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Publications by Jeremy L. Freeman
Rare Copy Number Variants Are an Important Cause of Epileptic Encephalopathies
Annals of Neurology
Neurology
Fine-Needle Aspiration Biopsy of the Thyroid
Archives of Otolaryngology–Head & Neck Surgery
Related publications
A New Method for Detecting Associations With Rare Copy-Number Variants
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
An Interaction-Based Model for Neuropsychiatric Features of Copy-Number Variants
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Copy Number Variants Are Frequent in Genetic Generalized Epilepsy With Intellectual Disability
Neurology
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Ketogenic Diet in Epileptic Encephalopathies
Epilepsy Research and Treatment
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Epileptic Encephalopathies – Next Generation Diagnostics
Child Neurology
Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections
PLoS ONE
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Copy Number Variation at 22q11.2: From Rare Variants to Common Mechanisms of Developmental Neuropsychiatric Disorders
Molecular Psychiatry
Psychiatry
Molecular Neuroscience
Mental Health
Molecular Biology
Cellular
Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases
Biological Psychiatry
Biological Psychiatry
Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy
PLoS ONE
Multidisciplinary