verified SJR 4,531 · Q1 • database Scopus / SJR & Web of Science indexed

United States · Cell Press

workspace_premium Q1 — Genetics lock_open Open Access Unclaimed

American Journal of Human Genetics

American Journal of Human Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 339. It has a price of 4598 €. It has an SJR impact factor of 4,531 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 4,531.

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

ISSN: 0002-9297

Editorial: Cell Press

Category: Genetics

Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

open_in_new Portal NPD menu_book Guidelines NPD

schedule Datos CoP · solo campos en BD

SJR Impact Factor trending_up

4,531 Q1

H-index 339

Tasa de Aceptación pie_chart

17% Selectiva

Fuente Acceptance_Rate

Tiempo a publicación hourglass_top

NPD

Campo Sin dato

Coste de Publicación (APC) payments

4.598 € Open Access

Ruta Non-OA 0 €

Metrics

Campos Scimago / CoP — sin series inventadas

Scopus / SJR Web of Science

SJR Impact

4,531

H-index

339

Docs (year)

197

Docs 3y

522

Total refs

11618

Cites 3y

4223

Citable 3y

493

Cites/Doc 2y

7.17

Ref/Doc

58.97

Immediate OA

4598 €

Embargoed OA

0 €

Non OA / Submission

0 €

shield Researcher voice

Name good journals. Call out predatory ones.

Share what peer review, fees, and timelines were really like. Praise fair editors. Flag APC traps, fake metrics, or spam solicitations — with facts from your submission.

Fair & fast peer review Clear APC / no surprise fees Suspected predatory Fake impact claims

rate_review Write an honest review

Researcher reviews

sentiment_dissatisfied No reviews yet — be the first to share an honest experience.

Publication speed *

Review quality *

Edition and editorial team *

Institutional email or ORCID * * Only to validate authenticity — identity is not shown publicly.

Best articles by citations

Cystic Fibrosis Transmembrane-Conductance Regulator Mutations among African Americans

Why Boys Will Be Boys: Two Pathways of Fetal Testicular Androgen Biosynthesis Are Needed for Male Sexual Differentiation

Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis

Efficient Strategies for Genome Scanning with Affected Sib Pairs

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

Dynamic Interrelationships between DNA Replication, Methylation, and Repair

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

DNA Variation and Language Affinities

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

Determinism and Mass-Media Portrayals of Genetics

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

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

SHOW MORE ARTICLES

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

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

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

Childhood Cancer and Neural Tube Defects

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

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

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

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

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

A Test Statistic to Detect Errors in Sib-Pair Relationships

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

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

FAQS

In Country of Papers you can find SJR impact factor and other metrics to help you decide on a Journal.