Stephen W. Scherer
0000-0002-8326-1999
Publication & Citation Trends
Publications
1,019 total
75. Investigation of Compound Heterozygous Events Involving Deletions and Sequence-Level Variants in Autism Etiology
Cited by 0
Semantic Scholar
74. Genome-Wide Significance Reconsidered: Low-Frequency Variants and Regulatory Networks in Autism
Cited by 0
Semantic Scholar
82. CHARACTERIZING GENE DOSAGE EFFECT IN SIX MAJOR PSYCHIATRIC CONDITIONS AT PATHWAY AND CELL TYPE LEVELS ALONG THE SENSORIMOTOR-ASSOCIATION CORTICAL GRADIENT
Cited by 0
Semantic Scholar
367. Inspire 7: Intellectual Disability Polygenic Risk Evaluation in 7q11.23 Deletion Syndrome
Cited by 0
Semantic Scholar
M54. RARE VARIANTS IN SMALL NUCLEAR RNA GENES REVEAL A SPLICING-RELATED GENETIC MECHANISM IN AUTISM SPECTRUM DISORDER
Cited by 0
Semantic Scholar
Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex OA
Cited by 1
Semantic Scholar
41. Variants in DENND2B Are Associated With Vulnerability for Neurodevelopmental Impairment, Psychosis and Catatonia
Cited by 0
Semantic Scholar
EAGLE-AI: A large language model workflow for automated extraction and scoring of literature evidence linking genes to autism spectrum disorder
Cited by 0
Semantic Scholar
Advancing Human Population Genomics with DNA Foundation Models
Cited by 0
Semantic Scholar
Research Topics
Genomic variations and chromosomal abnormalities
(313)
Genetics and Neurodevelopmental Disorders
(231)
Autism Spectrum Disorder Research
(197)
Genomics and Rare Diseases
(191)
Congenital heart defects research
(129)
Affiliations
University of New Brunswick
Broad Institute
Canadian Institute for Advanced Research
Northwestern University
Ontario Institute for Cancer Research