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Beta-Thalassemia Intermedia: A Single Thalassemia Center Experience from Northeastern Iraq

BioMed research international, 2020, Vol.2020, p.2807120-11

2020

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Effect of EGLN1 Genetic Polymorphisms on Hemoglobin Concentration in Andean Highlanders

BioMed research international, 2020, Vol.2020, p.3436581-16

2020

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Identification of Differential Gene Expression Pattern in Lens Epithelial Cells Derived from Cataractous and Noncataractous Lenses of Shumiya Cataract Rat

BioMed research international, 2020, Vol.2020, p.7319590-9

2020

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Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations

BioMed research international, 2019-01, Vol.2019, p.3457898-7

2019

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First Record Mutations in the Genes ASPA and ARSA Causing Leukodystrophy in Jordan

BioMed research international, 2019-01, Vol.2019, p.7235914-7

2019

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Bta-miR-124a Affects Lipid Metabolism by Regulating PECR Gene

BioMed research international, 2019, Vol.2019, p.2596914-9

2019

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Identification of Candidate Genes Associated with Charcot-Marie-Tooth Disease by Network and Pathway Analysis

BioMed research international, 2020, Vol.2020, p.1353516-13

2020

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Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate

BioMed research international, 2020, Vol.2020, p.8790531-6

2020

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Targeting N-Terminal Huntingtin with a Dual-sgRNA Strategy by CRISPR/Cas9

BioMed research international, 2019, Vol.2019, p.1039623-10

2019

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Detection of False-Positive Deletions from the Database of Genomic Variants

BioMed research international, 2019-01, Vol.2019, p.8420547-8

2019

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes

PLoS genetics, 2011-11, Vol.7 (11), p.e1002334

2011

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Copy Number Variations in Children with Tourette Syndrome: Systematic Investigation in a Clinical Setting

Genes, 2023-02, Vol.14 (2), p.500

2023

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Trait − driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes

Genes & Genomics, 2023, 45(4), , pp.491-505

2023

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Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis

BioMed research international, 2015-01, Vol.2015, p.426379-9

2015

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Sox11 is required to maintain proper levels of Hedgehog signaling during vertebrate ocular morphogenesis

PLoS genetics, 2014-07, Vol.10 (7), p.e1004491-e1004491

2014

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Discriminatory Weight of SNPs in Spike SARS-CoV-2 Variants: A Technically Rapid, Unambiguous, and Bioinformatically Validated Laboratory Approach

Viruses, 2022-01, Vol.14 (1), p.123

2022

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MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability

Journal of human genetics, 2016-02, Vol.61 (2), p.95-101

2016

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The Correlation-Base-Selection Algorithm for Diagnostic Schizophrenia Based on Blood-Based Gene Expression Signatures

BioMed research international, 2017-01, Vol.2017, p.7860506-7

2017

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Targeted next-generation sequencing identifies the disruption of the SHANK3 and RYR2 genes in a patient carrying a de novo t(1;22)(q43;q13.3) associated with signs of Phelan-McDermid syndrome

Molecular cytogenetics, 2020-06, Vol.13 (1), p.22-8, Article 22

2020

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Guidelines for Optimisation of a Multiplex Oligonucleotide Ligation-PCR for Characterisation of Microbial Pathogens in a Microsphere Suspension Array

BioMed research international, 2015-01, Vol.2015, p.790170-10

2015

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ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data

BioMed research international, 2017-01, Vol.2017, p.9631282-11

2017

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A Novel -72 (T→A) β-Promoter Mutation Causing Slightly Elevated HbA2 in a Vietnamese Heterozygote

BioMed research international, 2017, Vol.2017, p.4537409-4537409

2017

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In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients

BioMed research international, 2015-01, Vol.2015, p.341986-8

2015

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The embryo battle against adverse genomes: Are de novo terminal deletions the rescue of unfavorable zygotic imbalances?

European journal of medical genetics, 2022-08, Vol.65 (8), p.104532-104532, Article 104532

2022

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Antitumoural activity of a cytotoxic peptide of Lactobacillus casei peptidoglycan and its interaction with mitochondrial-bound hexokinase

Anti-cancer drugs, 2016-08, Vol.27 (7), p.609-619

2016

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Beta-Thalassemia Intermedia: A Single Thalassemia Center Experience from Northeastern Iraq

Effect of EGLN1 Genetic Polymorphisms on Hemoglobin Concentration in Andean Highlanders

Identification of Differential Gene Expression Pattern in Lens Epithelial Cells Derived from Cataractous and Noncataractous Lenses of Shumiya Cataract Rat

Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations

First Record Mutations in the Genes ASPA and ARSA Causing Leukodystrophy in Jordan

Bta-miR-124a Affects Lipid Metabolism by Regulating PECR Gene

Identification of Candidate Genes Associated with Charcot-Marie-Tooth Disease by Network and Pathway Analysis

Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate

Targeting N-Terminal Huntingtin with a Dual-sgRNA Strategy by CRISPR/Cas9

Detection of False-Positive Deletions from the Database of Genomic Variants

Relative burden of large CNVs on a range of neurodevelopmental phenotypes

Copy Number Variations in Children with Tourette Syndrome: Systematic Investigation in a Clinical Setting

Trait − driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes

Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis

Sox11 is required to maintain proper levels of Hedgehog signaling during vertebrate ocular morphogenesis

Discriminatory Weight of SNPs in Spike SARS-CoV-2 Variants: A Technically Rapid, Unambiguous, and Bioinformatically Validated Laboratory Approach

MECP2 missense mutations outside the canonical MBD and TRD domains in males with intellectual disability

The Correlation-Base-Selection Algorithm for Diagnostic Schizophrenia Based on Blood-Based Gene Expression Signatures

Targeted next-generation sequencing identifies the disruption of the SHANK3 and RYR2 genes in a patient carrying a de novo t(1;22)(q43;q13.3) associated with signs of Phelan-McDermid syndrome

Guidelines for Optimisation of a Multiplex Oligonucleotide Ligation-PCR for Characterisation of Microbial Pathogens in a Microsphere Suspension Array

ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data

A Novel -72 (T→A) β-Promoter Mutation Causing Slightly Elevated HbA2 in a Vietnamese Heterozygote

In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients

The embryo battle against adverse genomes: Are de novo terminal deletions the rescue of unfavorable zygotic imbalances?

Antitumoural activity of a cytotoxic peptide of Lactobacillus casei peptidoglycan and its interaction with mitochondrial-bound hexokinase

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