Rabi Tawil - Concepedia

Author

Rabi Tawil

University of Rochester Medical Center ORCID

Also Known As

Al-Rabi Tawil, Jeffrey M. Statland, Mathula Thangarajh, Muscle Study Group, Nuran Dilek, R C Griggs, R Tawil, R. Tawil, RABI TAWIL, Rabi N Tawil

305

Publications

20.1K

Citations

H-Index

137

Concepts

All Affiliations

University of Rochester Medical Center Leiden University Medical Center University of Rochester Fred Hutch Cancer Center Radboud University Nijmegen

About

Rabi Tawil is an author at University of Rochester Medical Center specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	49	7.7K
2	Health Sciences	10	10	1.1K
3	Natural Sciences	10	10	777
4	Arts	1	1	23
5	Engineering	1	1	65

Rabi Tawil

147

Publications

16.9K

Citations

H-Index

Page 1

	Year	Citations
Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome Nikki Plaster, Rabi Tawil, Martin Tristani‐Firouzi, Cell Episodic Electrical PhenotypesDevelopmental BiologyGenetic DisorderGeneticsPhysiology	2001	991
A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy Richard J.L.F. Lemmers, Patrick J. van der Vliet, Rinse Klooster, Science Facioscapulohumeral Muscular DystrophyDevelopmental BiologyMendelian DisorderFshd PatientsGenetic Disorder	2010	756
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2 Richard J.L.F. Lemmers, Rabi Tawil, Lisa M. Petek, Nature Genetics Rare DiseasesDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2012	641
Interferon‐α/β–mediated innate immune mechanisms in dermatomyositis Steven A. Greenberg, Jack L. Pinkus, Geraldine S. Pinkus, Annals of Neurology	2005	602
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) Martin Tristani‐Firouzi, Judy L. Jensen, Matthew R. Donaldson, Journal of Clinical Investigation	2002	537
Facioscapulohumeral Dystrophy: Incomplete Suppression of a Retrotransposed Gene Lauren Snider, Linda N. Geng, Richard J.L.F. Lemmers, PLoS Genetics Skeletal Muscle CellsTranscriptional RegulationMendelian DisorderSkeletal MuscleGenetic Disorder	2010	479
DUX4 Activates Germline Genes, Retroelements, and Immune Mediators: Implications for Facioscapulohumeral Dystrophy Linda N. Geng, Zizhen Yao, Lauren Snider, Developmental Cell Immune MediatorsGenetic DisorderGeneticsFacioscapulohumeral DystrophyGenomic Mechanism	2011	464
A phase I/IItrial of MYO‐029 in adult subjects with muscular dystrophy Kathryn R. Wagner, James L. Fleckenstein, Anthony A. Amato, Annals of Neurology	2008	457
Identification of a mutation in the gene causing hyperkalemic periodic paralysis Louis J. Ptáček, Alfred L. George, Robert C. Griggs, Cell Mendelian DisorderGenetic DisorderGeneticsPhysiologyMedicine	1991	388
An expanded version of the Hammersmith Functional Motor Scale for SMA II and III patients Jessica O’Hagen, Allan M. Glanzman, Michael McDermott, Neuromuscular Disorders Stroke RehabilitationSpinal Cord InjurySma IiApplied PhysiologyRehabilitation	2007	380

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