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Padhraig Gormley

Showing results (11-20 of 28) with videos related to

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Circulation|October 7, 2017
Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide SignalingConnor A Emdin, Amit V Khera, Derek Klarin, et al.
Nature Communications|January 26, 2019
Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern FinlandMitja I Kurki, Elmo Saarentaus, Olli Pietiläinen, et al.
Journal of Medical Genetics|July 31, 2017
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsiesEduardo Pérez-Palma, Ingo Helbig, Karl Martin Klein, et al.
Plos One|March 19, 2016
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy SyndromesDennis Lal, Eva M Reinthaler, Borislav Dejanovic, et al.
Genome Medicine|March 19, 2020
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disordersDennis Lal, Patrick May, Eduardo Perez-Palma, et al.
Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Ebiomedicine|October 27, 2015
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in EpilepsyCostin Leu, Simona Balestrini, Bridget Maher, et al.
Nature Genetics|April 22, 2014
De novo mutations in HCN1 cause early infantile epileptic encephalopathyCaroline Nava, Carine Dalle, Agnès Rastetter, et al.
Neuron|September 7, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
Neuron|May 8, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Circulation|October 7, 2017
Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide SignalingConnor A Emdin, Amit V Khera, Derek Klarin, et al.
Nature Communications|January 26, 2019
Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern FinlandMitja I Kurki, Elmo Saarentaus, Olli Pietiläinen, et al.
Journal of Medical Genetics|July 31, 2017
Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsiesEduardo Pérez-Palma, Ingo Helbig, Karl Martin Klein, et al.
Plos One|March 19, 2016
Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy SyndromesDennis Lal, Eva M Reinthaler, Borislav Dejanovic, et al.
Genome Medicine|March 19, 2020
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disordersDennis Lal, Patrick May, Eduardo Perez-Palma, et al.
Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Ebiomedicine|October 27, 2015
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in EpilepsyCostin Leu, Simona Balestrini, Bridget Maher, et al.
Nature Genetics|April 22, 2014
De novo mutations in HCN1 cause early infantile epileptic encephalopathyCaroline Nava, Carine Dalle, Agnès Rastetter, et al.
Neuron|September 7, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
Neuron|May 8, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
Pageof 3