Morad Khayat

879 total citations
11 papers, 311 citations indexed

About

Morad Khayat is a scholar working on Molecular Biology, Oncology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Morad Khayat has authored 11 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Oncology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Morad Khayat's work include Peptidase Inhibition and Analysis (4 papers), Metabolism and Genetic Disorders (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Morad Khayat is often cited by papers focused on Peptidase Inhibition and Analysis (4 papers), Metabolism and Genetic Disorders (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Morad Khayat collaborates with scholars based in Israel, United States and Netherlands. Morad Khayat's co-authors include Tzipora C. Falik‐Zaccai, Bella Gross, Vladimir M. Berginer, Hanna Mandel, Ruth Gershoni‐Baruch, Stanley H. Korman, Ron A. Wevers, Anthony Luder, Zalman Weintraub and Dan Geiger and has published in prestigious journals such as PEDIATRICS, The Journal of Pediatrics and Journal of Investigative Dermatology.

In The Last Decade

Morad Khayat

11 papers receiving 304 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Morad Khayat Israel	7	118	86	69	55	48	11	311
Akatsuki Kubota Japan	11	215 1.8×	42 0.5×	77 1.1×	10 0.2×	45 0.9×	35	442
Suna Önengüt United States	11	396 3.4×	71 0.8×	33 0.5×	30 0.5×	34 0.7×	11	551
Natividad Villa Spain	4	267 2.3×	23 0.3×	67 1.0×	27 0.5×	48 1.0×	7	409
Anna Abramowicz Poland	6	440 3.7×	52 0.6×	44 0.6×	22 0.4×	17 0.4×	8	636
Jun‐ichi Suehiro Japan	13	346 2.9×	101 1.2×	41 0.6×	56 1.0×	31 0.6×	22	526
Peiwen Kuo United States	8	179 1.5×	99 1.2×	49 0.7×	16 0.3×	22 0.5×	16	370
Ting-Chun Liu United States	6	273 2.3×	42 0.5×	73 1.1×	68 1.2×	29 0.6×	8	392
Chengyu Prince United States	11	333 2.8×	78 0.9×	18 0.3×	25 0.5×	12 0.3×	20	540
E. Natt Germany	10	314 2.7×	54 0.6×	59 0.9×	38 0.7×	10 0.2×	13	510
Mingchao Ma United States	7	221 1.9×	73 0.8×	10 0.1×	56 1.0×	21 0.4×	9	351

Countries citing papers authored by Morad Khayat

Since Specialization

Citations

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

Fields of papers citing papers by Morad Khayat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morad Khayat

This figure shows the co-authorship network connecting the top 25 collaborators of Morad Khayat. A scholar is included among the top collaborators of Morad Khayat 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 Morad Khayat. Morad Khayat is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Khayat, Morad, et al.. (2020). SAM症候群の研究により明らかにされたギャップ結合ターンオーバーにおけるデスモグレイン1の役割【JST・京大機械翻訳】. Journal of Investigative Dermatology. 140(3). 556–567. 4 indexed citations

Kalfon, Limor, et al.. (2017). [OXALATE STONES ARE PREVALENT AMONG DRUZE AND MUSLIM ARABS IN THE GALILEE].. PubMed. 156(3). 156–162. 6 indexed citations

Westbroek, Wendy, Nehama Cohen Kfir, Morad Khayat, et al.. (2012). A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis. Journal of Medical Genetics. 49(7). 462–472. 53 indexed citations

Khayat, Morad, et al.. (2010). Mammary-digital-nail (MDN) syndrome: a novel phenotype maps to human chromosome 22q12.3–13.1. European Journal of Human Genetics. 18(6). 662–667. 6 indexed citations

Klar, Aharon, Alan Rubinow, David Branski, et al.. (2009). Prolidase deficiency: it looks like systemic lupus erythematosus but it is not. European Journal of Pediatrics. 169(6). 727–732. 24 indexed citations

Falik‐Zaccai, Tzipora C., Morad Khayat, Anthony Luder, et al.. (2009). A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 46–56. 33 indexed citations

Falik‐Zaccai, Tzipora C., et al.. (2008). Population screening in a Druze community: the challenge and the reward. Genetics in Medicine. 10(12). 903–909. 31 indexed citations

Khayat, Morad, et al.. (2008). PNPO deficiency: An under diagnosed inborn error of pyridoxine metabolism. Molecular Genetics and Metabolism. 94(4). 431–434. 44 indexed citations

Berginer, Vladimir M., et al.. (2008). Chronic Diarrhea and Juvenile Cataracts: Think Cerebrotendinous Xanthomatosis and Treat. PEDIATRICS. 123(1). 143–147. 62 indexed citations

10.

Luder, Anthony, et al.. (2007). Chronic Lung Disease and Cystic Fibrosis Phenotype in Prolidase Deficiency: A Newly Recognized Association. The Journal of Pediatrics. 150(6). 656–658.e1. 6 indexed citations

11.

Indelman, Margarita, Ellen G Pfendner, Tzipora C. Falik‐Zaccai, et al.. (2006). Molecular Epidemiology of Hereditary Epidermolysis Bullosa in a Middle Eastern Population. Journal of Investigative Dermatology. 126(4). 777–781. 42 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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