ResearcherThe University of Texas MD Anderson Cancer CenterActive in the last 2 years

Chad Daniel Huff

ORCID-verified (high confidence, 0.95), identity_conf@1As of 7 November 2026

Matched on ORCID iD 0000-0002-1100-9364; OpenAlex author ID A5066045984, A5112189507; NIH RePORTER profile ID 10854751. Sources: OpenAlex.

Their work

Papers: 2 (first author 0, last author 1)
Trials: 0
Grants: 1
Labs led: 0
Collaborators: 8

Papers, trials and grants by year

2019: 1 grant · 2020: none · 2021: none · 2022: 1 paper · 2023: none · 2024: none · 2025: none · 2026: 1 paper

Papers 2

Grants 1

Discovery of Risk Loci and Genomics of Pancreatic Cancer through Exome Sequencing R01CA181244 ↗

Closest collaborators

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

Paul A Scheet · 1 shared paper, 1 shared grant, 2019–2022 · strength 0.52
- Grant Discovery of Risk Loci and Genomics of Pancreatic Cancer through Exome Sequencing R01CA181244 ↗
- 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 ↗
Yao Yu · 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.