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The Journal of Clinical Endocrinology and Metabolism|May 22, 2008
A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronineVijay Panicker, Christie Cluett, Beverley Shields, et al.
American Journal of Human Genetics|May 16, 2007
Type 2 diabetes TCF7L2 risk genotypes alter birth weight: a study of 24,053 individualsRachel M Freathy, Michael N Weedon, Amanda Bennett, et al.
Neurobiology of Disease|November 5, 2023
Phenotypic effect of GBA1 variants in individuals with and without Parkinson's disease: The RAPSODI studyMarco Toffoli, Harneek Chohan, Stephen Mullin, et al.
Diabetes|February 21, 2009
Type 2 diabetes risk alleles are associated with reduced size at birthRachel M Freathy, Amanda J Bennett, Susan M Ring, et al.
EMBO Molecular Medicine|January 3, 2026
A new form of diabetes caused by INS mutations defined by zygosity, stem cell and population dataYue Tong, Marianne Becker, Ulrike Schierloh, et al.
Diabetes|March 19, 2008
Common variation in the FTO gene alters diabetes-related metabolic traits to the extent expected given its effect on BMIRachel M Freathy, Nicholas J Timpson, Debbie A Lawlor, et al.
Science (New York, N.Y.)|April 28, 2007
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetesEleftheria Zeggini, Michael N Weedon, Cecilia M Lindgren, et al.
Nature Genetics|September 4, 2007
A common variant of HMGA2 is associated with adult and childhood height in the general populationMichael N Weedon, Guillaume Lettre, Rachel M Freathy, et al.
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