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Ana M Valdes
Ana M Valdes
Verified email at nottingham.ac.uk - Homepage
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Cited by
Year
Mutational processes of simple-sequence repeat loci in human populations.
A Di Rienzo, AC Peterson, JC Garza, AM Valdes, M Slatkin, NB Freimer
Proceedings of the National Academy of Sciences 91 (8), 3166-3170, 1994
18741994
Obesity, cigarette smoking, and telomere length in women
AM Valdes, T Andrew, JP Gardner, M Kimura, E Oelsner, LF Cherkas, ...
The lancet 366 (9486), 662-664, 2005
15322005
Real-time tracking of self-reported symptoms to predict potential COVID-19
C Menni, AM Valdes, MB Freidin, CH Sudre, LH Nguyen, DA Drew, ...
Nature medicine 26 (7), 1037-1040, 2020
10782020
Role of the gut microbiota in nutrition and health
AM Valdes, J Walter, E Segal, TD Spector
Bmj 361, 2018
10082018
An atlas of genetic influences on human blood metabolites
SY Shin, EB Fauman, AK Petersen, J Krumsiek, R Santos, J Huang, ...
Nature genetics 46 (6), 543-550, 2014
8832014
Allele frequencies at microsatellite loci: the stepwise mutation model revisited.
AM Valdes, M Slatkin, NB Freimer
Genetics 133 (3), 737-749, 1993
8381993
Identification of seven loci affecting mean telomere length and their association with disease
V Codd, CP Nelson, E Albrecht, M Mangino, J Deelen, JL Buxton, ...
Nature genetics 45 (4), 422-427, 2013
8262013
HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: analysis of the type 1 diabetes genetics consortium families
H Erlich, AM Valdes, J Noble, JA Carlson, M Varney, P Concannon, ...
Diabetes 57 (4), 1084-1092, 2008
7822008
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study
JB Richards, F Rivadeneira, M Inouye, TM Pastinen, N Soranzo, ...
The Lancet 371 (9623), 1505-1512, 2008
7462008
Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior
TE Thorgeirsson, DF Gudbjartsson, I Surakka, JM Vink, N Amin, F Geller, ...
Nature genetics 42 (5), 448-453, 2010
7432010
Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains
VK Rakyan, TA Down, S Maslau, T Andrew, TP Yang, H Beyan, ...
Genome research 20 (4), 434-439, 2010
7202010
Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population
JT Bell, PC Tsai, TP Yang, R Pidsley, J Nisbet, D Glass, M Mangino, ...
PLoS genetics 8 (4), e1002629, 2012
6792012
The role of HLA class II genes in insulin-dependent diabetes mellitus: molecular analysis of 180 Caucasian, multiplex families.
JA Noble, AM Valdes, M Cook, W Klitz, G Thomson, HA Erlich
American journal of human genetics 59 (5), 1134, 1996
5471996
Vaccine side-effects and SARS-CoV-2 infection after vaccination in users of the COVID Symptom Study app in the UK: a prospective observational study
C Menni, K Klaser, A May, L Polidori, J Capdevila, P Louca, CH Sudre, ...
The Lancet Infectious Diseases 21 (7), 939-949, 2021
4732021
Genetics of the HLA region in the prediction of type 1 diabetes
JA Noble, AM Valdes
Current diabetes reports 11 (6), 533-542, 2011
3972011
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
arcOGEN Consortium, arcOGEN Collaborators
The Lancet 380 (9844), 815-823, 2012
3942012
The effects of social status on biological aging as measured by white‐blood‐cell telomere length
LF Cherkas, A Aviv, AM Valdes, JL Hunkin, JP Gardner, GL Surdulescu, ...
Aging cell 5 (5), 361-365, 2006
3912006
The fecal metabolome as a functional readout of the gut microbiome
J Zierer, MA Jackson, G Kastenmüller, M Mangino, T Long, A Telenti, ...
Nature genetics 50 (6), 790-795, 2018
3422018
Common variants near TERC are associated with mean telomere length
V Codd, M Mangino, P Van Der Harst, PS Braund, M Kaiser, AJ Beveridge, ...
Nature genetics 42 (3), 197-199, 2010
3352010
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ...
Nature communications 6 (1), 1-9, 2015
3332015
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