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A novel embryo biopsy morphological analysis and genetic integrality criterion system significantly improves the outcome of preimplantation genetic testing
PurposeWhile efforts have been made to establish blastocyst grading systems in the past decades, little research has examined the quality of biopsy...
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Genetic susceptibility of urolithiasis: comprehensive results from genome-wide analysis
BackgroundThe pathogenesis of urolithiasis is multi-factorial and genetic factors have been shown to play a significant role in the development of...
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Genetic influence of meningioma on cisplatin resistance: a Mendelian randomization analysis
BackgroundAlthough various aspects of cisplatin resistance have been studied, the impact of genetic variations still needs to be explored.
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Genetic and histological analysis intraplacental choriocarcinoma: a case report
We report on single case of intraplacental choriocarcinoma (IC) coexisting with feto-maternal hemorrhage from our hospital, a rare malignant tumor...
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The genetic epidemiology of obsessive-compulsive disorder: a systematic review and meta-analysis
The first systematic review and meta-analysis of obsessive-compulsive disorder (OCD) genetic epidemiology was published approximately 20 years ago....
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Postnatal genetic umbilical cord analysis for earliest possible detection of inherited hearing impairment
IntroductionThe most common sensorineural disorder in humans is hearing impairment and approximately 60% of prelingual hearing disorders are genetic....
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Clinical features and genetic analysis of Dandy-Walker syndrome
BackgroundDandy-Walker syndrome (DWS) is a rare congenital malformation of the central nervous system (CNS), characterized by underdevelopment or...
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Genetic and observational associations of lung function with gastrointestinal tract diseases: pleiotropic and mendelian randomization analysis
BackgroundThe two-way communications along the gut-lung axis influence the immune function in both gut and lung. However, the shared genetic...
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Clinicopathological analysis of thyroid carcinomas with the RET and NTRK fusion genes: characterization for genetic analysis
Thyroid carcinomas exhibit various genetic alterations, including the RET and NTRK fusion genes that are targets for molecular therapies. Thus,...
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Phylogenetically evolutionary analysis provides insights into the genetic diversity and adaptive evolution of porcine deltacoronavirus
BackgroundPorcine deltacoronavirus (PDCoV) is one of the emerging swine enteric coronaviruses (SECoVs), which has been widely prevalent in the North...
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Pancreatic Cyst Fluid Assessment: Updates in Genetic Analysis and Risk for Progression
Purpose of ReviewGiven some pancreatic cysts require surveillance due to established malignant potential, efforts are being made to develop precise...
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Clinical and genetic analysis of methylmalonic aciduria in 60 patients from Southern China: a single center retrospective study
BackgroundMethylmalonic aciduria (MMA) is a group of rare genetic metabolic disorders resulting from defects in methylmalonyl coenzyme A mutase (MCM)...
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Genetic etiology of agenesis of the corpus callosum: a retrospective single-center cohort analysis of 114 fetuses
PurposeThe identification and prognosis of the agenesis of the corpus callosum (ACC) for prenatal consultation are complex and currently unclear....
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A meta-analysis and review on genetic map** of type 2 diabetes mellitus in Iraq
BackgroundThe prevalence of type 2 diabetes mellitus (T2DM) has been increasing rapidly in Iraq over the past few decades. Identifying the most...
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Polygenic Risk Score-Based Association Analysis Identifies Genetic Comorbidities Associated with Age-Related Hearing Difficulty in Two Independent Samples
PurposeAge-related hearing loss is the most common form of permanent hearing loss that is associated with various health traits, including...
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Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients
BackgroundPrimary periodic paralysis (PPP) is an inherited disorders of ion channel dysfunction characterized by recurrent episodes of flaccid muscle...
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Genetic analysis for mucinous ovarian carcinoma with infiltrative and expansile invasion and mucinous borderline tumor: a retrospective analysis
BackgroundMucinous carcinoma (MC) is a histological subtype of ovarian cancer that has a worse prognosis at advanced stages than the most prevalent...
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Post-mortem genetic analysis of sudden unexplained death in a young cohort: a whole-exome sequencing study
Sudden unexplained death (SUD) constitutes a considerable portion of unexpected sudden death in the young. Molecular autopsy has proved to be an...
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Genetic analysis of familial predisposition in the pathogenesis of malignant pleural mesothelioma
PurposeMesothelioma is the primary tumor of the mesothelial cell membrane. The most important etiology is asbestos exposure. The development of...
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Bayesian cost-effectiveness analysis of Whole genome sequencing versus Whole exome sequencing in a pediatric population with suspected genetic disorders
Genetic diseases are medical conditions caused by sequence or structural changes in an individual’s genome. Whole exome sequencing (WES) and whole...
