Search research articles
Contact Us
Filters
Showing results (121-130 of 239) with videos related to
Page
of 24
Sort By:
Plos Genetics
|
July 7, 2020
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits
Andrew D Bretherick, Oriol Canela-Xandri, Peter K Joshi, et al.
Investigative Ophthalmology & Visual Science
|
October 18, 2011
Complement factor D in age-related macular degeneration
Chloe 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 acids
Adam 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 project
Fabio 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 pigmentosa
Debra K Breuer, Beverly M Yashar, Elena Filippova, et al.
American Journal of Human Genetics
|
September 2, 2008
Runs of homozygosity in European populations
Ruth 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 Europe
Colm 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, Croatia
Ozren Polasek, Ana Marusić, Kresimir Rotim, et al.
Kidney International
|
April 24, 2009
Genome-wide linkage analysis of serum creatinine in three isolated European populations
Cristian 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.
Page
of 24
Search research articles
Search
Showing results (121-130 of 239) with videos related to
Sort By:
Page
of 24
Plos Genetics
|
July 7, 2020
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits
Andrew D Bretherick, Oriol Canela-Xandri, Peter K Joshi, et al.
Investigative Ophthalmology & Visual Science
|
October 18, 2011
Complement factor D in age-related macular degeneration
Chloe 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 acids
Adam 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 project
Fabio 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 pigmentosa
Debra K Breuer, Beverly M Yashar, Elena Filippova, et al.
American Journal of Human Genetics
|
September 2, 2008
Runs of homozygosity in European populations
Ruth 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 Europe
Colm 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, Croatia
Ozren Polasek, Ana Marusić, Kresimir Rotim, et al.
Kidney International
|
April 24, 2009
Genome-wide linkage analysis of serum creatinine in three isolated European populations
Cristian 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.
Page
of 24