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Judith Conroy

Showing results (21-30 of 33) with videos related to

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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.
Epilepsia|December 10, 2015
Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansionNicholas M Allen, Judith Conroy, Amre Shahwan, et al.
Inflammatory Bowel Diseases|June 28, 2024
HLA-DQA1*05 Allele Carriage and Anti-TNF Therapy Persistence in Inflammatory Bowel DiseaseJayne Doherty, Anthony W Ryan, Emma Quinn, et al.
Epilepsia|May 16, 2014
Towards the identification of a genetic basis for Landau-Kleffner syndromeJudith Conroy, Paul A McGettigan, Dara McCreary, et al.
Human Mutation|September 9, 2011
First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotypeJillian Casey, Riki Kawaguchi, Maria Morrissey, et al.
Clinical Transplantation|February 26, 2013
A genome-wide association study of recipient genotype and medium-term kidney allograft functionRobert P O'Brien, Paul J Phelan, Judith Conroy, et al.
European Journal of Human Genetics : EJHG|April 30, 2015
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility lociCiara Coleman, Emma M Quinn, Anthony W Ryan, et al.
Nature Genetics|March 25, 2014
TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural functionFernando Gómez-Herreros, Janneke H M Schuurs-Hoeijmakers, Mark McCormack, et al.
Brain : a Journal of Neurology|October 21, 2017
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathiesSilvia Masnada, Ulrike B S Hedrich, Elena Gardella, et al.
American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
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.
Epilepsia|December 10, 2015
Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansionNicholas M Allen, Judith Conroy, Amre Shahwan, et al.
Inflammatory Bowel Diseases|June 28, 2024
HLA-DQA1*05 Allele Carriage and Anti-TNF Therapy Persistence in Inflammatory Bowel DiseaseJayne Doherty, Anthony W Ryan, Emma Quinn, et al.
Epilepsia|May 16, 2014
Towards the identification of a genetic basis for Landau-Kleffner syndromeJudith Conroy, Paul A McGettigan, Dara McCreary, et al.
Human Mutation|September 9, 2011
First implication of STRA6 mutations in isolated anophthalmia, microphthalmia, and coloboma: a new dimension to the STRA6 phenotypeJillian Casey, Riki Kawaguchi, Maria Morrissey, et al.
Clinical Transplantation|February 26, 2013
A genome-wide association study of recipient genotype and medium-term kidney allograft functionRobert P O'Brien, Paul J Phelan, Judith Conroy, et al.
European Journal of Human Genetics : EJHG|April 30, 2015
Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility lociCiara Coleman, Emma M Quinn, Anthony W Ryan, et al.
Nature Genetics|March 25, 2014
TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural functionFernando Gómez-Herreros, Janneke H M Schuurs-Hoeijmakers, Mark McCormack, et al.
Brain : a Journal of Neurology|October 21, 2017
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathiesSilvia Masnada, Ulrike B S Hedrich, Elena Gardella, et al.
American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.
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