M Chaâbouni - Concepedia

Author

M Chaâbouni

Also Known As

A Ivanoff, M Chaabouni, M Chaâbouni, M N Chaabouni, M. Chaabouni, M.N. Chaabouni, Malak Chaabouni, Malek Chaabouni, Melek Chaabouni, Mohamed Nejib Chaabouni

Publications

519

Citations

H-Index

Concepts

All Affiliations

Hôpital Charles-Nicolle Hopital Universitaire Hedi Chaker Hôpital La Rabta Faculté de médecine de Tunis Tunis University

About

M Chaâbouni is an author at Hôpital Charles-Nicolle specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	123
2	Public Health	3	3	53
3	Biochemistry	1	1	30
4	Biology	1	1	27
5	Epidemiology	1	1	10

M Chaâbouni

Publications

375

Citations

H-Index

Page 1

	Year	Citations
A novel <i>UBE3A</i> truncating mutation in large Tunisian Angelman syndrome pedigree Leila Abaied, Médiha Trabelsi, M Chaâbouni, American Journal of Medical Genetics Part A	2009	77
[Blepharitis due to Demodex: myth or reality?]. B. Kamoun, Meriem Fourati, M Mlik, PubMed	1999	48
Incidence of mucopolysaccharidoses in Tunisia. Ben Turkia H, Néji Tebib, Hatem Azzouz, PubMed	2009	42
Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis O. M'hamdi, Claire Redin, Corinne Stoetzel, Clinical Genetics	2013	31
Only two mutations detected in 15 Tunisian patients with 11β‐hydroxylase deficiency: the p.Q356X and the novel p.G379V Maher Kharrat, Saoussen Trabelsi, M Chaâbouni, Clinical Genetics Steroid 11β-Hydroxylase DeficiencyGeneticsGenetic EpidemiologyPathologyMolecular Genetics	2010	30
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region M Chaâbouni, M. Le Merrer, O Raoul, European Journal of Medical Genetics BiologyCytogeneticsGenetic DisorderGeneticsBrachydactyly Candidate Region	2005	27
Mucopolysaccharidosis I: α‐<scp>L</scp>‐Iduronidase mutations in three Tunisian families Sandrine Laradi, Turgut Tükel, Mónica Erazo, Journal of Inherited Metabolic Disease	2005	25
Mucopolysaccharidosis type IV: N-Acetylgalactosamine-6-sulfatase mutations in Tunisian patients Sandrine Laradi, Turgut Tükel, S. Khediri, Molecular Genetics and Metabolism Genetic DisorderMedicinePathogenesisPathologyTunisian Patients	2005	22
[Childhood plaque milia of the inner canthus]. S. Bouassida, Meziou Tj, H Mlik, PubMed	1998	18
Y chromosome microdeletions in Tunisian infertile males Imen Rejeb, Ridha Mrad, Faouzi Mâazoul, Pathologie Biologie InfertilityFertilityCytogeneticsGeneticsReproductive Health	2007	13

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