E. H. Kolodny

921 total citations
11 papers, 675 citations indexed

About

E. H. Kolodny is a scholar working on Physiology, Cell Biology and Molecular Biology. According to data from OpenAlex, E. H. Kolodny has authored 11 papers receiving a total of 675 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Physiology, 5 papers in Cell Biology and 4 papers in Molecular Biology. Recurrent topics in E. H. Kolodny's work include Lysosomal Storage Disorders Research (5 papers), Cellular transport and secretion (3 papers) and Trypanosoma species research and implications (3 papers). E. H. Kolodny is often cited by papers focused on Lysosomal Storage Disorders Research (5 papers), Cellular transport and secretion (3 papers) and Trypanosoma species research and implications (3 papers). E. H. Kolodny collaborates with scholars based in United States, United Kingdom and Germany. E. H. Kolodny's co-authors include Jean J. Rebeiz, E. P. Richardson, Hermann Mascher, Ulrike Grittner, Arseni Markoff, Wolfgang Meyer, Karl J. Lackner, Jan Lukáš, Anne‐Katrin Giese and Viatcheslav Saviouk and has published in prestigious journals such as Neurology, Journal of Neurology Neurosurgery & Psychiatry and PLoS Genetics.

In The Last Decade

E. H. Kolodny

11 papers receiving 653 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E. H. Kolodny United States	8	329	306	184	118	111	11	675
Andres Deik United States	16	379 1.2×	224 0.7×	87 0.5×	140 1.2×	188 1.7×	33	722
Tatiana Brémovà-Ertl Germany	16	142 0.4×	239 0.8×	349 1.9×	199 1.7×	145 1.3×	37	764
Silvia Jesús Spain	17	510 1.6×	143 0.5×	153 0.8×	175 1.5×	194 1.7×	40	766
Pilar Gómez‐Garre Spain	20	363 1.1×	201 0.7×	81 0.4×	271 2.3×	159 1.4×	46	875
Isabelle Le Ber France	18	507 1.5×	320 1.0×	241 1.3×	125 1.1×	119 1.1×	33	873
Makio Takahashi Japan	13	409 1.2×	162 0.5×	92 0.5×	141 1.2×	208 1.9×	42	650
Simona Petrucci Italy	16	453 1.4×	135 0.4×	102 0.6×	132 1.1×	195 1.8×	43	755
Jun Kimura Japan	14	220 0.7×	129 0.4×	86 0.5×	109 0.9×	137 1.2×	17	547
Zygmunt Jamrozik Poland	13	359 1.1×	108 0.4×	90 0.5×	162 1.4×	125 1.1×	49	557
N. Gouider‐Khouja Tunisia	16	496 1.5×	98 0.3×	167 0.9×	236 2.0×	271 2.4×	47	879

Countries citing papers authored by E. H. Kolodny

Since Specialization

Citations

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

Fields of papers citing papers by E. H. Kolodny

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. H. Kolodny. 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 E. H. Kolodny. The network helps show where E. H. Kolodny may publish in the future.

Co-authorship network of co-authors of E. H. Kolodny

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

All Works

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11 of 11 papers shown

Lukáš, Jan, Anne‐Katrin Giese, Arseni Markoff, et al.. (2013). Functional Characterisation of Alpha-Galactosidase A Mutations as a Basis for a New Classification System in Fabry Disease. PLoS Genetics. 9(8). e1003632–e1003632. 129 indexed citations

Graber, Jerome, et al.. (2010). Vitamin B12-responsive severe leukoencephalopathy and autonomic dysfunction in a patient with "normal" serum B12 levels. Journal of Neurology Neurosurgery & Psychiatry. 81(12). 1369–1371. 25 indexed citations

Kolodny, E. H., et al.. (2007). Very long chain acyl‐CoA dehydrogenase deficiency in a pair of mildly affected monozygotic twin sister in their late fifties. Journal of Inherited Metabolic Disease. 30(5). 817–817. 6 indexed citations

Zeng, Bai Jin, Zijian Wang, Paola Torres, et al.. (2006). Rapid detection of three large novel deletions of the aspartoacylase gene in non-Jewish patients with Canavan disease. Molecular Genetics and Metabolism. 89(1-2). 156–163. 8 indexed citations

Zeng, Bai Jin, H. Shibuya, Gary S. Johnson, et al.. (2000). Isolation and characterization of the normal canine β‐galactosidase gene and its mutation in a dog model of GM1‐gangliosidosis. Journal of Inherited Metabolic Disease. 23(6). 593–606. 30 indexed citations

Scott, C. Ronald, GM Pastores, Hanna Andersson, et al.. (2000). The clinical expression of Gaucher disease correlates with genotype: Data from 570 patients. Genetics in Medicine. 2(1). 65–65. 2 indexed citations

Gasperi, Rita De, Miguel A. Gama Sosa, Stefania Battistini, et al.. (1996). Late-onset G sub M2 gangliosidosis. Neurology. 47(2). 547–552. 18 indexed citations

Russo, Mirella, Richard Perry, E. H. Kolodny, & Christopher Gillberg. (1996). Heller syndrome in a pre-school boy. Proposed medical evaluation and hypothesized pathogenesis. European Child & Adolescent Psychiatry. 5(3). 172–177. 9 indexed citations

DeGasperi, R, Miguel A. Gama Sosa, Eugene E. Grebner, et al.. (1995). Substitution of Alanine543 with a Threonine Residue at the Carboxy Terminal End of the β-Chain Is Associated with Thermolabile Hexosaminidase B in a Jewish Family of Oriental Ancestry. Biochemical and Molecular Medicine. 56(1). 31–36. 7 indexed citations

10.

Gasperi, Rita De, et al.. (1995). Late-onset GM2-gangliosidosis in two siblings of Ashkenazi Jewish ancestry results from a mutation in the HEXA gene causing abnormal thermolability of Hexosaminidase A.. Use Siena air (University of Siena). 1375–1375. 2 indexed citations

11.

Rebeiz, Jean J., E. H. Kolodny, & E. P. Richardson. (1968). Corticodentatonigral Degeneration With Neuronal Achromasia. Archives of Neurology. 18(1). 20–33. 439 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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