Publications | Lund University Publications

61 – 70 of 109

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/publication?embed=1&q=keywords+exact+%22genome-wide+association+study%22&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

« previous
1
…
6
7
8
9
…
11
next »

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 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 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 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
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
2019
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 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 Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration
Wilman, Henry R. ; Atabaki Pasdar, Naeimeh ^LU ; Franks, Paul ^LU ; Giordano, Giuseppe ^LU ; Pomares-Millan, Hugo ^LU ; Fitipaldi, Hugo ^LU ; Mutie, Pascal ^LU ; Klintenberg, Maria ^LU and Yaghootkar, Hanieh (2019) In Journal of Hepatology 71(3). p.594-602
- 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
Mark GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways
López-Isac, Elena ; Hesselstrand, Roger ^LU and Martin, Javier (2019) In Nature Communications 10(1).
- Contribution to journal › Article

« previous
1
…
6
7
8
9
…
11
next »

your query:: Remove keywords: genome-wide association study