Hannah J Park,Cassidy J Scott,Hadley Stevens Smith et al.
Hannah J Park et al.
Purpose: Social media provides an opportunity for the expression of people with rare conditions and may provide valuable insight into lived experiences to inform genomic care. Our objective was to describe the nature and ...
Association of HFE genotypes with hemochromatosis-related phenotypes in the All of Us research program [0.03%]
All of Us研究计划中与血色素沉着症相关表型的HFE基因型关联分析
Nandana D Rao,Ramal Moonesinghe,Lu Shi et al.
Nandana D Rao et al.
Purpose: Type 1 hereditary hemochromatosis (HH) can result in iron overload and liver disease if not detected and treated early. Most cases are found among people homozygous for HFE p.Cys282Tyr variants. Compound heterozy...
Reclassification of VUS in BRCA1 and BRCA2 using the new BRCA1/ BRCA2 ENIGMA track set demonstrates the superiority of ClinGen ENIGMA Expert Panel specifications over the standard ACMG/AMP classification system [0.03%]
使用新的BRCA1 / BRCA2 ENIGMA轨迹集对BRCA1和BRCA2中的VUS进行重新分类，证明ClinGen ENIGMA专家小组规范优于标准的ACMG / AMP分类系统
Anna Benet-Pagès,Andreas Laner,Luis R Nassar et al.
Anna Benet-Pagès et al.
Purpose: Variants of uncertain significance (VUS) are considered one of the most significant impediments to the translation of genetic test results into precise clinical recommendations. The 2015 American College of Medic...
Lessons learned in migrating from one commercial genetics clinical decision-making tool to another: Assessment of data integrity and utilization [0.03%]
在迁移到另一种商业遗传学临床决策工具时学到的经验教训：数据完整性和使用评估
Calvin Le,Kevin Tatunay,Wayne Liu et al.
Calvin Le et al.
Purpose: Rapid advancements in information technology have greatly influenced clinicians' engagement with patient data for health maintenance. The electronic health record often contains multiple ways to record risk facto...
CFTR haplotype phasing using long-read genome sequencing from ultralow input DNA [0.03%]
使用超低输入DNA的长读基因组测序进行CFTR单倍型排序
Neeru Gandotra,Antariksh Tyagi,Irina Tikhonova et al.
Neeru Gandotra et al.
Purpose: Newborn screening identifies rare diseases that result from the recessive inheritance of pathogenic variants in both copies of a gene. Long-read genome sequencing (LRS) is used for identifying and phasing genomic...
An evaluation of practices and policies used in genetics clinics across the United States to manage referrals for Ehlers-Danlos and hypermobility syndromes [0.03%]
美国遗传诊所用于管理埃勒斯-当洛斯和高关节活动度综合症转诊的实践和政策评估
Lauren Boucher,Berkley Nestler,Daniel Groepper et al.
Lauren Boucher et al.
Purpose: Hypermobile Ehlers-Danlos syndrome (hEDS) and joint hypermobility syndrome (JHS), among other conditions, comprise a collection of heritable disorders of connective tissue. There are recognized challenges in diag...
Genome sequencing enhances the diagnostic yield and expands the genetic landscape of male breast cancer [0.03%]
基因组测序提高诊断率并扩大了男性乳腺癌的遗传图谱范围
Wen Wen,Sen Zhao,Yiwen Jiang et al.
Wen Wen et al.
Purpose: To understand the broader genetic landscape of male breast cancer (MBC), focusing on the utility of genome sequencing (GS) beyond BRCA1/2 (HGNC: 1100, 1101) variants. ...
College of American Pathologists (CAP)/American College of Medical Genetics and Genomics (ACMG) proficiency testing for urinary glycosaminoglycan analysis: A summary of performance [0.03%]
美国病理学家协会（CAP）/医学遗传与基因组学会（ACMG）尿糖胺聚糖分析能力验证：表现概述
Kristina Cusmano-Ozog,Dietrich Matern,Thomas Long et al.
Kristina Cusmano-Ozog et al.
Purpose: Glycosaminoglycans (GAGs) accumulate in patients with mucopolysaccharidoses (MPS), multiple sulfatase deficiency, and mucolipidoses; measurement of total GAGs and the specific excretion pattern by fractionation c...
Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia [0.03%]
SLC13A1双等位基因丢失功能变异导致硫酸盐转运障碍及骨骼异常包括身材矮小、脊柱侧弯和骨骼发育不良等症状
Christina G Tise,Katie Ashton,Lachlan de Hayr et al.
Christina G Tise et al.
Purpose: Sulfate is vital for many physiological processes, including the structural and functional maintenance of macromolecules and formation of sulfur-containing compounds essential for cartilage and bone development. ...
Refining the interpretation of variants of uncertain significance in hereditary cancer screening through integrated RNA sequencing [0.03%]
通过整合RNA测序 refine 肿瘤遗传筛查中意义未明变异的解释
Youbao Sha,J Bryce Ortiz,Sara L Bristow et al.
Youbao Sha et al.
Purpose: Although up to 25% of germline variants are predicted to affect splicing, most are classified as variants of uncertain significance (VUS) because of the limited understanding of their functional consequences. Her...