Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Judith Conroy

Showing results (11-20 of 33) with videos related to

Pageof 4
Sort By:
Geroscience|January 7, 2023
Genes encoding agrin (AGRN) and neurotrypsin (PRSS12) are associated with muscle mass, strength and plasma C-terminal agrin fragment concentrationJedd Pratt, Laura Whitton, Anthony Ryan, et al.
Plos One|November 29, 2012
HGDP and HapMap analysis by Ancestry Mapper reveals local and global population relationshipsTiago R Magalhães, Jillian P Casey, Judith Conroy, et al.
American Journal of Human Genetics|December 29, 2005
Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorderZiarih Hawi, Ricardo Segurado, Judith Conroy, et al.
Journal of Human Genetics|May 20, 2016
Novel European SLC1A4 variant: infantile spasms and population ancestry analysisJudith Conroy, Nicholas M Allen, Kathleen Gorman, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|May 1, 2013
High-resolution genome-wide copy-number analyses identify localized copy-number alterations in Ewing sarcomaMiriam Lynn, Yuexiang Wang, Jaime Slater, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected childrenKatharina Domschke, Karen Sheehan, Naomi Lowe, et al.
Molecular Genetics and Metabolism|May 22, 2012
Identification of a mutation in LARS as a novel cause of infantile hepatopathyJillian P Casey, Paul McGettigan, Niamh Lynam-Lennon, et al.
European Journal of Human Genetics : EJHG|August 29, 2013
A novel locus for episodic ataxia:UBR4 the likely candidateJudith Conroy, Paul McGettigan, Raymond Murphy, et al.
Epilepsy & Behavior Case Reports|August 10, 2016
Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorderNicholas M Allen, Judith Conroy, Thierry Deonna, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2009
Association of the alpha4 integrin subunit gene (ITGA4) with autismCatarina Correia, Ana M Coutinho, Joana Almeida, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Geroscience|January 7, 2023
Genes encoding agrin (AGRN) and neurotrypsin (PRSS12) are associated with muscle mass, strength and plasma C-terminal agrin fragment concentrationJedd Pratt, Laura Whitton, Anthony Ryan, et al.
Plos One|November 29, 2012
HGDP and HapMap analysis by Ancestry Mapper reveals local and global population relationshipsTiago R Magalhães, Jillian P Casey, Judith Conroy, et al.
American Journal of Human Genetics|December 29, 2005
Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorderZiarih Hawi, Ricardo Segurado, Judith Conroy, et al.
Journal of Human Genetics|May 20, 2016
Novel European SLC1A4 variant: infantile spasms and population ancestry analysisJudith Conroy, Nicholas M Allen, Kathleen Gorman, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|May 1, 2013
High-resolution genome-wide copy-number analyses identify localized copy-number alterations in Ewing sarcomaMiriam Lynn, Yuexiang Wang, Jaime Slater, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected childrenKatharina Domschke, Karen Sheehan, Naomi Lowe, et al.
Molecular Genetics and Metabolism|May 22, 2012
Identification of a mutation in LARS as a novel cause of infantile hepatopathyJillian P Casey, Paul McGettigan, Niamh Lynam-Lennon, et al.
European Journal of Human Genetics : EJHG|August 29, 2013
A novel locus for episodic ataxia:UBR4 the likely candidateJudith Conroy, Paul McGettigan, Raymond Murphy, et al.
Epilepsy & Behavior Case Reports|August 10, 2016
Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorderNicholas M Allen, Judith Conroy, Thierry Deonna, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 5, 2009
Association of the alpha4 integrin subunit gene (ITGA4) with autismCatarina Correia, Ana M Coutinho, Joana Almeida, et al.
Pageof 4