Search research articles
Contact Us
Filters
Showing results (1-10 of 7) with videos related to
Page
of 1
Sort By:
Journal of Experimental Child Psychology
|
October 1, 1985
Infants' search for visible objects: implications for the interpretation of early search errors
C Sophian, L Yengo
International Journal of Obesity (2005)
|
October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population
S Robiou-du-Pont, A Bonnefond, L Yengo, et al.
Diabetes & Metabolism
|
April 9, 2013
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family
A Bonnefond, E Vaillant, J Philippe, et al.
Diabetes & Metabolism
|
April 3, 2012
European genetic variants associated with type 2 diabetes in North African Arabs
S Cauchi, I Ezzidi, Y El Achhab, et al.
Diabetologia
|
December 11, 2012
Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes
A Bonnefond, L Yengo, J Philippe, et al.
NPJ Genomic Medicine
|
February 27, 2025
Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height
A Papadopoulou, E M Litkowski, M Graff, et al.
Diabetologia
|
November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
A Albrechtsen, N Grarup, Y Li, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Journal of Experimental Child Psychology
|
October 1, 1985
Infants' search for visible objects: implications for the interpretation of early search errors
C Sophian, L Yengo
International Journal of Obesity (2005)
|
October 24, 2012
Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population
S Robiou-du-Pont, A Bonnefond, L Yengo, et al.
Diabetes & Metabolism
|
April 9, 2013
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family
A Bonnefond, E Vaillant, J Philippe, et al.
Diabetes & Metabolism
|
April 3, 2012
European genetic variants associated with type 2 diabetes in North African Arabs
S Cauchi, I Ezzidi, Y El Achhab, et al.
Diabetologia
|
December 11, 2012
Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes
A Bonnefond, L Yengo, J Philippe, et al.
NPJ Genomic Medicine
|
February 27, 2025
Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height
A Papadopoulou, E M Litkowski, M Graff, et al.
Diabetologia
|
November 20, 2012
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
A Albrechtsen, N Grarup, Y Li, et al.
Page
of 1