Nagwa Abdel Meguid

Nagwa Abdel Meguid's AcademicInfluence.com Rankings

Nagwa Abdel Meguid

Biology

#13414

World Rank

#16959

Historical Rank

Genetics

#1497

World Rank

#1599

Historical Rank

biology Degrees

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Biology

Nagwa Abdel Meguid's Degrees

Bachelors Genetics Cairo University
Masters Genetics Cairo University
PhD Genetics Cairo University

Why Is Nagwa Abdel Meguid Influential?

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According to Wikipedia, Nagwa Abdel Meguid is an Egyptian geneticist and 2002 winner of the L’Oreal UNESCO Award for Women in Science for Africa and the Middle East. Her research has "identified several genetic mutations that cause common syndromes such as the fragile X syndrome and Autism".

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Nagwa Abdel Meguid's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy (2012) (266)
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders (2017) (156)
Reduced serum levels of 25-hydroxy and 1,25-dihydroxy vitamin D in Egyptian children with autism. (2010) (139)
Evaluation of Oxidative Stress in Autism: Defective Antioxidant Enzymes and Increased Lipid Peroxidation (2011) (126)
Role of polyunsaturated fatty acids in the management of Egyptian children with autism. (2008) (123)
Oxidative Stress in Autism Spectrum Disorder (2020) (120)
MTHFR Genetic Polymorphism As a Risk Factor in Egyptian Mothers with Down Syndrome Children (2007) (56)
Dietary adequacy of Egyptian children with autism spectrum disorder compared to healthy developing children (2017) (49)
A new multiple congenital anomaly, mental retardation syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies. (1998) (37)
Novel Robinow syndrome causing mutations in the proximal region of the frizzled-like domain of ROR2 are retained in the endoplasmic reticulum (2007) (36)
Impact of Clostridium Bacteria in Children with Autism Spectrum Disorder and Their Anthropometric Measurements (2020) (28)
Diagnostic and Severity-Tracking Biomarkers for Autism Spectrum Disorder (2018) (28)
Altered urinary porphyrins and mercury exposure as biomarkers for autism severity in Egyptian children with autism spectrum disorder (2016) (28)
Homocysteine and oxidative stress in Egyptian children with Down syndrome. (2010) (28)
Gastrointestinal alterations in autism spectrum disorder: What do we know? (2020) (27)
Dietary Patterns of Children with Autism Spectrum Disorder: A Study Based in Egypt (2015) (25)
Hypogenitalism in the acrocallosal syndrome. (1989) (24)
Growth charts of Egyptian children with Down syndrome (0-36 months). (2004) (21)
The role of zinc supplementation on the metallothionein system in children with autism spectrum disorder (2019) (21)
Cognition and lobar morphology in full mutation boys with fragile X syndrome (2011) (21)
Haplotypes and mutations of the PAH locus in Egyptian families with PKU (1999) (20)
Methylenetetrahydrofolate reductase gene polymorphisms and the risk of colorectal carcinoma in a sample of Egyptian individuals. (2009) (18)
Brain Morphology in Autism and Fragile X Syndrome Correlates With Social IQ: First Report From the Canadian-Swiss-Egyptian Neurodevelopmental Study (2010) (18)
PREVALENCE OF CONSANGUINEOUS MARRIAGES IN SOUTH SINAI, EGYPT (2012) (17)
Evaluation of superoxide dismutase and glutathione peroxidase enzymes and their cofactors in egyptian children with down’s syndrome (2001) (17)
Handling autism imbalanced data using synthetic minority over-sampling technique (SMOTE) (2015) (17)
HFE Gene Polymorphisms and the Risk for Autism in Egyptian Children and Impact on the Effect of Oxidative Stress (2011) (16)
Williams syndrome: a relationship between genetics, brain morphology and behaviour. (2012) (16)
Prevalence of fragile X syndrome among school-age Egyptian males (2007) (16)
Expression of Reactive Oxygen Species–Related Transcripts in Egyptian Children With Autism (2017) (16)
A study of blood serotonin and serotonin transporter promoter variant (5-HTTLPR) polymorphism in Egyptian autistic children (2015) (13)
Feed regimen affects growth, condition index, proximate analysis and myocyte ultrastructure of juvenile spinefoot rabbitfish Siganus rivulatus (2011) (13)
Transposition of external genitalia and associated malformations (2003) (12)
Lenz microphthalmia syndrome: three additional cases with rare associated anomalies. (2000) (11)
Genetic Disorders in Egypt (2010) (11)
Study of 35delG in Congenital Sensorineural non-syndromic Hearing Loss in Egypt (2008) (11)
Altered S100 Calcium-Binding Protein B and Matrix Metallopeptidase 9 as Biomarkers of Mesial Temporal Lobe Epilepsy with Hippocampus Sclerosis (2018) (11)
Toxic Effect of Some Heavy Metals in Egyptian Autistic Children (2015) (11)
Frontal theta/beta ratio changes during TOVA in Egyptian ADHD children (2017) (10)
Evaluation of MTHFR Genetic Polymorphism as a Risk Factor in EgyptianAutistic Children and Mothers (2015) (10)
Frequency of risk factors and coexisting abnormalities in a population of Egyptian children with autism spectrum disorder. (2018) (9)
Genetic Variants in the Methylenetetrahydrofolate Reductase Gene in Egyptian Children with Conotruncal Heart Defects and their Mothers (2012) (8)
Anthropometric assessment of a Middle Eastern group of autistic children (2014) (8)
Salivary Cortisol Levels in Abused Children with Attention Deficit Hyperactivity Disorder (2015) (7)
Efficacy of selected treadmill training programme on oxidative stress in adolescents with Down syndrome. (2013) (7)
Intellectual disability secondary to a 16p13 duplication in a 1;16 translocation. Extended phenotype in a four‐generation family (2015) (7)
Protective effect of ashwagandha (Withania somnifera) against neurotoxicity induced by aluminum chloride in rats (2018) (7)
GABA synaptopathy promotes the elevation of caspases 3 and 9 as pro-apoptotic markers in Egyptian patients with autism spectrum disorder (2019) (6)
Plasma levels of nerve growth factor in Egyptian autistic children: Relation to hyperserotonemia and autoimmunity (2021) (6)
Simple molecular diagnostic method for fragile X syndrome in Egyptian patients: pilot study. (2014) (6)
Polymorphism in Variable Number of Tandem Repeats of Dopamine D4 Gene Is a Genetic Risk Factor in Attention Deficit Hyperactive Egyptian Children: Pilot Study (2015) (5)
Specialized Diet Therapies: Exploration for Improving Behavior in Autism Spectrum Disorder (ASD). (2020) (5)
The neuroanatomy of the autistic phenotype (2012) (5)
Isodicentric chromosome 18 in an abnormal infant using chromosome specific DNA probe. (1992) (5)
Orodental, ear and eye anomalies in Egyptian Brachmann de Lange syndrome cases. (1994) (4)
Mucopolysaccharidosis type I: clinical and biochemical study. (2000) (4)
Seasonal histological changes in the ovary of Sparus aurata, a hermaphrodite teleost marine fish (family: Sparidae). (1987) (3)
Genetic diagnosis of Prader–Willi syndrome (2016) (3)
Copy number variations of SHANK3 and related sensory profiles in Egyptian children with autism spectrum disorder (2020) (3)
Impact of Oxidative Stress on Autism Spectrum Disorder Behaviors in Children with Autism (2016) (2)
Influence of COVID-19 pandemic lockdown on a sample of Egyptian children with Down syndrome (2022) (2)
Contribution of chromosomal abnormalities at 10q and 22q to autism (2018) (2)
Role of amino acids in the pathophysiology of autism spectrum disorders in Saudi and Egyptian population samples (2014) (2)
ELECTROPHYSIOLOGIC ASSESSMENT OF AUDITORY FUNCTION IN CHILDREN WITH AUTISM AND ATTENTIONDEFICIT AND HYPERACTIVITY DISORDER (2014) (2)
The Link between Genetic Abnormalities in the Monogenic Disorders and the Behavioral Phenotype of Polygenic Disorders Has Yet To Be Addressed in Research (2012) (1)
Evaluation of Branched-Chain Amino Acids in Children with Autism Spectrum Disorder and Epilepsy (2023) (1)
Annelid nerve cells. III. Topographic relationship of the Golgi apparatus and alkaline phosphatase and the problem of neurosecretion in Allolobophora. (1979) (1)
Nonmosaic partial duplication 12p: clinical and cytogenetic findings and review of the literature 12p duplication: clinical and cytogenetic description (2014) (1)
Egypt and Autism (2021) (1)
Heterozygous expression of Lesch-Nyhan syndrome clinical and ultrastructural studies. (1990) (1)
MRI Surface-Based Brain Morphometry in Egyptian Autistic and Typically Developing Children (2015) (1)
Evaluation of plasma neurotransmitters in children living with Attention-Deficit Hyperactivity Disorder (ADHD) (2018) (1)
Prevalence of autism spectrum disorder among children referred to special needs clinic in Giza (2023) (1)
Anterior to posterior limb of the internal capsule morphology in fragile X syndrome (2009) (1)
Role of Plasma Fatty Acids in Egyptian Children with Attention Deficit Hyperactivity Disorder (2016) (1)
Spermatogenesis in the marine hermaphrodite teleost fish Sparus aurata. (1987) (1)
Seasonal changes in the cytology and cytochemistry of the pituitary gland of Sparus aurata. (1987) (1)
Autism and Fragile X: Is There a Neurochemical Link? (2014) (1)
Molecular Characterization of Probiotics and Their Influence on Children with Autism Spectrum Disorder (2022) (1)
Awareness and risk factors of autism spectrum disorder in an Egyptian population (2021) (1)
Severity-tracking biomarkers for ASD (2019) (0)
The distribution of lipids and carbohydrates in normal and methotrexate (MTX)-treated mouse Mus musculus testes. (1986) (0)
Annelid nerve cells. II. Mitochondria and neurosecretion in Allolobophora. (1979) (0)
Cyclic histological changes in the pituitary gland of Sparus aurata in correlation to the gonadal cycle. (1988) (0)
Prevalence of Intimate Partner Violence Against Arab Women in Consanguineous Marriages (2020) (0)
Corrigendum (2010) (0)
The histopathological effect induced by methotrexate (MTX) on the testes of Mus musculus. (1987) (0)
Cytological and cytochemical changes in the ovary of Sparus aurata during the annual reproductive cycle. (1987) (0)
Effect of methotrexate (MTX) on the testicular proteins, DNA and RNA of Mus musculus. (1986) (0)
Psoriasis before and after methotrexate (MXT) treatment: II. Localization of mitochondria and dehydrogenases. (1983) (0)
A Novel Mutation in the GJB 2 ( Connexin 26 ) Gene in Egyptian Children with Non-syndromic Sensorineural Hearing Loss (2013) (0)
Do autism and fragile X syndrome share neurobiological markers (2013) (0)
Epilepsy and autistic manifestations in an Egyptian child with ring 14 (2014) (0)
Oxidative Stress in Autism Spectrum Disorder (2020) (0)
Dietary adequacy of Egyptian children with autism spectrum disorder compared to healthy developing children (2017) (0)
Mothering A Child with Mental Disability in Egyptian Culture: Perceptions of Stigma (2020) (0)
Psoriasis before and after methotrexate (MXT) treatment. 3. Localization of dopa oxidase. (1984) (0)
A Novel Mutation in the GJB2 (Connexin 26) Gene in Egyptian Children with Non-syndromic Sensorineural Hearing Loss (2013) (0)
Disturbed Cellular Iron Metabolism Genes in Neurodevelopmental Disorders is Different from Neurodegenerative Disorders (2015) (0)
Cytological study of normal and methotrexate (MTX)-treated testes of Mus musculus. (1986) (0)
Shared behavioral and neurobiological markers in autism and fragile × syndrome with autistic features, however…. (2009) (0)
Seasonal histological changes in the pituitary gland of Sparus aurata. (1987) (0)
Differential expression of cystathionine beta synthase in adolescents with Down syndrome: impact on adiposity (2022) (0)
Diagnostic and Severity-Tracking Biomarkers for Autism Spectrum Disorder (2018) (0)
Role of S-100B as a Serum Biochemical Marker for Brain Injury in Egyptian Patients with Phenylketonuria (2010) (0)
PREVALENCE O F C ONSANGUINEOUS MARRIAGES IN S OUTH SINAI, EGYPT (2012) (0)
Altered urinary porphyrins and mercury exposure as biomarkers for autism severity in Egyptian children with autism spectrum disorder (2016) (0)
Review for "Three novel patients with epileptic encephalopathy due to biallelic mutations in the PLCB1 gene" (2019) (0)
Evaluation of circulating miRNAs and mRNAs expression patterns in autism spectrum disorder (2021) (0)
Psoriasis before and after methotrexate (MXT) treatment. 1. The Golgi apparatus and phosphatases. (1984) (0)
Neurodevelpomental disorders: Clinical, genetic and neuroimaging approach (2013) (0)
Overview in the etiopathogenesis of different phenotypes of autism (2018) (0)
Minor dysmorphism in a child with inherited ring chromosome 18 (2013) (0)
Johnson‑McMillin Microtia Syndrome: New Additional Family Case (0)
Linguistic phenotype in a sample of Arabic speaking children with Williams and fragile X syndromes (2018) (0)
Antioxidant activity in Egyptian children with Down syndrome before and after nutritional supplementation (2015) (0)
Microtia: A Combined Approach by Genetics and Audiology (2016) (0)
The role of zinc supplementation on the metallothionein system in children with autism spectrum disorder (2019) (0)
Altered S100 Calcium-Binding Protein B and Matrix Metallopeptidase 9 as Biomarkers of Mesial Temporal Lobe Epilepsy with Hippocampus Sclerosis (2018) (0)
Fundamental Role of Neurochemicals Aberration in the Pathogenesis of Autism Spectrum Disorders (2020) (0)
Seasonal changes in the testis of the marine teleost fish Sparus aurata. (1987) (0)
Recent advances in molecular medicine: Changing the practice of neurology (2014) (0)
A comparative study of two reptile muscles. III. A cytological study of cardiac and striated muscles. (1985) (0)
Double Chromosomal Abnormalities in Live Birth Infants (2013) (0)
Behaviour and fertility of albino Swiss mice after the administration of MTX. (1986) (0)
Study of sensory processing deficits in autism spectrum disorder symptom triad: an Egyptian sample (2021) (0)

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Nagwa Abdel Meguid's Academic­Influence.com Rankings