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Sarah Pickett (nee Campbell)
Sarah Pickett (nee Campbell)
Mitochondrial Research Group, Newcastle University
Verified email at ncl.ac.uk
Title
Cited by
Cited by
Year
Detecting recent positive selection in the human genome from haplotype structure
PC Sabeti, DE Reich, JM Higgins, HZP Levine, DJ Richter, SF Schaffner, ...
Nature 419 (6909), 832-837, 2002
22702002
A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis
CC Khor, SJ Chapman, FO Vannberg, A Dunne, C Murphy, EY Ling, ...
Nature genetics 39 (4), 523-528, 2007
5592007
mt DNA heteroplasmy level and copy number indicate disease burden in m. 3243A> G mitochondrial disease
JP Grady, SJ Pickett, YS Ng, CL Alston, EL Blakely, SA Hardy, CL Feeney, ...
EMBO molecular medicine 10 (6), e8262, 2018
2212018
Vitamin D receptor polymorphisms and susceptibility to tuberculosis in West Africa: a case-control and family study
L Bornman, SJ Campbell, K Fielding, B Bah, J Sillah, P Gustafson, ...
Journal of Infectious Diseases 190 (9), 1631-1641, 2004
2062004
Association of a Polymorphism in the P2X7 Gene with Tuberculosis in a Gambian Population
CM Li, SJ Campbell, DS Kumararatne, R Bellamy, C Ruwende, ...
The Journal of infectious diseases 186 (10), 1458-1462, 2002
1922002
Polymorphism within the interferon-γ/receptor complex is associated with pulmonary tuberculosis
GS Cooke, SJ Campbell, J Sillah, P Gustafson, B Bah, G Sirugo, ...
American journal of respiratory and critical care medicine 174 (3), 339-343, 2006
1772006
Variants in the SP110 gene are associated with genetic susceptibility to tuberculosis in West Africa
K Tosh, SJ Campbell, K Fielding, J Sillah, B Bah, P Gustafson, K Manneh, ...
Proceedings of the National Academy of Sciences 103 (27), 10364-10368, 2006
1532006
A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study
BHF Family Heart Study Research Group
The American Journal of Human Genetics 77 (6), 1011-1020, 2005
1422005
Polymorphisms of the CYP2D6 gene increase susceptibility to ankylosing spondylitis
MA Brown, S Edwards, E Hoyle, S Campbell, S Laval, AK Daly, KD Pile, ...
Human molecular genetics 9 (11), 1563-1566, 2000
1312000
Phenotypic heterogeneity in m. 3243A> G mitochondrial disease: the role of nuclear factors
SJ Pickett, JP Grady, YS Ng, GS Gorman, AM Schaefer, IJ Wilson, ...
Annals of clinical and translational neurology 5 (3), 333-345, 2018
1152018
Mapping of a novel susceptibility locus suggests a role for MC3R and CTSZ in human tuberculosis
GS Cooke, SJ Campbell, S Bennett, C Lienhardt, KPWJ McAdam, ...
American journal of respiratory and critical care medicine 178 (2), 203-207, 2008
1152008
Resolving complexity in mitochondrial disease: Towards precision medicine
RM Boggan, A Lim, RW Taylor, R McFarland, SJ Pickett
Molecular genetics and metabolism 128 (1-2), 19-29, 2019
412019
Response heterogeneity of human macrophages to ATP is associated with P2X7 receptor expression but not to polymorphisms in the P2RX7 promoter1
CM Li, SJ Campbell, DS Kumararatne, AVS Hill, DA Lammas
FEBS letters 531 (2), 127-131, 2002
372002
Interleukin-8 polymorphism is not associated with pulmonary tuberculosis in the gambia
GS Cooke, SJ Campbell, K Fielding, J Sillah, K Manneh, G Sirugo, ...
The Journal of infectious diseases 189 (8), 1545-1546, 2004
322004
Mitochondrial donation—which women could benefit?
SJ Pickett, A Blain, YS Ng, IJ Wilson, RW Taylor, R McFarland, ...
New England Journal of Medicine 380 (20), 1971-1972, 2019
292019
The molecular pathology of pathogenic mitochondrial tRNA variants
U Richter, R McFarland, RW Taylor, SJ Pickett
FEBS letters 595 (8), 1003-1024, 2021
282021
Height as a clinical biomarker of disease burden in adult mitochondrial disease
RL Boal, YS Ng, SJ Pickett, AM Schaefer, C Feeney, A Bright, RW Taylor, ...
The Journal of Clinical Endocrinology & Metabolism 104 (6), 2057-2066, 2019
242019
Variants of the CD40 ligand gene are not associated with increased susceptibility to tuberculosis in West Africa
SJ Campbell, P Sabeti, K Fielding, J Sillah, B Bah, P Gustafson, ...
Immunogenetics 55, 502-507, 2003
232003
Mitochondrial DNA disorders: from pathogenic variants to preventing transmission
TM Bernardino Gomes, YS Ng, SJ Pickett, DM Turnbull, AE Vincent
Human Molecular Genetics 30 (R2), R245-R253, 2021
192021
Imaging mass cytometry reveals generalised deficiency in OXPHOS complexes in Parkinson’s disease
C Chen, D McDonald, A Blain, A Sachdeva, L Bone, ALM Smith, ...
npj Parkinson's Disease 7 (1), 39, 2021
172021
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