Home › Researcher directory › Karim Ouldim
Karim Ouldim
Affiliation : Centre Hospitalier Universitaire Hassan II · Sidi Mohamed Ben Abdellah University
- 95Publications (affiliation in Morocco)
- 111Total publications
- 1072Citations
- 17h-index
Research profile
Karim Ouldim has 95 indexed publications (2007–2026). Their work appears mainly in “Cureus”, “Molecular Biology Reports” and “American Journal of Medical Genetics Part A”. Their most cited article, “Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus” (2007), has been cited 100 times. 31 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in United States.
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Create my free profile Add my publicationsResearch areas
- 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
Publication venues
- 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 per year
- 202615
- 20259
- 20247
- 20235
- 20227
- 20215
- 20206
- 20191
- 20186
- 20176
Collaborations
Partner institutions : 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
Co-authors’ countries : United States
Co-authors
- 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
Bibliographic data from OpenAlex (open database).
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