American Journal of Human Genetics

ISSN: 0002-9297

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American Journal of Human Genetics Q1 Unclaimed

Cell Press United States
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American Journal of Human Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 302. It has a price of 4598 €. It has an SJR impact factor of 6,661 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 6,661.

American Journal of Human Genetics focuses its scope in these topics and keywords: mutations, gene, syndrome, caused, genetic, mitochondrial, disease, association, pigmentosa, prediction, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -


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American Journal of Human Genetics


SJR Impact factor


H Index


Total Docs (Last Year)


Total Docs (3 years)


Total Refs


Total Cites (3 years)


Citable Docs (3 years)


Cites/Doc (2 years)



Aims and Scope

mutations, gene, syndrome, caused, genetic, mitochondrial, disease, association, pigmentosa, prediction, oxidase, identification, variant, variants, xlinked, progressive, neonatalonset, mutation, mental, congenital, disorder, dominant, eastern, ectodermal, encoding, heart, identifies, loci, locus, maps, mecp,

Best articles

A Causative Relationship between Mutant IFNgR1 Alleles and Impaired Cellular Response to IFN gamma in a Compound Heterozygous Child

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A De Novo Mutation (Gln2Stop) at the 5' End of the SRY Gene Leads to Sex Reversal with Partial Ovarian Function

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A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter

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A Presenilin-1 Truncating Mutation Is Present in Two Cases with Autopsy-Confirmed Early-Onset Alzheimer Disease

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A Test Statistic to Detect Errors in Sib-Pair Relationships

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A Tobit Variance-Component Method for Linkage Analysis of Censored Trait Data

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Affected-Sib-Pair Data Can Be Used to Distinguish Two-Locus Heterogeneity from Two-Locus Epistasis

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Atypical Forms of Incontinentia Pigmenti in Male Individuals Result from Mutations of a Cytosine Tract in Exon 10 of NEMO (IKK- gamma)

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CARD15: a Pleiotropic Autoimmune Gene That Confers Susceptibility to Psoriatic Arthritis

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Characterization of 10p Deletions Suggests Two Nonoverlapping Regions Contribute to the DiGeorge Syndrome Phenotype

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Childhood Cancer and Neural Tube Defects

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Comparison of Nonparametric Statistics for Detection of Linkage in Nuclear Families: Single-Marker Evaluation

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Cystic Fibrosis Transmembrane-Conductance Regulator Mutations among African Americans

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D4 Dopamine-Receptor (DRD4) Alleles and Novelty Seeking in Substance-Dependent, Personality-Disorder, and Control Subjects

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David M. Danks, M.D., A.O. (June 4, 1931-July 8, 2003):Founder, Murdoch Childrens Research Institute

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Detection of Gene-Environment Interactions in Joint Segregation and Linkage Analysis

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Determinism and Mass-Media Portrayals of Genetics

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Disruption of Autoregulatory Feedback by a Mutation in a Remote, Ultraconserved PAX6 Enhancer Causes Aniridia

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DNA Variation and Language Affinities

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Dominant Intermediate Charcot-Marie-Tooth Type C Maps to Chromosome 1p34-p35

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Dynamic Interrelationships between DNA Replication, Methylation, and Repair

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Effect of Genetic Heterogeneity and Assortative Mating on Linkage Analysis: A Simulation Study

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Efficient Strategies for Genome Scanning with Affected Sib Pairs

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Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis

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