Joanna Elson
Joanna Elson
Verified email at ncl.ac.uk - Homepage
Title
Cited by
Cited by
Year
Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups
C Herrnstadt, JL Elson, E Fahy, G Preston, DM Turnbull, C Anderson, ...
The American Journal of Human Genetics 70 (5), 1152-1171, 2002
6162002
Strong purifying selection in transmission of mammalian mitochondrial DNA
JB Stewart, C Freyer, JL Elson, A Wredenberg, Z Cansu, A Trifunovic, ...
PLoS biology 6 (1), e10, 2008
4132008
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA–haplogroup background
G Hudson, V Carelli, L Spruijt, M Gerards, C Mowbray, A Achilli, A Pyle, ...
The American Journal of Human Genetics 81 (2), 228-233, 2007
3262007
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age
JL Elson, DC Samuels, DM Turnbull, PF Chinnery
The American Journal of Human Genetics 68 (3), 802-806, 2001
3062001
Accumulation of mitochondrial DNA mutations in ageing, cancer, and mitochondrial disease: is there a common mechanism?
PF Chinnery, DC Samuels, J Elson, DM Turnbull
The Lancet 360 (9342), 1323-1325, 2002
2552002
Comparative genomics and the evolution of human mitochondrial DNA: assessing the effects of selection
JL Elson, DM Turnbull, N Howell
The American Journal of Human Genetics 74 (2), 229-238, 2004
2192004
Assigning pathogenicity to mitochondrial tRNA mutations: when ‘definitely maybe’is not good enough
R McFarland, JL Elson, RW Taylor, N Howell, DM Turnbull
TRENDS in Genetics 20 (12), 591-596, 2004
1772004
Mitochondrial DNA and survival after sepsis: a prospective study
SV Baudouin, D Saunders, W Tiangyou, JL Elson, J Poynter, A Pyle, ...
The Lancet 366 (9503), 2118-2121, 2005
1742005
Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease
JB Stewart, C Freyer, JL Elson, NG Larsson
Nature Reviews Genetics 9 (9), 657-662, 2008
1582008
A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations
JW Yarham, M Al‐Dosary, EL Blakely, CL Alston, RW Taylor, JL Elson, ...
Human mutation 32 (11), 1319-1325, 2011
1492011
Analysis of European mtDNAs for recombination
JL Elson, RM Andrews, PF Chinnery, RN Lightowlers, DM Turnbull, ...
The American Journal of Human Genetics 68 (1), 145-153, 2001
1412001
Mitochondrial tRNA mutations and disease
JW Yarham, JL Elson, EL Blakely, R McFarland, RW Taylor
Wiley Interdisciplinary Reviews: RNA 1 (2), 304-324, 2010
1342010
Nature of mitochondrial DNA deletions in substantia nigra neurons
AK Reeve, KJ Krishnan, JL Elson, CM Morris, A Bender, RN Lightowlers, ...
The American Journal of Human Genetics 82 (1), 228-235, 2008
1312008
Mitochondrial disease in adults: a scale to monitor progression and treatment
AM Schaefer, C Phoenix, JL Elson, R McFarland, PF Chinnery, ...
Neurology 66 (12), 1932-1934, 2006
1202006
Sequence variation in mitochondrial complex I genes: mutation or polymorphism?
AL Mitchell, JL Elson, N Howell, RW Taylor, DM Turnbull
Journal of medical genetics 43 (2), 175-179, 2006
1202006
Does the mitochondrial genome play a role in the etiology of Alzheimer’s disease?
JL Elson, C Herrnstadt, G Preston, L Thal, CM Morris, JA Edwardson, ...
Human genetics 119 (3), 241-254, 2006
1182006
mtDNA mutations and common neurodegenerative disorders
N Howell, JL Elson, PF Chinnery, DM Turnbull
Trends in Genetics 21 (11), 583-586, 2005
992005
Urine heteroplasmy is the best predictor of clinical outcome in the m. 3243A> G mtDNA mutation
RG Whittaker, JK Blackwood, CL Alston, EL Blakely, JL Elson, ...
Neurology 72 (6), 568-569, 2009
932009
Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing
LC Greaves, M Nooteboom, JL Elson, HAL Tuppen, GA Taylor, ...
PLoS Genet 10 (9), e1004620, 2014
822014
Mitochondrial DNA disease: new options for prevention
L Craven, JL Elson, L Irving, HA Tuppen, LM Lister, GD Greggains, ...
Human molecular genetics 20 (R2), R168-R174, 2011
682011
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