Deborah Raymond

7.5k citations

82 papers · 4.0k · 1 hit paper · h-index 34

Impact in

Neurology top 0.2%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
- Botulinum Toxin and Related Neurological Disorders
Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders

Papers in

Neurology 56
- Neurological disorders and treatments 36
- Parkinson's Disease Mechanisms and Treatments 27
- Botulinum Toxin and Related Neurological Disorders 4
Cellular and Molecular Neuroscience 27
- Genetic Neurodegenerative Diseases 22
- Hereditary Neurological Disorders 5

Co-authors: Susan Bressman (70 shared papers)Laurie J. Ozelius (46 shared papers)Rachel Saunders‐Pullman (61 shared papers)Neil Risch (11 shared papers)Stanley Fahn (7 shared papers)Mitchell F. Brin (8 shared papers)Tania Fuchs (5 shared papers)Christine Klein (9 shared papers)
Journals: Neurology (22 papers)Movement Disorders (13 papers)Annals of Neurology (5 papers)Parkinsonism & Related Disorders (5 papers)Nature Genetics (3 papers)
Partner nations: United States Israel Germany

In The Last Decade

Deborah Raymond

81 papers receiving 3.9k citations

Deborah Raymond's Hit Papers

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The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein 1997 · 771 citations

Peers

Countries citing papers authored by Deborah Raymond

Since Specialization

Citations

This map shows the geographic impact of Deborah Raymond's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Deborah Raymond with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deborah Raymond more than expected).

Fields of papers citing papers by Deborah Raymond

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah Raymond. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Deborah Raymond. The network helps show where Deborah Raymond may publish in the future.

Co-authors

The 25 scholars most cited alongside Deborah Raymond, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Deborah Raymond Line = papers co-authored together Deborah Raymond links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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#	Work
1	The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein Nature Genetics ·Laurie J. Ozelius, Jeffrey Hewett, Curtis E. Page, Susan Bressman, Patricia L. Kramer, Christo Shalish, Deborah de Leon, Mitchell F. Brin, Deborah Raymond, David P. Corey, Stanley Fahn, Neil Risch, Alan Buckler, James F. Gusella, Xandra O. Breakefield Hit paper breakdown →	1997	771
2	The DYT1 phenotype and guidelines for diagnostic testing Neurology ·Susan Bressman, Chiara Sabatti, Deborah Raymond, D. de Leon, Christine Klein, P. L. Kramer, Mitchell F. Brin, Stanley Fahn, Xandra O. Breakefield, Laurie J. Ozelius, Neil Risch	2000	242
3	Mutations in GNAL cause primary torsion dystonia Nature Genetics ·Tania Fuchs, Rachel Saunders‐Pullman, Ikuo Masuho, Marta San Luciano, Deborah Raymond, Stewart A. Factor, Anthony E. Lang, Tsao‐Wei Liang, Richard Trosch, Sierra R. White, E Ainehsazan, Denis Hervé, Nutan Sharma, Michelle E. Ehrlich, Kirill A. Martemyanov, Susan Bressman, Laurie J. Ozelius	2012	212
4	Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia Nature Genetics ·Tania Fuchs, Sophie Gavarini, Rachel Saunders‐Pullman, Deborah Raymond, Michelle E. Ehrlich, Susan Bressman, Laurie J. Ozelius	2009	210
5	The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene Brain ·Alison Brashear, William B. Dobyns, Patrícia de Carvalho Aguiar, Michael Borg, Catharina J.M. Frijns, Seema Gollamudi, Andrew Green, João Tiago Guimarães, Birgit-Gaye Haake, Christine Klein, Gurutz Linazasoro, A. Münchau, Deborah Raymond, David E. Riley, R. Saunders-Pullman, Marina A.J. Tijssen, David Webb, Jacek Zaremba, Susan Bressman, Laurie J. Ozelius	2007	168
6	The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease Neurology ·Ziv Gan‐Or, Laurie J. Ozelius, Anat Bar‐Shira, Rachel Saunders‐Pullman, Anat Mirelman, Ruth Kornreich, Mali Gana‐Weisz, Deborah Raymond, Liron Rozenkrantz, Andres Deik, Tanya Gurevich, Susan J. Gross, Nicole Schreiber‐Agus, Nir Giladi, Susan Bressman, Avi Orr‐Urtreger	2013	131
7	Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study The Lancet Neurology ·Susan Bressman, Deborah Raymond, Tania Fuchs, Gary A. Heiman, Laurie J. Ozelius, Rachel Saunders‐Pullman	2009	119
8	Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families Annals of Neurology ·Laura Almasy, Susan Bressman, Deborah Raymond, P. L. Kramer, P. Greene, Gary A. Heiman, B. Ford, J. Yount, D. de Leon, Sylvain Chouinard, Rachel Saunders‐Pullman, Mitchell F. Brin, Rahul Kapoor, A. C. Jones, Hongzhe Shen, Stanley Fahn, Neil Risch, Torbjoern G. Nygaard	1997	116
9	Progression in the LRRK2-Associated Parkinson Disease Population JAMA Neurology ·Rachel Saunders‐Pullman, Anat Mirelman, Roy N. Alcalay, Cuiling Wang, (unknown), Deborah Raymond, Helen Mejia‐Santana, Martha Orbe‐Reilly, Brooke Johannes, Avner Thaler, Laurie J. Ozelius, Avi Orr‐Urtreger, Karen Marder, Nir Giladi, Susan Bressman	2018	100
10	Regional metabolism in primary torsion dystonia Neurology ·Maren Carbon, Sherwin L. Su, Vijay Dhawan, Deborah Raymond, Susan Bressman, David Eidelberg	2004	97
11	Myoclonus dystonia Neurology ·Rachel Saunders‐Pullman, Janet Shriberg, Gary A. Heiman, Deborah Raymond, Kristin J. Wendt, P. L. Kramer, Karla Schilling, Roger Kurlan, Christine Klein, Laurie J. Ozelius, Neil Risch, Susan Bressman	2002	90
12	Primary dystonia: Is abnormal functional brain architecture linked to genotype? Annals of Neurology ·Maja Trošt, Maren Carbon, Christine Edwards, Yilong Ma, Deborah Raymond, Marc J. Mentis, James R. Moeller, Susan Bressman, David Eidelberg	2002	86
13	Abnormal striatal and thalamic dopamine neurotransmission Neurology ·Maren Carbon, Martin Niethammer, Shoujiao Peng, Deborah Raymond, Vijay Dhawan, Thomas Chaly, Yilong Ma, Susan Bressman, David Eidelberg	2009	86
14	Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31 Annals of Neurology ·Torbjoern G. Nygaard, Deborah Raymond, Caiping Chen, Ichizo Nishino, Paul Greene, Danna Jennings, Gary A. Heiman, Christine Klein, Rachel J. Saunders-Pullman, Patricia Kramer, Laurie J. Ozelius, Susan Bressman	1999	72
15	Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites Neurology ·Rachel Saunders‐Pullman, Deborah Raymond, A. Jon Stoessl, Douglas E. Hobson, Toshitaka Nakamura, Seth L. Pullman, D Lefton, Michael S. Okun, Ryan J. Uitti, Rivka Sachdev, Kaili Stanley, (unknown), J. Hagenah, Richard A. Gatti, Laurie J. Ozelius, Susan Bressman	2012	66
16	Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers Neurology ·Christopher W. Hess, Deborah Raymond, Patrícia de Carvalho Aguiar, Steven J. Frucht, Janet Shriberg, Gary A. Heiman, Roger Kurlan, Christine Klein, Susan Bressman, Laurie J. Ozelius, Rachel Saunders‐Pullman	2007	66
17	High mutation rate in dopa-responsive dystonia: Detection with comprehensive GCHI screening Neurology ·J. Hagenah, Rachel Saunders‐Pullman, Katja Hedrich, Kemal Kabakci, Kristin Habermann, Karin Wiegers, K. Mohrmann, Thora Lohnau, Deborah Raymond, P. Vieregge, T G Nygaard, L. J. Ozelius, S. B. Bressman, Christine Klein	2005	65
18	Age at onset as a factor in determining the phenotype of primary torsion dystonia Neurology ·Séan O’Riordan, Deborah Raymond, Timothy Lynch, Rachel Saunders‐Pullman, Susan Bressman, L. Daly, Michael Hutchinson	2004	63
19	Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression JAMA Network Open ·(unknown), Cuiling Wang, Deborah Raymond, Nicole Bryant, Clemens R. Scherzer, Avner Thaler, Roy N. Alcalay, Andrew B. West, Anat Mirelman, Yuliya I. Kuras, Karen Marder, Nir Giladi, Laurie J. Ozelius, Susan Bressman, Rachel Saunders‐Pullman	2021	56
20	Diagnostic criteria for dystonia in DYT1 families Neurology ·Susan Bressman, Deborah Raymond, Kristin J. Wendt, Rachel Saunders‐Pullman, D. de Leon, Stanley Fahn, Laurie J. Ozelius, Neil Risch	2002	54

About Deborah Raymond

Deborah Raymond is a scholar working on Neurology, Cellular and Molecular Neuroscience, Physiology, Molecular Biology and Rheumatology, having authored 82 papers that have together received 4.0k indexed citations. Recurring topics across this work include Neurological disorders and treatments (36 papers), Parkinson's Disease Mechanisms and Treatments (27 papers), Genetic Neurodegenerative Diseases (22 papers), Lysosomal Storage Disorders Research (11 papers), Glycogen Storage Diseases and Myoclonus (9 papers), Hereditary Neurological Disorders (5 papers), Autism Spectrum Disorder Research (4 papers) and Botulinum Toxin and Related Neurological Disorders (4 papers). The work is most often cited by research in Neurology (3.0k citations), Cellular and Molecular Neuroscience (1.9k citations), Neurology (299 citations), Clinical Biochemistry (115 citations) and Cell Biology (271 citations). Deborah Raymond has collaborated with scholars based in United States, Israel and Germany. Frequent co-authors include Susan Bressman, Laurie J. Ozelius, Rachel Saunders‐Pullman, Neil Risch, Stanley Fahn, Mitchell F. Brin, Tania Fuchs, Christine Klein, Gary A. Heiman and James F. Gusella. Their work appears in journals such as Neurology, Movement Disorders, Annals of Neurology, Parkinsonism & Related Disorders and Nature Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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