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Susan L. Santangelo

Researcher at Maine Medical Center

Publications -  95
Citations -  17971

Susan L. Santangelo is an academic researcher from Maine Medical Center. The author has contributed to research in topics: Autism & Autism spectrum disorder. The author has an hindex of 43, co-authored 89 publications receiving 15274 citations. Previous affiliations of Susan L. Santangelo include Tufts Medical Center & Massachusetts Mental Health Center.

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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

Jordan W. Smoller, +33 more
- 20 Apr 2013 - 
TL;DR: The findings show that specific SNPs are associated with a range of psychiatric disorders of childhood onset or adult onset, and variation in calcium-channel activity genes seems to have pleiotropic effects on psychopathology.
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

S. Hong Lee, +405 more
- 01 Sep 2013 - 
TL;DR: Empirical evidence of shared genetic etiology for psychiatric disorders can inform nosology and encourages the investigation of common pathophysiologies for related disorders.
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Association between Microdeletion and Microduplication at 16p11.2 and Autism

Lauren A. Weiss, +28 more
- 14 Feb 2008 - 
TL;DR: A novel, recurrent microdeletion and a reciprocal microduplication that carry substantial susceptibility to autism and appear to account for approximately 1% of cases are identified.
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Analysis of shared heritability in common disorders of the brain

Verneri Anttila, +720 more
- 22 Jun 2018 - 
TL;DR: It is demonstrated that, in the general population, the personality trait neuroticism is significantly correlated with almost every psychiatric disorder and migraine, and it is shown that both psychiatric and neurological disorders have robust correlations with cognitive and personality measures.
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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

F. Kyle Satterstrom, +201 more
- 06 Feb 2020 - 
TL;DR: The largest exome sequencing study of autism spectrum disorder (ASD) to date, using an enhanced analytical framework to integrate de novo and case-control rare variation, identifies 102 risk genes at a false discovery rate of 0.1 or less, consistent with multiple paths to an excitatory-inhibitory imbalance underlying ASD.