Search filters

Authors whose works are in public domain in at least one jurisdiction

List of works by Erin Turbitt

A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development

scientific article published on 9 November 2011

A primer in genomics for social and behavioral investigators

scientific article published on 22 February 2019

A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study

scientific article published on 16 February 2018

Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery

scientific article published on 5 December 2017

Australians' perspectives on support around use of personal genomic testing: Findings from the Genioz study

scientific article published on 13 November 2018

Australians' views and experience of personal genomic testing: survey findings from the Genioz study

scientific article published on 21 January 2019

Australians' views on personal genomic testing: focus group findings from the Genioz study

article

Availability of treatment drives decisions of genetic health professionals about disclosure of incidental findings

scientific article

CITED2 mutations potentially cause idiopathic premature ovarian failure.

scientific article published on 16 June 2012

Characterization of Escherichia coli O157:H7 in New Zealand using multiple-locus variable-number tandem-repeat analysis.

scientific article

Children referred for specialty care: Parental perspectives and preferences on referral, follow-up and primary care

scientific article

Considerations for reporting genome results to patients

scientific article published on 01 January 2013

Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis

scientific article

Defining personal utility in genomics: A Delphi study

scientific article published on 20 February 2017

Ethnic identity and engagement with genome sequencing research

scientific article published on 20 December 2018

Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation

scientific article published on 26 November 2014

Feasibility of Coping Effectiveness Training for Caregivers of Children with Autism Spectrum Disorder: a Genetic Counseling Intervention.

scientific article published on 6 September 2017

Fragile X syndrome clinical trials: exploring parental decision-making

scientific article published on 12 February 2019

General practitioner referrals to paediatric specialist outpatient clinics: referral goals and parental influence

scientific article published on 01 March 2018

Genetic counseling, genetic testing, and risk perceptions for breast and colorectal cancer: Results from the 2015 National Health Interview Survey

scientific article published on 25 February 2019

Identification of SOX3 as an XX male sex reversal gene in mice and humans

scientific article

Intentions to share exome sequencing results with family members: exploring spousal beliefs and attitudes.

scientific article published on 23 February 2018

Key informants' perspectives of implementing chromosomal microarrays into clinical practice in Australia

scientific article

Lower urgency paediatric injuries: Parent preferences for emergency department or general practitioner care

scientific article published on 31 July 2016

Managing the need to tell: Triggers and strategic disclosure of thalassemia major in Singapore

scientific article published on 01 March 2019

Molecular phylogenetic analysis of New Zealand mosquito species

scientific article published on 22 June 2020

Motivators and barriers for paediatricians discharging patients

scientific article published on 30 November 2016

Multiple-locus variable-number tandem-repeat analysis for discriminating within Salmonella enterica serovar Typhimurium definitive types and investigation of outbreaks.

scientific article published on 8 September 2010

Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women

scientific article published on 25 March 2015

Paediatric emergency department referrals from primary care.

scientific article published on 9 March 2016

Paediatrician perceptions of patient referral and discharge

scientific article published on 26 September 2016

Parent perspectives and reasons for lower urgency paediatric presentations to emergency departments.

scientific article

Parental decision making about clinical trial enrollment: A survey of parents of children with Fragile X syndrome

scientific article published on 01 December 2020

Parental preferences for paediatric specialty follow-up care.

scientific article

Personal utility in genomic testing: a systematic literature review.

scientific article published on 15 March 2017

Perspectives of Australian general practitioners on shared care for paediatric patients

scientific article published on 05 September 2016

Preferences for results from genomic microarrays: comparing parents and health care providers.

scientific article published on 29 April 2014

Public or private care: where do specialists spend their time?

scientific article published on 5 September 2016

Regular source of primary care and emergency department use of children in Victoria.

scientific article published on 26 November 2015

SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype.

scientific article

The many faces of MLPA

scientific article published on 01 January 2011

Use of a telenursing triage service by Victorian parents attending the emergency department for their child's lower urgency condition

scientific article

Web Platform vs In-Person Genetic Counselor for Return of Carrier Results From Exome Sequencing: A Randomized Clinical Trial.

scientific article published on 22 January 2018

What proportion of paediatric specialist referrals originates from general practitioners?

scientific article published on 6 September 2017

Paulina is supported by:

About Paulina

Help