Takip et
Carlo Sidore
Carlo Sidore
Regeneron Genetics Center
irgb.cnr.it üzerinde doğrulanmış e-posta adresine sahip
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
163902015
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
89872010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
85942012
Next-generation genotype imputation service and methods
S Das, L Forer, S Schönherr, C Sidore, AE Locke, A Kwong, SI Vrieze, ...
Nature genetics 48 (10), 1284-1287, 2016
37542016
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
31882016
Discovery and refinement of loci associated with lipid levels
CJ Willer, EM Schmidt, S Sengupta, GM Peloso, S Gustafsson, S Kanoni, ...
Nature genetics 45 (11), 1274, 2013
3112*2013
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
13212011
Common variants associated with plasma triglycerides and risk for coronary artery disease
R Do, CJ Willer, EM Schmidt, S Sengupta, C Gao, GM Peloso, ...
Nature genetics 45 (11), 1345-1352, 2013
10732013
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
RA Scott, V Lagou, RP Welch, E Wheeler, ME Montasser, J Luan, R Mägi, ...
Nature genetics 44 (9), 991-1005, 2012
9162012
Diversity of human copy number variation and multicopy genes
PH Sudmant, JO Kitzman, F Antonacci, C Alkan, M Malig, A Tsalenko, ...
Science 330 (6004), 641-646, 2010
8262010
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
7382011
Variation in genome-wide mutation rates within and between human families
Nature genetics 43 (7), 712-714, 2011
7022011
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
6312021
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy
V Orrù, M Steri, C Sidore, M Marongiu, V Serra, S Olla, G Sole, S Lai, ...
Nature genetics 52 (10), 1036-1045, 2020
6222020
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits
BF Voight, HM Kang, J Ding, CD Palmer, C Sidore, PS Chines, NP Burtt, ...
Public Library of Science 8 (8), e1002793, 2012
6152012
Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
P Zanoni, SA Khetarpal, DB Larach, WF Hancock-Cerutti, JS Millar, ...
Science 351 (6278), 1166-1171, 2016
6002016
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
5552022
FTO genotype is associated with phenotypic variability of body mass index
J Yang, RJF Loos, JE Powell, SE Medland, EK Speliotes, DI Chasman, ...
Nature 490 (7419), 267-272, 2012
5222012
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 3934, 2014
4692014
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 1235587, 2013
4272013
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