Mary D. King - Concepedia

Author

Mary D. King

Temple Street Children's University Hospital

Also Known As

Chinnamma Chakiath, Claudio M de Gusmão, King, Mary, M King, MARY D KING, Martyn King, Mary Clavey, Mary D King, Mary D. King, Mary Dolores King

140

Publications

9.3K

Citations

H-Index

Concepts

All Affiliations

Temple Street Children's University Hospital University College Dublin University College London Children's Health Ireland at Crumlin Our Lady's Hospital

About

Mary D. King is an author at Temple Street Children's University Hospital specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	30	3.5K
2	Social Sciences	5	5	324
3	Public Health	4	4	669
4	Health Sciences	3	3	191
5	Nursing	1	1	96

Mary D. King

Publications

7.6K

Citations

H-Index

Page 1

	Year	Citations
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection Yanick J. Crow, Andrea Leitch, Bruce E. Hayward, Nature Genetics Ribonuclease H2Viral EvolutionGenetic DisorderNeurovirologyGenetics	2006	666
Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i> Yanick J. Crow, Diana Chase, Johanna L. Schmidt, American Journal of Medical Genetics Part A	2015	589
Balance and Strength Training in Older Adults: Intervention Gains and Tai Chi Maintenance Leslie Wolfson, Robert Whipple, Carol A. Derby, Journal of the American Geriatrics Society	1996	516
Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome Gillian Rice, Teresa Patrick, Rekha Parmar, The American Journal of Human Genetics CardiomyopathyHeart FailureCardiorenal SyndromesCardiovascular DiseaseMolecular Phenotype	2007	442
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Nature Genetics Rare DiseasesMendelian DisorderGenetic DisorderGeneticsPathology	2012	417
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy Mikko Muona, Samuel F. Berkovic, Leanne M. Dibbens, Nature Genetics GeneticsNeuroscienceCentral Nervous SystemMedicinePotassium Homeostasis	2014	311
Effect of Dissemination of Evidence in Reducing Injuries from Falls Mary E. Tinetti, Dorothy I. Baker, Mary D. King, New England Journal of Medicine	2008	255
Improving Delivery of Acute Stroke Therapy Lewis B. Morgenstern, Lara Staub, Wenyaw Chan, Stroke	2002	252
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia Yasmin Namavar, P. G. Barth, Paul R. Kasher, Brain	2010	222
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 A. Reghan Foley, Manoj P. Menezes, Amelie Pandraud, Brain Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMendelian DisorderNeurological DisorderGenetic Disorder	2013	179

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