Detalhe da pesquisa
1.
An Organismal CNV Mutator Phenotype Restricted to Early Human Development.
Cell
; 168(5): 830-842.e7, 2017 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28235197
2.
Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function.
Cell
; 157(3): 636-50, 2014 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-24766809
3.
Integrative multi-omics analyses to identify the genetic and functional mechanisms underlying ovarian cancer risk regions.
Am J Hum Genet
; 2024 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38723632
4.
Ethnic inequities in use of breast conserving surgery and radiation therapy in Aotearoa/New Zealand: which factors contribute?
Breast Cancer Res Treat
; 205(3): 641-653, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38536575
5.
Ultrasmall and Highly Dispersed Pt Entities Deposited on Mesoporous N-doped Carbon Nanospheres by Pulsed CVD for Improved HER.
Small
; : e2311260, 2024 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38634299
6.
A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgery.
Platelets
; 35(1): 2290108, 2024 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38099325
7.
Contribution of large genomic rearrangements in PALB2 to familial breast cancer: implications for genetic testing.
J Med Genet
; 60(2): 112-118, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396271
8.
Population-based BRCA1/2 testing programmes are highly acceptable in the Jewish community: results of the JeneScreen Study.
J Med Genet
; 60(3): 265-273, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36763037
9.
The role of truth and bias in parents' judgments of children's science interests.
J Exp Child Psychol
; 244: 105949, 2024 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38705097
10.
Emergency Department Take-Home Naloxone Improves Access Compared with Pharmacy-Dispensed Naloxone.
J Emerg Med
; 66(4): e457-e462, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38461132
11.
From secularisations to political religions.
Hist Eur Ideas
; 50(1): 86-107, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38384988
12.
Radiation doses and fractionation schedules in non-low-risk ductal carcinoma in situ in the breast (BIG 3-07/TROG 07.01): a randomised, factorial, multicentre, open-label, phase 3 study.
Lancet
; 400(10350): 431-440, 2022 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35934006
13.
Impact of diabetes on surgery and radiotherapy for breast cancer.
Breast Cancer Res Treat
; 199(2): 305-314, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36997750
14.
Association of diabetes and breast cancer characteristics at diagnosis.
Cancer Causes Control
; 34(2): 103-111, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36409455
15.
Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression.
Clin Genet
; 103(1): 109-113, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36075864
16.
Fish and macroinvertebrate assemblages reveal extensive degradation of the world's rivers.
Glob Chang Biol
; 29(2): 355-374, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36131677
17.
Receipt of mastectomy and adjuvant radiotherapy following breast conserving surgery (BCS) in New Zealand women with BCS-eligible breast cancer, 2010-2015: an observational study focusing on ethnic differences.
BMC Cancer
; 23(1): 766, 2023 Aug 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37592208
18.
Validated biomarker assays confirm that ARID1A loss is confounded with MMR deficiency, CD8+ TIL infiltration, and provides no independent prognostic value in endometriosis-associated ovarian carcinomas.
J Pathol
; 256(4): 388-401, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34897700
19.
Universal genetic testing for women with newly diagnosed breast cancer in the context of multidisciplinary team care.
Med J Aust
; 218(8): 368-373, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37005005
20.
Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDH.
J Med Genet
; 59(3): 270-278, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33461977