Suchergebnisse - "Dueñas, Núria"

PubPharm (20)

1

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

enthalten in: bioRxiv.org | 2024

von Hassanin, E. | Spier, I. | Bobbili, D. | +15

2

Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome

enthalten in: bioRxiv.org | 2024

von Dueñas, N. | Klinkhammer, H. | Bonifaci, N. | +10

3

Tumor analysis of MMR genes in Lynch-like syndrome : Challenges associated with results interpretation

enthalten in: Cancer medicine | 2024

von Rofes, P. | Dueñas, N. | Del Valle, J. | +10

4

Tumor analysis of MMR genes in Lynch‐like syndrome : Challenges associated with results interpretation

enthalten in: Cancer Medicine | 2024

von Rofes, P. | Dueñas, N. | Valle, J. | +10

5

Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome

enthalten in: Journal of medical genetics | 2023

von Dueñas, N. | Klinkhammer, H. | Bonifaci, N. | +10

6

MTHFR C677T and A1298C polymorphism's effect on risk of colorectal cancer in Lynch syndrome

enthalten in: Scientific reports | 2023

von Wiik, M. | Negline, M. | Beisvåg, V. | +16

7

Evaluation of somatic mutations in cervicovaginal samples as a non-invasive method for the detection and molecular classification of endometrial cancer

enthalten in: EBioMedicine | 2023

von Pelegrina, B. | Paytubi, S. | Marin, F. | +25

8

Highly Sensitive Microsatellite Instability and Immunohistochemistry Assessment in Endometrial Aspirates as a Tool for Cancer Risk Individualization in Lynch Syndrome

enthalten in: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc | 2023

von Canet-Hermida, J. | Marín, F. | Dorca, E. | +20

9

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database

enthalten in: EClinicalMedicine | 2023

von Dominguez-Valentin, M. | Haupt, S. | Seppälä, T. | +98

10

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

enthalten in: BMC medical genomics | 2023

von Hassanin, E. | Spier, I. | Bobbili, D. | +15