American Journal of Medical Genetics Part B: Neuropsychiatric Genetics


Publication Venue For

  • Functional characterization and potential therapeutic avenues for variants in the NTRK2 gene causing developmental and epileptic encephalopathies.  189:37-47. 2022
  • Genes known to escape X chromosome inactivation predict co-morbid chronic musculoskeletal pain and posttraumatic stress symptom development in women following trauma exposure.  180:415-427. 2019
  • The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.  180:55-67. 2019
  • Developmental trajectories for young children with 16p11.2 copy number variation.  174:367-380. 2017
  • Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility.  156:11-18. 2011
  • Genetic association between α-synuclein and idiopathic Parkinson's disease.  147:1222-1230. 2008
  • A genomic scan for age at onset of Alzheimer's disease in 437 families from the NIMH genetic initiative.  147:784-792. 2008
  • Glutathione S-transferase polymorphisms and onset age in α-synuclein A53T mutant Parkinson's disease.  144:254-258. 2007
  • Abnormalities of cholesterol metabolism in autism spectrum disorders.  141:666-668. 2006
  • Association studies of transforming growth factor-β1 and Alzheimer's disease.  139 B:38-41. 2005
  • Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses.  139 B:28-32. 2005
  • Lack of Evidence for An Association between WNT2 and RELN Polymorphisms and Auitism.  126 B:51-57. 2004
  • Behavioral phenotypic variation in autism multiplex families: Evidence for a continuous severity gradient.  114:129-136. 2002
  • Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.  114:24-30. 2002
  • Environmental, medical, and family history risk factors for Parkinson's disease: A new England-based case control study.  88:742-749. 1999
  • Sex-exclusive quantitative trait loci influences in alcohol-related phenotypes.  88:647-652. 1999
  • Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.  88:551-556. 1999
  • 17q Inversion involving the neurofibromatosis type one locus in a family with neurofibromatosis type one.  60:312-316. 1995
  • International Standard Serial Number (issn)

  • 1552-4841
  • Electronic International Standard Serial Number (eissn)

  • 1552-485X