Works by Wood, Andrew R.
Results: 82
Unclassified endogenous eczema.
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- Contact Dermatitis (01051873), 1999, v. 41, n. 1, p. 18, doi. 10.1111/j.1600-0536.1999.tb06202.x
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- Article
Genetically defined favourable adiposity is not associated with a clinically meaningful difference in clinical course in people with type 2 diabetes but does associate with a favourable metabolic profile.
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- Diabetic Medicine, 2021, v. 38, n. 9, p. 1, doi. 10.1111/dme.14531
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Assessing the Causal Role of Sleep Traits on Glycated Hemoglobin: A Mendelian Randomization Study.
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- 2022
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- journal article
Development and Standardization of an Improved Type 1 Diabetes Genetic Risk Score for Use in Newborn Screening and Incident Diagnosis.
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- 2019
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- journal article
Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis.
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- 2019
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- journal article
Evidence of a causal relationship between body mass index and psoriasis: A mendelian randomization study.
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- 2019
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- journal article
Hundreds of variants clustered in genomic loci and biological pathways affect human height.
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- Nature, 2010, v. 467, n. 7317, p. 832, doi. 10.1038/nature09410
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- Article
Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling.
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- Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-024-55761-2
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Itraconazole and HIV protease inhibitors: an important interaction.
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- Medical Journal of Australia, 1999, v. 170, n. 1, p. 46, doi. 10.5694/j.1326-5377.1999.tb126872.x
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Another explanation for apparent epistasis.
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- Nature, 2014, v. 514, n. 7520, p. E3, doi. 10.1038/nature13691
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- Article
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association.
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- Human Molecular Genetics, 2011, v. 20, n. 20, p. 4082, doi. 10.1093/hmg/ddr328
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- Article
Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-25805-y
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- Article
Evidence of a causal relationship between body mass index and psoriasis: a Mendelian randomization study.
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- Norsk Epidemiologi, 2018, v. 28, n. Supplement 1, p. 25
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- Article
The splice site variant rs11078928 may be associated with a genotype-dependent alteration in expression of GSDMB transcripts.
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- BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-627
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- Article
The impact of Mendelian sleep and circadian genetic variants in a population setting.
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- PLoS Genetics, 2022, v. 18, n. 9, p. 1, doi. 10.1371/journal.pgen.1010356
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- Article
A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor.
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- PLoS Genetics, 2021, v. 17, n. 6, p. 1, doi. 10.1371/journal.pgen.1009577
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- Article
Does physical activity moderate the association between shorter leukocyte telomere length and incident coronary heart disease? Data from 54,180 UK Biobank participants.
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- GeroScience, 2024, v. 46, n. 1, p. 1331, doi. 10.1007/s11357-023-00890-7
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- Article
Prosaposin is a regulator of progranulin levels and oligomerization.
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- Nature Communications, 2016, v. 7, n. 6, p. 11992, doi. 10.1038/ncomms11992
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Biological interpretation of genome-wide association studies using predicted gene functions.
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- Nature Communications, 2015, v. 6, n. 1, p. 5890, doi. 10.1038/ncomms6890
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Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.
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- 2016
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- journal article
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08917-4
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- Article
Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08259-7
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- Article
Clinical Features and Genetic Risk of Demyelination Following Anti-TNF Treatment.
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- Journal of Crohn's & Colitis, 2020, v. 14, n. 12, p. 1653, doi. 10.1093/ecco-jcc/jjaa104
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- Article
Genome-Wide Association Study of Microscopic Colitis in the UK Biobank Confirms Immune-Related Pathogenesis.
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- Journal of Crohn's & Colitis, 2019, v. 13, n. 12, p. 1578, doi. 10.1093/ecco-jcc/jjz104
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- Article
Multiple Loci Are Associated with White Blood Cell Phenotypes.
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- PLoS Genetics, 2011, v. 7, n. 6, p. 1, doi. 10.1371/journal.pgen.1002113
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Causal Relationship between Obesity and Vitamin D Status: Bi-Directional Mendelian Randomization Analysis of Multiple Cohorts.
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- PLoS Medicine, 2013, v. 10, n. 2, p. 1, doi. 10.1371/journal.pmed.1001383
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- Article
Influence of cell distribution and diabetes status on the association between mitochondrial DNA copy number and aging phenotypes in the InCHIANTI study.
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- Aging Cell, 2018, v. 17, n. 1, p. 1, doi. 10.1111/acel.12683
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- Article
Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing.
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- Aging Cell, 2011, v. 10, n. 5, p. 868, doi. 10.1111/j.1474-9726.2011.00726.x
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- Article
Hyperglycaemia is a causal risk factor for upper limb pathologies.
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- International Journal of Epidemiology, 2024, v. 53, n. 1, p. 1, doi. 10.1093/ije/dyad187
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Simulated distributions from negative experiments highlight the importance of the body mass index distribution in explaining depression-body mass index genetic risk score interactions.
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- 2022
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- journal article
Effects of body mass index on relationship status, social contact and socio-economic position: Mendelian randomization and within-sibling study in UK Biobank.
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- 2020
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- journal article
Genetic evidence that higher central adiposity causes gastro-oesophageal reflux disease: a Mendelian randomization study.
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- 2020
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- journal article
Using genetics to understand the causal influence of higher BMI on depression.
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- 2019
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- journal article
Gene-obesogenic environment interactions in the UK Biobank study.
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- 2017
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- journal article
Mendelian randomization study of height and risk of colorectal cancer.
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- International Journal of Epidemiology, 2015, v. 44, n. 2, p. 662, doi. 10.1093/ije/dyv082
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- Article
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19.
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- BMC Proceedings, 2016, v. 10, p. 71, doi. 10.1186/s12919-016-0008-y
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Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.
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- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0185083
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A 3D Renal Proximal Tubule on Chip Model Phenocopies Lowe Syndrome and Dent II Disease Tubulopathy.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 10, p. 5361, doi. 10.3390/ijms22105361
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Defining the role of common variation in the genomic and biological architecture of adult human height.
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- Nature Genetics, 2014, v. 46, n. 11, p. 1173, doi. 10.1038/ng.3097
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Common maternal and fetal genetic variants show expected polygenic effects on risk of small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies.
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- PLoS Genetics, 2020, v. 16, n. 12, p. 1, doi. 10.1371/journal.pgen.1009191
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Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation.
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- eLife, 2022, p. 1, doi. 10.7554/eLife.72452
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Pyogenic granuloma-like lesions in a patient using topical tretinoin.
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- Australasian Journal of Dermatology, 1998, v. 39, n. 4, p. 248, doi. 10.1111/j.1440-0960.1998.tb01483.x
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Melanoma: Accuracy of clinical diagnosis.
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- Australasian Journal of Dermatology, 1998, v. 39, n. 1, p. 31, doi. 10.1111/j.1440-0960.1998.tb01238.x
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- Article
Severe allergy to sorbolene cream.
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- Australasian Journal of Dermatology, 1997, v. 38, n. 1, p. 33, doi. 10.1111/j.1440-0960.1997.tb01096.x
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Office radiotherapy in dermatology: A contemporary perspective.
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- Australasian Journal of Dermatology, 1996, v. 37, n. 2, p. 71, doi. 10.1111/j.1440-0960.1996.tb01009.x
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Genetically proxied therapeutic prolyl-hydroxylase inhibition and cardiovascular risk.
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- Human Molecular Genetics, 2023, v. 32, n. 3, p. 496, doi. 10.1093/hmg/ddac215
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- Article
Fetal alleles predisposing to metabolically favorable adiposity are associated with higher birth weight.
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- Human Molecular Genetics, 2022, v. 31, n. 11, p. 1762, doi. 10.1093/hmg/ddab356
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Corrigendum to: A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin–creatinine ratio.
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- Human Molecular Genetics, 2022, v. 31, n. 9, p. 1544, doi. 10.1093/hmg/ddac022
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Higher adiposity and mental health: causal inference using Mendelian randomization.
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- Human Molecular Genetics, 2021, v. 30, n. 24, p. 2371, doi. 10.1093/hmg/ddab204
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Mitochondrial genetic variation is enriched in G-quadruplex regions that stall DNA synthesis in vitro.
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- Human Molecular Genetics, 2020, v. 29, n. 8, p. 1292, doi. 10.1093/hmg/ddaa043
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