Concepedia

Author

Sellama Nadifi

University of Hassan II CasablancaORCID

Also Known As

Abdelatif Benider, Brehima Diakite, NADIFI, Sellama, Nadifi Sellama, Nadifi,Sellama, S Nadifi, S. Nadifi, SELLAMA NADIFI, Sellama Nadif, Sellama Nadifi

215

Publications

2.3K

Citations

25

H-Index

95

Concepts

All Affiliations

University of Hassan II CasablancaCentre Hospitalier Universitaire Ibn RochdInstitut Pasteur du MarocInsermUniversité Sultan Moulay Slimane
SN

About

Sellama Nadifi is an author at University of Hassan II Casablanca specializing in medicine, genetics, and public health.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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2

Public Health

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10

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3

Arts

2

2

63

4

Natural Sciences

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5

Health Sciences

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Sellama Nadifi

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62

Publications

1.6K

Citations

23

H-Index

YearCitations

Hypomorphic homozygous mutations in phosphoglucomutase 3 (PGM3) impair immunity and increase serum IgE levels

Atfa Sassi, Sandra Lazaroski, Gang Wu,

Journal of Allergy and Clinical Immunology

2014

188

The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population

Klaus Dieterich, Raoudha Zouari, Radu Harbuz,

Human Molecular Genetics

2009

107

A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco

Ahmed Belmouden, Rahma Melki, M. Hamdani,

Clinical Genetics

2002

70

BRCA1 and BRCA2 germline mutations in Moroccan breast/ovarian cancer families: Novel mutations and unclassified variants

Amal Tazzite, H. Jouhadi, Sellama Nadifi,

Gynecologic Oncology

2012

62

Anti-inflammatory potential of Capparis spinosa L. in vivo in mice through inhibition of cell infiltration and cytokine gene expression

Khadija El Azhary, Nadia Tahiri Jouti, Meryam El Khachibi,

BMC Complementary and Alternative Medicine

2017

51

The polymorphism G894 T of endothelial nitric oxide synthase (eNOS) gene is associated with susceptibility to essential hypertension (EH) in Morocco

Sanaa Nassereddine, Hind Hassani Idrissi, Rachida Habbal,

BMC Medical Genetics

2018

36

Autosomal recessive and sporadic deafness in Morocco: High frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant

Bouchaïb Gazzaz, Dominique Weil, Leïla Raïs,

Hearing Research

2005

35

Large scale meta-analysis of genetic studies in ischemic stroke: Five genes involving 152,297 individuals

Khalil Hamzi, Brehima Diakité, Amal Tazzite,

Indian journal of human genetics

2013

29

Association of inflammatory cytokine gene polymorphisms with inflammatory bowel disease in a Moroccan cohort

Nezha Senhaji, Aurelio Serrano, W. Badre,

Genes and Immunity

2015

29

Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss

Amina Bakhchane, Amale Bousfiha, Hicham Charoute,

European Journal of Medical Genetics

2016

28

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