Works by Duffy, David L.

Results: 97

Erratum.

Published in:

Genetic Epidemiology, 2007, v. 31, n. 7, p. 801, doi. 10.1002/gepi.20268

By:

Visscher, Peter M.;
Duffy, David L.

Publication type:

Article

The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits.

Published in:

Genetic Epidemiology, 2006, v. 30, n. 1, p. 30, doi. 10.1002/gepi.20124

By:

Peter M. Visscher;
David L. Duffy

Publication type:

Article

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities.

Published in:

Genetic Epidemiology, 2004, v. 26, n. 3, p. 231, doi. 10.1002/gepi.10311

By:

Dale R. Nyholt;
Nathan G. Gillespie;
Andrew C. Heath;
Kathleen R. Merikangas;
David L. Duffy;
Nicholas G. Martin

Publication type:

Article

Screening a 2 cM genetic map for allelic association: A simulated oligogenic trait.

Published in:

Genetic Epidemiology, 1995, v. 12, n. 6, p. 595, doi. 10.1002/gepi.1370120612

By:

Duffy, David L.

Publication type:

Article

Direction of causation: Reply to commentaries.

Published in:

Genetic Epidemiology, 1994, v. 11, n. 6, p. 463, doi. 10.1002/gepi.1370110603

By:

Neale, Michael C.;
Duffy, David L.;
Martin, Nicholas G.

Publication type:

Article

Inferring the direction of causation in cross-sectional twin data: Theoretical and empirical considerations.

Published in:

Genetic Epidemiology, 1994, v. 11, n. 6, p. 483, doi. 10.1002/gepi.1370110606

By:

Duffy, David L.;
Martin, Nicholas G.

Publication type:

Article

Risk factors for atherosclerosis in twins.

Published in:

Genetic Epidemiology, 1993, v. 10, n. 6, p. 557, doi. 10.1002/gepi.1370100638

By:

Duffy, David L.;
O'Connell, Dianne L.;
Heller, Richard F.;
Martin, Nicholas G.

Publication type:

Article

Informativeness of twin-nuclear family and nuclear family designs for segregation analysis.

Published in:

Genetic Epidemiology, 1991, v. 8, n. 4, p. 231, doi. 10.1002/gepi.1370080404

By:

Duffy, David L.;
Eaves, Lindon J.;
Vogler, G. P.

Publication type:

Article

Towards the full spectrum of genes for human skin colour.

Published in:

Pigment Cell & Melanoma Research, 2018, v. 31, n. 4, p. 457, doi. 10.1111/pcmr.12691

By:

Sturm, Richard A.;
Duffy, David L.

Publication type:

Article

Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits.

Published in:

Pigment Cell & Melanoma Research, 2014, v. 27, n. 4, p. 552, doi. 10.1111/pcmr.12253

By:

Jagirdar, Kasturee;
Smit, Darren J.;
Ainger, Stephen A.;
Lee, Katie J.;
Brown, Darren L.;
Chapman, Brett;
Zhen Zhao, Zhen;
Montgomery, Grant W.;
Martin, Nicholas G.;
Stow, Jennifer L.;
Duffy, David L.;
Sturm, Richard A.

Publication type:

Article

Human pigmentation: painting by numbers or ancestry?

Published in:

Pigment Cell & Melanoma Research, 2013, v. 26, n. 5, p. 605, doi. 10.1111/pcmr.12135

By:

Sturm, Richard A.;
Duffy, David L.

Publication type:

Article

Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.

Published in:

2011

By:

Ferreira, Manuel A R;
McRae, Allan F;
Medland, Sarah E;
Nyholt, Dale R;
Gordon, Scott D;
Wright, Margaret J;
Henders, Anjali K;
Madden, Pamela A;
Visscher, Peter M;
Wray, Naomi R;
Heath, Andrew C;
Montgomery, Grant W;
Duffy, David L;
Martin, Nicholas G

Publication type:

Correction Notice

Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 4, p. 458, doi. 10.1038/ejhg.2010.191

By:

Ferreira, Manuel A. R.;
McRae, Allan F.;
Medland, Sarah E.;
Nyholt, Dale R.;
Gordon, Scott D.;
Wright, Margaret J.;
Henders, Anjali K.;
Madden, Pamela A.;
Visscher, Peter M.;
Wray, Naomi R.;
Heath, Andrew C.;
Montgomery, Grant W.;
Duffy, David L.;
Martin, Nicholas G.

Publication type:

Article

Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 6, p. 700, doi. 10.1038/ejhg.2009.224

By:

Bouzigon, Emmanuelle;
Forabosco, Paola;
Koppelman, Gerard H.;
Cookson, William O. C. M.;
Dizier, Marie-Hélène;
Duffy, David L.;
Evans, David M.;
Ferreira, Manuel A. R.;
Kere, Juha;
Laitinen, Tarja;
Malerba, Giovanni;
Meyers, Deborah A.;
Moffatt, Miriam;
Martin, Nicholas G.;
Ng, Mandy Y.;
Pignatti, Pier Franco;
Wjst, Mathias;
Kauffmann, Francine;
Demenais, Florence;
Lewis, Cathryn M.

Publication type:

Article

A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 1, p. 94, doi. 10.1038/sj.ejhg.5201729

By:

Gu Zhu;
Montgomery, Grant W;
James, Michael R;
Trent, Jeff M;
Hayward, Nicholas K;
Martin, Nicholas G;
Duffy, David L

Publication type:

Article

ADAM33 haplotypes are associated with asthma in a large Australian population.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1027, doi. 10.1038/sj.ejhg.5201662

By:

Kedda, Mary-Anne;
Duffy, David L.;
Bradley, Bernadette;
O'Hehir, Robyn E.;
Thompson, Philip J.

Publication type:

Article

A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 8, p. 953, doi. 10.1038/sj.ejhg.5201646

By:

Ferreira, Manuel A. R.;
Visscher, Peter M.;
Martin, Nicholas G.;
Duffy, David L.

Publication type:

Article

Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 10, p. 835, doi. 10.1038/sj.ejhg.5201248

By:

Evans, David M;
Zhu, Gu;
Duffy, David L;
Montgomery, Grant W;
Frazer, Ian H;
Martin, Nicholas G

Publication type:

Article

Germline and somatic albinism variants in amelanotic/hypomelanotic melanoma: Increased carriage of TYR and OCA2 variants.

Published in:

PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0238529

By:

Rayner, Jenna E.;
Duffy, David L.;
Smit, Darren J.;
Jagirdar, Kasturee;
Lee, Katie J.;
De'Ambrosis, Brian;
Smithers, B. Mark;
McMeniman, Erin K.;
McInerney-Leo, Aideen M.;
Schaider, Helmut;
Stark, Mitchell S.;
Soyer, H. Peter;
Sturm, Richard A.

Publication type:

Article

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.

Published in:

Nature Genetics, 2011, v. 43, n. 11, p. 1114, doi. 10.1038/ng.958

By:

MacGregor, Stuart;
Montgomery, Grant W;
Liu, Jimmy Z;
Zhao, Zhen Zhen;
Henders, Anjali K;
Stark, Mitchell;
Schmid, Helen;
Holland, Elizabeth A;
Duffy, David L;
Zhang, Mingfeng;
Painter, Jodie N;
Nyholt, Dale R;
Maskiell, Judith A;
Jetann, Jodie;
Ferguson, Megan;
Cust, Anne E;
Jenkins, Mark A;
Whiteman, David C;
Olsson, Håkan;
Puig, Susana

Publication type:

Article

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.

Published in:

Nature Genetics, 2009, v. 41, n. 8, p. 915, doi. 10.1038/ng.410

By:

Falchi, Mario;
Bataille, Veronique;
Hayward, Nicholas K.;
Duffy, David L.;
Bishop, Julia A. Newton;
Pastinen, Tomi;
Cervino, Alessandra;
Zhao, Zhen Z.;
Deloukas, Panos;
Soranzo, Nicole;
Elder, David E.;
Barrett, Jennifer H.;
Martin, Nicholas G.;
Bishop, D. Timothy;
Montgomery, Grant W.;
Spector, Timothy D.

Publication type:

Article

Common sequence variants on 20q11.22 confer melanoma susceptibility.

Published in:

Nature Genetics, 2008, v. 40, n. 7, p. 838, doi. 10.1038/ng.163

By:

Brown, Kevin M.;
MacGregor, Stuart;
Montgomery, Grant W.;
Craig, David W.;
Zhen Zhen Zhao;
Iyadurai, Kelly;
Anjali K. Henders;
Homer, Nils;
Campbell, Megan J.;
Stark, Mitchell;
Thomas, Shane;
Schmid, Helen;
Holland, Elizabeth A.;
Gillanders, Elizabeth M.;
Duffy, David L.;
Maskiell, Judith A.;
Jetann, Jodie;
Ferguson, Megan;
Stephan, Dietrich A.;
Cust, Anne E.

Publication type:

Article

Familial aggregation of albuminuria and arterial hypertension in an Aboriginal Australian community and the contribution of variants in ACE and TP53.

Published in:

BMC Nephrology, 2016, v. 17, p. 1, doi. 10.1186/s12882-016-0396-2

By:

Duffy, David L.;
McDonald, Stephen P.;
Hayhurst, Beverley;
Panagiotopoulos, Sianna;
Smith, Trudy J.;
Wang, Xing L.;
Wilcken, David E.;
Duarte, Natalia L.;
Mathews, John;
Hoy, Wendy E.

Publication type:

Article

Evaluation of Candidate Stromal Epithelial Cross-Talk Genes Identifies Association between Risk of Serous Ovarian Cancer and TERT, a Cancer Susceptibility "Hot- Spot''.

Published in:

PLoS Genetics, 2010, v. 6, n. 7, p. 1, doi. 10.1371/journal.pgen.1001016

By:

Johnatty, Sharon E.;
Beesley, Jonathan;
Xiaoqing Chen;
Macgregor, Stuart;
Duffy, David L.;
Spurdle, Amanda B.;
deFazio, Anna;
Gava, Natalie;
Webb, Penelope M.;
Rossing, Mary Anne;
Doherty, Jennifer Anne;
Goodman, Marc T.;
Lurie, Galina;
Thompson, Pamela J.;
Wilkens, Lynne R.;
Ness, Roberta B.;
Moysich, Kirsten B.;
Chang-Claude, Jenny;
Shan Wang-Gohrke;
Cramer, Daniel W.

Publication type:

Article

Digital Quantification of Human Eye Color Highlights Genetic Association of Three New Loci.

Published in:

PLoS Genetics, 2010, v. 6, n. 5, p. 1, doi. 10.1371/journal.pgen.1000934

By:

Fan Liu;
Wollstein, Andreas;
Hysi, Pirro G.;
Ankra-Badu, Georgina A.;
Spector, Timothy D.;
Park, Daniel;
Gu Zhu;
Larsson, Mats;
Duffy, David L.;
Montgomery, Grant W.;
Mackey, David A.;
Walsh, Susan;
Lao, Oscar;
Hofman, Albert;
Rivadeneira, Fernando;
Vingerling, Johannes R.;
Uitterlinden, André G.;
Martin, Nicholas G.;
Hammond, Christopher J.;
Kayser, Manfred

Publication type:

Article

A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation.

Published in:

PLoS Genetics, 2008, v. 4, n. 5, p. 1, doi. 10.1371/journal.pgen.1000074

By:

Han, Jiali;
Kraft, Peter;
Nan, Hongmei;
Guo, Qun;
Chen, Constance;
Qureshi, Abrar;
Hankinson, Susan E.;
Hu, Frank B.;
Duffy, David L.;
Zhao, Zhen Zhen;
Martin, Nicholas G.;
Montgomery, Grant W.;
Hayward, Nicholas K.;
Thomas, Gilles;
Hoover, Robert N.;
Chanock, Stephen;
Hunter, David J.

Publication type:

Article

Germline variants are associated with increased primary melanoma tumor thickness at diagnosis.

Published in:

Human Molecular Genetics, 2020, v. 29, n. 21, p. 3578, doi. 10.1093/hmg/ddaa222

By:

Mangantig, Ernest;
MacGregor, Stuart;
Iles, Mark M;
Scolyer, Richard A;
Cust, Anne E;
Hayward, Nicholas K;
Montgomery, Grant W;
Duffy, David L;
Thompson, John F;
Henders, Anjali;
Bowdler, Lisa;
Rowe, Casey;
Cadby, Gemma;
Mann, Graham J;
Whiteman, David C;
Long, Georgina V;
Ward, Sarah V;
Khosrotehrani, Kiarash;
Barrett, Jennifer H;
Law, Matthew H

Publication type:

Article

Multiplex melanoma families are enriched for polygenic risk.

Published in:

Human Molecular Genetics, 2020, v. 29, n. 17, p. 2976, doi. 10.1093/hmg/ddaa156

By:

Law, Matthew H;
Aoude, Lauren G;
Duffy, David L;
Long, Georgina V;
Johansson, Peter A;
Pritchard, Antonia L;
Khosrotehrani, Kiarash;
Mann, Graham J;
Montgomery, Grant W;
Iles, Mark M;
Cust, Anne E;
Palmer, Jane M;
Consortium, Melanoma GWAS;
Shannon, Kerwin F;
Spillane, Andrew J;
Stretch, Jonathan R;
Thompson, John F;
Saw, Robyn P M;
Scolyer, Richard A;
Martin, Nicholas G

Publication type:

Article

Association between polymorphisms in the progesterone receptor gene and endometriosis.

Published in:

Molecular Human Reproduction, 2005, v. 11, n. 9, p. 641, doi. 10.1093/molehr/gah221

By:

Treloar, Susan A.;
Zhao, Zhen Zhen;
Armitage, Trudi;
Duffy, David L.;
Wicks, Jacqueline;
O’Connor, Daniel T.;
Martin, Nicholas G.;
Montgomery, Grant W.

Publication type:

Article

Head Motion and Inattention/Hyperactivity Share Common Genetic Influences: Implications for fMRI Studies of ADHD.

Published in:

PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0146271

By:

Couvy-Duchesne, Baptiste;
Ebejer, Jane L.;
Gillespie, Nathan A.;
Duffy, David L.;
Hickie, Ian B.;
Thompson, Paul M.;
Martin, Nicholas G.;
de Zubicaray, Greig I.;
McMahon, Katie L.;
Medland, Sarah E.;
Wright, Margaret J.

Publication type:

Article

Phenotypic Characterization of Nevus and Tumor Patterns in MITF E318K Mutation Carrier Melanoma Patients.

Published in:

Journal of Investigative Dermatology, 2014, v. 134, n. 1, p. 141, doi. 10.1038/jid.2013.272

By:

Sturm, Richard A;
Fox, Carly;
McClenahan, Phil;
Jagirdar, Kasturee;
Ibarrola-Villava, Maider;
Banan, Parastoo;
Abbott, Nicola C;
Ribas, Gloria;
Gabrielli, Brian;
Duffy, David L;
Soyer, H Peter

Publication type:

Article

Noncoding Variations in the Gene Encoding Ceramide Synthase 6 are Associated with Type 2 Diabetes in a Large Indigenous Australian Pedigree.

Published in:

2019

By:

Good, David A.;
Duffy, David L.;
Good, Manuela;
Xia Guo, Cheng;
Busfield, Frances;
Shaw, Anthony;
Shaw, Joanne T. E.

Publication type:

journal article

Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.

Published in:

2013

By:

Ebejer, Jane L;
Duffy, David L;
van der Werf, Julius;
Wright, Margaret J;
Montgomery, Grant;
Gillespie, Nathan A;
Hickie, Ian B;
Martin, Nicholas G;
Medland, Sarah E

Publication type:

Journal Article

Genome-Wide Association Study of Inattention and Hyperactivity–Impulsivity Measured as Quantitative Traits.

Published in:

Twin Research & Human Genetics, 2013, v. 16, n. 2, p. 560, doi. 10.1017/thg.2013.12

By:

Ebejer, Jane L.;
Duffy, David L.;
van der Werf, Julius;
Wright, Margaret J.;
Montgomery, Grant;
Gillespie, Nathan A.;
Hickie, Ian B.;
Martin, Nicholas G.;
Medland, Sarah E.

Publication type:

Article

Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma.

Published in:

2011

By:

Kvaskoff, Marina;
Whiteman, David C;
Zhao, Zhen Z;
Montgomery, Grant W;
Martin, Nicholas G;
Hayward, Nicholas K;
Duffy, David L

Publication type:

journal article

Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning.

Published in:

2011

By:

Luong, Hien T. T;
Chaplin, Justin;
McRae, Allan F;
Medland, Sarah E;
Willemsen, Gonneke;
Nyholt, Dale R;
Henders, Anjali K;
Hoekstra, Chantal;
Duffy, David L;
Martin, Nicholas G;
Boomsma, Dorret I;
Montgomery, Grant W;
Painter, Jodie N

Publication type:

journal article

Report of Endometrial Cancer in Australian BRCA1 and BRCA2 mutation-positive Families.

Published in:

2011

By:

Duffy, David L;
Antill, Yoland C;
Stewart, Colin J;
Young, Joanne P;
Spurdle, Amanda B;
kConFab

Publication type:

journal article

Heritability and linkage analysis of appendicitis utilizing age at onset.

Published in:

2009

By:

Oldmeadow, Christopher;
Mengersen, Kerrie;
Martin, Nicholas;
Duffy, David L.

Publication type:

journal article

The Queensland Study of Melanoma: environmental and genetic associations (Q-MEGA); study design, baseline characteristics, and repeatability of phenotype and sun exposure measures.

Published in:

2008

By:

Baxter, Amanda J.;
Hughes, Maria Celia;
Kvaskoff, Marina;
Siskind, Victor;
Shekar, Sri;
Aitken, Joanne F.;
Green, Adele C.;
Duffy, David L.;
Hayward, Nicholas K.;
Martin, Nicholas G.;
Whiteman, David C.

Publication type:

journal article

A study of diabetes mellitus within a large sample of Australian twins.

Published in:

2008

By:

Condon, Julianne;
Shaw, Joanne E.;
Luciano, Michelle;
Kyvik, Kirsten O.;
Martin, Nicholas G.;
Duffy, David L.

Publication type:

journal article

Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 23, p. 2988, doi. 10.1093/hmg/ddm268

By:

Beaumont, Kimberley A.;
Shekar, Sri N.;
Newton, Richard A.;
James, Michael R.;
Stow, Jennifer L.;
Duffy, David L.;
Sturm, Richard A.

Publication type:

Article

Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles.

Published in:

Human Molecular Genetics, 2007, v. 16, n. 18, p. 2249, doi. 10.1093/hmg/ddm177

By:

Beaumont, Kimberley A.;
Shekar, Sri L.;
Newton, Richard A.;
James, Michael R.;
Stow, Jennifer L.;
Duffy, David L.;
Sturm, Richard A.

Publication type:

Article

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes.

Published in:

Human Molecular Genetics, 2004, v. 13, n. 4, p. 447

By:

Duffy, David L.;
Box, Neil F.;
Chen, Wei;
Palmer, James S.;
Montgomery, Grant W.;
James, Michael R.;
Hayward, Nicholas K.;
Martin, Nicholas G.;
Sturm, Richard A.

Publication type:

Article

Classifying dermoscopic patterns of naevi in a case-control study of melanoma.

Published in:

PLoS ONE, 2017, v. 12, n. 10, p. 1, doi. 10.1371/journal.pone.0186647

By:

McWhirter, Seamus R.;
Duffy, David L.;
Lee, Katie J.;
Wimberley, Glen;
McClenahan, Philip;
Ling, Natalie;
Ardigo, Marco;
Schaider, Helmut;
Soyer, H. Peter;
Sturm, Richard A.

Publication type:

Article

Novel variants in growth differentiation factor 9 in mothers of dizygotic twins.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 11, p. 4713, doi. 10.1210/jc.2006-0970

By:

Palmer, James S.;
Zhen Zhen Zhao;
Hoekstra, Chantal;
Hayward, Nicholas K.;
Webb, Penelope M.;
Whiteman, David C.;
Martin, Nicholas G.;
Boomsma, Dorret I.;
Duffy, David L.;
Montgomery, Grant W.

Publication type:

Article

Dizygotic Twinning Is Not Linked to Variation at the a-Inhibin Locus on Human Chromosome 2.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 9, p. 3391, doi. 10.1210/jcem.85.9.6831

By:

MONTGOMERY, GRANT W.;
DUFFY, DAVID L.;
HALL, JEFF;
HADDON, BARBARA R.;
KUDO, MASATAKA;
MCGEE, ELIZABETH A.;
PALMER, JAMES S.;
HSUEH, AARON J.;
BOOMSMA, DORRET I.;
MARTIN, NICHOLAS G.

Publication type:

Article

Hazard and density estimation from bivariate censored data.

Published in:

Journal of Nonparametric Statistics, 1998, v. 10, n. 1, p. 67, doi. 10.1080/10485259808832754

By:

Dabrowska, Dorota M.;
Duffy, David L.;
Zhang, Zhongwei D.

Publication type:

Article

GWAS of Dizygotic Twinning in an Enlarged Australian Sample of Mothers of DZ Twins.

Published in:

Twin Research & Human Genetics, 2023, v. 26, n. 6, p. 327, doi. 10.1017/thg.2023.45

By:

Gordon, Scott D.;
Duffy, David L.;
Whiteman, David C.;
Olsen, Catherine M.;
McAloney, Kerrie;
Adsett, Jessica M.;
Garden, Natalie A.;
Cross, Simone M.;
List-Armitage, Susan E.;
Brown, Joy;
Beck, Jeffrey J.;
Mbarek, Hamdi;
Medland, Sarah E.;
Montgomery, Grant W.;
Martin, Nicholas G.

Publication type:

Article

The Heritability of Twinning in Seven Large Historic Pedigrees.

Published in:

2022

By:

Duffy, David L.;
Martin, Nicholas G.

Publication type:

journal article

'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers.

Published in:

2021

By:

Loesch, Danuta Z.;
Duffy, David L.;
Martin, Nicholas G.;
Tassone, Flora;
Atkinson, Anna;
Storey, Elsdon

Publication type:

journal article