Wallace DC - Search Results

1

The dual origin and Siberian affinities of Native American Y chromosomes.

Lell JT, Sukernik RI, Starikovskaya YB, Su B, Jin L, Schurr TG, Underhill PA, Wallace DC. Lell JT, et al. Among authors: wallace dc. Am J Hum Genet. 2002 Jan;70(1):192-206. doi: 10.1086/338457. Epub 2001 Nov 30. Am J Hum Genet. 2002. PMID: 11731934 Free PMC article.

2

A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.

Brown MD, Yang CC, Trounce I, Torroni A, Lott MT, Wallace DC. Brown MD, et al. Among authors: wallace dc. Am J Hum Genet. 1992 Aug;51(2):378-85. Am J Hum Genet. 1992. PMID: 1322638 Free PMC article.

3

Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations.

Ballinger SW, Schurr TG, Torroni A, Gan YY, Hodge JA, Hassan K, Chen KH, Wallace DC. Ballinger SW, et al. Among authors: wallace dc. Genetics. 1992 Jan;130(1):139-52. doi: 10.1093/genetics/130.1.139. Genetics. 1992. PMID: 1346259 Free PMC article.

4

American Indian prehistory as written in the mitochondrial DNA: a review.

Wallace DC, Torroni A. Wallace DC, et al. Hum Biol. 1992 Jun;64(3):403-16. Hum Biol. 1992. PMID: 1351474

5

The structure of human mitochondrial DNA variation.

Merriwether DA, Clark AG, Ballinger SW, Schurr TG, Soodyall H, Jenkins T, Sherry ST, Wallace DC. Merriwether DA, et al. Among authors: wallace dc. J Mol Evol. 1991 Dec;33(6):543-55. doi: 10.1007/BF02102807. J Mol Evol. 1991. PMID: 1685753

6

Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages.

Schurr TG, Ballinger SW, Gan YY, Hodge JA, Merriwether DA, Lawrence DN, Knowler WC, Weiss KM, Wallace DC. Schurr TG, et al. Among authors: wallace dc. Am J Hum Genet. 1990 Mar;46(3):613-23. Am J Hum Genet. 1990. PMID: 1968708 Free PMC article.

7

Oxidative phosphorylation diseases. Disorders of two genomes.

Shoffner JM 4th, Wallace DC. Shoffner JM 4th, et al. Among authors: wallace dc. Adv Hum Genet. 1990;19:267-330. Adv Hum Genet. 1990. PMID: 2193491 Review. No abstract available.

8

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2nd, Nikoskelainen EK. Wallace DC, et al. Science. 1988 Dec 9;242(4884):1427-30. doi: 10.1126/science.3201231. Science. 1988. PMID: 3201231

9

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. Among authors: wallace dc. Am J Hum Genet. 1995 Jul;57(1):133-49. Am J Hum Genet. 1995. PMID: 7611282 Free PMC article.

10

African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba. Cuba Neuropathy Field Investigation Team.

Torroni A, Brown MD, Lott MT, Newman NJ, Wallace DC. Torroni A, et al. Among authors: wallace dc. Hum Mutat. 1995;5(4):310-7. doi: 10.1002/humu.1380050407. Hum Mutat. 1995. PMID: 7627185

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