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Alan F Wright

Showing results (121-130 of 239) with videos related to

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Plos Genetics|July 7, 2020
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traitsAndrew D Bretherick, Oriol Canela-Xandri, Peter K Joshi, et al.
Investigative Ophthalmology & Visual Science|October 18, 2011
Complement factor D in age-related macular degenerationChloe M Stanton, John R W Yates, Anneke I den Hollander, et al.
American Journal of Human Genetics|April 17, 2012
Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acidsAdam Ameur, Stefan Enroth, Asa Johansson, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN projectFabio Marroni, Arne Pfeufer, Yurii S Aulchenko, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
American Journal of Human Genetics|September 2, 2008
Runs of homozygosity in European populationsRuth McQuillan, Anne-Louise Leutenegger, Rehab Abdel-Rahman, et al.
European Journal of Human Genetics : EJHG|June 24, 2010
Genes predict village of origin in rural EuropeColm O'Dushlaine, Ruth McQuillan, Michael E Weale, et al.
Croatian Medical Journal|March 5, 2009
Genome-wide association study of anthropometric traits in Korcula Island, CroatiaOzren Polasek, Ana Marusić, Kresimir Rotim, et al.
Kidney International|April 24, 2009
Genome-wide linkage analysis of serum creatinine in three isolated European populationsCristian Pattaro, Yurii S Aulchenko, Aaron Isaacs, et al.
American Journal of Human Genetics|January 14, 2003
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)Kirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
Pageof 24

Showing results (121-130 of 239) with videos related to

Sort By:
Pageof 24
Plos Genetics|July 7, 2020
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traitsAndrew D Bretherick, Oriol Canela-Xandri, Peter K Joshi, et al.
Investigative Ophthalmology & Visual Science|October 18, 2011
Complement factor D in age-related macular degenerationChloe M Stanton, John R W Yates, Anneke I den Hollander, et al.
American Journal of Human Genetics|April 17, 2012
Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acidsAdam Ameur, Stefan Enroth, Asa Johansson, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN projectFabio Marroni, Arne Pfeufer, Yurii S Aulchenko, et al.
American Journal of Human Genetics|May 7, 2002
A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosaDebra K Breuer, Beverly M Yashar, Elena Filippova, et al.
American Journal of Human Genetics|September 2, 2008
Runs of homozygosity in European populationsRuth McQuillan, Anne-Louise Leutenegger, Rehab Abdel-Rahman, et al.
European Journal of Human Genetics : EJHG|June 24, 2010
Genes predict village of origin in rural EuropeColm O'Dushlaine, Ruth McQuillan, Michael E Weale, et al.
Croatian Medical Journal|March 5, 2009
Genome-wide association study of anthropometric traits in Korcula Island, CroatiaOzren Polasek, Ana Marusić, Kresimir Rotim, et al.
Kidney International|April 24, 2009
Genome-wide linkage analysis of serum creatinine in three isolated European populationsCristian Pattaro, Yurii S Aulchenko, Aaron Isaacs, et al.
American Journal of Human Genetics|January 14, 2003
Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)Kirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
Pageof 24