ResearcherThe University of Texas MD Anderson Cancer CenterNo recent work listed

Yao Yu

ORCID-verified (high confidence, 0.95), identity_conf@1As of 8 November 2026

Matched on ORCID iD 0000-0002-2727-1746; OpenAlex author ID A5083562088. Sources: OpenAlex.

Their work

Papers: 1
Trials: 0
Grants: 0
Labs led: 0
Collaborators: 8

Papers, trials and grants by year

2022: 1 paper

Papers 1

A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic cancer risk. Co-author DOI 10.1016/j.xhgg.2021.100078 ↗

Closest collaborators

The 8 strongest of 8 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.

Chad Daniel Huff · 1 shared paper, 2022 · strength 0.12
- Paper A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic ca… DOI 10.1016/j.xhgg.2021.100078 ↗
Paul A Scheet · 1 shared paper, 2022 · strength 0.12
- Paper A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic ca… DOI 10.1016/j.xhgg.2021.100078 ↗
Xifeng Wu · 1 shared paper, 2022 · strength 0.12
- Paper A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic ca… DOI 10.1016/j.xhgg.2021.100078 ↗
Huamin Wang · 1 shared paper, 2022 · strength 0.12
- Paper A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic ca… DOI 10.1016/j.xhgg.2021.100078 ↗
Lisa Cannon‐Albright · 1 shared paper, 2022 · strength 0.12
- Paper A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic ca… DOI 10.1016/j.xhgg.2021.100078 ↗
Ping Chang · 1 shared paper, 2022 · strength 0.12
- Paper A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic ca… DOI 10.1016/j.xhgg.2021.100078 ↗
Donghui Li · 1 shared paper, 2022 · strength 0.12
- Paper A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic ca… DOI 10.1016/j.xhgg.2021.100078 ↗
Jennifer B. Permuth · 1 shared paper, 2022 · strength 0.12
- Paper A whole-exome case-control association study to characterize the contribution of rare coding variation to pancreatic ca… DOI 10.1016/j.xhgg.2021.100078 ↗

How to reach this person

A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.