Default: American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics

ISSN: 1552-4841

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American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics Q1 Unclaimed

Wiley-Liss Inc. United States
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

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: -

Metrics

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics

1,567

SJR Impact factor

124

H Index

59

Total Docs (Last Year)

262

Total Docs (3 years)

3721

Total Refs

882

Total Cites (3 years)

251

Citable Docs (3 years)

3,68

Cites/Doc (2 years)

63,07

Ref/Doc


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)

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"Replicated" genome wide association for dependence on illegal substances: Genomic regions identified by overlapping clusters of nominally positive SNPs

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5HTTLPR polymorphism in schizophrenic patients: Further support for association with violent suicide attempts

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A cautionary note on the use of simulation procedures for analyzing contingency tables containing small expected cell frequencies

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A genome-wide linkage analysis of dementia in the Amish

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A 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

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A novel homeobox mutation in thePITX2gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes

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A phenotype-based genetic association study reveals the contribution of neuregulin1 gene variants to age of onset and positive symptom severity in schizophrenia

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A twin study of the common vulnerability between heightened sensitivity to hypercapnia and panic disorder

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An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population

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Analysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 region

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Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD)

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Association of ANK3 with bipolar disorder confirmed in East Asia

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Association of genetic variants of ABCA1 with Alzheimer's disease risk

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Association of the phosphatase and tensin homolog gene (PTEN) with smoking initiation and nicotine dependence

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Association study ofCREB1 and childhood-onset mood disorders

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Behavioral phenotype in Costello syndrome with atypical mutation: A case report

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CAG repeat polymorphisms in KCNN3 (HSKCa3) and PPP2R2B show no association or linkage to schizophrenia

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CAG repeats in restless legs syndrome

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Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm

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Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression

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Cognitive effects of genetic variation in monoamine neurotransmitter systems: A population-based study of COMT, MAOA, and 5HTTLPR

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Common genetic variation in the GAD1 gene and the entire family of DLX homeobox genes and autism spectrum disorders

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Complete maternal uniparental isodisomy of chromosome 4 in a subject with major depressive disorder detected by high density SNP genotyping arrays

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