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Journal of Hospital Medicine|November 11, 2025
Low-value care and variation in practice in the care of children hospitalized with bronchiolitis in Canada (CareBEST): Protocol for a multi-center prospective cohort studyBranden Bonham, Tamara Perez, Michelle Bailey, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
<i>FRMPD4</i> , a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing lossDaniel Liedtke, Kristen Rak, Katrina M Schrode, et al.
Ebiomedicine|October 12, 2020
A CRISPR-Cas12a-based specific enhancer for more sensitive detection of SARS-CoV-2 infectionWeiren Huang, Lei Yu, Donghua Wen, et al.
Clinical Genetics|July 23, 2019
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration systemJia Rao, Xiaorong Liu, Jianhua Mao, et al.
Phenomics (Cham, Switzerland)|March 20, 2023
Genetic Architecture of Childhood Kidney and Urological Diseases in ChinaYe Fang, Hua Shi, Tianchao Xiang, et al.
The Lancet. Respiratory Medicine|December 2, 2023
Low-dose CT screening among never-smokers with or without a family history of lung cancer in Taiwan: a prospective cohort studyGee-Chen Chang, Chao-Hua Chiu, Chong-Jen Yu, et al.
The Journal of Clinical Investigation|July 3, 2019
Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapyJason D Roberts, Nathaniel P Murphy, Robert M Hamilton, et al.
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