M. Sherr

2.6k total citations
11 papers, 1.1k citations indexed

About

M. Sherr is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, M. Sherr has authored 11 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 8 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in M. Sherr's work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (8 papers) and Neurological disorders and treatments (7 papers). M. Sherr is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (8 papers) and Neurological disorders and treatments (7 papers). M. Sherr collaborates with scholars based in United States, Canada and United Kingdom. M. Sherr's co-authors include O. Colin Stine, Neal G. Ranen, Patrick E. Barta, Godfrey D. Pearlson, Elizabeth Aylward, Adam Rosenblatt, C A Ross, Mary L. Franz, F. Bylsma and Margaret H. Abbott and has published in prestigious journals such as Neurology, Movement Disorders and Journal of Medical Genetics.

In The Last Decade

M. Sherr

11 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Sherr United States	10	896	699	624	70	69	11	1.1k
Olivier Didierjean France	10	1.5k 1.6×	1.4k 2.0×	697 1.1×	119 1.7×	80 1.2×	13	1.7k
Nayana Lahiri United Kingdom	15	575 0.6×	610 0.9×	206 0.3×	113 1.6×	57 0.8×	27	1.0k
Astrid Lunkes Germany	12	1.5k 1.7×	1.4k 2.1×	648 1.0×	96 1.4×	99 1.4×	18	1.8k
Randi Jones United States	7	830 0.9×	745 1.1×	425 0.7×	75 1.1×	32 0.5×	7	1.1k
Laure Jamot France	11	946 1.1×	908 1.3×	333 0.5×	37 0.5×	83 1.2×	17	1.3k
Lena E. Hjermind Denmark	18	403 0.4×	405 0.6×	388 0.6×	100 1.4×	98 1.4×	47	904
J. J. Martin Belgium	15	729 0.8×	269 0.4×	366 0.6×	318 4.5×	68 1.0×	33	1.1k
John D. Schwankhaus United States	13	192 0.2×	257 0.4×	269 0.4×	72 1.0×	83 1.2×	25	674
Gilles David France	11	1.8k 2.0×	1.7k 2.5×	598 1.0×	91 1.3×	127 1.8×	15	1.9k
Orsolya Kántor Hungary	16	427 0.5×	343 0.5×	86 0.1×	52 0.7×	21 0.3×	34	725

Countries citing papers authored by M. Sherr

Since Specialization

Citations

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

Fields of papers citing papers by M. Sherr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Sherr

This figure shows the co-authorship network connecting the top 25 collaborators of M. Sherr. A scholar is included among the top collaborators of M. Sherr 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 M. Sherr. M. Sherr is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

Rosenblatt, Adam, Ryan R. Brinkman, Kaili Liang, et al.. (2001). Familial influence on age of onset among siblings with Huntington disease. American Journal of Medical Genetics. 105(5). 399–403. 4 indexed citations

Rosenblatt, Adam, Ryan R. Brinkman, Kung‐Yee Liang, et al.. (2001). Familial influence on age of onset among siblings with Huntington disease*. American Journal of Medical Genetics. 105(5). 399–403. 68 indexed citations

Aylward, Elizabeth, Ann Marie Codori, Adam Rosenblatt, et al.. (2000). Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease. Movement Disorders. 15(3). 552–560. 160 indexed citations

Margolis, Russell L., O. Colin Stine, Mary L. Franz, et al.. (1999). Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expression. Journal of Medical Genetics. 36(1). 62–64. 11 indexed citations

Rosenblatt, Adam, Neal G. Ranen, David C. Rubinsztein, et al.. (1998). Patients with features similar to Huntington's disease, without CAG expansion in huntingtin. Neurology. 51(1). 215–220. 17 indexed citations

Aylward, Elizabeth, F. Bylsma, Molly V. Wagster, et al.. (1998). Frontal lobe volume in patients with Huntington's disease. Neurology. 50(1). 252–258. 145 indexed citations

Aylward, Elizabeth, Qing Li, O. Colin Stine, et al.. (1997). Longitudinal change in basal ganglia volume in patients with Huntington's disease. Neurology. 48(2). 394–399. 165 indexed citations

Bêcher, Mark W., David C. Rubinsztein, Jayne Leggo, et al.. (1997). Dentatorubral and pallidoluysian atrophy (DRPLA) Clinical and neuropathological findings in genetically confirmed north american and european pedigrees. Movement Disorders. 12(4). 519–530. 72 indexed citations

Ranen, Neal G., Carol E. Peyser, Joseph Coyle, et al.. (1996). A controlled trial of idebenone in Huntington's disease. Movement Disorders. 11(5). 549–554. 78 indexed citations

10.

Chotai, Kokila, David Curtis, Marina Frontali, et al.. (1996). Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.. PubMed. 59(1). 16–22. 171 indexed citations

11.

Ranen, Neal G., O. Colin Stine, Margaret H. Abbott, et al.. (1995). Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease.. PubMed Central. 57(3). 593–602. 184 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.

Explore authors with similar magnitude of impact