Tirza Cohen

1.8k total citations
40 papers, 1.4k citations indexed

About

Tirza Cohen is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Tirza Cohen has authored 40 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Hematology. Recurrent topics in Tirza Cohen's work include Sexual Differentiation and Disorders (5 papers), Hormonal and reproductive studies (3 papers) and dental development and anomalies (3 papers). Tirza Cohen is often cited by papers focused on Sexual Differentiation and Disorders (5 papers), Hormonal and reproductive studies (3 papers) and dental development and anomalies (3 papers). Tirza Cohen collaborates with scholars based in Israel, United States and Switzerland. Tirza Cohen's co-authors include Rita Müller, Shigeki Shibahara, Tadashi Yoshida, A Chosack, Eliecer Eidelman, Michal Sagi, Esther Leiberman, Ariel Rösler, Joël Zlotogora and Chaim Brautbar and has published in prestigious journals such as Nucleic Acids Research, American Journal of Epidemiology and Human Molecular Genetics.

In The Last Decade

Tirza Cohen

40 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tirza Cohen Israel 19 800 308 271 174 174 40 1.4k
Nancy E. Maestri United States 19 855 1.1× 107 0.3× 723 2.7× 253 1.5× 155 0.9× 39 1.9k
Isabelle Gennero France 18 474 0.6× 90 0.3× 261 1.0× 62 0.4× 104 0.6× 49 1.1k
Daniel Zeve United States 16 720 0.9× 113 0.4× 206 0.8× 136 0.8× 50 0.3× 26 2.1k
Elizabeth Cho United States 16 656 0.8× 74 0.2× 166 0.6× 172 1.0× 134 0.8× 42 2.0k
Núria Torán Spain 24 608 0.8× 63 0.2× 339 1.3× 179 1.0× 137 0.8× 71 1.5k
Anitta Mahonen Finland 25 497 0.6× 84 0.3× 399 1.5× 86 0.5× 84 0.5× 46 1.6k
Maurice F. Attie United States 22 705 0.9× 159 0.5× 319 1.2× 37 0.2× 67 0.4× 34 2.1k
Frédéric Jehan France 20 388 0.5× 102 0.3× 379 1.4× 81 0.5× 116 0.7× 35 1.4k
S Refsum Norway 22 439 0.5× 66 0.2× 95 0.4× 50 0.3× 96 0.6× 76 1.3k
Hatem El‐Shanti United States 28 1.7k 2.1× 325 1.1× 618 2.3× 111 0.6× 604 3.5× 84 2.7k

Countries citing papers authored by Tirza Cohen

Since Specialization
Citations

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

Fields of papers citing papers by Tirza Cohen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tirza Cohen

This figure shows the co-authorship network connecting the top 25 collaborators of Tirza Cohen. A scholar is included among the top collaborators of Tirza Cohen 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 Tirza Cohen. Tirza Cohen 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.
Lerer, Israela, Michal Sagi, Vardiella Meiner, et al.. (2005). Deletion of the ANKRD15 gene at 9p24.3 causes parent-of-origin-dependent inheritance of familial cerebral palsy. Human Molecular Genetics. 14(24). 3911–3920. 106 indexed citations
2.
Levi, Haya, et al.. (2004). Sensorineural hearing loss in Jewish children born in Jerusalem. International Journal of Pediatric Otorhinolaryngology. 68(10). 1245–1250. 17 indexed citations
3.
Baldwin, Clinton T., et al.. (1994). Mutations in PAX3 associated with waardenburg syndrome type I. Human Mutation. 3(3). 205–211. 53 indexed citations
4.
Zlotogora, Joël, Michal Sagi, & Tirza Cohen. (1994). Familial hydrocephalus of prenatal onset. American Journal of Medical Genetics. 49(2). 202–204. 24 indexed citations
5.
Sagi, Michal, Shoshana Shiloh, & Tirza Cohen. (1992). Application of the health belief model in a study on parents' intentions to utilize prenatal diagnosis of cleft lip and/or palate. American Journal of Medical Genetics. 44(3). 326–333. 46 indexed citations
6.
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
7.
Zlotogora, Joël, David BenEzra, Tirza Cohen, & Évelyne Cohen. (1990). Syndrome of brittle cornea, blue sclera, and joint hyperextensibility. American Journal of Medical Genetics. 36(3). 269–272. 16 indexed citations
8.
Cohen, Tirza, et al.. (1990). Nucleotide sequence of the cDNA encoding human tyrosinase-related protein. Nucleic Acids Research. 18(9). 2807–2808. 87 indexed citations
9.
Shibahara, Shigeki, Yasushi Tomita, Hachiro Tagami, Rita Müller, & Tirza Cohen. (1988). Molecular basis for the heterogeneity of human tyrosinase.. The Tohoku Journal of Experimental Medicine. 156(4). 403–414. 90 indexed citations
10.
Friedlander, Yechiel, Jeremy D. Kark, Tirza Cohen, et al.. (1984). Admixture Analysis of Plasma Cholesterol Levels in a Jewish Population Sample in Jerusalem. Human Heredity. 34(2). 82–95. 1 indexed citations
11.
Naparstek, Yaakov, Ayala Abrahamov, Tirza Cohen, & Chaim Brautbar. (1984). Familial hereditary thrombocytopenia and HLA. American Journal of Hematology. 17(2). 113–116. 3 indexed citations
12.
Rösler, Ariel, Esther Leiberman, Joseph Sack, et al.. (1983). Clinical Variability of Congenital Adrenal Hyperplasia Due to 11 β-Hydroxylase Deficiency. Obstetrical & Gynecological Survey. 38(4). 222–222. 6 indexed citations
13.
Brautbar, Chaim, Joseph Sack, C. Levene, et al.. (1981). HLA in a Selective Aldosterone Biosynthetic Defect due to Type 2 Corticosterone Methyl‐Oxidase Deficiency. Tissue Antigens. 17(2). 212–216. 2 indexed citations
14.
Brautbar, Chaim, et al.. (1980). HLA–DRw4 in Pemphigus Vulgaris Patients in Israel. Tissue Antigens. 16(3). 238–243. 57 indexed citations
15.
Chosack, A, et al.. (1979). Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta. Oral Surgery Oral Medicine Oral Pathology. 47(2). 148–156. 77 indexed citations
16.
Sandler, S. Gerald, et al.. (1979). The Day Blood Group System in Israeli Jews and Arabs. Vox Sanguinis. 37(1). 41–46. 17 indexed citations
17.
Eidelman, Eliecer, A Chosack, & Tirza Cohen. (1976). Scrotal tongue and geographic tongue: Polygenic and associated traits. Oral Surgery Oral Medicine Oral Pathology. 42(5). 591–596. 48 indexed citations
18.
Robin, Gordon C. & Tirza Cohen. (1975). FAMILIAL SCOLIOSIS. Journal of Bone and Joint Surgery - British Volume. 57-B(2). 146–147. 23 indexed citations
19.
Deckelbaum, Richard J., et al.. (1972). Type III glycogenosis: Atypical enzyme activities in blood cells in two siblings. The Journal of Pediatrics. 81(5). 955–961. 5 indexed citations
20.
Cohen, Tirza, et al.. (1968). Incidence of Hemoglobin Bart’s in a Sample of Newborn from Israel. Human Heredity. 18(4). 361–368. 3 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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