F. El Kerch

442 total citations
8 papers, 182 citations indexed

About

F. El Kerch is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, F. El Kerch has authored 8 papers receiving a total of 182 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Genetics. Recurrent topics in F. El Kerch's work include Muscle Physiology and Disorders (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Genetic Neurodegenerative Diseases (1 paper). F. El Kerch is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Genetic Neurodegenerative Diseases (1 paper). F. El Kerch collaborates with scholars based in Morocco and France. F. El Kerch's co-authors include Abdelaziz Sefiani, Aziza Sbiti, Asma Smahi, Karim Ouldim, Lekbir Baala, Gilles Courtois, France Leturcq, Arnold Münnich, Céline Cluzeau and K. Azibi and has published in prestigious journals such as BioMed Research International, Journal of Medical Genetics and Human Mutation.

In The Last Decade

F. El Kerch

7 papers receiving 173 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. El Kerch Morocco	6	154	35	33	33	31	8	182
Lisa G. Shaffer United States	9	148 1.0×	205 5.9×	18 0.5×	6 0.2×	31 1.0×	10	302
Thomas Smol France	10	129 0.8×	70 2.0×	36 1.1×	22 0.7×	17 0.5×	34	224
Marjan De Rademaeker Belgium	9	152 1.0×	101 2.9×	22 0.7×	14 0.4×	56 1.8×	14	250
Dirk Korthaus Germany	7	143 0.9×	39 1.1×	22 0.7×	51 1.5×	8 0.3×	9	220
Anne Katrin Lampe United Kingdom	2	142 0.9×	32 0.9×	26 0.8×	30 0.9×	17 0.5×	2	176
Deborah A. Nickerson United States	3	118 0.8×	112 3.2×	49 1.5×	9 0.3×	7 0.2×	3	202
Christa van den Elzen Netherlands	8	264 1.7×	60 1.7×	27 0.8×	34 1.0×	40 1.3×	8	328
Marija Guć‐Šćekić Serbia	9	230 1.5×	76 2.2×	54 1.6×	16 0.5×	17 0.5×	23	299
Hayley Goullée Australia	9	123 0.8×	39 1.1×	16 0.5×	26 0.8×	30 1.0×	17	230
Julien Bouckenheimer France	5	223 1.4×	46 1.3×	8 0.2×	7 0.2×	14 0.5×	5	284

Countries citing papers authored by F. El Kerch

Since Specialization

Citations

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

Fields of papers citing papers by F. El Kerch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. El Kerch. 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 F. El Kerch. The network helps show where F. El Kerch may publish in the future.

Co-authorship network of co-authors of F. El Kerch

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

All Works

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8 of 8 papers shown

1.

Kerch, F. El, et al.. (2014). Carrier Frequency of the c.525delT Mutation in the SGCG Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population. Genetic Testing and Molecular Biomarkers. 18(4). 253–256. 20 indexed citations

2.

Kerch, F. El, et al.. (2011). Confirmation de la forte prévalence au Maroc de la mutation homozygote c.144delC du gène aurora kinase C (AURKC) dans les tératozoospermies avec spermatozoïdes macrocéphales. Journal de gynécologie, obstétrique et biologie de la reproduction. Supplément. 40(4). 329–333. 18 indexed citations

3.

Jaouad, Imane Cherkaoui, et al.. (2009). MYH Associated Polyposis with a p.Tyr165Cys Mutation in a Moroccan Patient. Balkan Journal of Medical Genetics. 12(2). 65–67. 1 indexed citations

4.

Bal, Élodie, Lekbir Baala, Céline Cluzeau, et al.. (2007). Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus. Human Mutation. 28(7). 703–709. 61 indexed citations

5.

Sbiti, Aziza, F. El Kerch, & Abdelaziz Sefiani. (2002). Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients. BioMed Research International. 2(3). 158–160. 25 indexed citations

6.

Azibi, K., Abderrezak Reghis, F. El Kerch, et al.. (1997). Genetic and allelic heterogeneity of LGMD in North Africa. Neuromuscular Disorders. 7(6-7). 441–441. 1 indexed citations

7.

Kerch, F. El, Abdelaziz Sefiani, K. Azibi, et al.. (1994). Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa.. Journal of Medical Genetics. 31(4). 342–343. 22 indexed citations

8.

Romero, Norma B., F.M.S. Tomé, France Leturcq, et al.. (1994). Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.. PubMed. 317(1). 70–6. 34 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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