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The Journal of Clinical Endocrinology and Metabolism
|
February 5, 2009
Common variation in the DIO2 gene predicts baseline psychological well-being and response to combination thyroxine plus triiodothyronine therapy in hypothyroid patients
Vijay Panicker, Ponnusamy Saravanan, Bijay Vaidya, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 2, 2022
PLIN1 Haploinsufficiency Causes a Favorable Metabolic Profile
Kashyap A Patel, Shivang Burman, Thomas W Laver, et al.
The Journal of Allergy and Clinical Immunology
|
September 2, 2008
Filaggrin gene mutations are associated with asthma and eczema in later life
Neil E Rice, Bipen D Patel, Iain A Lang, et al.
American Journal of Human Genetics
|
June 14, 2022
Rare genetic variants in genes and loci linked to dominant monogenic developmental disorders cause milder related phenotypes in the general population
Rebecca Kingdom, Marcus Tuke, Andrew Wood, et al.
Diabetes
|
October 27, 2006
No evidence of association of ENPP1 variants with type 2 diabetes or obesity in a study of 8,089 U.K. Caucasians
Michael N Weedon, Beverley Shields, Graham Hitman, et al.
Diabetes
|
March 3, 2009
Interrogating type 2 diabetes genome-wide association data using a biological pathway-based approach
John R B Perry, Mark I McCarthy, Andrew T Hattersley, et al.
Aging Cell
|
October 20, 2017
Influence of cell distribution and diabetes status on the association between mitochondrial DNA copy number and aging phenotypes in the InCHIANTI study
Ann Zenobia Moore, Jun Ding, Marcus A Tuke, et al.
Plos Genetics
|
December 30, 2025
Getting to GRIPS with MR-Egger: Modelling directional pleiotropy independently of allele coding
Frank Dudbridge, Bethany Voller, Ruby M Woodward, et al.
Journal of Negative Results in Biomedicine
|
November 28, 2006
A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian population
Rachel M Freathy, Simon M S Mitchell, Beatrice Knight, et al.
Genetic Epidemiology
|
December 30, 2009
A powerful approach to sub-phenotype analysis in population-based genetic association studies
Andrew P Morris, Cecilia M Lindgren, Eleftheria Zeggini, et al.
Page
of 31
Search research articles
Search
Showing results (31-40 of 307) with videos related to
Sort By:
Page
of 31
The Journal of Clinical Endocrinology and Metabolism
|
February 5, 2009
Common variation in the DIO2 gene predicts baseline psychological well-being and response to combination thyroxine plus triiodothyronine therapy in hypothyroid patients
Vijay Panicker, Ponnusamy Saravanan, Bijay Vaidya, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 2, 2022
PLIN1 Haploinsufficiency Causes a Favorable Metabolic Profile
Kashyap A Patel, Shivang Burman, Thomas W Laver, et al.
The Journal of Allergy and Clinical Immunology
|
September 2, 2008
Filaggrin gene mutations are associated with asthma and eczema in later life
Neil E Rice, Bipen D Patel, Iain A Lang, et al.
American Journal of Human Genetics
|
June 14, 2022
Rare genetic variants in genes and loci linked to dominant monogenic developmental disorders cause milder related phenotypes in the general population
Rebecca Kingdom, Marcus Tuke, Andrew Wood, et al.
Diabetes
|
October 27, 2006
No evidence of association of ENPP1 variants with type 2 diabetes or obesity in a study of 8,089 U.K. Caucasians
Michael N Weedon, Beverley Shields, Graham Hitman, et al.
Diabetes
|
March 3, 2009
Interrogating type 2 diabetes genome-wide association data using a biological pathway-based approach
John R B Perry, Mark I McCarthy, Andrew T Hattersley, et al.
Aging Cell
|
October 20, 2017
Influence of cell distribution and diabetes status on the association between mitochondrial DNA copy number and aging phenotypes in the InCHIANTI study
Ann Zenobia Moore, Jun Ding, Marcus A Tuke, et al.
Plos Genetics
|
December 30, 2025
Getting to GRIPS with MR-Egger: Modelling directional pleiotropy independently of allele coding
Frank Dudbridge, Bethany Voller, Ruby M Woodward, et al.
Journal of Negative Results in Biomedicine
|
November 28, 2006
A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian population
Rachel M Freathy, Simon M S Mitchell, Beatrice Knight, et al.
Genetic Epidemiology
|
December 30, 2009
A powerful approach to sub-phenotype analysis in population-based genetic association studies
Andrew P Morris, Cecilia M Lindgren, Eleftheria Zeggini, et al.
Page
of 31