Orit Reish

3.1k total citations · 1 hit paper
72 papers, 1.8k citations indexed

About

Orit Reish is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Orit Reish has authored 72 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 27 papers in Molecular Biology and 24 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Orit Reish's work include Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (11 papers) and Metabolism and Genetic Disorders (6 papers). Orit Reish is often cited by papers focused on Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (11 papers) and Metabolism and Genetic Disorders (6 papers). Orit Reish collaborates with scholars based in Israel, United States and United Kingdom. Orit Reish's co-authors include Arie Herman, Susan A. Berry, Ron Maymon, Aliza Amiel, Zvi Vaknin, Eli Heyman, Moshe Fejgin, Richard A. King, Heather Etchevers and Christelle Golzio and has published in prestigious journals such as Cancer, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Orit Reish

72 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations

2009 294 citations Orit Reish et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Orit Reish Israel	25	880	516	425	165	146	72	1.8k
Ishwar C. Verma India	20	625 0.7×	386 0.7×	325 0.8×	246 1.5×	65 0.4×	139	1.7k
Tülay Güran Türkiye	25	833 0.9×	452 0.9×	222 0.5×	86 0.5×	61 0.4×	131	2.3k
Thomas P. Foley United States	29	655 0.7×	502 1.0×	498 1.2×	126 0.8×	98 0.7×	85	2.8k
Mimi S. Kim United States	24	825 0.9×	241 0.5×	153 0.4×	140 0.8×	174 1.2×	66	1.6k
Boleslaw Goldman Israel	22	746 0.8×	575 1.1×	246 0.6×	45 0.3×	74 0.5×	74	1.7k
Kirk Aleck United States	18	775 0.9×	566 1.1×	815 1.9×	86 0.5×	51 0.3×	31	2.0k
Michael Pike United Kingdom	24	459 0.5×	385 0.7×	179 0.4×	51 0.3×	91 0.6×	61	1.9k
David B. Flannery United States	18	381 0.4×	599 1.2×	337 0.8×	102 0.6×	58 0.4×	45	1.2k
Adda Grimberg United States	28	1.1k 1.3×	505 1.0×	550 1.3×	60 0.4×	421 2.9×	85	3.0k
Christiane Theda Australia	16	774 0.9×	520 1.0×	181 0.4×	158 1.0×	50 0.3×	24	1.3k

Countries citing papers authored by Orit Reish

Since Specialization

Citations

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

Fields of papers citing papers by Orit Reish

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Orit Reish

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

All Works

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20 of 20 papers shown

Laitman, Yael, Rachel Michaelson‐Cohen, Rakefet Chen‐Shtoyerman, et al.. (2020). Age at diagnosis of cancer in 185delAG BRCA1 mutation carriers of diverse ethnicities: tentative evidence for modifier factors. Familial Cancer. 20(3). 189–194. 1 indexed citations

Michaelson‐Cohen, Rachel, Rakefet Chen‐Shtoyerman, Orit Reish, et al.. (2018). Uterine cancer in Jewish Israeli BRCA1/2 mutation carriers. Cancer. 125(5). 698–703. 24 indexed citations

Paluch–Shimon, Shani, Addie Dvir, Luna Kadouri, et al.. (2015). Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel. Breast Cancer Research and Treatment. 155(1). 133–138. 17 indexed citations

Reish, Orit, et al.. (2011). Sporadic Aneuploidy in PHA-Stimulated Lymphocytes of Trisomies 21, 18, and 13. Cytogenetic and Genome Research. 133(2-4). 184–189. 25 indexed citations

Spiegel, Ronen, Annick Raas‐Rothschild, Orit Reish, et al.. (2009). The clinical spectrum of fetal Niemann–Pick type C. American Journal of Medical Genetics Part A. 149A(3). 446–450. 68 indexed citations

Strassburger, D., Shevach Friedler, A. Raziel, et al.. (2009). The cytogenetic constitution of embryos derived from immature (metaphase I) oocytes obtained after ovarian hyperstimulation. Fertility and Sterility. 94(3). 971–978. 34 indexed citations

Saada, Ann, Rutger O. Vogel, Saskia J.G. Hoefs, et al.. (2009). Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease. The American Journal of Human Genetics. 84(6). 718–727. 135 indexed citations

Reish, Orit, et al.. (2006). Sporadic aneuploidy in PHA-stimulated lymphocytes of Turner’s syndrome patients. Chromosome Research. 14(5). 527–534. 15 indexed citations

Ben‐Ami, Ido, et al.. (2005). Is there an increased rate of anencephaly in twins?. Prenatal Diagnosis. 25(11). 1007–1010. 8 indexed citations

10.

Herman, Arie, et al.. (2003). Correlation and Overlapping between Nuchal Translucency and Triple Test among Down Syndrome-Affected Pregnancies. Fetal Diagnosis and Therapy. 18(3). 196–200. 6 indexed citations

11.

Shohat, Mordechai, Z. Appelman, Ziva Ben‐Neriah, et al.. (2003). Prenatal diagnosis of Down syndrome: Ten year experience in the Israeli population. American Journal of Medical Genetics Part A. 122A(3). 215–222. 24 indexed citations

12.

Reish, Orit, et al.. (2003). Modified allelic replication in lymphocytes of patients with neurofibromatosis type 1. Cancer Genetics and Cytogenetics. 143(2). 133–139. 12 indexed citations

13.

Maymon, Ron, Gratiana Hermann, Orit Reish, et al.. (2003). Chorioangioma and its severe infantile sequelae: case report. Prenatal Diagnosis. 23(12). 976–980. 18 indexed citations

14.

Reish, Orit, Israela Lerer, Aliza Amiel, et al.. (2002). Wiedemann‐Beckwith syndrome: Further prenatal characterization of the condition. American Journal of Medical Genetics. 107(3). 209–213. 45 indexed citations

15.

Reish, Orit, et al.. (2002). Asynchronous replication of biallelically expressed loci: A new phenomenon in Turner syndrome. Genetics in Medicine. 4(6). 439–443. 9 indexed citations

16.

Erez, Ilan, et al.. (2001). Congenital Short-Bowel and Malrotation: Clinical Presentation and Outcome of Six Affected Offspring in Three Related Families. European Journal of Pediatric Surgery. 11(5). 331–334. 39 indexed citations

17.

Amiel, Aliza, et al.. (2000). Replication Asynchrony Increases in Women at Risk for Aneuploid Offspring. Chromosome Research. 8(2). 141–150. 15 indexed citations

18.

Reish, Orit, Robert J. Gorlin, Maria Hordinsky, et al.. (1997). Brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia BRESEK/BRESHECK: New X-link. American Journal of Medical Genetics. 68(4). 386–390. 28 indexed citations

19.

Reish, Orit, Robert Plante, & M. Tuchman. (1993). Four New Mutations in the Ornithine Transcarbamylase Gene. Biochemical Medicine and Metabolic Biology. 50(2). 169–175. 18 indexed citations

20.

Harel, Liora, et al.. (1990). MUMPS ARTHRITIS IN CHILDREN. The Pediatric Infectious Disease Journal. 9(12). 928–928. 5 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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