M Shohat

1.3k total citations
29 papers, 911 citations indexed

About

M Shohat is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, M Shohat has authored 29 papers receiving a total of 911 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in M Shohat's work include Connective tissue disorders research (5 papers), Prenatal Screening and Diagnostics (4 papers) and Metabolism and Genetic Disorders (3 papers). M Shohat is often cited by papers focused on Connective tissue disorders research (5 papers), Prenatal Screening and Diagnostics (4 papers) and Metabolism and Genetic Disorders (3 papers). M Shohat collaborates with scholars based in Israel, United States and Netherlands. M Shohat's co-authors include David L. Rimoin, Helen E. Gruber, Lutfi Jaber, BL Weber, Gila Hornreich, Uziel Beller, Jerome I. Rotter, Ephrat Levy‐Lahad, D. Halle and Bella Kaufman and has published in prestigious journals such as Neurology, The Journal of Pediatrics and Journal of Investigative Dermatology.

In The Last Decade

M Shohat

27 papers receiving 862 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M Shohat Israel 15 387 329 134 105 88 29 911
Stavit A. Shalev Israel 19 416 1.1× 519 1.6× 84 0.6× 60 0.6× 107 1.2× 44 962
Olaf Rittinger Austria 17 384 1.0× 433 1.3× 81 0.6× 47 0.4× 66 0.8× 40 785
Paolo Simi Italy 22 571 1.5× 633 1.9× 138 1.0× 64 0.6× 145 1.6× 82 1.4k
Marie‐Louise Briard France 21 418 1.1× 630 1.9× 137 1.0× 94 0.9× 287 3.3× 55 1.4k
Joyce Turner United States 13 274 0.7× 301 0.9× 91 0.7× 160 1.5× 539 6.1× 29 1.0k
Naomi Fitch Canada 22 585 1.5× 479 1.5× 186 1.4× 119 1.1× 262 3.0× 44 1.1k
Sylvie Manouvrier France 16 359 0.9× 529 1.6× 110 0.8× 52 0.5× 124 1.4× 52 921
I. Christopher Lloyd United Kingdom 23 482 1.2× 807 2.5× 153 1.1× 53 0.5× 75 0.9× 47 1.7k
A. Moseley United States 5 890 2.3× 834 2.5× 92 0.7× 91 0.9× 133 1.5× 10 1.6k
Sarah Smithson United Kingdom 16 731 1.9× 767 2.3× 73 0.5× 54 0.5× 109 1.2× 55 1.5k

Countries citing papers authored by M Shohat

Since Specialization
Citations

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

Fields of papers citing papers by M Shohat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M Shohat

This figure shows the co-authorship network connecting the top 25 collaborators of M Shohat. A scholar is included among the top collaborators of M Shohat 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 M Shohat. M Shohat 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.
Reinstein, Eyal, Valerie Drasinover, Rachel Lotan, et al.. (2017). Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type. Clinical Genetics. 93(1). 160–163. 8 indexed citations
2.
Avrahami, Limor, Saskia M. Maas, Metsada Pasmanik‐Chor, et al.. (2008). Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype. Clinical Genetics. 74(1). 47–53. 40 indexed citations
3.
Basel‐Vanagaite, Lina, et al.. (2006). Expanding the phenotypic spectrum of L1CAM‐associated disease. Clinical Genetics. 69(5). 414–419. 25 indexed citations
4.
Gorsky, Meir, et al.. (1998). Genetic influence on the prevalence of Torus palatinus. American Journal of Medical Genetics. 75(2). 138–140. 50 indexed citations
5.
Shohat, M, Rachel Lotan, Nurit Magal, et al.. (1998). Amyloidosis in Familial Mediterranean Fever Is Associated with a Specific Ancestral Haplotype in the MEFV Locus. Molecular Genetics and Metabolism. 65(3). 197–202. 6 indexed citations
6.
Jaber, Lutfi, Tamar Shohat, Jerome I. Rotter, & M Shohat. (1997). Consanguinity and common adult diseases in Israeli Arab communities. American Journal of Medical Genetics. 70(4). 346–348. 36 indexed citations
7.
Levy‐Lahad, Ephrat, Raphael Catane, Shlomit Eisenberg, et al.. (1997). Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families.. PubMed. 60(5). 1059–67. 245 indexed citations
8.
Braverman, Itzhak, Lutfi Jaber, Cahtia Adelman, et al.. (1996). Audiovestibular Findings in Patients With Deafness Caused by a Mitochondrial Susceptibility Mutation and Precipitated by an Inherited Nuclear Mutation or Aminoglycosides. Archives of Otolaryngology - Head and Neck Surgery. 122(9). 1001–1004. 41 indexed citations
9.
Shohat, M, et al.. (1996). Breast cancer and BRCA1 mutations.. PubMed. 334(18). 1199; author reply 1199–1200. 5 indexed citations
10.
Mimouni, Marc, Aviva Mimouni-Bloch, Joseph Schachter, & M Shohat. (1996). Familial hypothyroidism with autosomal dominant inheritance.. Archives of Disease in Childhood. 75(3). 245–246. 8 indexed citations
11.
Shohat, M, et al.. (1995). The gene for familial Mediterranean fever is mapped to 16p 13.3- p13.1 with evidence for homogeneity.. PubMed. 371B. 901–3.
12.
Appelman, Z., Moshe Manor, Nurit Magal, et al.. (1994). Prenatal diagnosis of twin zygosity by DNA ‘fingerprint’ analysis. Prenatal Diagnosis. 14(4). 307–309. 7 indexed citations
13.
Ikeda, Shigaku, Anne R. Haake, Nicholas N. Ewing, et al.. (1994). Localization of the Gene for Darier Disease to a 5-cM Interval on Chromosome 12q. Journal of Investigative Dermatology. 103(4). 478–481. 13 indexed citations
14.
Shohat, M, et al.. (1993). New form of spondyloepimetaphyseal dysplasia (SEMD) in Jewish family of Iraqi Origin. American Journal of Medical Genetics. 46(4). 358–362. 10 indexed citations
15.
Merlob, Paul, N. Naor, & M Shohat. (1991). Phenotypic expression of the first liveborn 68,XX triploid newborn.. Journal of Medical Genetics. 28(12). 886–887. 4 indexed citations
16.
Shohat, M, David L. Rimoin, Helen E. Gruber, & Ralph S. Lachman. (1991). Perinatal lethal hypophosphatasia; Clinical, radiologic and morphologic findings. Pediatric Radiology. 21(6). 421–427. 51 indexed citations
17.
Shohat, M, et al.. (1990). Geleophysic dysplasia: A storage disorder affecting the skin, bone, liver, heart, and trachea. The Journal of Pediatrics. 117(2). 227–232. 22 indexed citations
18.
Shohat, M, Ralph Lachman, Helen E. Gruber, & David L. Rimoin. (1989). Brachyolmia: Radiographic and genetic evidence of heterogeneity. American Journal of Medical Genetics. 33(2). 209–219. 47 indexed citations
19.
Shohat, M, et al.. (1989). Autosomal dominant transmission of isolated congenital vertical talus.. PubMed. 36(6). 427–30. 22 indexed citations
20.
Shohat, M, Tami Shohat, M Nitzan, et al.. (1988). Growth and ethnicity in scoliosis. Acta Orthopaedica Scandinavica. 59(3). 310–313. 27 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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