E-LIB Suche - Ergebnisse für: Venner, Eric

1

O01: Using multiplexed functional data to reduce the VUS bu..:

Dawood, Moez ; Fayer, Shawn ; Post, Mason...
Genetics in Medicine Open. 2 (2024) - p. 101010 , 2024

Link: https://doi.org/10.1016/..

2

Genetic sex validation for sample tracking in next-generati..:

Hu, Jianhong ; Korchina, Viktoriya ; Zouk, Hana...
BMC Research Notes. 17 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

3

Tracking updates in clinical databases increases efficiency..:

Li, Lele ; Tian, Xia ; Woodzell, Vaughan...
Genetics in Medicine Open. 2 (2024) - p. 101841 , 2024

Link: https://doi.org/10.1016/..

4

The frequency of pathogenic variation in the All of Us coho..:

Venner, Eric ; Patterson, Karynne ; Kalra, Divya...
Communications Biology. 7 (2024) 1 - p. , 2024

Link: https://doi.org/10.1038/..

5

Empowering personalized pharmacogenomics with generative AI..:

Murugan, Mullai ; Yuan, Bo ; Venner, Eric...
Journal of the American Medical Informatics Association. 31 (2024) 6 - p. 1356-1366 , 2024

Link: https://doi.org/10.1093/..

6

Precision Neurology for Dementia (P2-6.002):

Shulman, Joshua ; Vanegas-Arroyave, Nora ; Fong, Jamie...
Neurology. 100 (2023) 17_supplement_2 - p. , 2023

Link: https://doi.org/10.1212/..

7

Implementation of preemptive DNA sequence–based pharmacogen..:

Wang, Liewei ; Scherer, Steven E. ; Bielinski, Suzette J....
Genetics in Medicine. 24 (2022) 5 - p. 1062-1072 , 2022

Link: https://doi.org/10.1016/..

8

OP039: Best practices for the interpretation and reporting ..:

Austin-Tse, Chrissy ; Jobanputra, Vaidehi ; Perry, Denise...
Genetics in Medicine. 24 (2022) 3 - p. S365-S366 , 2022

Link: https://doi.org/10.1016/..

9

Artificial Intelligence and Cardiovascular Genetics:

Krittanawong, Chayakrit ; Johnson, Kipp W. ; Choi, Edward...
Life. 12 (2022) 2 - p. 279 , 2022

Link: https://doi.org/10.3390/..

10

Best practices for the interpretation and reporting of clin..:

Austin-Tse, Christina A. ; Jobanputra, Vaidehi ; Perry, Denise L....
npj Genomic Medicine. 7 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

11

Whole-genome sequencing as an investigational device for re..:

Venner, Eric ; Muzny, Donna ; Smith, Joshua D....
Genome Medicine. 14 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

12

Harmonizing variant classification for return of results in..:

Harrison, Steven M. ; Austin‐Tse, Christina A. ; Kim, Serra...
Human Mutation. 43 (2021) 8 - p. 1114-1121 , 2021

Link: https://doi.org/10.1002/..

13

Improving reporting standards for polygenic scores in risk ..:

Wand, Hannah ; Lambert, Samuel A. ; Tamburro, Cecelia...
Nature. 591 (2021) 7849 - p. 211-219 , 2021

Link: https://doi.org/10.1038/..

14

Genomic considerations for FHIR®; eMERGE implementation les..:

Murugan, Mullai ; Babb, Lawrence J. ; Overby Taylor, Casey...
Journal of Biomedical Informatics. 118 (2021) - p. 103795 , 2021

Link: https://doi.org/10.1016/..

15

The Implementation Science for Genomic Health Translation (..:

Feofanova, Elena Valeryevna ; Zhang, Guo-Qiang ; Lhatoo, Samden...
JMIR Research Protocols. 10 (2021) 3 - p. e25576 , 2021

Link: https://doi.org/10.2196/..