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Scientific Reports
|
October 30, 2013
GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus
Patrick Sleiman, Dai Wang, Joseph Glessner, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 2, 2021
Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries
Hui-Qi Qu, James Snyder, John Connolly, et al.
Frontiers in Psychiatry
|
April 7, 2022
Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data
Yichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Molecular Oncology
|
August 14, 2024
Copy number variations contribute to malignant tumor development in children with serious birth defects
Yichuan Liu, Joseph Glessner, Hui-Qi Qu, et al.
Genome Research
|
October 9, 2007
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
Kai Wang, Mingyao Li, Dexter Hadley, et al.
Journal of Psychiatric Research
|
March 18, 2019
Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa
Xiao Chang, Huiqi Qu, Yichuan Liu, et al.
Metabolomics : Official Journal of the Metabolomic Society
|
December 2, 2022
Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium
Hui-Qi Qu, Joseph Glessner, Jingchun Qu, et al.
Translational Psychiatry
|
November 3, 2020
Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans
Xiao Chang, Yichuan Liu, Frank Mentch, et al.
Innovation (Cambridge (Mass.))
|
May 4, 2021
Genetic correlations between COVID-19 and a variety of traits and diseases
Xiao Chang, Yun Li, Kenny Nguyen, et al.
Congenital Heart Disease
|
October 21, 2011
Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies
Elizabeth Goldmuntz, Prasuna Paluru, Joseph Glessner, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 95) with videos related to
Sort By:
Page
of 10
Scientific Reports
|
October 30, 2013
GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus
Patrick Sleiman, Dai Wang, Joseph Glessner, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 2, 2021
Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries
Hui-Qi Qu, James Snyder, John Connolly, et al.
Frontiers in Psychiatry
|
April 7, 2022
Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data
Yichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Molecular Oncology
|
August 14, 2024
Copy number variations contribute to malignant tumor development in children with serious birth defects
Yichuan Liu, Joseph Glessner, Hui-Qi Qu, et al.
Genome Research
|
October 9, 2007
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
Kai Wang, Mingyao Li, Dexter Hadley, et al.
Journal of Psychiatric Research
|
March 18, 2019
Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa
Xiao Chang, Huiqi Qu, Yichuan Liu, et al.
Metabolomics : Official Journal of the Metabolomic Society
|
December 2, 2022
Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium
Hui-Qi Qu, Joseph Glessner, Jingchun Qu, et al.
Translational Psychiatry
|
November 3, 2020
Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans
Xiao Chang, Yichuan Liu, Frank Mentch, et al.
Innovation (Cambridge (Mass.))
|
May 4, 2021
Genetic correlations between COVID-19 and a variety of traits and diseases
Xiao Chang, Yun Li, Kenny Nguyen, et al.
Congenital Heart Disease
|
October 21, 2011
Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies
Elizabeth Goldmuntz, Prasuna Paluru, Joseph Glessner, et al.
Page
of 10