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Sarah Ennis
Sarah Ennis
在 soton.ac.uk 的电子邮件经过验证
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引用次数
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Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
G Thorleifsson, GB Walters, AW Hewitt, G Masson, A Helgason, A DeWan, ...
Nature genetics 42 (10), 906-909, 2010
4572010
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ...
Nature genetics 45 (2), 155-163, 2013
3562013
Vitrectomy outcomes in eyes with diabetic macular edema and vitreomacular traction
Diabetic Retinopathy Clinical Research Network
Ophthalmology 117 (6), 1087, 2010
3322010
Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis
C Gast, RJ Pengelly, M Lyon, DJ Bunyan, EG Seaby, N Graham, ...
Nephrology Dialysis Transplantation 31 (6), 961-970, 2016
2832016
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ...
Nature genetics 46 (10), 1126-1130, 2014
2562014
The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis
N Maniatis, A Collins, CF Xu, LC McCarthy, DR Hewett, W Tapper, ...
Proceedings of the National Academy of Sciences 99 (4), 2228-2233, 2002
2282002
Association between the SERPING1 gene and age-related macular degeneration: a two-stage case–control study
S Ennis, C Jomary, R Mullins, A Cree, X Chen, A MacLeod, S Jones, ...
The Lancet 372 (9652), 1828-1834, 2008
1932008
Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers
S Ennis, D Ward, A Murray
European Journal of Human Genetics 14 (2), 253-255, 2006
1922006
A systematic review of the applications of artificial intelligence and machine learning in autoimmune diseases
IS Stafford, M Kellermann, E Mossotto, RM Beattie, BD MacArthur, S Ennis
NPJ digital medicine 3 (1), 30, 2020
1902020
Evidence of association of APOE with age‐related macular degeneration ‐ a pooled analysis of 15 studies
GJ McKay, CC Patterson, U Chakravarthy, S Dasari, CC Klaver, ...
Human mutation 32 (12), 1407-1416, 2011
1672011
Reproductive and menstrual history of females with fragile X expansions
A Murray, S Ennis, F MacSwiney, J Webb, NE Morton
European Journal of Human Genetics 8 (4), 247-252, 2000
1542000
Classification of paediatric inflammatory bowel disease using machine learning
E Mossotto, JJ Ashton, T Coelho, RM Beattie, BD MacArthur, S Ennis
Scientific reports 7 (1), 2427, 2017
1522017
Clinical presentation of 6q24 transient neonatal diabetes mellitus (6q24 TNDM) and genotype–phenotype correlation in an international cohort of patients
LE Docherty, S Kabwama, A Lehmann, E Hawke, L Harrison, ...
Diabetologia 56, 758-762, 2013
1512013
The optimal measure of allelic association
NE Morton, W Zhang, P Taillon-Miller, S Ennis, PY Kwok, A Collins
Proceedings of the National Academy of Sciences 98 (9), 5217-5221, 2001
1462001
Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes
K Christodoulou, AE Wiskin, J Gibson, W Tapper, C Willis, NA Afzal, ...
Gut 62 (7), 977-984, 2013
1432013
Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited
JA Crolla, SA Youings, S Ennis, PA Jacobs
European Journal of Human Genetics 13 (2), 154-160, 2005
1332005
FRAXA and FRAXE: the results of a five year survey
SA Youings, A Murray, N Dennis, S Ennis, C Lewis, N McKechnie, ...
Journal of Medical Genetics 37 (6), 415-421, 2000
1312000
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
H Springelkamp, R Höhn, A Mishra, PG Hysi, CC Khor, SJ Loomis, ...
Nature communications 5 (1), 4883, 2014
1172014
Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people
GJ McKay, G Silvestri, U Chakravarthy, S Dasari, LG Fritsche, BH Weber, ...
American journal of epidemiology 173 (12), 1357-1364, 2011
1162011
Exome sequence read depth methods for identifying copy number changes
L Kadalayil, S Rafiq, MJJ Rose-Zerilli, RJ Pengelly, H Parker, D Oscier, ...
Briefings in bioinformatics 16 (3), 380-392, 2015
1102015
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