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Global Medical Genetics|June 16, 2022
Analysis of Genetic Variations in Connexin 26 ( GJB2 ) Gene among Nonsyndromic Hearing Impairment: Familial StudySmita Hegde, Rajat Hegde, Suyamindra S Kulkarni, et al.
Global Medical Genetics|June 16, 2022
Genetic Variants and Drug Efficacy in Tuberculosis: A Step toward Personalized TherapyAlmas Khan, Mohammad Abbas, Sushma Verma, et al.
Global Medical Genetics|June 16, 2022
Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal HypertrophyAyca Kocaaga, Sevgi Yimenicioglu
Global Medical Genetics|December 19, 2022
Advances in Organoid Culture ResearchZhiyuan Xie, Linghao Wang, Yan Zhang
Global Medical Genetics|March 11, 2021
Inconsistency of Karyotyping and Array Comparative Genomic Hybridization (aCGH) in a Mosaic Turner Syndrome CasePinar Tulay, Mahmut Cerkez Ergoren, Ahmet Alkaya, et al.
Global Medical Genetics|July 25, 2022
A New 12q21 Deletion Syndrome: A Case Report and Literature ReviewAlessandra Di Nora, Greta De Costa, Alessia Di Mari, et al.
Global Medical Genetics|April 1, 2025
Significant PK variability of plasma-derived FIX concentrates in chinese children with Haemophilia B: A fixed single-dose study of factor IX-CTBBGuoqing Liu, Di Ai, Gang Li, et al.
Global Medical Genetics|June 18, 2025
Generating a database by calculating the pathogenic variants and allele frequencies detected in hereditary cancers using genomic data: A nation studyManal Salah Babiker Ali, Polat Olgun, Ömer Diker, et al.
Global Medical Genetics|February 9, 2026
Mediating role of the weight-adjusted-waist index in the association between sedentary behavior and depression: A cross-sectional studyXinxuan Lyu, Wei Jin, Zhaoshun Lyu, et al.
Global Medical Genetics|February 3, 2026
Genetic link between metabolic syndrome and coronary artery disease: Insights from genome-wide cross-trait analysisPengcheng Yi, Quanting Yin, Huanhuan Zhang, et al.
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