Aziza Sbiti

577 total citations
19 papers, 387 citations indexed

About

Aziza Sbiti is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Aziza Sbiti has authored 19 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Aziza Sbiti's work include Genomic variations and chromosomal abnormalities (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Muscle Physiology and Disorders (3 papers). Aziza Sbiti is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Muscle Physiology and Disorders (3 papers). Aziza Sbiti collaborates with scholars based in Morocco, France and Germany. Aziza Sbiti's co-authors include Abdelaziz Sefiani, Imane Cherkaoui Jaouad, Abdelhafid Natiq, Siham Chafai Elalaoui, F. El Kerch, Lekbir Baala, Stanislas Lyonnet, Arnold Münnich, Jeanne Amiel and Tania Attié‐Bitach and has published in prestigious journals such as Nature Genetics, Fertility and Sterility and Clinica Chimica Acta.

In The Last Decade

Aziza Sbiti

18 papers receiving 367 citations

Peers

Aziza Sbiti

GENET

PPCH

GENET

Preeti Paliwal India

SG Ahmed Nigeria

Elisa Biamino Italy

Chantal Missirian France

Petra Muschke Germany

Chad Haldeman‐Englert United States

Ray E. Shenefelt United States

Gülen Eda Ütine Türkiye

Silvia Maitz Italy

João Facucho-Oliveira Portugal

Preeti Paliwal India

Aziza Sbiti

238 ×1.1

74 ×0.6

GENET

30 ×0.4

PPCH

42 ×0.6

GENET

28 ×0.6

Citations per year, relative to Aziza Sbiti Aziza Sbiti (= 1×) peers Preeti Paliwal

Countries citing papers authored by Aziza Sbiti

Since Specialization

Citations

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

Fields of papers citing papers by Aziza Sbiti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aziza Sbiti

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

All Works

Sort: Min cites: Since: Top N: Style:

19 of 19 papers shown

Elalaoui, Siham Chafai, et al.. (2022). Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability. Ophthalmic Genetics. 43(5). 689–692. 1 indexed citations

Leeuw, Nicole de, et al.. (2021). 15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review. The Italian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 188–188. 7 indexed citations

Ratbi, Ilham, et al.. (2020). Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutations. Clinica Chimica Acta. 506. 28–32. 1 indexed citations

Natiq, Abdelhafid, et al.. (2019). Constitutional Partial Proximal Trisomy 14q11.2 to 14q21: Two New Moroccan Cases and Review of the Literature. 3(3). 1–17.

Natiq, Abdelhafid, et al.. (2017). Familial X/Y Translocation Encompassing <b><i>ARSE</i></b> in Two Moroccan Siblings with Sensorineural Deafness. Cytogenetic and Genome Research. 153(2). 66–72. 3 indexed citations

Natiq, Abdelhafid, Aziza Sbiti, Jaber Lyahyai, et al.. (2016). 20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature. BMC Research Notes. 9(1). 5–5. 5 indexed citations

Natiq, Abdelhafid, et al.. (2016). Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report. Journal of Medical Case Reports. 10(1). 122–122. 5 indexed citations

Ratbi, Ilham, et al.. (2016). Cytogenetic Investigation in a Group of Ten Infertile Men with Non-Obstructive Azoospermia: First Algerian 46, XX Syndrome.. PubMed. 45(6). 739–47. 4 indexed citations

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

10.

Jaouad, Imane Cherkaoui, et al.. (2012). Cytogenetic Analysis of 5572 Patients Referred for Suspected Chromosomal Abnormalities in Morocco. Genetic Testing and Molecular Biomarkers. 16(6). 569–573. 10 indexed citations

11.

Lyahyai, Jaber, Aziza Sbiti, Amina Barkat, Ilham Ratbi, & Abdelaziz Sefiani. (2011). Spinal Muscular Atrophy Carrier Frequency and Estimated Prevalence of the Disease in Moroccan Newborns. Genetic Testing and Molecular Biomarkers. 16(3). 215–218. 20 indexed citations

12.

Sbiti, Aziza, Ilham Ratbi, Yamna Kriouile, & Abdelaziz Sefiani. (2011). L’amyotrophie spinale infantile : cause fréquente des hypotonies congénitales au Maroc. Archives de Pédiatrie. 18(12). 1261–1264. 2 indexed citations

13.

Jaouad, Imane Cherkaoui, et al.. (2010). Cytogenetic and epidemiological profiles of Down syndrome in a Moroccan population: a report of 852 cases.. PubMed. 51(2). 133–6. 15 indexed citations

14.

Jaouad, Imane Cherkaoui, et al.. (2009). CONSANGUINEOUS MARRIAGES IN MOROCCO AND THE CONSEQUENCE FOR THE INCIDENCE OF AUTOSOMAL RECESSIVE DISORDERS. Journal of Biosocial Science. 41(5). 575–581. 93 indexed citations

15.

Ouldim, Karim, et al.. (2008). Unexpected fertility and paternal UPD 22. Fertility and Sterility. 90(5). 2013.e13–2013.e15. 18 indexed citations

16.

Baala, Lekbir, Sylvain Briault, Heather Etchevers, et al.. (2007). Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis. Nature Genetics. 39(4). 454–456. 148 indexed citations

17.

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

18.

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

19.

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

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.

Explore authors with similar magnitude of impact