Journal Report

AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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Journal Information
Journal Title
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Publisher
WILEY
ISSN
1552-4825
E-ISSN
1552-4833
Database
Clarivate
Domain
Health Sciences, Life Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Recurrent Neurodevelopmental Disorder Associated With a Dominant‐Negative <scp> <i>TOP2B</i> H63Y </scp> Variant
Zong Yi Ha, Leticia Dinatto, Kirsten Meagher et al.
2026-10-30
DOI: 10.1002/ajmg.a.70343
Recurrent Reactions to Enzyme Replacement Therapy in Infantile‐Onset Pompe Disease: A Case of Immunologic Barriers to Drug Tolerance
Nikhil A. Crain, Priya Chopra, Michael Q. Sanderson et al.
2026-10-30
DOI: 10.1002/ajmg.a.70349
Microduplication Overlapping <scp> <i>YY1</i> </scp> at 14q32.2 Narrows the Candidate Interval for Cortical Malformation and Early‐Onset Arterial Ischemic Stroke
Michal Bar‐Hakim, Lauren A. Beslow, Ayala Frumkin et al.
2026-10-30
DOI: 10.1002/ajmg.a.70337
A Rare Cause of Intellectual Disability: Novel Mutation of <i>ALKBH8</i> Gene in Two Different Families and Review of the Literature
Ceren Yılmaz Uzman, Semra Gürsoy, Durdugül Ayyıldız Emecen et al.
2026-10-28
DOI: 10.1002/ajmg.a.70341
Characterization of Families Adopting Children With Down Syndrome and Exploratory Associations With Neuropsychiatric Outcomes
Maeve C. Lucas, Stephanie Thompson, Nazek Queder et al.
2026-10-25
DOI: 10.1002/ajmg.a.70322
Genotype–Phenotype Correlations in <scp> <i>KRT17</i> </scp> ‐ <scp>PEDD</scp> : The Critical Role of Codon 88
Hande Nur Cesur Baltacı, Merve Aygün Alizada, Ayşe Boyvat et al.
2026-10-22
DOI: 10.1002/ajmg.a.70336
Brachydactyly Type A2 as A Presenting Feature of <i>NADSYN1</i> ‐Related Congenital NAD Deficiency Disorder
Sonia Lomuscio, Federica Russo, Lucia Micale et al.
2026-10-22
DOI: 10.1002/ajmg.a.70339
Correction to “A Novel Homozygous Splice Variant in the <scp> <i>NUP188</i> </scp> Gene Causing Sandestig‐Stefanova Syndrome in a Saudi Patient”
2026-10-21
DOI: 10.1002/ajmg.a.70326
Meier‐GORLIN Syndrome Caused by Compound Heterozygous <scp> <i>CDC6</i> </scp> Variants
Raquel Neves, Meghan R. Mulligan, Amie Siemonek et al.
2026-10-21
DOI: 10.1002/ajmg.a.70334
Expanding the Genotypic and Phenotypic Spectrum of Li–Campeau Syndrome: A Homozygous Single‐Exon Deletion in <scp>UBR7</scp>
Tarik Duzenli, Damla Yıldız, Gulsum Kayhan et al.
2026-10-19
DOI: 10.1002/ajmg.a.70342
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Printed: November 1, 2026 20:14