Detalhe da pesquisa
1.
Acquired mutations in BAX confer resistance to BH3-mimetic therapy in acute myeloid leukemia.
Blood
; 141(6): 634-644, 2023 02 09.
Artigo
Inglês
| MEDLINE | ID: mdl-36219880
2.
Clonal hematopoiesis, myeloid disorders and BAX-mutated myelopoiesis in patients receiving venetoclax for CLL.
Blood
; 139(8): 1198-1207, 2022 02 24.
Artigo
Inglês
| MEDLINE | ID: mdl-34469514
3.
Health economic evidence for the use of molecular biomarker tests in hematological malignancies: A systematic review.
Eur J Haematol
; 108(6): 469-485, 2022 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-35158410
4.
Development of a machine learning model to predict mild cognitive impairment using natural language processing in the absence of screening.
BMC Med Inform Decis Mak
; 22(1): 129, 2022 05 12.
Artigo
Inglês
| MEDLINE | ID: mdl-35549702
5.
What Are We Missing?: Evaluating an Intimate Partner Violence Screening Program in a Pediatric Emergency Department.
Pediatr Emerg Care
; 38(2): e462-e467, 2022 Feb 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35100751
6.
Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes.
Haematologica
; 106(1): 64-73, 2021 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32054657
7.
Erratum to: Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes.
Haematologica
; 109(4): 1311, 2024 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38562077
8.
Evaluating the breast cancer predisposition role of rare variants in genes associated with low-penetrance breast cancer risk SNPs.
Breast Cancer Res
; 20(1): 3, 2018 01 09.
Artigo
Inglês
| MEDLINE | ID: mdl-29316957
9.
Oral Health Promotion and Smoking Cessation Program Delivered via Tobacco Quitlines: The Oral Health 4 Life Trial.
Am J Public Health
; 108(5): 689-695, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29565660
10.
Canary: an atomic pipeline for clinical amplicon assays.
BMC Bioinformatics
; 18(1): 555, 2017 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29246107
11.
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
Hum Mol Genet
; 24(18): 5345-55, 2015 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-26130695
12.
Methyl-CpG binding domain 4, DNA glycosylase (MBD4)-associated neoplasia syndrome associated with a homozygous missense variant in MBD4: Expansion of an emerging phenotype.
Br J Haematol
; 198(1): 196-199, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35381620
13.
Multiple BCL2 mutations cooccurring with Gly101Val emerge in chronic lymphocytic leukemia progression on venetoclax.
Blood
; 135(10): 773-777, 2020 03 05.
Artigo
Inglês
| MEDLINE | ID: mdl-31951646
14.
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
J Med Genet
; 53(5): 298-309, 2016 05.
Artigo
Inglês
| MEDLINE | ID: mdl-26921362
15.
Reevaluation of RINT1 as a breast cancer predisposition gene.
Breast Cancer Res Treat
; 159(2): 385-92, 2016 09.
Artigo
Inglês
| MEDLINE | ID: mdl-27544226
16.
Clonal independence of JAK2 and CALR or MPL mutations in comutated myeloproliferative neoplasms demonstrated by single cell DNA sequencing.
Haematologica
; 106(1): 313-315, 2021 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32817290
17.
Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls.
Breast Cancer Res
; 17: 111, 2015 Aug 19.
Artigo
Inglês
| MEDLINE | ID: mdl-26283626
18.
A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variability.
Br J Haematol
; 190(5): e297-e301, 2020 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32488879
19.
Copy number analysis of ductal carcinoma in situ with and without recurrence.
Mod Pathol
; 28(9): 1174-84, 2015 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-26321097
20.
Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles.
PLoS Genet
; 8(9): e1002894, 2012 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-23028338