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Neda Gharani

Showing results (1-10 of 20) with videos related to

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Human Fertility (Cambridge, England)|February 15, 2002
Pathogenesis of polycystic ovary syndrome: evidence for a genetically determined disorder of ovarian androgen productionStephen Franks, Carole Gilling-Smith, Neda Gharani, et al.
American Journal of Human Genetics|March 20, 2003
Estimation and testing of parent-of-origin effects for quantitative traitsJohn C Whittaker, Neda Gharani, Peter Hindmarsh, et al.
Frontiers in Bioinformatics|March 27, 2024
ursaPGx: a new R package to annotate pharmacogenetic star alleles using phased whole-genome sequencing dataGennaro Calendo, Dara Kusic, Jozef Madzo, et al.
Journal of Personalized Medicine|March 6, 2021
Common Treatment, Common Variant: Evolutionary Prediction of Functional Pharmacogenomic VariantsLaura B Scheinfeldt, Andrew Brangan, Dara M Kusic, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|March 8, 2005
Three autism candidate genes: a synthesis of human genetic analysis with other disciplinesChristopher W Bartlett, Neda Gharani, James H Millonig, et al.
Behavior Genetics|December 13, 2005
Cognitive traits link to human chromosomal regionsSteven Buyske, Marsha E Bates, Neda Gharani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2011
Genetic risk estimation in the Coriell Personalized Medicine CollaborativeCatharine B Stack, Neda Gharani, Erynn S Gordon, et al.
Biological Psychiatry|July 21, 2009
Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2Rym Benayed, Jiyeon Choi, Paul G Matteson, et al.
Genome Medicine|October 19, 2013
The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation systemNeda Gharani, Margaret A Keller, Catharine B Stack, et al.
Biorxiv : the Preprint Server for Biology|July 16, 2025
New iPSC resource with long-read whole genome sequencing characterizations for enhanced in vitro modelingLaura Scheinfeldt, Anthony Pompetti, Gennaro Calendo, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Human Fertility (Cambridge, England)|February 15, 2002
Pathogenesis of polycystic ovary syndrome: evidence for a genetically determined disorder of ovarian androgen productionStephen Franks, Carole Gilling-Smith, Neda Gharani, et al.
American Journal of Human Genetics|March 20, 2003
Estimation and testing of parent-of-origin effects for quantitative traitsJohn C Whittaker, Neda Gharani, Peter Hindmarsh, et al.
Frontiers in Bioinformatics|March 27, 2024
ursaPGx: a new R package to annotate pharmacogenetic star alleles using phased whole-genome sequencing dataGennaro Calendo, Dara Kusic, Jozef Madzo, et al.
Journal of Personalized Medicine|March 6, 2021
Common Treatment, Common Variant: Evolutionary Prediction of Functional Pharmacogenomic VariantsLaura B Scheinfeldt, Andrew Brangan, Dara M Kusic, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|March 8, 2005
Three autism candidate genes: a synthesis of human genetic analysis with other disciplinesChristopher W Bartlett, Neda Gharani, James H Millonig, et al.
Behavior Genetics|December 13, 2005
Cognitive traits link to human chromosomal regionsSteven Buyske, Marsha E Bates, Neda Gharani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2011
Genetic risk estimation in the Coriell Personalized Medicine CollaborativeCatharine B Stack, Neda Gharani, Erynn S Gordon, et al.
Biological Psychiatry|July 21, 2009
Autism-associated haplotype affects the regulation of the homeobox gene, ENGRAILED 2Rym Benayed, Jiyeon Choi, Paul G Matteson, et al.
Genome Medicine|October 19, 2013
The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation systemNeda Gharani, Margaret A Keller, Catharine B Stack, et al.
Biorxiv : the Preprint Server for Biology|July 16, 2025
New iPSC resource with long-read whole genome sequencing characterizations for enhanced in vitro modelingLaura Scheinfeldt, Anthony Pompetti, Gennaro Calendo, et al.
Pageof 2