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Journal of Community Genetics
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September 12, 2023
The Circassians and the Chechens in Jordan: results of a decade of epidemiological and genetic studies
Sara Abudahab, Nancy Hakooz, Laith Al-Etian, et al.
The Journal of Gene Medicine
|
August 20, 2025
Single-Cell RNA Sequencing of Peripheral Blood Mononuclear Cells in Patients With Single Ventricle/Hypoplastic Left Heart Syndrome
Hui-Qi Qu, Kayleigh Ostberg, Diana J Slater, et al.
Metabolism: Clinical and Experimental
|
November 6, 2020
Association of DLL1 with type 1 diabetes in patients characterized by low polygenic risk score
Jingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Genes
|
January 21, 2023
Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples
Hui-Qi Qu, Charlly Kao, James Garifallou, et al.
Diabetes Research and Clinical Practice
|
February 22, 2026
Sex specific genomic insights into type 1 diabetes through GWAS and single cell transcriptome analysis
Hui-Qi Qu, Kayleigh Ostberg, Diana J Slater, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine
|
November 21, 2023
High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations
Hui-Qi Qu, Joseph T Glessner, Jingchun Qu, et al.
Gastroenterology
|
January 23, 2013
Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene
Shuang Cui, Melissa Leyva-Vega, Ellen A Tsai, et al.
Scientific Reports
|
August 22, 2015
CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations
Rana Dajani, Jin Li, Zhi Wei, et al.
Scientific Reports
|
August 7, 2021
Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients
Jingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Genome Medicine
|
December 2, 2017
Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders
Joseph T Glessner, Jin Li, Dai Wang, et al.
Page
of 13
Search research articles
Search
Showing results (21-30 of 124) with videos related to
Sort By:
Page
of 13
Journal of Community Genetics
|
September 12, 2023
The Circassians and the Chechens in Jordan: results of a decade of epidemiological and genetic studies
Sara Abudahab, Nancy Hakooz, Laith Al-Etian, et al.
The Journal of Gene Medicine
|
August 20, 2025
Single-Cell RNA Sequencing of Peripheral Blood Mononuclear Cells in Patients With Single Ventricle/Hypoplastic Left Heart Syndrome
Hui-Qi Qu, Kayleigh Ostberg, Diana J Slater, et al.
Metabolism: Clinical and Experimental
|
November 6, 2020
Association of DLL1 with type 1 diabetes in patients characterized by low polygenic risk score
Jingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Genes
|
January 21, 2023
Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples
Hui-Qi Qu, Charlly Kao, James Garifallou, et al.
Diabetes Research and Clinical Practice
|
February 22, 2026
Sex specific genomic insights into type 1 diabetes through GWAS and single cell transcriptome analysis
Hui-Qi Qu, Kayleigh Ostberg, Diana J Slater, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine
|
November 21, 2023
High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations
Hui-Qi Qu, Joseph T Glessner, Jingchun Qu, et al.
Gastroenterology
|
January 23, 2013
Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene
Shuang Cui, Melissa Leyva-Vega, Ellen A Tsai, et al.
Scientific Reports
|
August 22, 2015
CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations
Rana Dajani, Jin Li, Zhi Wei, et al.
Scientific Reports
|
August 7, 2021
Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients
Jingchun Qu, Hui-Qi Qu, Jonathan P Bradfield, et al.
Genome Medicine
|
December 2, 2017
Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders
Joseph T Glessner, Jin Li, Dai Wang, et al.
Page
of 13