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Stephen W Scherer

Showing results (61-70 of 499) with videos related to

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Seminars in Pediatric Neurology|May 18, 2011
The Cerebral Palsy Demonstration Project: a multidimensional research approach to cerebral palsyMichael Shevell, Steven P Miller, Stephen W Scherer, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 19, 2026
Large Models for Small Tables: Adapting Tabular Foundation Models to EHR DataRui Zhu, Xiaopu Zhou, Ivy Liang, et al.
Human Mutation|October 23, 2012
Mechanisms of formation of structural variation in a fully sequenced human genomeAndy Wing Chun Pang, Ohsuke Migita, Jeffrey R Macdonald, et al.
Cell|December 28, 2020
Phase Separation as a Missing Mechanism for Interpretation of Disease MutationsBrian Tsang, Iva Pritišanac, Stephen W Scherer, et al.
International Journal of Cardiology|November 10, 2015
Rare copy number variations in an adult with transposition of the great arteries emphasize the importance of updated genetic assessments in syndromic congenital cardiac diseaseGregory Costain, S Lucy Roche, Stephen W Scherer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autismJohn B Vincent, Sandy Thevarkunnel, Debbie Kolozsvari, et al.
BMC Bioinformatics|May 27, 2011
A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV dataTakeshi Nishiyama, Kunihiko Takahashi, Toshiro Tango, et al.
Human Molecular Genetics|August 8, 2002
Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genomeXavier Estivill, Joseph Cheung, Miguel Angel Pujana, et al.
Human Molecular Genetics|August 6, 2008
Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissuesLayla Parker-Katiraee, Eleni Bousiaki, David Monk, et al.
Genome Biology|September 12, 2025
Diverse short tandem repeat sequences influence gene regulation in human populationsAleksandra Mitina, Worrawat Engchuan, Brett Trost, et al.
Pageof 50

Showing results (61-70 of 499) with videos related to

Sort By:
Pageof 50
Seminars in Pediatric Neurology|May 18, 2011
The Cerebral Palsy Demonstration Project: a multidimensional research approach to cerebral palsyMichael Shevell, Steven P Miller, Stephen W Scherer, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 19, 2026
Large Models for Small Tables: Adapting Tabular Foundation Models to EHR DataRui Zhu, Xiaopu Zhou, Ivy Liang, et al.
Human Mutation|October 23, 2012
Mechanisms of formation of structural variation in a fully sequenced human genomeAndy Wing Chun Pang, Ohsuke Migita, Jeffrey R Macdonald, et al.
Cell|December 28, 2020
Phase Separation as a Missing Mechanism for Interpretation of Disease MutationsBrian Tsang, Iva Pritišanac, Stephen W Scherer, et al.
International Journal of Cardiology|November 10, 2015
Rare copy number variations in an adult with transposition of the great arteries emphasize the importance of updated genetic assessments in syndromic congenital cardiac diseaseGregory Costain, S Lucy Roche, Stephen W Scherer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autismJohn B Vincent, Sandy Thevarkunnel, Debbie Kolozsvari, et al.
BMC Bioinformatics|May 27, 2011
A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV dataTakeshi Nishiyama, Kunihiko Takahashi, Toshiro Tango, et al.
Human Molecular Genetics|August 8, 2002
Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genomeXavier Estivill, Joseph Cheung, Miguel Angel Pujana, et al.
Human Molecular Genetics|August 6, 2008
Dynamic variation in allele-specific gene expression of Paraoxonase-1 in murine and human tissuesLayla Parker-Katiraee, Eleni Bousiaki, David Monk, et al.
Genome Biology|September 12, 2025
Diverse short tandem repeat sequences influence gene regulation in human populationsAleksandra Mitina, Worrawat Engchuan, Brett Trost, et al.
Pageof 50