Elena Michaelovsky

2.1k total citations
38 papers, 1.4k citations indexed

About

Elena Michaelovsky is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Psychology. According to data from OpenAlex, Elena Michaelovsky has authored 38 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 15 papers in Cellular and Molecular Neuroscience and 11 papers in Clinical Psychology. Recurrent topics in Elena Michaelovsky's work include Neurotransmitter Receptor Influence on Behavior (14 papers), Congenital heart defects research (12 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Elena Michaelovsky is often cited by papers focused on Neurotransmitter Receptor Influence on Behavior (14 papers), Congenital heart defects research (12 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Elena Michaelovsky collaborates with scholars based in Israel, United States and Sweden. Elena Michaelovsky's co-authors include Amos Frisch, Abraham Weizman, Alan Apter, Miri Carmel, Rivka Rockah, Doron Gothelf, R. Weizman, Michael Poyurovsky, Omer Zarchi and Nathaniel Laor and has published in prestigious journals such as Biological Psychiatry, Molecular Psychiatry and Psychophysiology.

In The Last Decade

Elena Michaelovsky

38 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elena Michaelovsky Israel 23 541 430 418 356 275 38 1.4k
Araceli Rosa Spain 22 243 0.4× 320 0.7× 308 0.7× 612 1.7× 403 1.5× 69 1.7k
Julie Taubman United States 8 289 0.5× 655 1.5× 466 1.1× 312 0.9× 122 0.4× 10 1.5k
Branimir Jernej Croatia 19 318 0.6× 504 1.2× 151 0.4× 235 0.7× 154 0.6× 47 1.1k
Jana Strohmaier Germany 21 307 0.6× 218 0.5× 175 0.4× 362 1.0× 380 1.4× 42 1.3k
Zhifeng Zhou China 17 302 0.6× 392 0.9× 131 0.3× 156 0.4× 163 0.6× 38 1.1k
В. Е. Голимбет Russia 17 388 0.7× 286 0.7× 181 0.4× 312 0.9× 297 1.1× 202 1.2k
Hisashi Tanii Japan 24 269 0.5× 229 0.5× 380 0.9× 324 0.9× 134 0.5× 70 1.4k
Olga Okladnova Germany 15 398 0.7× 555 1.3× 224 0.5× 243 0.7× 238 0.9× 21 1.2k
Paweł Kapelski Poland 20 351 0.6× 380 0.9× 120 0.3× 387 1.1× 285 1.0× 66 1.2k
Dubravka Hranilović Croatia 18 302 0.6× 445 1.0× 131 0.3× 210 0.6× 186 0.7× 44 1.0k

Countries citing papers authored by Elena Michaelovsky

Since Specialization
Citations

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

Fields of papers citing papers by Elena Michaelovsky

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Michaelovsky

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Michaelovsky. A scholar is included among the top collaborators of Elena Michaelovsky 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 Elena Michaelovsky. Elena Michaelovsky 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.
Melhem, Nadine, Sami Hamdan, Lambertus Klei, et al.. (2017). Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred. Psychiatric Genetics. 27(5). 169–177. 3 indexed citations
2.
Gothelf, Doron, Amos Frisch, Abraham Weizman, et al.. (2015). Thymic and bone marrow output in individuals with 22q11.2 deletion syndrome. Pediatric Research. 77(4). 579–585. 20 indexed citations
3.
Carmel, Miri, Omer Zarchi, Elena Michaelovsky, et al.. (2014). Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects. Journal of Psychiatric Research. 56. 28–35. 24 indexed citations
4.
Zarchi, Omer, Adele Diamond, Ronnie Weinberger, et al.. (2013). A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: Velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes. European Psychiatry. 29(4). 203–210. 23 indexed citations
5.
Zarchi, Omer, Miri Carmel, J. Attias, et al.. (2013). Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes. Journal of Psychiatric Research. 47(11). 1623–1629. 31 indexed citations
6.
Michaelovsky, Elena, Amos Frisch, Miri Carmel, et al.. (2012). Genotype-phenotype correlation in 22q11.2 deletion syndrome. BMC Medical Genetics. 13(1). 122–122. 71 indexed citations
7.
Gothelf, Doron, Amos Frisch, Elena Michaelovsky, Abraham Weizman, & Robert J. Shprintzen. (2009). Velocardiofacial Syndrome. Journal of Mental Health Research in Intellectual Disabilities. 2(2). 149–167. 48 indexed citations
8.
Wasserman, Danuta, T. Geijer, Marcus Sokolowski, et al.. (2006). Association of the serotonin transporter promotor polymorphism with suicide attempters with a high medical damage. European Neuropsychopharmacology. 17(3). 230–233. 34 indexed citations
9.
Zalsman, Gil, Amos Frisch, Leo Sher, et al.. (2005). Family-based association study of 5-HT2A receptor T102C polymorphism and suicidal behavior in Ashkenazi inpatient adolescents. International Journal of Adolescent Medicine and Health. 17(3). 231–238. 18 indexed citations
10.
Zalsman, Gil, George M. Anderson, Amos Frisch, et al.. (2005). Relationships between serotonin transporter promoter polymorphism, platelet serotonin transporter binding and clinical phenotype in suicidal and non-suicidal adolescent inpatients. Journal of Neural Transmission. 112(2). 309–315. 26 indexed citations
11.
Poyurovsky, Michael, Elena Michaelovsky, Amos Frisch, et al.. (2005). COMT Val158Met polymorphism in schizophrenia with obsessive-compulsive disorder: A case–control study. Neuroscience Letters. 389(1). 21–24. 32 indexed citations
12.
Koronyo‐Hamaoui, Maya, Amos Frisch, David Stein, et al.. (2005). Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca2+-activated K+ channel to genetic predisposition to anorexia nervosa. Journal of Psychiatric Research. 41(1-2). 160–167. 22 indexed citations
13.
Michaelovsky, Elena, Amos Frisch, Dan J. Stein, et al.. (2005). Haplotype analysis of the COMT‐ARVCF gene region in Israeli anorexia nervosa family trios. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 139B(1). 45–50. 18 indexed citations
14.
Koronyo‐Hamaoui, Maya, Eva Gak, Dan J. Stein, et al.. (2004). CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: A case‐control study of female patients and several ethnic groups in the Israeli Jewish population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 131B(1). 76–80. 15 indexed citations
15.
16.
Zalsman, Gil, Amos Frisch, Robyn Lewis, et al.. (2004). DRD4 receptor gene exon III polymorphism in inpatient suicidal adolescents. Journal of Neural Transmission. 111(12). 1593–1603. 20 indexed citations
17.
Zalsman, Gil, Amos Frisch, Michal Bromberg, et al.. (2001). Family‐based association study of serotonin transporter promoter in suicidal adolescents: No association with suicidality but possible role in violence traits. American Journal of Medical Genetics. 105(3). 239–245. 66 indexed citations
18.
Frisch, Amos, Elena Michaelovsky, Rivka Rockah, et al.. (2000). Association between obsessive-compulsive disorder and polymorphisms of genes encoding components of the serotonergic and dopaminergic pathways. European Neuropsychopharmacology. 10(3). 205–209. 99 indexed citations
19.
Persson, Malin, T. Geijer, Amos Frisch, et al.. (2000). Dopamine D4 receptor gene polymorphism and personality traits in healthy volunteers. European Archives of Psychiatry and Clinical Neuroscience. 250(4). 203–206. 23 indexed citations
20.
Persson, Malin, T. Geijer, Danuta Wasserman, et al.. (1999). Lack of association between suicide attempt and a polymorphism at the dopamine receptor D4 locus. Psychiatric Genetics. 9(2). 97–100. 15 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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