Christina M. Hultman
0000-0002-0327-2410
Publication & Citation Trends
Publications
0 total
Deleterious coding variation associated with autism is shared across ancestries
Cited by 0
Semantic Scholar
Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database
Cited by 2
Semantic Scholar
Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder OA
Cited by 30
Semantic Scholar
Contribution of autosomal rare and de novo variants to sex differences in autism
Cited by 7
Semantic Scholar
Cell-type specific methylation changes in the newborn child associated to obstetric pain relief OA
Cited by 0
Semantic Scholar
4. SWEDEN SCHIZOPHRENIA STUDY HIGHLIGHTS NOVEL COMMON VARIATION ASSOCIATED WITH SCHIZOPHRENIA
Cited by 0
Semantic Scholar
Investigating neonatal health risk variables through cell-type specific methylome-wide association studies OA
Cited by 0
Semantic Scholar
Research Topics
Autism Spectrum Disorder Research
(64)
Genetic Associations and Epidemiology
(54)
Genomics and Rare Diseases
(39)
Genomic variations and chromosomal abnormalities
(37)
Genetics and Neurodevelopmental Disorders
(36)
Affiliations
Broad Institute
University of North Carolina at Chapel Hill
Uppsala University
Statistics Sweden
Brigham and Women's Hospital