Robert L. Wollmann

6.8k total citations
118 papers, 5.4k citations indexed

About

Robert L. Wollmann is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Robert L. Wollmann has authored 118 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Neurology, 40 papers in Molecular Biology and 25 papers in Cellular and Molecular Neuroscience. Recurrent topics in Robert L. Wollmann's work include Myasthenia Gravis and Thymoma (20 papers), Cellular transport and secretion (14 papers) and Ion channel regulation and function (13 papers). Robert L. Wollmann is often cited by papers focused on Myasthenia Gravis and Thymoma (20 papers), Cellular transport and secretion (14 papers) and Ion channel regulation and function (13 papers). Robert L. Wollmann collaborates with scholars based in United States, France and Germany. Robert L. Wollmann's co-authors include Kāri Stefánsson, Raymond P. Roos, Ricardo A. Maselli, Blake W. Moore, M. Jerković, B. G. W. Arnason, Elaine Fuchs, James J. Dowling, Raphael C. Lee and L. Philip River and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Robert L. Wollmann

118 papers receiving 5.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert L. Wollmann United States 38 2.2k 1.4k 888 770 610 118 5.4k
Juha Peltonen Finland 49 2.3k 1.1× 1.9k 1.4× 1.3k 1.5× 701 0.9× 772 1.3× 224 7.5k
Ursula Schlötzer‐Schrehardt Germany 63 3.6k 1.7× 809 0.6× 1.3k 1.5× 527 0.7× 777 1.3× 308 13.4k
Dov Soffer Israel 30 3.3k 1.5× 864 0.6× 343 0.4× 610 0.8× 229 0.4× 105 6.7k
G. Diane Shelton United States 43 3.2k 1.5× 1.1k 0.8× 842 0.9× 925 1.2× 130 0.2× 282 6.5k
Takashi Nakajima Japan 36 2.1k 1.0× 883 0.6× 391 0.4× 389 0.5× 644 1.1× 213 5.7k
Klaus Addicks Germany 50 3.7k 1.7× 315 0.2× 941 1.1× 1.2k 1.6× 543 0.9× 199 8.4k
Michael C. Brown United States 46 3.7k 1.7× 533 0.4× 2.0k 2.3× 2.2k 2.9× 310 0.5× 160 8.2k
Thomas O. Crawford United States 59 5.4k 2.5× 1.8k 1.3× 952 1.1× 2.3k 3.0× 563 0.9× 160 10.8k
Barry G.W. Arnason United States 46 1.2k 0.5× 1.7k 1.2× 179 0.2× 1.0k 1.3× 1.8k 2.9× 157 6.6k
Matthias Reinhard Germany 42 1.5k 0.7× 2.3k 1.6× 1.4k 1.6× 703 0.9× 100 0.2× 132 6.5k

Countries citing papers authored by Robert L. Wollmann

Since Specialization
Citations

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

Fields of papers citing papers by Robert L. Wollmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert L. Wollmann. 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 Robert L. Wollmann. The network helps show where Robert L. Wollmann may publish in the future.

Co-authorship network of co-authors of Robert L. Wollmann

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

All Works

20 of 20 papers shown
1.
Sacher, Adrian G., et al.. (2010). Long-Term Survival of a Patient with Glioblastoma. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 37(2). 289–292. 4 indexed citations
2.
Maselli, Ricardo A., et al.. (2010). Mutations in MUSK causing congenital myasthenic syndrome impair MuSK–Dok-7 interaction. Human Molecular Genetics. 19(12). 2370–2379. 73 indexed citations
3.
MacLeod, Heather, Peter Pytel, Robert L. Wollmann, et al.. (2007). A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex. Neuromuscular Disorders. 17(4). 285–289. 16 indexed citations
4.
Spencer, Melissa J., Bula J. Bhattacharyya, Elena Kudryashova, et al.. (2007). Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome. Journal of Clinical Investigation. 117(10). 2903–2912. 25 indexed citations
5.
Chen, Xiangjun, Eleni N. Levedakou, Kathleen J. Millen, et al.. (2007). Proprioceptive Sensory Neuropathy in Mice with a Mutation in the Cytoplasmic Dynein Heavy Chain 1 Gene. Journal of Neuroscience. 27(52). 14515–14524. 127 indexed citations
6.
Vohra, Bhupinder P. S., et al.. (2004). Focal caspase activation underlies the endplate myopathy in slow‐channel syndrome. Annals of Neurology. 55(3). 347–352. 26 indexed citations
7.
Maselli, Ricardo A., et al.. (2003). Rapsyn mutations in myasthenic syndrome due to impaired receptor clustering. Muscle & Nerve. 28(3). 293–301. 33 indexed citations
8.
Maselli, Ricardo A., et al.. (2002). Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesis. Muscle & Nerve. 27(2). 180–187. 51 indexed citations
9.
Munshi, Ilyas, et al.. (2001). Traumatic aneurysm resulting from insertion of an intracranial pressure monitor. Journal of neurosurgery. 95(4). 720–720. 13 indexed citations
10.
Zhu, Xiaolei, et al.. (2001). Overexpression of γ-Sarcoglycan Induces Severe Muscular Dystrophy. Journal of Biological Chemistry. 276(24). 21785–21790. 50 indexed citations
11.
Wong, K., Regina C. Armstrong, Kymberly A. Gyure, et al.. (2000). Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome. Acta Neuropathologica. 100(6). 635–646. 78 indexed citations
12.
Freiburg, Alexandra, Geir Skeie, Bernhard Kolmerer, et al.. (1998). Striational autoantibodies in myasthenia gravis patients recognize I-band titin epitopes. Journal of Neuroimmunology. 81(1-2). 98–108. 18 indexed citations
13.
Gómez, Christopher M., et al.. (1998). Genetic Manipulation of AChR Responses Suggests Multiple Causes of Weakness in Slow‐Channel Syndromea. Annals of the New York Academy of Sciences. 841(1). 167–180. 6 indexed citations
14.
Dowling, James J., Yanmin Yang, Robert L. Wollmann, Louis F. Reichardt, & Elaine Fuchs. (1997). Developmental Expression of BPAG1-n: Insights into the Spastic Ataxia and Gross Neurologic Degeneration inDystonia MusculorumMice. Developmental Biology. 187(2). 131–142. 51 indexed citations
15.
Sato, Shigeru, Liang Zhang, Jong Kim, et al.. (1996). A Neutralization Site of DA Strain of Theiler's Murine Encephalomyelitis Virus Important for Disease Phenotype. Virology. 226(2). 327–337. 26 indexed citations
16.
Krishnasamy, Swarna, Everett E. Vokes, George J. Dohrmann, et al.. (1995). Concomitant Chemoradiotherapy, Neutron Boost, and Adjuvant Chemotherapy for Anaplastic Astrocytoma and Glioblastoma Multiforme. Cancer Investigation. 13(5). 453–459. 11 indexed citations
17.
Maselli, Ricardo A., Robert L. Wollmann, & Raymond P. Roos. (1995). Function and Ultrastructure of the Neuromuscular Junction in Post‐Polio Syndrome. Annals of the New York Academy of Sciences. 753(1). 129–137. 11 indexed citations
18.
Chelmicka‐Schorr, Ewa, et al.. (1992). Sympathectomy augments adoptively transferred experimental allergic encephalomyelitis. Journal of Neuroimmunology. 37(1-2). 99–103. 33 indexed citations
19.
Huttenlocher, Peter R. & Robert L. Wollmann. (1991). Cellular Neuropathology of Tuberous Sclerosisa. Annals of the New York Academy of Sciences. 615(1). 140–148. 26 indexed citations
20.
Kohrman, Michael, et al.. (1986). A variant of Fukuyama congenital muscular dystrophy in a non-Japanese child. Pediatric Neurology. 2(5). 290–293. 5 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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