Abdelaziz Sefiani

3.5k citations

123 papers · 1.8k indexed · h-index 21

Genetics top 5%
- Genomic variations and chromosomal abnormalities 18
- Genetics and Neurodevelopmental Disorders 10
- Neurogenetic and Muscular Disorders Research 9
- Genomics and Rare Diseases 7
- Connective tissue disorders research 7
Molecular Biology top 10%
- Muscle Physiology and Disorders 7
- RNA regulation and disease 7
- RNA modifications and cancer 7
Genetics top 10%
- Genomic variations and chromosomal abnormalities 18
- Genetics and Neurodevelopmental Disorders 10
- Neurogenetic and Muscular Disorders Research 9
- Genomics and Rare Diseases 7
- Connective tissue disorders research 7
Clinical Biochemistry top 5%
Developmental Neuroscience top 10%

Co-authors: Ilham Ratbi Siham Chafai Elalaoui Aziza Sbiti Imane Cherkaoui Jaouad Jaber Lyahyai Lekbir Baala F. El Kerch Abdelhafid Natiq
Cited by: Genetics Molecular Biology
Journals: Nucleic Acids Research (1 paper)Nature Genetics (1 paper)SHILAP Revista de lepidopterología (4 papers)
Partner nations: Morocco France Netherlands

In The Last Decade

Abdelaziz Sefiani

115 papers receiving 1.7k citations

Peers

Countries citing papers authored by Abdelaziz Sefiani

Since Specialization

Citations

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

Fields of papers citing papers by Abdelaziz Sefiani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Abdelaziz Sefiani, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Abdelaziz Sefiani Line = papers co-authored together Abdelaziz Sefiani links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	First application of next-generation sequencing in four families with Wilson disease in Morocco SHILAP Revista de lepidopterología ·Maryem Sahli,Abdelali Zrhidri,Youssef El Kadiri,Imane Cherkaoui Jaouad,Toufik Meskini,Abdelaziz Sefiani	2023	1
2	Mutational spectrum of BRCA1/2 genes in Moroccan patients with hereditary breast and/or ovarian cancer, and review of BRCA mutations in the MENA region Breast Cancer Research and Treatment ·Siham Chafai Elalaoui,Fatima Zahra Laarabi,Lamiae Afif,Jaber Lyahyai,Ilham Ratbi,Imane Cherkaoui Jaouad,Yassamine Doubaj,Meryem Sahli,Mouna Ouhenach,Abdelaziz Sefiani	2022	4
3	Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndrome African Health Sciences ·Siham Chafai Elalaoui,Wiam Smaili,Julien Van‐Gils,Patricia Fergelot,Ilham Ratbi,Mariam Tajir,Benoı̂t Arveiler,Didier Lacombe,Abdelaziz Sefiani	2021	1
4	Identification of a novel LAMA2 c.2217G > A, p.(Trp739) mutation in a Moroccan patient with congenital muscular dystrophy: a case report BMC Medical Genomics* ·Youssef El Kadiri,Ilham Ratbi,Fatima Zahra Laarabi,Yamna Kriouile,Abdelaziz Sefiani,Jaber Lyahyai	2021	6
5	Familial X/Y Translocation Encompassing <b><i>ARSE</i></b> in Two Moroccan Siblings with Sensorineural Deafness Cytogenetic and Genome Research ·Saadia Amasdl,Wiam Smaili,Abdelhafid Natiq,A. Belkhayyat Hassani,Aziza Sbiti,Aomar Agadr,Damien Sanlaville,Abdelaziz Sefiani	2017	3
6	Further evidence of POP1 mutations as the cause of anauxetic dysplasia American Journal of Medical Genetics Part A ·Siham Chafai Elalaoui,Fatima Zahra Laarabi,Maria Mansouri,Nidal Alaoui Mrani,Gen Nishimura,Abdelaziz Sefiani	2016	14
7	AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population Genetic Testing and Molecular Biomarkers ·Lamiae Boualla,Mariam Tajir,N. Oulahiane,Jaber Lyahyai,Fatima Zahra Laarabi,Siham Chafai Elalaoui,Kenza Soulami,Hassan Ait Ouamar,Abdelaziz Sefiani	2015	15
8	Clinical and molecular findings in a Moroccan patient with popliteal pterygium syndrome: a case report Journal of Medical Case Reports ·Ilham Ratbi,Nawfal Fejjal,Marie Legendre,Nathalie Collot,Serge Amselem,Abdelaziz Sefiani	2014	3
9	Syndrome de Silver Russell: A propos de 3 cas et revue de la litterature Pan African Medical Journal ·Afaf Lamzouri,Ilham Ratbi,Abdelaziz Sefiani	2013	2
10	Germline mosaicism in Rubinstein–Taybi syndrome Gene ·Mariam Tajir,Patricia Fergelot,Guenaëlle Lancelot,Siham Chafai Elalaoui,Benoı̂t Arveiler,Didier Lacombe,Abdelaziz Sefiani	2013	10
11	Cytogenetic Analysis of 5572 Patients Referred for Suspected Chromosomal Abnormalities in Morocco Genetic Testing and Molecular Biomarkers ·Nisrine Aboussair,Imane Cherkaoui Jaouad,Souad Cherkaoui Dequaqui,Aziza Sbiti,Fatiha El-Kerch,Benbouchta Yahya,Abdelhafid Natiq,Abdelaziz Sefiani	2012	10
12	Frequencies of CYP3A51/3 Variants in a Moroccan Population and Effect on Tacrolimus Daily Dose Requirements in Renal Transplant Patients Genetic Testing and Molecular Biomarkers ·Mustapha Elmachad,Driss Elkabbaj,Fatiha Elkerch,Fatima Zahra Laarabi,Amina Barkat,Zouhir Oualim,Abdelaziz Sefiani	2012	14
13	Frequency of IL28B rs12979860 Single-Nucleotide Polymorphism Alleles in Newborn Infants and in Patients with Chronic Hepatitis C in Morocco Genetic Testing and Molecular Biomarkers ·Mariam Tajir,Mustapha Elmachad,Nawal Kabbaj,Fatima Zahra Laarabi,Amina Barkat,N. Amrani,Abdelaziz Sefiani	2012	3
14	An inherited LMNA gene mutation in atypical Progeria syndrome American Journal of Medical Genetics Part A ·Yassamine Doubaj,Annachiara De Sandre‐Giovannoli,Esteves‐Vieira Vera,Claire Navarro,Siham Chafai Elalaoui,Mariam Tajir,Nicolas Lévy,Abdelaziz Sefiani	2012	36
15	MEFV mutations in Moroccan patients suffering from familial Mediterranean Fever Rheumatology International ·Latifa Belmahi,Imane Jaouad Cherkaoui,Iman Hama,Abdelaziz Sefiani	2011	14
16	Homozygous Inactivating Mutations in the NKX3-2 Gene Result in Spondylo-Megaepiphyseal-Metaphyseal Dysplasia The American Journal of Human Genetics ·Jan Hellemans,Marleen Simon,Annelies Dheedene,Yasemin Alanay,Ercan Mıhçı,Laïla Rifai,Abdelaziz Sefiani,Yolande van Bever,M. Meradji,Andrea Superti‐Furga,Geert Mortier	2009	28
17	Cystic fibrosis carrier frequency and estimated prevalence of the disease in Morocco Journal of Cystic Fibrosis ·Ilham Ratbi,Emmanuelle Génin,Marie Legendre,Annick Le Floch,Cathérine Costa,Souad Cherkaoui-Deqqaqi,Michel Goossens,Abdelaziz Sefiani,Emmanuelle Girodon	2008	15
18	Unexpected fertility and paternal UPD 22 Fertility and Sterility ·Karim Ouldim,Aziza Sbiti,Abdelbafid Natiq,Fatiha El-Kerch,S. Cherkaoui,Abdelaziz Sefiani	2008	18
19	La mutation 35delG du gène de la connexine 26, une cause fréquente des surdités non syndromiques autosomiques récessives au Maroc Archives de Pédiatrie ·Ilham Ratbi,S. Hajji,Karim Ouldim,Nisrine Aboussair,D Feldmann,Abdelaziz Sefiani	2007	4
20	Mowat-Wilson syndrome in a Moroccan consanguineous family Indian journal of human genetics ·Ilham Ratbi,ChafaiSiham Elalaoui,MoalFlorence Dastot-Le,Michel Goossens,Irina Giurgea,Abdelaziz Sefiani	2007	3

About Abdelaziz Sefiani

Abdelaziz Sefiani is a scholar working on Developmental Biology, Genetics and Genetics, having authored 123 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Genetics and Neurodevelopmental Disorders (10 papers), Neurogenetic and Muscular Disorders Research (9 papers), Genomics and Rare Diseases (7 papers), Muscle Physiology and Disorders (7 papers), Connective tissue disorders research (7 papers), RNA regulation and disease (7 papers) and RNA modifications and cancer (7 papers). The work is most often cited by research in Genetics (526 citations), Molecular Biology (964 citations) and Genetics (142 citations). Abdelaziz Sefiani has collaborated with scholars based in Morocco, France and Netherlands. Frequent co-authors include Ilham Ratbi, Siham Chafai Elalaoui, Aziza Sbiti, Imane Cherkaoui Jaouad, Jaber Lyahyai, Lekbir Baala, F. El Kerch, Abdelhafid Natiq, Arnold Münnich and Amina Barkat. Their work appears in journals such as Nucleic Acids Research, Nature Genetics and SHILAP Revista de lepidopterología.

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