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Bo Isomaa

Showing results (31-40 of 73) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|November 21, 2007
[Not Available]Leif Groop, Antti Virkamäki, Bo Isomaa, et al.
American Journal of Human Genetics|June 15, 2006
Comprehensive association testing of common mitochondrial DNA variation in metabolic diseaseRicha Saxena, Paul I W de Bakker, Karyn Singer, et al.
European Journal of Endocrinology|February 12, 2009
Genetic variation in the ADIPOR2 gene is associated with liver fat content and its surrogate markers in three independent cohortsAnna Kotronen, Hannele Yki-Järvinen, Anna Aminoff, et al.
Genetic Epidemiology|February 11, 2011
Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variantsLin T Guey, Jasmina Kravic, Olle Melander, et al.
Diabetes|September 28, 2006
Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individualsRicha Saxena, Lauren Gianniny, Noël P Burtt, et al.
Cell Metabolism|May 18, 2016
Increased Melatonin Signaling Is a Risk Factor for Type 2 DiabetesTiinamaija Tuomi, Cecilia L F Nagorny, Pratibha Singh, et al.
Diabetes|January 26, 2013
Link between GIP and osteopontin in adipose tissue and insulin resistanceEmma Ahlqvist, Peter Osmark, Tiina Kuulasmaa, et al.
Plos Genetics|December 19, 2014
Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerinAnke Tönjes, Markus Scholz, Jana Breitfeld, et al.
Nature Genetics|December 9, 2008
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretionValeriya Lyssenko, Cecilia L F Nagorny, Michael R Erdos, et al.
Human Molecular Genetics|November 30, 2017
Genome-wide meta-analysis identifies novel determinants of circulating serum progranulinAnke Tönjes, Markus Scholz, Jacqueline Krüger, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Duodecim; Laaketieteellinen Aikakauskirja|November 21, 2007
[Not Available]Leif Groop, Antti Virkamäki, Bo Isomaa, et al.
American Journal of Human Genetics|June 15, 2006
Comprehensive association testing of common mitochondrial DNA variation in metabolic diseaseRicha Saxena, Paul I W de Bakker, Karyn Singer, et al.
European Journal of Endocrinology|February 12, 2009
Genetic variation in the ADIPOR2 gene is associated with liver fat content and its surrogate markers in three independent cohortsAnna Kotronen, Hannele Yki-Järvinen, Anna Aminoff, et al.
Genetic Epidemiology|February 11, 2011
Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variantsLin T Guey, Jasmina Kravic, Olle Melander, et al.
Diabetes|September 28, 2006
Common single nucleotide polymorphisms in TCF7L2 are reproducibly associated with type 2 diabetes and reduce the insulin response to glucose in nondiabetic individualsRicha Saxena, Lauren Gianniny, Noël P Burtt, et al.
Cell Metabolism|May 18, 2016
Increased Melatonin Signaling Is a Risk Factor for Type 2 DiabetesTiinamaija Tuomi, Cecilia L F Nagorny, Pratibha Singh, et al.
Diabetes|January 26, 2013
Link between GIP and osteopontin in adipose tissue and insulin resistanceEmma Ahlqvist, Peter Osmark, Tiina Kuulasmaa, et al.
Plos Genetics|December 19, 2014
Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerinAnke Tönjes, Markus Scholz, Jana Breitfeld, et al.
Nature Genetics|December 9, 2008
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretionValeriya Lyssenko, Cecilia L F Nagorny, Michael R Erdos, et al.
Human Molecular Genetics|November 30, 2017
Genome-wide meta-analysis identifies novel determinants of circulating serum progranulinAnke Tönjes, Markus Scholz, Jacqueline Krüger, et al.
Pageof 8