Michael A. Simpson - Concepedia

Author

Michael A. Simpson

Also Known As

Alan H. Beggs, B M Mount, Crina Samarghitean, EuroEPINOMICS RES myoclonic astatic epilepsy working group, Hanns-Ulrich Marschall, Jonathan N. Barker, Katri Pylkäs, Lam C Tsoi, Lam C. Tsoi, Lara Abulhoul

391

Publications

38.8K

Citations

H-Index

223

Concepts

All Affiliations

King's College London Guy's Hospital University College London St George's, University of London Guy's and St Thomas' NHS Foundation Trust

About

Michael A. Simpson is an author at King's College London specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	43	67	7.8K
2	Education	3	3	98
3	Health Sciences	1	1	72
4	Language Studies	1	1	10
5	Law	1	1	10

Michael A. Simpson

154

Publications

14.9K

Citations

H-Index

Page 1

	Year	Citations
Assessment of Minimal Residual Disease in Standard-Risk AML Adam Ivey, Robert K. Hills, Michael A. Simpson, New England Journal of Medicine	2016	812
Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis Alexandros Onoufriadis, Michael A. Simpson, Andrew Pink, The American Journal of Human Genetics InflammationRheumatologyAutoimmune DiseaseGeneralized Pustular PsoriasisMedicine	2011	521
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) Pia Østergaard, Michael A. Simpson, Fiona Connell, Nature Genetics Hematological MalignancyGenetic DisorderMixed-phenotype Acute LeukemiaMalignant Blood DisorderHematology	2011	494
Structural Insights into Histone Demethylation by JMJD2 Family Members Zhongzhou Chen, Jianye Zang, Johnathan R. Whetstine, Cell Histone ModificationsChromatinChromatin StructureChromatin RemodelingNatural Sciences	2006	399
Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase Michael A. Simpson, Christos Proukakis, David A. Priestman, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsHomozygous Loss-of-function MutationNeuroscience	2004	381
Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting Liat Samuelov, Ofer Sarig, Robert M. Harmon, Nature Genetics AllergyAutoimmune DiseaseAtopic DermatitisDesmoglein 1Allergen	2013	330
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis Elisavet Fotiou, Silvia Martin‐Almedina, Michael A. Simpson, Nature Communications	2015	316
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia Karin Tuschl, Esther Meyer, Leonardo E. Valdivia, Nature Communications	2016	312
Novel Mutation in Desmoplakin Causes Arrhythmogenic Left Ventricular Cardiomyopathy Mark Norman, Michael A. Simpson, Jens Mogensen, Circulation	2005	307
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss Michael A. Simpson, Melita Irving, Esra Asilmaz, Nature Genetics Progressive Bone LossCraniofacial DisorderGenetic DisorderHematologyPathology	2011	306

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