K. Azibi

1.2k citations

18 papers · 770 indexed · h-index 14

Cellular and Molecular Neuroscience top 10%
Cell Biology top 10%
- Biotin and Related Studies 2
Molecular Biology
- Muscle Physiology and Disorders 7
Molecular Medicine top 10%
- Antibiotic Resistance in Bacteria 2
Genetics top 10%
- Neurogenetic and Muscular Disorders Research 3
Physiology
- Nitric Oxide and Endothelin Effects 2
- Lysosomal Storage Disorders Research 2
Public Health, Environmental and Occupational Health
- Reproductive Biology and Fertility 2
Reproductive Medicine
- Ovarian function and disorders 2

Co-authors: Kevin P. Campbell Michel Fardeau F.M.S. Tomé H. Barry Collin Malika Chaouch Jean‐Claude Kaplan Kiichiro Matsumura France Leturcq
Cited by: Cellular and Molecular Neuroscience Cell Biology Molecular Biology
Journals: Neuromuscular Disorders (3 papers)Antimicrobial Agents and Chemotherapy (2 papers)Journal of Medical Genetics (2 papers)
Partner nations: France United States Algeria

In The Last Decade

K. Azibi

18 papers receiving 748 citations

Peers

Countries citing papers authored by K. Azibi

Since Specialization

Citations

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

Fields of papers citing papers by K. Azibi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside K. Azibi, 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 K. Azibi Line = papers co-authored together K. Azibi links everyone, so they are left out of the graph.

All Works

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18 of 18 papers shown

#	Work
1	Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency The Journal of Clinical Endocrinology & Metabolism ·Justine Bouilly,Isabelle Beau,Sara Barraud,Valérie Bernard,K. Azibi,Jérôme Fagart,Anne Fèvre,Anne‐Laure Todeschini,Reiner A. Veitia,Chérif Beldjord,Brigitte Delemer,Catherine Dodé,Jacques Young,Nadine Binart	2016	88
2	New NOBOX Mutations Identified in a Large Cohort of Women With Primary Ovarian Insufficiency Decrease KIT-L Expression The Journal of Clinical Endocrinology & Metabolism ·Justine Bouilly,Florence Roucher‐Boulez,Anne Gompel,Hélène Bry‐Gauillard,K. Azibi,Chérif Beldjord,Catherine Dodé,Jérôme Bouligand,H KRETZSCHMAR,A.C. Hécart,Brigitte Delemer,Jacques Young,Nadine Binart	2014	42
3	Relationship of eNOS gene variants to diseases that have in common an endothelial cell dysfunction Journal of Cellular and Molecular Medicine ·C Helţianu,şehnaz bodur,Anca Violeta Gafencu,Mihaela Diaconu,Lucia Maria Costiug,Wilhelm Geißler,K. Azibi,Livia Poënaru,Maya Simionescu	2005	34
4	Endothelial nitric oxide synthase gene polymorphisms in Fabry's disease Clinical Genetics ·C Helţianu,şehnaz bodur,K. Azibi,Livia Poënaru,Maya Simionescu	2002	18
5	Identification of a novelde novo mutation (G373D) in the ?-galactosidase A gene (GLA) in a patient affected with Fabry disease Human Mutation ·Dominique P. Germain,敏平方,Florence Fellmann,K. Azibi,Catherine Caillaud,Marie‐Charlotte Bernard,Livia Poënaru	2001	11
6	Nucleotide Sequence of the bla _RTG-2 (CARB-5) Gene and Phylogeny of a New Group of Carbenicillinases Antimicrobial Agents and Chemotherapy ·Xinrui Zou,Marie‐France Szajnert,Marie‐Laure Joly‐Guillou,K. Azibi,Marc Delpech,Jagadindra Ray Choudhury	2000	22
7	Characterization and Nucleotide Sequence of CARB-6, a New Carbenicillin-Hydrolyzing β-Lactamase from Vibrio cholerae Antimicrobial Agents and Chemotherapy ·Xinrui Zou,G. Aubert,Marie‐France Szajnert,K. Azibi,Marc Delpech,Jagadindra Ray Choudhury	1999	21
8	Genetic and allelic heterogeneity of LGMD in North Africa Neuromuscular Disorders ·K. Azibi,Rolf Syrdal,Abderrezak Reghis,F. El Kerch,Aziza Sbiti,A. Sefiani,France Leturcq,Marc Jeanpierre,Alain Carrié,Fédérica Piccolo,C. Beldjord,Meng-ting Lu	1997	1
9	Primary adhalinopathy (α‐sarcoglycanopathy) Neurology ·B. Eymard,Norma B. Romero,France Leturcq,Fédérica Piccolo,Alain Carrié,Marc Jeanpierre,H. Barry Collin,Nathalie Deburgrave,K. Azibi,M. Chaouch,Luciano Merlini,Christine Thémar-Noël,Esperança Batlles Pagès,M Mayer,(unknown),Kevin P. Campbell,Josseline Kaplan,F.M.S. Tomé,Michel Fardeau	1997	95
10	Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). Journal of Medical Genetics ·Alain Carrié,Fédérica Piccolo,France Leturcq,Claudia de Toma,K. Azibi,C. Beldjord,Jean‐Michel Vallat,Luciano Merlini,Thomas Voit,Caroline A. Sewry,J.A. Urtizberea,Norma B. Romero,F.M.S. Tomé,Michel Fardeau,Yoshihide Sunada,Kevin P. Campbell,J.‐C. Kaplan,Marc Jeanpierre	1997	97
11	Absence of γ‐sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12 FEBS Letters ·Daniel Jung,France Leturcq,Yoshihide Sunada,Franck Duclos,F.M.S. Tomé,Carolyn R. Moomaw,Luciano Merlini,K. Azibi,Malika Chaouch,Clive A. Slaughter,Michel Fardeau,Ruth Monica Palacios Ayala,Kevin P. Campbell	1996	46
12	From adhalinopathies to alpha-sarcoglycanopathies: An overview Neuromuscular Disorders ·Marc Jeanpierre,Alain Carrié,Fédérica Piccolo,France Leturcq,K. Azibi,Claudia de Toma,C. Beldjord,Luciano Merlini,Thomas Voit,Norma B. Romero,Yoshihide Sunada,F.M.S. Tomé,Michel Fardeau,Kevin P. Campbell,J.‐C. Kaplan	1996	13
13	Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan) Neuromuscular Disorders ·Josseline Kaplan,Fédérica Piccolo,K. Azibi,Alain Carrié,France Leturcq,Claudia de Toma,C. Beldjord,M. Chaouch,A. Sefiani,Luciano Merlini,T. Voit,C. Sewry,Yoshihide Sunada,Raouf Bouchilaoun,Shelli Brunswick,F.M.S. Tomé,Michel Fardeau,学白石,Marc Jeanpierre	1996	1
14	Laminin abnormality in severe childhood autosomal recessive muscular dystrophy. PubMed ·Hirotsugu Yamada,正明西木,I. Higuchi,H Kawai,K. Azibi,M. Chaouch,Steven L. Roberds,Takeshi Tanaka,Joilyn D. Bush,Takao Mitsui	1995	18
15	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 ·F. El Kerch,Abdelaziz Sefiani,K. Azibi,Nadia Boutaleb,M. Yahyaoui,Kewal Krishna Dewett,Marie Claude Vinet,France Leturcq,L Bachner,J. Beckmann	1994	22
16	Adhalin gene polymorphism Human Molecular Genetics ·Valérie Allamand,France Leturcq,Kenneth Lytts,Marc Jeanpierre,K. Azibi,Steven L. Roberds,Louis Lim,Kevin P. Campbell,J. Beckmann,Kaplan Jc	1994	7
17	Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency. PubMed ·Norma B. Romero,F.M.S. Tomé,France Leturcq,F. El Kerch,K. Azibi,L Bachner,Richard D. Anderson,Steven L. Roberds,Kevin P. Campbell,Michel Fardeau	1994	34
18	Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy Nature ·Kiichiro Matsumura,F.M.S. Tomé,H. Barry Collin,K. Azibi,Malika Chaouch,Jean‐Claude Kaplan,Michel Fardeau,Kevin P. Campbell	1992	200

About K. Azibi

K. Azibi is a scholar working on Molecular Medicine, Genetics, Reproductive Medicine, Physiology and Endocrinology, having authored 18 papers that have together received 770 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (7 papers), Neurogenetic and Muscular Disorders Research (3 papers), Nitric Oxide and Endothelin Effects (2 papers), Reproductive Biology and Fertility (2 papers), Ovarian function and disorders (2 papers), Antibiotic Resistance in Bacteria (2 papers), Biotin and Related Studies (2 papers) and Lysosomal Storage Disorders Research (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (220 citations), Cell Biology (158 citations), Molecular Biology (583 citations), Molecular Medicine (39 citations) and Genetics (81 citations). K. Azibi has collaborated with scholars based in France, United States and Algeria. Frequent co-authors include Kevin P. Campbell, Michel Fardeau, F.M.S. Tomé, H. Barry Collin, Malika Chaouch, Jean‐Claude Kaplan, Kiichiro Matsumura, France Leturcq, Luciano Merlini and Norma B. Romero. Their work appears in journals such as Neuromuscular Disorders, Antimicrobial Agents and Chemotherapy, Journal of Medical Genetics, The Journal of Clinical Endocrinology & Metabolism and Human Mutation.

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