# Kai Wang

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/kai-wang-2/

## Facts

| Field | Value |
| --- | --- |
| Citations | 221,275 |
| Field | Cancer Genomics and Diagnostics |
| h-index | 173 |
| i10-index | 3,017 |
| Last Known Institution | Qingdao University |
| OpenAlex ID | https://openalex.org/A5100437036 |
| ORCID iD | 0000-0002-6170-4744 |
| Works | 7,187 |

## Researcher papers

Showing 12 of 21.

- [ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data](https://scholariq.org/papers/annovar-functional-annotation-of-genetic-variants-from-high-throughput/)
- [Circular RNAs are abundant, conserved, and associated with ALU repeats](https://scholariq.org/papers/circular-rnas-are-abundant-conserved-and-associated-with-alu-repeats/)
- [Pembrolizumab versus chemotherapy for previously untreated, PD-L1-expressing, locally advanced or metastatic non-small-cell lung cancer (KEYNOTE-042): a randomised, open-label, controlled, phase 3 trial](https://scholariq.org/papers/pembrolizumab-versus-chemotherapy-for-previously-untreated-pd-l1-expressing/)
- [Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis](https://scholariq.org/papers/genetic-risk-and-a-primary-role-for-cell-mediated-immune-mechanisms-in-multiple/)
- [The MicroRNA Spectrum in 12 Body Fluids](https://scholariq.org/papers/the-microrna-spectrum-in-12-body-fluids/)
- [Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus](https://scholariq.org/papers/candidate-gene-for-the-chromosome-1-familial-alzheimer-s-disease-locus/)
- [Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing](https://scholariq.org/papers/development-and-validation-of-a-clinical-cancer-genomic-profiling-test-based-on/)
- [Functional impact of global rare copy number variation in autism spectrum disorders](https://scholariq.org/papers/functional-impact-of-global-rare-copy-number-variation-in-autism-spectrum/)
- [PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data](https://scholariq.org/papers/penncnv-an-integrated-hidden-markov-model-designed-for-high-resolution-copy/)
- [Autism genome-wide copy number variation reveals ubiquitin and neuronal genes](https://scholariq.org/papers/autism-genome-wide-copy-number-variation-reveals-ubiquitin-and-neuronal-genes/)
- [Common genetic variants on 5p14.1 associate with autism spectrum disorders](https://scholariq.org/papers/common-genetic-variants-on-5p14-1-associate-with-autism-spectrum-disorders/)
- [Reduced default mode network functional connectivity in patients with recurrent major depressive disorder](https://scholariq.org/papers/reduced-default-mode-network-functional-connectivity-in-patients-with-recurrent/)

## Researcher topics

- [Cancer Genomics and Diagnostics](https://scholariq.org/topics/cancer-genomics-and-diagnostics/)
- [Cancer-related molecular mechanisms research](https://scholariq.org/topics/cancer-related-molecular-mechanisms-research/)
- [Crystallization and Solubility Studies](https://scholariq.org/topics/crystallization-and-solubility-studies/)
- [Functional Brain Connectivity Studies](https://scholariq.org/topics/functional-brain-connectivity-studies/)
- [X-ray Diffraction in Crystallography](https://scholariq.org/topics/x-ray-diffraction-in-crystallography/)

## Researcher university

- [Qingdao University](https://scholariq.org/institutions/qingdao-university/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.