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Common variants in breast cancer risk loci predispose to distinct tumor subtypes

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DOI
10.1186/s13058-021-01484-x
Ahearn, Thomas U.; Zhang, Haoyu; Michailidou, Kyriaki; Milne, Roger L.; Bolla, Manjeet K.; Dennis, J...
Breast cancer research2022Publicationer information ikon

Common genetic variants influence human subcortical brain structures

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DOI
10.1038/nature14101
Hibar Derrek P, Stein Jason L, Renteria Miguel E, Arias-Vasquez Alejandro, Desrivières Sylvane, Jaha...
NATURE (LONDON)2015Publicationer information ikon

Common genetic variants influence human subcortical brain structures.

Hibar DP; ...; Boks MP; Bralten J; ...; Chen Q; Ching CR; Cuellar-Partida G; den Braber A; Giddaluru...
Nature (london)2015Publicationer information ikon

Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants

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10.1164/rccm.202207-1331OC
NHLBI Trans-Omics Precision Med; Peljto, Anna L.; Blumhagen, Rachel Z.; Walts, Avram D.; Cardwell, J...
American journal of respiratory and critical care medicine2023Publicationer information ikon

FUT2 Variants Confer Susceptibility to Familial Otitis Media

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10.1016/j.ajhg.2018.09.010
UWCMG; Santos-Cortez, Regie Lyn P.; Chiong, Charlotte M.; Frank, Daniel N.; Ryan, Allen F.; Giese, A...
American journal of human genetics2018Publicationer information ikon

Identification of common genetic risk variants for autism spectrum disorder

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10.1038/s41588-019-0344-8
Psychiat Genomics Consortium; BUPGEN; 23andMe Res Team; Grove, Jakob; Ripke, Stephan; Als, Thomas D....
Nature Genetics2019Publicationer information ikon

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

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DOI
10.1093/hmg/ddr325
Steinberg, S.; Pietiläinen, Olli; Palotie, Leena; Stefansson, Kari; ,
Human molecular genetics2011Publicationer information ikon

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

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DOI
10.1038/ng.980
Shi, Yongyong; Li, Zhiqiang; Xu, Qi; Wang, Ti; Li, Tao; Shen, Jiawei; Zhang, Fengyu; Chen, Jianhua; ...
Nature genetics2011Publicationer information ikon

Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

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10.1016/j.biopsych.2018.11.024
CHD Exome Consortium; Consortium Genetics Smoking; EPIC-CVD Consortium; Understanding Soc Sci Grp; B...
Biological psychiatry2019Publicationer information ikon

The impact of common and rare genetic variants on bradyarrhythmia development

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10.1038/s41588-024-01978-2
FinnGen; Million Veteran Program; Regeneron Genetics Center; Weng, Lu-Chen; Rämö, Joel T.; Jurgens, ...
Nature Genetics2025

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Referentgranskad
Öppen tillgång
DOI
10.1186/s13058-021-01484-x
2022

Common genetic variants influence human subcortical brain structures

Referentgranskad
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DOI
10.1038/nature14101
2015

Common genetic variants influence human subcortical brain structures.

2015

Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants

Referentgranskad
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DOI
10.1164/rccm.202207-1331OC
2023

FUT2 Variants Confer Susceptibility to Familial Otitis Media

Referentgranskad
Öppen tillgång
DOI
10.1016/j.ajhg.2018.09.010
2018

Identification of common genetic risk variants for autism spectrum disorder

Referentgranskad
Öppen tillgång
DOI
10.1038/s41588-019-0344-8
2019

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

Referentgranskad
DOI
10.1093/hmg/ddr325
2011

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

Referentgranskad
DOI
10.1038/ng.980
2011

Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

Referentgranskad
Öppen tillgång
DOI
10.1016/j.biopsych.2018.11.024
2019

The impact of common and rare genetic variants on bradyarrhythmia development

Referentgranskad
Öppen tillgång
DOI
10.1038/s41588-024-01978-2
2025