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2015
Mark Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Dondorp, Wybo ; de Wert, Guido ; Bombard, Yvonne ; Bianchi, Diana W ; Bergmann, Carsten ; Borry, Pascal ; Chitty, Lyn S ; Fellmann, Florence ; Forzano, Francesca and Hall, Alison , et al. (2015) In European Journal of Human Genetics 23(11). p.1438-1450
- Contribution to journal › Article
Mark Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
Dondorp, Wybo ; de Wert, Guido ; Bombard, Yvonne ; Bianchi, Diana W ; Bergmann, Carsten ; Borry, Pascal ; Chitty, Lyn S ; Fellmann, Florence ; Forzano, Francesca and Hall, Alison , et al. (2015) In European Journal of Human Genetics
- Contribution to journal › Article
Mark A genetic risk score for hypertension associates with the risk of ischemic stroke in a Swedish case-control study.
Fava, Cristiano ^LU ; Sjögren, Marketa ^LU ; Olsson, Sandra ; Lövkvist, Håkan ^LU ; Jood, Katarina ; Engström, Gunnar ^LU ; Hedblad, Bo ^LU ; Norrving, Bo ^LU ; Jern, Christina and Lindgren, Arne ^LU , et al. (2015) In European Journal of Human Genetics 23(7). p.969-974
- Contribution to journal › Article
Mark Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach.
Thomsen, Hauke ^LU ; da Silva Filho, Miguel Inacio ; Försti, Asta ^LU ; Fuchs, Michael ; Ponader, Sabine ; von Strandmann, Elke Pogge ; Eisele, Lewin ; Herms, Stefan ; Hofmann, Per and Sundquist, Jan ^LU , et al. (2015) In European Journal of Human Genetics 23(6). p.824-830
- Contribution to journal › Article
Mark Reply to Mendez et al : the 'extremely ancient' chromosome that still isn't
Elhaik, Eran ^LU ; Tatarinova, Tatiana V ; Klyosov, Anatole A and Graur, Dan (2015) In European Journal of Human Genetics 23(5). p.8-567
- Contribution to journal › Letter
Mark Whole-genome sequencing in newborn screening? : A statement on the continued importance of targeted approaches in newborn screening programmes
Howard, Heidi Carmen ^LU ; Knoppers, Bartha Maria ; Cornel, Martina C ; Wright Clayton, Ellen ; Sénécal, Karine and Borry, Pascal (2015) In European Journal of Human Genetics 23(12). p.1593-1600
- Contribution to journal › Article
2014
Mark The 'extremely ancient' chromosome that isn't : a forensic bioinformatic investigation of Albert Perry's X-degenerate portion of the Y chromosome
Elhaik, Eran ^LU ; Tatarinova, Tatiana V ; Klyosov, Anatole A and Graur, Dan (2014) In European Journal of Human Genetics 22(9). p.1111-1116
- Contribution to journal › Article
2013
Mark Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations
Wang, Chuan ; Ahlford, Annika ; Jarvinen, Tiina M. ; Nordmark, Gunnel ; Eloranta, Maija-Leena ; Gunnarsson, Iva ; Svenungsson, Elisabet ; Padyukov, Leonid ; Sturfelt, Gunnar ^LU and Jönsen, Andreas ^LU , et al. (2013) In European Journal of Human Genetics 21(9). p.994-999
- Contribution to journal › Article
Mark Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders
Travaglini, Lorena ; Brancati, Francesco ; Silhavy, Jennifer ; Iannicelli, Miriam ; Nickerson, Elizabeth ; Elkhartoufi, Nadia ; Scott, Eric ; Spencer, Emily ; Gabriel, Stacey and Thomas, Sophie , et al. (2013) In European Journal of Human Genetics 21(10). p.8-1074
- Contribution to journal › Article
2012
Mark A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene.
Lövkvist, Håkan ^LU ; Olsson, Sandra ^LU ; Höglund, Peter ^LU ; Melander, Olle ^LU ; Jern, Christina ; Sjögren, Marketa ^LU ; Engström, Gunnar ^LU ; Smith, Gustav ^LU ; Hedblad, Bo ^LU and Andsberg, Gunnar ^LU , et al. (2012) In European Journal of Human Genetics 20(7). p.783-789
- Contribution to journal › Article

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