Mohammed Zarhrate

6.6k total citations
14 papers, 376 citations indexed

About

Mohammed Zarhrate is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Mohammed Zarhrate has authored 14 papers receiving a total of 376 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Genetics. Recurrent topics in Mohammed Zarhrate's work include Neurogenetic and Muscular Disorders Research (4 papers), RNA modifications and cancer (3 papers) and RNA Research and Splicing (3 papers). Mohammed Zarhrate is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), RNA modifications and cancer (3 papers) and RNA Research and Splicing (3 papers). Mohammed Zarhrate collaborates with scholars based in France, United Kingdom and United States. Mohammed Zarhrate's co-authors include Arnold Münnich, Laurence Colleaux, Sarah Boissel, Jean‐Marc Egly, Marlène Rio, Satoru Hashimoto, Alain Fischer, Bénédicte Neven, Frédéric Rieux‐Laucat and Marie‐Claude Stolzenberg and has published in prestigious journals such as Science, Journal of Clinical Investigation and Neurology.

In The Last Decade

Mohammed Zarhrate

14 papers receiving 373 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mohammed Zarhrate France	9	213	120	103	102	37	14	376
Isabela Batista Oliva United States	5	274 1.3×	53 0.4×	128 1.2×	39 0.4×	16 0.4×	8	396
Anna Maria Ranzoni United Kingdom	8	303 1.4×	83 0.7×	75 0.7×	34 0.3×	14 0.4×	12	451
Fernanda Gabriella De Angelis Italy	11	648 3.0×	80 0.7×	104 1.0×	174 1.7×	15 0.4×	13	766
Laura A. Penny United States	7	151 0.7×	131 1.1×	36 0.3×	116 1.1×	27 0.7×	9	420
Lan Hoang-Minh United States	11	223 1.0×	77 0.6×	62 0.6×	134 1.3×	15 0.4×	21	383
Astrid Nümann Germany	10	223 1.0×	34 0.3×	94 0.9×	84 0.8×	31 0.8×	13	469
Shoichi Tani Japan	6	438 2.1×	90 0.8×	45 0.4×	99 1.0×	21 0.6×	12	558
Steve Dingwall Canada	7	297 1.4×	50 0.4×	34 0.3×	33 0.3×	21 0.6×	9	372
Simone Bach Italy	8	221 1.0×	104 0.9×	259 2.5×	30 0.3×	28 0.8×	18	525
Bret Duffin United States	8	270 1.3×	109 0.9×	34 0.3×	80 0.8×	18 0.5×	10	440

Countries citing papers authored by Mohammed Zarhrate

Since Specialization

Citations

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

Fields of papers citing papers by Mohammed Zarhrate

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohammed Zarhrate

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

All Works

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14 of 14 papers shown

Mayeur, Anne, Nicolas Cagnard, Mohammed Zarhrate, et al.. (2023). A shared pattern of altered gene expression in human embryos affected by mitochondrial diseases. Human Reproduction. 38(5). 992–1002. 3 indexed citations

Stolzenberg, Marie‐Claude, Jérôme Hadjadj, Laura Barnabei, et al.. (2023). L’haploinsuffisance en SHARPIN est responsable d’un déficit partiel en LUBAC, de manifestations inflammatoires, d’une auto-immunité et d’un défaut de production d’anticorps. La Revue de Médecine Interne. 44. A329–A329. 1 indexed citations

Huber, Céline, Geneviève Baujat, Caroline Michot, et al.. (2022). Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals. Journal of Medical Genetics. 60(4). 337–345. 8 indexed citations

Perrault, Isabelle, Sylvain Hanein, Xavier Gérard, et al.. (2021). Whole Locus Sequencing Identifies a Prevalent Founder Deep Intronic RPGRIP1 Pathologic Variant in the French Leber Congenital Amaurosis Cohort. Genes. 12(2). 287–287. 4 indexed citations

About, Frédégonde, Stéphanie Bibert, Emmanuelle Jouanguy, et al.. (2019). Identification of an Endoglin Variant Associated With HCV-Related Liver Fibrosis Progression by Next-Generation Sequencing. Frontiers in Genetics. 10. 1024–1024. 7 indexed citations

Pelet, Anna, Ulrike Steuerwald, Veronika Barešová, et al.. (2019). PAICS deficiency, a new defect of de novo purine synthesis resulting in multiple congenital anomalies and fatal outcome. Human Molecular Genetics. 28(22). 3805–3814. 23 indexed citations

Cagnard, Nicolas, Marine Gil, Fernando E. Sepulveda, et al.. (2018). Tetratricopeptide repeat domain 7A is a nuclear factor that modulates transcription and chromatin structure. Cell Discovery. 4(1). 61–61. 11 indexed citations

Lévy, E, Marie‐Claude Stolzenberg, Julie Bruneau, et al.. (2016). LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis. Clinical Immunology. 168. 88–93. 40 indexed citations

Hashimoto, Satoru, Sarah Boissel, Mohammed Zarhrate, et al.. (2011). MED23 Mutation Links Intellectual Disability to Dysregulation of Immediate Early Gene Expression. Science. 333(6046). 1161–1163. 98 indexed citations

10.

Magérus, Aude, Bénédicte Neven, Marie‐Claude Stolzenberg, et al.. (2010). Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation. Journal of Clinical Investigation. 121(1). 106–112. 83 indexed citations

11.

Maystadt, Isabelle, Mohammed Zarhrate, B. Estournet, et al.. (2006). A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36. Neurology. 67(1). 120–124. 8 indexed citations

12.

Viollet, Louis, Mohammed Zarhrate, Isabelle Maystadt, et al.. (2004). Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families. European Journal of Human Genetics. 12(6). 483–488. 12 indexed citations

13.

Maystadt, Isabelle, Mohammed Zarhrate, P. Landrieu, et al.. (2004). Allelic heterogeneity of SMARD1 at the IGHMBP2 locus. Human Mutation. 23(5). 525–526. 43 indexed citations

14.

Viollet, Louis, A Barois, Ziad Rifai, et al.. (2002). Mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13. Annals of Neurology. 51(5). 585–592. 35 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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