Các bài viết có thể truy cập công khai - Mari NelisTìm hiểu thêm
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Đánh giá
Endometriosis and irritable bowel syndrome: similarities and differences in the spectrum of comorbidities
M Peters, I Mikeltadze, H Karro, M Saare, ...
Human Reproduction 37 (9), 2186-2196, 2022
Các cơ quan ủy nhiệm: European Commission
Có tại một số nơi: 60
Đánh giá
Heart disease and stroke statistics—2017 update: a report from the American Heart Association
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
circulation 135 (10), e146-e603, 2017
Các cơ quan ủy nhiệm: US National Institutes of Health, American Heart Association
Đánh giá
Biological insights from 108 schizophrenia-associated genetic loci
C Pantelis, GN Papadimitriou, S Papiol, E Parkhomenko, MT Pato, ...
Nature 511 (7510), 421-427, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
Đánh giá
Genetic studies of body mass index yield new insights for obesity biology
AE Locke, B Kahali, SI Berndt, AE Justice, TH Pers, FR Day, C Powell, ...
Nature 518 (7538), 197-206, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, British Heart Foundation, Cancer Research …
Đánh giá
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
EK Speliotes, CJ Willer, SI Berndt, KL Monda, G Thorleifsson, AU Jackson, ...
Nature genetics 42 (11), 937-948, 2010
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, German …
Đánh giá
Hundreds of variants clustered in genomic loci and biological pathways affect human height
H Lango Allen, K Estrada, G Lettre, SI Berndt, MN Weedon, F Rivadeneira, ...
Nature 467 (7317), 832-838, 2010
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, German …
Đánh giá
Defining the role of common variation in the genomic and biological architecture of adult human height
AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ...
Nature genetics 46 (11), 1173-1186, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, British Heart Foundation, UK Medical …
Đánh giá
FinnGen provides genetic insights from a well-phenotyped isolated population
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ...
Nature 613 (7944), 508-518, 2023
Các cơ quan ủy nhiệm: Business Finland
Đánh giá
Systematic identification of trans eQTLs as putative drivers of known disease associations
HJ Westra, MJ Peters, T Esko, H Yaghootkar, C Schurmann, J Kettunen, ...
Nature genetics 45 (10), 1238-1243, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health, German Research Foundation, UK Medical …
Đánh giá
New genetic loci link adipose and insulin biology to body fat distribution
D Shungin, TW Winkler, DC Croteau-Chonka, T Ferreira, AE Locke, ...
Nature 518 (7538), 187-196, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, British Heart Foundation, Cancer Research …
Đánh giá
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
Các cơ quan ủy nhiệm: US National Institutes of Health, Danish Council for Independent Research …
Đánh giá
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
IM Heid, AU Jackson, JC Randall, TW Winkler, L Qi, V Steinthorsdottir, ...
Nature genetics 42 (11), 949-960, 2010
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, German …
Đánh giá
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
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
Các cơ quan ủy nhiệm: US National Institutes of Health, National Health and Medical Research …
Đánh giá
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases
A Gusev, SH Lee, G Trynka, H Finucane, BJ Vilhjálmsson, H Xu, C Zang, ...
The American Journal of Human Genetics 95 (5), 535-552, 2014
Các cơ quan ủy nhiệm: US National Institutes of Health, Australian Research Council, National …
Đánh giá
A new highly penetrant form of obesity due to deletions on chromosome 16p11. 2
RG Walters, S Jacquemont, A Valsesia, AJ De Smith, D Martinet, ...
Nature 463 (7281), 671-675, 2010
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health, Genome …
Đánh giá
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
CE Elks, JRB Perry, P Sulem, DI Chasman, N Franceschini, C He, ...
Nature genetics 42 (12), 1077-1085, 2010
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health …
Đánh giá
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma
MT Landi, N Chatterjee, K Yu, LR Goldin, AM Goldstein, M Rotunno, ...
The american journal of human genetics 85 (5), 679-691, 2009
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
Common variants in KCNN3 are associated with lone atrial fibrillation
PT Ellinor, KL Lunetta, NL Glazer, A Pfeufer, A Alonso, MK Chung, ...
Nature genetics 42 (3), 240-244, 2010
Các cơ quan ủy nhiệm: US National Institutes of Health
Đánh giá
The trans-ancestral genomic architecture of glycemic traits
J Chen, CN Spracklen, G Marenne, A Varshney, LJ Corbin, J Luan, ...
Nature genetics 53 (6), 840-860, 2021
Các cơ quan ủy nhiệm: US National Institutes of Health, Canadian Institutes of Health Research …
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