Mark McCormack - Concepedia

Author

Mark McCormack

Royal College of Surgeons in Ireland ORCID

Also Known As

Andreja Avbersek, Arif Shukralla, J McCormack, James McCormack, M McCormack, M. McCormack, M. T. McCormack, Marissa J McCormack, Mark McCormack, McCormack, M

Publications

Citations

H-Index

Concepts

All Affiliations

Royal College of Surgeons in Ireland Beaumont Hospital University Medical Center Utrecht University College London Université Libre de Bruxelles

About

Mark McCormack is an author at Royal College of Surgeons in Ireland specializing in medicine, neurogenetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	3.1K
2	Natural Sciences	2	2	627
3	Public Health	1	1	2K
4	Social Sciences	1	1	49
5	Allergy	1	1	152

Mark McCormack

Publications

5.6K

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
HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans Mark McCormack, Ana Alfirevic, Stéphane Bourgeois, New England Journal of Medicine	2011	899
Natural selection on <i>EPAS1</i> ( <i>HIF2α</i> ) associated with low hemoglobin concentration in Tibetan highlanders Cynthia M. Beall, Gianpiero L. Cavalleri, Libin Deng, Proceedings of the National Academy of Sciences	2010	824
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek, Nature Communications Epilepsy TherapiesGeneticsGenetic EpidemiologyMolecular GeneticsMonogenic Epilepsy Genes	2018	493
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott, The American Journal of Human Genetics Allelic VariantUltra-rare Genetic VariationWhole-exome Sequencing StudyGeneticsGenetic Disorder	2019	298
Distinct HLA associations of LGI1 and CASPR2-antibody diseases Sophie Binks, James Varley, Wanseon Lee, Brain HlaHistocompatibilityClinical ImmunologyImmunohematologyImmunodeficiencies	2018	152
TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function Fernando Gómez-Herreros, Janneke Schuurs-Hoeijmakers, Mark McCormack, Nature Genetics Molecular NeuroscienceMolecular RegulationNatural SciencesMolecular BiologyCell Death	2014	134
Tibetans living at sea level have a hyporesponsive hypoxia-inducible factor system and blunted physiological responses to hypoxia Nayia Petousi, Quentin P. P. Croft, Gianpiero L. Cavalleri, Journal of Applied Physiology	2013	133
Exome Sequencing Followed by Large-Scale Genotyping Fails to Identify Single Rare Variants of Large Effect in Idiopathic Generalized Epilepsy Erin L. Heinzen, Chantal Depondt, Gianpiero L. Cavalleri, The American Journal of Human Genetics	2012	100
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia Ida E. Sønderby, Ómar Gústafsson, Nhat Trung Doan, Molecular Psychiatry	2018	73

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