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2023
Mark A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
Middha, Pooja ; Wang, Xiaoliang ; Behrens, Sabine ; Bolla, Manjeet K ; Wang, Qin ; Dennis, Joe ; Michailidou, Kyriaki ; Ahearn, Thomas U ; Andrulis, Irene L and Anton-Culver, Hoda , et al. (2023) In Breast cancer research : BCR 25(1). p.1-13
- Contribution to journal › Article
2021
Mark Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment
Morra, Anna ; Escala-Garcia, Maria ; Beesley, Jonathan ; Keeman, Renske ; Canisius, Sander ; Ahearn, Thomas U. ; Andrulis, Irene L. ; Anton-Culver, Hoda ; Arndt, Volker and Auer, Paul L. , et al. (2021) In Breast cancer research : BCR 23(1). p.86-86
- Contribution to journal › Article
Mark Combined associations of a polygenic risk score and classical risk factors with breast cancer risk
Kapoor, Pooja Middha ; Mavaddat, Nasim ; Choudhury, Parichoy Pal ; Wilcox, Amber N ; Lindström, Sara ^LU ; Behrens, Sabine ; Michailidou, Kyriaki ; Dennis, Joe ; Bolla, Manjeet K and Wang, Qin , et al. (2021) In Journal of the National Cancer Institute 113(3). p.329-337
- Contribution to journal › Article
2020
Mark Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Zhang, Haoyu ; Ahearn, Thomas U ; Lecarpentier, Julie ; Barnes, Daniel ; Beesley, Jonathan ; Qi, Guanghao ; Jiang, Xia ; O'Mara, Tracy A ; Zhao, Ni and Bolla, Manjeet K , et al. (2020) In Nature Genetics 52(6). p.572-581
- Contribution to journal › Letter
2018
Mark A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
Wu, Lang ; Shi, Wei ; Long, Jirong ; Guo, Xingyi ; Michailidou, Kyriaki ; Beesley, Jonathan ; Bolla, Manjeet K. ; Shu, Xiao Ou ; Lu, Yingchang and Cai, Qiuyin , et al. (2018) In Nature Genetics 50(7). p.968-978
- Contribution to journal › Article
2017
Mark Rare and low-frequency coding variants alter human adult height
Marouli, Eirini ; Graff, Mariaelisa ; Medina-Gomez, Carolina ; Lo, Ken Sin ; Wood, Andrew R ; Kjaer, Troels R. ; Fine, Rebecca S. ; Lu, Yingchang ; Schurmann, Claudia and Highland, Heather M , et al. (2017) In Nature 542(7640). p.186-190
- Contribution to journal › Article
Mark Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Webb, Thomas R. ; Erdmann, Jeanette ; Stirrups, Kathleen E. ; Stitziel, Nathan O. ; Masca, Nicholas G D ; Jansen, Henning ; Kanoni, Stavroula ; Nelson, Christopher P ; Ferrario, Paola G. and König, Inke R. , et al. (2017) In Journal of the American College of Cardiology 69(7). p.823-836
- Contribution to journal › Article
2016
Mark Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits
Chami, Nathalie ; Chen, Ming Huei ; Slater, Andrew J. ; Eicher, John D. ; Evangelou, Evangelos ; Tajuddin, Salman M. ; Love-Gregory, Latisha ; Kacprowski, Tim ; Schick, Ursula M. and Nomura, Akihiro , et al. (2016) In American Journal of Human Genetics 99(1). p.8-21
- Contribution to journal › Article
Mark Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease
Stitziel, Nathan O. ; Stirrups, Kathleen E. ; Masca, Nicholas G D ; Erdmann, Jeanette ; Ferrario, Paola G. ; König, Inke R. ; Weeke, Peter E. ; Webb, Thomas R. ; Auer, Paul L. and Schick, Ursula M. , et al. (2016) In New England Journal of Medicine 374(12). p.1134-1144
- Contribution to journal › Article
2015
Mark Association of exome sequences with plasma C-reactive protein levels in >9000 participants.
Schick, Ursula M ; Auer, Paul L ; Bis, Joshua C ; Lin, Honghuang ; Wei, Peng ; Pankratz, Nathan ; Lange, Leslie A ; Brody, Jennifer ; Stitziel, Nathan O and Kim, Daniel S , et al. (2015) In Human Molecular Genetics 24(2). p.559-571
- Contribution to journal › Article

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