Padhraig Gormley - Concepedia

Author

Padhraig Gormley

Also Known As

Analysis Team, Bridget Riley-Gillis, Denis Baird, Ellen Tsai, Emily Holzinger, Genetic Commission of the Italian League against Epilepsy, Geoff Kerchner, Gormley, P., John Eicher, Marjo-Riitta Järvelin

Publications

12.1K

Citations

H-Index

Concepts

All Affiliations

Massachusetts General Hospital Harvard University Institute for Molecular Medicine Finland University of Helsinki Broad Institute

About

Padhraig Gormley is an author at Massachusetts General Hospital specializing in medicine, neurogenetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	4.3K
2	Public Health	4	4	2.1K
3	Social Sciences	3	3	1.9K
4	Biostatistics	1	1	19
5	Cognitive Science	1	1	14

Padhraig Gormley

Publications

5.8K

Citations

H-Index

Page 1

	Year	Citations
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
De novo mutations in schizophrenia implicate synaptic networks Menachem Fromer, Andrew Pocklington, David H. Kavanagh, Nature Synaptic PlasticityPsychotic DisorderPsychiatric GeneticsSchizophreniaConnectomics	2014	1.7K
The phenotypic spectrum of <i>SCN8A</i> encephalopathy Jan Larsen, Gemma L. Carvill, Elena Gardella, Neurology	2015	282
De novo mutations in HCN1 cause early infantile epileptic encephalopathy Caroline Nava, Carine Dalle, Agnès Rastetter, Nature Genetics Genetic DisorderGeneticsNeuroscienceNeurologyNeuropathology	2014	230
De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome Arvid Suls, Johanna A. Jaehn, Angéla Kecskés, The American Journal of Human Genetics Chd2 CauseDravet SyndromeMolecular NeuroscienceNeurobiology Of DiseaseGenetic Disorder	2013	219
Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling Connor A. Emdin, Amit V. Khera, Derek Klarin, Circulation	2017	109
<i>CHD2</i> myoclonic encephalopathy is frequently associated with self-induced seizures Rhys H. Thomas, Lin Mei Zhang, Gemma L. Carvill, Neurology	2015	98
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families Padhraig Gormley, Mitja Kurki, Marjo Hiekkala, Neuron Family MedicineCluster HeadacheGenetic EpidemiologyNeurologyMedicine	2018	94
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy Costin Leu, Simona Balestrini, Bridget H. Maher, EBioMedicine	2015	84
Analysis of Shared Heritability in Common Disorders of the Brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2016	83

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