About the journal
HGG Advances is an open-access journal published by Elsevier in United States, publishing in english. It is listed in DOAJ and MEDLINE and PUBMED according to the sources read. Declared publication charge: 2,640 USD. Declared review time at DOAJ: 23 weeks. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Elsevier
- ISSN
- 2666-2477
- Country
- United States
- Languages
- english
- Access
- Open access
- Declared publication charge
- 2,640 USD
- Articles in DOAJ
- 382
- Declared review time
- 23 weeks
- Declared peer-review model
- peer_review
Index listings
- DOAJ · 2021-03-15
- MEDLINE · 2023-01-01
- PUBMED · 2020-10-22
- Indexing
- DOAJ · MEDLINE · PUBMED
- APC
- 2,640 USD
- Declared review time (DOAJ)
- 23 weeks
- Actual review time (measured)
- 136 days received→accepted — computed from PubMed (n=100)
- Activity (OpenAlex)
- Active — latest works 2026
- PublishLens list status
- Shown after sign-in
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Methodology signals (dated facts from their sources)
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Descriptive metadata from public sources (DOAJ, OpenAlex, PubMed) as of the capture date shown — contains no assessment or judgment.
Articles in DOAJ
382
Most recent article
3 months ago
Average review time (journal-declared via DOAJ)
23weeks
Works in OpenAlex
515
Last recorded publication year
2026
h-index
27
i10-index
120
From OpenAlex open data (CC0).
Editorial & policy12
- Last DOAJ review date
- 2026-04-27
- Added to DOAJ
- 2021-03-15
- Declared plagiarism screening
- Not declared
- Other fees beyond APC
- No
- Declared digital preservation
- CLOCKSSPMCPortico
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Editorial board
- Official page ↗
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 97%
- ORCID iDs in current deposits
- 83%
- Deposits licence metadata at Crossref
- ✓
- APC waiver policy
- View policy
- Peer-review policy
- View policy
Identity & continuity3
- Alternate titles
- Human Genetics and Genomics advances
- Source type
- journal
- NLM unique ID (PubMed)
- 101772885
Classification2
Subjects (DOAJ)
LCC codes
Subject areas
- Genomics and Rare Diseases
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genetic Associations and Epidemiology
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
Show all subjects (50)
- RNA modifications and cancer
- RNA modifications and cancer
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- Congenital heart defects research
- Congenital heart defects research
- Genetic Mapping and Diversity in Plants and Animals
- RNA Research and Splicing
- RNA Research and Splicing
- Genetic Mapping and Diversity in Plants and Animals
- Bioinformatics and Genomic Networks
- Bioinformatics and Genomic Networks
- Genetic factors in colorectal cancer
- Genetic factors in colorectal cancer
- Cancer Genomics and Diagnostics
- RNA and protein synthesis mechanisms
- RNA regulation and disease
- Cancer Genomics and Diagnostics
- RNA and protein synthesis mechanisms
- RNA regulation and disease
- Ethics in Clinical Research
- Ethics in Clinical Research
- Genetic Neurodegenerative Diseases
- Race, Genetics, and Society
- Genetic Neurodegenerative Diseases
- Race, Genetics, and Society
- Genomics and Phylogenetic Studies
- Genetic Syndromes and Imprinting
- Genomics and Phylogenetic Studies
- CRISPR and Genetic Engineering
- Prenatal Screening and Diagnostics
- Genetic Syndromes and Imprinting
- CRISPR and Genetic Engineering
- Mitochondrial Function and Pathology
- Prenatal Screening and Diagnostics
- Genetic and phenotypic traits in livestock
- Connective tissue disorders research
- Mitochondrial Function and Pathology
- Genetic and phenotypic traits in livestock
- Connective tissue disorders research
Keywords (DOAJ)
- human genetics
- rare disease
- genomic variation
- genetic medicine
- genomics
Community confirmations — what users saw in MJL or Scopus Sources; not platform verification and never part of any score.
The journal's record in other sources:Web of Science MJLDOAJ