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2021
Mark Systems biology analysis of human genomes points to key pathways conferring spina bifida risk
Aguiar-Pulido, Vanessa ; Wolujewicz, Paul ; Martinez-Fundichely, Alexander ; Elhaik, Eran ^LU ; Thareja, Gaurav ; Abdel Aleem, Alice ; Chalhoub, Nader ; Cuykendall, Tawny ; Al-Zamer, Jamel and Lei, Yunping , et al. (2021) In Proceedings of the National Academy of Sciences of the United States of America 118(51).
- Contribution to journal › Article
2020
Mark A new efficient method to detect genetic interactions for lung cancer GWAS
Luyapan, Jennifer ; Ji, Xuemei ; Li, Siting ; Xiao, Xiangjun ; Zhu, Dakai ; Duell, Eric J. ; Christiani, David C. ; Schabath, Matthew B. ; Arnold, Susanne M. and Zienolddiny, Shanbeh , et al. (2020) In BMC Medical Genomics 13(1).
- Contribution to journal › Article
Mark Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus
van Zuydam, Natalie R. ; Groop, Leif ^LU and Palmer, Colin N. A. (2020) In Circulation: Genomic and Precision Medicine p.640-648
- Contribution to journal › Article
Mark Genome-wide association meta-analysis of single-nucleotide polymorphisms and symptomatic venous thromboembolism during therapy for acute lymphoblastic leukemia and lymphoma in caucasian children
Mateos, Marion K. ; Tulstrup, Morten ; Quinn, Michael C.J. ; Tuckuviene, Ruta ; Marshall, Glenn M. ; Gupta, Ramneek ; Mayoh, Chelsea ; Wolthers, Benjamin O. ; Barbaro, Pasquale M. and Ruud, Ellen , et al. (2020) In Cancers 12(5).
- Contribution to journal › Article
Mark Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
Lahrouchi, Najim ; Platonov, Pyotr ^LU and Bezzina, Connie R. (2020) In Circulation 142(4). p.324-338
- Contribution to journal › Article
Mark Genetic risk factors for venous thromboembolism
Zöller, Bengt ^LU ; Svensson, Peter J. ^LU ; Dahlbäck, Björn ^LU ; Lind-Hallden, Christina ^LU ; Hallden, Christer ^LU and Elf, Johan ^LU (2020) In Expert Review of Hematology 13(9). p.971-981
- Contribution to journal › Scientific review
Mark Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
Rheinbay, Esther ; Nielsen, Morten Muhlig ; Abascal, Federico ; Wala, Jeremiah A ; Shapira, Ofer ; Tiao, Grace ; Hornshøj, Henrik ; Hess, Julian M ; Juul, Randi Istrup and Lin, Ziao , et al. (2020) In Nature 578(7793). p.102-111
- Contribution to journal › Article
2019
Mark PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome
Mola-Caminal, Marina ; Lindgren, Arne ^LU ; Fernandez-Cadenas, Israel and Jimenez-Conde, Jordi (2019) In Circulation Research 124(1). p.114-120
- Contribution to journal › Article
Mark A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes : results from an exome-wide association study of albuminuria
Ahluwalia, Tarunveer S. ; Schulz, Christina Alexandra ^LU ; Waage, Johannes ; Skaaby, Tea ; Sandholm, Niina ; van Zuydam, Natalie ; Charmet, Romain ; Bork-Jensen, Jette ; Almgren, Peter ^LU and Thuesen, Betina H. , et al. (2019) In Diabetologia 62(2). p.292-305
- Contribution to journal › Article
Mark Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
Aragam, Krishna G. ; Chaffin, Mark ; Levinson, Rebecca T. ; McDermott, Gregory ; Choi, Seung Hoan ; Shoemaker, M. Benjamin ; Haas, Mary E. ; Weng, Lu Chen ; Lindsay, Mark E. and Smith, J. Gustav ^LU , et al. (2019) In Circulation 139(4). p.489-501
- Contribution to journal › Article

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