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Qi Ni
Qi Ni
Boston Children's Hospital
Genetics
Biology
Medicine
Gene
Neonatal intensive care unit
4
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17
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An automatic diagnostic system for pediatric genetic disorders developed by linking genotype and phenotype information
2021
medRxiv
Xinran Dong
Bingbing Wu
Huijun Wang
Lin Yang
Xiang Chen
Qi Ni
Yaqiong Wang
Bo Liu
Yulan Lu
Wenhao Zhou
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Apparent homozygosity for a novel splicing variant in EPS8 causes congenital profound hearing loss.
2021
European Journal of Medical Genetics
Sha Yu
Wen-xia Chen
Yun-Fei Zhang
Yihua Ni
Ping Lu
Bin Wang
Yan Wang
Bingbing Wu
Qi Ni
Huijun Wang
Zheng-min Xu
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Overdosage of HNF1B Gene Associated With Annular Pancreas Detected in Neonate Patients With 17q12 Duplication
2021
Frontiers in Genetics
Feifan Xiao
Xiuyun Liu
Yulan Lu
Bingbing Wu
Renchao Liu
Bo Liu
Kai Yan
Huiyao Chen
Guoqiang Cheng
Laishuan Wang
Qi Ni
Gang Li
Ping Zhang
Xiaomin Peng
Yun Cao
Chun Shen
Huijun Wang
Wenhao Zhou
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Optimized trio genome sequencing (OTGS) as a first-tier genetic test in critically ill infants: practice in China
2020
Human Genetics
Huijun Wang
Yulan Lu
Xinran Dong
Guoping Lu
Guoqiang Cheng
Yanyan Qian
Qi Ni
Ping Zhang
Lin Yang
Bingbing Wu
Wenhao Zhou
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Citations (17)
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