User profiles for X Jian

Xian Jian

- Verified email at uestc.edu.cn - Cited by 4356

Xing Jian

- Verified email at wustl.edu - Cited by 2637

Electrocatalytic hydrogen evolution under neutral pH conditions: current understandings, recent advances, and future prospects

Z Zhou, Z Pei, L Wei, S Zhao, X Jian… - Energy & Environmental …, 2020 - pubs.rsc.org
… CoP x was further extended to synthesize Mo phosphides (MoP x )… x electrodes have a
similar local structure as that of CoP x . However, MoP x displayed higher HER activity than CoP x

[HTML][HTML] In silico tools for splicing defect prediction: a survey from the viewpoint of end users

X Jian, E Boerwinkle, X Liu - Genetics in Medicine, 2014 - nature.com
… Xueqiu Jian MPH … Xueqiu Jian MPH … & Liu, X. In silico tools for splicing defect
prediction: a survey from the viewpoint of end users. Genet Med 16, 497–503 (2014). …

Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

…, AV Smith, L Qu, D Bacq, N Denning, X Jian… - Nature …, 2019 - nature.com
Risk for late-onset Alzheimer’s disease (LOAD), the most prevalent dementia, is partially
driven by genetics. To identify LOAD risk loci, we performed a large genome-wide association …

Selective chemical labeling reveals the genome-wide distribution of 5-hydroxymethylcytosine

…, C Yi, X Li, Y Li, CH Chen, W Zhang, X Jian… - Nature …, 2011 - nature.com
In contrast to 5-methylcytosine (5-mC), which has been studied extensively 1 , 2 , 3 , little is
known about 5-hydroxymethylcytosine (5-hmC), a recently identified epigenetic modification …

Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies

C Dong, P Wei, X Jian, R Gibbs… - Human molecular …, 2015 - academic.oup.com
Accurate deleteriousness prediction for nonsynonymous variants is crucial for distinguishing
pathogenic mutations from background polymorphisms in whole exome sequencing (WES) …

dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions

X Liu, X Jian, E Boerwinkle - Human mutation, 2011 - Wiley Online Library
With the advance of sequencing technologies, whole exome sequencing has increasingly
been used to identify mutations that cause human diseases, especially rare Mendelian …

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

…, HI Hyacinth, MA Ikram, E Ingelsson, MR Irvin, X Jian… - Nature …, 2018 - nature.com
Stroke has multiple etiologies, but the underlying genes and pathways are largely unknown.
We conducted a multiancestry genome-wide-association meta-analysis in 521,612 …

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

…, P Whitehead, L Fratiglioni, C Medway, X Jian… - Nature …, 2017 - nature.com
We identified rare coding variants associated with Alzheimer's disease in a three-stage case–control
study of 85,133 subjects. In stage 1, we genotyped 34,174 samples using a whole-…

dbNSFP v2. 0: a database of human non‐synonymous SNVs and their functional predictions and annotations

X Liu, X Jian, E Boerwinkle - Human mutation, 2013 - Wiley Online Library
dbNSFP is a database developed for functional prediction and annotation of all potential
non‐synonymous single‐nucleotide variants (nsSNVs) in the human genome. This database …

Effect of power ultrasound on solidification of aluminum A356 alloy

X Jian, H Xu, TT Meek, Q Han - Materials letters, 2005 - Elsevier
The present investigation attempted to evaluate the effect of ultrasonic vibration on the
nucleation and growth of aluminum alloy A356 melt. A356 melt was treated at various solid …