Xueqiu Jian
Molecular Biology · 2011–2019
A researcher in the Science corpus: 6 papers; trusts 35 researchers and is trusted by 20 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 141 citations into it; #1,841 of 17,773 by trust here, #4,951 by citations
- Genetics — 115 citations into it; #747 of 6,854 by trust here, #1,113 by citations
- Computational Biology & Bioinformatics — 15 citations into it
- Cancer Research — 10 citations into it
Whom Xueqiu Jian trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Kai Wang
- Pauline Crystal Ng
- Yoav Freund
- Gene W. Yeo
- Andy Liaw
- Xiaoming Liu
- Prateek Kumar
- Steven Henikoff
- Mihaela Pertea
- Mingyao Li
Who trusts Xueqiu Jian overall
- Xiaoming Liu
- Xiaoming Liu
- Abhishek Niroula
- B. Feng
- Chunlei Wu
- Chang Li
- Eric Boerwinkle
- Rajarshi Ghosh
- Chang Li
- Xiao-Xia Chang
Papers from Xueqiu Jian's perspective
Ordered by how strongly the researchers Xueqiu Jian trusts endorse each paper. Same corpus, a different order for every researcher.
- The Human Gene Mutation Database: 2008 update
- Detection of nonneutral substitution rates on mammalian phylogenies.
- Predicting the effects of amino acid substitutions on protein function.
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
- dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (Human Mutation)
- Exome sequencing identifies the cause of a Mendelian disorder (Nature Genetics)
- A general framework for estimating the relative pathogenicity of human genetic variants
- dbSNP: the NCBI database of genetic variation
- The UCSC Genome Browser database: extensions and updates 2013 (Nucleic Acids Res.)
- Performance of mutation pathogenicity prediction methods on missense variants (Human Mutation)
Their papers
- dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (2011) — 817 citations
- Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies. (2015) — 1,063 citations
- dbNSFP v2.0: A Database of Human Non-synonymous SNVs and Their Functional Predictions and Annotations (2013) — 625 citations
- In silico prediction of splice-altering single nucleotide variants in the human genome (2014) — 481 citations
- Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (2019) — 2,422 citations
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations