Journal Report

CLINICAL GENETICS

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Journal Information
Journal Title
CLINICAL GENETICS
Publisher
WILEY
ISSN
0009-9163
E-ISSN
1399-0004
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
Mosaic <i>KRAS</i> Variant as a Cause of Developmental Eye Anomalies in an Individual With <scp>EncephaloCranioCutaneous</scp> Lipomatosis
Karthikah Jeganathan, Fabiola Ceroni, Samuel J. H. Clokie et al.
2026-10-29
DOI: 10.1111/cge.70274
Expanding the Biochemical Phenotype of <scp>ReNU</scp> Syndrome: A Case Report
Irene De Biase, McKall Johnson, Qinwen Mao et al.
2026-10-28
DOI: 10.1111/cge.70272
Novel <i>LOX</i> Start‐Loss Variant Mimicking Arterial Tortuosity Syndrome in Neonatal Cutis Laxa: A Diagnostic Challenge
Pallavi Sinha, Varun Holla, Kishan Singh Rawat et al.
2026-10-27
DOI: 10.1111/cge.70270
Fatal Neonatal <scp>mTORopathy</scp> : Expanding the Phenotypic Spectrum of <i>RRAGC</i> ‐Associated <scp>L</scp> ong– <scp>O</scp> lsen– <scp>D</scp> istelmaier Syndrome
Juliana Lores, Valentina Botia‐Arciniegas, Diana Ramirez‐Montaño et al.
2026-10-25
DOI: 10.1111/cge.70263
Challenges in Gene‐Directed Therapies for Rare Neurodevelopmental Disorders Using <scp>HNRNPU</scp> as an Exemplar
Daniel Aiyedun, Susan F. Rogers, Doaa M. Taha et al.
2026-10-22
DOI: 10.1111/cge.70267
Silent Ears, Failing Heart: Dilated Cardiomyopathy in an Infant With <scp> <i>LARS2</i> </scp> ‐Related Perrault Syndrome Type 4 ( <scp>PRLTS4</scp> )
Faten Ahmad Alkateb, Reham Aljohani, Mohammed S. Alkahmous et al.
2026-10-22
DOI: 10.1111/cge.70268
Clinical Spectrum of Chromosome 15q11–q13 Duplication Syndrome: A Scoping Review of Neurodevelopmental and Multisystem Manifestations
Cortés‐Cruz Jorge Baruch, Cerda‐Mireles Odette Carolina, Sánchez‐Sánchez Luz María et al.
2026-10-22
DOI: 10.1111/cge.70269
Cerebral Ventriculomegaly With Abnormality of the Aqueduct of Sylvius: A Case Series
Romain Nicolle, Laurence Loeuillet, Bettina Bessieres et al.
2026-10-20
DOI: 10.1111/cge.70265
A Familial Case of Thauvin–Robinet–Faivre Syndrome ( <scp>TROFAS</scp> ), Presenting With Postaxial Polydactyly and Upper Lip Vascular Malformation
Federica Ruscitti, Xenia Latypova, Faustine Ageorges et al.
2026-10-18
DOI: 10.1111/cge.70264
Expanding Clinical and Variant Spectrum of <scp> <i>CBX1</i> </scp> ‐Related Syndrome: Report of Three Novel Cases
Graciela Carrillo, Shuhei Fujino, Harrison Higgs et al.
2026-10-13
DOI: 10.1111/cge.70262
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Printed: November 1, 2026 19:35