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
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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 126. It has an SJR impact factor of 1,393 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,393.

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics focuses its scope in these topics and keywords: schizophrenia, disorder, gene, susceptibility, family, factor, genesevidence, genetics, intrachromosomal, impact, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics

1,393

SJR Impact factor

126

H Index

50

Total Docs (Last Year)

201

Total Docs (3 years)

3023

Total Refs

685

Total Cites (3 years)

196

Citable Docs (3 years)

3,22

Cites/Doc (2 years)

60,46

Ref/Doc

Aims and Scope


schizophrenia, disorder, gene, susceptibility, family, factor, genesevidence, genetics, intrachromosomal, impact, familysexually, implicates, independent, influences, insertions, metaanalysissubstance, mthfr, nowmethylenetetrahydrofolate, evidence, effect, duration, age, benzodiazepine, bipolar, birth, canadian, cohortautistic, combined, ct, data, dimorphic, disease, disorderline, disorderthe, dopamine,



Best articles by citations

The New England family study high-risk project: Neurological impairments among offspring of parents with schizophrenia and other psychoses

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Possible association of the alpha-2A adrenergic receptor gene (ADRA2A) with symptoms of attention-deficit/hyperactivity disorder

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

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Serotonergic polymorphisms and psychotic disorders in populations from North Spain

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What should be said to the lay public regarding ADHD etiology

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

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Genome-wide association study of hoarding traits

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Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness

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The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects

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Relationship of MAO-A promoter (u-VNTR) and COMT (V158M) gene polymorphisms to CSF monoamine metabolites levels in a psychiatric sample of caucasians: A preliminary report

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Expression and genetic variability ofPCDH11Y, a gene specific toHomo sapiens and candidate for susceptibility to psychiatric disorders

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New Huntington disease mutation arising from a paternal CAG34allele showing somatic length variation in serially passaged lymphoblasts

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Differentially methylated regions in bipolar disorder and suicide

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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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Mutations in the TSGA14 gene in families with autism spectrum disorders

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Effect of model choice in genetic association studies: DRD4 exon III VNTR and cigarette use in young adults

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Developmental trajectories for young children with 16p11.2 copy number variation

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

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Neuregulin 3 and its roles in schizophrenia risk and presentation

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

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Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation

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