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Exploring hTERT promoter methylation in cutaneous T‐cell lymphomas

Molecular oncology, 2022-05, Vol.16 (9), p.1931-1946

2022

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CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population

Annals of human genetics, 2022-03, Vol.86 (2), p.80-86

2022

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A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

European journal of human genetics : EJHG, 2021-06, Vol.29 (6), p.988-997

2021

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BRCA mutations in a cohort of Iraqi patients presenting to a tertiary referral center

BMC medical genetics, 2019-09, Vol.20 (1), p.154-154, Article 154

2019

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Targeting Epigenetic Modifiers Can Reduce the Clonogenic Capacities of Sézary Cells

Frontiers in oncology, 2021-10, Vol.11, p.775253-775253

2021

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Telomeric Repeat-Containing RNA (TERRA): A Review of the Literature and First Assessment in Cutaneous T-Cell Lymphomas

Genes, 2022-03, Vol.13 (3), p.539

2022

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Analysis of ASS1 gene in ten unrelated middle eastern families with citrullinemia type 1 identifies rare and novel variants

Molecular genetics & genomic medicine, 2023-02, Vol.11 (2), p.e2058-n/a

2023

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An unusual case of chronic lymphocytic leukemia with trisomy 12 and t(14;18) and a favorable response to ibrutinib

Leukemia research reports, 2021-01, Vol.15, p.100245, Article 100245

2021

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Genomic analysis of Meckel-Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes

European journal of human genetics : EJHG, 2013-07, Vol.21 (7), p.762-768

2013

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Pediatric M5 acute myeloid leukemia with MLL-SEPT6 fusion and a favorable outcome

Leukemia research reports, 2021-01, Vol.16, p.100277, Article 100277

2021

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Novel pleiotropic BRCA2 pathogenic variants in Lebanese families

Cancer genetics, 2019-02, Vol.231-232, p.32-35

2019

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PI4K2A deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy

Annals of clinical and translational neurology, 2022-09, Vol.9 (9), p.1345-1358

2022

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BRCA mutation screening and patterns among high-risk Lebanese subjects

Hereditary cancer in clinical practice, 2019-01, Vol.17 (1), p.4-4, Article 4

2019

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Chloroquine and the potential adverse outcome in undiagnosed G6PD-deficient cases infected with COVID-19

Journal of medical screening, 2021-03, Vol.28 (1), p.54-54

2021

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A novel cystic fibrosis gene mutation c.2490insT in a Palestinian patient: A case report and review of the literature

Annals of thoracic medicine, 2017-10, Vol.12 (4), p.290-293

2017

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A rare case of acute myeloid leukemia with t(12;19)(q13;q13)

Leukemia research reports, 2020-01, Vol.14, p.100216, Article 100216

2020

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Changing frequency of equivocal HER-2/neu scores and factors predictive of negative HER 2/neu fluorescent in situ hybridisation in invasive carcinomas of the breast

Journal of clinical pathology, 2014-03, Vol.67 (3), p.204-209

2014

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De novo exceptional complex chromosomal rearrangement in a healthy fertile male: case report and review of the literature

Fertility and sterility, 2011-11, Vol.96 (5), p.1160-1164

2011

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An investigational ovarian stimulation protocol increased significantly the psychological burden in women with premature ovarian failure

Acta obstetricia et gynecologica Scandinavica, 2012-11, Vol.91 (11), p.1273-1278

2012

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Novel intronic JAG1 variant associated with Alagille syndrome in a three-generation Lebanese family with variable features

Clinical dysmorphology, 2023-04, Vol.32 (2), p.80

2023

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DNMT3B deficiency presenting as severe combined immune deficiency: A case report

Clinical immunology (Orlando, Fla.), 2020-06, Vol.215, p.108453-108453, Article 108453

2020

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Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropenia

Pediatric hematology and oncology, 2019-10, Vol.36 (7), p.432-437

2019

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Novel SCN9A variant associated with congenital insensitivity to pain

Molecular biology reports, 2023-07, Vol.50 (7), p.6293-6298

2023

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Exploring hTERT promoter methylation in cutaneous T‐cell lymphomas

CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population

A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing

BRCA mutations in a cohort of Iraqi patients presenting to a tertiary referral center

Targeting Epigenetic Modifiers Can Reduce the Clonogenic Capacities of Sézary Cells

Telomeric Repeat-Containing RNA (TERRA): A Review of the Literature and First Assessment in Cutaneous T-Cell Lymphomas

Characterization of Apparently Balanced Chromosomal Rearrangements from the Developmental Genome Anatomy Project

Duplication of 10q24 locus: broadening the clinical and radiological spectrum

Analysis of ASS1 gene in ten unrelated middle eastern families with citrullinemia type 1 identifies rare and novel variants

An unusual case of chronic lymphocytic leukemia with trisomy 12 and t(14;18) and a favorable response to ibrutinib

Genomic analysis of Meckel-Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes

Pediatric M5 acute myeloid leukemia with MLL-SEPT6 fusion and a favorable outcome

Novel pleiotropic BRCA2 pathogenic variants in Lebanese families

PI4K2A deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy

BRCA mutation screening and patterns among high-risk Lebanese subjects

Chloroquine and the potential adverse outcome in undiagnosed G6PD-deficient cases infected with COVID-19

A novel cystic fibrosis gene mutation c.2490insT in a Palestinian patient: A case report and review of the literature

A rare case of acute myeloid leukemia with t(12;19)(q13;q13)

Changing frequency of equivocal HER-2/neu scores and factors predictive of negative HER 2/neu fluorescent in situ hybridisation in invasive carcinomas of the breast

De novo exceptional complex chromosomal rearrangement in a healthy fertile male: case report and review of the literature

An investigational ovarian stimulation protocol increased significantly the psychological burden in women with premature ovarian failure

Novel intronic JAG1 variant associated with Alagille syndrome in a three-generation Lebanese family with variable features

DNMT3B deficiency presenting as severe combined immune deficiency: A case report

Acquired centromeric heteromorphism of chromosome 7 yields discordant results between fluorescent in situ hybridization and karyotype analysis in a child with severe congenital neutropenia

Novel SCN9A variant associated with congenital insensitivity to pain

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