A. Sefiani

603 total citations
15 papers, 233 citations indexed

About

A. Sefiani is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, A. Sefiani has authored 15 papers receiving a total of 233 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in A. Sefiani's work include Genetic and rare skin diseases. (5 papers), Hedgehog Signaling Pathway Studies (3 papers) and Glycosylation and Glycoproteins Research (1 paper). A. Sefiani is often cited by papers focused on Genetic and rare skin diseases. (5 papers), Hedgehog Signaling Pathway Studies (3 papers) and Glycosylation and Glycoproteins Research (1 paper). A. Sefiani collaborates with scholars based in France, Morocco and Canada. A. Sefiani's co-authors include M. C. Hors‐Cayla, S. Heuertz, Damian Labuda, Laurent Abel, Daniel Sinnett, J Frézal, Karim Ouldim, B. Le Marec, M Guilloud-Bataille and P Maroteaux and has published in prestigious journals such as Gene, Genomics and Human Genetics.

In The Last Decade

A. Sefiani

15 papers receiving 225 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Sefiani France	8	181	130	44	30	22	15	233
Francesca Fusco Italy	9	198 1.1×	181 1.4×	45 1.0×	60 2.0×	16 0.7×	14	338
Hironao Numabe Japan	11	177 1.0×	136 1.0×	12 0.3×	11 0.4×	6 0.3×	32	281
Pola Smirin‐Yosef Israel	10	160 0.9×	178 1.4×	22 0.5×	7 0.2×	18 0.8×	15	309
Poustka Annemarie Germany	8	287 1.6×	431 3.3×	31 0.7×	4 0.1×	15 0.7×	9	514
Mariem Ben Rekaya Tunisia	12	102 0.6×	195 1.5×	15 0.3×	7 0.2×	35 1.6×	25	276
C. Rasberry United Kingdom	11	361 2.0×	383 2.9×	30 0.7×	6 0.2×	4 0.2×	15	536
C. Linch United States	5	101 0.6×	109 0.8×	12 0.3×	13 0.4×	17 0.8×	15	201
Jennifer M. Huang United States	8	160 0.9×	256 2.0×	47 1.1×	20 0.7×	12 0.5×	12	330
Sorath Noorani Siddiqui Pakistan	10	61 0.3×	156 1.2×	18 0.4×	7 0.2×	6 0.3×	25	245
Emine Bolat Netherlands	4	173 1.0×	206 1.6×	35 0.8×	14 0.5×	12 0.5×	6	246

Countries citing papers authored by A. Sefiani

Since Specialization

Citations

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

Fields of papers citing papers by A. Sefiani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Sefiani

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

All Works

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15 of 15 papers shown

Ouldim, Karim, et al.. (2016). Genetics and genomic medicine in Morocco: the present hope can make the future bright. Molecular Genetics & Genomic Medicine. 4(6). 588–598. 9 indexed citations

Jaouad, Imane Cherkaoui, et al.. (2012). The first mutations in the MYH gene reported in Moroccan colon cancer patients. Gene. 496(1). 55–58. 5 indexed citations

Elalaoui, Siham Chafai, et al.. (2011). Syndrome d’Hutchinson-Gilford (progéria). À propos de 3 cas. Archives de Pédiatrie. 18(2). 156–159. 3 indexed citations

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

Jaouad, Imane Cherkaoui, et al.. (2008). Omenn Syndrome with Mutation in RAG1 Gene. The Indian Journal of Pediatrics. 75(9). 944–946. 4 indexed citations

Sefiani, A., et al.. (2007). Incontinentia pigmenti : à propos d’un cas. Journal Français d Ophtalmologie. 30(8). 844.e1–844.e7. 1 indexed citations

Forner, Joachim, Aziza Sbiti, C. Beldjord, et al.. (1998). A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11.. PubMed. 41(1). 11–6. 9 indexed citations

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

Benomar, Ali, Farid Meggouh, Olivier Didierjean, et al.. (1996). Autosomal dominant cerebellar ataxia type I in Morocco: presence of the SCA1 and SCA3/MJD mutations. European Journal of Neurology. 3(4). 369–372. 2 indexed citations

10.

Kaplan, Josseline, Fédérica Piccolo, K. Azibi, et al.. (1996). Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan). Neuromuscular Disorders. 6(2). S8–S8. 1 indexed citations

11.

Sefiani, A., Ridha Mrad, Louise R. Simard, et al.. (1991). Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers. Human Genetics. 86(3). 297–9. 32 indexed citations

12.

Sefiani, A., Laurent Abel, S. Heuertz, et al.. (1989). The gene for incontinentia pigmenti is assigned to Xq28. Genomics. 4(3). 427–429. 85 indexed citations

13.

Sefiani, A., et al.. (1989). Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations.. PubMed. 32(3). 149–51. 9 indexed citations

14.

Sefiani, A., Daniel Sinnett, Laurent Abel, et al.. (1988). Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11. Human Genetics. 80(3). 282–286. 25 indexed citations

15.

Sefiani, A., M Guilloud-Bataille, S. Heuertz, et al.. (1988). Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome. Human Genetics. 81(1). 61–63. 29 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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