Kai Wang
Genetics · Nature · 2007–2011
A researcher in the Science corpus: 11 papers; trusts 13 researchers and is trusted by 9 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 144 citations into it; #1,185 of 6,854 by trust here, #186 by citations
- Molecular Biology — 91 citations into it; #3,756 of 17,773 by trust here, #1,887 by citations
- Immunology — 14 citations into it
Whom Kai Wang trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- C. Dong
- Johan T. den Dunnen
- Phil Hyoun Lee
- Frank Steemers
- Kim D. Pruitt
- V. Ramensky
- Kevin L. Gunderson
- Katherine S. Pollard
- Tong Tong Wu
- Adam C. Siepel
Who trusts Kai Wang overall
- Xiaoming Liu
- Xueqiu Jian
- Hui Yang
- Eric Boerwinkle
- Kai Wang
- Xiao-Xia Chang
- Karen Eilbeck
- A. Young
- Umadevi Paila
- Xiaoming Liu
Papers from Kai Wang's perspective
Ordered by how strongly the researchers Kai Wang trusts endorse each paper. Same corpus, a different order for every researcher.
- BLAT--the BLAST-like alignment tool. (Genome Research)
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
- Fine-scale structural variation of the human genome (Nature Genetics)
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Segmental duplications: organization and impact within the current human genome project assembly. (Genome Research)
- NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins (Nucleic Acids Res.)
- Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes.
- Human non-synonymous SNPs: server and survey. (Nucleic Acids Research)
- Detection of large-scale variation in the human genome (Nature Genetics)
- Detection of nonneutral substitution rates on mammalian phylogenies.
Their papers
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data (2010) — 13,554 citations
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- Analysing biological pathways in genome-wide association studies (2010) — 815 citations
- Rare Variants Create Synthetic Genome-Wide Associations (2010) — 920 citations
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007) — 1,861 citations
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) — 2,780 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
- Meta-Analysis Increases to 71 the Tally of Confirmed Crohn’s Disease Susceptibility Loci (2010) — 2,611 citations
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes (2009) — 1,451 citations
- Common genetic variants on 5p14.1 associate with autism spectrum disorders (2009) — 1,008 citations
- Genotype, haplotype and copy-number variation in worldwide human populations (2008) — 881 citations