Gabriel Cohn

1.2k total citations
42 papers, 793 citations indexed

About

Gabriel Cohn is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Gabriel Cohn has authored 42 papers receiving a total of 793 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Physiology, 8 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Gabriel Cohn's work include Lysosomal Storage Disorders Research (8 papers), BRCA gene mutations in cancer (5 papers) and Prenatal Screening and Diagnostics (5 papers). Gabriel Cohn is often cited by papers focused on Lysosomal Storage Disorders Research (8 papers), BRCA gene mutations in cancer (5 papers) and Prenatal Screening and Diagnostics (5 papers). Gabriel Cohn collaborates with scholars based in United States, Israel and Serbia. Gabriel Cohn's co-authors include Lameh Fananapazir, Nava Epstein, Marinos C. Dalakas, Deborah Elstein, David B. Seifer, Ari Zimran, Nan Wang, David M. Zahrieh, Maher Deeb and David M. Poppel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and Blood.

In The Last Decade

Gabriel Cohn

35 papers receiving 756 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gabriel Cohn United States	13	299	294	219	153	112	42	793
Thomas Fitzmaurice United States	6	128 0.4×	112 0.4×	301 1.4×	196 1.3×	92 0.8×	11	526
Alexandra Sullivan United States	14	124 0.4×	736 2.5×	48 0.2×	101 0.7×	134 1.2×	19	1.3k
Myra Wick United States	16	83 0.3×	397 1.4×	30 0.1×	56 0.4×	22 0.2×	55	1.1k
Luis A. Barrera Colombia	17	11 0.0×	191 0.6×	603 2.8×	278 1.8×	122 1.1×	27	830
Ari Bernstein United States	8	21 0.1×	151 0.5×	127 0.6×	29 0.2×	35 0.3×	34	656
Silvia Sebastiani Italy	13	42 0.1×	95 0.3×	243 1.1×	26 0.2×	11 0.1×	42	1.3k
Satoshi Sohda Japan	18	70 0.2×	187 0.6×	23 0.1×	26 0.2×	7 0.1×	43	964
Hussein A. Abbas United States	18	25 0.1×	524 1.8×	41 0.2×	48 0.3×	36 0.3×	79	1.1k
Ibtissam Youlyouz‐Marfak Morocco	14	17 0.1×	136 0.5×	72 0.3×	61 0.4×	19 0.2×	38	695
Anders Glomstein Denmark	20	44 0.1×	245 0.8×	78 0.4×	77 0.5×	14 0.1×	42	1.4k

Countries citing papers authored by Gabriel Cohn

Since Specialization

Citations

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

Fields of papers citing papers by Gabriel Cohn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gabriel Cohn

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

Cohn, Gabriel, et al.. (2020). PIN1 Provides Dynamic Control of MYC in Response to Extrinsic Signals. Frontiers in Cell and Developmental Biology. 8. 224–224. 12 indexed citations

Heath, Jessica L., Gabriel Cohn, Sayyed K. Zaidi, & Gary S. Stein. (2019). The role of cell adhesion in hematopoiesis and leukemogenesis. Journal of Cellular Physiology. 234(11). 19189–19198. 7 indexed citations

Cohn, Gabriel, et al.. (2013). Development of a mnemonic screening tool for identifying subjects with Hunter syndrome. European Journal of Pediatrics. 172(7). 965–970. 10 indexed citations

Pastores, Gregory M., Barry E. Rosenbloom, Neal J. Weinreb, et al.. (2013). A multicenter open-label treatment protocol (HGT-GCB-058) of velaglucerase alfa enzyme replacement therapy in patients with Gaucher disease type 1: safety and tolerability. Genetics in Medicine. 16(5). 359–366. 26 indexed citations

Lavalle, Adrián Gurza, et al.. (2011). GIGANTE PELA PROPRIA NATUREZA. 1 indexed citations

Elstein, Deborah, et al.. (2010). Early achievement and maintenance of the therapeutic goals using velaglucerase alfa in type 1 Gaucher disease. Blood Cells Molecules and Diseases. 46(1). 119–123. 27 indexed citations

Zimran, Ari, Gheona Altarescu, Drorit Attias, et al.. (2010). Phase 1/2 and extension study of velaglucerase alfa replacement therapy in adults with type 1 Gaucher disease: 48-month experience. Blood. 115(23). 4651–4656. 91 indexed citations

Cohn, Gabriel. (2004). Indiferença, nova forma de barbárie. 1 indexed citations

Cohn, Gabriel. (2003). Renovando os problemas nas ciências sociais. Editora FIOCRUZ eBooks. 35–46. 4 indexed citations

10.

Markenson, Glenn, et al.. (2000). Parvoviral Infection Associated With Increased Nuchal Translucency: A Case Report. Journal of Perinatology. 20(2). 129–131. 18 indexed citations

11.

Byrne, Timothy, et al.. (2000). Immunohistochemical analysis of BRCA2 expression in normal human buccal cells.. Oncology Reports. 7(5). 955–8. 1 indexed citations

12.

Naeem, Rizwan, et al.. (2000). De novo translocation (8;12) and frontofacionasal dysplasia in a newborn boy. American Journal of Medical Genetics. 94(3). 179–183. 3 indexed citations

13.

Byrne, T. J., et al.. (2000). An antibody assay predictive of BRCA1 mutations in ovarian tumors and normal tissue.. Oncology Reports. 7(5). 949–53. 8 indexed citations

14.

Byrne, T. J., et al.. (1999). A minimally invasive assay detects BRCA 1 germline mutations. Genetics in Medicine. 1(2). 53–53.

15.

Naeem, Rizwan, et al.. (1998). Reproduction in a patient with trisomy 8 mosaicism: Case report and literature review. American Journal of Medical Genetics. 75(4). 382–385. 12 indexed citations

16.

Cohn, Gabriel, et al.. (1996). The usefulness of a prenatal genetic questionnaire in genetic risk assessment. Obstetrics and Gynecology. 88(5). 806–810. 5 indexed citations

17.

Epstein, Nava, et al.. (1992). Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation.. Circulation. 86(2). 345–352. 176 indexed citations

18.

Cohn, Gabriel. (1986). Informacao e tecnologia. 3. 1 indexed citations

19.

Cohn, Gabriel, et al.. (1981). Valor e renda da terra: o movimento do capital no campo. 1 indexed citations

20.

Cohn, Gabriel. (1968). Petróleo e nacionalismo. 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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