ISSN: 0003-4800

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Annals of Human Genetics Q3 Unclaimed

Wiley-Blackwell Publishing Ltd United Kingdom

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Annals of Human Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 79. It has a price of 3000 €. It has an SJR impact factor of 0,629 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,629.

Annals of Human Genetics focuses its scope in these topics and keywords: genetic, gene, south, distribution, dfnb, diversity, epistatic, ets, evaluationthe, f, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Genetics (Q3) Genetics (clinical) (Q3) Genetics (clinical) (Q3)

Price

3000 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0,629

SJR Impact factor

79

H Index

37

Total Docs (Last Year)

139

Total Docs (3 years)

1288

Total Refs

255

Total Cites (3 years)

134

Citable Docs (3 years)

2.04

Cites/Doc (2 years)

34.81

Ref/Doc

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Molecular genetics & genomic medicine Q3
Immunogenetics Q3
BMC Medical Genetics Q3
Cancer genetics Q3
Human gene therapy. Clinical development Q3

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Aims and Scope

Best articles by citations

Increased parental age and number of pregnancies in Klippel-Trenaunay-Weber syndrome

Diversity of the human Y chromosome of South American Amerindians: a comparison with Blacks, Whites, and Japanese from Brazil

Alpha coat protein COPA (HEP-COP): presence of an Alu repeat in cDNA and identity of the amino terminus to xenin

Recombination, interference and sequence: comparison of chromosomes 21 and 22

X-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred

The evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination

Information provided by pairs of distantly affected relatives to search for genes involved in rare autosomal dominant diseases

The correlation between relatives under assortative mating for an X-linked and autosomal trait.

Biochemical genetics of the pentose phosphate cycle: human ribose 5-phosphate isomerase (RPI) and ribulose 5-phosphate 3-epimerase (RPE)

Mucopolysaccharidosis type I: characterization of a common mutation that causes Hurler syndrome in Moroccan subjects

Assessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cells

Genetic history of cystic fibrosis mutations in Italy. I. Regional distribution

SHOW MORE ARTICLES

Molecular Analysis of Myophosphorylase Deficiency in Dutch Patients with McArdle's Disease

Accelerated Gene Counting for Haplotype Frequency Estimation

Wilson's Disease, vol. 30 in the series Major Problems in Neurology. By Tjaard Hoogenraad. London, Philadelphia, Toronto, Sydney, Tokyo: W. B. Saunders. Co Ltd. Pp. 209. ¬£45.00.

On Fisher's exact test for detecting gametic disequilibrium between DNA polymorphisms

Assignment of the human cardiac/slow skeletal muscle troponin C gene (TNNC1) between D3S3118 and GCT4B10 on the short arm of chromosome 3 by somatic cell hybrid analysis

Testing the Genetic Relation Between Two Individuals Using a Panel of Frequency-unknown Single Nucleotide Polymorphisms

Tests for Candidate-Gene Association Using Case-Parents Design

Analysis of BRCA1 and BRCA2 in breast and breast/ovarian cancer families shows population substructure in the Iberian peninsula

Evidence for a major gene for bone mineral density/content in human pedigrees identified via probands with extreme bone mineral density

Cloning and chromosome assignment of the human CDX2 gene

Environmental Mutagenesis. Edited by D. H. Phillips and S. Venitt, Bios Scientific Publishers, Oxford, U.K., 1995, Pp. 403.

Nonsyndromic cleft lip and palate: Complex genetics and environmental effects