John Wolff

1.2k total citations
23 papers, 844 citations indexed

About

John Wolff is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, John Wolff has authored 23 papers receiving a total of 844 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in John Wolff's work include Genetic Neurodegenerative Diseases (8 papers), Hereditary Neurological Disorders (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). John Wolff is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Hereditary Neurological Disorders (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). John Wolff collaborates with scholars based in United States, Australia and Netherlands. John Wolff's co-authors include Wendy H. Raskind, Mark Matsushita, Hillary Lipe, Thomas D. Bird, Dong-Hui Chen, Magali Fernandez, Zoran Brkanac, Thomas D. Bird, David Nochlin and Patrick J. Cimino and has published in prestigious journals such as Blood, PLoS ONE and Neurology.

In The Last Decade

John Wolff

23 papers receiving 830 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John Wolff United States 18 481 411 154 137 101 23 844
Sherryl A. Taylor Canada 16 455 0.9× 318 0.8× 181 1.2× 137 1.0× 131 1.3× 35 768
Friedmar R. Kreuz Germany 17 498 1.0× 441 1.1× 129 0.8× 197 1.4× 71 0.7× 30 923
Thalia Antoniadi Greece 16 327 0.7× 217 0.5× 61 0.4× 155 1.1× 89 0.9× 28 850
B. Müller Germany 15 272 0.6× 269 0.7× 334 2.2× 158 1.2× 41 0.4× 23 744
V. Volpini Spain 17 571 1.2× 369 0.9× 167 1.1× 222 1.6× 19 0.2× 33 996
Alice B. Schindler United States 15 607 1.3× 396 1.0× 202 1.3× 104 0.8× 16 0.2× 37 1.0k
Hideji Hashida Japan 19 672 1.4× 520 1.3× 434 2.8× 81 0.6× 31 0.3× 49 1.2k
Andrée Robaglia‐Schlupp France 16 399 0.8× 419 1.0× 138 0.9× 140 1.0× 11 0.1× 30 1.0k
Kristina Friberg Sweden 11 347 0.7× 400 1.0× 42 0.3× 106 0.8× 86 0.9× 19 1.1k
A. V. Polyakov Russia 14 415 0.9× 312 0.8× 146 0.9× 188 1.4× 11 0.1× 133 976

Countries citing papers authored by John Wolff

Since Specialization
Citations

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

Fields of papers citing papers by John Wolff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John Wolff

This figure shows the co-authorship network connecting the top 25 collaborators of John Wolff. A scholar is included among the top collaborators of John Wolff 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 John Wolff. John Wolff 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.
Chen, Donghui, Mena Scavina, Elizabeth Blue, et al.. (2017). An 8‐generation family with X‐linked Charcot–Marie–Tooth: Confirmation Of the pathogenicity Of a 3′ untranslated region mutation in GJB1 and its clinical features. Muscle & Nerve. 57(5). 859–862. 2 indexed citations
2.
Chen, Dong-Hui, Jennifer E. Below, Akiko Shimamura, et al.. (2016). Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L. The American Journal of Human Genetics. 98(6). 1146–1158. 119 indexed citations
3.
Peter, Beate, Ellen M. Wijsman, Alejandro Q. Nato, et al.. (2016). Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. PLoS ONE. 11(4). e0153864–e0153864. 31 indexed citations
4.
Chen, Dong-Hui, Wendy H. Raskind, William W. Parson, et al.. (2010). A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations. Journal of the Neurological Sciences. 296(1-2). 22–29. 32 indexed citations
5.
Poorkaj, Parvoneh, Wendy H. Raskind, James B. Leverenz, et al.. (2010). A novel X‐linked four‐repeat tauopathy with Parkinsonism and spasticity. Movement Disorders. 25(10). 1409–1417. 17 indexed citations
6.
Sul, Youngmee, Allen Hillel, Hillary Lipe, et al.. (2010). CMT2C with vocal cord paresis associated with short stature and mutations in the TRPV4 gene. Neurology. 75(22). 1968–1975. 55 indexed citations
7.
Raskind, Wendy H., Mark Matsushita, Beate Peter, et al.. (2008). Familial dyskinesia and facial myokymia (FDFM): Follow‐up of a large family and linkage to chromosome 3p21‐3q21. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(4). 570–574. 7 indexed citations
8.
Chen, Dong-Hui, Mark Matsushita, Shirley Rainier, et al.. (2005). Presence of Alanine-to-Valine Substitutions in Myofibrillogenesis Regulator 1 in Paroxysmal Nonkinesigenic Dyskinesia. Archives of Neurology. 62(4). 597–597. 34 indexed citations
9.
Wolff, John, et al.. (2004). Extreme leucocytosis and splenomegaly in metastasised melanoma.. PubMed. 62(5). 164–7. 7 indexed citations
10.
Chen, Dong-Hui, Zoran Brkanac, Christophe L. M. J. Verlinde, et al.. (2003). Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia. The American Journal of Human Genetics. 72(4). 839–849. 174 indexed citations
11.
Brkanac, Zoran, Magali Fernandez, Mark Matsushita, et al.. (2002). A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qter. Archives of Neurology. 59(8). 1291–1291. 53 indexed citations
12.
Syme, Rachel, et al.. (2002). Storage of blood for in vitro generation of dendritic cells. Cytotherapy. 4(3). 271–276. 7 indexed citations
13.
Brkanac, Zoran, Magali Fernandez, Mark Matsushita, et al.. (2002). Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22‐q32. American Journal of Medical Genetics. 114(4). 450–457. 47 indexed citations
14.
Raskind, Wendy H., et al.. (2001). Hereditary benign chorea. Neurology. 57(1). 106–110. 20 indexed citations
15.
Chansky, Howard A., et al.. (1999). Evidence for a polyclonal etiology of palmar fibromatosis. The Journal Of Hand Surgery. 24(2). 339–344. 8 indexed citations
16.
Benson, Kathleen F., Marshall S. Horwitz, John Wolff, et al.. (1998). CAG Repeat Expansion in Autosomal Dominant Familial Spastic Paraparesis: Novel Expansion in a Subset of Patients. Human Molecular Genetics. 7(11). 1779–1786. 20 indexed citations
17.
Raskind, Wendy H., John Wolff, John K. Fink, et al.. (1998). Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34. Human Genetics. 102(1). 93–97. 22 indexed citations
18.
Horwitz, Marshall S., Kathleen F. Benson, John Wolff, et al.. (1997). Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2. The American Journal of Human Genetics. 61(4). 873–881. 32 indexed citations
19.
Raskind, Wendy H., Margaret A. Pericak‐Vance, Felicia Lennon, et al.. (1997). Familial spastic paraparesis: Evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2. American Journal of Medical Genetics. 74(1). 26–36. 21 indexed citations
20.
Rc, Smith, et al.. (1983). A rating scale for tardive dyskinesia and Parkinsonian symptoms.. PubMed. 19(2). 266–76. 22 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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