Significance of native title to the petroleum industryYOUNG, Doug; MACGREGOR, Stuart.APPEA journal. 2002, issn 1326-4966, 2Vol, vol 2, 163-173Conference Paper

Use of phenotypic covariates in association analysis by sequential addition of casesMACGREGOR, Stuart; CRADDOCK, Nick; HOLMANS, Peter A et al.European journal of human genetics. 2006, Vol 14, Num 5, pp 529-534, issn 1018-4813, 6 p.Article

Computational study of the mechanism of cyclometalation by palladium acetateDAVIES, David L; DONALD, Steven M. A; MACGREGOR, Stuart A et al.Journal of the American Chemical Society. 2005, Vol 127, Num 40, pp 13754-13755, issn 0002-7863, 2 p.Article

Obesity and Risk of Esophageal Adenocarcinoma and Barrett's Esophagus: A Mendelian Randomization StudyTHRIFT, Aaron P; SHAHEEN, Nicholas J; CORLEY, Douglas A et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 11, issn 0027-8874, 252.1-252.8Article

Genome-wide association identifies ATOH7 as a major gene determining human optic disc sizeMACGREGOR, Stuart; HEWITT, Alex W; CARBONARO, Francis et al.Human molecular genetics (Print). 2010, Vol 19, Num 13, pp 2716-2724, issn 0964-6906, 9 p.Article

Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in EuropeansMEDLAND, Sarah E; NYHOLT, Dale R; CAMPBELL, Megan J et al.American journal of human genetics. 2009, Vol 85, Num 5, pp 750-755, issn 0002-9297, 6 p.Article

Genome partitioning of genetic variation for height from 11,214 sibling pairsVISSCHER, Peter M; MACGREGOR, Stuart; LIU, Yao-Zhong et al.American journal of human genetics. 2007, Vol 81, Num 5, pp 1104-1110, issn 0002-9297, 7 p.Article

Bias, precision and heritability of self-reported and clinically measured height in Australian twinsMACGREGOR, Stuart; COMES, Belinda K; MARTIN, Nicholas G et al.Human genetics. 2006, Vol 120, Num 4, pp 571-580, issn 0340-6717, 10 p.Article

Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorderGREEN, Elaine K; RAYBOULD, Rachel; O'DONOVAN, Michael C et al.Archives of general psychiatry. 2005, Vol 62, Num 6, pp 642-648, issn 0003-990X, 7 p.Article

ABCATransporter Gene Expression and Poor Outcome in Epithelial Ovarian CancerHEDDITCH, Ellen L; GAO, Bo; WILLIAMS, Rebekka T et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 7, issn 0027-8874, dju149.1-dju149.11Article

Meta-Analysis Combining New and Existing Data Sets Confirms that the TERT-CLPTM1L Locus Influences Melanoma RiskLAW, Matthew H; MONTGOMERY, Grant W; BROWN, Kevin M et al.Journal of investigative dermatology. 2012, Vol 132, Num 2, pp 485-487, issn 0022-202X, 3 p.Article

Association Between In Vivo Alcohol Metabolism and Genetic Variation in Pathways that Metabolize the Carbon Skeleton of Ethanol and NADH Reoxidation in the Alcohol Challenge Twin StudyLIND, Penelope A; MACGREGOR, Stuart; HEATH, Andrew C et al.Alcoholism, clinical and experimental research. 2012, Vol 36, Num 12, pp 2074-2085, issn 0145-6008, 12 p.Article

A novel recurrent mutation in MITF predisposes to familial and sporadic melanomaYOKOYAMA, Satoru; WOODS, Susan L; TAYLOR, John C et al.Nature (London). 2011, Vol 480, Num 7375, pp 99-103, issn 0028-0836, 5 p.Article

A 3p26-3p25 Genetic Linkage Finding for DSM-IV Major Depression in Heavy Smoking FamiliesPERGADIA, Michele L; GLOWINSKI, Anne L; NELSON, Elliot C et al.The American journal of psychiatry. 2011, Vol 168, Num 8, pp 848-852, issn 0002-953X, 5 p.Article

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucomaTHORLEIFSSON, Gudmar; BRAGI WALTERS, G; STEFANSSON, Hreinn et al.Nature genetics. 2010, Vol 42, Num 10, pp 906-909, issn 1061-4036, 4 p.Article

Genome-wide association meta-analysis identifies new endometriosis risk lociNYHOLT, Dale R; LOW, Siew-Kee; ATTIA, John et al.Nature genetics. 2012, Vol 44, Num 12, pp 1355-1359, issn 1061-4036, 5 p.Article

Genome-wide association study identifies a locus at 7p15.2 associated with endometriosisPAINTER, Jodie N; ANDERSON, Carl A; GORDON, Scott D et al.Nature genetics. 2011, Vol 43, Num 1, pp 51-54, issn 1061-4036, 4 p.Article

Platinum Sensitivity-Related Germline Polymorphism Discovered via a Cell-Based Approach and Analysis of Its Association with Outcome in Ovarian Cancer PatientsHUANG, R. Stephanie; JOHNATTY, Sharon E; SHUANGLI MI et al.Clinical cancer research (Print). 2011, Vol 17, Num 16, pp 5490-5500, issn 1078-0432, 11 p.Article

Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence : an integrated analysisMACGREGOR, Stuart; LIND, Penelope A; BUCHOLZ, Kathleen K et al.Human molecular genetics (Print). 2009, Vol 18, Num 3, pp 580-593, issn 0964-6906, 14 p.Article

A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's diseaseHAROLD, Denise; MACGREGOR, Stuart; JONES, Lesley et al.Pharmacogenetics and genomics (Print). 2006, Vol 16, Num 2, pp 75-77, issn 1744-6872, 3 p.Article

Familiality of postpartum depression in unipolar disorder : Results of a family studyFORTY, Liz; JONES, Lisa; BREWSTER, Shyama et al.The American journal of psychiatry. 2006, Vol 163, Num 9, pp 1549-1553, issn 0002-953X, 5 p.Article

Genetic variation of brain-derived neurotrophic factor (BDNF) in bipolar disorder : Case-control study of over 3000 individuals from the UKGREEN, Elaine K; RAYBOULD, Rachel; CRADDOCK, Nick et al.British journal of psychiatry (Print). 2006, Vol 188, Num JAN, pp 21-25, issn 0007-1250, 5 p.Article

The Effect on Melanoma Risk of Genes Previously Associated With Telomere LengthILES, Mark M; BISHOP, D. Timothy; ANDRESEN, Per A et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 10, issn 0027-8874, 267.1-267.5Article

Germline Genetic Contributions to Risk for Esophageal Adenocarcinoma, Barrett's Esophagus, and Gastroesophageal RefluxEK, Weronica E; LEVINE, David M; ROMERO, Yvonne et al.Journal of the National Cancer Institute. 2013, Vol 105, Num 22, pp 1711-1718, issn 0027-8874, 8 p.Article

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibilityCOX, Hannah C; LEA, Rod A; RIDKER, Paul M et al.Neurogenetics (Oxford. Print). 2012, Vol 13, Num 3, pp 261-266, issn 1364-6745, 6 p.Article