John Wolff

1.2k citations

23 papers · 844 indexed · h-index 18

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Neurology top 10%
- Neurological disorders and treatments
- Neurological diseases and metabolism

Papers in ⓘ

Cellular and Molecular Neuroscience 10
- Genetic Neurodegenerative Diseases 8
- Hereditary Neurological Disorders 5
Neurology 3
- Neurological diseases and metabolism 3

Co-authors: Wendy H. Raskind (20 shared papers)Mark Matsushita (12 shared papers)Hillary Lipe (10 shared papers)Thomas D. Bird (9 shared papers)Dong-Hui Chen (5 shared papers)Magali Fernandez (3 shared papers)Zoran Brkanac (3 shared papers)Thomas D. Bird (6 shared papers)
Journals: Neurology (3 papers)The American Journal of Human Genetics (3 papers)Blood (1 paper)Human Molecular Genetics (1 paper)Movement Disorders (1 paper)
Partner nations: United States Australia Netherlands

In The Last Decade

John Wolff

23 papers receiving 830 citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia The American Journal of Human Genetics ·Dong-Hui Chen, Zoran Brkanac, Christophe L. M. J. Verlinde, Xiao-Jian Tan, Laura Bylenok, David Nochlin, Mark Matsushita, Hillary Lipe, John Wolff, Magali Fernandez, Patrick J. Cimino, D. Thomas Bird, Wendy H. Raskind	2003	174
2	Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L The American Journal of Human Genetics ·Dong-Hui Chen, Jennifer E. Below, Akiko Shimamura, Sioḃán Keel, Mark Matsushita, John Wolff, Youngmee Sul, Emily Bonkowski, María Castellà, Toshiyasu Taniguchi, Deborah A. Nickerson, Thalia Papayannopoulou, Thomas D. Bird, Wendy H. Raskind	2016	119
3	The clinical and genetic spectrum of spinocerebellar ataxia 14 Neurology ·D. -H. Chen, Patrick J. Cimino, Laura P.W. Ranum, Huda Y. Zoghbi, Ichiro Yabe, Lawrence J. Schut, Russel L. Margolis, Hillary Lipe, Abreham Feleke, Megumi Matsushita, John Wolff, Caurnel Morgan, Douglas Lau, (unknown), Hidenao Sasaki, Wendy H. Raskind, Thomas D. Bird	2005	56
4	CMT2C with vocal cord paresis associated with short stature and mutations in the TRPV4 gene Neurology ·D.-H. Chen, Youngmee Sul, MaryAnn Weiss, Allen Hillel, Hillary Lipe, John Wolff, Megumi Matsushita, Wendy H. Raskind, Thomas D. Bird	2010	55
5	A New Dominant Spinocerebellar Ataxia Linked to Chromosome 19q13.4-qter Archives of Neurology ·Zoran Brkanac, Laura Bylenok, Magali Fernandez, Mark Matsushita, Hillary Lipe, John Wolff, David Nochlin, Wendy H. Raskind, Thomas D. Bird	2002	53
6	Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22‐q32 American Journal of Medical Genetics ·Zoran Brkanac, Magali Fernandez, Mark Matsushita, Hilary Lipe, John Wolff, Thomas D. Bird, Wendy H. Raskind	2002	47
7	Two Novel Mutations inABHD12: Expansion of the Mutation Spectrum in PHARC and Assessment of Their Functional Effects Human Mutation ·Dong-Hui Chen, Alipi V. Naydenov, Jacqueline L. Blankman, Heather C. Mefford, Marie Y. Davis, Youngmee Sul, A. Samuel Barloon, Emily Bonkowski, John Wolff, Mark Matsushita, Corrine Smith, Benjamin F. Cravatt, Ken Mackie, Wendy H. Raskind, Nephi Stella, Thomas D. Bird	2013	41
8	Presence of Alanine-to-Valine Substitutions in Myofibrillogenesis Regulator 1 in Paroxysmal Nonkinesigenic Dyskinesia Archives of Neurology ·Dong-Hui Chen, Mark Matsushita, Shirley Rainier, Brandon Meaney, Lisa M. Tisch, Abreham Feleke, John Wolff, Hillary Lipe, John K. Fink, Thomas D. Bird, Wendy H. Raskind	2005	34
9	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 ·Dong-Hui Chen, Wendy H. Raskind, William W. Parson, Joshua A. Sonnen, Tiffany Vu, Yunlin Zheng, Mark Matsushita, John Wolff, Hillary Lipe, Thomas D. Bird	2010	32
10	Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2 The American Journal of Human Genetics ·Marshall S. Horwitz, Kathleen F. Benson, Feng-Qian Li, John Wolff, Mark Leppert, Lynne Hobson, Marie Mangelsdorf, Sui Yu, D. Hewett, Robert I. Richards, Wendy H. Raskind	1997	32
11	Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech PLoS ONE ·Beate Peter, Ellen M. Wijsman, Alejandro Q. Nato, Mark Matsushita, Kathy Chapman, Ian B. Stanaway, John Wolff, Kaori Oda, Virginia B. Gabo, Wendy H. Raskind	2016	31
12	Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34 Human Genetics ·Wendy H. Raskind, Tamara Bolin, John Wolff, John K. Fink, Mark Matsushita, M. Litt, Hillary Lipe, Thomas D. Bird	1998	22
13	A rating scale for tardive dyskinesia and Parkinsonian symptoms. PubMed ·Smith Rc, Richard P. Allen, Jennifer Gordon, John Wolff	1983	22
14	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 ·Wendy H. Raskind, Margaret A. Pericak‐Vance, Felicia Lennon, John Wolff, Hillary Lipe, Thomas D. Bird	1997	21
15	CAG Repeat Expansion in Autosomal Dominant Familial Spastic Paraparesis: Novel Expansion in a Subset of Patients Human Molecular Genetics ·Kathleen F. Benson, Marshall S. Horwitz, John Wolff, K. Friend, Elizabeth Thompson, S. White, Robert I. Richards, Wendy H. Raskind, Thomas D. Bird	1998	20
16	Hereditary benign chorea Neurology ·(unknown), Wendy H. Raskind, Megumi Matsushita, John Wolff, Hillary Lipe, Thomas D. Bird	2001	20
17	A novel X‐linked four‐repeat tauopathy with Parkinsonism and spasticity Movement Disorders ·Parvoneh Poorkaj, Wendy H. Raskind, James B. Leverenz, Mark Matsushita, Cyrus P. Zabetian, Ali Samii, Sophia Kim, Nayiry Gazi, John G. Nutt, John Wolff, Dora Yearout, J. Lynne Greenup, Ellen J. Steinbart, Thomas D. Bird	2010	17
18	Mapping of a syndrome of X-linked thrombocytopenia with thalassemia to band Xp11-12: further evidence of genetic heterogeneity of X-linked thrombocytopenia Blood ·Wendy H. Raskind, Kathy K. Niakan, John Wolff, Mark Matsushita, Ty Vaughan, George Stamatoyannopoulos, Chiaki Watanabe, J. W. Huamán Ríos, Hans D. Ochs	2000	17
19	Evidence for a polyclonal etiology of palmar fibromatosis The Journal Of Hand Surgery ·Howard A. Chansky, Thomas E. Trumble, Ernest U. Conrad, John Wolff, Lorne W. Murray, Wendy H. Raskind	1999	8
20	Storage of blood for in vitro generation of dendritic cells Cytotherapy ·Rachel Syme, D. Callaghan, Peter Duggan, S. Bitner, Michelle Anne Kelly, John Wolff, Doug Stewart, Stefan Glück	2002	7

About John Wolff

John Wolff is a scholar working on Cellular and Molecular Neuroscience, Neurology, Clinical Biochemistry, Hematology and Neurology, having authored 23 papers that have together received 844 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (8 papers), Hereditary Neurological Disorders (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), DNA Repair Mechanisms (4 papers), Neurological diseases and metabolism (3 papers), Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (2 papers) and Acute Myeloid Leukemia Research (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (411 citations), Neurology (154 citations), Neurology (81 citations), Hematology (101 citations) and Sensory Systems (40 citations). John Wolff has collaborated with scholars based in United States, Australia and Netherlands. Frequent 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. Their work appears in journals such as Neurology, The American Journal of Human Genetics, Blood, Human Molecular Genetics and Movement 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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