Suchergebnisse - "Grove, Megan E"

PubPharm (37)

1

Regional Variation in Cardiovascular Genes Enables a Tractable Genome Editing Strategy

enthalten in: Circulation. Genomic and precision medicine | 2024

von Krysov, V. | Wilson, R. | Ten, N. | +9

2

Knowledge and attitudes on implementing cardiovascular pharmacogenomic testing

enthalten in: Clinical and translational science | 2024

von Russell, C. | Campion, M. | Grove, M. | +6

3

Knowledge and attitudes on implementing cardiovascular pharmacogenomic testing

enthalten in: Clinical and Translational Science | 2024

von Russell, C. | Campion, M. | Grove, M. | +6

4

Regional variation in cardiovascular genes enables a tractable genome editing strategy

enthalten in: bioRxiv.org | 2023

von Krysov, V. | Wilson, R. | Ten, N. | +9

5

Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing

enthalten in: Nature biotechnology | 2022

von Goenka, S. | Gorzynski, J. | Shafin, K. | +26

6

Ultra-Rapid Nanopore Whole Genome Genetic Diagnosis of Dilated Cardiomyopathy in an Adolescent With Cardiogenic Shock

enthalten in: Circulation. Genomic and precision medicine | 2022

von Gorzynski, J. | Goenka, S. | Shafin, K. | +25

7

PPA2-associated sudden cardiac death : extending the clinical and allelic spectrum in 20 new families

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

von Guimier, A. | Achleitner, M. | Moreau de Bellaing, A. | +57

ErratumFor: Genet Med. 2021 Dec;23(12):2415-2425. - PMID 34400813

8

Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting

enthalten in: The New England journal of medicine | 2022

von Gorzynski, J. | Goenka, S. | Shafin, K. | +34

9

PPA2-associated sudden cardiac death : extending the clinical and allelic spectrum in 20 new families

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2021

von Guimier, A. | Achleitner, M. | Moreau de Bellaing, A. | +57

ErratumIn: Genet Med. 2022 Apr;24(4):967. - PMID 35394429

10

Clinical utility of genomic sequencing : a measurement toolkit

enthalten in: NPJ genomic medicine | 2020

von Hayeems, R. | Dimmock, D. | Bick, D. | +10