verified SJR 0,658 · Q2 • database Scopus / SJR & Web of Science indexed

United States · Wiley-Liss Inc.

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American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics

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 140. It has an SJR impact factor of 0,658 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,658.

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics focuses its scope in these topics and keywords: schizophrenia, disorder, susceptibility, gene, polymorphisms, ofbdnfon, canadian, combined, dopamine, insertions, ...

ISSN: 1552-4841

Editorial: Wiley-Liss Inc.

Category: Genetics (clinical)

Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

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schedule Datos CoP · solo campos en BD

SJR Impact Factor trending_up

0,658 Q2

H-index 140

Tasa de Aceptación pie_chart

22% Selectiva

Fuente Acceptance_Rate

Tiempo a publicación hourglass_top

NPD

Campo Sin dato

Coste de Publicación (APC) payments

NPD Open Access

Ruta Non-OA 0 €

Metrics

Campos Scimago / CoP — sin series inventadas

Scopus / SJR Web of Science

SJR Impact

0,658

H-index

140

Docs (year)

Docs 3y

Total refs

2098

Cites 3y

171

Citable 3y

Cites/Doc 2y

1.88

Ref/Doc

51.17

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

0 €

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Best articles by citations

Association of ANK3 with bipolar disorder confirmed in East Asia

What should be said to the lay public regarding ADHD etiology based on unbiased systematic quantitative empirical evidence

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

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

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

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

Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm

CAG repeats in restless legs syndrome

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

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

Association study ofCREB1 and childhood-onset mood disorders

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

SHOW MORE ARTICLES

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

"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)

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

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

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

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

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

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

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

A genome-wide linkage analysis of dementia in the Amish

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

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

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