Mordechai Shohat

5.0k total citations · 1 hit paper
83 papers, 2.9k citations indexed

About

Mordechai Shohat is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mordechai Shohat has authored 83 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 32 papers in Genetics and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mordechai Shohat's work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (15 papers) and Mitochondrial Function and Pathology (10 papers). Mordechai Shohat is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (15 papers) and Mitochondrial Function and Pathology (10 papers). Mordechai Shohat collaborates with scholars based in Israel, United States and Canada. Mordechai Shohat's co-authors include Nathan Fischel‐Ghodsian, Lutfi Jaber, Jerome I. Rotter, Xiangdong Bu, Marlene C. Bohlman, Toni R. Prezant, Gino Cortopassi, Sı́tkı́ Öztaş, Kathleen S. Arnos and John Agapian and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Mordechai Shohat

77 papers receiving 2.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

1993 903 citations Lutfi Jaber, Jerome I. Rotter et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mordechai Shohat Israel	26	1.7k	540	512	432	331	83	2.9k
Annick Raas‐Rothschild Israel	34	1.7k 1.0×	898 1.7×	290 0.6×	197 0.5×	190 0.6×	108	3.8k
Andreas Janecke Austria	37	2.2k 1.3×	1.3k 2.4×	309 0.6×	194 0.4×	62 0.2×	132	4.4k
Célia Bádenas Spain	33	2.2k 1.3×	1.4k 2.7×	234 0.5×	400 0.9×	78 0.2×	139	3.9k
Mohammed Al‐Owain Saudi Arabia	25	1.1k 0.7×	595 1.1×	103 0.2×	133 0.3×	267 0.8×	87	2.0k
Marco Seri Italy	38	2.3k 1.4×	1.4k 2.5×	133 0.3×	202 0.5×	121 0.4×	193	5.3k
Stavit A. Shalev Israel	29	1.8k 1.1×	709 1.3×	68 0.1×	126 0.3×	287 0.9×	88	2.6k
Ziva Ben‐Neriah Israel	20	774 0.5×	404 0.7×	206 0.4×	195 0.5×	152 0.5×	40	1.4k
H.J.M. Smeets Netherlands	30	1.5k 0.9×	501 0.9×	53 0.1×	110 0.3×	301 0.9×	63	2.4k
Mohnish Suri United Kingdom	24	1.2k 0.7×	736 1.4×	158 0.3×	180 0.4×	52 0.2×	82	2.2k
L.‐C. Tsui Canada	26	1.3k 0.8×	547 1.0×	154 0.3×	109 0.3×	71 0.2×	50	2.5k

Countries citing papers authored by Mordechai Shohat

Since Specialization

Citations

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

Fields of papers citing papers by Mordechai Shohat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mordechai Shohat

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

Birnbaum, R., G. Malinger, Liat Ben‐Sira, et al.. (2024). Identification of a Mosaic Variant in the SYNCRIP Gene Causing Foetal Periventricular Nodular Heterotopia, Abnormal Sulcation and Infratentorial Anomaly. Prenatal Diagnosis. 44(13). 1659–1662. 1 indexed citations

Levy, Michal, Lily Bazak, Uri Hamiel, et al.. (2024). Exome sequencing in every pregnancy? Results of trio exome sequencing in structurally normal fetuses. Prenatal Diagnosis. 45(3). 276–286. 12 indexed citations

Haratz, Karina Krajden, et al.. (2024). A de novo pathogenic variant in DHX30 gene in a fetus with isolated dysgenesis of the corpus callosum. Prenatal Diagnosis. 44(3). 357–359.

Siegelmann‐Danieli, Nava, Victoria Neiman, Avital Bareket‐Samish, et al.. (2023). Whole exome germline sequencing in early‐onset prostate cancer patients: Genomic findings and clinical outcomes. The Prostate. 84(1). 39–46. 2 indexed citations

Levy, Michal, et al.. (2023). Proximal 1q21 duplication: A syndrome or a susceptibility locus?. American Journal of Medical Genetics Part A. 191(10). 2551–2557.

Malinger, G., et al.. (2022). Prenatal diagnosis of microcephaly as shown by plateauing of head circumference growth during the 3rd trimester in a fetus with a CCND2 inverse growth variant. Prenatal Diagnosis. 42(10). 1343–1345. 4 indexed citations

Maya, Idit, Reuven Sharony, Shiri Yacobson, et al.. (2017). When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations. Genetics in Medicine. 20(1). 128–131. 46 indexed citations

Reinstein, Eyal, Ana Gutiérrez‐Fernández, Shay Tzur, et al.. (2016). Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C. European Journal of Human Genetics. 24(12). 1792–1796. 33 indexed citations

Smirin‐Yosef, Pola, Ayelet Halevy, Metsada Pasmanik‐Chor, et al.. (2013). Microcephaly Thin Corpus Callosum Intellectual Disability Syndrome Caused by Mutated TAF2. Pediatric Neurology. 49(6). 411–416.e1. 23 indexed citations

10.

Basel‐Vanagaite, Lina, Noam Zevit, Liang Guo, et al.. (2012). Transient Infantile Hypertriglyceridemia, Fatty Liver, and Hepatic Fibrosis Caused by Mutated GPD1, Encoding Glycerol-3-Phosphate Dehydrogenase 1. The American Journal of Human Genetics. 90(1). 49–60. 73 indexed citations

11.

Maya, Idit, Bella Davidov, Liron Gershovitz, et al.. (2010). Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting. Prenatal Diagnosis. 30(12-13). 1131–1137. 61 indexed citations

12.

Saada, Ann, Rutger O. Vogel, Saskia J.G. Hoefs, et al.. (2009). Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease. The American Journal of Human Genetics. 84(6). 718–727. 135 indexed citations

13.

Bykhovskaya, Yelena, Emebet Mengesha, Dai Wang, et al.. (2004). Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3. Molecular Genetics and Metabolism. 83(3). 199–206. 51 indexed citations

14.

Bykhovskaya, Yelena, Huiying Yang, Kent D. Taylor, et al.. (2001). Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness. Genetics in Medicine. 3(3). 177–180. 46 indexed citations

15.

Cohn, Daniel H., et al.. (2000). A Locus for an Autosomal Dominant Form of Progressive Renal Failure and Hypertension at Chromosome 1q21. The American Journal of Human Genetics. 67(3). 647–651. 39 indexed citations

16.

Bykhovskaya, Yelena, Xavier Estivill, Kent D. Taylor, et al.. (2000). Candidate Locus for a Nuclear Modifier Gene for Maternally Inherited Deafness. The American Journal of Human Genetics. 66(6). 1905–1910. 82 indexed citations

17.

Warner, Laura E., Mordechai Shohat, Zamir Shorer, & James R. Lupski. (1997). Multiplede novo MPZ (P0) point mutations in a sporadic Dejerine-Sottas case. Human Mutation. 10(1). 21–24. 21 indexed citations

18.

Shohat, Mordechai, Rona Lotan, Nurit Magal, et al.. (1997). A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter. The American Journal of Human Genetics. 61(5). 1139–1143. 18 indexed citations

19.

Yang, Huiying, et al.. (1992). Two‐locus mitochondrial and nuclear gene models for mitochondrial disorders. Genetic Epidemiology. 9(1). 27–44. 29 indexed citations

20.

Shohat, Mordechai, Salomon H. Reisner, R. Krikler, et al.. (1983). Retinopathy of Prematurity: Incidence and Risk Factors. PEDIATRICS. 72(2). 159–163. 134 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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