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1.
A randomized multicenter trial of a chronic disease management intervention for decompensated cirrhosis. The Australian Liver Failure (ALFIE) trial.
Hepatology
; 2024 Mar 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-38825975
2.
Longitudinal studies examining the impact of prenatal and subsequent episodes of maternal depression on offspring antisocial behaviour.
Eur Child Adolesc Psychiatry
; 30(1): 5-40, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-31792693
3.
Clinical factors leading to a change in management in chronic hepatitis B patients managed in a tertiary setting.
Intern Med J
; 50(2): 177-184, 2020 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31449717
4.
Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta.
Am J Hum Genet
; 91(3): 565-71, 2012 Sep 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-22901946
5.
Health-related physical fitness assessment in a community-based cancer rehabilitation setting.
Support Care Cancer
; 23(9): 2525-33, 2015 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-25617069
6.
Adolescent male hazardous drinking and participation in organised activities: involvement in team sports is associated with less hazardous drinking in young offenders.
Crim Behav Ment Health
; 25(1): 28-41, 2015 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24839197
7.
Robust diagnostic genetic testing using solution capture enrichment and a novel variant-filtering interface.
Hum Mutat
; 35(4): 434-41, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24307375
8.
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects.
Hum Mol Genet
; 21(4): 776-83, 2012 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-22068589
9.
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Am J Hum Genet
; 89(3): 464-73, 2011 Sep 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-21907015
10.
Mutation detection by clonal sequencing of PCR amplicons and grouped read typing is applicable to clinical diagnostics.
Hum Mutat
; 34(1): 248-54, 2013 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22915446
11.
Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data.
Hum Mutat
; 34(7): 945-52, 2013 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-23554237
12.
A computational index derived from whole-genome copy number analysis is a novel tool for prognosis in early stage lung squamous cell carcinoma.
Genomics
; 99(1): 18-24, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22050995
13.
A high ratio of linoleic acid (n-6 PUFA) to alpha-linolenic acid (n-3 PUFA) adversely affects early stage of human neuronal differentiation and electrophysiological activity of glutamatergic neurons in vitro.
Front Cell Dev Biol
; 11: 1166808, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37255597
14.
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis.
Hum Mutat
; 33(8): 1175-81, 2012 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-22553128
15.
Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens.
Nucleic Acids Res
; 38(14): e151, 2010 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-20525786
16.
Illuminator, a desktop program for mutation detection using short-read clonal sequencing.
Genomics
; 98(4): 302-9, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-21621601
17.
Anxiety and depression in Australian chronic hepatitis C outpatients: prevalence and predictors.
Australas Psychiatry
; 20(6): 496-500, 2012 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-23099509
18.
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing.
NAR Genom Bioinform
; 4(4): lqac089, 2022 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-36478959
19.
Comparison of mouse models reveals a molecular distinction between psychotic illness in PWS and schizophrenia.
Transl Psychiatry
; 11(1): 433, 2021 08 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-34417445
20.
CSF-resident CD4+ T-cells display a distinct gene expression profile with relevance to immune surveillance and multiple sclerosis.
Brain Commun
; 3(3): fcab155, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34761221