M. Gribaa

I. Touitou, M. Gribaa, C. Rittore, 2011, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Distinguishing the four genetic causes of jouberts syndrome–related disorders

E. Bertini, M. Koenig, H. Kayserili, 2005, Annals of neurology.

Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotonia.

M. Gribaa, A. Saâd, D. Sanlaville, 2012, European journal of medical genetics.

Cytogenetic analysis in 139 Tunisian patients with de novo acute myeloid leukemia.

M. Gribaa, A. Saâd, Haifa Hichri, 2002, Annales de genetique.

Cytogenetic survey of 117 Tunisian patients with de novo myelodysplastic syndrome.

M. Gribaa, A. Saâd, Haifa Hichri, 2002, Annales de genetique.

Clinical and Genetic Heterogeneity of Familial Early-Onset Diabetes: Case of Six Tunisian Patients Suspected of Maturity-Onset Diabetes of the Young 12

M. Gribaa, A. Saâd, A. Hai, 2020 .

Challenges for Molecular Diagnosis of Familial Early-Onset Diabetes in Unexplored Populations

M. Gribaa, A. Saâd, A. Amara, 2014, Iranian journal of public health.

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms.

M. Gribaa, A. Saâd, E. Clauser, 2012, Gene.

Clinical, biological, radiological, and genetic study of LPAC syndrome in Tunisian patients.

M. Gribaa, Y. Halleb, R. Ghrissi, 2022, Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology.

Hypomagnesemia with Secondary Hypocalcemia Linked to a Novel TRPM6 Gene Mutation

M. Gribaa, B. Dworniczak, A. Marzouk, 2016 .

The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patients

M. Gribaa, S. Laradi, S. Ferchichi, 2019, BMC Medical Genetics.

Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer

M. Gribaa, G. Plotz, S. Zeuzem, 2022, PLoS ONE.

Molecular characterization of piebaldism in a Tunisian family.

M. Gribaa, S. Boubaker, H. Besbès, 2015, Pathologie-biologie.

Y chromosome microdeletions in azoospermic and oligozoospermic Tunisian men

M. Gribaa, A. Saâd, G. Saad, 2018, Middle East Fertility Society Journal.

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

T. Yuen, M. Gribaa, S. Haider, 2017, Proceedings of the National Academy of Sciences.

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency in a Tunisian family

M. Gribaa, G. Saad, A. Maaroufi, 2020, The Pan African medical journal.

Identification and functional consequences of a novel MRE11 mutation affecting 10 Saudi Arabian patients with the ataxia telangiectasia-like disorder.

M. Koenig, M. Gribaa, M. Fernet, 2005, Human molecular genetics.

Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population

M. Gribaa, A. Saâd, J. Bouguila, 2015, Hemoglobin.

Progressive pseudorheumatoid dysplasia in North and West Africa: Clinical description in ten patients with mutations of WISP3

E. Chouery, A. Mégarbané, G. Lefranc, 2017 .

A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23.

N. Drouot, M. Koenig, M. Gribaa, 2007, Brain : a journal of neurology.

Placental mesenchymal dysplasia with beckwith-wiedemann syndrome fetus in the context of biparental and androgenic cell lines.

M. Gribaa, A. Saâd, H. Elghezal, 2008, Placenta.

The usefulness of p57(KIP2) immunohistochemical staining and genotyping test in the diagnosis of the hydatidiform mole.

M. Gribaa, S. Brahem, M. Yacoubi, 2011, Pathology, research and practice.

Assessment of the role of histopathology and DNA image analysis in the diagnosis of molar and non-molar abortion: a study of 89 cases in the center of Tunisia.

M. Gribaa, M. Mokni, Moez Gribaa, 2009, Pathology, research and practice.

Cryptic Rearrangements in Idiopathic Intellectual Disability Diagnosed by Molecular Cytogenetic Analysis

M. Gribaa, A. Saâd, L. B. Jemaa, 2012 .

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma

G. Barton, M. Akiyama, H. Shimizu, 2012, Nature Genetics.

Sanjad-Sakati syndrome in a Tunisian child.

M. Gribaa, N. Ghedira, K. Monastiri, 2015, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Frequency of HNF4A-P.I463V Variant in the Tunisian North-African Population and Its Relation with Diabetes Mellitus

M. Gribaa, A. Saâd, I. Ben Charfeddine, 2015, Iranian journal of public health.

A c.3216_3217delGA mutation in AGL gene in Tunisian patients with a glycogen storage disease type III: evidence of a founder effect

M. Gribaa, A. Saâd, J. Bouguila, 2012, Clinical genetics.

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III

Ali Saad, G. Comi, M. Gribaa, 2011, Journal of Human Genetics.

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development

M. Gribaa, K. McElreavey, A. Saâd, 2023, Reproductive Biology and Endocrinology.

Homozygosity mapping of a third Joubert syndrome locus to 6q23

M. Koenig, M. Gribaa, E. Boltshauser, 2004, Journal of Medical Genetics.

Cytogenetic and molecular aspects of absolute teratozoospermia: comparison between polymorphic and monomorphic forms.

M. Gribaa, A. Saâd, Abdelbacet Amara, 2011, Urology.

Multiple Self-Healing Palmoplantar Carcinoma: A Familial Predisposition to Skin Cancer with Primary Palmoplantar and Conjunctival Lesions

B. Merriman, G. Stevanin, M. Gribaa, 2014, The Journal of investigative dermatology.

Homozygosity mapping of Marinesco–Sjögren syndrome to 5q31

M. Koenig, M. Gribaa, H. Dollfus, 2003, European Journal of Human Genetics.

Screening of Angelman Syndrome deletion and methylation aberration using MS-MLPA assay in a Tunisian population

M. Gribaa, A. Saâd, I. Turki, 2019, Biomedical Research and Clinical Practice.

[Clinical and genetic characteristics of Buschke-Fischer-Brauer's disease in a Tunisian family].

M. Gribaa, A. Saâd, L. Adala, 2010, Annales de dermatologie et de vénéréologie.

Corrigendum to “Reduction of palmoplantar keratoderma Buschke–Fischer–Brauer locus to only 0.967 Mb” [J. Dermatol. Sci. 67(September (3)) (2012) 210–212]

M. Gribaa, A. Saâd, B. Sriha, 2012 .

Reduction of palmoplantar keratoderma Buschke-Fischer-Brauer locus to only 0.967 Mb.

M. Gribaa, A. Saâd, B. Sriha, 2012, Journal of dermatological science.

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.

M. Gribaa, T. B. Lazreg, A. Saâd, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Targeted next generation sequencing screening of Lynch syndrome in Tunisian population

H. Morreau, T. van Wezel, M. Gribaa, 2019, Familial Cancer.

Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population

M. Gribaa, A. Saâd, I. Ben Charfeddine, 2015, Journal of Assisted Reproduction and Genetics.

Familial early-onset diabetes is not a typical MODY in several Tunisian patients.

P. Froguel, M. Vaxillaire, M. Gribaa, 2012, La Tunisie medicale.

Prostatic tissue in 46XX congenital adrenal hyperplasia: Case report and literature review

M. Gribaa, G. Saad, A. Maaroufi, 2021, Clinical case reports.

Targeted next generation sequencing screening of Lynch syndrome in Tunisian population

H. Morreau, T. van Wezel, M. Gribaa, 2019, Familial Cancer.

Modulation at Age of Onset in Tunisian Huntington Disease Patients: Implication of New Modifier Genes

M. Gribaa, A. Saâd, Marwa Chourabi, 2014, Genetics research international.

Association of the OPRM1 and COMT genes' polymorphisms with the efficacy of morphine in Tunisian cancer patients: Impact of the high genetic heterogeneity in Tunisia?

M. Gribaa, A. Saâd, J. Woillard, 2016, Therapie.