ISSN: 0003-4800
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Annals of Human Genetics Q3 Unclaimed
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 0,609 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,609.
Annals of Human Genetics focuses its scope in these topics and keywords: gene, genetic, south, founderhaplotype, fmr, families, f, evaluationthe, ets, epistatic, ...
Type: Journal
Type of Copyright:
Languages: English
Open Access Policy: Open Choice
Type of publications:
Publication frecuency: -
3000 €
Inmediate OANPD
Embargoed OA0 €
Non OAMetrics
0,609
SJR Impact factor79
H Index36
Total Docs (Last Year)118
Total Docs (3 years)1387
Total Refs206
Total Cites (3 years)113
Citable Docs (3 years)1.23
Cites/Doc (2 years)38.53
Ref/DocOther journals with similar parameters
Stem Cell Investigation Q3
Molecular Genetics and Metabolism Reports Q3
Molecular genetics & genomic medicine Q3
BMC Medical 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
View moreDiversity of the human Y chromosome of South American Amerindians: a comparison with Blacks, Whites, and Japanese from Brazil
View moreAlpha coat protein COPA (HEP-COP): presence of an Alu repeat in cDNA and identity of the amino terminus to xenin
View moreRecombination, interference and sequence: comparison of chromosomes 21 and 22
View moreX-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred
View moreThe evolution and population genetics of the ALDH2 locus: random genetic drift, selection, and low levels of recombination
View moreInformation provided by pairs of distantly affected relatives to search for genes involved in rare autosomal dominant diseases
View moreThe correlation between relatives under assortative mating for an X-linked and autosomal trait.
View moreBiochemical genetics of the pentose phosphate cycle: human ribose 5-phosphate isomerase (RPI) and ribulose 5-phosphate 3-epimerase (RPE)
View moreMucopolysaccharidosis type I: characterization of a common mutation that causes Hurler syndrome in Moroccan subjects
View moreAssessment of diagnostic quantitative fluorescent multiplex polymerase chain reaction assays performed on single cells
View moreGenetic history of cystic fibrosis mutations in Italy. I. Regional distribution
View moreMolecular Analysis of Myophosphorylase Deficiency in Dutch Patients with McArdle's Disease
View moreAccelerated Gene Counting for Haplotype Frequency Estimation
View moreWilson'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.
View moreOn Fisher's exact test for detecting gametic disequilibrium between DNA polymorphisms
View moreAssignment 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
View moreTesting the Genetic Relation Between Two Individuals Using a Panel of Frequency-unknown Single Nucleotide Polymorphisms
View moreTests for Candidate-Gene Association Using Case-Parents Design
View moreAnalysis of BRCA1 and BRCA2 in breast and breast/ovarian cancer families shows population substructure in the Iberian peninsula
View moreEvidence for a major gene for bone mineral density/content in human pedigrees identified via probands with extreme bone mineral density
View moreCloning and chromosome assignment of the human CDX2 gene
View moreEnvironmental Mutagenesis. Edited by D. H. Phillips and S. Venitt, Bios Scientific Publishers, Oxford, U.K., 1995, Pp. 403.
View moreNonsyndromic cleft lip and palate: Complex genetics and environmental effects
View more
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