About the journal
American Journal of Medical Genetics Part A is a journal published by Wiley in United States. It is listed in MEDLINE and PUBMED according to the sources read. Facts are reproduced as recorded at their sources with their capture dates; PublishLens indicators are available after sign-in.
Basic facts
- Publisher
- Wiley
- ISSN
- 1552-4825 · 1552-4833
- Country
- United States
- Access
- Not open access / not declared
- Declared peer-review model
- peer_review
- Official website
- https://onlinelibrary.wiley.com/journal/15524833
Index listings
- MEDLINE · 2003-01-01
- PUBMED · 2003-01-01
- Indexing
- MEDLINE · PUBMED
- APC
- —
- Declared review time (DOAJ)
- —
- Actual review time (measured)
- 128 days received→accepted — computed from PubMed (n=98)
- 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.
Works in OpenAlex
13211
Last recorded publication year
2026
h-index
162
i10-index
7027
From OpenAlex open data (CC0).
Editorial & policy5
- Observed digital preservation (Keepers registry)— snapshot 2026-10-05
- CLOCKSSPortico
- Norwegian register (HK-dir)— 2026
- Level 1 — approved scholarly channel
- Open references deposited at Crossref
- 90%
- ORCID iDs in current deposits
- 83%
- Enrolled in Crossref Similarity Check
- ✓
- Deposits licence metadata at Crossref
- ✓
Identity & continuity2
- Source type
- journal
- NLM unique ID (PubMed)
- 101235741
Classification(no data)
No data available to the platform for this group
No platform data for: Classification — absence is not a judgment about the journal.
Subject areas
- Genomic variations and chromosomal abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetics and Neurodevelopmental Disorders
- Prenatal Screening and Diagnostics
- Prenatal Screening and Diagnostics
- Genomics and Rare Diseases
- Genomics and Rare Diseases
Show all subjects (50)
- Congenital heart defects research
- Congenital heart defects research
- Connective tissue disorders research
- Connective tissue disorders research
- Genetic Syndromes and Imprinting
- Genetic Syndromes and Imprinting
- RNA modifications and cancer
- RNA modifications and cancer
- Congenital Ear and Nasal Anomalies
- Congenital Ear and Nasal Anomalies
- Chromosomal and Genetic Variations
- Chromosomal and Genetic Variations
- Craniofacial Disorders and Treatments
- Craniofacial Disorders and Treatments
- Hedgehog Signaling Pathway Studies
- Hedgehog Signaling Pathway Studies
- Cleft Lip and Palate Research
- Cleft Lip and Palate Research
- Epigenetics and DNA Methylation
- Epigenetics and DNA Methylation
- RNA regulation and disease
- RNA regulation and disease
- Neurogenetic and Muscular Disorders Research
- Neurogenetic and Muscular Disorders Research
- Congenital limb and hand anomalies
- Congenital limb and hand anomalies
- Fetal and Pediatric Neurological Disorders
- Fetal and Pediatric Neurological Disorders
- BRCA gene mutations in cancer
- BRCA gene mutations in cancer
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Protein Tyrosine Phosphatases
- Protein Tyrosine Phosphatases
- Congenital Anomalies and Fetal Surgery
- Congenital Anomalies and Fetal Surgery
- Metabolism and Genetic Disorders
- Metabolism and Genetic Disorders
- Autism Spectrum Disorder Research
- Autism Spectrum Disorder Research
- Genomics and Chromatin Dynamics
- Genomics and Chromatin Dynamics
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