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Publications by Sandra K. Loo

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay

American Journal of Human Genetics
Genetics
2019English

IRF2BPL Is Associated With Neurological Phenotypes

American Journal of Human Genetics
Genetics
2018English

De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

American Journal of Human Genetics
Genetics
2019English

Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes

American Journal of Human Genetics
Genetics
2019English

Electrophysiological Biomarkers of Diagnosis and Outcome in Neurodevelopmental Disorders

Current Opinion in Neurology
Neurology
2015English

Atypical EEG Beta Asymmetry in Adults With ADHD

Neuropsychologia
Cognitive NeuroscienceBehavioral NeuroscienceExperimentalCognitive Psychology
2010English

A Parietal Biomarker for ADHD Liability: As Predicted by the Distributed Effects Perspective Model of ADHD

Frontiers in Psychiatry
PsychiatryMental Health
2015English

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