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Simon G Gregory

Showing results (81-90 of 142) with videos related to

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Journal of Child Psychology and Psychiatry, and Allied Disciplines|January 19, 2026
Evaluating placebo responses to intranasal oxytocin in autism: findings from the placebo lead-in phase of a randomised controlled trialKelsie A Boulton, Rinku Thapa, Yun Ju Song, et al.
Human Molecular Genetics|January 22, 2008
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasetsBeth S Sutton, David R Crosslin, Svati H Shah, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 3, 2008
Refinement of 2q and 7p loci in a large multiplex NTD familyDemetra S Stamm, Deborah G Siegel, Lorraine Mehltretter, et al.
Oncotarget|November 30, 2010
Integrated genomic analyses identify ERRFI1 and TACC3 as glioblastoma-targeted genesChristopher G Duncan, Patrick J Killela, Cathy A Payne, et al.
Plos One|May 3, 2011
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophyYi-Ju Li, Mollie A Minear, Jacqueline Rimmler, et al.
Clinical Epigenetics|January 31, 2021
Genetic, epigenetic, and environmental factors controlling oxytocin receptor gene expressionJoshua S Danoff, Kelly L Wroblewski, Andrew J Graves, et al.
Nucleic Acids Research|August 10, 2022
Resistance of mitochondrial DNA to cadmium and Aflatoxin B1 damage-induced germline mutation accumulation in C. elegansTess C Leuthner, Laura Benzing, Brendan F Kohrn, et al.
American Journal of Human Genetics|December 29, 2009
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9pS Amer Riazuddin, Norann A Zaghloul, Amr Al-Saif, et al.
International Journal of Cancer|September 15, 2005
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGHCaroline Jarbo, Patrick G Buckley, Arkadiusz Piotrowski, et al.
BMC Genetics|February 29, 2012
Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5Daniel K Nolan, Beth Sutton, Carol Haynes, et al.
Pageof 15

Showing results (81-90 of 142) with videos related to

Sort By:
Pageof 15
Journal of Child Psychology and Psychiatry, and Allied Disciplines|January 19, 2026
Evaluating placebo responses to intranasal oxytocin in autism: findings from the placebo lead-in phase of a randomised controlled trialKelsie A Boulton, Rinku Thapa, Yun Ju Song, et al.
Human Molecular Genetics|January 22, 2008
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasetsBeth S Sutton, David R Crosslin, Svati H Shah, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 3, 2008
Refinement of 2q and 7p loci in a large multiplex NTD familyDemetra S Stamm, Deborah G Siegel, Lorraine Mehltretter, et al.
Oncotarget|November 30, 2010
Integrated genomic analyses identify ERRFI1 and TACC3 as glioblastoma-targeted genesChristopher G Duncan, Patrick J Killela, Cathy A Payne, et al.
Plos One|May 3, 2011
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophyYi-Ju Li, Mollie A Minear, Jacqueline Rimmler, et al.
Clinical Epigenetics|January 31, 2021
Genetic, epigenetic, and environmental factors controlling oxytocin receptor gene expressionJoshua S Danoff, Kelly L Wroblewski, Andrew J Graves, et al.
Nucleic Acids Research|August 10, 2022
Resistance of mitochondrial DNA to cadmium and Aflatoxin B1 damage-induced germline mutation accumulation in C. elegansTess C Leuthner, Laura Benzing, Brendan F Kohrn, et al.
American Journal of Human Genetics|December 29, 2009
Missense mutations in TCF8 cause late-onset Fuchs corneal dystrophy and interact with FCD4 on chromosome 9pS Amer Riazuddin, Norann A Zaghloul, Amr Al-Saif, et al.
International Journal of Cancer|September 15, 2005
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGHCaroline Jarbo, Patrick G Buckley, Arkadiusz Piotrowski, et al.
BMC Genetics|February 29, 2012
Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5Daniel K Nolan, Beth Sutton, Carol Haynes, et al.
Pageof 15