Dvorah Abeliovich

1.2k total citations · 1 hit paper
15 papers, 965 citations indexed

About

Dvorah Abeliovich is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Dvorah Abeliovich has authored 15 papers receiving a total of 965 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Dvorah Abeliovich's work include Genomic variations and chromosomal abnormalities (4 papers), Cystic Fibrosis Research Advances (3 papers) and Cancer Genomics and Diagnostics (3 papers). Dvorah Abeliovich is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Cystic Fibrosis Research Advances (3 papers) and Cancer Genomics and Diagnostics (3 papers). Dvorah Abeliovich collaborates with scholars based in Israel, Germany and United States. Dvorah Abeliovich's co-authors include Tamar Peretz, Jeffery P. Struewing, Michael M. Kaback, Francis S. Collins, Lawrence C. Brody, Israela Lerer, Michal Sagi, Annick Raas‐Rothschild, EA Rachmilewitz and Haya Levi and has published in prestigious journals such as Nature Genetics, Blood and Human Molecular Genetics.

In The Last Decade

Dvorah Abeliovich

15 papers receiving 929 citations

Hit Papers

The carrier frequency of ... 1995 2026 2005 2015 1995 100 200 300 400 500
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.

  1. The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals
    1995 512 citations Jeffery P. Struewing, Dvorah Abeliovich et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dvorah Abeliovich Israel 12 557 443 189 186 110 15 965
A M van den Ouweland Netherlands 13 286 0.5× 312 0.7× 186 1.0× 52 0.3× 122 1.1× 19 737
Kelly Gonzalez United States 13 423 0.8× 413 0.9× 248 1.3× 110 0.6× 267 2.4× 18 943
Christina Evers Germany 16 274 0.5× 293 0.7× 62 0.3× 78 0.4× 110 1.0× 33 743
Jacob A. Reiss United States 19 514 0.9× 273 0.6× 45 0.2× 111 0.6× 87 0.8× 43 1.0k
Marloes Steehouwer Netherlands 13 740 1.3× 719 1.6× 217 1.1× 115 0.6× 72 0.7× 18 1.4k
L A Brueton United Kingdom 19 693 1.2× 728 1.6× 93 0.5× 41 0.2× 163 1.5× 25 1.3k
Jan Murken Germany 17 633 1.1× 535 1.2× 65 0.3× 84 0.5× 62 0.6× 51 1.1k
Rocío Acuña‐Hidalgo United States 7 340 0.6× 443 1.0× 162 0.9× 60 0.3× 40 0.4× 8 824
Hanna Davies Sweden 8 348 0.6× 447 1.0× 148 0.8× 48 0.3× 106 1.0× 13 856
Veronique Duke United Kingdom 14 202 0.4× 384 0.9× 84 0.4× 74 0.4× 83 0.8× 22 923

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

15 of 15 papers shown
1.
Lerer, Israela, et al.. (2000). Contribution of connexin 26 mutations to nonsyndromic deafness in Ashkenazi patients and the variable phenotypic effect of the mutation 167delT. American Journal of Medical Genetics. 95(1). 53–56. 68 indexed citations
2.
Sagi, Michal, et al.. (1999). Cystic fibrosis mutations in Israeli Arab patients. Human Mutation. 14(6). 543–543. 29 indexed citations
3.
Augarten, Arie, et al.. (1999). A large deletion mutation in the CFTR gene (3120+1Kbdel8.6Kb): A founder mutation in the Palestinian Arabs. Human Mutation. 13(4). 337–337. 39 indexed citations
4.
Kaduri, Luna, Ayala Hubert, Michal Sagi, et al.. (1999). Genetic testing of breast and ovarian cancer patients: clinical characteristics and hormonal risk modifiers. European Journal of Obstetrics & Gynecology and Reproductive Biology. 85(1). 75–80. 9 indexed citations
5.
Abeliovich, Dvorah, et al.. (1996). Microsatellite instability and p53 mutations in therapy-related leukemia suggest mutator phenotype. Blood. 88(11). 4296–4303. 18 indexed citations
6.
Abeliovich, Dvorah, et al.. (1996). Predominant 45,X,-Y karyotype in donor cells after allogeneic BMT: Cytogenetic and molecular analysis. Cancer Genetics and Cytogenetics. 86(1). 1–7. 12 indexed citations
7.
Bar‐David, Shirli, et al.. (1996). Localization of two X-linked mental retardation (XLMR) genes to Xp: MRX37 gene at Xp22.31-p22.32 and a putative MRX gene on Xp22.11-p22.2. American Journal of Medical Genetics. 64(1). 83–88. 12 indexed citations
8.
Abeliovich, Dvorah, et al.. (1996). t(15;21)(q15;q22.1)pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring. American Journal of Medical Genetics. 66(1). 45–51. 5 indexed citations
9.
Abeliovich, Dvorah, et al.. (1996). Cystic Fibrosis Heterozygote Screeningin the Orthodox Community ofAshkenazi Jews: The Dor YesharimApproach and Heterozygote Frequency. European Journal of Human Genetics. 4(6). 338–341. 25 indexed citations
10.
Abeliovich, Dvorah, et al.. (1996). Microsatellite instability and p53 mutations in therapy-related leukemia suggest mutator phenotype. Blood. 88(11). 4296–4303. 146 indexed citations
11.
Struewing, Jeffery P., Dvorah Abeliovich, Tamar Peretz, et al.. (1995). The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nature Genetics. 11(2). 198–200. 512 indexed citations breakdown →
12.
Abeliovich, Dvorah, et al.. (1995). Simultaneous Formation of invdup(15) and dup(15q) in a Girl withDevelopmental Delay: Origin ofthe Abnormal Chromosomes. European Journal of Human Genetics. 3(1). 49–55. 7 indexed citations
13.
Abeliovich, Dvorah, et al.. (1994). Loss of Y chromosome. Cancer Genetics and Cytogenetics. 76(1). 70–71. 18 indexed citations
14.
Buiting, Karin, Bärbel Dittrich, Wendy P. Robinson, et al.. (1994). Detection of aberrant DNA methylation in unique Prader — Willi syndrome patients and its diagnostic implications. Human Molecular Genetics. 3(6). 893–895. 36 indexed citations
15.
Abeliovich, Dvorah, et al.. (1993). Negative expansion of the myotonic dystrophy unstable sequence.. PubMed. 52(6). 1175–81. 29 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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