ISSN: 0002-9297

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American Journal of Human Genetics Q1 Unclaimed

Cell Press United States

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

American Journal of Human Genetics is a journal indexed in SJR in Genetics and Genetics (clinical) with an H index of 293. It has a price of 4598 €. It has an SJR impact factor of 7,376 and it has a best quartile of Q1. It is published in English.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Genetics (Q1) Genetics (clinical) (Q1) Genetics (clinical) (Q1)

Price

4598 €

Gold OA

-

Green OA

0 €

Non OA

Metrics

7,376

SJR Impact factor

293

H Index

224

Total Docs (Last Year)

638

Total Docs (3 years)

10197

Total Refs

6055

Total Cites (3 years)

553

Citable Docs (3 years)

10,67

Cites/Doc (2 years)

45,52

Ref/Doc

Aims and Scope

Other journals with similar parameters

Genome Biology Q1
Cell Stem Cell Q1
Genome Research Q1
Annual Review of Genetics Q1
Nucleic Acids Research Q1

Best articles

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

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

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

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

A Test Statistic to Detect Errors in Sib-Pair Relationships

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

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

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

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

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

Childhood Cancer and Neural Tube Defects

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

SHOW MORE ARTICLES

Cystic Fibrosis Transmembrane-Conductance Regulator Mutations among African Americans

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

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

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

Determinism and Mass-Media Portrayals of Genetics

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

DNA Variation and Language Affinities

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

Dynamic Interrelationships between DNA Replication, Methylation, and Repair

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

Efficient Strategies for Genome Scanning with Affected Sib Pairs

Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis

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