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Resistance trends and risk factors of extended spectrum β-lactamases in Escherichia coli infections in Aleppo, Syria

American journal of infection control, 2013-07, Vol.41 (7), p.597-600

2013

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Prevalence of antibiotic resistance among Acinetobacter baumannii isolates from Aleppo, Syria

American journal of infection control, 2012-10, Vol.40 (8), p.776-777

2012

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Identification of a novel CTCF mutation responsible for syndromic intellectual disability - a case report

BMC medical genetics, 2017-06, Vol.18 (1), p.68-68, Article 68

2017

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Characterization of an Emirati TMEM138 mutation leading to Joubert syndrome

Pediatrics international, 2017-01, Vol.59 (1), p.113-114

2017

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A Novel Variant in the Endothelin-Converting Enzyme-Like 1 (ECEL1) Gene in an Emirati Child

Medical principles and practice, 2017, Vol.26 (2), p.195-198

2017

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Association of Myoinositol Transporters with Schizophrenia and Bipolar Disorder: Evidence from Human and Animal Studies

Complex psychiatry, 2019-10, Vol.5 (4), p.200-211

2019

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Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa

Oman journal of ophthalmology, 2017-09, Vol.10 (3), p.228-231

2017

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Novel splice-site mutation in WDR62 revealed by whole-exome sequencing in a Sudanese family with primary microcephaly

Congenital anomalies, 2016-05, Vol.56 (3), p.135-137

2016

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Catechol-O-methyltransferase Val 108/158 Met polymorphism and breast cancer risk: a case control study in Syria

Breast cancer (Tokyo, Japan), 2013, Vol.20 (1), p.62-66

2013

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Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing

Methods in molecular biology (Clifton, N.J.), 2021-01, Vol.2243, p.1

2021

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L-plastin associated syndrome of immune deficiency and hematologic cytopenia

Journal of allergy and clinical immunology, 2024-09, Vol.154 (3), p.767-777

2024

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Expanded PCH1D phenotype linked to EXOSC9 mutation

European journal of medical genetics, 2020-01, Vol.63 (1), p.103622-103622, Article 103622

2020

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Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis

Metabolic brain disease, 2016-10, Vol.31 (5), p.1189-1192

2016

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Melanin Concentrating Hormone Signaling Deficits in Schizophrenia: Association With Memory and Social Impairments and Abnormal Sensorimotor Gating

The international journal of neuropsychopharmacology, 2020-03, Vol.23 (1), p.53-65

2020

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Single‐center experience of N‐linked Congenital Disorders of Glycosylation with a Summary of Molecularly Characterized Cases in Arabs

Annals of human genetics, 2018-01, Vol.82 (1), p.35-47

2018

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Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1

Science immunology, 2020-07, Vol.5 (49)

2020

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Identification of a novel homozygous UNC80 variant in a child with infantile hypotonia with psychomotor retardation and characteristic facies-2 (IHPRF2)

Metabolic brain disease, 2018-06, Vol.33 (3), p.869-873

2018

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A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis–lymphedema–telangiectasia syndrome by Whole Exome Sequencing

Molecular and cellular probes, 2016-02, Vol.30 (1), p.18-21

2016

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Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates

Hormone research in paediatrics, 2017-01, Vol.87 (1), p.64-68

2017

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Meta‐analyses of the association of HLA‐DRB1 alleles with rheumatoid arthritis among Arabs

International journal of rheumatic diseases, 2017-07, Vol.20 (7), p.832-838

2017

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Characterization of an Emirati TMEM 138 mutation leading to Joubert syndrome

Pediatrics international, 2017-01, Vol.59 (1), p.113-114

2017

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Erratum to: Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis

Metabolic brain disease, 2016-10, Vol.31 (5), p.1193-1193

2016

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Summary of mutations underlying autosomal recessive congenital ichthyoses (ARCI) in Arabs with four novel mutations in ARCI‐related genes from the United Arab Emirates

International journal of dermatology, 2017-05, Vol.56 (5), p.514-523

2017

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Resistance trends and risk factors of extended spectrum [Beta]-lactamases in Escherichia coli infections in Aleppo, Syria

American journal of infection control, 2013-07, Vol.41 (7), p.597

2013

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Multidrug resistance in Pseudomonas aeruginosa isolated from nosocomial respiratory and urinary infections in Aleppo, Syria

Journal of infection in developing countries, 2015-02, Vol.9 (2), p.210-213

2015

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Resistance trends and risk factors of extended spectrum β-lactamases in Escherichia coli infections in Aleppo, Syria

Prevalence of antibiotic resistance among Acinetobacter baumannii isolates from Aleppo, Syria

Identification of a novel CTCF mutation responsible for syndromic intellectual disability - a case report

Characterization of an Emirati TMEM138 mutation leading to Joubert syndrome

A Novel Variant in the Endothelin-Converting Enzyme-Like 1 (ECEL1) Gene in an Emirati Child

Association of Myoinositol Transporters with Schizophrenia and Bipolar Disorder: Evidence from Human and Animal Studies

Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa

Novel splice-site mutation in WDR62 revealed by whole-exome sequencing in a Sudanese family with primary microcephaly

Catechol-O-methyltransferase Val 108/158 Met polymorphism and breast cancer risk: a case control study in Syria

Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing

L-plastin associated syndrome of immune deficiency and hematologic cytopenia

Expanded PCH1D phenotype linked to EXOSC9 mutation

Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis

Melanin Concentrating Hormone Signaling Deficits in Schizophrenia: Association With Memory and Social Impairments and Abnormal Sensorimotor Gating

Single‐center experience of N‐linked Congenital Disorders of Glycosylation with a Summary of Molecularly Characterized Cases in Arabs

Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1

Identification of a novel homozygous UNC80 variant in a child with infantile hypotonia with psychomotor retardation and characteristic facies-2 (IHPRF2)

A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis–lymphedema–telangiectasia syndrome by Whole Exome Sequencing

Identification of a Novel Homozygous INSR Variant in a Patient with Rabson-Mendenhall Syndrome from the United Arab Emirates

Meta‐analyses of the association of HLA‐DRB1 alleles with rheumatoid arthritis among Arabs

Characterization of an Emirati TMEM 138 mutation leading to Joubert syndrome

Erratum to: Novel ECHS1 mutation in an Emirati neonate with severe metabolic acidosis

Summary of mutations underlying autosomal recessive congenital ichthyoses (ARCI) in Arabs with four novel mutations in ARCI‐related genes from the United Arab Emirates

Resistance trends and risk factors of extended spectrum [Beta]-lactamases in Escherichia coli infections in Aleppo, Syria

Multidrug resistance in Pseudomonas aeruginosa isolated from nosocomial respiratory and urinary infections in Aleppo, Syria

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