Chen YS - Search Results

1

mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations.

Chen YS, Olckers A, Schurr TG, Kogelnik AM, Huoponen K, Wallace DC. Chen YS, et al. Am J Hum Genet. 2000 Apr;66(4):1362-83. doi: 10.1086/302848. Epub 2000 Mar 28. Am J Hum Genet. 2000. PMID: 10739760 Free PMC article.

2

Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups.

Chen YS, Torroni A, Excoffier L, Santachiara-Benerecetti AS, Wallace DC. Chen YS, et al. Am J Hum Genet. 1995 Jul;57(1):133-49. Am J Hum Genet. 1995. PMID: 7611282 Free PMC article.

3

mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.

Torroni A, Lott MT, Cabell MF, Chen YS, Lavergne L, Wallace DC. Torroni A, et al. Among authors: chen ys. Am J Hum Genet. 1994 Oct;55(4):760-76. Am J Hum Genet. 1994. PMID: 7942855 Free PMC article. Clinical Trial.

4

mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico.

Torroni A, Chen YS, Semino O, Santachiara-Beneceretti AS, Scott CR, Lott MT, Winter M, Wallace DC. Torroni A, et al. Among authors: chen ys. Am J Hum Genet. 1994 Feb;54(2):303-18. Am J Hum Genet. 1994. PMID: 8304347 Free PMC article.

5

Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.

Brown MD, Torroni A, Huoponen K, Chen YS, Lott MT, Wallace DC. Brown MD, et al. Among authors: chen ys. Am J Hum Genet. 1994 Aug;55(2):410-2. Am J Hum Genet. 1994. PMID: 8037217 Free PMC article. No abstract available.

6

Expression and sequence analysis of the mouse adenine nucleotide translocase 1 and 2 genes.

Levy SE, Chen YS, Graham BH, Wallace DC. Levy SE, et al. Among authors: chen ys. Gene. 2000 Aug 22;254(1-2):57-66. doi: 10.1016/s0378-1119(00)00252-3. Gene. 2000. PMID: 10974536

7

Mitochondrial DNA sequence diversity in bipolar affective disorder.

McMahon FJ, Chen YS, Patel S, Kokoszka J, Brown MD, Torroni A, DePaulo JR, Wallace DC. McMahon FJ, et al. Among authors: chen ys. Am J Psychiatry. 2000 Jul;157(7):1058-64. doi: 10.1176/appi.ajp.157.7.1058. Am J Psychiatry. 2000. PMID: 10873911

8

Defining haplotype blocks and tag single-nucleotide polymorphisms in the human genome.

Schulze TG, Zhang K, Chen YS, Akula N, Sun F, McMahon FJ. Schulze TG, et al. Among authors: chen ys. Hum Mol Genet. 2004 Feb 1;13(3):335-42. doi: 10.1093/hmg/ddh035. Epub 2003 Dec 17. Hum Mol Genet. 2004. PMID: 14681300

9

Can long-range microsatellite data be used to predict short-range linkage disequilibrium?

Schulze TG, Chen YS, Akula N, Hennessy K, Badner JA, McInnis MG, DePaulo JR, Schumacher J, Cichon S, Propping P, Maier W, Rietschel M, Nöthen MM, McMahon FJ. Schulze TG, et al. Among authors: chen ys. Hum Mol Genet. 2002 Jun 1;11(12):1363-72. doi: 10.1093/hmg/11.12.1363. Hum Mol Genet. 2002. PMID: 12023978

10

Neither single-marker nor haplotype analyses support an association between genetic variation near NOTCH4 and bipolar disorder.

Prathikanti S, Schulze TG, Chen YS, Harr B, Akula N, Hennessy K, Potluri S, Lyons J, Nguyen T, McMahon FJ. Prathikanti S, et al. Among authors: chen ys. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):10-5. doi: 10.1002/ajmg.b.20123. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15384085

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