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Erin Turbitt
Erin Turbitt
Geverifieerd e-mailadres voor uts.edu.au
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Identification of SOX3 as an XX male sex reversal gene in mice and humans
E Sutton, J Hughes, S White, R Sekido, J Tan, V Arboleda, N Rogers, ...
The Journal of clinical investigation 121 (1), 328-341, 2011
2942011
Copy number variation in patients with disorders of sex development due to 46, XY gonadal dysgenesis
S White, T Ohnesorg, A Notini, K Roeszler, J Hewitt, H Daggag, C Smith, ...
PloS one 6 (3), e17793, 2011
1602011
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
MR Hart, BB Biesecker, CL Blout, KD Christensen, LM Amendola, ...
Genetics in Medicine 21 (5), 1100-1110, 2019
1452019
Personal utility in genomic testing: a systematic literature review
JN Kohler, E Turbitt, BB Biesecker
European Journal of Human Genetics 25 (6), 662-668, 2017
1342017
Defining personal utility in genomics: A Delphi study
B Kohler, J., Turbitt, E., Lewis, K., Wilfond, B., Jamal, L., Peay, H ...
Clinical Genetics, 2017
782017
Web platform vs in-person genetic counselor for return of carrier results from exome sequencing: a randomized clinical trial
BB Biesecker, KL Lewis, KL Umstead, JJ Johnston, E Turbitt, KP Fishler, ...
JAMA Internal Medicine 178 (3), 338-346, 2018
732018
A multi-exon deletion within WWOX is associated with a 46, XY disorder of sex development
S White, J Hewitt, E Turbitt, Y Van Der Zwan, R Hersmus, S Drop, ...
European journal of human genetics 20 (3), 348-351, 2012
622012
Addressing underrepresentation in genomics research through community engagement
AA Lemke, ED Esplin, AJ Goldenberg, C Gonzaga-Jauregui, ...
The American Journal of Human Genetics 109 (9), 1563-1571, 2022
392022
Evaluation of recipients of positive and negative secondary findings evaluations in a hybrid CLIA-research sequencing pilot
JC Sapp, JJ Johnston, K Driscoll, AR Heidlebaugh, AM Sagardia, ...
The American Journal of Human Genetics 103 (3), 358-366, 2018
392018
Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women
KM Cornish, CM Kraan, QM Bui, MA Bellgrove, SA Metcalfe, JN Trollor, ...
Neurology 84 (16), 1631-1638, 2015
362015
Advancing precision public health using human genomics: examples from the field and future research opportunities
MC Roberts, AE Fohner, L Landry, DL Olstad, AK Smit, E Turbitt, CG Allen
Genome medicine 13 (1), 97, 2021
302021
SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype
R Hersmus, H Stoop, E Turbitt, JW Oosterhuis, SLS Drop, AH Sinclair, ...
BMC medical genetics 13, 1-7, 2012
292012
CITED2 mutations potentially cause idiopathic premature ovarian failure
DJ Fonseca, D Ojeda, B Lakhal, R Braham, S Eggers, E Turbitt, S White, ...
Translational Research 160 (5), 384-388, 2012
262012
Australians’ perspectives on support around use of personal genomic testing: findings from the Genioz study
SA Metcalfe, C Hickerton, J Savard, E Stackpoole, R Tytherleigh, E Tutty, ...
European Journal of Medical Genetics 62 (5), 290-299, 2019
222019
Preferences for results from genomic microarrays: comparing parents and health care providers
E Turbitt, JL Halliday, DJ Amor, SA Metcalfe
Clinical Genetics 87 (1), 21-29, 2015
212015
Australians’ views on personal genomic testing: focus group findings from the Genioz study
SA Metcalfe, C Hickerton, J Savard, B Terrill, E Turbitt, C Gaff, K Gray, ...
European Journal of Human Genetics 26 (8), 1101-1112, 2018
182018
Public or private care: where do specialists spend their time?
GL Freed, E Turbitt, A Allen
Australian Health Review 41 (5), 541-545, 2016
182016
Feasibility of coping effectiveness training for caregivers of children with autism spectrum disorder: A genetic counseling intervention
C Haakonsen Smith, E Turbitt, J Muschelli, L Leonard, KL Lewis, ...
Journal of genetic counseling 27, 252-262, 2018
162018
General practitioner perspectives on referrals to paediatric public specialty clinics
GL Freed, E Turbitt, M Kunin, S Gafforini, L Sanci, N Spike
Australian Family Physician 45 (10), 747-753, 2016
162016
Lower urgency paediatric injuries: Parent preferences for emergency department or general practitioner care
S Gafforini, E Turbitt, GL Freed
Emergency Medicine Australasia 28 (5), 564-568, 2016
162016
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Artikelen 1–20