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Scientific Reports
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August 29, 2024
Identification of genetic variants associated with clinical features of sickle cell disease
Katharine Tsukahara, Xiao Chang, Frank Mentch, et al.
Journal of Neurodevelopmental Disorders
|
June 11, 2022
An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities
Isabella Slaby, Heather S Hain, Debra Abrams, et al.
BMC Genomics
|
February 25, 2021
MONTAGE: a new tool for high-throughput detection of mosaic copy number variation
Joseph T Glessner, Xiao Chang, Yichuan Liu, et al.
Frontiers in Genetics
|
March 28, 2014
Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts
John J Connolly, Joseph T Glessner, Berta Almoguera, et al.
Frontiers in Cell and Developmental Biology
|
August 30, 2021
Discovery of Novel Host Molecular Factors Underlying HBV/HCV Infection
Xubo Huang, Joseph T Glessner, Jinxia Huang, et al.
Frontiers in Genetics
|
September 2, 2022
COVID-19 in pediatrics: Genetic susceptibility
Joseph T Glessner, Xiao Chang, Frank Mentch, et al.
Human Molecular Genetics
|
August 21, 2014
Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations
Laura E Mitchell, A J Agopian, Angela Bhalla, et al.
Briefings in Bioinformatics
|
January 11, 2021
DeepCNV: a deep learning approach for authenticating copy number variations
Joseph T Glessner, Xiurui Hou, Cheng Zhong, et al.
Obesity (Silver Spring, Md.)
|
May 25, 2013
A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls
Wei-Dong Li, Hongxiao Jiao, Kai Wang, et al.
Plos One
|
May 10, 2011
A genome-wide association study on obesity and obesity-related traits
Kai Wang, Wei-Dong Li, Clarence K Zhang, et al.
Page
of 13
Search research articles
Search
Showing results (11-20 of 124) with videos related to
Sort By:
Page
of 13
Scientific Reports
|
August 29, 2024
Identification of genetic variants associated with clinical features of sickle cell disease
Katharine Tsukahara, Xiao Chang, Frank Mentch, et al.
Journal of Neurodevelopmental Disorders
|
June 11, 2022
An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities
Isabella Slaby, Heather S Hain, Debra Abrams, et al.
BMC Genomics
|
February 25, 2021
MONTAGE: a new tool for high-throughput detection of mosaic copy number variation
Joseph T Glessner, Xiao Chang, Yichuan Liu, et al.
Frontiers in Genetics
|
March 28, 2014
Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts
John J Connolly, Joseph T Glessner, Berta Almoguera, et al.
Frontiers in Cell and Developmental Biology
|
August 30, 2021
Discovery of Novel Host Molecular Factors Underlying HBV/HCV Infection
Xubo Huang, Joseph T Glessner, Jinxia Huang, et al.
Frontiers in Genetics
|
September 2, 2022
COVID-19 in pediatrics: Genetic susceptibility
Joseph T Glessner, Xiao Chang, Frank Mentch, et al.
Human Molecular Genetics
|
August 21, 2014
Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations
Laura E Mitchell, A J Agopian, Angela Bhalla, et al.
Briefings in Bioinformatics
|
January 11, 2021
DeepCNV: a deep learning approach for authenticating copy number variations
Joseph T Glessner, Xiurui Hou, Cheng Zhong, et al.
Obesity (Silver Spring, Md.)
|
May 25, 2013
A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls
Wei-Dong Li, Hongxiao Jiao, Kai Wang, et al.
Plos One
|
May 10, 2011
A genome-wide association study on obesity and obesity-related traits
Kai Wang, Wei-Dong Li, Clarence K Zhang, et al.
Page
of 13