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Publications by Hussein Daoud

De Novo Mutations in FOXP1 in Cases With Intellectual Disability, Autism, and Language Impairment

American Journal of Human Genetics

English

Detailed Biochemical and Bioenergetic Characterization of FBXL4-Related Encephalomyopathic Mitochondrial DNA Depletion

Internal Medicine

Molecular Biology

English

Related publications

Mutations in RAB39B in Individuals With Intellectual Disability, Autism Spectrum Disorder, and Macrocephaly

Molecular Autism

Developmental Neuroscience

Developmental Biology

Molecular Biology

English

Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability

American Journal of Human Genetics

English

Visual Impairment in Persons With Intellectual Disability

Specijalna Edukacija i Rehabilitacija

Educational Psychology

English

Recessive Truncating Mutations in ALKBH8 Cause Intellectual Disability and Severe Impairment of Wobble Uridine Modification

American Journal of Human Genetics

English

Macrocephaly-Intellectual Disability-Autism Syndrome

English

De Novo Truncating Variants in PHF21A Cause Intellectual Disability and Craniofacial Anomalies

European Journal of Human Genetics

English

The Role of Every-Day Executive Function in Social Impairment and Adaptive Skills in Autism Spectrum Disorder With Intellectual Disability

Research in Autism Spectrum Disorders

Clinical Psychology

Educational Psychology

English

Autism and Intellectual Disability Associated With Mitochondrial Disease and Hyperlactacidemia

International Journal of Molecular Sciences

Organic Chemistry

Molecular Biology

Theoretical Chemistry

Inorganic Chemistry

Computer Science Applications

English

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

American Journal of Human Genetics

English