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Molecular Genetics & Genomic Medicine|October 23, 2019
Effects of early trauma and corticotropin-releasing factor receptor 1 gene polymorphism on adult visual spatial memoryFei-Fei Sun, Ran Wang, Na Li, et al.
Molecular Genetics & Genomic Medicine|April 25, 2020
CASC15 polymorphisms are correlated with cervical cancer susceptibility in Chinese womenZiying Gao, Zichao Xiong, Yao Sun, et al.
Molecular Genetics & Genomic Medicine|April 25, 2020
Two novel deleterious variants of Angiotensin-I-converting Enzyme gene identified in a family with recurrent anhydramniosJingwei Wang, Qiao Bin, Biheng Cheng, et al.
Molecular Genetics & Genomic Medicine|April 25, 2020
Clinical performance of DNA-based prenatal screening using single-nucleotide polymorphisms approach in Thai women with singleton pregnancyTachjaree Panchalee, Naravat Poungvarin, Warisa Amornrit, et al.
Molecular Genetics & Genomic Medicine|April 25, 2020
Failure to follow up on a medically actionable finding from direct to consumer genetic testing: A case reportRamin Garmany, Christopher J Lee, Richard R Sharp, et al.
Molecular Genetics & Genomic Medicine|April 25, 2020
A novel homozygous nonsense ZP1 variant causes human female infertility associated with empty follicle syndrome (EFS)Qianhua Xu, Xiaoli Zhu, Madiha Maqsood, et al.
Molecular Genetics & Genomic Medicine|April 22, 2020
A novel PCDH19 missense mutation, c.812G>A (p.Gly271Asp), identified using whole-exome sequencing in a Chinese family with epilepsy female restricted mental retardation syndromeXuechao Zhao, Yanhong Wang, Shiyue Mei, et al.
Molecular Genetics & Genomic Medicine|September 7, 2021
Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing dataGerman Demidov, Joohyun Park, Sorin Armeanu-Ebinger, et al.
Molecular Genetics & Genomic Medicine|September 19, 2025
Frequency and Spectrum of Actionable Secondary Findings in the Maltese PopulationLaura Grech, Celine Ann Grech, Jasmine Spiteri, et al.
Molecular Genetics & Genomic Medicine|September 23, 2025
Genetic Analysis of Familial Developmental Dysplasia of the Hip Associated With a Heterozygous Variant in the COMP Gene: A Case ReportYan Miao, Jiashan Li, Siying Liang, et al.
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