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Nature Genetics
|
October 31, 2023
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing
Yasminka A Jakubek, Ying Zhou, Adrienne Stilp, et al.
Scientific Data
|
January 20, 2023
Deep phenotyping and genomic data from a nationally representative study on dementia in India
Jinkook Lee, Sarah Petrosyan, Pranali Khobragade, et al.
BMC Genetics
|
December 30, 2014
Genetic diversity is a predictor of mortality in humans
Nathan A Bihlmeyer, Jennifer A Brody, Albert Vernon Smith, et al.
Human Molecular Genetics
|
November 29, 2022
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease
Yang Pan, Xiao Sun, Xuenan Mi, et al.
Diabetes Care
|
January 27, 2022
Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts
Daniel DiCorpo, Jessica LeClair, Joanne B Cole, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point Mutations
Joshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Brain : a Journal of Neurology
|
August 9, 2022
Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI
Yunju Yang, Maria J Knol, Ruiqi Wang, et al.
Translational Psychiatry
|
December 5, 2021
Association of low-frequency and rare coding variants with information processing speed
Jan Bressler, Gail Davies, Albert V Smith, et al.
Human Genetics
|
January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
Karen Y He, Xiaoyin Li, Tanika N Kelly, et al.
Blood
|
July 26, 2018
DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis
Cavin K Ward-Caviness, Jennifer E Huffman, Karl Everett, et al.
Page
of 42
Search research articles
Search
Showing results (261-270 of 414) with videos related to
Sort By:
Page
of 42
Nature Genetics
|
October 31, 2023
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing
Yasminka A Jakubek, Ying Zhou, Adrienne Stilp, et al.
Scientific Data
|
January 20, 2023
Deep phenotyping and genomic data from a nationally representative study on dementia in India
Jinkook Lee, Sarah Petrosyan, Pranali Khobragade, et al.
BMC Genetics
|
December 30, 2014
Genetic diversity is a predictor of mortality in humans
Nathan A Bihlmeyer, Jennifer A Brody, Albert Vernon Smith, et al.
Human Molecular Genetics
|
November 29, 2022
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease
Yang Pan, Xiao Sun, Xuenan Mi, et al.
Diabetes Care
|
January 27, 2022
Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts
Daniel DiCorpo, Jessica LeClair, Joanne B Cole, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point Mutations
Joshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Brain : a Journal of Neurology
|
August 9, 2022
Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI
Yunju Yang, Maria J Knol, Ruiqi Wang, et al.
Translational Psychiatry
|
December 5, 2021
Association of low-frequency and rare coding variants with information processing speed
Jan Bressler, Gail Davies, Albert V Smith, et al.
Human Genetics
|
January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data
Karen Y He, Xiaoyin Li, Tanika N Kelly, et al.
Blood
|
July 26, 2018
DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis
Cavin K Ward-Caviness, Jennifer E Huffman, Karl Everett, et al.
Page
of 42