Suchergebnisse - "Kemppainen, Jennifer L."

PubPharm (30)

1

Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)

enthalten in: ResearchSquare.com | 2023

von Vairo, F. | Kemppainen, J. | Vitek, C. | +60

2

Risk of Syndrome-Associated Cancers Among First-Degree Relatives of Patients With Pancreatic Ductal Adenocarcinoma With Pathogenic or Likely Pathogenic Germline Variants

enthalten in: JAMA oncology | 2023

von Chen, X. | Meyer, M. | Kemppainen, J. | +5

3

Implementation of genomic medicine for rare disease in a tertiary healthcare system : Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)

enthalten in: Journal of translational medicine | 2023

von Pinto E Vairo, F. | Kemppainen, J. | Vitek, C. | +60

4

Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)

enthalten in: Journal of translational medicine | 2023

von Pinto e Vairo, F. | Kemppainen, J. | Vitek, C. | +60

5

Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)

enthalten in: Journal of translational medicine | 2023

von Pinto e Vairo, F. | Kemppainen, J. | Vitek, C. | +60

6

Impact of integrated translational research on clinical exome sequencing

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

von Klee, E. | Cousin, M. | Pinto E Vairo, F. | +57

ErratumFor: Genet Med. 2021 Mar;23(3):498-507. - PMID 33144682

7

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability

enthalten in: Journal of medical genetics | 2022

von Schalk, A. | Cousin, M. | Dsouza, N. | +69

8

Pancreatic cancer risk to siblings of probands in bilineal cancer settings

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

von Rabe, K. | Stevens, M. | Hernández, A. | +5

9

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability

enthalten in: bioRxiv.org | 2022

von Schalk, A. | Cousin, M. | Challman, T. | +69

10

Genomics Integration Into Nephrology Practice

enthalten in: Kidney medicine | 2021

von Pinto E Vairo, F. | Prochnow, C. | Kemppainen, J. | +23