Accueil › Annuaire des chercheurs › Karim Ouldim
Karim Ouldim
Affiliation : Centre Hospitalier Universitaire Hassan II · Sidi Mohamed Ben Abdellah University
- 95Publications (affiliation marocaine)
- 111Publications au total
- 1072Citations
- 17Indice h
Profil de recherche
Karim Ouldim compte 95 publications référencées (2007–2026). Ses travaux paraissent principalement dans « Cureus », « Molecular Biology Reports » et « American Journal of Medical Genetics Part A ». Son article le plus cité, « Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus » (2007), a été cité 100 fois. 31 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de États-Unis.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Genomics and Rare Diseases
- Genetic factors in colorectal cancer
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Publications (95)
- Idiopathic Pulmonary Fibrosis: A Comprehensive Review of Risk Factors, Genetics, Diagnosis, and Therapeutic Approaches
- First combined analysis of SMN1, SMN2, and NAIP copy numbers in Moroccan SMA patients and their correlation with disease severity
- Melanin-free DNA extraction: a rapid and high-efficiency protocol for molecular studies
- A novel missense variant in Sterol-sensing domain related to Niemann-Pick type C1: case report and comprehensive analysis
- Clinical and neuroimaging features in a case of cerebrotendinous xanthomatosis with a CYP27A1 genotype newly identified in morocco: a literature review of African cases
- The genetic landscape of breast cancer in young women from Morocco: implications for diagnosis and treatment
- Novel Perspectives on ATP8A2 Regulation: Evidence for Parental Imprinting and Chimeric Transcript Formation
- Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families
- Prevalence and spectrum of AZFc copy number variations in infertile Moroccan men
- Pediatric hypertrophic cardiomyopathy: current diagnostic strategies, genetic insights, and challenges in risk stratification (a literature review)
- Molecular etiology and therapeutic advances in retinoblastoma
- Clinical and Genetic Insights into Angelman Syndrome: A Retrospective Study of 26 Cases in Morocco
- Progressive ataxia and orolingual chorea revealing a novel VPS13A variant: a case report of chorea-acanthocytosis without peripheral acanthocytosis with a literature review
- High frequency of LRRK2 p.Gly2019Ser in Moroccan Parkinson’s disease: RFLP as a reliable genotyping approach
- Next Generation Sequencing in the Diagnosis of Multiple Myeloma
- A novel homozygous loss-of-function NOTCH3 variant in a Moroccan patient: expanding the spectrum beyond CADASIL
- Expanding the spectrum of ATP8A2 mutations: a new splicing variant and systematic review of CAMRQ4 syndrome
- Unveiling a novel AIMP2 c.157 C>T variant in a Moroccan patient with hypomyelinating leukodystrophy type 17: A case report and insights from a literature review
- Whole Exome Sequencing Identifies Novel Homozygous LGI1 Variant Mimicking ADAM22 -Related Pathologies in a Moroccan Family
- 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
- MUC5B Polymorphism and Susceptibility to Idiopathic Pulmonary Fibrosis in Morocco
- MCLMR Syndrome: A Case Report and Systematic Review
- A rare case of mosaic monosomy 21 in a Moroccan patient: clinical findings and insights from a systematic review
- Novel Variant in the NLRP12 Gene: Insights From a Case Report and Systematic Review
- RAS Mutations Predict Recurrence-Free Survival and Recurrence Patterns in Colon Cancer: A Unicenter Study in Morocco
- A novel homozygous missense variant identified in the myosin VIIA motor domain of a Moroccan patient with usher syndrome
- Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population
- Update on prostate cancer epidemiology in Morocco
- Novel ABL1 mutation in a Moroccan CML patient with Imatinib resistance
- Exploring Splice-Site Mutations in LAMA2-Related Muscular Dystrophies: A Comprehensive Analysis of Genotypic and Phenotypic Patterns
- Conventional and molecular cytogenetic characterization of a Moroccan patient with WAGR syndrome
- The Diagnosis and Genetic Mechanisms of Prader-Willi Syndrome: Findings From a Moroccan Population Study
- A homozygous missense variant in the PLCB4 gene causes severe phenotype of auriculocondylar syndrome type 2
- Next Generation Sequencing in Diagnosis of Multiple Myeloma
- Rare and Atypical Case of Turner Syndrome With Three Cell Lines
- 149P Rare RAS mutations are associated with recurrence patterns and recurrence-free survival in colon cancer: First results from Morocco
- Review of prostate cancer genomic studies in Africa
- Dietary Fat Intake and KRAS Mutations in Colorectal Cancer in a Moroccan Population
- Molecular Diagnosis of Primary Hyperoxaluria Type 1 and Distal Renal Tubular Acidosis in Moroccan Patients With Nephrolithiasis and/or Nephrocalcinosis
- Detection of a new deleterious SGCE gene variant in Moroccan family with inherited myoclonus–dystonia
- Molecular classification of soft tissue sarcomas for adequate diagnosis: A study on the northeast population of Morocco
- Initiation of the Pharmacogenetics of Capecitabine in Morocco
- Molecular Diagnosis of Primary Hyperoxaluria Type 1 and Distal Renal Tubular Acidosis in Moroccan Patients With Nephrolithiasis and/or Nephrocalcinosis
- Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
- Molecular and clinical assessment of maturity-onset diabetes of the young revealed low mutational rate in Moroccan families
- 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
- Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
- Detection of a new deleterious SGCE gene variant in Moroccan family with inherited Myoclonic-dystonia
- Empowering newborn screening programs in African countries through establishment of an international collaborative effort
- Analysis of Molecular Pretreated Tumor Profiles as Predictive Biomarkers of Therapeutic Response and Survival Outcomes after Neoadjuvant Therapy for Rectal Cancer in Moroccan Population
- Cytogenetic and FISH analysis of 93 multiple myeloma Moroccan patients
- Associations between nutritional factors and KRAS mutations in colorectal cancer: a systematic review
- 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
- Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age
- Implication of Microsatellite Instability Pathway in Outcome of Colon Cancer in Moroccan Population
- Gut microbiome of Moroccan colorectal cancer patients
- Williams–Beuren syndrome in diverse populations
- GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot
- The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational Prevalence
- Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation
- Cover Image, Volume 176A, Number 5, May 2018
- Noonan syndrome in diverse populations
- 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
- Novel NKX2-5 germline mutation in a Moroccan child with transitional atrio-ventricular septal defect (tAVSD)
- The detection of a novel insertion mutation in exon 2 of the MEFV gene associated with familial mediterranean fever in a moroccan family
- Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations
- Cover Image, Volume 173A, Number 9, September 2017
- Noonan syndrome-causing genes
- Genetics and genomic medicine in Morocco: the present hope can make the future bright
- Syndrome de Lynch: à propos d’un cas et revue de la litterature
- Epigenetics could explain some Moroccan population colorectal cancers peculiarities: microsatellite instability pathway exploration
- TPMT alleles in the Moroccans
- L’exploration moléculaire du gène NKX2.5 dans deux populations atteintes de communication inter-auriculaire (CIA) et de tétralogie de Fallot (TOF)
- Caractérisation épidémiologique de la communication interventriculaire (CIV) dans la population marocaine
- Agénésie bilatérale des vésicules séminales et des canaux déférents
- [Etiologic profile of severe and profound sensorineural hearing loss in children in the region of north-central Morocco].
- Pharmacogenetics and prediction of side effects of drugs
- Improving medical research in the Arab world
- Pharmacogénétique qu’en est-il au Maroc?
- Marqueurs chromosomiques: à propos d'un cas
- The first mutations in the MYH gene reported in Moroccan colon cancer patients
- [Microdeletion syndromes (Williams syndrome and deletion syndrome 22q11) at CHU Hassan II of Fez: report of 3 observations].
- [The Cri du Chat syndrome: report of an observation].
- Consanguinité et prédisposition aux néphropathies dans la population marocaine (à propos de 265 cas)
- Prévalence de la mutation 35delG dans les surdités génétiques autosomiques récessives non syndromiques au Maroc
- Genetic testing and first presymptomatic diagnosis in Moroccan families at high risk for breast/ovarian cancer
- Multiple synostosis syndrome
- Maladie des synostoses multiples
- Gonadal Dysgenesis 46, XX Associated with Mayer‐Rokitansky‐Kuster‐Hauser Syndrome: One Case Report
- Microdélétion 22q11.2 révélée par une hypocalcémie néonatale avec une dysmorphie faciale mineure
- Unexpected fertility and paternal UPD 22
- Omenn Syndrome with Mutation in RAG1 Gene
- Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus
- La mutation 35delG du gène de la connexine 26, une cause fréquente des surdités non syndromiques autosomiques récessives au Maroc
- Tetrasomy 15q11-q13 Diagnosed by FISH in a Patient with Autistic Disorder
Revues de publication
- Cureus × 6
- Molecular Biology Reports × 5
- American Journal of Medical Genetics Part A × 5
- Neurogenetics × 4
- Pan African Medical Journal × 4
- Egyptian Journal of Medical Human Genetics × 3
Publications par année
- 202615
- 20259
- 20247
- 20235
- 20227
- 20215
- 20206
- 20191
- 20186
- 20176
Collaborations
Établissements partenaires : Institut National d'Hygiène du Maroc · Université Mohammed VI des Sciences et de la Santé · Mohammed V University · Institut Pasteur du Maroc · National Institutes of Health
Pays des co-auteurs : États-Unis
Co-auteurs
- Laila Bouguenouch
- Ihssane El Bouchikhi
- Khadija Belhassan
- Imane Samri
- Fatima Zohra Moufid
- Amal Ouskri
- Mohamed Ahakoud
- Samir Atmani
- Sana Chaouki
- Mohammed Iraqui Houssaïni
- Abdelhamid Bouramtane
- Badreddine Elmakhzen
Données bibliographiques issues d’OpenAlex (base ouverte).
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