. PMID: 8477259

3

Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism.

Oetting WS, King RA. Oetting WS, et al. Hum Mutat. 1999;13(2):99-115. doi: 10.1002/(SICI)1098-1004(1999)13:2<99::AID-HUMU2>3.0.CO;2-C. Hum Mutat. 1999. PMID: 10094567 Review.

4

New insights into ocular albinism type 1 (OA1): Mutations and polymorphisms of the OA1 gene.

Oetting WS. Oetting WS. Hum Mutat. 2002 Feb;19(2):85-92. doi: 10.1002/humu.10034. Hum Mutat. 2002. PMID: 11793467 Review.

5

A call for mutations.

Cotton RG, Auerbach AD, Oetting WS; Human GenomeVariation Society. Cotton RG, et al. Among authors: oetting ws. Genet Med. 2005 May-Jun;7(5):370. doi: 10.1097/01.GIM.0000164550.87307.11. Genet Med. 2005. PMID: 15915089 Free article. No abstract available.

6

The 2004 Human Genome Variation Society scientific meeting.

Oetting WS, Tabone T. Oetting WS, et al. Hum Mutat. 2005 Aug;26(2):160-3. doi: 10.1002/humu.20194. Hum Mutat. 2005. PMID: 15971230

7

2005 Human Genome Variation Society Scientific Meeting.

Oetting WS. Oetting WS. Hum Mutat. 2006 Mar;27(3):286-9. doi: 10.1002/humu.20297. Hum Mutat. 2006. PMID: 16419082

8

The 2006 Human Genome Variation Society scientific meeting.

Oetting WS. Oetting WS. Hum Mutat. 2007 May;28(5):517-21. doi: 10.1002/humu.20489. Hum Mutat. 2007. PMID: 17357128

9

Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR).

Chan PA, Duraisamy S, Miller PJ, Newell JA, McBride C, Bond JP, Raevaara T, Ollila S, Nyström M, Grimm AJ, Christodoulou J, Oetting WS, Greenblatt MS. Chan PA, et al. Among authors: oetting ws. Hum Mutat. 2007 Jul;28(7):683-93. doi: 10.1002/humu.20492. Hum Mutat. 2007. PMID: 17370310

10

Large scale DNA sequencing: new challenges emerge--the 2007 Human Genome Variation Society scientific meeting.

Oetting WS. Oetting WS. Hum Mutat. 2008 May;29(5):765-8. doi: 10.1002/humu.20729. Hum Mutat. 2008. PMID: 18348287

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