John K. Fink

9.0k total citations
102 papers, 5.7k citations indexed

About

John K. Fink is a scholar working on Cellular and Molecular Neuroscience, Neurology and Genetics. According to data from OpenAlex, John K. Fink has authored 102 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Cellular and Molecular Neuroscience, 34 papers in Neurology and 24 papers in Genetics. Recurrent topics in John K. Fink's work include Neurological diseases and metabolism (34 papers), Hereditary Neurological Disorders (34 papers) and Neurogenetic and Muscular Disorders Research (23 papers). John K. Fink is often cited by papers focused on Neurological diseases and metabolism (34 papers), Hereditary Neurological Disorders (34 papers) and Neurogenetic and Muscular Disorders Research (23 papers). John K. Fink collaborates with scholars based in United States, Russia and United Kingdom. John K. Fink's co-authors include Peter Hedera, George J. Brewer, Shirley Rainier, James T. Warren, Karen J. Kluin, Michael L. Peacock, Robert D. Dick, Virginia Johnson, Fred Askari and Robert Dick and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

John K. Fink

100 papers receiving 5.5k citations

Peers

Countries citing papers authored by John K. Fink

Since Specialization

Citations

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

Fields of papers citing papers by John K. Fink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John K. Fink

This figure shows the co-authorship network connecting the top 25 collaborators of John K. Fink. A scholar is included among the top collaborators of John K. Fink 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 K. Fink. John K. Fink 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

#	Work	Indexed citations
1	Diagenesis of fossil gar fish scales with implications for geochronology and paleoenvironmental applications 2024 ·Geochimica et Cosmochimica Acta ·John K. Fink, Marissa M. Tremblay, Thomas Tobin, Lisa D. Stockli, Daniel F. Stöckli, Ryan B. Ickert	1
2	Primary lateral sclerosis: consensus diagnostic criteria 2020 ·Journal of Neurology Neurosurgery & Psychiatry ·Martin R. Turner, Richard J. Barohn, Philippe Corcia, John K. Fink, Matthew B. Harms, Matthew C. Kiernan, John Ravits, Vincenzo Silani, Zachary Simmons, Jeffrey Statland, Leonard H. van den Berg, Hiroshi Mitsumoto, (unknown)	125
3	Docker: a Software as a Service, Operating System-Level Virtualization Framework 2014 ·SHILAP Revista de lepidopterología ·John K. Fink	38
4	Neuropathy target esterase (NTE): overview and future 2012 ·Chemico-Biological Interactions ·Rudy J. Richardson, Nichole D. Hein, Sanjeeva J. Wijeyesakere, John K. Fink, Галина Ф. Махаева	77
5	Constructs of human neuropathy target esterase catalytic domain containing mutations related to motor neuron disease have altered enzymatic properties 2010 ·Toxicology Letters ·Nichole D. Hein, Jeanne A. Stuckey, Shirley Rainier, John K. Fink, Rudy J. Richardson	16
6	Hereditary spastic paraplegia 2006 ·Current Neurology and Neuroscience Reports ·John K. Fink	217
7	Cerebrotendinous Xanthomatosis 2005 ·Archives of Neurology ·Matthew T. Lorincz, Shirley Rainier, Donald A. Thomas, John K. Fink	80
8	Porphyric neuropathy 2004 ·Muscle & Nerve ·James W. Albers, John K. Fink	70
9	NIPA1 Gene Mutations Cause Autosomal Dominant Hereditary Spastic Paraplegia (SPG6) 2003 ·The American Journal of Human Genetics ·Shirley Rainier, (unknown), Debra A. Tokarz, Robert D. Nicholls, John K. Fink	146
10	Myelopolyneuropathy and Pancytopenia Due to Copper Deficiency and High Zinc Levels of Unknown Origin 2003 ·Archives of Neurology ·Peter Hedera, John K. Fink, Paula Bockenstedt, George J. Brewer	72
11	Advances in the hereditary spastic paraplegias 2003 ·Experimental Neurology ·John K. Fink	94
12	Aerosol therapy for children 2001 ·PubMed ·Bruce K. Rubin, John K. Fink	42
13	Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia 2001 ·Nature Genetics ·Xinping Zhao, David M. Alvarado, Shirley Rainier, Rosemary Lemons, Peter Hedera, Christian Weber, Turgut Tükel, Memnune Yüksel Apak, Terry Heiman‐Patterson, Ming Lei, (unknown), John K. Fink	255
14	Prenatal diagnosis of hereditary spastic paraplegia 2001 ·Prenatal Diagnosis ·Peter Hedera, (unknown), Shirley Rainier, David M. Alvarado, Turgut Tükel, Memnune Yüksel Apak, John K. Fink	3
15	Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8q 1999 ·The American Journal of Human Genetics ·Peter Hedera, Shirley Rainier, David M. Alvarado, Xinping Zhao, (unknown), Brith Otterud, Mark Leppert, John K. Fink	71
16	Advances in hereditary spastic paraplegia 1997 ·Current Opinion in Neurology ·John K. Fink	48
17	Hereditary Spastic Paraplegia 1996 ·Neurology ·John K. Fink, Terry Heiman‐Patterson, Thomas D. Bird, Franca Cambi, Marie‐Pierre Dubé, Denise A. Figlewicz, (unknown), Afif Hentati, Margaret A. Pericak‐Vance, Wendy H. Raskind, Guy A. Rouleau, Teepu Siddique	147
18	Novel amyloid precursor protein gene mutation (codon 665^Asp) in a patient with late‐onset Alzheimer's disease 1994 ·Annals of Neurology ·Michael L. Peacock, Daniel L. Murman, Anders A. F. Sima, James T. Warren, A D Roses, John K. Fink	21
19	Clinical and Genetic Analysis of Progressive Dystonia With Diurnal Variation 1991 ·Archives of Neurology ·John K. Fink, Paula Ravin, Michele R. Filling‐Katz, Charles E. Argoff, Mark Hallett	11
20	Tetrahydrobiopterin administration in biopterin‐deflcient progressive dystonia with diurnal variation 1989 ·Neurology ·John K. Fink, Paula Ravin, Charles E. Argoff, Robert A. Levine, Brady Ro, Mark Hallett, Norman W. Barton	25

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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