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Homozygous deletion of exons 2–7 within TGFB3 gene in a child with severe Loeys‐Dietz syndrome and Marfan‐like features

American journal of medical genetics. Part A, 2020-05, Vol.182 (5), p.1230-1235

2020

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Developmental delay, intellectual disability, short stature, subglottic stenosis, hearing impairment, onychodysplasia of the index fingers, and distinctive facial features: A newly reported autosomal recessive syndrome

American journal of medical genetics. Part A, 2020-08, Vol.182 (8), p.1865-1872

2020

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Antiproliferative and Proapoptotic Effects of Topotecan in Combination With Thymoquinone on Acute Myelogenous Leukemia

Clinical lymphoma, myeloma and leukemia, 2014-09, Vol.14, p.S46-S55

2014

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Follicle-stimulating hormone regulates expression and activity of epidermal growth factor receptor in the murine ovarian follicle

Proceedings of the National Academy of Sciences - PNAS, 2014-11, Vol.111 (47), p.16778-16783

2014

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A Report on a Family with TMTC3-Related Syndrome and Review

Case reports in medicine, 2020-11, Vol.2020 (2020), p.1-6

2020

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Epidermal growth factor receptor signaling uncouples germ cells from the somatic follicular compartment at ovulation

Nature communications, 2021-03, Vol.12 (1), p.1438-1438, Article 1438

2021

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Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases

Molecular genetics & genomic medicine, 2018-11, Vol.6 (6), p.1041-1052

2018

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Active Fluctuations of the Nuclear Envelope Shape the Transcriptional Dynamics in Oocytes

Developmental cell, 2019-10, Vol.51 (2), p.145-157.e10

2019

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Control of Oocyte Growth and Development by Intercellular Communication Within the Follicular Niche

Molecular Mechanisms of Cell Differentiation in Gonad Development, 2016-01, Vol.58, p.191-224

2016

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Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database

Frontiers in genetics, 2023-05, Vol.14, p.1177204-1177204

2023

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Follicle-Stimulating Hormone Increases Gap Junctional Communication Between Somatic and Germ-Line Follicular Compartments During Murine Oogenesis1

Biology of reproduction, 2015-08, Vol.93 (2)

2015

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A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort

Journal of neuromuscular diseases, 2022-01, Vol.9 (1), p.193-210

2022

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Mammalian Oocytes Locally Remodel Follicular Architecture to Provide the Foundation for Germline-Soma Communication

Current biology, 2018-04, Vol.28 (7), p.1124-1131.e3

2018

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Follicle-Stimulating Hormone Increases Gap Junctional Communication Between Somatic and Germ-Line Follicular Compartments During Murine Oogenesis

Biology of reproduction, 2015-08, Vol.93 (2), p.47-47

2015

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MAMMALIAN OOCYTES LOCALLY REMODEL FOLLICULAR ARCHITECTURE TO PROVIDE THE FOUNDATION FOR GERM LINE-SOMA COMMUNICATION

Current biology, 2018-03, Vol.28 (7), p.1124-1131.e3

2018

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SIX6-related anophthalmia/microphthalmia: second report on a deletion in a consanguineous family

Ophthalmic genetics, 2021-01, Vol.42 (1), p.88-91

2021

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Growth In Vitro of Granulosa Cell-Oocyte Complexes of the Mouse

Methods in molecular biology (Clifton, N.J.), 2018, Vol.1818, p.1

2018

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Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders

Genes, 2021-09, Vol.12 (10), p.1518

2021

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Recessive marfanoid syndrome with herniation associated with a homozygous mutation in Fibulin-3

European journal of medical genetics, 2020-05, Vol.63 (5), p.103869-103869, Article 103869

2020

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Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes

Journal of pediatric hematology/oncology, 2021-07, Vol.43 (5), p.e727-e735

2021

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SOX11-related syndrome: report on a new case and review

Clinical dysmorphology, 2021-01, Vol.30 (1), p.44-49

2021

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A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22)

European journal of medical genetics, 2019-11, Vol.62 (11), p.103576-103576, Article 103576

2019

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Kefir exhibits anti‐proliferative and pro‐apoptotic effects on colon adenocarcinoma cells with no significant effects on cell migration and invasion (647.24)

The FASEB journal, 2014-04, Vol.28 (S1), p.n/a

2014

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The Lebanese Allele in the PET100 Gene: Report on Two New Families with Cytochrome c Oxidase Deficiency

Journal of pediatric genetics (Birmingham, Ala.), 2019-09, Vol.8 (3), p.172-178

2019

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Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome

Molecular syndromology, 2021-10, Vol.12 (6), p.342-350

2021

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Homozygous deletion of exons 2–7 within TGFB3 gene in a child with severe Loeys‐Dietz syndrome and Marfan‐like features

Developmental delay, intellectual disability, short stature, subglottic stenosis, hearing impairment, onychodysplasia of the index fingers, and distinctive facial features: A newly reported autosomal recessive syndrome

Antiproliferative and Proapoptotic Effects of Topotecan in Combination With Thymoquinone on Acute Myelogenous Leukemia

Follicle-stimulating hormone regulates expression and activity of epidermal growth factor receptor in the murine ovarian follicle

A Report on a Family with TMTC3-Related Syndrome and Review

Epidermal growth factor receptor signaling uncouples germ cells from the somatic follicular compartment at ovulation

Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases

Active Fluctuations of the Nuclear Envelope Shape the Transcriptional Dynamics in Oocytes

Control of Oocyte Growth and Development by Intercellular Communication Within the Follicular Niche

Spectrum of genetic disorders and gene variants in the United Arab Emirates national population: insights from the CTGA database

Follicle-Stimulating Hormone Increases Gap Junctional Communication Between Somatic and Germ-Line Follicular Compartments During Murine Oogenesis1

A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort

Mammalian Oocytes Locally Remodel Follicular Architecture to Provide the Foundation for Germline-Soma Communication

Follicle-Stimulating Hormone Increases Gap Junctional Communication Between Somatic and Germ-Line Follicular Compartments During Murine Oogenesis

MAMMALIAN OOCYTES LOCALLY REMODEL FOLLICULAR ARCHITECTURE TO PROVIDE THE FOUNDATION FOR GERM LINE-SOMA COMMUNICATION

SIX6-related anophthalmia/microphthalmia: second report on a deletion in a consanguineous family

Growth In Vitro of Granulosa Cell-Oocyte Complexes of the Mouse

Catalogue for Transmission Genetics in Arabs (CTGA) Database: Analysing Lebanese Data on Genetic Disorders

Recessive marfanoid syndrome with herniation associated with a homozygous mutation in Fibulin-3

Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes

SOX11-related syndrome: report on a new case and review

A novel PDE6D mutation in a patient with Joubert syndrome type 22 (JBTS22)

Kefir exhibits anti‐proliferative and pro‐apoptotic effects on colon adenocarcinoma cells with no significant effects on cell migration and invasion (647.24)

The Lebanese Allele in the PET100 Gene: Report on Two New Families with Cytochrome c Oxidase Deficiency

Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome

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