Michael Korostishevsky

1.2k total citations
27 papers, 718 citations indexed

About

Michael Korostishevsky is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Michael Korostishevsky has authored 27 papers receiving a total of 718 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Rheumatology. Recurrent topics in Michael Korostishevsky's work include Autoimmune Bullous Skin Diseases (3 papers), Congenital heart defects research (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Michael Korostishevsky is often cited by papers focused on Autoimmune Bullous Skin Diseases (3 papers), Congenital heart defects research (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Michael Korostishevsky collaborates with scholars based in Israel, United States and United Kingdom. Michael Korostishevsky's co-authors include Asaf Levy, Uri Nir, Eitan Friedman, Batsheva Bonné‐Tamir, Dvir Dahary, Doron Lancet, Edna Ben‐Asher, Yaël Ratner, Michael S. Ritsner and Ruth Navon and has published in prestigious journals such as Biological Psychiatry, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Michael Korostishevsky

26 papers receiving 698 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael Korostishevsky Israel 15 357 148 101 95 83 27 718
Barry A. Chioza United Kingdom 20 551 1.5× 222 1.5× 43 0.4× 76 0.8× 40 0.5× 39 1.1k
Vı́ctor Volpini Spain 23 605 1.7× 188 1.3× 33 0.3× 41 0.4× 34 0.4× 45 1.2k
Melissa A. Landek‐Salgado United States 18 330 0.9× 127 0.9× 26 0.3× 122 1.3× 12 0.1× 31 1.1k
Melissa B. Gingrich United States 8 370 1.0× 52 0.4× 98 1.0× 68 0.7× 15 0.2× 9 1.2k
Bernhard Weschke Germany 13 547 1.5× 152 1.0× 41 0.4× 164 1.7× 114 1.4× 23 985
Hidetoshi Kassai Japan 16 465 1.3× 105 0.7× 46 0.5× 99 1.0× 17 0.2× 29 751
Judith Mallolas Spain 9 291 0.8× 85 0.6× 71 0.7× 66 0.7× 33 0.4× 13 547
Maria Kousi United States 12 621 1.7× 340 2.3× 25 0.2× 374 3.9× 18 0.2× 15 1.2k
Matthew Covey United States 15 332 0.9× 104 0.7× 70 0.7× 58 0.6× 26 0.3× 17 807

Countries citing papers authored by Michael Korostishevsky

Since Specialization
Citations

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

Fields of papers citing papers by Michael Korostishevsky

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael Korostishevsky. 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 Michael Korostishevsky. The network helps show where Michael Korostishevsky may publish in the future.

Co-authorship network of co-authors of Michael Korostishevsky

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Korostishevsky. A scholar is included among the top collaborators of Michael Korostishevsky 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 Michael Korostishevsky. Michael Korostishevsky 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.
Korostishevsky, Michael, Claire J. Steves, Ida Malkin, et al.. (2015). Genomics and metabolomics of muscular mass in a community-based sample of UK females. European Journal of Human Genetics. 24(2). 277–283. 39 indexed citations
2.
Korostishevsky, Michael, Daniel Kurnik, Eleni Aklillu, et al.. (2014). The VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populations. Journal of Applied Genetics. 55(2). 163–171. 5 indexed citations
3.
Korostishevsky, Michael, Amos Frisch, Yoram Cohen, et al.. (2013). Association between a common CYP17A1 haplotype and anxiety in female anorexia nervosa. Archives of Women s Mental Health. 16(5). 423–428. 2 indexed citations
4.
Korostishevsky, Michael, Ida Malkin, Svetlana Trofimov, et al.. (2012). Significant association between body composition phenotypes and the osteocalcin genomic region in normative human population. Bone. 51(4). 688–694. 19 indexed citations
5.
Korostishevsky, Michael, Frances M. K. Williams, Deborah Hart, et al.. (2012). Implementation of the simplified stochastic model of ageing for longitudinal osteoarthritis data assessment. Annals of Human Biology. 39(3). 214–222. 1 indexed citations
6.
Levy, Asaf, et al.. (2009). Single nucleotide polymorphisms in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high‐risk women. International Journal of Cancer. 127(3). 589–597. 103 indexed citations
7.
Korostishevsky, Michael, Ida Malkin, Tim D. Spector, & Gregory Livshits. (2009). Parametric model‐based statistics for possible genotyping errors and sample stratification in sibling‐pair SNP data. Genetic Epidemiology. 34(1). 26–33. 2 indexed citations
8.
Korostishevsky, Michael, et al.. (2008). Anthropometric and bone-related biochemical factors are associated with different haplotypes of ANKH locus. Annals of Human Biology. 35(5). 535–546. 4 indexed citations
9.
Kalichman, Leonid, Michael Korostishevsky, & Eugene Kobyliansky. (2008). Laterality indices in the Chuvashian population. Anthropologischer Anzeiger. 66(4). 409–418. 4 indexed citations
10.
Michaelovsky, Elena, Doron Gothelf, Michael Korostishevsky, et al.. (2007). Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS. The International Journal of Neuropsychopharmacology. 11(3). 351–63. 40 indexed citations
11.
Gothelf, Doron, Elena Michaelovsky, Amos Frisch, et al.. (2006). Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome. The International Journal of Neuropsychopharmacology. 10(3). 301–301. 55 indexed citations
12.
Ostrovsky, Olga, Michael Korostishevsky, Merav Leiba, et al.. (2006). Characterization of HPSE Gene Single Nucleotide Polymorphisms in Jewish Populations of Israel. Acta Haematologica. 117(1). 57–64. 21 indexed citations
13.
Gazit, Ephraim, et al.. (2004). Erroneous identification in a mixed population: simulation using Israeli STR data. International Journal of Legal Medicine. 118(2). 111–114. 1 indexed citations
14.
Ostrovsky, Olga, Arnon Nagler, Michael Korostishevsky, Ephraim Gazit, & Hanan Galski. (2004). Genotype and Allele Frequencies of C3435T Polymorphism of the MDR1 Gene in Various Jewish Populations of Israel. Therapeutic Drug Monitoring. 26(6). 679–684. 18 indexed citations
15.
Korostishevsky, Michael, Yaël Ratner, Dvir Dahary, et al.. (2004). Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis. Biological Psychiatry. 56(3). 169–176. 151 indexed citations
16.
Loewenthal, Ron, et al.. (2003). Pemphigus vulgaris in Jewish patients is associated with HLA-A region genes. Human Immunology. 64(8). 771–779. 26 indexed citations
17.
18.
Tamary, Hannah, Lea Shalmon, Hanna Shalev, et al.. (1998). Localization of the Gene for Congenital Dyserythropoietic Anemia Type I to a <1-cM Interval on Chromosome 15q15.1-15.3. The American Journal of Human Genetics. 62(5). 1062–1069. 42 indexed citations
19.
Baldwin, Clinton T., et al.. (1995). Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Human Molecular Genetics. 4(9). 1637–1642. 72 indexed citations
20.
Bonné‐Tamir, Batsheva, et al.. (1994). Genetic Mapping of the Gene for Usher Syndrome: Linkage Analysis in a Large Samaritan Kindred. Genomics. 20(1). 36–42. 20 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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