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2014
Mark Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Arking, Dan E ; Pulit, Sara L ; Crotti, Lia ; van der Harst, Pim ; Munroe, Patricia B ; Koopmann, Tamara T ; Sotoodehnia, Nona ; Rossin, Elizabeth J ; Morley, Michael and Wang, Xinchen , et al. (2014) In Nature Genetics 46(8). p.826-836
- Contribution to journal › Article
Mark Meta-analysis of gene-level tests for rare variant association.
Liu, Dajiang J ; Peloso, Gina M ; Zhan, Xiaowei ; Holmen, Oddgeir L ; Zawistowski, Matthew ; Feng, Shuang ; Nikpay, Majid ; Auer, Paul L ; Goel, Anuj and Zhang, He , et al. (2014) In Nature Genetics 46(2). p.200-200
- Contribution to journal › Article
Mark Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
Flannick, Jason ; Thorleifsson, Gudmar ; Beer, Nicola L ; Jacobs, Suzanne B R ; Grarup, Niels ; Burtt, Noël P ; Mahajan, Anubha ; Fuchsberger, Christian ; Atzmon, Gil and Benediktsson, Rafn , et al. (2014) In Nature Genetics 46(4). p.357-357
- Contribution to journal › Article
Mark Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
Thompson, Bryony A ; Spurdle, Amanda B ; Plazzer, John-Paul ; Greenblatt, Marc S ; Akagi, Kiwamu ; Al-Mulla, Fahd ; Bapat, Bharati ; Bernstein, Inge ; Capellá, Gabriel and den Dunnen, Johan T , et al. (2014) In Nature Genetics 46. p.107-115
- Contribution to journal › Article
Mark Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Mahajan, Anubha ; Go, Min Jin ; Zhang, Weihua ; Below, Jennifer E. ; Gaulton, Kyle J. ; Ferreira, Teresa ; Horikoshi, Momoko ; Johnson, Andrew D. ; Ng, Maggie C. Y. and Prokopenko, Inga , et al. (2014) In Nature Genetics 46(3). p.234-234
- Contribution to journal › Article
2013
Mark Homozygosity for a null allele of SMIM1 defines the Vel-negative blood group phenotype.
Storry, Jill ^LU ; Jöud, Magnus ^LU ; Christophersen, Mikael Kronborg ^LU ; Thuresson, Britt ^LU ; Åkerström, Bo ^LU ; Sojka, Birgitta Nilsson ; Nilsson, Björn ^LU and Olsson, Martin L ^LU (2013) In Nature Genetics 45(5). p.109-537
- Contribution to journal › Article
Mark Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk
Chubb, Daniel ; Weinhold, Niels ; Broderick, Peter ; Chen, Bowang ^LU ; Johnson, David C. ; Försti, Asta ^LU ; Vijayakrishnan, Jayaram ; Migliorini, Gabriele ; Dobbins, Sara E. and Holroyd, Amy , et al. (2013) In Nature Genetics 45(10). p.366-1221
- Contribution to journal › Article
Mark The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma
Weinhold, Niels ; Johnson, David C. ; Chubb, Daniel ; Chen, Bowang ^LU ; Försti, Asta ^LU ; Hosking, Fay J. ; Broderick, Peter ; Ma, Yussanne P. ; Dobbins, Sara E. and Hose, Dirk , et al. (2013) In Nature Genetics 45(5). p.522-525
- Contribution to journal › Article
Mark A functional variant in the CFI gene confers a high risk of age-related macular degeneration
van de Ven, Johannes P. H. ; Nilsson, Sara ^LU ; Tan, Perciliz L. ; Buitendijk, Gabrille H. S. ; Ristau, Tina ; Mohlin, Frida ^LU ; Nabuurs, Sander B. ; Schoenmaker-Koller, Frederieke E. ; Smailhodzic, Dzenita and Campochiaro, Peter A. , et al. (2013) In Nature Genetics 45(7). p.813-813
- Contribution to journal › Article
Mark Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Bojesen, Stig E. ; Pooley, Karen A. ; Johnatty, Sharon E. ; Beesley, Jonathan ; Michailidou, Kyriaki ; Tyrer, Jonathan P. ; Edwards, Stacey L. ; Pickett, Hilda A. ; Shen, Howard C. and Smart, Chanel E. , et al. (2013) In Nature Genetics 45(4). p.371-384
- Contribution to journal › Article

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