European Neuropsychopharmacology

THE ALLELIC ARCHITECTURE OF RARE VARIATION IN AUTISM AND OTHER NEURODEVELOPMENTAL CONDITIONS.

CROSS-DISORDER RARE VARIANT ANALYSIS OF AUTISM AND ADHD.

T63. CROSS-DISORDER ANALYSIS OF AUTISM AND ADHD USING RARE VARIANTS: INSIGHTS FROM DANISH IPSYCH EXOMES.

CHARACTERIZING ASSOCIATIONS BETWEEN DISRUPTIVE DE NOVO RARE VARIANT BURDENS AND PHENOTYPIC COMBINATIONS IN OVER 3,000 AUTISTIC CHILDREN: TOWARDS BUILDING A PUBLIC CLINICAL GENETIC RESOURCE.

THE FEMALE PROTECTIVE EFFECT AGAINST AUTISM SPECTRUM DISORDER.

47. GENE DISCOVERY FROM EXOME SEQUENCING IN AUTISM AND COMPARISON TO DEVELOPMENTAL DELAY AND SCHIZOPHRENIA.

INSIGHTS INTO THE CONTRIBUTION OF RARE NONCODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING.

29 BRAINVAR DATA SET: WHOLE-GENOME AND RNA SEQUENCING REVEAL VARIATION AND TRANSCRIPTOMIC COORDINATION IN THE DEVELOPING HUMAN PREFRONTAL CORTEX.

De Novo Coding Variants Are Strongly Associated with Tourette Syndrome.

9 LIMITED CONTRIBUTION OF RARE, NONCODING VARIATION TO AUTISM SPECTRUM DISORDER FROM SEQUENCING OF 2,076 GENOMES IN QUARTET FAMILIES.

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