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 330. It has a price of 4598 €. It has an SJR impact factor of 4,516 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 4,516.

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


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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 by citations

Localization of a Gene for Migraine without Aura to Chromosome 4q21

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Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia

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

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

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Human Phenylalanine Hydroxylase Mutations and Hyperphenylalaninemia Phenotypes: A Metanalysis of Genotype-Phenotype Correlations

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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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Goosecoid-Like Sequences and the Smallest Region of Deletion Overlap in DiGeorge and Velocardiofacial Syndromes

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The Quantitative LOD Score: Test Statistic and Sample Size for Exclusion and Linkage of Quantitative Traits in Human Sibships

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Reply to Gill

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NCALD Antisense Oligonucleotide Therapy in Addition to Nusinersen further Ameliorates Spinal Muscular Atrophy in Mice

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Paraoxonase-Gene Polymorphisms Associated with Coronary Heart Disease: Support for the Oxidative Damage Hypothesis?

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Familial Multiple-System Tauopathy with Presenile Dementia Is Localized to Chromosome 17

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

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Familial Nontoxic Multinodular Thyroid Goiter Locus Maps to Chromosome 14q but Does Not Account for Familial Nonmedullary Thyroid Cancer

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

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Genetic Heterogeneity of Mannose-Binding Proteins: The Jekyll and Hyde of Innate Immunity?

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Power, Mode of Inheritance, and Type I Error in Lod Scores and Affecteds-Only Methods: Reply to Kruglyak

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

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The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease

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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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Molecular Analysis of the Androgen-Receptor Gene in a Family with Receptor-Positive Partial Androgen Insensitivity: An Unusual Type of Intronic Mutation

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Reply to Little

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Gene Localization for an Autosomal Dominant Familial Periodic Fever to 12p13

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Use of a Quantitative Trait to Map a Locus Associated with Severity of Positive Symptoms in Familial Schizophrenia to Chromosome 6p

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