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Edwin H Cook

Showing results (121-130 of 205) with videos related to

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American Journal of Medical Genetics|September 5, 2002
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA networkBernie Devlin, Pamela Bennett, Edwin H Cook, et al.
Plos One|December 16, 2016
A Quantitative Electrophysiological Biomarker of Duplication 15q11.2-q13.1 SyndromeJoel Frohlich, Damla Senturk, Vidya Saravanapandian, et al.
European Journal of Human Genetics : EJHG|August 5, 2004
Genome-wide association study identifies ITGB3 as a QTL for whole blood serotoninLauren A Weiss, Jeremy Veenstra-Vanderweele, Dina L Newman, et al.
Neuroscience Letters|September 17, 2005
Family-based association study of DAT1 and DRD4 polymorphism in Korean children with ADHDYoung Shin Kim, Bennett L Leventhal, Soo-Jeong Kim, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 14, 2003
Homocysteine, pharmacogenetics, and neurotoxicity in children with leukemiaShinji Kishi, James Griener, Cheng Cheng, et al.
Blood|September 13, 2003
Effects of prednisone and genetic polymorphisms on etoposide disposition in children with acute lymphoblastic leukemiaShinji Kishi, Wenjian Yang, Benoit Boureau, et al.
Journal of Child and Adolescent Psychopharmacology|August 12, 2015
Pharmacogenetic Study of Serotonin Transporter and 5HT2A Genotypes in AutismFedra Najjar, Thomas Owley, Matthew W Mosconi, et al.
JAACAP Open|September 9, 2025
Maternal Serotonin Levels and Neurodevelopmental Severity in Autistic Children: A Partial Replication and ExtensionAmandeep Jutla, Lauren C Shuffrey, Stephen J Guter, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 20, 2010
Effect of dopamine transporter genotype on caudate volume in childhood ADHD and controlsDevon Shook, Colin Brady, Philip S Lee, et al.
Journal of Medical Genetics|June 24, 2009
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autismRavinesh A Kumar, Jyotsna Sudi, Timothy D Babatz, et al.
Pageof 21

Showing results (121-130 of 205) with videos related to

Sort By:
Pageof 21
American Journal of Medical Genetics|September 5, 2002
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA networkBernie Devlin, Pamela Bennett, Edwin H Cook, et al.
Plos One|December 16, 2016
A Quantitative Electrophysiological Biomarker of Duplication 15q11.2-q13.1 SyndromeJoel Frohlich, Damla Senturk, Vidya Saravanapandian, et al.
European Journal of Human Genetics : EJHG|August 5, 2004
Genome-wide association study identifies ITGB3 as a QTL for whole blood serotoninLauren A Weiss, Jeremy Veenstra-Vanderweele, Dina L Newman, et al.
Neuroscience Letters|September 17, 2005
Family-based association study of DAT1 and DRD4 polymorphism in Korean children with ADHDYoung Shin Kim, Bennett L Leventhal, Soo-Jeong Kim, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|August 14, 2003
Homocysteine, pharmacogenetics, and neurotoxicity in children with leukemiaShinji Kishi, James Griener, Cheng Cheng, et al.
Blood|September 13, 2003
Effects of prednisone and genetic polymorphisms on etoposide disposition in children with acute lymphoblastic leukemiaShinji Kishi, Wenjian Yang, Benoit Boureau, et al.
Journal of Child and Adolescent Psychopharmacology|August 12, 2015
Pharmacogenetic Study of Serotonin Transporter and 5HT2A Genotypes in AutismFedra Najjar, Thomas Owley, Matthew W Mosconi, et al.
JAACAP Open|September 9, 2025
Maternal Serotonin Levels and Neurodevelopmental Severity in Autistic Children: A Partial Replication and ExtensionAmandeep Jutla, Lauren C Shuffrey, Stephen J Guter, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 20, 2010
Effect of dopamine transporter genotype on caudate volume in childhood ADHD and controlsDevon Shook, Colin Brady, Philip S Lee, et al.
Journal of Medical Genetics|June 24, 2009
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autismRavinesh A Kumar, Jyotsna Sudi, Timothy D Babatz, et al.
Pageof 21