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Plos One
|
January 30, 2020
Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach
Tripti Agarwal, Tanica Lyngdoh, Frank Dudbridge, et al.
Genome Biology
|
March 29, 2020
Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
Benjamin H Mullin, Jennifer Tickner, Kun Zhu, et al.
BMC Genomics
|
February 26, 2016
Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density
Benjamin H Mullin, John P Walsh, Hou-Feng Zheng, et al.
Pain
|
September 3, 2025
Genome-wide association study of neuropathic pain phenotypes implicates loci involved in neural cell adhesion, channels, collagen matrix formation, and immune regulation
Richard Packer, Kayesha Coley, Alexander T Williams, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 23, 2020
Proportion of Idiopathic Pulmonary Fibrosis Risk Explained by Known Common Genetic Loci in European Populations
Olivia C Leavy, Shwu-Fan Ma, Philip L Molyneaux, et al.
European Journal of Human Genetics : EJHG
|
January 5, 2006
Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort
Scott G Wilson, Gail Adam, Maria Langdown, et al.
The Journal of Infectious Diseases
|
April 5, 2012
Transmission of human herpesvirus type 8 infection within families in american indigenous populations from the Brazilian Amazon
Jaila D Borges, Vanda A U F Souza, Claudia Giambartolomei, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 14, 2023
Epigenome-wide Association Study Shows Differential DNA Methylation of MDC1, KLF9, and CUTA in Autoimmune Thyroid Disease
Nicole Lafontaine, Christopher J Shore, Purdey J Campbell, et al.
Plos One
|
August 6, 2009
Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia
Roberta Pastorino, Cristina Menni, Monserrata Barca, et al.
Genetics
|
August 14, 2023
Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis
Benjamin H Mullin, Kun Zhu, Suzanne J Brown, et al.
Page
of 20
Search research articles
Search
Showing results (101-110 of 193) with videos related to
Sort By:
Page
of 20
Plos One
|
January 30, 2020
Causal relationships between lipid and glycemic levels in an Indian population: A bidirectional Mendelian randomization approach
Tripti Agarwal, Tanica Lyngdoh, Frank Dudbridge, et al.
Genome Biology
|
March 29, 2020
Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
Benjamin H Mullin, Jennifer Tickner, Kun Zhu, et al.
BMC Genomics
|
February 26, 2016
Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density
Benjamin H Mullin, John P Walsh, Hou-Feng Zheng, et al.
Pain
|
September 3, 2025
Genome-wide association study of neuropathic pain phenotypes implicates loci involved in neural cell adhesion, channels, collagen matrix formation, and immune regulation
Richard Packer, Kayesha Coley, Alexander T Williams, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 23, 2020
Proportion of Idiopathic Pulmonary Fibrosis Risk Explained by Known Common Genetic Loci in European Populations
Olivia C Leavy, Shwu-Fan Ma, Philip L Molyneaux, et al.
European Journal of Human Genetics : EJHG
|
January 5, 2006
Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort
Scott G Wilson, Gail Adam, Maria Langdown, et al.
The Journal of Infectious Diseases
|
April 5, 2012
Transmission of human herpesvirus type 8 infection within families in american indigenous populations from the Brazilian Amazon
Jaila D Borges, Vanda A U F Souza, Claudia Giambartolomei, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 14, 2023
Epigenome-wide Association Study Shows Differential DNA Methylation of MDC1, KLF9, and CUTA in Autoimmune Thyroid Disease
Nicole Lafontaine, Christopher J Shore, Purdey J Campbell, et al.
Plos One
|
August 6, 2009
Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia
Roberta Pastorino, Cristina Menni, Monserrata Barca, et al.
Genetics
|
August 14, 2023
Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis
Benjamin H Mullin, Kun Zhu, Suzanne J Brown, et al.
Page
of 20