Stanley H. Korman

3.7k total citations
94 papers, 2.3k citations indexed

About

Stanley H. Korman is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry. According to data from OpenAlex, Stanley H. Korman has authored 94 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Clinical Biochemistry, 43 papers in Molecular Biology and 24 papers in Biochemistry. Recurrent topics in Stanley H. Korman's work include Metabolism and Genetic Disorders (48 papers), Amino Acid Enzymes and Metabolism (22 papers) and Biochemical and Molecular Research (17 papers). Stanley H. Korman is often cited by papers focused on Metabolism and Genetic Disorders (48 papers), Amino Acid Enzymes and Metabolism (22 papers) and Biochemical and Molecular Research (17 papers). Stanley H. Korman collaborates with scholars based in Israel, United States and Netherlands. Stanley H. Korman's co-authors include Alisa Gutman, Richard J. Deckelbaum, Sylvie M. Le Blancq, Orly Elpeleg, Hanna Mandel, Avraham Shaag, Ann Saada, John M. Gomori, Simon Edvardson and Lex H.T. Van der Ploeg and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Stanley H. Korman

90 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stanley H. Korman Israel 30 1.2k 828 337 250 235 94 2.3k
Wendy E. Smith United States 20 1.1k 0.9× 806 1.0× 132 0.4× 710 2.8× 41 0.2× 40 2.3k
María Luisa Campo Spain 18 1.0k 0.9× 249 0.3× 89 0.3× 222 0.9× 48 0.2× 32 1.8k
Diane Kepka‐Lenhart United States 19 665 0.6× 127 0.2× 340 1.0× 717 2.9× 120 0.5× 24 2.3k
Nigar Fatma United States 25 1.1k 1.0× 106 0.1× 70 0.2× 122 0.5× 88 0.4× 45 1.6k
Ashish Jain Norway 26 2.5k 2.1× 65 0.1× 87 0.3× 258 1.0× 358 1.5× 46 4.3k
P H Pekala United States 23 1.4k 1.2× 75 0.1× 184 0.5× 1.1k 4.3× 307 1.3× 28 3.1k
Alessandra Romagnoli Italy 20 1.5k 1.3× 79 0.1× 55 0.2× 286 1.1× 254 1.1× 28 3.1k
R Kang United States 5 1.3k 1.1× 198 0.2× 40 0.1× 172 0.7× 368 1.6× 8 2.6k
Grégory Bellot Singapore 15 1.4k 1.2× 124 0.1× 62 0.2× 169 0.7× 671 2.9× 22 2.5k
Ekaterina Loginicheva United States 9 1.7k 1.4× 70 0.1× 86 0.3× 579 2.3× 538 2.3× 9 3.9k

Countries citing papers authored by Stanley H. Korman

Since Specialization
Citations

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

Fields of papers citing papers by Stanley H. Korman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stanley H. Korman

This figure shows the co-authorship network connecting the top 25 collaborators of Stanley H. Korman. A scholar is included among the top collaborators of Stanley H. Korman 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 Stanley H. Korman. Stanley H. Korman 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.
Besien, Koen van, Parameswaran Hari, Wendy Stock, et al.. (2016). Reduced intensity haplo plus single cord transplant compared to double cord transplant: improved engraftment and graft-versus-host disease-free, relapse-free survival. Haematologica. 101(5). 634–643. 26 indexed citations
2.
Edvardson, Simon, Stanley H. Korman, A. Livne, et al.. (2010). l-arginine:glycine amidinotransferase (AGAT) deficiency: Clinical presentation and response to treatment in two patients with a novel mutation. Molecular Genetics and Metabolism. 101(2-3). 228–232. 32 indexed citations
3.
Fernández‐Irigoyen, Joaquín, Enrique Santamaría, Yin‐Hsiu Chien, et al.. (2010). Enzymatic activity of methionine adenosyltransferase variants identified in patients with persistent hypermethioninemia. Molecular Genetics and Metabolism. 101(2-3). 172–177. 24 indexed citations
4.
Edvardson, Simon, Hiroko Hama, Avraham Shaag, et al.. (2008). Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia. The American Journal of Human Genetics. 83(5). 643–648. 154 indexed citations
5.
Boneh, Avihu, Sonia Allan, Danuta Mendelson, et al.. (2008). Clinical, ethical and legal considerations in the treatment of newborns with non-ketotic hyperglycinaemia. Molecular Genetics and Metabolism. 94(2). 143–147. 20 indexed citations
6.
Kure, Shigeo, Stanley H. Korman, Junko Kanno, et al.. (2006). Rapid diagnosis of glycine encephalopathy by 13C‐glycine breath test. Annals of Neurology. 59(5). 862–867. 14 indexed citations
7.
Korman, Stanley H.. (2006). Inborn errors of isoleucine degradation: A review. Molecular Genetics and Metabolism. 89(4). 289–299. 50 indexed citations
8.
Korman, Stanley H., James Pitt, Avihu Boneh, et al.. (2006). A novel SLC25A20 splicing mutation in patients of different ethnic origin with neonatally lethal carnitine-acylcarnitine translocase (CACT) deficiency. Molecular Genetics and Metabolism. 89(4). 332–338. 15 indexed citations
9.
Ribes, Antònia, Bernd A. Neubauer, Stanley H. Korman, et al.. (2005). L-2-hydroxyglutaric aciduria: novel mutations in the L-2-hydroxyglutarate dehydrogenase gene. Journal of Inherited Metabolic Disease. 28. 93–93. 1 indexed citations
10.
Boneh, Avihu, Stanley H. Korman, Ken‐ichi Sato, et al.. (2005). A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem. Journal of Human Genetics. 50(5). 230–234. 19 indexed citations
11.
Flusser, Hagit, Stanley H. Korman, K. Satō, et al.. (2005). Mild glycine encephalopathy (NKH) in a large kindred due to a silent exonic GLDC splice mutation. Neurology. 64(8). 1426–1430. 29 indexed citations
12.
Korman, Stanley H. & Alisa Gutman. (2004). N-acetyl Tyrosyluria Caused by Parenteral or Enteral Administration of N-acetyl-L-tyrosine: Differentiation From Hereditary and Acquired Tyrosinemias. Journal of Pediatric Gastroenterology and Nutrition. 39(1). 95–100.
13.
14.
Wang, Yuhuan, Stanley H. Korman, Jing Ye, et al.. (2001). Phenotype and genotype variation in primary carnitine deficiency. Genetics in Medicine. 3(6). 387–392. 59 indexed citations
15.
Levy‐Khademi, Floris, Stanley H. Korman, & Yona Amitai. (2000). Henoch–Schönlein Purpura: Simultaneous Occurrence in Two Siblings. Pediatric Dermatology. 17(2). 139–140. 9 indexed citations
16.
Blancq, Sylvie M. Le, Stanley H. Korman, & Lex H.T. Van der Ploeg. (1992). Spontaneous chromosome rearrangements in the protozoanGiardia lamblia: estimation of mutation rates. Nucleic Acids Research. 20(17). 4539–4545. 21 indexed citations
17.
Korman, Stanley H., et al.. (1991). Pancreatic Pseudocyst. Journal of Pediatric Gastroenterology and Nutrition. 12(3). 372–375. 1 indexed citations
18.
Korman, Stanley H., et al.. (1989). Asymptomatic giardiasis in children. The Pediatric Infectious Disease Journal. 8(11). 773–779. 64 indexed citations
19.
Korman, Stanley H., et al.. (1988). Subacute meningitis caused by Brucella: a diagnostic challenge. European Journal of Pediatrics. 148(2). 120–121. 7 indexed citations
20.
Granot, Esther, et al.. (1986). Functional Gastrointestinal Obstruction in a Child with Chronic Granulomatous Disease. Journal of Pediatric Gastroenterology and Nutrition. 5(2). 321–323. 6 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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