ISSN: 1552-4841
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American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics Q1 Unclaimed
American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics is a journal indexed in SJR in Genetics (clinical) and Cellular and Molecular Neuroscience with an H index of 124. It has an SJR impact factor of 1,567 and it has a best quartile of Q1. It is published in English.
Type: Journal
Type of Copyright:
Languages: English
Open Access Policy: Open Choice
Type of publications:
Publication frecuency: -
- €
Gold OA-
Green OA- €
Non OAMetrics
1,567
SJR Impact factor124
H Index59
Total Docs (Last Year)262
Total Docs (3 years)3721
Total Refs882
Total Cites (3 years)251
Citable Docs (3 years)3,68
Cites/Doc (2 years)63,07
Ref/DocAims and Scope
Other journals with similar parameters
Genome Research Q1
American Journal of Human Genetics Q1
Genome Medicine Q1
Annual Review of Genomics and Human Genetics Q1
Genetics in Medicine Q1
Best articles
"Association study of a functional promoter polymorphism in theXBP1 gene and schizophrenia," American Journal Of Medical Genetics Part B (Neuropsychiatric Genetics) 141B:71-75 (2006)
View more"Replicated" genome wide association for dependence on illegal substances: Genomic regions identified by overlapping clusters of nominally positive SNPs
View more5HTTLPR polymorphism in schizophrenic patients: Further support for association with violent suicide attempts
View moreA cautionary note on the use of simulation procedures for analyzing contingency tables containing small expected cell frequencies
View moreA genome-wide linkage analysis of dementia in the Amish
View moreA genome-wide search for risk genes using homozygosity mapping and microarrays with 1,494 single-nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder
View moreA novel homeobox mutation in thePITX2gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes
View moreA phenotype-based genetic association study reveals the contribution of neuregulin1 gene variants to age of onset and positive symptom severity in schizophrenia
View moreA twin study of the common vulnerability between heightened sensitivity to hypercapnia and panic disorder
View moreAn association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population
View moreAnalysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 region
View moreAssociation of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD)
View moreAssociation of ANK3 with bipolar disorder confirmed in East Asia
View moreAssociation of genetic variants of ABCA1 with Alzheimer's disease risk
View moreAssociation of the phosphatase and tensin homolog gene (PTEN) with smoking initiation and nicotine dependence
View moreAssociation study ofCREB1 and childhood-onset mood disorders
View moreBehavioral phenotype in Costello syndrome with atypical mutation: A case report
View moreCAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia
View moreCAG repeats in restless legs syndrome
View moreClock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm
View moreCognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression
View moreCognitive effects of genetic variation in monoamine neurotransmitter systems: A population-based study of COMT, MAOA, and 5HTTLPR
View moreCommon genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders
View moreComplete maternal uniparental isodisomy of chromosome 4 in a subject with major depressive disorder detected by high density SNP genotyping arrays
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