Susan Bressman

27.6k citations

212 papers · 14.7k indexed · 4 hit papers · h-index 64

Neurology top 0.02%
- Neurological disorders and treatments 133
- Parkinson's Disease Mechanisms and Treatments 91
- Botulinum Toxin and Related Neurological Disorders 49
- Neurological diseases and metabolism 11
Cellular and Molecular Neuroscience top 0.1%
- Genetic Neurodegenerative Diseases 85
- Hereditary Neurological Disorders 21
Neurology top 0.2%
- Neurological disorders and treatments 133
- Parkinson's Disease Mechanisms and Treatments 91
- Botulinum Toxin and Related Neurological Disorders 49
- Neurological diseases and metabolism 11
Physiology top 1%
- Lysosomal Storage Disorders Research 21
Cognitive Neuroscience top 2%
Rheumatology
- Glycogen Storage Diseases and Myoclonus 11

Co-authors: Stanley Fahn Laurie J. Ozelius Deborah Raymond Rachel Saunders‐Pullman Neil Risch Christine Klein Mitchell F. Brin Robert E. Burke
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Movement Disorders (40 papers)Neurology (39 papers)Annals of Neurology (16 papers)
Partner nations: United States Israel Germany

In The Last Decade

Susan Bressman

209 papers receiving 14.3k citations

Hit Papers

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Peers

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

The 25 scholars most cited alongside Susan Bressman, 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 Susan Bressman Line = papers co-authored together Susan Bressman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Disordered network structure and function in dystonia: pathological connectivity vs. adaptive responses Cerebral Cortex ·An Vo,Nha Nguyen,Koji Fujita,Katharina A. Schindlbeck,Natalia Gozzano,Susan Bressman,Martin Niethammer,David Eidelberg	2023	6
2	Sex-Related Longitudinal Change of Motor, Non-Motor, and Biological Features in Early Parkinson’s Disease Journal of Parkinson s Disease ·Marina Picillo,(unknown),David-Erick Lafontant,Susan Bressman,Chelsea Caspell‐Garcia,Christopher S. Coffey,Phillipp Euskirchen,C. Dauccia,Nabila Dahodwala,Rachel Saunders‐Pullman,Caroline M. Tanner,Amy W. Amara	2021	21
3	Benign SLC39A14 Course of Dystonia‐Parkinsonism Secondary to Inherited Manganese Accumulation Movement Disorders Clinical Practice ·Aleksandra Pacowska,Bayu Witopo,Hagar Mor‐Shaked,Susan Bressman,Deborah Raymond,Laurie J. Ozelius,David Arkadir	2020	6
4	Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition Neurobiology of Disease ·Elena Arystarkhova,Ihtsham Haq,TR Soares,Fanny Mochel,Rachel Saunders‐Pullman,Susan Bressman,Konstantinos Varvarousis,Nitin Gupta,Jared Cook,Scott Demarest,Allison Brashear,Laurie J. Ozelius,Kathleen J. Sweadner	2019	28
5	High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation Human Genetics ·Todd Lencz,Jin Yu,Cameron D. Palmer,Shai Carmi,Danny Ben‐Avraham,Nir Barzilai,Susan Bressman,Ariel Darvasi,Judy H. Cho,Lorraine N. Clark,Zeynep H. Gümüş,Joseph Vijai,Robert J. Klein,Steven M. Lipkin,Kenneth Offit,Harry Ostrer,Laurie J. Ozelius,Inga Peter,Gil Atzmon,Itsik Pe’er	2018	15
6	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	94
7	Disruption of network for visual perception of natural motion in primary dystonia Human Brain Mapping ·Koji Fujita,Wataru Sako,An Vo,Susan Bressman,David Eidelberg	2017	4
8	Peripheral ß-glucocerebrosidase enzyme activity and lipidomics in ß-glucocerebrosidase (GBA1) mutation Parkinson disease (P2.149) Neurology ·G W Linse,Olaf A. Bodamer,Britt Johnson,William C. Nichols,Mariel Pullman,Robert Ortega,Brooke Johannes,Deborah Raymond,Laurie J. Ozelius,Jacek Bielawski,Susan Bressman,Lina M. Obeid,Yusuf A. Hannun,Rachel Saunders‐Pullman	2015	2
9	Parkinson Disease Phenotype in Ashkenazi Jews with and without LRRK2 Mutations (S13.004) Neurology ·Roy N. Alcalay,Anat Mirelman,Rachel Saunders‐Pullman,Ming‐Xin Tang,Helen Mejia‐Santana,Deborah Raymond,Sabine Kosub,Martha Orbe‐Reilly,Llency Rosado,Tanya Gurevich,Ziv Gan‐Or,Harshal Tamboli,Avi Orr‐Urtreger,Laurie J. Ozelius,Lorraine N. Clark,Nir Giladi,Susan Bressman,Karen Marder	2013	1
10	Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease Parkinsonism & Related Disorders ·Matthew J. Barrett,J. Hagenah,Vijay Dhawan,Shichun Peng,Kaili Stanley,Deborah Raymond,Andres Deik,Susan J. Gross,Nicole Schreiber‐Agus,Anat Mirelman,Karen Marder,Laurie J. Ozelius,David Eidelberg,Susan Bressman,Rachel Saunders‐Pullman	2012	21
11	Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism Brain ·Bart F.L. van Nuenen,Rick C. Helmich,Murielle Ferraye,Avner Thaler,Talma Hendler,Avi Orr‐Urtreger,Anat Mirelman,Susan Bressman,Karen Marder,Nir Giladi,Bart P.C. van de Warrenburg,Bastiaan R. Bloem,Ivan Toni	2012	25
12	Gender differences in the IL6 −174G>C and ESR2 1730G>A polymorphisms and the risk of Parkinson's disease Neuroscience Letters ·Marta San Luciano,Laurie J. Ozelius,Richard B. Lipton,Deborah Raymond,Susan Bressman,Rachel Saunders‐Pullman	2011	14
13	Pallidal deep brain stimulation for DYT6 dystonia Journal of Neurology Neurosurgery & Psychiatry ·Fedor Panov,Michele Tagliati,Laurie J. Ozelius,Tania Fuchs,Yakov Gologorsky,Tyler Cheung,Marat V. Avshalumov,Susan Bressman,Rachel Saunders‐Pullman,Donald J. Weisz,Ron L. Alterman	2011	60
14	Gender differences in the risk of familial parkinsonism: Beyond LRRK2? Neuroscience Letters ·Rachel Saunders‐Pullman,Kaili Stanley,Marta San Luciano,Matthew J. Barrett,Vicki Shanker,Deborah Raymond,Laurie J. Ozelius,Susan Bressman	2011	20
15	The TOR1A (DYT1) Gene Family and Its Role in Early Onset Torsion Dystonia Genomics ·Laurie J. Ozelius,M. L. Napolitano,Christine Klein,Jeffrey Hewett,Mari Mineta,Joanne Leung,Christo Shalish,Susan Bressman,Deborah de Leon,Mitchell F. Brin,Stanley Fahn,David P. Corey,Xandra O. Breakefield	1999	119
16	De Novo Mutations (GAG Deletion) in the DYT1 Gene in Two Non-Jewish Patients with Early-onset Dystonia Human Molecular Genetics ·Mattias Jonsson,Mitchell F. Brin,D. de Leon,Limborskaia Sa,I. A. Ivanova‐Smolenskaya,Susan Bressman,Alon Friedman,Elena D. Markova,Neil Risch,Xandra O. Breakefield,Laurie J. Ozelius	1998	47
17	The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding proteinbreakdown → Nature Genetics ·Laurie J. Ozelius,Jeffrey Hewett,M. L. Napolitano,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	1997	770
18	Teaching tape for the motor section of the toronto western spasmodic torticollis scale Movement Disorders ·Cynthia Comella,Glenn T. Stebbins,Christopher G. Goetz,Teresa A. Chmura,Susan Bressman,Anthony E. Lang	1997	139
19	Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34 Annals of Neurology ·Patricia L. Kramer,Deborah de Leon,Laurie J. Ozelius,Neil Risch,Susan Bressman,Mitchell F. Brin,Deborah E. Schuback,Robert E. Burke,David J. Kwiatkowski,Heidi Shale,James F. Gusella,Xandra O. Breakefield,Stanley Fahn	1990	109
20	Clonazepam, Haloperidol, and Clonidine in Tic Disorders Southern Medical Journal ·Eileen Dowse,Susan Bressman,Heidi Shale,S Fahn	1988	23

About Susan Bressman

Susan Bressman is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology, having authored 212 papers that have together received 14.7k indexed citations. Recurring topics across this work include Neurological disorders and treatments (133 papers), Parkinson's Disease Mechanisms and Treatments (91 papers), Genetic Neurodegenerative Diseases (85 papers), Botulinum Toxin and Related Neurological Disorders (49 papers), Hereditary Neurological Disorders (21 papers), Lysosomal Storage Disorders Research (21 papers), Neurological diseases and metabolism (11 papers) and Glycogen Storage Diseases and Myoclonus (11 papers). The work is most often cited by research in Neurology (11.4k citations), Cellular and Molecular Neuroscience (7.1k citations) and Neurology (1.7k citations). Susan Bressman has collaborated with scholars based in United States, Israel and Germany. Frequent 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. Their work appears in journals such as Movement Disorders, Neurology, Annals of Neurology, Brain and Parkinsonism & Related Disorders.

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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