Dvorah Abeliovich

4.8k total citations
98 papers, 3.0k citations indexed

About

Dvorah Abeliovich is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Dvorah Abeliovich has authored 98 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 39 papers in Genetics and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Dvorah Abeliovich's work include Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (15 papers) and Genetic Syndromes and Imprinting (13 papers). Dvorah Abeliovich is often cited by papers focused on Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (15 papers) and Genetic Syndromes and Imprinting (13 papers). Dvorah Abeliovich collaborates with scholars based in Israel, United States and United Kingdom. Dvorah Abeliovich's co-authors include Israela Lerer, Joël Zlotogora, Michal Sagi, Tamar Peretz, N. Weinberg, M. Sagi, Ziva Ben‐Neriah, Vardiella Meiner, Luna Kaduri and Norman Heching and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and The American Journal of Human Genetics.

In The Last Decade

Dvorah Abeliovich

97 papers receiving 2.9k citations

Peers

Dvorah Abeliovich

GENET

PPCH

SURGE

PRM

Israela Lerer Israel

Andreas Winterpacht Germany

Peter D. Turnpenny United Kingdom

Oliver Bartsch Germany

Margherita Silengo Italy

Peter Wieacker Germany

Frances Flinter United Kingdom

Hirofumi Ohashi Japan

Irene M. Janssen Netherlands

S Malcolm United Kingdom

Israela Lerer Israel

Dvorah Abeliovich

1.2k ×0.9

972 ×0.7

GENET

301 ×0.7

PPCH

238 ×0.7

SURGE

343 ×1.2

PRM

Citations per year, relative to Dvorah Abeliovich Dvorah Abeliovich (= 1×) peers Israela Lerer

Countries citing papers authored by Dvorah Abeliovich

Since Specialization

Citations

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

Fields of papers citing papers by Dvorah Abeliovich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dvorah Abeliovich

This figure shows the co-authorship network connecting the top 25 collaborators of Dvorah Abeliovich. A scholar is included among the top collaborators of Dvorah Abeliovich 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 Dvorah Abeliovich. Dvorah Abeliovich 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

Goldberg, Yael, Rinnat M. Porat, Inbal Kedar, et al.. (2009). An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC. Familial Cancer. 9(2). 141–150. 21 indexed citations

Sagi, M., N. Weinberg, Elias Aizenman, et al.. (2009). Preimplantation genetic diagnosis for BRCA1/2—a novel clinical experience. Prenatal Diagnosis. 29(5). 508–513. 46 indexed citations

Molho‐Pessach, Vered, Israela Lerer, Dvorah Abeliovich, et al.. (2008). The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3. The American Journal of Human Genetics. 83(4). 529–534. 129 indexed citations

Steiner, Israel, Marc Gotkine, Bettina Steiner‐Birmanns, et al.. (2008). Increased severity over generations of Charcot-Marie-Tooth disease type 1A. Journal of Neurology. 255(6). 813–819. 13 indexed citations

Kadouri, Luna, Dani Bercovich, Israela Lerer, et al.. (2007). A novel BRCA-1 mutation in Arab kindred from east Jerusalem with breast and ovarian cancer. BMC Cancer. 7(1). 14–14. 30 indexed citations

Ben‐Chetrit, Eldad, et al.. (2003). Molecular diagnosis of FMF: lessons from a study of 446 unrelated individuals.. PubMed. 20(4 Suppl 26). S25–9. 29 indexed citations

Lotem, Michal, et al.. (2003). Cytogenetic analysis of melanoma cell lines. Cancer Genetics and Cytogenetics. 142(2). 87–91. 9 indexed citations

Cividalli, Gabriel, et al.. (2002). Fluorescence in situ hybridization analysis of the cryptic t(12;21) (p13;q22) in childhood B-lineage acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 132(1). 61–64. 12 indexed citations

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

10.

Lerer, Israela, et al.. (2001). The 28-kb Deletion Spanning D15S63 Is a Polymorphic Variant in the Ashkenazi Jewish Population. The American Journal of Human Genetics. 68(1). 261–263. 4 indexed citations

11.

Buiting, Karin, Bärbel Dittrich, Bernd Dworniczak, et al.. (1999). A 28-kb Deletion Spanning D15S63 (PW71) in Five Families: A Rare Neutral Variant?. The American Journal of Human Genetics. 65(6). 1588–1594. 7 indexed citations

12.

Abeliovich, Dvorah, Susana Ben‐Neriah, Rachel E. Cohen, et al.. (1999). Clinical Implications of Fluorescence In Situ Hybridization Analysis in 13 Chronic Myeloid Leukemia Cases. Cancer Genetics and Cytogenetics. 114(2). 100–107. 27 indexed citations

13.

Bar, Merav, et al.. (1997). Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel‐Lindau and RET genes. Clinical Endocrinology. 47(6). 707–712. 42 indexed citations

14.

Ariel, I M, Dvorah Abeliovich, Jacob Bar‐Ziv, & Abraham Hochberg. (1996). Renal Pathology in Wagr Syndrome. Pediatric Pathology & Laboratory Medicine. 16(6). 1013–1021. 4 indexed citations

15.

Maarel, Silvère M. van der, D. Olde Weghuis, I Huber, et al.. (1995). Cloning of candidate genes for X-linked mental retardation by use of chromosome aberrations. American Journal of Medical Genetics Part A. 64(1). 19. 1 indexed citations

16.

Abeliovich, Dvorah, et al.. (1995). Reversed BCR/ABL rearrangement detected by FISH in Philadelphia negative chronic myelocytic leukemia. Cancer Genetics and Cytogenetics. 81(2). 115–117. 14 indexed citations

17.

Abeliovich, Dvorah, Judith Dagan, Chava Kimchi‐Sarfaty, & Joël Zlotogora. (1995). Paracentric inversion X(q21.2q24) associated with mental retardation in males and normal ovarian function in females. American Journal of Medical Genetics. 55(3). 359–362. 9 indexed citations

18.

Schiff, Elena, Joël Zlotogora, Dvorah Abeliovich, M. Zeigler, & Gideon Bach. (1994). Hunter syndrome among Jews in Israel. Biomedicine & Pharmacotherapy. 48(8-9). 381–384. 5 indexed citations

19.

Abeliovich, Dvorah, Iris Lavon, Israela Lerer, et al.. (1992). Screening for five mutations detects 97% of cystic fibrosis (CF) chromosomes and predicts a carrier frequency of 1:29 in the Jewish Ashkenazi population.. PubMed. 51(5). 951–6. 114 indexed citations

20.

Rosenthal, Joseph, Dvorah Abeliovich, Rivka Carmi, John M. Opitz, & James F. Reynolds. (1987). Clinical variability of partial duplication 1q: A clinical report and literature review. American Journal of Medical Genetics. 27(4). 787–792. 11 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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