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  1. Investigation of Floating Peat Wetlands, Sacramento–San Joaquin Delta, California

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  2. Feature Cover: Light‐Activated Nucleic Acid Amplification Systems Using Photo‐Caged DNA Polymerase or Primers (Advanced Genetics 2/07)

    Published in Advanced Genetics (2026)
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  3. Light‐Activated Nucleic Acid Amplification Systems Using Photo‐Caged DNA Polymerase or Primers

    Published in Advanced Genetics (2026)
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  4. Locus‐Specific Genetic Associations at the DAOA Gene in Schizophrenia and Bipolar Disorder

    Published in Advanced Genetics (2026)
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  5. Front Cover: PDMSA: A Web‐Based Tool for Pan‐Cancer Survival Analysis Using DNA Methylation Levels as Biomarkers (Advanced Genetics 2/07)

    Published in Advanced Genetics (2026)
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  6. Issue Information: (Advanced Genetics 2/07)

    Published in Advanced Genetics (2026)
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  7. Biomaterial Physical Cues as Gene Regulators for Cellular Agriculture

    Published in Advanced Genetics (2026)
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  8. A Case of Pallister–Killian Syndrome in a Newborn

    Published in Case Reports in Genetics (2026)
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  9. A Case of Nonimmune Hydrops Fetalis With a Duct-Dependent Systemic Circulation and a Novel Mutation of Kabuki Syndrome

    Published in Case Reports in Genetics (2026)
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  10. A Case Highlighting the Importance of Timely Intervention for a Male With AZFb + c Microdeletion

    Published in Case Reports in Genetics (2026)
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  11. Clinical Heterogeneity of a TP53 Variant in a Consanguineous Omani Family: A Case Report Featuring a Homozygous Pathogenic Variant

    Published in Case Reports in Genetics (2026)
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  12. Prolonged Survival With Homozygous Deletion of Exon 9 in Perlman Syndrome: A Case Report

    Published in Case Reports in Genetics (2026)
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  13. Complete Androgen Insensitivity Syndrome (CAIS) Genetic Counseling: Navigating Germline Mosaicism Concerns

    Published in Case Reports in Genetics (2026)
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  14. Camptodactyly and Early-Onset Scoliosis in Snijders Blok–Campeau Syndrome

    Published in Case Reports in Genetics (2026)
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  15. Novel MYH11 Splice Site Variant Causing Exon Skipping in a Family With Thoracic Aortic Aneurysms and Dissections

    Published in Case Reports in Genetics (2026)
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  16. A Rare Case of Concurrent SNRPB Mutation and 22q11.2 Microduplication in a Child With Cerebro-Costo-Mandibular Syndrome

    Published in Case Reports in Genetics (2026)
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  17. Hereditary Myopathy With Early Respiratory Failure Associated With an Incidental COL4A5 Variant: A Case Report

    Published in Case Reports in Genetics (2026)
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