Brown MD - Search Results

1

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

Brown MD, Starikovskaya E, Derbeneva O, Hosseini S, Allen JC, Mikhailovskaya IE, Sukernik RI, Wallace DC. Brown MD, et al. Hum Genet. 2002 Feb;110(2):130-8. doi: 10.1007/s00439-001-0660-8. Epub 2002 Jan 24. Hum Genet. 2002. PMID: 11935318

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. Am J Hum Genet. 1992 Aug;51(2):378-85. Am J Hum Genet. 1992. PMID: 1322638 Free PMC article.

3

Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.

Brown MD, Sun F, Wallace DC. Brown MD, et al. Am J Hum Genet. 1997 Feb;60(2):381-7. Am J Hum Genet. 1997. PMID: 9012411 Free PMC article.

4

Y chromosome polymorphisms in native American and Siberian populations: identification of native American Y chromosome haplotypes.

Lell JT, Brown MD, Schurr TG, Sukernik RI, Starikovskaya YB, Torroni A, Moore LG, Troup GM, Wallace DC. Lell JT, et al. Among authors: brown md. Hum Genet. 1997 Oct;100(5-6):536-43. doi: 10.1007/s004390050548. Hum Genet. 1997. PMID: 9341867

5

mtDNA haplogroup X: An ancient link between Europe/Western Asia and North America?

Brown MD, Hosseini SH, Torroni A, Bandelt HJ, Allen JC, Schurr TG, Scozzari R, Cruciani F, Wallace DC. Brown MD, et al. Am J Hum Genet. 1998 Dec;63(6):1852-61. doi: 10.1086/302155. Am J Hum Genet. 1998. PMID: 9837837 Free PMC article.

6

Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation.

Brown MD, Trounce IA, Jun AS, Allen JC, Wallace DC. Brown MD, et al. J Biol Chem. 2000 Dec 22;275(51):39831-6. doi: 10.1074/jbc.M006476200. J Biol Chem. 2000. PMID: 10976107 Free article.

7

Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families.

Brown MD, Zhadanov S, Allen JC, Hosseini S, Newman NJ, Atamonov VV, Mikhailovskaya IE, Sukernik RI, Wallace DC. Brown MD, et al. Hum Genet. 2001 Jul;109(1):33-9. doi: 10.1007/s004390100538. Hum Genet. 2001. PMID: 11479733

8

Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.

Brown MD, Allen JC, Van Stavern GP, Newman NJ, Wallace DC. Brown MD, et al. Am J Med Genet. 2001 Dec 15;104(4):331-8. Am J Med Genet. 2001. PMID: 11754070

9

Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups.

Starikovskaya EB, Sukernik RI, Derbeneva OA, Volodko NV, Ruiz-Pesini E, Torroni A, Brown MD, Lott MT, Hosseini SH, Huoponen K, Wallace DC. Starikovskaya EB, et al. Among authors: brown md. Ann Hum Genet. 2005 Jan;69(Pt 1):67-89. doi: 10.1046/j.1529-8817.2003.00127.x. Ann Hum Genet. 2005. PMID: 15638829 Free PMC article.

10

Natural selection shaped regional mtDNA variation in humans.

Mishmar D, Ruiz-Pesini E, Golik P, Macaulay V, Clark AG, Hosseini S, Brandon M, Easley K, Chen E, Brown MD, Sukernik RI, Olckers A, Wallace DC. Mishmar D, et al. Among authors: brown md. Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):171-6. doi: 10.1073/pnas.0136972100. Epub 2002 Dec 30. Proc Natl Acad Sci U S A. 2003. PMID: 12509511 Free PMC article.

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