Susan Bressman

27.6k total citations · 4 hit papers
212 papers, 14.7k citations indexed

About

Susan Bressman is a scholar working on Neurology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Susan Bressman has authored 212 papers receiving a total of 14.7k indexed citations (citations by other indexed papers that have themselves been cited), including 179 papers in Neurology, 103 papers in Cellular and Molecular Neuroscience and 28 papers in Physiology. Recurrent topics in Susan Bressman's work include Neurological disorders and treatments (133 papers), Parkinson's Disease Mechanisms and Treatments (91 papers) and Genetic Neurodegenerative Diseases (85 papers). Susan Bressman is often cited by papers focused on Neurological disorders and treatments (133 papers), Parkinson's Disease Mechanisms and Treatments (91 papers) and Genetic Neurodegenerative Diseases (85 papers). Susan Bressman collaborates with scholars based in United States, Israel and Germany. Susan Bressman's co-authors include Stanley Fahn, Laurie J. Ozelius, Deborah Raymond, Rachel Saunders‐Pullman, Neil Risch, Christine Klein, Mitchell F. Brin, Robert E. Burke, David Eidelberg and Alberto Albanese and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and Nature Genetics.

In The Last Decade

Susan Bressman

209 papers receiving 14.3k 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.

Phenomenology and classification of dystonia: A consensus update

2013 1.5k citations Susan Bressman, Stanley Fahn et al. Movement Disorders profile →
Validity and reliability of a rating scale for the primary torsion dystonias

1985 848 citations Robert E. Burke, Stanley Fahn et al. Neurology profile →
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 →
Anti–Tumor Necrosis Factor Therapy and Incidence of Parkinson Disease Among Patients With Inflammatory Bowel Disease

2018 286 citations Inga Peter, Susan Bressman et al. JAMA Neurology profile →

Peers

Susan Bressman

NEURO

CMN

NEURO

PHYSI

Alberto Albanese Italy

Marie Vidailhet France

Vladimir Kostić Serbia

Christine Klein Germany

A. Destée France

Lüdger Schöls Germany

Elan D. Louis United States

Timothy Schallert United States

Paolo Barone Italy

Janice L. Holton United Kingdom

Alberto Albanese Italy

Susan Bressman

12.0k ×1.1

NEURO

5.7k ×0.8

CMN

1.8k ×0.9

2.2k ×1.3

NEURO

1.5k ×1.0

PHYSI

Citations per year, relative to Susan Bressman Susan Bressman (= 1×) peers Alberto Albanese

Countries citing papers authored by Susan Bressman

Since Specialization

Citations

This map shows the geographic impact of Susan Bressman'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 Susan Bressman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Susan Bressman more than expected).

Fields of papers citing papers by Susan Bressman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susan Bressman. 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 Susan Bressman. The network helps show where Susan Bressman may publish in the future.

Co-authorship network of co-authors of Susan Bressman

This figure shows the co-authorship network connecting the top 25 collaborators of Susan Bressman. A scholar is included among the top collaborators of Susan Bressman 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 Susan Bressman. Susan Bressman 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

Vo, An, Nha Nguyen, Koji Fujita, et al.. (2023). Disordered network structure and function in dystonia: pathological connectivity vs. adaptive responses. Cerebral Cortex. 33(11). 6943–6958. 6 indexed citations

Picillo, Marina, David-Erick Lafontant, Susan Bressman, et al.. (2021). Sex-Related Longitudinal Change of Motor, Non-Motor, and Biological Features in Early Parkinson’s Disease. Journal of Parkinson s Disease. 12(1). 421–436. 21 indexed citations

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

Arystarkhova, Elena, Ihtsham Haq, Fanny Mochel, et al.. (2019). Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition. Neurobiology of Disease. 132. 104577–104577. 28 indexed citations

Lencz, Todd, Jin Yu, Cameron D. Palmer, et al.. (2018). High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation. Human Genetics. 137(4). 343–355. 15 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

Fujita, Koji, Wataru Sako, An Vo, Susan Bressman, & David Eidelberg. (2017). Disruption of network for visual perception of natural motion in primary dystonia. Human Brain Mapping. 39(3). 1163–1174. 4 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

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.

Nuenen, Bart F.L. van, Rick C. Helmich, Murielle Ferraye, et al.. (2012). Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism. Brain. 135(12). 3687–3698. 25 indexed citations

12.

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

13.

Panov, Fedor, Michele Tagliati, Laurie J. Ozelius, et al.. (2011). Pallidal deep brain stimulation for DYT6 dystonia. Journal of Neurology Neurosurgery & Psychiatry. 83(2). 182–187. 60 indexed citations

14.

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

15.

Ozelius, Laurie J., Christine Klein, Jeffrey Hewett, et al.. (1999). The TOR1A (DYT1) Gene Family and Its Role in Early Onset Torsion Dystonia. Genomics. 62(3). 377–384. 119 indexed citations

16.

Brin, Mitchell F., D. de Leon, Limborskaia Sa, et al.. (1998). De Novo Mutations (GAG Deletion) in the DYT1 Gene in Two Non-Jewish Patients with Early-onset Dystonia. Human Molecular Genetics. 7(7). 1133–1136. 47 indexed citations

17.

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 →

18.

Comella, Cynthia, Glenn T. Stebbins, Christopher G. Goetz, et al.. (1997). Teaching tape for the motor section of the toronto western spasmodic torticollis scale. Movement Disorders. 12(4). 570–575. 139 indexed citations

19.

Kramer, Patricia L., Deborah de Leon, Laurie J. Ozelius, et al.. (1990). Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34. Annals of Neurology. 27(2). 114–120. 109 indexed citations

20.

Bressman, Susan, et al.. (1988). Clonazepam, Haloperidol, and Clonidine in Tic Disorders. Southern Medical Journal. 81(9). 1103–1105. 23 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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