Hanna Dar

1.1k total citations
53 papers, 796 citations indexed

About

Hanna Dar is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Hanna Dar has authored 53 papers receiving a total of 796 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 17 papers in Pediatrics, Perinatology and Child Health and 10 papers in Molecular Biology. Recurrent topics in Hanna Dar's work include Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Dermatoglyphics and Human Traits (8 papers). Hanna Dar is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Dermatoglyphics and Human Traits (8 papers). Hanna Dar collaborates with scholars based in Israel, United States and Netherlands. Hanna Dar's co-authors include Zvi Borochowitz, Rina Schmidt, Harold M. Nitowsky, R. Gonen, М Шарф, Nicole Israël, Arieh Riskin, Shimon Degani, A. Tamir and Matthias David and has published in prestigious journals such as The Lancet, Annals of Oncology and British Journal of Haematology.

In The Last Decade

Hanna Dar

49 papers receiving 736 citations

Peers

Hanna Dar

PPCH

GENET

SURGE

M. G. J. Jahoda Netherlands

Robert Saura France

G Pescia Switzerland

M J Mahoney United States

Constantinos Pángalos Greece

Robert M. Greenstein United States

Iris Bartels Germany

Kamal K. Naguib Kuwait

Peining Li United States

A.J. Rutherford United Kingdom

M. G. J. Jahoda Netherlands

Hanna Dar

648 ×2.4

PPCH

283 ×1.1

GENET

238 ×0.9

103 ×0.8

149 ×1.7

SURGE

Citations per year, relative to Hanna Dar Hanna Dar (= 1×) peers M. G. J. Jahoda

Countries citing papers authored by Hanna Dar

Since Specialization

Citations

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

Fields of papers citing papers by Hanna Dar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanna Dar

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

Tadmor, Tamar, et al.. (2006). Hemophagocytic Syndrome Preceding Acute Myeloid Leukemia With der t [7:17][q12; q11], Monosomy, 17 and 5p-. Journal of Pediatric Hematology/Oncology. 28(8). 544–546. 12 indexed citations

Riskin, Arieh, Ilana Koren, David Bader, et al.. (2006). The Approach to a Neonate with a Possible Prenatal Diagnosis of Androgen Insensitivity Syndrome. Journal of Pediatric Endocrinology and Metabolism. 19(12). 1437–43. 1 indexed citations

Stoupel, E, Z. Appelman, Ziva Ben‐Neriah, et al.. (2005). Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990–2000. International Journal of Biometeorology. 50(1). 1–5. 20 indexed citations

Bader, David, Arieh Riskin, A. Tamir, et al.. (2004). Alpha-fetoprotein in the early neonatal period—a large study and review of the literature. Clinica Chimica Acta. 349(1-2). 15–23. 100 indexed citations

Dar, Hanna, et al.. (2003). Detection of X Chromosome Aneuploidy Using Southern Blot Analysis During Routine Population-Based Screening for Fragile X Syndrome. Genetic Testing. 7(4). 345–346. 1 indexed citations

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

Dar, Hanna, et al.. (2000). Detection of translocation (16;16) in acute myeloid leukaemia (AML) patients by fluorescence in situ hybridization (FISH) using 16 telomer's probes. British Journal of Haematology. 110(2). 247–247. 1 indexed citations

Dar, Hanna, et al.. (1996). Maternal serum markers levels in consecutive pregnancies: A possible genetic predisposition to abnormal levels. American Journal of Medical Genetics. 61(2). 154–157. 16 indexed citations

Gershoni‐Baruch, Ruth, et al.. (1996). Interstitial deletion (6)q13q15. American Journal of Medical Genetics. 62(4). 345–347. 10 indexed citations

10.

Israël, Nicole, et al.. (1996). Unconjugated Estriol as Maternal Serum Marker for the Detection of Down Syndrome Pregnancies. Fetal Diagnosis and Therapy. 11(2). 99–105. 7 indexed citations

11.

David, M, et al.. (1995). Very Low Maternal Serum Unconjugated Estriol and Prenatal Diagnosis of Steroid Sulfatase Deficiency. Fetal Diagnosis and Therapy. 10(2). 76–80. 20 indexed citations

12.

Shohat, Mordechai, Bella Davidov, Gad Barkai, et al.. (1995). Amniocentesis rate and the detection of down syndrome and other chromosomal anomalies in Israel. Prenatal Diagnosis. 15(10). 967–970. 12 indexed citations

13.

Shapira, M., et al.. (1994). Deletion of the short arm of chromosome 10 (10p13): Report of a patient and review. American Journal of Medical Genetics. 52(1). 34–38. 27 indexed citations

14.

Degani, S., R. Gonen, I. Shapiro, et al.. (1992). Sonographic indications for karyotyping procedures. An international questionnaire. Ultrasound in Obstetrics and Gynecology. 2(1). 11–14. 3 indexed citations

15.

Borochowitz, Zvi, et al.. (1992). New multiple congenital anomalies: Mental retardation syndrome (MCA/MR) with facio‐cutaneous‐skeletal involvement. American Journal of Medical Genetics. 43(4). 678–685. 39 indexed citations

16.

Doron, Y., et al.. (1990). Brain tumor as a second malignant neoplasm following neuroblastoma stage IV S. Medical and Pediatric Oncology. 18(3). 240–245. 2 indexed citations

17.

Chemke, Juan, R. Voss, Z. Appelman, et al.. (1989). The dilemma of chromosomal mosaicism in chorionic villus sampling—‘direct’ versus long‐term cultures. Prenatal Diagnosis. 9(4). 223–226. 11 indexed citations

18.

Dar, Hanna, et al.. (1988). Paracentric inversion of Xq and ovarian dysfunction. American Journal of Medical Genetics. 29(1). 167–170. 18 indexed citations

19.

Dar, Hanna & Sarah Winter. (1970). A Study of Dermatoglyphics and the Simian Crease in Familial Deafness. Human Heredity. 20(5). 493–506. 5 indexed citations

20.

Dar, Hanna & Susann Winter. (1969). A cytogenetic study of familial deafness.. Journal of Medical Genetics. 6(3). 298–303. 8 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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