Search details
1.
Unusual suspects in hereditary melanoma: POT1, POLE, BAP1.
Trends Genet
; 38(12): 1204-1207, 2022 12.
Article
in English
| MEDLINE | ID: mdl-35811174
2.
POT1 and multiple primary melanomas: the dermatological phenotype.
J Med Genet
; 2024 May 08.
Article
in English
| MEDLINE | ID: mdl-38724174
3.
The ATM Ser49Cys Variant Effects ATM Function as a Regulator of Oncogene-Induced Senescence.
Int J Mol Sci
; 25(3)2024 Jan 29.
Article
in English
| MEDLINE | ID: mdl-38338943
4.
Germline ERBB3 mutation in familial non-small-cell lung carcinoma: expanding ErbB's role in oncogenesis.
Hum Mol Genet
; 30(24): 2393-2401, 2021 11 30.
Article
in English
| MEDLINE | ID: mdl-34274969
5.
Models of communication for polygenic scores and associated psychosocial and behavioral effects on recipients: A systematic review.
Genet Med
; 25(1): 1-11, 2023 01.
Article
in English
| MEDLINE | ID: mdl-36322150
6.
Development and evaluation of a novel educational program for providers on the use of polygenic risk scores.
Genet Med
; 25(8): 100876, 2023 08.
Article
in English
| MEDLINE | ID: mdl-37149760
7.
The MC1R r allele does not increase melanoma risk in MITF E318K carriers.
Br J Dermatol
; 188(6): 770-776, 2023 05 24.
Article
in English
| MEDLINE | ID: mdl-36879448
8.
A step forward, but still inadequate: Australian health professionals' views on the genetics and life insurance moratorium.
J Med Genet
; 59(8): 817-826, 2022 08.
Article
in English
| MEDLINE | ID: mdl-34544841
9.
Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia.
Twin Res Hum Genet
; 26(2): 184-187, 2023 04.
Article
in English
| MEDLINE | ID: mdl-37226735
10.
The emerging field of polygenic risk scores and perspective for use in clinical care.
Hum Mol Genet
; 29(R2): R165-R176, 2020 10 20.
Article
in English
| MEDLINE | ID: mdl-32620971
11.
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Hum Mol Genet
; 29(22): 3662-3678, 2020 12 04.
Article
in English
| MEDLINE | ID: mdl-33276377
12.
The impact of Marfan syndrome on an Aboriginal Australian family: 'I don't like it as much as I don't like cancer'.
J Genet Couns
; 31(3): 620-630, 2022 06.
Article
in English
| MEDLINE | ID: mdl-34713948
13.
A Systematic Review on the Impact of Genetic Testing for Familial Melanoma II: Psychosocial Outcomes and Attitudes.
Dermatology
; 237(5): 816-826, 2021.
Article
in English
| MEDLINE | ID: mdl-33508831
14.
A Systematic Review on the Impact of Genetic Testing for Familial Melanoma I: Primary and Secondary Preventative Behaviours.
Dermatology
; 237(5): 806-815, 2021.
Article
in English
| MEDLINE | ID: mdl-33588421
15.
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
N Engl J Med
; 377(6): 544-552, 2017 08 10.
Article
in English
| MEDLINE | ID: mdl-28792876
16.
Factors influencing cancer genetic somatic mutation test ordering by cancer physician.
J Transl Med
; 18(1): 431, 2020 11 12.
Article
in English
| MEDLINE | ID: mdl-33183308
17.
Comprehensive genetic screening: The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohort.
Pediatr Diabetes
; 20(1): 57-64, 2019 02.
Article
in English
| MEDLINE | ID: mdl-30191644
18.
GOLM1: expanding our understanding of melanoma susceptibility.
J Med Genet
; 60(9): 835-837, 2023 09.
Article
in English
| MEDLINE | ID: mdl-37487699
19.
Human Genetics Society of Australasia Position Statement: Genetic Testing and Personal Insurance Products in Australia - CORRIGENDUM.
Twin Res Hum Genet
; : 1, 2023 Aug 29.
Article
in English
| MEDLINE | ID: mdl-37640686
20.
Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects.
Hum Mol Genet
; 24(5): 1234-42, 2015 Mar 01.
Article
in English
| MEDLINE | ID: mdl-25343988