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Medrxiv : the Preprint Server for Health Sciences
|
November 19, 2025
Robust Mixed Model Association Test for Gene-Environment Interactions
Mengyu Zhang, Jingxian Tang, Michael R Brown, et al.
Biological Research for Nursing
|
January 5, 2018
Effects of Gender-Specific Differences, Inflammatory Response, and Genetic Variation on the Associations Among Depressive Symptoms and the Risk of Major Adverse Coronary Events in Patients With Acute Coronary Syndrome
Jennifer Sanner, Megan L Grove, Erica Yu, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
January 22, 2011
Association of retinoic acid receptor genes with meningomyelocele
Phong X Tran, Kit Sing Au, Alanna C Morrison, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2017
Mutations in folate transporter genes and risk for human myelomeningocele
Tina O Findley, Joy C Tenpenny, Michelle R O'Byrne, et al.
American Journal of Obstetrics and Gynecology
|
August 18, 2009
Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida
Carla A Martinez, Hope Northrup, Jone-Ing Lin, et al.
Epigenetics
|
May 6, 2025
DNA methylation markers of insulin resistance surrogate measures in the Atherosclerosis Risk in Communities (ARIC) study
Jeewoen Shin, Jan Bressler, Megan L Grove, et al.
Molecular Genetics & Genomic Medicine
|
September 22, 2020
Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks
Paul Hillman, Craig Baker, Luke Hebert, et al.
Plos One
|
December 11, 2012
Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients
Catherine J Spellicy, Hope Northrup, Jack M Fletcher, et al.
International Journal of Hypertension
|
March 26, 2019
Association of <i>FMO3</i> Variants with Blood Pressure in the Atherosclerosis Risk in Communities Study
Tyler S Bryant, Priya Duggal, Bing Yu, et al.
Plos One
|
September 24, 2020
Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients
Luke Hebert, Paul Hillman, Craig Baker, et al.
Page
of 33
Search research articles
Search
Showing results (31-40 of 325) with videos related to
Sort By:
Page
of 33
Medrxiv : the Preprint Server for Health Sciences
|
November 19, 2025
Robust Mixed Model Association Test for Gene-Environment Interactions
Mengyu Zhang, Jingxian Tang, Michael R Brown, et al.
Biological Research for Nursing
|
January 5, 2018
Effects of Gender-Specific Differences, Inflammatory Response, and Genetic Variation on the Associations Among Depressive Symptoms and the Risk of Major Adverse Coronary Events in Patients With Acute Coronary Syndrome
Jennifer Sanner, Megan L Grove, Erica Yu, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
January 22, 2011
Association of retinoic acid receptor genes with meningomyelocele
Phong X Tran, Kit Sing Au, Alanna C Morrison, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2017
Mutations in folate transporter genes and risk for human myelomeningocele
Tina O Findley, Joy C Tenpenny, Michelle R O'Byrne, et al.
American Journal of Obstetrics and Gynecology
|
August 18, 2009
Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida
Carla A Martinez, Hope Northrup, Jone-Ing Lin, et al.
Epigenetics
|
May 6, 2025
DNA methylation markers of insulin resistance surrogate measures in the Atherosclerosis Risk in Communities (ARIC) study
Jeewoen Shin, Jan Bressler, Megan L Grove, et al.
Molecular Genetics & Genomic Medicine
|
September 22, 2020
Identification of novel candidate risk genes for myelomeningocele within the glucose homeostasis/oxidative stress and folate/one-carbon metabolism networks
Paul Hillman, Craig Baker, Luke Hebert, et al.
Plos One
|
December 11, 2012
Folate metabolism gene 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with ADHD in myelomeningocele patients
Catherine J Spellicy, Hope Northrup, Jack M Fletcher, et al.
International Journal of Hypertension
|
March 26, 2019
Association of <i>FMO3</i> Variants with Blood Pressure in the Atherosclerosis Risk in Communities Study
Tyler S Bryant, Priya Duggal, Bing Yu, et al.
Plos One
|
September 24, 2020
Burden of rare deleterious variants in WNT signaling genes among 511 myelomeningocele patients
Luke Hebert, Paul Hillman, Craig Baker, et al.
Page
of 33