Deborah Raymond

7.4k total citations · 1 hit paper
81 papers, 4.0k citations indexed

About

Deborah Raymond is a scholar working on Neurology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Deborah Raymond has authored 81 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Neurology, 37 papers in Cellular and Molecular Neuroscience and 15 papers in Physiology. Recurrent topics in Deborah Raymond's work include Neurological disorders and treatments (45 papers), Parkinson's Disease Mechanisms and Treatments (38 papers) and Genetic Neurodegenerative Diseases (31 papers). Deborah Raymond is often cited by papers focused on Neurological disorders and treatments (45 papers), Parkinson's Disease Mechanisms and Treatments (38 papers) and Genetic Neurodegenerative Diseases (31 papers). Deborah Raymond collaborates with scholars based in United States, Israel and Germany. Deborah Raymond's co-authors include Susan Bressman, Laurie J. Ozelius, Rachel Saunders‐Pullman, Neil Risch, Stanley Fahn, Mitchell F. Brin, Tania Fuchs, Gary A. Heiman, James F. Gusella and Christine Klein and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Deborah Raymond

79 papers receiving 3.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

1997 770 citations Laurie J. Ozelius, Jeffrey Hewett et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Deborah Raymond United States	34	3.2k	2.3k	680	453	381	81	4.0k
Alexander Zimprich Austria	32	1.6k 0.5×	1.4k 0.6×	1.1k 1.7×	551 1.2×	504 1.3×	76	3.3k
Niccolò E. Mencacci United Kingdom	25	1.3k 0.4×	798 0.4×	675 1.0×	426 0.9×	245 0.6×	58	2.1k
Grazia Annesi Italy	27	1.2k 0.4×	1.2k 0.6×	1.1k 1.6×	263 0.6×	259 0.7×	94	2.7k
Jørgen E. Nielsen Denmark	31	1.6k 0.5×	1.4k 0.6×	1.6k 2.4×	964 2.1×	683 1.8×	150	3.8k
Katja Hedrich Germany	25	1.7k 0.5×	1.1k 0.5×	436 0.6×	199 0.4×	421 1.1×	35	2.1k
Patricia L. Kramer United States	20	1.6k 0.5×	1.3k 0.6×	483 0.7×	220 0.5×	264 0.7×	31	2.3k
Katrin Bürk Germany	37	1.6k 0.5×	2.8k 1.3×	2.4k 3.5×	175 0.4×	477 1.3×	73	3.7k
Marina Frontali Italy	29	1.3k 0.4×	2.0k 0.9×	1.8k 2.6×	156 0.3×	314 0.8×	81	3.0k
Nutan Sharma United States	27	1.8k 0.6×	1.4k 0.6×	618 0.9×	256 0.6×	246 0.6×	90	2.6k
E. R. Brunt Netherlands	35	1.2k 0.4×	2.6k 1.2×	2.7k 4.0×	165 0.4×	291 0.8×	55	3.7k

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-authorship network of co-authors of Deborah Raymond

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah Raymond. A scholar is included among the top collaborators of Deborah Raymond based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Deborah Raymond. Deborah Raymond is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Raymond, Deborah, Emma L Thorn, David Russell, et al.. (2024). Multiple sclerosis in LRRK2 G2019S Parkinson’s disease and isolated nigral degeneration in a homozygous variant carrier. Frontiers in Neurology. 15. 1450654–1450654. 2 indexed citations

Raymond, Deborah, Barbara Plitnick, Jennifer Brons, et al.. (2024). Supplemental ambient lighting intervention to improve sleep in Parkinson's disease: A pilot trial. Parkinsonism & Related Disorders. 129. 107149–107149. 3 indexed citations

Raymond, Deborah, Rachel S. Gerber, Barbara Plitnick, et al.. (2023). Pilot Tailored Lighting Intervention on Sleep Disturbances in Parkinson disease (P7-11.014). Neurology. 100(17_supplement_2).

Mor‐Shaked, Hagar, et al.. (2020). Benign SLC39A14 Course of Dystonia‐Parkinsonism Secondary to Inherited Manganese Accumulation. Movement Disorders Clinical Practice. 7(5). 569–570. 6 indexed citations

Saunders‐Pullman, Rachel, Anat Mirelman, Roy N. Alcalay, et al.. (2018). Progression in the LRRK2-Associated Parkinson Disease Population. JAMA Neurology. 75(3). 312–312. 94 indexed citations

Bodamer, Olaf A., Britt Johnson, William C. Nichols, et al.. (2015). Peripheral ß-glucocerebrosidase enzyme activity and lipidomics in ß-glucocerebrosidase (GBA1) mutation Parkinson disease (P2.149). Neurology. 84(14_supplement). 2 indexed citations

Saunders‐Pullman, Rachel, Anat Mirelman, Cuiling Wang, et al.. (2014). Olfactory identification in LRRK 2 G2019S mutation carriers: a relevant marker?. Annals of Clinical and Translational Neurology. 1(9). 670–678. 27 indexed citations

Marder, Karen, Ming‐Xin Tang, Roy N. Alcalay, et al.. (2014). Age Specific Penetrance of the LRRK2 G2019S Mutation in the Michael J Fox Ashkenazi Jewish (AJ) LRRK2 Consortium (S17.002). Neurology. 82(10_supplement). 3 indexed citations

Alcalay, Roy N., Anat Mirelman, Rachel Saunders‐Pullman, et al.. (2013). Parkinson Disease Phenotype in Ashkenazi Jews with and without LRRK2 Mutations (S13.004). Neurology. 80(7_supplement). 1 indexed citations

10.

Barrett, Matthew J., J. Hagenah, Vijay Dhawan, et al.. (2012). Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease. Parkinsonism & Related Disorders. 19(2). 186–191. 21 indexed citations

11.

Luciano, Marta San, Laurie J. Ozelius, Richard B. Lipton, et al.. (2011). Gender differences in the IL6 −174G>C and ESR2 1730G>A polymorphisms and the risk of Parkinson's disease. Neuroscience Letters. 506(2). 312–316. 14 indexed citations

12.

Saunders‐Pullman, Rachel, Kaili Stanley, Marta San Luciano, et al.. (2011). Gender differences in the risk of familial parkinsonism: Beyond LRRK2?. Neuroscience Letters. 496(2). 125–128. 20 indexed citations

13.

Brüggemann, Norbert, Johann Hagenah, Kaili Stanley, et al.. (2011). Substantia nigra hyperechogenicity with LRRK2 G2019S mutations. Movement Disorders. 26(5). 885–888. 29 indexed citations

14.

Bressman, Susan, Deborah Raymond, Tania Fuchs, et al.. (2009). Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study. The Lancet Neurology. 8(5). 441–446. 119 indexed citations

15.

Fuchs, Tania, Sophie Gavarini, Rachel Saunders‐Pullman, et al.. (2009). Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia. Nature Genetics. 41(3). 286–288. 207 indexed citations

16.

Raymond, Deborah, Rachel Saunders‐Pullman, Patrícia de Carvalho Aguiar, et al.. (2008). Phenotypic spectrum and sex effects in eleven myoclonus‐dystonia families with ε‐sarcoglycan mutations. Movement Disorders. 23(4). 588–592. 35 indexed citations

17.

Saunders‐Pullman, Rachel, Deborah Raymond, Geetha Senthil, et al.. (2007). Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish–Mennonites. American Journal of Medical Genetics Part A. 143A(18). 2098–2105. 48 indexed citations

18.

Nygaard, Torbjoern G., Deborah Raymond, Caiping Chen, et al.. (1999). Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31. Annals of Neurology. 46(5). 794–798. 71 indexed citations

19.

Ozelius, Laurie J., Jeffrey Hewett, Susan Bressman, et al.. (1997). The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nature Genetics. 17(1). 40–48. 770 indexed citations breakdown →

20.

Almasy, Laura, Susan Bressman, Deborah Raymond, et al.. (1997). Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families. Annals of Neurology. 42(4). 670–673. 116 indexed citations

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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