关注
Carlo Sidore
Carlo Sidore
Regeneron Genetics Center
在 irgb.cnr.it 的电子邮件经过验证
标题
引用次数
引用次数
年份
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
153402015
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
88262010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
83382012
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
34412016
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
3002*2013
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
29922016
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
12962011
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
10412013
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
8992012
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
8012010
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
7212011
Variation in genome-wide mutation rates within and between human families
Nature genetics 43 (7), 712-714, 2011
6922011
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
6112012
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
5712016
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
5112012
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
4982021
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
4542014
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
4232013
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
4042022
Overexpression of the cytokine BAFF and autoimmunity risk
M Steri, V Orrù, ML Idda, M Pitzalis, M Pala, I Zara, C Sidore, V Faà, ...
New England Journal of Medicine 376 (17), 1615-1626, 2017
3842017
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