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American Journal of Human Genetics (AJHG)

Publisher :

Cell Press

Scopus Profile
Peer reviewed only
Scopus Profile
Open Access
  • Medicine
  • Genetics
  • Biochemistry
e-ISSN :

1537-6605

Issue Frequency :

Monthly

Impact Factor :

8.1

p-ISSN :

0002-9297

Est. Year :

1949

Mobile :

6173972800

Country :

United States

Language :

English

APC :

YES

Impact Factor Assignee :

Google Scholar

Email :

JournalCustomerService-usa@elsevier.com

Journal Descriptions

AJHG provides a record of research and review relating to heredity in humans and to the application of genetic principles in medicine and public policy, as well as in related areas of molecular and cell biology. Topics explored by AJHG include behavioral genetics, biochemical genetics, clinical genetics, cytogenetics, dysmorphology, gene therapy, genetic counseling, genetic epidemiology, genomics, immunogenetics, molecular genetics, neurogenetics, and population genetics. AJHG welcomes submissions of articles and reports on timely subjects concerning all aspects of human genetics, including studies of model organisms that are of direct relevance to human genetics. Manuscripts should be written in a manner accessible to investigators representing diverse backgrounds in human genetics. Descriptions of new statistical methods of general interest to the genetics community are welcome. New methods should be compared to existing methods with the use of real data and/or simulations with parameters (e.g., haplotype frequencies, effect sizes) that are based on a real data example (e.g., marker or haplotype data from the HapMap project). All novel computer programs must be made publicly available by the time that the manuscript is published, and a URL for the website must be included in the Web Resources section of the manuscript. Letters commenting on material previously published in AJHG are also welcome. AJHG does not publish reports of either single mutations or mutational surveys of previously identified loci unless they have unusual significance and substantial insight. Descriptions of new linkage assignments will be considered only if they are of special interest. Reports of negative data will not normally be considered.


American Journal of Human Genetics (AJHG) is :

International, Peer-Reviewed, Open Access, Refereed, Medicine, Genetics, Biochemistry , Online or Print, Monthly Journal

UGC Approved, ISSN Approved: P-ISSN - 0002-9297, E-ISSN - 1537-6605, Established in - 1949, Impact Factor - 8.1

Not Provide Crossref DOI

Indexed in Scopus, PubMed

Not indexed in WoS, DOAJ, UGC CARE

Indexing

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Scopus
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PubMed
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Elsevier

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Publications of AJHG

  • dott image June, 2017

Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

Deep sequence-based imputation can enhance the discovery power of genome-wide association studies by assessing previously unexplored variation across the common- and low-frequency spectra. W...

  • dott image January, 2003

Association between the Severity of Angiographic Coronary Artery Disease and Paraoxonase Gene Polymorphisms in the National Heart, Lung, and Blood Ins...

Paraoxonase (PON), a high-density lipoprotein–associated enzyme, is believed to protect against low-density lipoprotein oxidation and thus affects the risk of coronary artery disease (CAD)...

  • dott image November, 2018

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

Inflammation plays a key role in the development of complex diseases, such as cardiovascular disease,1 type 2 diabetes,2 Alzheimer disease,3 and schizophrenia.4 C-reactive protein (CRP) is a...

  • dott image Zhong Zheng
  • dott image February, 2014

Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

Elevated low-density lipoprotein cholesterol (LDL-C) is a treatable, heritable risk factor for cardiovascular disease. Genome-wide association studies (GWASs) have identified 157 variants as...

  • dott image September, 2012

Burden of Rare Sarcomere Gene Variants in the Framingham and Jackson Heart Study Cohorts

Rare sarcomere protein variants cause dominant hypertrophic and dilated cardiomyopathies. To evaluate whether allelic variants in eight sarcomere genes are associated with cardiac morphology...

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