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
Incidence and Cancer Morbidity of Xeroderma Pigmentosum: A Swedish Population‐Based Register Study
Theofanis Zagoras, Roope A. Kallionpää, Sam Polesie et al.
2026-11-11
DOI: 10.1002/ajmg.a.70359
Comb‐Like <scp>EEG</scp> Pattern as an Early Diagnostic Clue in Maple Syrup Urine Disease ( <scp>MSUD</scp> ): A Systematic Review
Yutaka Furuta, Mingyu Li, Guojun Zhang et al.
2026-11-10
DOI: 10.1002/ajmg.a.70355
A Unique Case of <scp>PPP1R12A</scp> ‐Related Urogenital and Brain Malformation Syndrome Phenotypically Overlapping With <scp>VACTERL</scp> Association, With Additional Literature Review of Previously Described Phenotypes
Elliot Horn, Mindy Kolodziejski, Evangelia Kalaitzoglou et al.
2026-11-9
DOI: 10.1002/ajmg.a.70340
Diverse Phenotypic Consequences of the Differential Splicing of <i>FLNA</i> Intronic Variants
David J. Bunyan, Nicola Foulds, Gabriela Jones et al.
2026-11-5
DOI: 10.1002/ajmg.a.70353
Neurodevelopmental Regression in <scp>SMG9</scp> ‐Related Heart and Brain Syndrome
Alan David, Kym Boycott, Gabrielle Lemire et al.
2026-11-5
DOI: 10.1002/ajmg.a.70350
From Cognitive Processing to Daily Functioning: Language, Visuomotor Integration, and Adaptive Behavior in Children With Coffin‐Siris Syndrome
Myrthe R. M. Kamphof, Sophie van Rijn, Gijs W. E. Santen et al.
2026-11-5
DOI: 10.1002/ajmg.a.70347
Associations of Attention‐Deficit/Hyperactivity Disorder Symptoms With Quality of Life and Real‐Life Functioning in Adults With Neurofibromatosis Type 1: A Nationwide Questionnaire Study in Denmark
Cecilie Ejerskov, Jens R. M. Jepsen, Anja Krøyer et al.
2026-11-5
DOI: 10.1002/ajmg.a.70356
Atypical X‐Linked Severe Combined Immunodeficiency in a Patient With Early‐Onset Inflammatory Bowel Disease
Agustina Fainguersch, Jennah Foltz, Theodore E. Wilson et al.
2026-11-2
DOI: 10.1002/ajmg.a.70352
Table of Contents, Volume 200A, Number 12, December 2026
2026-11-2 Vol. 200 Issue 12 Pages 2597-2600
DOI: 10.1002/ajmg.a.70345
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
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Printed: November 12, 2026 11:51