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Joseph Glessner

Showing results (71-80 of 95) with videos related to

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Gene|October 11, 2025
Genome-wide association study and HLA genotyping for beryllium disease susceptibility in a European descent populationShu-Yi Liao, Tasha E Fingerlin, Sean Jacobson, et al.
Journal of Medical Genetics|March 5, 2024
<i>NASP</i> gene contributes to autism by epigenetic dysregulation of neural and immune pathwaysSipeng Zhang, Jie Yang, Dandan Ji, et al.
Frontiers in Immunology|June 15, 2026
Identification of <i>IL7R</i> as a key genetic risk locus in childhood steroid-sensitive nephrotic syndrome and IgA nephropathyCong Wang, Yue Jiang, Yingchao Song, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCsCarolina Gracia-Diaz, Jonathan E Perdomo, Munir E Khan, et al.
Plos One|September 18, 2015
The Role of ARF6 in Biliary AtresiaMylarappa Ningappa, Juhoon So, Joseph Glessner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participantsAmir Hossein Saeidian, Michael E March, Leila Youssefian, et al.
Nature Communications|September 20, 2017
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma riskXiao Chang, Yan Zhao, Cuiping Hou, et al.
Human Molecular Genetics|January 4, 2015
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemiaMinal J Menezes, Yiran Guo, Jianguo Zhang, et al.
Genetics in Medicine Open|March 5, 2026
Single vs dual genetic disease in children with congenital anomalies and solid tumorsDeborah J Watson, Amir Hossein Saeidian, Xiang Wang, et al.
The Journal of Allergy and Clinical Immunology|August 8, 2009
17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestryJames H Flory, Patrick M Sleiman, Jason D Christie, et al.
Pageof 10

Showing results (71-80 of 95) with videos related to

Sort By:
Pageof 10
Gene|October 11, 2025
Genome-wide association study and HLA genotyping for beryllium disease susceptibility in a European descent populationShu-Yi Liao, Tasha E Fingerlin, Sean Jacobson, et al.
Journal of Medical Genetics|March 5, 2024
<i>NASP</i> gene contributes to autism by epigenetic dysregulation of neural and immune pathwaysSipeng Zhang, Jie Yang, Dandan Ji, et al.
Frontiers in Immunology|June 15, 2026
Identification of <i>IL7R</i> as a key genetic risk locus in childhood steroid-sensitive nephrotic syndrome and IgA nephropathyCong Wang, Yue Jiang, Yingchao Song, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCsCarolina Gracia-Diaz, Jonathan E Perdomo, Munir E Khan, et al.
Plos One|September 18, 2015
The Role of ARF6 in Biliary AtresiaMylarappa Ningappa, Juhoon So, Joseph Glessner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participantsAmir Hossein Saeidian, Michael E March, Leila Youssefian, et al.
Nature Communications|September 20, 2017
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma riskXiao Chang, Yan Zhao, Cuiping Hou, et al.
Human Molecular Genetics|January 4, 2015
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemiaMinal J Menezes, Yiran Guo, Jianguo Zhang, et al.
Genetics in Medicine Open|March 5, 2026
Single vs dual genetic disease in children with congenital anomalies and solid tumorsDeborah J Watson, Amir Hossein Saeidian, Xiang Wang, et al.
The Journal of Allergy and Clinical Immunology|August 8, 2009
17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestryJames H Flory, Patrick M Sleiman, Jason D Christie, et al.
Pageof 10