Amalou G - Search Results

1

Missense variants weakening a SOX9 phosphodegron linked to odontogenesis defects, scoliosis and other skeletal features.

Ettaki I, Haseeb A, Karvande A, Amalou G, Saih A, AitRaise I, Hamdi S, Wakrim L, Barakat A, Fellah H, El Alloussi M, Lefebvre V. Ettaki I, et al. Among authors: amalou g. HGG Adv. 2025 Jan 9:100404. doi: 10.1016/j.xhgg.2025.100404. Online ahead of print. HGG Adv. 2025. PMID: 39797402 Free article.

2

Molecular Profile of BCR-ABL1 Negative Myeloproliferative Neoplasm in a Moroccan Population.

Soro SGC, Amalou G, Benchikh S, El Hamouchi A, Charoute H, Oukheda M, Abdelouaheb BB, Saile R, Lebrazi H, Nassereddine S. Soro SGC, et al. Among authors: amalou g. Asian Pac J Cancer Prev. 2024 Nov 1;25(11):4013-4025. doi: 10.31557/APJCP.2024.25.11.4013. Asian Pac J Cancer Prev. 2024. PMID: 39611926 Free article.

3

First report of an Ivorian family with nonsyndromic hearing loss caused by GJB2 compound heterozygous variants.

Toure M, Amalou G, Raise IA, Mobio NMA, Malki A, Barakat A. Toure M, et al. Among authors: amalou g. Ann Hum Genet. 2024 Aug 2. doi: 10.1111/ahg.12574. Online ahead of print. Ann Hum Genet. 2024. PMID: 39092543

4

Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.

Idyahia A, Redouan S, Amalou G, Charoute H, Harmak H, Bonnet C, Petit C, Benrahma H, Barakat A. Idyahia A, et al. Among authors: amalou g. Mol Biol Rep. 2024 Jul 25;51(1):850. doi: 10.1007/s11033-024-09740-x. Mol Biol Rep. 2024. PMID: 39052101

5

Novel pathogenic WHRN variant causing hearing loss in a moroccan family.

AitRaise I, Amalou G, Redouane S, Charoute H, Snoussi K, Abdelghaffar H, Bonnet C, Petit C, Barakat A. AitRaise I, et al. Among authors: amalou g. Mol Biol Rep. 2023 Dec;50(12):10663-10669. doi: 10.1007/s11033-023-08901-8. Epub 2023 Nov 4. Mol Biol Rep. 2023. PMID: 37924449

6

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.

AitRaise I, Amalou G, Bakhchane A, Bousfiha A, Abdelghaffar H, Majida C, Bonnet C, Petit C, Barakat A. AitRaise I, et al. Among authors: amalou g. Biochem Genet. 2024 Jun;62(3):1914-1924. doi: 10.1007/s10528-023-10515-5. Epub 2023 Oct 1. Biochem Genet. 2024. PMID: 37777971

7

A case report of two Moroccan patients with hereditary neurological disorders and molecular modeling study on the S72L de novo PMP22 variant.

Ait El Cadi C, Dafrallah L, Amalou G, Charif M, Charoute H, Araqi-Houssaini A, Lakhiari H, Lenaers G, Barakat A. Ait El Cadi C, et al. Among authors: amalou g. Rev Neurol (Paris). 2023 Oct;179(8):902-909. doi: 10.1016/j.neurol.2023.01.728. Epub 2023 Jun 7. Rev Neurol (Paris). 2023. PMID: 37296061

8

First characterization of LTBP3 variants in two Moroccan families with hypoplastic amelogenesis imperfecta.

Nouara F, Amalou G, Bouzidi A, Charif M, Charoute H, Lenaers G, El Arabi S, Bousfiha B, Barakat A. Nouara F, et al. Among authors: amalou g. Arch Oral Biol. 2022 Oct;142:105518. doi: 10.1016/j.archoralbio.2022.105518. Epub 2022 Aug 6. Arch Oral Biol. 2022. PMID: 35998423

9

Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies.

Bouzidi A, Charoute H, Charif M, Amalou G, Kandil M, Barakat A, Lenaers G. Bouzidi A, et al. Among authors: amalou g. Orphanet J Rare Dis. 2022 May 12;17(1):197. doi: 10.1186/s13023-022-02340-7. Orphanet J Rare Dis. 2022. PMID: 35551639 Free PMC article. Review.

10

A homozygous nonsense HECW2 variant is associated with neurodevelopmental delay and intellectual disability.

Krami AM, Bouzidi A, Charif M, Amalou G, Charoute H, Rouba H, Roky R, Lenaers G, Barakat A, Nahili H. Krami AM, et al. Among authors: amalou g. Eur J Med Genet. 2022 Jun;65(6):104515. doi: 10.1016/j.ejmg.2022.104515. Epub 2022 Apr 27. Eur J Med Genet. 2022. PMID: 35487419

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