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Seth I Berger

Showing results (11-20 of 61) with videos related to

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BMC Bioinformatics|October 6, 2007
Genes2Networks: connecting lists of gene symbols using mammalian protein interactions databasesSeth I Berger, Jeremy M Posner, Avi Ma'ayan
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2026
Response to Spurdle et alSeth I Berger, Georgia Pitsava, Changrui Xiao, et al.
Bioinformatics (Oxford, England)|August 17, 2010
ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experimentsAlexander Lachmann, Huilei Xu, Jayanth Krishnan, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Sequencing approaches in hereditary cancer testing: strengths, limitations and future directionsSami Belhadj, Christopher J Hatch, Holly LaDuca, et al.
Nanotechnology|June 26, 2025
Computer vision techniques for high-speed atomic force microscopy of DNA moleculesNicholas Driver, Andrey Mikheikin, Sean Koebley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 21, 2020
A systematic review of monogenic etiologies of nonimmune hydrops fetalisAndrea M Quinn, Breanna N Valcarcel, Mona M Makhamreh, et al.
Human Mutation|September 17, 2020
Functional analysis of Sonic Hedgehog variants associated with holoprosencephaly in humans using a CRISPR/Cas9 zebrafish modelSungkook Hong, Ping Hu, Jae Hee Jang, et al.
Prenatal Diagnosis|October 30, 2023
PIEZO1 is the most common monogenic etiology of non-immune hydrops fetalis detected by prenatal exome sequencingCasey J Brewer, Mona M Makhamreh, Kavya Shivashankar, et al.
Molecular Genetics and Metabolism|August 27, 2022
Fetal pharmacogenomics: A promising addition to complex neonatal careMegan Raymond, Elizabeth Critchlow, Stephanie M Rice, et al.
Orphanet Journal of Rare Diseases|July 10, 2025
Lysosomal storage disorders in nonimmune hydrops fetalis diagnosed by exome sequencingMona M Makhamreh, Kavya Shivashankar, Stephanie M Rice, et al.
Pageof 7

Showing results (11-20 of 61) with videos related to

Sort By:
Pageof 7
BMC Bioinformatics|October 6, 2007
Genes2Networks: connecting lists of gene symbols using mammalian protein interactions databasesSeth I Berger, Jeremy M Posner, Avi Ma'ayan
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2026
Response to Spurdle et alSeth I Berger, Georgia Pitsava, Changrui Xiao, et al.
Bioinformatics (Oxford, England)|August 17, 2010
ChEA: transcription factor regulation inferred from integrating genome-wide ChIP-X experimentsAlexander Lachmann, Huilei Xu, Jayanth Krishnan, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
Sequencing approaches in hereditary cancer testing: strengths, limitations and future directionsSami Belhadj, Christopher J Hatch, Holly LaDuca, et al.
Nanotechnology|June 26, 2025
Computer vision techniques for high-speed atomic force microscopy of DNA moleculesNicholas Driver, Andrey Mikheikin, Sean Koebley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 21, 2020
A systematic review of monogenic etiologies of nonimmune hydrops fetalisAndrea M Quinn, Breanna N Valcarcel, Mona M Makhamreh, et al.
Human Mutation|September 17, 2020
Functional analysis of Sonic Hedgehog variants associated with holoprosencephaly in humans using a CRISPR/Cas9 zebrafish modelSungkook Hong, Ping Hu, Jae Hee Jang, et al.
Prenatal Diagnosis|October 30, 2023
PIEZO1 is the most common monogenic etiology of non-immune hydrops fetalis detected by prenatal exome sequencingCasey J Brewer, Mona M Makhamreh, Kavya Shivashankar, et al.
Molecular Genetics and Metabolism|August 27, 2022
Fetal pharmacogenomics: A promising addition to complex neonatal careMegan Raymond, Elizabeth Critchlow, Stephanie M Rice, et al.
Orphanet Journal of Rare Diseases|July 10, 2025
Lysosomal storage disorders in nonimmune hydrops fetalis diagnosed by exome sequencingMona M Makhamreh, Kavya Shivashankar, Stephanie M Rice, et al.
Pageof 7