Suchergebnisse - "Domchek, Susan M"

PubPharm (518)

41

Care after premenopausal risk‐reducing salpingo‐oophorectomy in high‐risk women : Scoping review and international consensus recommendations

enthalten in: BJOG: An International Journal of Obstetrics & Gynaecology | 2023

von Nebgen, D. | Domchek, S. | Kotsopoulos, J. | +24

42

Development and Validation of a Breast Cancer Polygenic Risk Score on the Basis of Genetic Ancestry Composition

enthalten in: JCO precision oncology | 2022

von Hughes, E. | Wagner, S. | Pruss, D. | +26

43

Ruxolitinib and exemestane for estrogen receptor positive, aromatase inhibitor resistant advanced breast cancer

enthalten in: NPJ breast cancer | 2022

von Makhlin, I. | McAndrew, N. | Wileyto, E. | +14

44

Analysis of matched primary and recurrent BRCA1/2 mutation-associated tumors identifies recurrence-specific drivers

enthalten in: Nature communications | 2022

von Shah, J. | Pueschl, D. | Wubbenhorst, B. | +17

45

Impact of integrating genomic data into the electronic health record on genetics care delivery

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

von Lau-Min, K. | McKenna, D. | Asher, S. | +21

46

Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants

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

von Li, H. | Engel, C. | Hoya, M. | +59

ErratumFor: Genet Med. 2022 Jan;24(1):119-129. - PMID 34906479

47

Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

enthalten in: Communications biology | 2022

von Hakkaart, C. | Pearson, J. | Marquart, L. | +98

48

HRDex: a tool for deriving homologous recombination deficiency (HRD) scores from whole exome sequencing data

enthalten in: bioRxiv.org | 2022

von Pluta, J. | Hausler, R. | Wubbenhorst, B. | +4

49

Polygenic risk scores for prediction of breast cancer risk in women of African ancestry : a cross-ancestry approach

enthalten in: Human molecular genetics | 2022

von Gao, G. | Zhao, F. | Ahearn, T. | +54

50

Classification of BRCA2 Variants of Uncertain Significance (VUS) Using an ACMG/AMP Model Incorporating a Homology-Directed Repair (HDR) Functional Assay

enthalten in: Clinical cancer research : an official journal of the American Association for Cancer Research | 2022

von Hu, C. | Susswein, L. | Roberts, M. | +16