American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Publication Venue For
Genes known to escape X chromosome inactivation predict co-morbid chronic musculoskeletal pain and posttraumatic stress symptom development in women following trauma exposure
Developmental trajectories for young children with 16p11.2 copy number variation
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility
Genetic association between α-synuclein and idiopathic Parkinson's disease
A genomic scan for age at onset of Alzheimer's disease in 437 families from the NIMH genetic initiative
Glutathione S-transferase polymorphisms and onset age in α-synuclein A53T mutant Parkinson's disease
Abnormalities of cholesterol metabolism in autism spectrum disorders
Association studies of transforming growth factor-β1 and Alzheimer's disease
. 139 B:38-41.
Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses
. 139 B:28-32.
Lack of Evidence for An Association between WNT2 and RELN Polymorphisms and Auitism
. 126 B:51-57.
Behavioral phenotypic variation in autism multiplex families: Evidence for a continuous severity gradient
Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families
Environmental, medical, and family history risk factors for Parkinson's disease: A new England-based case control study
Sex-exclusive quantitative trait loci influences in alcohol-related phenotypes
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism
17q Inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one
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