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Genomic analysis of inherited hearing loss in the Palestinian population

Proceedings of the National Academy of Sciences - PNAS, 2020-08, Vol.117 (33), p.20070-20076

2020

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Using multi-scale genomics to associate poorly annotated genes with rare diseases

Genome medicine, 2024-01, Vol.16 (1), p.4-22, Article 4

2024

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Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection

Neurology, 2016-05, Vol.86 (21), p.2016

2016

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Sex-dependent neuronal effects of α-synuclein reveal that GABAergic transmission is neuroprotective of sleep-controlling neurons

Cell & bioscience, 2023-09, Vol.13 (1), p.1-16, Article 172

2023

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The Diagnostic Potential of JWST in Characterizing Elusive AGNs

The Astrophysical journal, 2021-01, Vol.906 (1), p.35

2021

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The noncoding genome and hearing loss

Human genetics, 2022-04, Vol.141 (3-4), p.323-333

2022

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Sex-dependent effects of monomeric α-synuclein on calcium and cell death of lateral hypothalamic mouse neurons are altered by orexin

Molecular and cellular neuroscience, 2024-06, Vol.129, p.103934, Article 103934

2024

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Inclusion of hemimegalencephaly into the phenotypic spectrum of NPRL3 pathogenic variants in familial focal epilepsy with variable foci

Epilepsia (Copenhagen), 2019-06, Vol.60 (6), p.e67-e73

2019

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Relics of Supermassive Black Hole Seeds: The Discovery of an Accreting Black Hole in an Optically Normal, Low Metallicity Dwarf Galaxy

Astrophysical journal. Letters, 2021-05, Vol.912 (1), p.L2

2021

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Improving search ranking of geospatial data based on deep learning using user behavior data

Computers & geosciences, 2020-09, Vol.142, p.104520, Article 104520

2020

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The combination of whole‐exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies

Acta ophthalmologica (Oxford, England), 2019-09, Vol.97 (6), p.e877-e886

2019

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Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53

International journal of cancer, 2017-08, Vol.141 (4), p.750-756

2017

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Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

Journal of medical genetics, 2015-09, Vol.52 (9), p.636-641

2015

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Inclusion of hemimegalencephaly into the phenotypic spectrum of NPRL 3 pathogenic variants in familial focal epilepsy with variable foci

Epilepsia (Copenhagen), 2019-06, Vol.60 (6)

2019

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Sex-dependent neuronal effects of [alpha]-synuclein reveal that GABAergic transmission is neuroprotective of sleep-controlling neurons

Cell & bioscience, 2023-09, Vol.13 (1)

2023

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Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families

European journal of human genetics : EJHG, 2016-10, Vol.24 (10), p.1430-1435

2016

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Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities

Cold Spring Harbor molecular case studies, 2020-10, Vol.6 (5), p.a005652

2020

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Nurturing compassion in schools: A randomized controlled trial of the effectiveness of a Compassionate Mind Training program for teachers

PloS one, 2022-03, Vol.17 (3), p.e0263480

2022

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Feasibility of a new multifactorial fall prevention assessment and personalized intervention among older people recently discharged from the emergency department

PloS one, 2022-06, Vol.17 (6), p.e0268682-e0268682

2022

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Dupilumab in children aged 6 months to younger than 6 years with uncontrolled atopic dermatitis: a randomised, double-blind, placebo-controlled, phase 3 trial

The Lancet (British edition), 2022-09, Vol.400 (10356), p.908-919

2022

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Long-distance dispersal patterns in the Cerulean Warbler: a case study from Indiana

Avian conservation and ecology, 2023-05, Vol.18 (1), p.19, Article art19

2023

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Psychosocial characteristics are associated with adherence to dietary, drugs and physical activity recommendations amongst cardiovascular disease patients in Lebanon

PloS one, 2023-10, Vol.18 (10), p.e0287844-e0287844

2023

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Identification of a Novel Pseudo‐Natural Product Type IV IDO1 Inhibitor Chemotype

Angewandte Chemie (International ed.), 2022-10, Vol.61 (40), p.e202209374-n/a

International ed. in English, 2022

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Genomic analysis of inherited hearing loss in the Palestinian population

Using multi-scale genomics to associate poorly annotated genes with rare diseases

Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection

Sex-dependent neuronal effects of α-synuclein reveal that GABAergic transmission is neuroprotective of sleep-controlling neurons

The Diagnostic Potential of JWST in Characterizing Elusive AGNs

The noncoding genome and hearing loss

Sex-dependent effects of monomeric α-synuclein on calcium and cell death of lateral hypothalamic mouse neurons are altered by orexin

Inclusion of hemimegalencephaly into the phenotypic spectrum of NPRL3 pathogenic variants in familial focal epilepsy with variable foci

Relics of Supermassive Black Hole Seeds: The Discovery of an Accreting Black Hole in an Optically Normal, Low Metallicity Dwarf Galaxy

Improving search ranking of geospatial data based on deep learning using user behavior data

The combination of whole‐exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies

Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53

Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

Inclusion of hemimegalencephaly into the phenotypic spectrum of NPRL 3 pathogenic variants in familial focal epilepsy with variable foci

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

Sex-dependent neuronal effects of [alpha]-synuclein reveal that GABAergic transmission is neuroprotective of sleep-controlling neurons

Mutation of KREMEN1, a modulator of Wnt signaling, is responsible for ectodermal dysplasia including oligodontia in Palestinian families

Helicase-inactivating BRIP1 mutation yields Fanconi anemia with microcephaly and other congenital abnormalities

Nurturing compassion in schools: A randomized controlled trial of the effectiveness of a Compassionate Mind Training program for teachers

Feasibility of a new multifactorial fall prevention assessment and personalized intervention among older people recently discharged from the emergency department

Dupilumab in children aged 6 months to younger than 6 years with uncontrolled atopic dermatitis: a randomised, double-blind, placebo-controlled, phase 3 trial

Effect of photobiomodulation combined with physical therapy on functional performance in children with myelomeningocele: A protocol randomized clinical blind study

Long-distance dispersal patterns in the Cerulean Warbler: a case study from Indiana

Psychosocial characteristics are associated with adherence to dietary, drugs and physical activity recommendations amongst cardiovascular disease patients in Lebanon

Identification of a Novel Pseudo‐Natural Product Type IV IDO1 Inhibitor Chemotype

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