Showing 1 - 15 results of 15 for search 'Gerton Lunter', query time: 0.02s
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Genome-wide identification of human functional DNA using a neutral indel model. by Gerton Lunter, Chris P Ponting, Jotun Hein
Published 2006-01-01Get full text
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A new isolation with migration model along complete genomes infers very different divergence processes among closely related great ape species. by Thomas Mailund, Anders E Halager, Michael Westergaard, Julien Y Dutheil, Kasper Munch, Lars N Andersen, Gerton Lunter, Kay Prüfer, Aylwyn Scally, Asger Hobolth, Mikkel H Schierup
Published 2012-01-01Get full text
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Lifestyle factors related to prevalent chronic disease multimorbidity: A population-based cross-sectional study. by Jacobien Niebuur, Judith M Vonk, Yihui Du, Geertruida H de Bock, Gerton Lunter, Paul F M Krabbe, Behrooz Z Alizadeh, Harold Snieder, Nynke Smidt, Marike Boezen, Eva Corpeleijn
Published 2023-01-01Get full text
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Genetic association studies in critically ill patients: a systematic reviewResearch in context by Wenbo Zhang, Nam Nguyen-Hoang, Sean C.S. Rivrud, Anne-Fleur Zandbergen, Yalan Yan, Eline G.M. Cox, Eva Suarez-Pajes, Amanda Y. Chong, Alexander J. Mentzer, Carlos Flores, Gerton Lunter, Frederik Keus, Harold Snieder
Published 2025-04-01Get full text
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The human pancreatic islet transcriptome: expression of candidate genes for type 1 diabetes and the impact of pro-inflammatory cytokines. by Décio L Eizirik, Michael Sammeth, Thomas Bouckenooghe, Guy Bottu, Giorgia Sisino, Mariana Igoillo-Esteve, Fernanda Ortis, Izortze Santin, Maikel L Colli, Jenny Barthson, Luc Bouwens, Linda Hughes, Lorna Gregory, Gerton Lunter, Lorella Marselli, Piero Marchetti, Mark I McCarthy, Miriam Cnop
Published 2012-01-01Get full text
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Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations. by Katherine R Bull, Andrew J Rimmer, Owen M Siggs, Lisa A Miosge, Carla M Roots, Anselm Enders, Edward M Bertram, Tanya L Crockford, Belinda Whittle, Paul K Potter, Michelle M Simon, Ann-Marie Mallon, Steve D M Brown, Bruce Beutler, Christopher C Goodnow, Gerton Lunter, Richard J Cornall
Published 2013-01-01Get full text
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Recessive mutations in SPTBN2 implicate β-III spectrin in both cognitive and motor development. by Stefano Lise, Yvonne Clarkson, Emma Perkins, Alexandra Kwasniewska, Elham Sadighi Akha, Ricardo Parolin Schnekenberg, Daumante Suminaite, Jilly Hope, Ian Baker, Lorna Gregory, Angie Green, Chris Allan, Sarah Lamble, Sandeep Jayawant, Gerardine Quaghebeur, M Zameel Cader, Sarah Hughes, Richard J E Armstrong, Alexander Kanapin, Andrew Rimmer, Gerton Lunter, Iain Mathieson, Jean-Baptiste Cazier, David Buck, Jenny C Taylor, David Bentley, Gilean McVean, Peter Donnelly, Samantha J L Knight, Mandy Jackson, Jiannis Ragoussis, Andrea H Németh
Published 2012-01-01Get full text
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