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Andrew Skol

Showing results (1-10 of 16) with videos related to

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Experimental and Clinical Psychopharmacology|December 9, 2009
Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: an exploratory study with d-amphetamine in healthy participantsAjna Hamidovic, Andrea Dlugos, Andrew Skol, et al.
Neurotoxicology and Teratology|September 26, 2013
Do dopamine gene variants and prenatal smoking interactively predict youth externalizing behavior?T Caitlin O'Brien, Brian S Mustanski, Andrew Skol, et al.
Gastroenterology|July 28, 2010
Genetic heterogeneity in colorectal cancer associations between African and European americansSonia S Kupfer, Jeffrey R Anderson, Stanley Hooker, et al.
American Journal of Medical Genetics. Part A|April 10, 2024
Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysisKunal Kanwar, Saffiya Bashey, Brenda L Bohnsack, et al.
Genes|June 27, 2024
A Case of Non-Syndromic Congenital Cataracts Caused by a Novel <i>MAF</i> Variant in the C-Terminal DNA-Binding Domain-Case Report and Literature ReviewSharon H Zhao, Kai Lee Yap, Valerie Allegretti, et al.
Genes|August 28, 2025
<i>GPR143</i>-Associated Ocular Albinism in a Hispanic Family and Review of the LiteratureAnushree Aneja, Brenda L Bohnsack, Valerie Allegretti, et al.
Ophthalmic Genetics|May 6, 2026
Evaluating gene-disease relationship strength in crystallin genes in association with pediatric cataractsAlexander Ing, Allison Goetsch Weisman, Andy Drackley, et al.
Plos One|November 3, 2011
Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and CaucasiansSonia S Kupfer, Jeffrey R Anderson, Anton E Ludvik, et al.
Genes|May 4, 2026
A Case of Aymé-Gripp Syndromic Congenital Cataracts and Pigmentary Retinopathy Caused by a Novel MAF Variant in the N-Terminal Transactivation Domain-A Case Report and Literature ReviewMax Chauhan, Kaersti L Rickels, Sudhi P Kurup, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 6, 2009
Common and rare variants of DAOA in bipolar disorderManjula Maheshwari, Jiajun Shi, Judith A Badner, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Experimental and Clinical Psychopharmacology|December 9, 2009
Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: an exploratory study with d-amphetamine in healthy participantsAjna Hamidovic, Andrea Dlugos, Andrew Skol, et al.
Neurotoxicology and Teratology|September 26, 2013
Do dopamine gene variants and prenatal smoking interactively predict youth externalizing behavior?T Caitlin O'Brien, Brian S Mustanski, Andrew Skol, et al.
Gastroenterology|July 28, 2010
Genetic heterogeneity in colorectal cancer associations between African and European americansSonia S Kupfer, Jeffrey R Anderson, Stanley Hooker, et al.
American Journal of Medical Genetics. Part A|April 10, 2024
Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysisKunal Kanwar, Saffiya Bashey, Brenda L Bohnsack, et al.
Genes|June 27, 2024
A Case of Non-Syndromic Congenital Cataracts Caused by a Novel <i>MAF</i> Variant in the C-Terminal DNA-Binding Domain-Case Report and Literature ReviewSharon H Zhao, Kai Lee Yap, Valerie Allegretti, et al.
Genes|August 28, 2025
<i>GPR143</i>-Associated Ocular Albinism in a Hispanic Family and Review of the LiteratureAnushree Aneja, Brenda L Bohnsack, Valerie Allegretti, et al.
Ophthalmic Genetics|May 6, 2026
Evaluating gene-disease relationship strength in crystallin genes in association with pediatric cataractsAlexander Ing, Allison Goetsch Weisman, Andy Drackley, et al.
Plos One|November 3, 2011
Genetic associations in the vitamin D receptor and colorectal cancer in African Americans and CaucasiansSonia S Kupfer, Jeffrey R Anderson, Anton E Ludvik, et al.
Genes|May 4, 2026
A Case of Aymé-Gripp Syndromic Congenital Cataracts and Pigmentary Retinopathy Caused by a Novel MAF Variant in the N-Terminal Transactivation Domain-A Case Report and Literature ReviewMax Chauhan, Kaersti L Rickels, Sudhi P Kurup, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 6, 2009
Common and rare variants of DAOA in bipolar disorderManjula Maheshwari, Jiajun Shi, Judith A Badner, et al.
Pageof 2