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Nature Genetics
|
March 9, 2010
Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Marc E Rothenberg, Jonathan M Spergel, Joseph D Sherrill, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 9, 2026
Age and the Diurnal Oscillatory Features of the Human Chronobiome
Carsten Skarke, Nicholas F Lahens, Antonijo Mrčela, et al.
Biological Psychiatry
|
December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism
Thomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.
American Journal of Human Genetics
|
March 3, 2009
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease
Kai Wang, Haitao Zhang, Subra Kugathasan, et al.
JAMA Psychiatry
|
May 11, 2022
Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort
Aaron Alexander-Bloch, Guillaume Huguet, Laura M Schultz, et al.
Frontiers in Physiology
|
November 16, 2020
Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and Laterality
Juhoon So, Mylarappa Ningappa, Joseph Glessner, et al.
Nature Communications
|
April 22, 2024
Clinical associations with a polygenic predisposition to benign lower white blood cell counts
Jonathan D Mosley, John P Shelley, Alyson L Dickson, et al.
Nature
|
December 3, 2010
Integrative genomics identifies LMO1 as a neuroblastoma oncogene
Kai Wang, Sharon J Diskin, Haitao Zhang, et al.
Human Molecular Genetics
|
March 23, 2011
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium
Xiaofeng Zhu, J H Young, Ervin Fox, et al.
Nature Communications
|
April 21, 2015
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells
Jin Li, Silje F Jørgensen, S Melkorka Maggadottir, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 95) with videos related to
Sort By:
Page
of 10
Nature Genetics
|
March 9, 2010
Common variants at 5q22 associate with pediatric eosinophilic esophagitis
Marc E Rothenberg, Jonathan M Spergel, Joseph D Sherrill, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 9, 2026
Age and the Diurnal Oscillatory Features of the Human Chronobiome
Carsten Skarke, Nicholas F Lahens, Antonijo Mrčela, et al.
Biological Psychiatry
|
December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism
Thomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.
American Journal of Human Genetics
|
March 3, 2009
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease
Kai Wang, Haitao Zhang, Subra Kugathasan, et al.
JAMA Psychiatry
|
May 11, 2022
Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort
Aaron Alexander-Bloch, Guillaume Huguet, Laura M Schultz, et al.
Frontiers in Physiology
|
November 16, 2020
Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and Laterality
Juhoon So, Mylarappa Ningappa, Joseph Glessner, et al.
Nature Communications
|
April 22, 2024
Clinical associations with a polygenic predisposition to benign lower white blood cell counts
Jonathan D Mosley, John P Shelley, Alyson L Dickson, et al.
Nature
|
December 3, 2010
Integrative genomics identifies LMO1 as a neuroblastoma oncogene
Kai Wang, Sharon J Diskin, Haitao Zhang, et al.
Human Molecular Genetics
|
March 23, 2011
Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium
Xiaofeng Zhu, J H Young, Ervin Fox, et al.
Nature Communications
|
April 21, 2015
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells
Jin Li, Silje F Jørgensen, S Melkorka Maggadottir, et al.
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of 10