B. E. Cohen

814 total citations
41 papers, 607 citations indexed

About

B. E. Cohen is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology. According to data from OpenAlex, B. E. Cohen has authored 41 papers receiving a total of 607 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Clinical Biochemistry, 11 papers in Genetics and 9 papers in Molecular Biology. Recurrent topics in B. E. Cohen's work include Metabolism and Genetic Disorders (17 papers), Neonatal Health and Biochemistry (6 papers) and Digestive system and related health (4 papers). B. E. Cohen is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Neonatal Health and Biochemistry (6 papers) and Digestive system and related health (4 papers). B. E. Cohen collaborates with scholars based in Israel, United States and United Kingdom. B. E. Cohen's co-authors include Hanan Costeff, Leonard Weller, J H Passwell, Richard M. Goodman, Gerard Schwartz, Savio L.C. Woo, Yosef Shiloh, Smadar Avigad, Mika Lidov and Kara Sheinart and has published in prestigious journals such as Nature, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

B. E. Cohen

39 papers receiving 539 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
B. E. Cohen Israel	15	171	125	119	108	93	41	607
Jean‐Michel Pedespan France	15	145 0.8×	35 0.3×	121 1.0×	35 0.3×	59 0.6×	34	536
E Tunçbilek Türkiye	15	175 1.0×	24 0.2×	195 1.6×	172 1.6×	198 2.1×	52	814
Erawati V. Bawle United States	17	562 3.3×	153 1.2×	442 3.7×	108 1.0×	91 1.0×	38	1.1k
Angelina Xavier Acosta Brazil	18	141 0.8×	48 0.4×	152 1.3×	139 1.3×	34 0.4×	79	850
Greetje de Jong South Africa	16	153 0.9×	17 0.1×	88 0.7×	70 0.6×	185 2.0×	36	762
Hermine M. Pashayan United States	16	180 1.1×	18 0.1×	375 3.2×	33 0.3×	126 1.4×	41	706
David J. Aughton United States	15	313 1.8×	27 0.2×	494 4.2×	22 0.2×	175 1.9×	30	815
Yavuz Renda Türkiye	16	215 1.3×	59 0.5×	55 0.5×	60 0.6×	49 0.5×	45	786
Rabah M. Shawky Egypt	13	184 1.1×	31 0.2×	173 1.5×	72 0.7×	102 1.1×	66	615
Vanessa Ramírez United States	16	239 1.4×	12 0.1×	75 0.6×	89 0.8×	57 0.6×	26	986

Countries citing papers authored by B. E. Cohen

Since Specialization

Citations

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

Fields of papers citing papers by B. E. Cohen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. E. Cohen

This figure shows the co-authorship network connecting the top 25 collaborators of B. E. Cohen. A scholar is included among the top collaborators of B. E. 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 B. E. Cohen. B. E. Cohen 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

Cohen, B. E., Arielle R. Nagler, & Miriam Keltz Pomeranz. (2016). Nonbacterial Causes of Lymphangitis with Streaking. The Journal of the American Board of Family Medicine. 29(6). 808–812. 7 indexed citations

Cohen, B. E., et al.. (2015). Phenylketonuria (PKU) in Israel. PubMed. 9. 95–101.

Maman, Ettie, Yuval Yung, B. E. Cohen, et al.. (2011). Expression and regulation of sFRP family members in human granulosa cells. Molecular Human Reproduction. 17(7). 399–404. 36 indexed citations

Sivakumar, Kumaraswamy, Kara Sheinart, Mika Lidov, & B. E. Cohen. (1995). Symptomatic spinal epidural lipomatosis in a patient with Cushing's disease. Neurology. 45(12). 2281–2283. 39 indexed citations

Avigad, Smadar, Sandra E. Kleiman, B. E. Cohen, et al.. (1991). Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuria.. PubMed. 49(2). 393–9. 26 indexed citations

Shafir, Raphael, et al.. (1983). Postoperative catheterization and prophylactic antimicrobials in children with hypospadias. Urology. 22(4). 391–393. 13 indexed citations

Costeff, Hanan, et al.. (1983). Relative importance of genetic and nongenetic etiologies in idiopathic mental retardation: estimates based on analysis of medical histories. Annals of Human Genetics. 47(1). 83–93. 24 indexed citations

Costeff, Hanan, B. E. Cohen, & Leonard Weller. (1983). BIOLOGICAL FACTORS IN MILD MENTAL RETARDATION. Developmental Medicine & Child Neurology. 25(5). 580–587. 30 indexed citations

Keren, G., Dan Duksin, B. E. Cohen, & Richard M. Goodman. (1981). Collagen synthesis by fibroblasts in a patient with the Cockayne syndrome. European Journal of Pediatrics. 137(3). 339–342. 2 indexed citations

10.

Laufer, J, et al.. (1981). Raised plasma renin activity in the hypertension of the Guillain-Barre syndrome.. BMJ. 282(6272). 1272–1273. 12 indexed citations

11.

Costeff, Hanan, et al.. (1981). Pathogenic Factors in Idiopathic Mental Retardation. Developmental Medicine & Child Neurology. 23(5). 484–493. 27 indexed citations

12.

Cohen, B. E., et al.. (1978). Ureteropelvic Junction Obstruction: Its Occurrence in 3 Members of a Single Family. The Journal of Urology. 120(3). 361–364. 18 indexed citations

13.

Passwell, J H, et al.. (1975). Congenital ichthyosis, mental retardation, dwarfism and renal impairment: A new syndrome. Clinical Genetics. 8(1). 59–65. 13 indexed citations

14.

Passwell, J H, et al.. (1973). A syndrom characterized by congenital ichthyosis with atrophy, mental retardation, dwarfism, and generalized aminoaciduria. The Journal of Pediatrics. 82(3). 467–471. 25 indexed citations

15.

Cohen, B. E., et al.. (1973). Cysteine peptiduria in a mentally retarded patient. Clinica Chimica Acta. 45(4). 335–339. 4 indexed citations

16.

Lebenthal, Emanuel, et al.. (1971). Glucose-galactose malabsorption in an Oriental-Iraqui Jewish family. The Journal of Pediatrics. 78(5). 844–850. 12 indexed citations

17.

Goodman, Richard M., et al.. (1971). GENETIC CONSIDERATIONS IN GIANT PIGMENTED HAIRY NAEVUS. British Journal of Dermatology. 85(2). 150–157. 16 indexed citations

18.

Cohen, B. E., et al.. (1969). MENTAL RETARDATION IN A FAMILY WITH PHENYLKETONURIA AND MILD HYPERPH ENYLALANINEMIA. PEDIATRICS. 44(5). 655–660. 10 indexed citations

19.

Cohen, B. E., et al.. (1963). PHENYLKETONURIA IN YEMENITE JEWS. PEDIATRICS. 32(6). 1069–1073. 4 indexed citations

20.

Steinberg, Anna, et al.. (1957). Amino-aciduria and Hypermetabolism in Progeria. Archives of Disease in Childhood. 32(165). 401–403. 14 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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