Categoría: ORIGINAL ARTICLE
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The Genetic Basis of Neurological Disorders: Missense and Nonsense Variants in Three Pakistani Families With Syndromic Intellectual Disability
Annals of Human Genetics, EarlyView.
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CFAP74 Variants Could Cause Male Infertility With the Asthenoteratozoospermia Phenotype
Annals of Human Genetics, EarlyView.
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Genetic Landscape of Pediatric Dyslipidemia in a Turkish Cohort: Insights From a Single‐Center Experience
Annals of Human Genetics, EarlyView.
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Causal Effects of Inflammatory Cytokines on Urethral Stricture Disease: A Bidirectional Mendelian Randomization Study
Annals of Human Genetics, Volume 89, Issue 6, Page 434-445, November 2025.
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Mendelian Randomization Identifies Putative Aging‐Related Causal Genes With Diagnostic Potential in Ulcerative Colitis
Annals of Human Genetics, Volume 89, Issue 6, Page 415-424, November 2025.
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Exploring the Causal Link Between Systemic Lupus Erythematosus and Stroke Risk Through Mendelian Randomization Study
Annals of Human Genetics, Volume 89, Issue 6, Page 407-414, November 2025.
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Novel SPTB Variations Cause Hereditary Spherocytosis With Cholangiolithiasis and Severe Intrahepatic Cholestasis
Annals of Human Genetics, Volume 89, Issue 6, Page 450-458, November 2025.
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Significant Association Among the Epigenetic Alterations in EGFR and ALK Genes and Non–Small Cell Lung Cancer: A Prospective Emerging Molecular Biomarker
Annals of Human Genetics, Volume 89, Issue 6, Page 425-433, November 2025.