Academic Journal
Quartile not availableAmerican Journal of Medical Genetics Part A
About American Journal of Medical Genetics Part A
About American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A is a peer-reviewed scholarly journal published by Wiley.
Key indicators: ISSN 15524825, 15524833.
Understanding This Journal's Metrics
Journal metrics help researchers assess fit, but they must be interpreted in context:
Publishing in American Journal of Medical Genetics Part A
When considering this journal, verify its current indexing status, editorial board, and recent publications to ensure it meets your needs for visibility and credibility.
- Author guidelines: Follow formatting, reference style, and article-type requirements exactly — non-compliant manuscripts may be returned without review.
- Submission: Submit via the official journal website.
Is This Journal Right for Your Paper?
- Audience match: Will the journal's readers cite and build on your findings?
- Timeline: Higher-tier journals mean longer review and higher rejection risk. Balance prestige against your schedule.
- Indexing: Confirm indexing in Web of Science, Scopus, and PubMed (if biomedical) meets your institutional requirements.
- Open access needs: Check funder mandates and whether the journal offers compliant OA options.
Frequently Asked Questions
What is the ISSN of American Journal of Medical Genetics Part A?
15524825, 15524833.
Who publishes American Journal of Medical Genetics Part A?
Wiley.
Where do I submit to American Journal of Medical Genetics Part A?
Via the official website.
Is American Journal of Medical Genetics Part A peer-reviewed?
Yes — it is a peer-reviewed scholarly journal indexed in major academic databases.
Journal Metrics
A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
Latest publications matched automatically by ISSN.
Novel Compound Heterozygous ATAD3A Variants in Harel‐Yoon Syndrome With Congenital Cataracts and Dilated Cardiomyopathy
Tingting Wen, Hongyu Chen, Lan Yu, Xianghong Zhang et al.
2026-10-12 · DOI: 10.1002/ajmg.a.70327Table of Contents, Volume 200A, Number 11, November 2026
2026-11 · DOI: 10.1002/ajmg.a.70310TTC21B : From Modifier to Causative Gene in Joubert Syndrome
Valentina Serpieri, Fulvio D'Abrusco, Anna Pichiecchio, Thouraya Ben Younes et al.
2026-10-08 · DOI: 10.1002/ajmg.a.70319The Value of Integrating Adult Genetic Services Into Pregnancy Care: Changing Fetal, Neonatal, and Maternal Management
Madeline J. Dyke, Emily E. Hardisty, Neeta L. Vora, Asha N. Talati et al.
2026-10-08 · DOI: 10.1002/ajmg.a.70329Systematic Review of Females With Intellectual Disability and MECP2 Duplication
Paul Malik, Davut Pehlivan, Cary Fu, Antonio F. Martinez‐Monseny et al.
2026-10-08 · DOI: 10.1002/ajmg.a.70318Height, Head Circumference, Sitting Height, Leg Length, and Body Proportions Growth References to the Argentinian and Spanish Population for Hypochondroplasia
Mariana del Pino, Mercedes León‐López, Sofía Chiaramonte, Silvia Modamio‐Hoybjor et al.
2026-10-07 · DOI: 10.1002/ajmg.a.70325Fracture Prevalence Among Those With Hypermobility Spectrum Disorder/Hypermobile Ehlers‐Danlos Syndrome
Brad T. Tinkle
2026-10-07 · DOI: 10.1002/ajmg.a.70324Correction to “Unraveling a Diagnostic Enigma: A TECPR2 Case Solved Through Multi‐Omic Genomics”
2026-10-06 · DOI: 10.1002/ajmg.a.70312Expanding the Phenotypic Spectrum of TXNDC15 ‐Related Ciliopathies to Include Joubert Syndrome
Zachary T. Sentell, Robert Geraghty, Juliana E. Arcila‐Galvis, Praveen Dhondurao‐Sudhindar et al.
2026-10-05 · DOI: 10.1002/ajmg.a.70317Clinical Spectrum, Genetic Profile, and Genotype–Phenotype Correlations in Microvillus Inclusion Disease: A Systematic Review
Xiang Pan, Zhi‐Jun Mo, Hui Lin, Jing‐Jing Ma et al.
2026-10-05 · DOI: 10.1002/ajmg.a.70314Fatal Dilated Cardiomyopathy and Monogenic Diabetes Mellitus as SMPD4 ‐Related Disorder
Takato Akiba, Shino Shimada, Ken Takahashi, Akimi Ishikawa et al.
2026-10-04 · DOI: 10.1002/ajmg.a.70323Computer‐Aided Facial Analysis and Non‐Coding Variants Detectable by Exome Sequencing Increase Its Diagnostic Yield: Results From the DECIPHERD Study
Daniela Böhme, Víctor Faundes, María Cecilia Poli, Boris Rebolledo‐Jaramillo et al.
2026-10-01 · DOI: 10.1002/ajmg.a.70320Correction to “De Novo 2.2 Mb 19q13.42–q13.43 Microdeletion Encompassing U2AF2 : Support for a Haploinsufficiency Model”
2026-09-29 · DOI: 10.1002/ajmg.a.70311Differential Diagnosis of Mucopolysaccharidoses Types I, II , III , IVA , and VI Through Analysis of Leukocytic Inclusions
Márcio A. W. Melo, Marcelo S. Kertenetzky, Cristina M. Silveira, Maíra M. Ribeiro et al.
2026-09-27 · DOI: 10.1002/ajmg.a.70316Guillouet‐Gordon Syndrome With Severe Microtia in an Infant With a Homozygous Variant in MED16
Sarah E. Seese, Linda M. Reis, Allison Genchanok, Hannah Brodner et al.
2026-09-25 · DOI: 10.1002/ajmg.a.70315A Systematic Review of Positron Emission Tomography ( PET ) in X‐Linked Adrenoleukodystrophy: Beyond Structural MRI
Yutaka Furuta, Hong Li, Stephanie R. Keller, John A. Phillips et al.
2026-09-25 · DOI: 10.1002/ajmg.a.70313A MORC2 Variant Associated With Severe Intellectual Disability and Unusual Phenotype
Harry Wilton‐Clark, Kati Kämpjärvi, Oksana Suchowersky, Shailly Jain‐Ghai et al.
2026-09-24 · DOI: 10.1002/ajmg.a.70307Syndromic Hirschsprung Disease With a Novel De Novo Sense Exonic SVA Insertion of TCF20
Briana O'Leary, Aditya Ramanujan, Aria Belle, Nina B. Gold et al.
2026-09-24 · DOI: 10.1002/ajmg.a.70306Reviews
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Version History
October 10, 2026 at 5:04 pm
October 9, 2026