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Publications by Christian Gilissen
Author Correction: Parent-Of-Origin-Specific Signatures of De Novo Mutations
Nature Genetics
Genetics
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial Dysmorphism
American Journal of Human Genetics
Genetics
Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway
American Journal of Human Genetics
Genetics
The Discovery of a LEMD2-Associated Nuclear Envelopathy With Early Progeroid Appearance Suggests Advanced Applications for AI-Driven Facial Phenotyping
American Journal of Human Genetics
Genetics
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder
American Journal of Human Genetics
Genetics
Truncating De Novo Mutations in the Krüppel-Type Zinc-Finger Gene ZNF148 in Patients With Corpus Callosum Defects, Developmental Delay, Short Stature, and Dysmorphisms
Genome Medicine
Molecular Medicine
Genetics
Molecular Biology
BTG1 Regulates Glucocorticoid Receptor Autoinduction in Acute Lymphoblastic Leukemia
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Accurate Distinction of Pathogenic From Benign CNVs in Mental Retardation
PLoS Computational Biology
Molecular Neuroscience
Evolution
Ecology
Genetics
Behavior
Molecular Biology
Systematics
Simulation
Cellular
Computational Theory
Mathematics
Modeling
Clinical Exome Sequencing for Cerebellar Ataxia and Spastic Paraplegia Uncovers Novel Gene–disease Associations and Unanticipated Rare Disorders
European Journal of Human Genetics
Genetics
1 in 38 Individuals at Risk of a Dominant Medically Actionable Disease
European Journal of Human Genetics
Genetics
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