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Harrison Brand

Showing results (31-40 of 87) with videos related to

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American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Genome Research|May 15, 2024
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Defining a tandem repeat catalog and variation clusters for genome-wide analysesBen Weisburd, Egor Dolzhenko, Mark F Bennett, et al.
HGG Advances|September 18, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2023
Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial cleftingKimberly K Diaz Perez, Sarah W Curtis, Alba Sanchis-Juan, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
American Journal of Human Genetics|April 23, 2026
Defining a tandem repeat catalog and variation clusters for genome-wide analyses and population databasesBen Weisburd, Egor Dolzhenko, Mark F Bennett, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
American Journal of Human Genetics|October 18, 2016
Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal DiagnosisZehra Ordulu, Tammy Kammin, Harrison Brand, et al.
Pageof 9

Showing results (31-40 of 87) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|October 7, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Genome Research|May 15, 2024
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Defining a tandem repeat catalog and variation clusters for genome-wide analysesBen Weisburd, Egor Dolzhenko, Mark F Bennett, et al.
HGG Advances|September 18, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 18, 2023
Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial cleftingKimberly K Diaz Perez, Sarah W Curtis, Alba Sanchis-Juan, et al.
Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palateKelsey Robinson, Trenell J Mosley, Kenneth S Rivera-González, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
American Journal of Human Genetics|April 23, 2026
Defining a tandem repeat catalog and variation clusters for genome-wide analyses and population databasesBen Weisburd, Egor Dolzhenko, Mark F Bennett, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disordersArthur S Lee, Lauren J Ayers, Michael Kosicki, et al.
American Journal of Human Genetics|October 18, 2016
Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal DiagnosisZehra Ordulu, Tammy Kammin, Harrison Brand, et al.
Pageof 9