Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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Dr Jodie Painter Email
Telephone: +61 7 3362 0214
Facsimile: +61 7 3362 0101
Email: Jodie.Painter@qimrberghofer.edu.au

Please contact Dr Jodie Painter for more information and a complete list of publications.

Publications
2015
 Painter JN, O'Mara TA, Batra J, Cheng T, Lose FA, Dennis J, Michailidou K, Tyrer JP, Ahmed S, Ferguson K, Healey CS, Kaufmann S, Hillman KM, Walpole C, Moya L, Pollock P, Jones A, Howarth K, Martin L, Gorman M, Hodgson S, National Study of Endometrial Cancer Genetics Group (NSECG), CHIBCHA Consortium, De Polanco MM, Sans M, Carracedo A, Castellvi-Bel S, Rojas-Martinez A, Santos E, Teixeira MR, Carvajal-Carmona L, Shu XO, Long J, Zheng W, Xiang YB, Australian National Endometrial Cancer Study Group (ANECS), Montgomery GW, Webb PM, Scott RJ, McEvoy M, Attia J, Holliday E, Martin NG, Nyholt DR, Henders AK, Fasching PA, Hein A, Beckmann MW, Renner SP, Dörk T, Hillemanns P, Dürst M, Runnebaum I, Lambrechts D, Coenegrachts L, Schrauwen S, Amant F, Winterhoff B, Dowdy SC, Goode EL, Teoman A, Salvesen HB, Trovik J, Njolstad TS, Werner HM, Ashton K, Proietto T, Otton G, Tzortzatos G, Mints M, Tham E, RENDOCAS, Hall P, Czene K, Liu J, Li J, Hopper JL, Southey MC, Australian Ovarian Cancer Study (AOCS), Ekici AB, Ruebner M, Johnson N, Peto J, Burwinkel B, Marme F, Brenner H, Dieffenbach AK, Meindl A, Brauch H, GENICA Network, Lindblom A, Depreeuw J, Moisse M, Chang-Claude J, Rudolph A, Couch FJ, Olson JE, Giles GG, Bruinsma F, Cunningham JM, Fridley BL, Børresen-Dale AL, Kristensen VN, Cox A, Swerdlow AJ, Orr N, Bolla MK, Wang Q, Weber RP, Chen Z, Shah M, French JD, Pharoah PD, Dunning AM, Tomlinson I, Easton DF, Edwards SL, Thompson DJ, Spurdle AB: Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human Molecular Genetics 24(5):1478-1492, 2015 [PDF] [OSI] [PubMed] [More...]
2014
 Painter JN, Nyholt DR, Krause L, Zhao ZZ, Chapman B, Zhang C, Medland S, Martin NG, Kennedy S, Treloar S, Zondervan K, Montgomery GW: Common variants in the CYP2C19 gene are associated with susceptibility to endometriosis. Fertility and Sterility 102(2):496-502.e5, 2014 [PDF] [N/OSI] [PubMed] [More...]
 McRae AF, Powell JE, Henders AK, Bowdler L, Hemani G, Shah S, Painter JN, Martin NG, Visscher PM, Montgomery GW: Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome biology 15(5):R73, 2014 [PDF] [PubMed] [More...]
2013
 Luong HT, Painter JN, Shakhbazov K, Chapman B, Henders AK, Powell JE, Nyholt DR, Montgomery GW: Fine mapping of variants associated with endometriosis in the WNT4 region on chromosome 1p36. International journal of molecular epidemiology and genetics 4(4):193-206, 2013 [PDF unavailable] [PubMed] [More...]
2012
 O'Callaghan ME, Maclennan AH, Gibson CS, McMichael GL, Haan EA, Broadbent JL, Goldwater PN, Painter JN, Montgomery GW, Dekker GA, Australian Collaborative Cerebral Palsy Research Group: Fetal and Maternal Candidate Single Nucleotide Polymorphism Associations With Cerebral Palsy: A Case-Control Study. Pediatrics 129(2):e414-e423, 2012 [PDF unavailable] [PubMed] [More...]
 Luong HT, Nyholt DR, Painter JN, Chapman B, Kennedy S, Treloar SA, Zondervan KT, Montgomery GW: No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis. Human reproduction (Oxford, England) 27:3616-3621, 2012 [PDF unavailable] [PubMed] [More...]
 Eggert SL, Huyck KL, Somasundaram P, Kavalla R, Stewart EA, Lu AT, Painter JN, Montgomery GW, Medland SE, Nyholt DR, Treloar SA, Zondervan KT, Heath AC, Madden PA, Rose L, Buring JE, Ridker PM, Chasman DI, Martin NG, Cantor RM, Morton CC: Genome-wide Linkage and Association Analyses Implicate FASN in Predisposition to Uterine Leiomyomata. American Journal of Human Genetics 91(4):621-628, 2012 [PDF] [OSI] [PubMed] [More...]
 Nyholt DR, Low SK, Anderson CA, Painter JN, Uno S, Morris AP, MacGregor S, Gordon SD, Henders AK, Martin NG, Attia J, Holliday EG, McEvoy M, Scott RJ, Kennedy SH, Treloar SA, Missmer SA, Adachi S, Tanaka K, Nakamura Y, Zondervan KT, Zembutsu H, Montgomery GW: Genome-wide association meta-analysis identifies new endometriosis risk loci. Nature Genetics 44(12):1355-1359, 2012 [PDF] [OSI] [PubMed] [More...]
2011
 Painter JN, Anderson CA, Nyholt DR, Macgregor S, Lin J, Lee SH, Lambert A, Zhao ZZ, Roseman F, Guo Q, Gordon SD, Wallace L, Henders AK, Visscher PM, Kraft P, Martin NG, Morris AP, Treloar SA, Kennedy SH, Missmer SA, Montgomery GW, Zondervan KT: Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics 43(1):51-54, 2011 [PDF] [OSI] [PubMed] [More...]
 Painter JN, Nyholt DR, Morris A, Zhao ZZ, Henders AK, Lambert A, Wallace L, Martin NG, Kennedy SH, Treloar SA, Zondervan KT, Montgomery GW: High-density fine-mapping of a chromosome 10q26 linkage peak suggests association between endometriosis and variants close to CYP2C19. Fertility and Sterility 95:2236-2240, 2011 [PDF] [PubMed] [More...]
 Painter JN, Nyholt DR, Montgomery GW: Association mapping. Methods in molecular biology (Clifton, N.J.) 760:35-52, 2011 [PDF unavailable] [PubMed] [More...]
 Luong HT, Chaplin J, McRae AF, Medland SE, Willemsen G, Nyholt DR, Henders AK, Hoekstra C, Duffy DL, Martin NG, Boomsma DI, Montgomery GW, Painter JN: Variation in BMPR1B, TGFRB1 and BMPR2 and Control of Dizygotic Twinning. Twin Research and Human Genetics 14(5):408-416, 2011 [PDF] [PubMed] [More...]
 Macgregor S, Montgomery GW, Liu JZ, Zhao ZZ, Henders AK, Stark M, Schmid H, Holland EA, Duffy DL, Zhang M, Painter JN, Nyholt DR, Maskiell JA, Jetann J, Ferguson M, Cust AE, Jenkins MA, Whiteman DC, Olsson H, Puig S, Bianchi-Scarrà G, Hansson J, Demenais F, Landi MT, Dębniak T, Mackie R, Azizi E, Bressac-de Paillerets B, Goldstein AM, Kanetsky PA, Gruis NA, Elder DE, Newton-Bishop JA, Bishop DT, Iles MM, Helsing P, Amos CI, Wei Q, Wang LE, Lee JE, Qureshi AA, Kefford RF, Giles GG, Armstrong BK, Aitken JF, Han J, Hopper JL, Trent JM, Brown KM, Martin NG, Mann GJ, Hayward NK: Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nature Genetics 43(11):1114-1118, 2011 [PDF] [OSI] [PubMed] [More...]
2010
 Painter JN, Willemsen G, Nyholt D, Hoekstra C, Duffy DL, Henders AK, Wallace L, Healey S, Cannon-Albright LA, Skolnick M, Martin NG, Boomsma DI, Montgomery GW: A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins. Human Reproduction 25(6):1569-1580, 2010 [PDF] [PubMed] [More...]
 Mosing MA, Verweij KJ, Medland SE, Painter J, Gordon SD, Heath AC, Madden PA, Montgomery GW, Martin NG: A genome-wide association study of self-rated health. Twin Research and Human Genetics 13(4):398-403, 2010 [PDF] [PubMed] [More...]
2009
 Medland SE, Nyholt DR, Painter JN, McEvoy BP, McRae AF, Zhu G, Gordon SD, Ferreira MA, Wright MJ, Henders AK, Campbell MJ, Duffy DL, Hansell NK, Macgregor S, Slutske WS, Heath AC, Montgomery GW, Martin NG: Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans. American Journal of Human Genetics 85:750-755, 2009 [PDF] [OSI] [PubMed] [More...]
2008
 Zhao ZZ, Painter JN, Palmer JS, Webb PM, Hayward NK, Whiteman DC, Boomsma DI, Martin NG, Duffy DL, Montgomery GW: Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning. Human Reproduction 23:2372-2379, 2008 [PDF] [PubMed] [More...]
 Montgomery GW, Nyholt DR, Zhao ZZ, Treloar SA, Painter JN, Missmer SA, Kennedy SH, Zondervan KT: The search for genes contributing to endometriosis risk. Human Reproduction Update 14(5):447-457, 2008 [PDF unavailable] [PubMed] [More...]
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