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Exploring the Germline Genetics of In Situ and Invasive Cutaneous Melanoma: A Genome-Wide Association Study Meta-Analysis.
- Published in:
- JAMA Dermatology, 2024, v. 160, n. 9, p. 964, doi. 10.1001/jamadermatol.2024.2601
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- Article
Association between polymorphisms in the progesterone receptor gene and endometriosis.
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- Molecular Human Reproduction, 2005, v. 11, n. 9, p. 641, doi. 10.1093/molehr/gah221
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- Article
Variation in Latent Classes of Adult Attention-Deficit Hyperactivity Disorder by Sex and Environmental Adversity.
- Published in:
- 2016
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- Publication type:
- journal article
GWAS of Dizygotic Twinning in an Enlarged Australian Sample of Mothers of DZ Twins.
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- Twin Research & Human Genetics, 2023, v. 26, n. 6, p. 327, doi. 10.1017/thg.2023.45
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- Article
The Heritability of Twinning in Seven Large Historic Pedigrees.
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- 2022
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- Publication type:
- journal article
'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers.
- Published in:
- 2021
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- Publication type:
- journal article
Variation at and Asthma on the Island of Tristan da Cunha.
- Published in:
- 2019
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- Publication type:
- journal 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
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- Publication type:
- journal article
Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.
- Published in:
- 2013
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- 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
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- Publication type:
- Article
Variation in BMPR1B, TGFRB1 and BMPR2 and control of dizygotic twinning.
- Published in:
- 2011
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- Publication type:
- journal article
Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma.
- Published in:
- 2011
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- Publication type:
- journal article
Report of Endometrial Cancer in Australian BRCA1 and BRCA2 mutation-positive Families.
- Published in:
- 2011
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- Publication type:
- journal article
Heritability and linkage analysis of appendicitis utilizing age at onset.
- Published in:
- 2009
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- Publication type:
- journal article
A study of diabetes mellitus within a large sample of Australian twins.
- Published in:
- 2008
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- 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
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- Publication type:
- journal article
Communication Skills of House Officers.
- Published in:
- Annals of Internal Medicine, 1980, v. 93, n. 2, p. 354, doi. 10.7326/0003-4819-93-2-354
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- 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
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- Publication type:
- Article
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
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- Nature Genetics, 2009, v. 41, n. 8, p. 915, doi. 10.1038/ng.410
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- Publication type:
- Article
Common sequence variants on 20q11.22 confer melanoma susceptibility.
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- Nature Genetics, 2008, v. 40, n. 7, p. 838, doi. 10.1038/ng.163
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- Publication type:
- Article
Familial aggregation of albuminuria and arterial hypertension in an Aboriginal Australian community and the contribution of variants in ACE and TP53.
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- BMC Nephrology, 2016, v. 17, p. 1, doi. 10.1186/s12882-016-0396-2
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- Article
GSTP1 does not modify MC1R effects on melanoma risk.
- Published in:
- Experimental Dermatology, 2017, v. 26, n. 8, p. 730, doi. 10.1111/exd.13114
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- Article
Attention Deficit Hyperactivity Disorder in Australian Adults: Prevalence, Persistence, Conduct Problems and Disadvantage.
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- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0047404
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- Publication type:
- Article
Genome-Wide Association Studies of Asthma in Population-Based Cohorts Confirm Known and Suggested Loci and Identify an Additional Association near HLA.
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- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0044008
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- Publication type:
- Article
A Non-Synonymous Mutation in the Canine Pkd1 Gene Is Associated with Autosomal Dominant Polycystic Kidney Disease in Bull Terriers.
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- PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022455
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- Article
Novel variants in growth differentiation factor 9 in mothers of dizygotic twins.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 11, p. 4713, doi. 10.1210/jc.2006-0970
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- Publication type:
- Article
Dizygotic Twinning Is Not Linked to Variation at the a-Inhibin Locus on Human Chromosome 2.
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- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 9, p. 3391, doi. 10.1210/jcem.85.9.6831
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- Article
The EPAS1 gene influences the aerobic–anaerobic contribution in elite endurance athletes.
- Published in:
- Human Genetics, 2005, v. 118, n. 3/4, p. 416, doi. 10.1007/s00439-005-0066-0
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- Publication type:
- Article
Assessing the genetic risk of nodular melanoma using a candidate gene approach.
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- British Journal of Dermatology, 2024, v. 190, n. 2, p. 199, doi. 10.1093/bjd/ljad365
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- Article
The MC1R r allele does not increase melanoma risk in MITF E318K carriers.
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- British Journal of Dermatology, 2023, v. 188, n. 6, p. 770, doi. 10.1093/bjd/ljad041
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- Article
Publisher Correction: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08078-w
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- Article
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06649-5
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- Publication type:
- Article
Genome-Wide Association Study Suggests the Variant rs7551288*A within the DHCR24 Gene Is Associated with Poor Overall Survival in Melanoma Patients.
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- Cancers, 2022, v. 14, n. 10, p. 2410, doi. 10.3390/cancers14102410
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- Article
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.
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- 2011
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- 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
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- Publication type:
- Article
Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy.
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- European Journal of Human Genetics, 2010, v. 18, n. 6, p. 700, doi. 10.1038/ejhg.2009.224
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- Publication type:
- Article
A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions.
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- European Journal of Human Genetics, 2007, v. 15, n. 1, p. 94, doi. 10.1038/sj.ejhg.5201729
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- Article
ADAM33 haplotypes are associated with asthma in a large Australian population.
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- European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1027, doi. 10.1038/sj.ejhg.5201662
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- Article
A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits.
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- European Journal of Human Genetics, 2006, v. 14, n. 8, p. 953, doi. 10.1038/sj.ejhg.5201646
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- Article
Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q.
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- European Journal of Human Genetics, 2004, v. 12, n. 10, p. 835, doi. 10.1038/sj.ejhg.5201248
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- Article
Evidence of Genetic Effects on Blood Lead Concentration.
- Published in:
- Environmental Health Perspectives, 2007, v. 115, n. 8, p. 1224, doi. 10.1289/ehp.8847
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- Publication type:
- Article
Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity.
- Published in:
- Human Reproduction, 2024, v. 39, n. 1, p. 240, doi. 10.1093/humrep/dead247
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- 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
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- Article
Identification of a melanoma susceptibility locus and somatic mutation in TET2.
- Published in:
- Carcinogenesis, 2014, v. 35, n. 9, p. 2097
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- Publication type:
- Article
Human pigmentation genes under environmental selection.
- Published in:
- Genome Biology, 2012, v. 13, n. 9, p. 248, doi. 10.1186/gb-2012-13-9-248
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- 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
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- Publication type:
- Article
Multiple Pigmentation Gene Polymorphisms Account for a Substantial Proportion of Risk of Cutaneous Malignant Melanoma.
- Published in:
- Journal of Investigative Dermatology, 2010, v. 130, n. 2, p. 520, doi. 10.1038/jid.2009.258
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- Publication type:
- Article
A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability.
- Published in:
- Journal of Investigative Dermatology, 2009, v. 129, n. 9, p. 2211, doi. 10.1038/jid.2009.48
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- Publication type:
- Article
Analysis of Cultured Human Melanocytes Based on Polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P Loci.
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- Journal of Investigative Dermatology, 2009, v. 129, n. 2, p. 392, doi. 10.1038/jid.2008.211
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- Publication type:
- Article
Linkage and Association Analysis of Spectrophotometrically Quantified Hair Color in Australian Adolescents: the Effect of OCA2 and HERC2.
- Published in:
- Journal of Investigative Dermatology, 2008, v. 128, n. 12, p. 2807, doi. 10.1038/jid.2008.147
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- Publication type:
- Article