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2023
Mark Ethnic, gender and other sociodemographic biases in genome-wide association studies for the most burdensome non-communicable diseases : 2005-2022
Fitipaldi, Hugo ^LU and Franks, Paul W ^LU (2023) In Human Molecular Genetics 32(3). p.520-532
- Contribution to journal › Article
Mark Novel pathological variants of NHP2 affect N-terminal domain flexibility, protein stability, H/ACA Ribonucleoprotein (RNP) complex formation and telomerase activity
Maliński, Bartosz ; Vertemara, Jacopo ; Faustini, Elena ; Ladenvall, Claes ; Norberg, Anna ; Zhang, Yuming ; Von Castelmur, Eleonore ; Baliakas, Panagiotis ; Tisi, Renata and Cammenga, Jörg ^LU , et al. (2023) In Human Molecular Genetics 32(19). p.2901-2912
- Contribution to journal › Article
Mark Circulating triglycerides are associated with human adipose tissue DNA methylation of genes linked to metabolic disease
Rönn, Tina ^LU ; Perfilyev, Alexander ^LU ; Jönsson, Josefine ^LU ; Eriksson, Karl-Fredrik ^LU ; Jørgensen, Sine W ; Brøns, Charlotte ^LU ; Gillberg, Linn ^LU ; Vaag, Allan ^LU ; Stener-Victorin, Elisabet and Ling, Charlotte ^LU (2023) In Human Molecular Genetics 32(11). p.1875-1887
- Contribution to journal › Article
2022
Mark Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes
Pervjakova, Natalia ; Moen, Gunn-Helen ; Borges, Maria-Carolina ; Ferreira, Teresa ; Cook, James P ; Allard, Catherine ; Beaumont, Robin N ; Canouil, Mickaël ; Hatem, Gad ^LU and Heiskala, Anni , et al. (2022) In Human Molecular Genetics 31(19). p.3377-3391
- Contribution to journal › Article
Mark Genomic editing of metformin efficacy-associated genetic variants in SLC47A1 does not alter SLC47A1 expression
Kalamajski, Sebastian ^LU ; Huang, Mi ^LU ; Dalla-Riva, Jonathan ^LU ; Keller, Maria ^LU ; Dawed, Adem Y ; Hansson, Ola ^LU ; Pearson, Ewan R ^LU ; Mulder, Hindrik ^LU and Franks, Paul W ^LU (2022) In Human Molecular Genetics 31(4). p.491-498
- Contribution to journal › Article
2020
Mark Demonstration of brain region-specific neuronal vulnerability in human iPSC-based model of familial Parkinson's disease
Brazdis, Razvan Marius ; Alecu, Julian E. ; Marsch, Daniel ; Dahms, Annika ; Simmnacher, Katrin ; Lörentz, Sandra ^LU ; Brendler, Anna ; Schneider, Yanni ; Marxreiter, Franz and Roybon, Laurent ^LU , et al. (2020) In Human Molecular Genetics 29(7). p.1180-1191
- Contribution to journal › Article
Mark Prostate cancer risk SNP rs10993994 is a trans-eQTL for SNHG11 mediated through MSMB
Bicak, Mesude ; Wang, Xing ; Gao, Xiaoni ; Xu, Xing ; Väänänen, Riina Minna ; Taimen, Pekka ; Lilja, Hans ^LU ; Pettersson, Kim and Klein, Robert J. (2020) In Human Molecular Genetics 29(10). p.1581-1591
- Contribution to journal › Article
Mark Effect of rare coding variants in the CFI gene on Factor I expression levels
de Jong, Sarah ^LU ; Volokhina, Elena B. ^LU ; de Breuk, Anita ; Nilsson, Sara C. ^LU ; de Jong, Eiko K. ; van der Kar, Nicole C.A.J. ; Bakker, Bjorn ; Hoyng, Carel B. ; van den Heuvel, Lambert P. and Blom, Anna M. ^LU , et al. (2020) In Human Molecular Genetics 29(14). p.2313-2324
- Contribution to journal › Article
2019
Mark Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis
Fadista, João ^LU ; Skotte, Line ; Geller, Frank ; Bybjerg-Grauholm, Jonas ; Gørtz, Sanne ; Romitti, Paul A. ; Caggana, Michele ; Kay, Denise M. ; Matsson, Hans and Boyd, Heather A. , et al. (2019) In Human Molecular Genetics 28(2). p.332-340
- Contribution to journal › Article
2018
Mark Consortium-based genome-wide meta-analysis for childhood dental caries traits
Haworth, Simon ; Shungin, Dmitry ^LU ; Van Der Tas, Justin T. ; Vucic, Strahinja ; Medina-Gomez, Carolina ; Yakimov, Victor ; Feenstra, Bjarke ; Shaffer, John R. ; Lee, Myoung Keun and Standl, Marie , et al. (2018) In Human Molecular Genetics 27(17). p.3113-3127
- Contribution to journal › Article

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