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Harrison Brand

Showing results (21-30 of 87) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Cell|September 2, 2022
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 triosMarta Byrska-Bishop, Uday S Evani, Xuefang Zhao, et al.
Human Genetics|October 3, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Nature Communications|June 14, 2020
Functional annotation of rare structural variation in the human brainLide Han, Xuefang Zhao, Mary Lauren Benton, et al.
American Journal of Human Genetics|November 9, 2024
Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assemblyYulia Mostovoy, Philip M Boone, Yongqing Huang, et al.
American Journal of Human Genetics|March 31, 2021
Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologiesXuefang Zhao, Ryan L Collins, Wan-Ping Lee, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Transcriptomic profiling uncovers mis-splicing and gene fusions in amyotrophic lateral sclerosisHuilin Xu, Tiziana Petrozziello, Adel Boudi, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
Pageof 9

Showing results (21-30 of 87) with videos related to

Sort By:
Pageof 9
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Cell|September 2, 2022
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 triosMarta Byrska-Bishop, Uday S Evani, Xuefang Zhao, et al.
Human Genetics|October 3, 2024
Genome-wide study of gene-by-sex interactions identifies risks for cleft palateKelsey Robinson, Randy Parrish, Wasiu Lanre Adeyemo, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 triosKelsey R Robinson, Sarah W Curtis, Justin E Paschall, et al.
Nature Communications|June 14, 2020
Functional annotation of rare structural variation in the human brainLide Han, Xuefang Zhao, Mary Lauren Benton, et al.
American Journal of Human Genetics|November 9, 2024
Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assemblyYulia Mostovoy, Philip M Boone, Yongqing Huang, et al.
American Journal of Human Genetics|March 31, 2021
Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologiesXuefang Zhao, Ryan L Collins, Wan-Ping Lee, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Transcriptomic profiling uncovers mis-splicing and gene fusions in amyotrophic lateral sclerosisHuilin Xu, Tiziana Petrozziello, Adel Boudi, et al.
Human Molecular Genetics|October 31, 2025
Haploinsufficiency of GRHL2 is associated with orofacial clefting in humansSarah W Curtis, Cinderella Yang, Alba Sanchis-Juan, et al.
Pageof 9