Journal Report

MOLECULAR SYNDROMOLOGY

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Journal Information
Journal Title
MOLECULAR SYNDROMOLOGY
Publisher
KARGER
ISSN
1661-8769
E-ISSN
1661-8777
Database
Clarivate
Domain
Health Sciences, Life Sciences, Physical Sciences, Social 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
Dual Molecular Diagnosis of CLP1-Related Pontocerebellar Hypoplasia Type 10 and Cystic Fibrosis in a Child: A Case Report
Ayse Büsra Pekal, Süheyl Önal, melike gümüs çoban et al.
2026-10-22
DOI: 10.1159/msy/adrag031
Large 7q21 Deletion Associated With SHFM1, Bilateral Cochlear Nerve Hypoplasia, and Severe Proportionate Short Stature: A Case Report
Irem Gokdemir, Gonul Buyukyilmaz, Duygu Deligozoglu et al.
2026-10-22
DOI: 10.1159/msy/adrag030
Implementation of a Multi-Tiered Missense Predictor Pipeline for Variant Prioritization in Sleep-Related Hypermotor Epilepsy
Elsa Morina, Nihan Bilge Satkin
2026-10-12
DOI: 10.1159/msy/adrag029
Sifrim-Hitz-Weiss Syndrome Caused by a Novel De Novo Nonsense Variant in CHD4: A Case Report
Damla Eker, Cisem Mail, Veysel Öz et al.
2026-10-10
DOI: 10.1159/msy/adrag025
Obesity as an Underrecognized Feature of White–Sutton Syndrome: A POGZ-Related Case Report
Sirmen Kizilcan Çetin, Elif Kelestemur, Safak Demirtas et al.
2026-10-10
DOI: 10.1159/msy/adrag028
Case Reports for Copy Number Variations in Pediatric Non-Syndromic Obesity: New Insights From 2 Patients With MC4R Deletions
André Weber, Rainer Wimmer, Sophie Engfer et al.
2026-10-10 Pages 1-1
DOI: 10.1159/msy/adrag026
Targeted Long-Read Sequencing Identifies Myotonic Dystrophy Type 1 in a Mildly Affected Elderly Patient with Negative Southern Blot Analysis: A Case Report
Juhee Chae, Jaehyeon Lee, Joonhong Park
2026-10-10
DOI: 10.1159/msy/adrag027
Molecularly Confirmed Dual Diagnosis of Sotos and Tenorio Syndromes in a Father and Son: A case report
Jair Tenorio-Castano, Sofia Catena, Angelica Kapely et al.
2026-10-7
DOI: 10.1159/msy/adrag015
Clinical, Biochemical, and Neuroimaging Characteristics of Glutaric Aciduria Type I, L-2-Hydroxyglutaric Aciduria, and Canavan Disease in Childhood
Burcu Koseci, Merve Yoldas Celik, Ezgi Burgac et al.
2026-10-5
DOI: 10.1159/msy/adrag024
Usher Syndrome Type 2A and Epileptic Encephalopathy with Spike-Wave Activation in Sleep: A Coincidental Dual Diagnosis? Case Report
Hande Gazeteci Tekin, Fatma Kuşgöz, Tayfun Cinleti et al.
2026-9-30 Pages 1-1
DOI: 10.1159/msy/adrag009
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Printed: November 4, 2026 04:25