Works matching AU Ouldim, Karim

Results: 40

The first PTPN11 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studies.

Published in:

Turkish Journal of Medical Sciences, 2015, v. 45, n. 2, p. 306, doi. 10.3906/sag-1310-50

By:

EL BOUCHIKHI, Ihssane;
SAMRI, Imane;
IRAQUI HOUSSAINI, Mohammed;
TRHANINT, Saaid;
BOUGUENOUCH, Laila;
SAYEL, Hanane;
HIDA, Moustapha;
ATMANI, Samir;
OULDIM, Karim

Publication type:

Article

Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1363

By:

Hamdaoui, Hasna;
Benlarroubia, Oumaima;
Ait Boujmia, Oum Kaltoum;
Mossafa, Hossein;
Ouldim, Karim;
Belkhayat, Aziza;
Smyej, Imane;
Benrahma, Houda;
Dehbi, Hind;
Chegdani, Fatima

Publication type:

Article

Genetics and genomic medicine in Morocco: the present hope can make the future bright.

Published in:

Molecular Genetics & Genomic Medicine, 2016, v. 4, n. 6, p. 588, doi. 10.1002/mgg3.255

By:

Belhassan, Khadija;
Ouldim, Karim;
Sefiani, Abdel Aziz

Publication type:

Article

RAS Mutations Predict Recurrence-Free Survival and Recurrence Patterns in Colon Cancer: A Unicenter Study in Morocco.

Published in:

Cancer Control: Journal of the Moffitt Cancer Center, 2024, p. 1, doi. 10.1177/10732748241229290

By:

El Agy, Fatima;
El Bardai, Sanae;
Boukansa, Sara;
Bouguenouch, Laila;
Benbrahim, Zineb;
Mazaz, Khalid;
Benjelloun, El Bachir;
Ousadden, Abdelmalek;
Ouldim, Karim;
Ibrahimi, Sidi Adil;
Chbani, Laila

Publication type:

Article

Gut microbiome of Moroccan colorectal cancer patients.

Published in:

Medical Microbiology & Immunology, 2018, v. 207, n. 3/4, p. 211, doi. 10.1007/s00430-018-0542-5

By:

Allali, Imane;
Boukhatem, Noureddine;
Bouguenouch, Leila;
Hardi, Hanaa;
Boudouaya, H. Abir;
Cadenas, M. Belen;
Ouldim, Karim;
Amzazi, Saaïd;
Azcarate-Peril, M. Andrea;
Ghazal, Hassan

Publication type:

Article

High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast-ovarian cancer prevention and control.

Published in:

BMC Research Notes, 2017, v. 10, p. 1, doi. 10.1186/s13104-017-2511-2

By:

Laarabi, Fatima-Zahra;
Ratbi, Ilham;
Elalaoui, Siham Chafai;
Mezzouar, Loubna;
Doubaj, Yassamine;
Bouguenouch, Laila;
Ouldim, Karim;
Benjaafar, Noureddine;
Sefiani, Abdelaziz

Publication type:

Article

An XPC and XPA genetic study on xeroderma pigmentosum patients in a Moroccan population.

Published in:

Our Dermatology Online / Nasza Dermatologia Online, 2020, v. 11, n. 4, p. 335, doi. 10.7241/ourd.20204.1

By:

Bay, Hanane Bay;
Rasso, Asmae;
Aqil, Niema;
Bouguenouch, Leila;
Ouldim, Karim;
Elloudi, Sara;
Douhi, Zakia;
Mernissi, Fatima Zahra

Publication type:

Article

Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome.

Published in:

Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00514-5

By:

Chbel, Faiza;
Hamdaoui, Hasna;
Mossafa, Houssein;
Ouldim, Karim;
Benrahma, Houda

Publication type:

Article

Tetrasomy 15q11-q13 Diagnosed by FISH in a Patient with Autistic Disorder.

Published in:

Journal of Biomedicine & Biotechnology, 2007, p. 1, doi. 10.1155/2007/61538

By:

Ouldim, Karim;
Natiq, Abdelhafid;
Jonveaux, Philippe;
Sefiani, Abdelaziz

Publication type:

Article

A novel homozygous missense variant identified in the myosin VIIA motor domain of a Moroccan patient with usher syndrome.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09603-5

By:

Ouarhache, Maryem;
Kettani, Oussama;
Fizazi, Khawla El;
Bouguenouch, Laila;
Ouldim, Karim

Publication type:

Article

Review of prostate cancer genomic studies in Africa.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.911101

By:

Samtal, Chaimae;
El Jaddaoui, Islam;
Hamdi, Salsabil;
Bouguenouch, Laila;
Ouldim, Karim;
Nejjari, Chakib;
Ghazal, Hassan;
Bekkari, Hicham

Publication type:

Article

Dietary Fat Intake and KRAS Mutations in Colorectal Cancer in a Moroccan Population.

Published in:

Nutrients, 2022, v. 14, n. 2, p. 318, doi. 10.3390/nu14020318

By:

El Asri, Achraf;
Ouldim, Karim;
Bouguenouch, Laila;
Sekal, Mohammed;
Moufid, Fatima Zahra;
Kampman, Ellen;
Huybrechts, Inge;
Gunter, Marc J.;
Abbaoui, Sanae;
Znati, Kaoutar;
Karkouri, Mehdi;
Kinany, Khaoula El;
Hatime, Zineb;
Deoula, Meimouna Mint Sidi;
Chbani, Laila;
Zarrouq, Btissame;
El Rhazi, Karima

Publication type:

Article

A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2.

Published in:

American Journal of Medical Genetics. Part A, 2023, v. 191, n. 11, p. 2673, doi. 10.1002/ajmg.a.63375

By:

El Fizazi, Khawla;
Bouramtane, Abdelhamid;
Abbassi, Meriame;
El Asri, Yasser Ali;
Askander, Omar;
El Fahime, Mustapha;
Ouldim, Karim;
Ridal, Mohammed;
Bouguenouch, Laila

Publication type:

Article

Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype.

Published in:

Egyptian Journal of Medical Human Genetics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s43042-021-00136-1

By:

EL Bouchikhi, Ihssane;
Belhassan, Khadija;
Moufid, Fatima Zohra;
Bouguenouch, Laila;
Samri, Imane;
Iraqui Houssaïni, Mohammed;
Ouldim, Karim;
Atmani, Samir

Publication type:

Article

Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age.

Published in:

Egyptian Journal of Medical Human Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s43042-020-0047-9

By:

El Bouchikhi, Ihssane;
Bouguenouch, Laila;
Moufid, Fatima Zohra;
Samri, Imane;
Abdouss, Fatima;
Melhouf, Moulay Abdelilah;
Iraqui Houssaini, Mohammed;
Belhassan, Khadija;
Atmani, Samir;
Ouldim, Karim

Publication type:

Article

Epigenetics could explain some Moroccan population colorectal cancers peculiarities: microsatellite instability pathway exploration.

Published in:

Diagnostic Pathology, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13000-015-0326-9

By:

Sekal, Mohammed;
Ameurtesse, Hassania;
Chbani, Laila;
Ouldim, Karim;
Bennis, Sanae;
Abkari, Mohammed;
Boulouz, Amal;
Benajah, Dafr Allah;
Benjelloun, Basher;
Ousadden, Abdelmalek;
Ait Taleb, Khalid;
Ait Laalim, Said;
Toghrai, Imane;
Mazaz, Khalid;
Arifi, Samia;
Mellas, Nawfel;
El Rhazi, Karima;
Harmouch, Taoufiq;
Ibrahimi, Sidi Adil;
Riffi, Afaf Amarti

Publication type:

Article

Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus–dystonia.

Published in:

2022

By:

Chbel, Faiza;
Charroute, Hicham;
Boulouiz, Redouane;
Hamdaoui, Hasna;
Mossafa, Houssein;
Benrahma, Houda;
Ouldim, Karim

Publication type:

Case Study

Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation.

Published in:

Turkish Journal of Gastroenterology, 2018, v. 29, n. 6, p. 701, doi. 10.5152/tjg.2018.17761

By:

Moufid, Fatima Zahra;
Bouguenouch, Laila;
El Bouchikhi, Ihssane;
Houssaini, Mohamed Iraqui;
Ouldim, Karim

Publication type:

Article

Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation.

Published in:

Turkish Journal of Gastroenterology, 2018, v. 29, n. 5, p. 1, doi. 10.5152/tjg.2018.17761

By:

Moufid, Fatima Zahra;
Bouguenouch, Laila;
El Bouchikhi, Ihssane;
Houssaini, Mohamed Iraqui;
Ouldim, Karim

Publication type:

Article

Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation.

Published in:

Turkish Journal of Gastroenterology, 2017, v. 28, p. 9, doi. 10.5152/tjg.2018.17761

By:

Moufid, Fatima Zahra;
Bouguenouch, Laila;
El Bouchikhi, Ihssane;
Houssaini, Mohamed Iraqui;
Ouldim, Karim

Publication type:

Article

Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation.

Published in:

Turkish Journal of Gastroenterology, 2017, v. 28, p. 12, doi. 10.5152/tjg.2018.17761

By:

Moufid, Fatima Zahra;
Bouguenouch, Laila;
Bouchikhi, Ihssane El;
Houssaini, Mohamed Iraqui;
Ouldim, Karim

Publication type:

Article

GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.

Published in:

African Health Sciences, 2018, v. 18, n. 4, p. 922, doi. 10.4314/ahs.v18i4.11

By:

EL Bouchikhi, Ihssane;
Belhassan, Khadija;
Moufid, Fatima Zohra;
Houssaini, Mohammed Iraqui;
Bouguenouch, Laila;
Samri, Imane;
Bouhrim, Mohamed;
Ouldim, Karim;
Atma, Samir

Publication type:

Article

NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population.

Published in:

Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2017, v. 17, n. 3, p. 217, doi. 10.14744/AnatolJCardiol.2016.7222

By:

El Bouchikhi, Ihssane;
Bouguenouch, Laila;
Moufid, Fatima Zohra;
Houssaini, Mohammed Iraqui;
Belhassan, Khadija;
Samri, Imane;
Joutei, Ayoub Tahri;
Ouldim, Karim;
Atmani, Samir

Publication type:

Article

Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects.

Published in:

Eurasian Journal of Medicine, 2020, v. 52, n. 3, p. 283, doi. 10.5152/eurasianjmed.2020.19237

By:

El Bouchikhi, Ihssane;
Bouguenouch, Laila;
Moufid, Fatima Zohra;
Belhassan, Khadija;
Samri, Imane;
Chaouti, Amal;
Houssaïni, Mohammed Iraqui;
Atmani, Samir;
Ouldim, Karim

Publication type:

Article

Expanding the spectrum of ATP8A2 mutations: a new splicing variant and systematic review of CAMRQ4 syndrome.

Published in:

Molecular Biology Reports, 2025, v. 52, n. 1, p. 1, doi. 10.1007/s11033-025-10546-8

By:

Abdelhamid, Bouramtane;
Badreddine, Elmakhzen;
Amal, Ouskri;
Rania, Bouchikhi;
El-asri, Yasser Ali;
Mohamed, Ahakoud;
Laila, Bouguenouch;
Karim, Ouldim;
Omar, Askander

Publication type:

Article

The first assessment of Angiotensin-Converting Enzyme 1 (ACE1) D/I polymorphism and demographic factors in association with COVID-19 outcomes in the Moroccan Population.

Published in:

Molecular Biology Reports, 2025, v. 52, n. 1, p. 1, doi. 10.1007/s11033-024-10211-6

By:

El Bouchikhi, Ihssane;
El Otmani, Ihsane;
Ahakoud, Mohamed;
Kettani, Oussama;
El Makhzen, Badreddine;
Yahyaoui, Ghita;
Oumokhtar, Bouchra;
Ouldim, Karim;
El-Azami-El-Idrissi, Mohammed;
Achour, Sanae;
Mahmoud, Mustapha;
Bouguenouch, Laila

Publication type:

Article

Cancer Omics in Africa: Present and Prospects.

Published in:

Frontiers in Oncology, 2020, v. 10, p. N.PAG, doi. 10.3389/fonc.2020.606428

By:

El Jaddaoui, Islam;
Allali, Imane;
Sehli, Sofia;
Ouldim, Karim;
Hamdi, Salsabil;
Al Idrissi, Najib;
Nejjari, Chakib;
Amzazi, Saaïd;
Bakri, Youssef;
Ghazal, Hassan

Publication type:

Article

Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations.

Published in:

Pan African Medical Journal, 2017, v. 28, p. 1, doi. 10.11604/pamj.2017.28.286.4372

By:

Bouguenouch, Laila;
Samri, Imane;
Abbassi, Meryem;
Hamdaoui, Hasna;
El Otmani, Ihssane;
Sayel, Hanane;
Trhanint, Said;
Benmiloud, Sara;
Amrani, Moncif;
Bennis, Sanae;
Ouldim, Karim;
Hida, Mustapha

Publication type:

Article

Syndrome de Lynch: à propos d'un cas et revue de la litterature.

Published in:

Pan African Medical Journal, 2016, v. 24, p. 1, doi. 10.11604/pamj.2016.24.142.4398

By:

Bouguenouch, Laila;
Samri, Imane;
Belhassan, Khadija;
Sayel, Hanane;
Abbassi, Meriame;
Bennis, Sanae;
Benajah, Dafr Allah;
Ibrahimi, Adil;
Amarti, Afaf;
Ouldim, Karim

Publication type:

Article

Profil étiologique des surdités neurosensorielle sévère et profonde de l'enfant dans la région du centre-nord du Maroc.

Published in:

Pan African Medical Journal, 2014, v. 17, p. 1, doi. 10.11604/pamj.2014.17.100.2331

By:

Ridal, Mohammed;
Outtasi, Naouar;
Taybi, Zainab;
Boulouiz, Redouan;
Chaouki, Sanae;
Boubou, Meryem;
Maaroufi, Mustapha;
Benmansour, Najib;
Zaki, Zouheir;
Ouldim, Karim;
Barakat, Hamid;
Hida, Mustapha;
Tizniti, Siham;
El Alami, Mohamed Noreddine

Publication type:

Article

Marqueurs chromosomiques: à propos d'un cas.

Published in:

Pan African Medical Journal, 2013, v. 15, p. 1, doi. 10.11604/pamj.2013.15.104.1993

By:

Samri, Imane;
Bouguenouch, Laila;
Hamdaoui, Hasna;
El Otmani, Ihsan;
El Omairi, Nissrine;
Chaouki, Sana;
Hida, Moustapha;
Ouldim, Karim

Publication type:

Article

Pharmacogénétique: qu'en est-il au Maroc?

Published in:

Pan African Medical Journal, 2013, v. 14, p. 1, doi. 10.11604/pamj.2013.14.143.2141

By:

Idrissi, Meryem Janati;
Ouldim, Karim;
Amarti, Afaf;
Hassouni, Mohamed El;
Khabbal, Youssef

Publication type:

Article

Le syndrome de Cri du Chat : A propos d'une observation.

Published in:

Pan African Medical Journal, 2012, v. 11, p. 1

By:

Ouldim, Karim;
Samri, Imane;
Bouguenouch, Laila;
Hamdaoui, Hasna;
Otmani, Ihsan El;
Hbibi, Mohamed;
Chaouki, Sana;
Hida, Moustapha

Publication type:

Article

Syndromes microdélétionnels (syndrome de Williams et syndrome de la délétion 22q11) au CHU Hassan II de Fès: à propos de 3 observations.

Published in:

Pan African Medical Journal, 2012, v. 11, p. 1

By:

Ouldim, Karim;
Bouguenouch, Laila;
Samri, Imane;
Otmani, Ihsan El;
Hamdaoui, Hasna;
Bennis, Sanae;
Lakhdar, Mounia Idrissi;
Chaouki, Sana;
Atmani, Samir;
Hida, Moustapha

Publication type:

Article

Update on prostate cancer epidemiology in Morocco.

Published in:

African Journal of Urology, 2024, v. 30, n. 1, p. 1, doi. 10.1186/s12301-024-00419-0

By:

Samtal, Chaimae;
Bouguenouch, Laila;
Ismaili, Nabil;
El Baldi, Marwa;
El Makhzen, Badreddine;
El Rhazi, Karima;
Mzyiene, Mohammed;
Farih, Moulay Hassan;
Ouldim, Karim;
Ghazal, Hassan;
Bekkari, Hicham

Publication type:

Article

Novel NKX2-5 germline mutation in a Moroccan child with transitional atrio-ventricular septal defect (tAVSD).

Published in:

Turkish Journal of Pediatrics, 2017, v. 59, n. 5, p. 610, doi. 10.24953/turkjped.2017.05.019

By:

El-Bouchikhi, Ihssane;
Belhassan, Khadija;
Zohra Moufid, Fatima;
Iraqui Houssaini, Mohammed;
Ouldim, Karim;
Atmani, Samir

Publication type:

Article

Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population.

Published in:

Audiology & Neurotology, 2024, v. 29, n. 3, p. 216, doi. 10.1159/000535346

By:

El Fizazi, Khawla;
Abbassi, Meriame;
Nmer, Samira;
Laamarti, Hajar;
ElAlami, Mohamed Noureddine;
Ouldim, Karim;
Bouguenouch, Laila;
Ridal, Mohammed

Publication type:

Article

OCPS 5: Molecular characterization of gastrointestinal stromal tumours: The experience of Hassan II University Hospital-Fez; Morocco.

Published in:

2015

By:

Samia, Arifi;
Sanae, El Bardai;
Ouldim, Karim;
Hostein, Isabelle;
Coindre, Jean Michel;
Afaf, Amarti;
Laila, Chbani

Publication type:

Abstract

OCPS 4: Molecular characterization of mlh1 and msh2 germline mutations among colorectal cancer patients showing extinction of MLH1 and MSH2 proteins.

Published in:

2015

By:

Moufid, Fatima Zohra;
Bouguenouch, Laila;
Elbouchikhi, Ihssane;
Houssaini, Mohamed Iraqui;
Belhassan, Khadija;
Samri, Iman;
Karim, Ouldim

Publication type:

Abstract

Associations between nutritional factors and KRAS mutations in colorectal cancer: a systematic review.

Published in:

2020

By:

El Asri, Achraf;
Zarrouq, Btissame;
El Kinany, Khaoula;
Bouguenouch, Laila;
Ouldim, Karim;
El Rhazi, Karima

Publication type:

journal article