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JAMA Pediatrics
|
September 22, 2025
Clinical Long-Read Sequencing Test for Genetic Disease Diagnosis
Isabelle Thiffault, Emily Farrow, Cassandra Barrett, et al.
Genome Research
|
August 6, 2009
Population genomics in a disease targeted primary cell model
Elin Grundberg, Tony Kwan, Bing Ge, et al.
American Journal of Human Genetics
|
September 8, 2009
Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease
Dominique J Verlaan, Soizik Berlivet, Gary M Hunninghake, et al.
Diabetes
|
December 6, 2013
Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity
Sarah Keildson, Joao Fadista, Claes Ladenvall, et al.
Nature Communications
|
May 29, 2023
Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort
Warren A Cheung, Adam F Johnson, William J Rowell, et al.
Nature Genetics
|
October 20, 2009
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis
Bing Ge, Dmitry K Pokholok, Tony Kwan, et al.
Genome Biology
|
March 12, 2017
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
Warren A Cheung, Xiaojian Shao, Andréanne Morin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 7, 2019
Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures
Jie Zheng, Winfried Maerz, Ingrid Gergei, et al.
Genome Biology
|
May 9, 2019
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
Warren A Cheung, Xiaojian Shao, Andréanne Morin, et al.
Plos Genetics
|
June 16, 2010
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits
Yi-Hsiang Hsu, M Carola Zillikens, Scott G Wilson, et al.
Page
of 21
Search research articles
Search
Showing results (171-180 of 208) with videos related to
Sort By:
Page
of 21
JAMA Pediatrics
|
September 22, 2025
Clinical Long-Read Sequencing Test for Genetic Disease Diagnosis
Isabelle Thiffault, Emily Farrow, Cassandra Barrett, et al.
Genome Research
|
August 6, 2009
Population genomics in a disease targeted primary cell model
Elin Grundberg, Tony Kwan, Bing Ge, et al.
American Journal of Human Genetics
|
September 8, 2009
Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease
Dominique J Verlaan, Soizik Berlivet, Gary M Hunninghake, et al.
Diabetes
|
December 6, 2013
Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity
Sarah Keildson, Joao Fadista, Claes Ladenvall, et al.
Nature Communications
|
May 29, 2023
Direct haplotype-resolved 5-base HiFi sequencing for genome-wide profiling of hypermethylation outliers in a rare disease cohort
Warren A Cheung, Adam F Johnson, William J Rowell, et al.
Nature Genetics
|
October 20, 2009
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis
Bing Ge, Dmitry K Pokholok, Tony Kwan, et al.
Genome Biology
|
March 12, 2017
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
Warren A Cheung, Xiaojian Shao, Andréanne Morin, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 7, 2019
Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures
Jie Zheng, Winfried Maerz, Ingrid Gergei, et al.
Genome Biology
|
May 9, 2019
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome
Warren A Cheung, Xiaojian Shao, Andréanne Morin, et al.
Plos Genetics
|
June 16, 2010
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits
Yi-Hsiang Hsu, M Carola Zillikens, Scott G Wilson, et al.
Page
of 21