Stanley H. Korman

3.7k citations

94 papers · 2.3k · h-index 30

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Biochemistry top 1%
- Amino Acid Enzymes and Metabolism

Papers in

Clinical Biochemistry 48
- Metabolism and Genetic Disorders 48
Molecular Biology 43
- Biochemical and Molecular Research 17
- Mitochondrial Function and Pathology 13
- Peroxisome Proliferator-Activated Receptors 9

Co-authors: Alisa Gutman (26 shared papers)Richard J. Deckelbaum (4 shared papers)Orly Elpeleg (9 shared papers)Sylvie M. Le Blancq (4 shared papers)Hanna Mandel (6 shared papers)Avraham Shaag (9 shared papers)Ann Saada (5 shared papers)John M. Gomori (3 shared papers)
Journals: Molecular Genetics and Metabolism (11 papers)Journal of Inherited Metabolic Disease (9 papers)Journal of Pediatric Gastroenterology and Nutrition (7 papers)Annals of Neurology (4 papers)Nucleic Acids Research (3 papers)
Partner nations: Israel United States Netherlands

In The Last Decade

Stanley H. Korman

90 papers receiving 2.2k citations

Peers

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-authors

The 25 scholars most cited alongside Stanley H. Korman, 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 Stanley H. Korman Line = papers co-authored together Stanley H. Korman 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 94 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis Nature ·Shiran Rabinovich, Lital N. Adler, Keren Yizhak, Alona Sarver, Alon Silberman, Shani Agron, Noa Stettner, Qin Sun, Alexander Brandis, Daniel Helbling, Stanley H. Korman, Shalev Itzkovitz, David Dimmock, Igor Ulitsky, Sandesh C.S. Nagamani, Eytan Ruppin, Ayelet Erez	2015	264
2	Mutations in the Fatty Acid 2-Hydroxylase Gene Are Associated with Leukodystrophy with Spastic Paraparesis and Dystonia The American Journal of Human Genetics ·Simon Edvardson, Hiroko Hama, Avraham Shaag, John M. Gomori, Itai Berger, Dov Soffer, Stanley H. Korman, I. Taustein, Ann Saada, Orly Elpeleg	2008	154
3	Hypobetalipoproteinemia Due to an Apolipoprotein B Gene Exon 21 Deletion Derived by Alu-Alu Recombination Journal of Biological Chemistry ·Lei Huang, M E Ripps, Stanley H. Korman, Richard J. Deckelbaum, Jan L. Breslow	1989	96
4	Elevated plasma citrulline and arginine due to consumption of Citrullus vulgaris (watermelon) Journal of Inherited Metabolic Disease ·Hanna Mandel, Nina S. Levy, S. Izkovitch, Stanley H. Korman	2004	65
5	Asymptomatic giardiasis in children The Pediatric Infectious Disease Journal ·MIRIAM ISH-HOROWICZ, Stanley H. Korman, Mervyn Shapiro, UDI HAR-EVEN, Israel Tamir, NURITH STRAUSS, Richard J. Deckelbaum	1989	64
6	Phenotype and genotype variation in primary carnitine deficiency Genetics in Medicine ·Yuhuan Wang, Stanley H. Korman, Jing Ye, J. Jay Gargus, Alisa Gutman, Franco Taroni, Barbara Garavaglia, Nicola Longo	2001	59
7	A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents The American Journal of Human Genetics ·Annick Raas‐Rothschild, Ronald J. A. Wanders, Petra A.W. Mooijer, Jeannette Gootjes, Hans R. Waterham, Alisa Gutman, Yasuyuki Suzuki, Nobuyuki Shimozawa, Naomi Kondo, Gideon Eshel, Marc Espeel, Frank Roels, Stanley H. Korman	2002	55
8	Agenesis of corpus callosum and optic nerve hypoplasia due to mutations in SLC25A1 encoding the mitochondrial citrate transporter Journal of Medical Genetics ·Simon Edvardson, Vito Porcelli, Chaim Jalas, Devorah Soiferman, Yuval Kellner, Avraham Shaag, Stanley H. Korman, Ciro Leonardo Pierri, Pasquale Scarcia, Nitay Fraenkel, Reeval Segel, Abraham Schechter, Ayala Frumkin, Ophry Pines, Ann Saada, Luigi Palmieri, Orly Elpeleg	2013	53
9	TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome Journal of Medical Genetics ·Ronen Spiegel, Morad Khayat, Stavit A. Shalev, Y. Horovitz, Hanna Mandel, Eli Hershkovitz, Flora Barghuti, Avraham Shaag, Ann Saada, Stanley H. Korman, Orly Elpeleg, Ido Yatsiv	2010	52
10	Inborn errors of isoleucine degradation: A review Molecular Genetics and Metabolism ·Stanley H. Korman	2006	50
11	Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin Molecular Genetics and Metabolism ·Ingrid Tein, Orly Elpeleg, Bruria Ben‐Zeev, Stanley H. Korman, Alexander Lossos, Dorit Lev, Tally Lerman‐Sagie, Esther Leshinsky‐Silver, Jerry Vockley, Gerard T. Berry, Anne‐Marie Lamhonwah, Dietrich Matern, Charles R. Roe, Niels Gregersen	2007	45
12	Pitfalls in the diagnosis of glycine encephalopathy (non-ketotic hyperglycinemia) Developmental Medicine & Child Neurology ·Stanley H. Korman, Alisa Gutman	2002	44
13	PNPO deficiency: An under diagnosed inborn error of pyridoxine metabolism Molecular Genetics and Metabolism ·Morad Khayat, Stanley H. Korman, Pnina Frankel, Zalman Weintraub, Sylvia Hershckowitz, Vered Fleisher Sheffer, Mordechai Ben Elisha, Ron A. Wevers, Tzipora C. Falik‐Zaccai	2008	44
14	Giardia lamblia: Identification of different strains from man Parasitology Research ·Stanley H. Korman, Sylvie M. Le Blancq, Dan T. Spira, J. El On, Ram Reifen, Richard J. Deckelbaum	1986	44
15	Frequent rearrangements of rRNA-encoding chromosomes inGiardia lamblia Nucleic Acids Research ·Sylvie M. Le Blancq, Stanley H. Korman, Lex H.T. Van der Ploeg	1991	43
16	Persistent NKH with transient or absent symptoms and a homozygous GLDC mutation Annals of Neurology ·Stanley H. Korman, Avihu Boneh, Akiko Ichinohe, Kanako Kojima, Ken‐ichi Sato, Zivanit Ergaz, John M. Gomori, Alisa Gutman, Shigeo Kure	2004	42
17	Treatment from birth of nonketotic hyperglycinemia due to a novel GLDC mutation Annals of Neurology ·Stanley H. Korman, Isaiah D. Wexler, Alisa Gutman, M. O. Rolland, Junko Kanno, Shigeo Kure	2006	41
18	Pitfalls in the diagnosis of glycine encephalopathy (non‐ketotic hyperglycinemia) Developmental Medicine & Child Neurology ·Stanley H. Korman, Alisa Gutman	2002	41
19	Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency Molecular Genetics and Metabolism ·Stanley H. Korman, Hans R. Waterham, Alisa Gutman, Cornelis Jakobs, Ronald J. A. Wanders	2005	38
20	Giardia lamblia: haploid genome size determined by pulsed field gel electrophoresis is less than 12 Mb Nucleic Acids Research ·Jian‐Bing Fan, Stanley H. Korman, Charles R. Cantor, Cassandra L. Smith	1991	35

About Stanley H. Korman

Stanley H. Korman is a scholar working on Clinical Biochemistry, Molecular Biology, Biochemistry, Rheumatology and Physiology, having authored 94 papers that have together received 2.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (48 papers), Amino Acid Enzymes and Metabolism (22 papers), Biochemical and Molecular Research (17 papers), Mitochondrial Function and Pathology (13 papers), Neonatal Health and Biochemistry (10 papers), Parasitic Infections and Diagnostics (10 papers), Peroxisome Proliferator-Activated Receptors (9 papers) and Diet and metabolism studies (8 papers). The work is most often cited by research in Clinical Biochemistry (828 citations), Biochemistry (337 citations), Parasitology (220 citations), Molecular Biology (1.2k citations) and Cancer Research (235 citations). Stanley H. Korman has collaborated with scholars based in Israel, United States and Netherlands. Frequent co-authors include Alisa Gutman, Richard J. Deckelbaum, Orly Elpeleg, Sylvie M. Le Blancq, Hanna Mandel, Avraham Shaag, Ann Saada, John M. Gomori, Simon Edvardson and Lex H.T. Van der Ploeg. Their work appears in journals such as Molecular Genetics and Metabolism, Journal of Inherited Metabolic Disease, Journal of Pediatric Gastroenterology and Nutrition, Annals of Neurology and Nucleic Acids Research.

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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