Howell N - Search Results

1

The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree rates.

Howell N, Smejkal CB, Mackey DA, Chinnery PF, Turnbull DM, Herrnstadt C. Howell N, et al. Am J Hum Genet. 2003 Mar;72(3):659-70. doi: 10.1086/368264. Epub 2003 Feb 4. Am J Hum Genet. 2003. PMID: 12571803 Free PMC article.

2

A high frequency of mtDNA polymorphisms in HeLa cell sublines.

Herrnstadt C, Preston G, Andrews R, Chinnery P, Lightowlers RN, Turnbull DM, Kubacka I, Howell N. Herrnstadt C, et al. Among authors: howell n. Mutat Res. 2002 Apr 25;501(1-2):19-28. doi: 10.1016/s0027-5107(01)00304-9. Mutat Res. 2002. PMID: 11934434

3

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. Among authors: howell n. 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.

4

Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutations.

Howell N, Miller NR, Mackey DA, Arnold A, Herrnstadt C, Williams IM, Kubacka I. Howell N, et al. J Neuroophthalmol. 2002 Dec;22(4):262-9. doi: 10.1097/00041327-200212000-00002. J Neuroophthalmol. 2002. PMID: 12464729

5

Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.

Howell N, Oostra RJ, Bolhuis PA, Spruijt L, Clarke LA, Mackey DA, Preston G, Herrnstadt C. Howell N, et al. Am J Hum Genet. 2003 Jun;72(6):1460-9. doi: 10.1086/375537. Epub 2003 May 6. Am J Hum Genet. 2003. PMID: 12736867 Free PMC article.

6

Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background.

Howell N, Herrnstadt C, Shults C, Mackey DA. Howell N, et al. Am J Med Genet A. 2003 Jun 1;119A(2):147-51. doi: 10.1002/ajmg.a.20135. Am J Med Genet A. 2003. PMID: 12749053

7

Comparative genomics and the evolution of human mitochondrial DNA: assessing the effects of selection.

Elson JL, Turnbull DM, Howell N. Elson JL, et al. Among authors: howell n. Am J Hum Genet. 2004 Feb;74(2):229-38. doi: 10.1086/381505. Epub 2004 Jan 7. Am J Hum Genet. 2004. PMID: 14712420 Free PMC article.

8

African Haplogroup L mtDNA sequences show violations of clock-like evolution.

Howell N, Elson JL, Turnbull DM, Herrnstadt C. Howell N, et al. Mol Biol Evol. 2004 Oct;21(10):1843-54. doi: 10.1093/molbev/msh184. Epub 2004 Jun 9. Mol Biol Evol. 2004. PMID: 15190127

9

Co-segregation and heteroplasmy of two coding-region mtDNA mutations within a matrilineal pedigree.

Howell N, Kubacka I, Keers SM, Turnbull DM, Chinnery PF. Howell N, et al. Hum Genet. 2005 Jan;116(1-2):28-32. doi: 10.1007/s00439-004-1203-x. Epub 2004 Nov 3. Hum Genet. 2005. PMID: 15599765

10

mtDNA mutations and common neurodegenerative disorders.

Howell N, Elson JL, Chinnery PF, Turnbull DM. Howell N, et al. Trends Genet. 2005 Nov;21(11):583-6. doi: 10.1016/j.tig.2005.08.012. Epub 2005 Sep 8. Trends Genet. 2005. PMID: 16154228 Review.

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