Judith Dagan

649 total citations
27 papers, 457 citations indexed

About

Judith Dagan is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Judith Dagan has authored 27 papers receiving a total of 457 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 11 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Judith Dagan's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (4 papers). Judith Dagan is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (5 papers) and Chromosomal and Genetic Variations (4 papers). Judith Dagan collaborates with scholars based in Israel, United States and Netherlands. Judith Dagan's co-authors include Joël Zlotogora, Dvorah Abeliovich, Gertrude Kohn, Maimon M. Cohen, Meira Shaham, B. Jacoby, Israela Lerer, Kyla Marks, Vardiella Meiner and Alina Levy and has published in prestigious journals such as The Lancet, Cancer Letters and Physiologia Plantarum.

In The Last Decade

Judith Dagan

27 papers receiving 423 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judith Dagan Israel 12 231 223 96 88 85 27 457
M.M. Aronson United States 13 264 1.1× 213 1.0× 90 0.9× 83 0.9× 75 0.9× 48 498
K. L. Ying United States 12 267 1.2× 252 1.1× 75 0.8× 81 0.9× 51 0.6× 18 497
Christa M. Lese United States 8 313 1.4× 438 2.0× 157 1.6× 168 1.9× 50 0.6× 12 598
M. F. Croquette France 11 274 1.2× 293 1.3× 49 0.5× 100 1.1× 56 0.7× 17 444
Philippe Coullin France 15 268 1.2× 208 0.9× 189 2.0× 76 0.9× 32 0.4× 28 526
Herman E. Wyandt United States 15 205 0.9× 359 1.6× 169 1.8× 108 1.2× 24 0.3× 40 517
J L Watt United Kingdom 13 191 0.8× 298 1.3× 161 1.7× 130 1.5× 47 0.6× 19 462
D L Van Dyke United States 9 282 1.2× 301 1.3× 72 0.8× 110 1.3× 76 0.9× 11 540
A. Rodewald Germany 17 218 0.9× 552 2.5× 170 1.8× 154 1.8× 50 0.6× 41 726
M.H. Breuning Netherlands 8 219 0.9× 157 0.7× 43 0.4× 77 0.9× 22 0.3× 13 385

Countries citing papers authored by Judith Dagan

Since Specialization
Citations

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

Fields of papers citing papers by Judith Dagan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Dagan

This figure shows the co-authorship network connecting the top 25 collaborators of Judith Dagan. A scholar is included among the top collaborators of Judith Dagan 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 Judith Dagan. Judith Dagan 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.
Kurolap, Alina, Israela Lerer, Judith Dagan, et al.. (2022). Unique Ataxia-Oculomotor Apraxia 2 (AOA2) in Israel with Novel Variants, Atypical Late Presentation, and Possible Identification of a Poison Exon. Journal of Molecular Neuroscience. 72(8). 1715–1723. 2 indexed citations
2.
Raas‐Rothschild, Annick, et al.. (2009). The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: Report on two patients and review of the literature. European Journal of Medical Genetics. 52(2-3). 140–144. 14 indexed citations
3.
Dagan, Judith, et al.. (2003). Establishment and characterization of pheochromocytoma tumor models expressing different levels of trkA receptors. Cancer Letters. 200(2). 177–185. 3 indexed citations
4.
Sagi, Michal, et al.. (2001). Prenatal diagnosis of sex chromosome aneuploidy: possible reasons for high rates of pregnancy termination. Prenatal Diagnosis. 21(6). 461–465. 43 indexed citations
5.
Dagan, Judith, et al.. (1999). Increased Spontaneous Chromosomal Breakage in Shwachman Syndrome. Journal of Pediatric Gastroenterology and Nutrition. 28(4). 449–450. 9 indexed citations
6.
Zlotogora, Joël, et al.. (1998). Transient neonatal diabetes mellitus in a child with invdup(6)(q22q23) of paternal origin.. PubMed. 5(6). 417–9. 33 indexed citations
7.
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
8.
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
9.
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
10.
Friling, Ronit, Y Yassur, Dvorah Abeliovich, et al.. (1995). A complex chromosome translocation resulting in deletion 11 p and associated with uveal colobomata. Ophthalmic Genetics. 16(2). 71–74. 4 indexed citations
11.
Nadjari, M., et al.. (1993). Nonimmune hydrops fetalis in a 49,XXXXY fetus at 16 menstrual weeks. American Journal of Medical Genetics. 47(4). 529–530. 5 indexed citations
12.
Abeliovich, Dvorah, Judith Dagan, Alina Levy, Avraham Steinberg, & Joël Zlotogora. (1993). Isochromosome 18p in a mother and her child. American Journal of Medical Genetics. 46(4). 392–393. 47 indexed citations
13.
Ziv, Yael, Galit Rotman, Moshe Frydman, et al.. (1991). The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22–q23. Genomics. 9(2). 373–375. 38 indexed citations
14.
Voss, R., Eva Gross‐Kieselstein, Haggit Hurvitz, et al.. (1984). A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.. Journal of Medical Genetics. 21(6). 454–459. 8 indexed citations
15.
Wahrman, J., et al.. (1978). A long unidentifiable extra chromosomal segment – a possible duplication of human 7q. Cytogenetic and Genome Research. 20(1-6). 160–168. 7 indexed citations
16.
Mm, Cohen, I. Ariel, & Judith Dagan. (1974). Chromosome deletion (46, XY, 20q-) in sideroblastic anemia.. PubMed. 10(11). 1393–6. 23 indexed citations
17.
Kohn, Gertrude, et al.. (1973). CHROMOSOMES IN ATAXIATELANGIECTASIA. The Lancet. 302(7844). 1500–1500. 14 indexed citations
18.
Dagan, Judith & Daniel Zohary. (1970). Wild tetraploid wheats from West Iran cytogenetically identical with Israeli T. dicoccoides.. 15–17. 11 indexed citations
19.
Jacoby, B. & Judith Dagan. (1970). Effects of 6N‐Benzyladenine on Primary Leaves of Intact Bean Plants and on their Sodium Absorption Capacity. Physiologia Plantarum. 23(2). 397–403. 11 indexed citations
20.
Jacoby, B. & Judith Dagan. (1967). A comparison of two methods of investigating sodium uptake by bean-leaf cells and the vitality of isolated leaf-cells. PROTOPLASMA. 64(3). 325–329. 9 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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