Suchergebnisse - "Ukaegbu, Chinedu"

PubPharm (43)

1

A Randomized Trial of Two Remote Health Care Delivery Models on the Uptake of Genetic Testing and Impact on Patient-Reported Psychological Outcomes in Families With Pancreatic Cancer : The Genetic Education, Risk Assessment, and Testing (GENERATE) Study

enthalten in: Gastroenterology | 2024

von Rodriguez, N. | Furniss, C. | Yurgelun, M. | +25

2

Mutational signature profiling classifies subtypes of clinically different mismatch repair deficient tumors with a differential immunogenic response potential

enthalten in: bioRxiv.org | 2023

von Giner-Calabuig, M. | De Leon, S. | Wang, J. | +20

3

Most people share genetic test results with relatives even if the findings are normal : Family communication in a diverse population

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2023

von Hunter, J. | Riddle, L. | Joseph, G. | +78

4

PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancer

enthalten in: Familial cancer | 2023

von Sandoval, R. | Horiguchi, M. | Ukaegbu, C. | +4

5

Risk management actions following genetic testing in the Cancer Health Assessments Reaching Many (CHARM) Study : A prospective cohort study

enthalten in: Cancer medicine | 2023

von Guo, B. | Knerr, S. | Kauffman, T. | +82

6

Clinical factors associated with skin neoplasms in individuals with Lynch syndrome in a longitudinal observational cohort

enthalten in: Journal of the American Academy of Dermatology | 2023

von Zhong, C. | Horiguchi, M. | Uno, H. | +6

7

MyLynch : A Patient-Facing Clinical Decision Support Tool for Genetically-Guided Personalized Medicine in Lynch Syndrome

enthalten in: Cancers | 2023

von Knapp, S. | Revette, A. | Underhill-Blazey, M. | +12

8

Development and Validation of the PREMMplus Model for Multigene Hereditary Cancer Risk Assessment

enthalten in: Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 2022

von Yurgelun, M. | Uno, H. | Furniss, C. | +7

CommentIn: J Clin Oncol. 2022 Dec 10;40(35):4040-4043. - PMID 36166722

9

A validation of models for prediction of pathogenic variants in mismatch repair genes

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2022

von Shyr, C. | Blackford, A. | Huang, T. | +21

10

Mutational signature profiling classifies subtypes of clinically different mismatch-repair-deficient tumours with a differential immunogenic response potential

enthalten in: British journal of cancer | 2022

von Giner-Calabuig, M. | De Leon, S. | Wang, J. | +20

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