Deborah Raymond - Concepedia

Author

Deborah Raymond

Also Known As

D R Raymond, D Raymond, D. Raymond, DANGO Julien Raymond, Dalton Raymond, Deborah Raymond, Farah Kausar, Misty Wethington, Raymond, Deborah

147

Publications

7.3K

Citations

H-Index

Concepts

All Affiliations

Mount Sinai Beth Israel Icahn School of Medicine at Mount Sinai Albert Einstein College of Medicine Columbia University Tel Aviv University

About

Deborah Raymond is an author at Mount Sinai Beth Israel specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	23	3K
2	Social Sciences	4	4	292
3	Health Sciences	2	2	110
4	Public Health	2	2	49
5	Natural Sciences	1	1	71

Deborah Raymond

Publications

6.9K

Citations

H-Index

Page 1

	Year	Citations
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein Laurie J. Ozelius, Jeffrey Hewett, Curtis E. Page, Nature Genetics Molecular NeuroscienceMolecular PhysiologyAtp-binding ProteinGeneticsPhysiology	1997	1K
The <i>DYT1</i> phenotype and guidelines for diagnostic testing Susan Bressman, Chiara Sabatti, Deborah Raymond, Neurology	2000	360
Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia Tania Fuchs, Sophie Gavarini, Rachel Saunders‐Pullman, Nature Genetics Thap1 GeneDevelopmental BiologyGeneticsMolecular GeneticsMedicine	2009	330
Mutations in GNAL cause primary torsion dystonia Tania Fuchs, Rachel Saunders‐Pullman, Ikuo Masuho, Nature Genetics Mendelian DisorderGenetic DisorderParkinson DiseaseGeneticsDegenerative Disease	2012	318
The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene Alison Brashear, William B. Dobyns, Patrícia de Carvalho Aguiar, Brain	2007	274
Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families Laura Almasy, Susan Bressman, Deborah Raymond, Annals of Neurology	1997	179
Arm swing as a potential new prodromal marker of Parkinson's disease Anat Mirelman, Hagar Bernad‐Elazari, Avner Thaler, Movement Disorders	2016	178
The p.L302P mutation in the lysosomal enzyme gene <i>SMPD1</i> is a risk factor for Parkinson disease Ziv Gan‐Or, Laurie J. Ozelius, Anat Bar‐Shira, Neurology	2013	175
Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study Susan Bressman, Deborah Raymond, Tania Fuchs, The Lancet Neurology Early-onset DystoniaGenetic DisorderGeneticsDegenerative DiseaseMotor Disorder	2009	172
Age-specific penetrance of<i>LRRK2</i>G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium Karen Marder, Yuanjia Wang, Roy N. Alcalay, Neurology	2015	164

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