Lior Cohen

1.4k total citations
27 papers, 755 citations indexed

About

Lior Cohen is a scholar working on Molecular Biology, Genetics and Atomic and Molecular Physics, and Optics. According to data from OpenAlex, Lior Cohen has authored 27 papers receiving a total of 755 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Atomic and Molecular Physics, and Optics. Recurrent topics in Lior Cohen's work include Genomics and Rare Diseases (4 papers), Mitochondrial Function and Pathology (4 papers) and Spectroscopy and Quantum Chemical Studies (3 papers). Lior Cohen is often cited by papers focused on Genomics and Rare Diseases (4 papers), Mitochondrial Function and Pathology (4 papers) and Spectroscopy and Quantum Chemical Studies (3 papers). Lior Cohen collaborates with scholars based in Israel, United States and Canada. Lior Cohen's co-authors include J. P. Valleau, Mark Last, Lina Basel‐Vanagaite, Abraham Kandel, Shay Tzur, Xun Xu, Laura Davis‐Keppen, Antonella Celluzzi, Bruno Dallapiccola and Mingyan Fang and has published in prestigious journals such as The Journal of Chemical Physics, Gastroenterology and The Journal of Physical Chemistry B.

In The Last Decade

Lior Cohen

27 papers receiving 735 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lior Cohen Israel 13 234 163 145 115 111 27 755
H. Christen Switzerland 13 118 0.5× 85 0.5× 129 0.9× 30 0.3× 45 0.4× 35 854
Benjamin P. Lee United States 19 355 1.5× 75 0.5× 194 1.3× 52 0.5× 19 0.2× 31 1.1k
Vladimir Makarov Russia 11 518 2.2× 96 0.6× 318 2.2× 13 0.1× 10 0.1× 30 826
Bryan Beresford‐Smith Australia 11 283 1.2× 204 1.3× 91 0.6× 21 0.2× 7 0.1× 21 684
Pietro L. Indovina Italy 18 333 1.4× 28 0.2× 54 0.4× 22 0.2× 6 0.1× 53 894
Omar Demerdash United States 19 440 1.9× 98 0.6× 296 2.0× 8 0.1× 23 0.2× 30 1.0k
Ioannis N. Demetropoulos Greece 11 84 0.4× 53 0.3× 112 0.8× 80 0.7× 8 0.1× 34 434
P. G. Sørensen Denmark 14 302 1.3× 24 0.1× 91 0.6× 9 0.1× 7 0.1× 25 764
Setsuko Nakagawa Japan 19 512 2.2× 101 0.6× 166 1.1× 9 0.1× 3 0.0× 81 1.1k

Countries citing papers authored by Lior Cohen

Since Specialization
Citations

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

Fields of papers citing papers by Lior Cohen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lior Cohen

This figure shows the co-authorship network connecting the top 25 collaborators of Lior Cohen. A scholar is included among the top collaborators of Lior 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 Lior Cohen. Lior 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.
Cohen, Lior, et al.. (2023). Uncommon Presentation of Cystic Fibrosis: A Case Report and Literature Review. Cureus. 15(9). e45186–e45186. 1 indexed citations
2.
Crippa, M., Silvia Maitz, Karin Weiss, et al.. (2020). SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome. Frontiers in Neurology. 11. 631–631. 12 indexed citations
3.
Tan, Tiong Yang, Jiří Sedmík, Mark P. Fitzgerald, et al.. (2020). Bi-allelic ADARB1 Variants Associated with Microcephaly, Intellectual Disability, and Seizures. The American Journal of Human Genetics. 106(4). 467–483. 34 indexed citations
4.
Weiss, Karin, Nina Ekhilevitch, Lior Cohen, et al.. (2019). Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population. European Journal of Medical Genetics. 63(2). 103643–103643. 6 indexed citations
5.
Bend, Renee, Lior Cohen, Melissa T. Carter, et al.. (2019). Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities. European Journal of Human Genetics. 28(1). 76–87. 18 indexed citations
6.
Cohen, Lior, et al.. (2019). Late diagnosis of Alstrom syndrome in a Yemenite-Jewish child. Ophthalmic Genetics. 40(1). 7–11. 7 indexed citations
7.
Cohen, Lior, et al.. (2018). Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardation. European Journal of Human Genetics. 27(2). 263–268. 19 indexed citations
8.
Sharony, Reuven, et al.. (2017). Prenatal course of metaphyseal anadysplasia associated with homozygous mutation in MMP9 identified by exome sequencing. Clinical Genetics. 92(6). 645–648. 7 indexed citations
9.
Straussberg, Rachel, Alexandros Onoufriadis, Osnat Konen, et al.. (2017). Novel homozygous missense mutation in NT5C2 underlying hereditary spastic paraplegia SPG45. American Journal of Medical Genetics Part A. 173(11). 3109–3113. 12 indexed citations
10.
Cohen, Lior, Shay Tzur, Nitza Goldenberg‐Cohen, et al.. (2016). Exome sequencing identified a novelde novo OPA1mutation in a consanguineous family presenting with optic atrophy. Genetics Research. 98. 5 indexed citations
11.
Kurolap, Alina, Naama Orenstein, Inbal Kedar, et al.. (2016). Is one diagnosis the whole story? patients with double diagnoses. American Journal of Medical Genetics Part A. 170(9). 2338–2348. 16 indexed citations
12.
Masotti, Andrea, Paolo Uva, Laura Davis‐Keppen, et al.. (2015). Keppen-Lubinsky Syndrome Is Caused by Mutations in the Inwardly Rectifying K+ Channel Encoded by KCNJ6. The American Journal of Human Genetics. 96(2). 295–300. 86 indexed citations
13.
Reinstein, Eyal, Katia Orvin, Einav Tayeb-Fligelman, et al.. (2015). Mutations inTAX1BP3Cause Dilated Cardiomyopathy with Septo-Optic Dysplasia. Human Mutation. 36(4). 439–442. 24 indexed citations
14.
Cohen, Lior, et al.. (2008). Info-fuzzy algorithms for mining dynamic data streams. Applied Soft Computing. 8(4). 1283–1294. 32 indexed citations
15.
Huppert, Dan, et al.. (2005). Excitation Wavelength Dependence of the Proton-Transfer Reaction of the Green Fluorescent Protein. The Journal of Physical Chemistry B. 109(9). 4241–4251. 6 indexed citations
16.
Cohen, Lior. (1993). A lower bound on the loss of graphite by atomic oxygen attack at asymptotic energy. The Journal of Chemical Physics. 99(12). 9652–9663. 17 indexed citations
17.
Cohen, Lior & H. O. Pritchard. (1986). Comparison of unimolecular rates calculated classically and quantally from the same potential surface. The Journal of Physical Chemistry. 90(6). 990–992. 6 indexed citations
18.
Burns, George & Lior Cohen. (1983). Nonequilibrium effects in the energy distribution function. The Journal of Chemical Physics. 78(6). 3245–3252. 2 indexed citations
19.
Valleau, J. P., et al.. (1980). Primitive model electrolytes. II. The symmetrical electrolyte. The Journal of Chemical Physics. 72(11). 5942–5954. 105 indexed citations
20.
Pitlik, Silvio, et al.. (1977). Portal Hypertension and Esophageal Varices in Hemangiomatosis of the Spleen. Gastroenterology. 72(5). 937–940. 12 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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