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Louise Gallagher

Showing results (81-90 of 140) with videos related to

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Plos One|March 31, 2017
Vector-free intracellular delivery by reversible permeabilizationShirley O'Dea, Valeria Annibaldi, Louise Gallagher, et al.
Digital Health|March 31, 2025
Designing digital conversational agents for youth with multiple mental health conditions: Insights on key features from a youth-engaged qualitative descriptive studyJingyi Hou, Jamie Gibson, Thalia Phi, et al.
European Journal of Human Genetics : EJHG|May 3, 2012
CNVs leading to fusion transcripts in individuals with autism spectrum disorderRichard Holt, Nuala H Sykes, Inês C Conceição, et al.
Stem Cell Research|December 29, 2020
Derivation of iPSC lines from three young healthy donors of Caucasian origin (NUIGi035-A; NUIGi036-A; NUIGi037-A)Yicheng Ding, Berta Marcó de la Cruz, Veronica McInerney, 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.
Journal of Neurodevelopmental Disorders|June 21, 2021
Behavioral features in Prader-Willi syndrome (PWS): consensus paper from the International PWS Clinical Trial ConsortiumLauren Schwartz, Assumpta Caixàs, Anastasia Dimitropoulos, et al.
Stem Cell Research|November 24, 2019
Derivation of familial iPSC lines from three ASD patients carrying NRXN1α<sup>+/-</sup> and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B)Yicheng Ding, Berta Marcó de la Cruz, Yawen Xia, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 30, 2012
No evidence that common genetic risk variation is shared between schizophrenia and autismJacob A S Vorstman, Richard J L Anney, Eske M Derks, et al.
Neuroscience Letters|March 23, 2010
Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studiesKatherine E Tansey, Keeley J Brookes, Matthew J Hill, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 11, 2008
Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32Judith Conroy, Lynne Cochrane, Richard J L Anney, et al.
Pageof 14

Showing results (81-90 of 140) with videos related to

Sort By:
Pageof 14
Plos One|March 31, 2017
Vector-free intracellular delivery by reversible permeabilizationShirley O'Dea, Valeria Annibaldi, Louise Gallagher, et al.
Digital Health|March 31, 2025
Designing digital conversational agents for youth with multiple mental health conditions: Insights on key features from a youth-engaged qualitative descriptive studyJingyi Hou, Jamie Gibson, Thalia Phi, et al.
European Journal of Human Genetics : EJHG|May 3, 2012
CNVs leading to fusion transcripts in individuals with autism spectrum disorderRichard Holt, Nuala H Sykes, Inês C Conceição, et al.
Stem Cell Research|December 29, 2020
Derivation of iPSC lines from three young healthy donors of Caucasian origin (NUIGi035-A; NUIGi036-A; NUIGi037-A)Yicheng Ding, Berta Marcó de la Cruz, Veronica McInerney, 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.
Journal of Neurodevelopmental Disorders|June 21, 2021
Behavioral features in Prader-Willi syndrome (PWS): consensus paper from the International PWS Clinical Trial ConsortiumLauren Schwartz, Assumpta Caixàs, Anastasia Dimitropoulos, et al.
Stem Cell Research|November 24, 2019
Derivation of familial iPSC lines from three ASD patients carrying NRXN1α<sup>+/-</sup> and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B)Yicheng Ding, Berta Marcó de la Cruz, Yawen Xia, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 30, 2012
No evidence that common genetic risk variation is shared between schizophrenia and autismJacob A S Vorstman, Richard J L Anney, Eske M Derks, et al.
Neuroscience Letters|March 23, 2010
Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studiesKatherine E Tansey, Keeley J Brookes, Matthew J Hill, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 11, 2008
Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32Judith Conroy, Lynne Cochrane, Richard J L Anney, et al.
Pageof 14