Search research articles
Contact Us
Filters
Showing results (41-50 of 95) with videos related to
Page
of 10
Sort By:
Human Molecular Genetics
|
June 1, 2022
Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing
Yichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Biomarker Research
|
November 17, 2022
Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing
Yichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Cancer Communications (London, England)
|
August 10, 2023
Genomic information of children with malignant brain tumors for the prediction of length of hospitalization
Yichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Diabetes, Obesity & Metabolism
|
May 5, 2021
Combined application of genetic and polygenic risk scores for type 1 diabetes risk prediction
Hui-Qi Qu, Jingchun Qu, Jonathan Bradfield, et al.
Genome Biology
|
July 10, 2026
Computational strategies for copy number variation detection, disease association, and beyond
Amir Hossein Saeidian, Hani Sabaie, Mahdi Akbarzadeh, et al.
Pediatric Diabetes
|
January 8, 2022
Improved genetic risk scoring algorithm for type 1 diabetes prediction
Hui-Qi Qu, Jingchun Qu, Joseph Glessner, et al.
Molecular Autism
|
August 4, 2010
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region
L Alison McInnes, Alisa Nakamine, Marion Pilorge, et al.
American Journal of Medical Genetics. Part A
|
December 28, 2020
Ciliopathies: Coloring outside of the lines
Alanna Strong, Dong Li, Frank Mentch, et al.
Inflammatory Bowel Diseases
|
December 17, 2009
Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease
Marla C Dubinsky, Ling Mei, Madison Friedman, et al.
Genome Research
|
January 15, 2009
Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy
Edward F Attiyeh, Sharon J Diskin, Marc A Attiyeh, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 95) with videos related to
Sort By:
Page
of 10
Human Molecular Genetics
|
June 1, 2022
Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing
Yichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Biomarker Research
|
November 17, 2022
Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing
Yichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Cancer Communications (London, England)
|
August 10, 2023
Genomic information of children with malignant brain tumors for the prediction of length of hospitalization
Yichuan Liu, Hui-Qi Qu, Xiao Chang, et al.
Diabetes, Obesity & Metabolism
|
May 5, 2021
Combined application of genetic and polygenic risk scores for type 1 diabetes risk prediction
Hui-Qi Qu, Jingchun Qu, Jonathan Bradfield, et al.
Genome Biology
|
July 10, 2026
Computational strategies for copy number variation detection, disease association, and beyond
Amir Hossein Saeidian, Hani Sabaie, Mahdi Akbarzadeh, et al.
Pediatric Diabetes
|
January 8, 2022
Improved genetic risk scoring algorithm for type 1 diabetes prediction
Hui-Qi Qu, Jingchun Qu, Joseph Glessner, et al.
Molecular Autism
|
August 4, 2010
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region
L Alison McInnes, Alisa Nakamine, Marion Pilorge, et al.
American Journal of Medical Genetics. Part A
|
December 28, 2020
Ciliopathies: Coloring outside of the lines
Alanna Strong, Dong Li, Frank Mentch, et al.
Inflammatory Bowel Diseases
|
December 17, 2009
Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease
Marla C Dubinsky, Ling Mei, Madison Friedman, et al.
Genome Research
|
January 15, 2009
Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy
Edward F Attiyeh, Sharon J Diskin, Marc A Attiyeh, et al.
Page
of 10