| human | Q5 |
| P496 | ORCID iD | 0000-0002-7535-006X |
| P1153 | Scopus author ID | 56189798900 |
| P69 | educated at | University of Utah | Q168515 |
| P108 | employer | University of Utah | Q168515 |
| P734 | family name | Young | Q12678727 |
| Young | Q12678727 | ||
| Young | Q12678727 | ||
| P735 | given name | Erin | Q770100 |
| Erin | Q770100 | ||
| P106 | occupation | researcher | Q1650915 |
| Q35053897 | Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions |
| Q88728614 | Improved, ACMG-compliant, in silico prediction of pathogenicity for missense substitutions encoded by TP53 variants |
| Q55443512 | Pancreatic cancer as a sentinel for hereditary cancer predisposition. |
| Q40070779 | Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families. |
| Q28652308 | Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study |
| Q28652056 | Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers |
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