PubMed (OMIM) for id: 1648371

Year	Number of Results
1978	1
1980	1
1981	4
1982	2
1983	2
1984	1
1985	1
1986	4
1992	2
2001	1
2002	1
2003	1
2004	2
2005	1
2024	0

1

Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.

Pyle A, Foltynie T, Tiangyou W, Lambert C, Keers SM, Allcock LM, Davison J, Lewis SJ, Perry RH, Barker R, Burn DJ, Chinnery PF. Pyle A, et al. Ann Neurol. 2005 Apr;57(4):564-7. doi: 10.1002/ana.20417. Ann Neurol. 2005. PMID: 15786469

2

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency.

Kirby DM, Salemi R, Sugiana C, Ohtake A, Parry L, Bell KM, Kirk EP, Boneh A, Taylor RW, Dahl HH, Ryan MT, Thorburn DR. Kirby DM, et al. J Clin Invest. 2004 Sep;114(6):837-45. doi: 10.1172/JCI20683. J Clin Invest. 2004. PMID: 15372108 Free PMC article.

3

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency.

McFarland R, Kirby DM, Fowler KJ, Ohtake A, Ryan MT, Amor DJ, Fletcher JM, Dixon JW, Collins FA, Turnbull DM, Taylor RW, Thorburn DR. McFarland R, et al. Ann Neurol. 2004 Jan;55(1):58-64. doi: 10.1002/ana.10787. Ann Neurol. 2004. PMID: 14705112

4

Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.

van der Walt JM, Nicodemus KK, Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Mastaglia F, Stajich JM, McLaurin AC, Middleton LT, Scott BL, Schmechel DE, Pericak-Vance MA, Vance JM. van der Walt JM, et al. Am J Hum Genet. 2003 Apr;72(4):804-11. doi: 10.1086/373937. Epub 2003 Feb 28. Am J Hum Genet. 2003. PMID: 12618962 Free PMC article.

5

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups.

Herrnstadt C, Elson JL, Fahy E, Preston G, Turnbull DM, Anderson C, Ghosh SS, Olefsky JM, Beal MF, Davis RE, Howell N. Herrnstadt C, et al. Am J Hum Genet. 2002 May;70(5):1152-71. doi: 10.1086/339933. Epub 2002 Apr 5. Am J Hum Genet. 2002. PMID: 11938495 Free PMC article.

6

Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene.

Taylor RW, Singh-Kler R, Hayes CM, Smith PE, Turnbull DM. Taylor RW, et al. Ann Neurol. 2001 Jul;50(1):104-7. doi: 10.1002/ana.1084. Ann Neurol. 2001. PMID: 11456298

7

tRNA punctuation model of RNA processing in human mitochondria.

Ojala D, Montoya J, Attardi G. Ojala D, et al. Nature. 1981 Apr 9;290(5806):470-4. doi: 10.1038/290470a0. Nature. 1981. PMID: 7219536

8

Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs.

Montoya J, Ojala D, Attardi G. Montoya J, et al. Nature. 1981 Apr 9;290(5806):465-70. doi: 10.1038/290465a0. Nature. 1981. PMID: 7219535

9

Sequence and organization of the human mitochondrial genome.

Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG. Anderson S, et al. Nature. 1981 Apr 9;290(5806):457-65. doi: 10.1038/290457a0. Nature. 1981. PMID: 7219534

10

Identification and mapping of human mitochondrial genes.

Attardi G, Chomyn A, Montoya J, Ojala D. Attardi G, et al. Cytogenet Cell Genet. 1982;32(1-4):85-98. doi: 10.1159/000131689. Cytogenet Cell Genet. 1982. PMID: 7140372 No abstract available.

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