ISSN: 1434-5161

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Journal of Human Genetics Q2 Unclaimed

Nature Publishing Group United Kingdom

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Journal of Human Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 92. It has a price of 3690 €. It has an SJR impact factor of 1,148 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 1,148.

Journal of Human Genetics focuses its scope in these topics and keywords: cutaneous, patients, gene, gstt, gstm, gioro, genes, familypharmacogenomics, fabry, evenness, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Genetics (Q2) Genetics (clinical) (Q2) Genetics (clinical) (Q2)

Price

3690 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

1,148

SJR Impact factor

92

H Index

120

Total Docs (Last Year)

373

Total Docs (3 years)

4469

Total Refs

1122

Total Cites (3 years)

359

Citable Docs (3 years)

2.69

Cites/Doc (2 years)

37.24

Ref/Doc

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Gene: X Q2
Advances in Biological Regulation Q2
Genes Chromosomes and Cancer Q2
Human Gene Therapy Q2
BMC Cancer Q2

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Aims and Scope

Best articles by citations

Structural basis of the GM2 gangliosidosis B variant

The interleukin 6 -174G/C Polymorphism is associated with indices of obesity in men

Preferential reduction of dicentrics in reciprocal exchanges due to the combination of the size of broken chromosome segments by radiation

Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms

Comparative study of the haplotype structure and linkage disequilibrium of chromosome 1p36.2 region in the Korean and Japanese populations

High heritability of bone size at the hip and spine in Chinese

Genomic structure and alternative splicing of the insulin receptor tyrosine kinase substrate of 53-kDa protein

Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome

Characterization of six base pair deletion in the putative HNF1-binding site of human PXR promoter

Isolation and characterization of a novel human NM23-H1B gene, a different transcript of NM23-H1

Deregulated expression of KRAP, a novel gene encoding actin-interacting protein, in human colon cancer cells

SHOW MORE ARTICLES

Novel mutations and phenotypic effect of the splice site modulator IVS3-48C in nine Swedish families with erythropoietic protoporphyria

A new sequenced allelic ladder marker for D1S80 typing

On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting?

High throughput multiple combination extraction from large scale polymorphism data by exact tree method

Novel mutations involving the NF1 gene coding sequence in neurofibromatosis type 1 patients from Taiwan

Novel mutations of EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis

A Biochemical analysis demonstrates that the BRCA1 intronic variant IVS10-2A=>C is a mutation

Homozygous mutation Arg768Trp in the ABC-transporter encoding gene MRP2/cMOAT/ABCC2 causes Dubin-Johnson syndrome in a Caucasian patient

Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease

A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy

Association of a polymorphism of the dopamine receptor D4 gene with bone mineral density in Japanese men

DNA polymorphism and mutations in CPN1, including the genomic basis of carboxypeptidase N deficiency