Informations du chercheur

Nom complet

ABOUSSAIR NISRINE

Grade

PES

Spécialité

Génétique

Thématique de recherche

Maladies génétiques/RARES

Laboratoire

Laboratoire de recherche l'enfance la santé et le développement

Établissement

Non affilié

Ouvrages (0 au total)

Aucun ouvrage disponible.

Projets (0 au total)

Aucun projet disponible.

Publications (20 au total)

The frequency of the homozygote 35delG mutation in the connexin 26 gene in North African with non-syndromic hearing loss: A meta-analysis study

Auteur: Moussaoui Abdelmajid ,MeriemEl Qabli, Latifa Adarmouch, Nisrine Aboussair

Revue: Meta Gene

Année: 2021

DOI: doi.org/10.1016/j.mgene.2021.100895

First characterization of LHON pedigrees in North Africa.

Auteur: Aymane Bouzidi, Nisrine Aboussair, Majida Charif, Ghita Amalou, David Goudenège, Valérie Desquiret-Dumas, Céline Bris, Najat Sifeddine, Halima Nahili, Meriem Elqabli, Kenza Dafir, Mostafa Kandil, Patrizia Amati-Bonneau, Vincent Procaccio, Abdelhamid Barakat ,Guy Lenaers

Revue: Eye (nature)

Année: 2020

DOI: https://doi.org/10.1038/s41433-019-0755-x

First Report of 2q37 Microdeletion Syndrome in Morocco

Auteur: Hanane Ait hammou , Mariam Tajir, Nisrine Aboussair

Revue: Scholars Journal of Medical Case Reports

Année: 2020

DOI: DOI: 10.36347/sjmcr.2020.v08i01.025

1p36 deletion syndrome: First case report in Morocco detected by fluorescence in situ hybridization.

Auteur: Kenza Dafir, Fatima Zahra Bouzid, Maria Mansouri, Nisrine Aboussair

Revue: The Pan African Medical Journal

Année: 2020

DOI: doi: 10.11604/pamj.2020.37.349.26166]

A Case of Complete Neu-Laxova Syndrome: Report and Literature Review

Auteur: Bouchra Fakhir1, Oussama Rachid, Amal Ait Benhassi, Nisrine Aboussair, Abderraouf Soummani

Revue: Open Journal of Obstetrics and Gynecology

Année: 2020

DOI: DOI: 10.4236/ojog.2020.1030031

BREASTFEEDING TYPE AND ITS RELATIONSHIP WITH THE DEVELOPMENT OF ALLERGIES IN CHILDREN

Auteur: Sanaa Sabour Alaoui | Jalal Ouirari | and | Nisrine Aboussair

Revue: American Journal of Innovative Research & Applied Sciences

Année: 2019

Oculo-auditory syndrome: ophtalmologic impairment screening in deaf children

Auteur: Raji, A.; Belhoucha, B.; Rochdi, Y.; Nouri, H.; Aboussair, N.; Hajji, B.; Moutaouakil, A.

Revue: Journal of Hearing Science

Année: 2018

Retard de croissance staturo-pondéral révélant un syndrome de Silver Russell associé à une composante inédite

Auteur: Ghizlane El Mghari1, Bouchra Rafiq1,&, Nawal El Ansari1, Nisrine Aboussair2

Revue: The Pan African Medical Journal.

Année: 2017

Treacher Collins syndrome: a clinical and molecular study based on a large series of patients

Auteur: Marie Vincent MD ,David Geneviève MD, PhD ,Agnès Ostertag PhD, Sandrine Marlin MD, Didier Lacombe MD, PhD, Dominique Martin-Coignard MD, Christine Coubes MD, Albert David MD, Stanislas Lyonnet MD, PhD, Catheline Vilain MD, Anne Dieux-Coeslier MD, Sylvie Manouvrier MD, PhD, Bertrand Isidor MD, Marie-Line Jacquemont MD, Sophie Julia MD, Valérie Layet MD, Sophie Naudion MD, Sylvie Odent MD, PhD, Laurent Pasquier MD, Sybille Pelras MD, Nicole Philip MD, PhD, Geneviève Pierquin MD, Fabienne Prieur MD, Nisrine Aboussair MD, Tania Attie-Bitach MD, PhD, Geneviève Baujat MD, Patricia Blanchet MD, Catherine Blanchet MD, Hélène Dollfus MD, PhD, Bérénice Doray MD, Elise Schaefer MD, Patrick Edery MD, PhD, Fabienne Giuliano MD, Alice Goldenberg MD, Cyril Goizet MD, PhD, Agnès Guichet MD, Christian Herlin MD, Laetitia Lambert MD, Bruno Leheup MD, PhD, Jelena Martinovic MD, Sandra Mercier MD, Cyril Mignot MD, Marie-Laure Moutard MD, Marie-José Perez MD, Lucile Pinson MD, Jacques Puechberty MD, Marjolaine Willems MD, Hanitra Randrianaivo MD, Kateline Szaskon MD, Annick Toutain MD, PhD, Alain Verloes MD, PhD, Jacqueline Vigneron MD, Elodie Sanchez, Pierre Sarda MD, PhD, Jean-Louis Laplanche PharmD, PhD & Corinne Collet PharmD, PhD

Revue: Genetics in Medicine

Année: 2016

Communications (118 au total)

Clinical and genetic aspects of Leber congenital amaurosis: First Moroccan series

Manifestation: The first international congress of the Moroccan Society of Genomics and Human Genetics (SM2GH) and the third of School of Immunogenetic December , 19th 2019

Date: 2019-12-19

Organisation: Agadir

Trisomy 18 : First Series of the Genetics Department of Marrakech

Manifestation: the first International Congress of the Moroccan Society of Genomics and Human Genetics (SM2GH) & Third School of Immunogenetics (SIG)

Date: 2019-12-19

Organisation: Agadir

Cytogenetic aspects of chronic myeloid leukemia: a series of 147 cases

Manifestation: The first international congress of the Moroccan Society of Genomics and Human Genetics (SM2GH) and the third of School of Immunogenetic December , 19th 2019

Date: 2019-12-19

Organisation: Agadir

1- Man with uterus: about three cases

Manifestation: First International Congress of the Moroccan Society of Genomic and Human Genetics and the third edition of the School of immunogenetics 19-21 December 2019

Date: 2019-12-19

Organisation: Agadir

Bilan génétique des surdités de l'enfant

Manifestation: Atelier ORL organisé par l'association de pédiatrie de la région Tensift Alhaouz

Date: 2019-12-14

Organisation: Marrakech

Oncogénétique et cancer de la prostate

Manifestation: Rencontre d'onco Urologie de Marrakech (ROUM)

Date: 2019-11-02

Organisation: Marrakech

The molecular diagnosis of duchene and becker myopathy by multipex-PCR : first series of the genetics department of Mohammed VI University Hospital of Marrakech.

Manifestation: 2nd International Scientific Conference for Research and Ethics

Date: 2019-04-19

Organisation: Taroudant

Syndrome de prader wili :première série du service de génétique du chu Mohammed VI de Marrakech

Manifestation: 2nd International Scientific Conference for Research and Ethics

Date: 2019-04-19

Organisation: Taroudant

Mutation faux sens du gène MECP2 chez 02 patients atteints du syndrome de RETT

Manifestation: 2nd International Scientific Conference for Research and Ethics

Date: 2019-04-19

Organisation: Taroudant