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Alan F Wright

Showing results (141-150 of 239) with videos related to

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Obesity (Silver Spring, Md.)|October 24, 2009
Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 geneAsa Johansson, Fabio Marroni, Caroline Hayward, et al.
Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
Human Molecular Genetics|July 23, 2013
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degenerationMorad Ansari, Paul M McKeigue, Christine Skerka, et al.
BMC Medical Genetics|March 13, 2010
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine levelCristian Pattaro, Alessandro De Grandi, Veronique Vitart, et al.
Human Molecular Genetics|October 28, 2008
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysisAsa Johansson, Fabio Marroni, Caroline Hayward, et al.
Human Molecular Genetics|June 15, 2012
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3Valentina Cipriani, Hin-Tak Leung, Vincent Plagnol, et al.
Nature Genetics|March 11, 2008
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and goutVeronique Vitart, Igor Rudan, Caroline Hayward, et al.
Diabetes|January 1, 2013
Mutations in HNF1A result in marked alterations of plasma glycan profileGaya Thanabalasingham, Jennifer E Huffman, Jayesh J Kattla, et al.
Plos Genetics|February 6, 2013
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancersGordan Lauc, Jennifer E Huffman, Maja Pučić, et al.
Nature Communications|April 1, 2015
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopiaMasahiro Miyake, Kenji Yamashiro, Yasuharu Tabara, et al.
Pageof 24

Showing results (141-150 of 239) with videos related to

Sort By:
Pageof 24
Obesity (Silver Spring, Md.)|October 24, 2009
Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 geneAsa Johansson, Fabio Marroni, Caroline Hayward, et al.
Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
Human Molecular Genetics|July 23, 2013
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degenerationMorad Ansari, Paul M McKeigue, Christine Skerka, et al.
BMC Medical Genetics|March 13, 2010
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine levelCristian Pattaro, Alessandro De Grandi, Veronique Vitart, et al.
Human Molecular Genetics|October 28, 2008
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysisAsa Johansson, Fabio Marroni, Caroline Hayward, et al.
Human Molecular Genetics|June 15, 2012
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3Valentina Cipriani, Hin-Tak Leung, Vincent Plagnol, et al.
Nature Genetics|March 11, 2008
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and goutVeronique Vitart, Igor Rudan, Caroline Hayward, et al.
Diabetes|January 1, 2013
Mutations in HNF1A result in marked alterations of plasma glycan profileGaya Thanabalasingham, Jennifer E Huffman, Jayesh J Kattla, et al.
Plos Genetics|February 6, 2013
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancersGordan Lauc, Jennifer E Huffman, Maja Pučić, et al.
Nature Communications|April 1, 2015
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopiaMasahiro Miyake, Kenji Yamashiro, Yasuharu Tabara, et al.
Pageof 24