Sharon Hassin‐Baer

8.0k total citations
127 papers, 2.8k citations indexed

About

Sharon Hassin‐Baer is a scholar working on Neurology, Cognitive Neuroscience and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sharon Hassin‐Baer has authored 127 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 88 papers in Neurology, 23 papers in Cognitive Neuroscience and 21 papers in Cellular and Molecular Neuroscience. Recurrent topics in Sharon Hassin‐Baer's work include Parkinson's Disease Mechanisms and Treatments (72 papers), Neurological disorders and treatments (33 papers) and Genetic Neurodegenerative Diseases (14 papers). Sharon Hassin‐Baer is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (72 papers), Neurological disorders and treatments (33 papers) and Genetic Neurodegenerative Diseases (14 papers). Sharon Hassin‐Baer collaborates with scholars based in Israel, United States and Canada. Sharon Hassin‐Baer's co-authors include Gilad Yahalom, Oren Cohen, Rivka Inzelberg, Simon Israeli‐Korn, Oren Cohen, Amos D. Korczyn, David Tanné, Oren S. Cohen, Gila Bronner and Zeev Nitsan and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Sharon Hassin‐Baer

123 papers receiving 2.7k citations

Peers

Sharon Hassin‐Baer

NEURO

CMN

NEURO

Giuseppe Moretto Italy

Vincenzo La Bella Italy

Ruwei Ou China

Jarosław Sławek Poland

Blair Ford United States

Sadako Kuno Japan

Roberta Marchese Italy

F. Carella Italy

Norbert Brüggemann Germany

Shigeki Kuzuhara Japan

Giuseppe Moretto Italy

Sharon Hassin‐Baer

1.2k ×0.7

NEURO

646 ×0.9

CMN

514 ×1.0

389 ×1.0

NEURO

250 ×0.7

Citations per year, relative to Sharon Hassin‐Baer Sharon Hassin‐Baer (= 1×) peers Giuseppe Moretto

Countries citing papers authored by Sharon Hassin‐Baer

Since Specialization

Citations

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

Fields of papers citing papers by Sharon Hassin‐Baer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sharon Hassin‐Baer. 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 Sharon Hassin‐Baer. The network helps show where Sharon Hassin‐Baer may publish in the future.

Co-authorship network of co-authors of Sharon Hassin‐Baer

This figure shows the co-authorship network connecting the top 25 collaborators of Sharon Hassin‐Baer. A scholar is included among the top collaborators of Sharon Hassin‐Baer 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 Sharon Hassin‐Baer. Sharon Hassin‐Baer 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

Senkevich, Konstantin, Eric Yu, Jamil Ahmad, et al.. (2024). Are rare heterozygous SYNJ1 variants associated with Parkinson’s disease?. npj Parkinson s Disease. 10(1). 201–201.

Lesman‐Segev, Orit H., Nofar Mor, Ortal Barel, et al.. (2023). Adult-onset Alexander disease among patients of Jewish Syrian descent. Neurogenetics. 24(4). 303–310. 3 indexed citations

Mardor, Yael, et al.. (2022). Advanced radiological investigation of levodopa- induced dyskinesia in Parkinson’s disease patients: assessment of blood brain barrier function. Neurology Asia. 27(2). 353–362. 1 indexed citations

Israeli‐Korn, Simon, et al.. (2020). Self‐motion perception in Parkinson's disease. European Journal of Neuroscience. 53(7). 2376–2387. 29 indexed citations

Wong, Darice Y., Claudio M. de Gusmão, May Sanyoura, et al.. (2020). Prevalence of RFC1 -mediated spinocerebellar ataxia in a North American ataxia cohort. Neurology Genetics. 6(3). e440–e440. 32 indexed citations

Israeli‐Korn, Simon, et al.. (2020). Visual self-motion cues are impaired yet overweighted during visual–vestibular integration in Parkinson’s disease. Brain Communications. 2(1). fcaa035–fcaa035. 30 indexed citations

Israeli‐Korn, Simon, et al.. (2020). Overconfidence in visual perception in parkinson's disease. European Journal of Neuroscience. 53(6). 2027–2039. 10 indexed citations

Rudakou, Uladzislau, Eric Yu, Lynne Krohn, et al.. (2020). Targeted sequencing of Parkinson’s disease loci genes highlights SYT11, FGF20 and other associations. Brain. 144(2). 462–472. 29 indexed citations

Yu, Eric, Uladzislau Rudakou, Lynne Krohn, et al.. (2020). Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease. Movement Disorders. 36(1). 178–187. 29 indexed citations

10.

Saini, Prabhjyot, Uladzislau Rudakou, Eric Yu, et al.. (2020). Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease. Neurobiology of Aging. 100. 119.e7–119.e13. 25 indexed citations

11.

Wong, Darice Y., Claudio M. de Gusmão, May Sanyoura, et al.. (2020). Prevalence of RFC1-Mediated Spinocerebellar Ataxia in a North American Ataxia Cohort. Annals of Neurology. 88. 3 indexed citations

12.

Hassin‐Baer, Sharon, et al.. (2019). The spectrum of tremor among carriers of the FMR1 premutation with or without the fragile X-associated tremor/ataxia syndrome (FXTAS). Parkinsonism & Related Disorders. 65. 32–38. 9 indexed citations

13.

Lerman, Sheera F., et al.. (2019). Catastrophizing mediates the relationship between non-motor symptoms and quality of life in Parkinson's disease. Disability and health journal. 12(4). 673–678. 10 indexed citations

14.

Laassri, Majid, Sharon Hassin‐Baer, Rachel Handsher, et al.. (2018). Evolution of echovirus 11 in a chronically infected immunodeficient patient. PLoS Pathogens. 14(3). e1006943–e1006943. 7 indexed citations

15.

Yahalom, Gilad, Lior Greenbaum, Simon Israeli‐Korn, et al.. (2018). Carriers of both GBA and LRRK2 mutations, compared to carriers of either, in Parkinson's disease: Risk estimates and genotype-phenotype correlations. Parkinsonism & Related Disorders. 62. 179–184. 60 indexed citations

16.

Yahalom, Gilad, et al.. (2018). AppTUG - A Smartphone Application of Instrumented ‘Timed Up and Go’ for Neurological Disorders. 10(8). 689–695. 6 indexed citations

17.

Elizur, Shai E., Michal Berkenstadt, Noah Gruber, et al.. (2018). [FMR1 PREMUTATION CARRIERS - ARE THEY REALLY ASYMPTOMATIC?]. PubMed. 157(4). 241–244. 1 indexed citations

18.

Yahalom, Gilad, et al.. (2015). Botulinum Toxin for Ocular Tics. 7(1). 9–11.

19.

Hassin‐Baer, Sharon, et al.. (2011). Phenotype of the 202 adenine deletion in the parkin gene: 40 years of follow‐up. Movement Disorders. 26(4). 719–722. 8 indexed citations

20.

Moro, Elena, Jens Volkmann, Inke R. König, et al.. (2008). Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism. Neurology. 70(14). 1186–1191. 50 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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