Detalhe da pesquisa
1.
Evidence for 28 genetic disorders discovered by combining healthcare and research data.
Nature
; 586(7831): 757-762, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057194
2.
Age-adjusted association of homologous recombination genes with ovarian cancer using clinical exomes as controls.
Hered Cancer Clin Pract
; 17: 19, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31341520
3.
Germline pathogenic variants identified in women with ovarian tumors.
Gynecol Oncol
; 151(3): 481-488, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30322717
4.
Differences in cancer prevalence among CHEK2 carriers identified via multi-gene panel testing.
Cancer Genet
; 246-247: 12-17, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32805687
5.
Annotation of Sequence Variants in Cancer Samples: Processes and Pitfalls for Routine Assays in the Clinical Laboratory.
J Mol Diagn
; 17(4): 339-51, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25977238
6.
A Transition Zone Showing Highly Discontinuous or Alternating Levels of Stem Cell and Proliferation Markers Characterizes the Development of PTEN-Haploinsufficient Colorectal Cancer.
PLoS One
; 10(6): e0131108, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26098881