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: -

Categories: Psychiatry and Mental Health (Q1) Cellular and Molecular Neuroscience (Q2) Genetics (clinical) (Q2)

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

Other journals with similar parameters

Genome Research Q1
American Journal of Human Genetics Q1
Annual Review of Genomics and Human Genetics Q1
Genome Medicine Q1
PLoS Genetics Q1

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Aims and Scope

Best articles by citations

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

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

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

Serotonergic polymorphisms and psychotic disorders in populations from North Spain

What should be said to the lay public regarding ADHD etiology

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

Genome-wide association study of hoarding traits

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

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

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

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

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

SHOW MORE ARTICLES

Differentially methylated regions in bipolar disorder and suicide

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

Mutations in the TSGA14 gene in families with autism spectrum disorders

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

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

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

Neuregulin 3 and its roles in schizophrenia risk and presentation

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

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

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

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

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

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