Suchergebnisse - "Danos, Arpad M"

PubPharm (39)

1

CIViCdb 2022 : evolution of an open-access cancer variant interpretation knowledgebase

enthalten in: Nucleic acids research | 2023

von Krysiak, K. | Danos, A. | Saliba, J. | +62

2

Evolution of the open-access CIViC knowledgebase is driven by the needs of the cancer variant interpretation community

enthalten in: bioRxiv.org | 2022

von Krysiak, K. | Danos, A. | Kiwala, S. | +49

3

Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease

enthalten in: Human mutation | 2022

von Chiorean, A. | Farncombe, K. | Delong, S. | +22

4

Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity) : Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)

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

von Horak, P. | Griffith, M. | Danos, A. | +44

ErratumFor: Genet Med. 2022 May;24(5):986-998. - PMID 35101336

5

Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity) : Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)

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

von Horak, P. | Griffith, M. | Danos, A. | +44

CommentIn: Genet Med. 2022 Sep;24(9):1986-1988. - PMID 35779071

6

A community approach to the cancer-variant-interpretation bottleneck

enthalten in: Nature cancer | 2022

von Krysiak, K. | Danos, A. | Kiwala, S. | +49

7

Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity) : joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)

enthalten in: Genetics in medicine | 29 January 2022

von Horak, P. | Griffith, M. | Danos, A. | +44

8

Large scale genotype‐ and phenotype‐driven machine learning in Von Hippel‐Lindau disease

enthalten in: Human mutation | 2022

von Chiorean, A. | Farncombe, K. | Delong, S. | +22

9

The CIViC knowledge model and standard operating procedures for curation and clinical interpretation of variants in cancer

enthalten in: bioRxiv.org | 2020

von Danos, A. | Krysiak, K. | Barnell, E. | +18

10

CIViCpy: a Python software development and analysis toolkit for the CIViC knowledgebase

enthalten in: bioRxiv.org | 2020

von Wagner, A. | Kiwala, S. | Coffman, A. | +8