Dr Rona Strawbridge

  • UKRI Innovation / Rutherford Fund Fellowship at HDR-UK (Mental Health & Wellbeing)

Biography

Dr Rona Strawbridge completed her BSc in Biochemistry with Medical Biochemistry at Cardiff University (UK) in 2003.  Subsequently, Dr Strawbridge moved to Karolinksa Institute (Sweden) to undertake her PhD studies and defended her PhD thesis on "Genetic Studies of Prostate Cancer and Type 2 Diabetes:  MUC1 and GHR" (2003-2008).

Remaining at Karolinksa Institute as a Post-Doctoral Fellow (2009-2011), Dr Strawbridge shifted her focus to genome-wide genetic studies of glucometabolic and cardiovascular traits, participating in many projects run through international genetics consortia, including MAGIC, GIANT and DIAGRAM.  Dr Strawbridge was appointed as a Research Associate Professor (2012-2016), where her research utilised genetics to explore causality of metabolic components on cardiovascular disease, and was awarded Associate Professorship in Molecular Medicine (Docent).  She continues to be affiliated with the Cardiovascular Medicine, Genetics and Genomics group at Karolinska Institute.  

In 2017 Dr Strawbridge moved to Glasgow University (UK) to join Professor Daniel Smith's team, where her focus is using genetics to investigate the link between psychiatric disorders and cardio-metabolic disease.


Research interests

People with schizophrenia, bipolar disorder and major depressive disorder have an increased incidence of cardiovascular disease compared to the general population, although the link is poorly understood.  Dr Strawbridge's research aims are to:

  1. Identify genetic determinants of cross-diagnostic traits associated with psychiatric diseases (following RDoc) criteria)
  2. Use established genetics to try to understand the relationship between serious mental illness and metabolic and cardiovascular diseases.

Grants

Grants and Awards listed are those received whilst working with the University of Glasgow.

  • Mental Health Data Pathfinder
    Medical Research Council
    2018 - 2020
     

Research datasets

Jump to: 2019
Number of items: 1.

2019

Johnston, K., Adams, M. J., Nicholl, B. , Ward, J., Strawbridge, R. , Ferguson, A., McIntosh, A. M., Bailey, M. and Smith, D. (2019) Genome-wide association summary statistics for a genome-wide association study of multisite chronic pain. [Data Collection]

This list was generated on Sun Aug 18 17:57:57 2019 BST.

Publications

List by: Type | Date

Jump to: 2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011 | 2010 | 2008 | 2007
Number of items: 82.

2019

Ward, J. et al. (2019) The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function. Molecular Psychiatry, (doi:10.1038/s41380-019-0439-8) (PMID:31168069) (Early Online Publication)

Lyall, D. M. et al. (2019) Assessing for interaction between APOE ε4, sex and lifestyle on cognitive abilities. Neurology, 92, e2691-e2698. (doi:10.1212/WNL.0000000000007551) (PMID:31028125) (PMCID:PMC6556094)

Johnston, K. J.A., Adams, M. J., Nicholl, B. I. , Ward, J., Strawbridge, R. , Ferguson, A., McIntosh, A., Bailey, M. E.S. and Smith, D. J. (2019) Genome-wide association study of multisite chronic pain in UK Biobank. PLoS Genetics, 15(6), e1008164. (doi:10.1371/journal.pgen.1008164) (PMID:31194737)

Morris, J. et al. (2019) Genetic variation in CADM2 as a link between psychological traits and obesity. Scientific Reports, 9, 7339. (doi:10.1038/s41598-019-43861-9) (PMID:31089183) (PMCID:PMC6517397)

Lyall, D. M. et al. (2019) Association between APOE e4 and white matter hyperintensity volume, but not total brain volume or white matter integrity. Brain Imaging and Behavior, (doi:10.1007/s11682-019-00069-9) (PMID:30903549) (Early Online Publication)

Strawbridge, R. J. et al. (2019) Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide. EBioMedicine, 41, pp. 517-525. (doi:10.1016/j.ebiom.2019.02.005) (PMID:30745170) (PMCID:PMC6442001)

2018

Franceschini, N. et al. (2018) GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes. Nature Communications, 9, 5141. (doi:10.1038/s41467-018-07340-5) (PMID:30510157) (PMCID:PMC6277418)

Evangelou, E. et al. (2018) Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics, 50, pp. 1412-1425. (doi:10.1038/s41588-018-0205-x) (PMID:30224653)

Ward, J. et al. (2018) Polygenic risk scores for major depressive disorder and neuroticism as predictors of antidepressant response: meta-analysis of three treatment cohorts. PLoS ONE, 13(9), e0203896. (doi:10.1371/journal.pone.0203896) (PMID:30240446) (PMCID:PMC6150505)

Strawbridge, R. et al. (2018) Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression. Translational Psychiatry, 8, 178. (doi:10.1038/s41398-018-0236-1) (PMID:30181555)

Ferguson, A. et al. (2018) Genome-wide association study of circadian rhythmicity in 71,500 UK Biobank participants and polygenic association with mood instability. EBioMedicine, 35, pp. 279-287. (doi:10.1016/j.ebiom.2018.08.004) (PMID:30120083) (PMCID:PMC6154782)

Strawbridge, R. J. and van Zuydam, N. R. (2018) Shared genetic contribution of type 2 diabetes and cardiovascular disease: Implications for prognosis and treatment. Current Diabetes Reports, 18(8), 59. (doi:10.1007/s11892-018-1021-5) (PMID:29938349) (PMCID:PMC6015804)

Lyall, L. M. et al. (2018) Association of disrupted circadian rhythmicity with mood disorders, subjective wellbeing, and cognitive function: a cross-sectional study of 91 105 participants from the UK Biobank. Lancet Psychiatry, 5(6), pp. 507-514. (doi:10.1016/S2215-0366(18)30139-1) (PMID:29776774)

Lundbäck, V., Kulyte, A., Strawbridge, R. J. , Ryden, M., Arner, P., Marcus, C. and Dahlman, I. (2018) FAM13A and POM121C are candidate genes for fasting insulin: functional follow-up analysis of a genome-wide association study. Diabetologia, 61(5), pp. 1112-1123. (doi:10.1007/s00125-018-4572-8) (PMID:29487953)

Lyall, L. M. et al. (2018) Seasonality of depressive symptoms in women but not in men: a cross-sectional study in the UK Biobank cohort. Journal of Affective Disorders, 229, pp. 296-305. (doi:10.1016/j.jad.2017.12.106) (PMID:29329063)

Strawbridge, R. J. et al. (2018) Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort. Translational Psychiatry, 8, 39. (doi:10.1038/s41398-017-0079-1) (PMID:29391395) (PMCID:PMC5804026)

2017

Ward, J. et al. (2017) Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia. Translational Psychiatry, 7, 1264. (doi:10.1038/s41398-017-0012-7) (PMID:29187730) (PMCID:PMC5802589)

Scott, R. A. et al. (2017) An expanded genome-wide association study of type 2 diabetes in Europeans. Diabetes, 66(11), pp. 2888-2902. (doi:10.2337/db16-1253) (PMID:28566273)

Strawbridge, R. J. et al. (2017) Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in subclinical vascular remodelling using Mendelian randomisation. Atherosclerosis, 266, pp. 196-204. (doi:10.1016/j.atherosclerosis.2017.09.031) (PMID:29040868)

Gregg, E. et al. (2017) Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: a transethnic genome-wide meta-analysis. PLoS Medicine, 14(9), e1002383. (doi:10.1371/journal.pmed.1002383) (PMID:28898252) (PMCID:PMC5595282)

Wain, L. V. et al. (2017) Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney. Hypertension, 70(3), e4-e19. (doi:10.1161/HYPERTENSIONAHA.117.09438) (PMID:28739976)

Saleheen, D. et al. (2017) Loss of cardio-protective effects at the ADAMTS7 locus due to gene-smoking interactions. Circulation, 135(24), pp. 2336-2353. (doi:10.1161/CIRCULATIONAHA.116.022069) (PMID:28461624)

Frånberg, M., Strawbridge, R. J. , Hamsten, A., de Faire, U., Lagergren, J. and Sennblad, B. (2017) Fast and general tests of genetic interaction for genome-wide association studies. PLoS Computational Biology, 13(6), e1005556. (doi:10.1371/journal.pcbi.1005556) (PMID:28586362) (PMCID:PMC5478145)

Justice, A. E. et al. (2017) Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nature Communications, 8, 14977. (doi:10.1038/ncomms14977) (PMID:28443625) (PMCID:PMC5414044)

Folkersen, L. et al. (2017) Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease. PLoS Genetics, 13(4), e1006706. (doi:10.1371/journal.pgen.1006706) (PMID:28369058) (PMCID:PMC5393901)

2016

Bruzelius, M. et al. (2016) PDGFB, a new candidate plasma biomarker for venous thromboembolism: results from the VEREMA affinity proteomics study. Blood, 128(23), e59-e66. (doi:10.1182/blood-2016-05-711846) (PMID:27742707)

Ehret, G. B. et al. (2016) The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nature Genetics, 48(10), pp. 1171-1184. (doi:10.1038/ng.3667) (PMID:27618452) (PMCID:PMC5042863)

Strawbridge, R. J. et al. (2016) Soluble CD93 is involved in metabolic dysregulation but does not influence carotid intima-media thickness. Diabetes, 65(10), pp. 2888-2899. (doi:10.2337/db15-1333) (PMID:27659228)

Kanoni, S. et al. (2016) Analysis with the exome array identifies multiple new independent variants in lipid loci. Human Molecular Genetics, 25(18), pp. 4094-4106. (doi:10.1093/hmg/ddw227) (PMID:27466198) (PMCID:PMC5291227)

McLeod, O. et al. (2016) Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease. Cytokine, 81, pp. 1-9. (doi:10.1016/j.cyto.2016.01.007) (PMID:26821299) (PMCID:PMC4837217)

Paramel Varghese, G. et al. (2016) NLRP3 inflammasome expression and activation in human atherosclerosis. Journal of the American Heart Association, 5(5), e003031. (doi:10.1161/JAHA.115.003031) (PMID:27207962) (PMCID:PMC4889178)

Strawbridge, R. J. , Laumen, H., Hamsten, A., Breier, M., Grallert, H., Hauner, H., Arner, P. and Dahlman, I. (2016) Effects of genetic loci associated with central obesity on adipocyte lipolysis. PLoS ONE, 11(4), e0153990. (doi:10.1371/journal.pone.0153990) (PMID:27104953) (PMCID:PMC4841524)

Zanoni, P. et al. (2016) Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease. Science, 351(6278), pp. 1166-1171. (doi:10.1126/science.aad3517) (PMID:26965621) (PMCID:PMC4889017)

Dahlman, I., Rydén, M., Brodin, D., Grallert, H., Strawbridge, R. J. and Arner, P. (2016) Numerous genes in loci associated with body fat distribution are linked to adipose function. Diabetes, 65(2), pp. 433-437. (doi:10.2337/db15-0828) (PMID:26798124)

Bruzelius, M. et al. (2016) F11 is associated with recurrent VTE in women: a prospective cohort study. Thrombosis and Haemostasis, 115(2), pp. 406-414. (doi:10.1160/TH15-06-0459) (PMID:26423325)

2015

Gaulton, K. J. et al. (2015) Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nature Genetics, 47(12), pp. 1415-1425. (doi:10.1038/ng.3437) (PMID:26551672) (PMCID:MC4666734)

Winkler, T. W. et al. (2015) The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study. PLoS Genetics, 11(10), e1005378. (doi:10.1371/journal.pgen.1005378) (PMID:26426971) (PMCID:PMC4591371)

Huffman, J. E. et al. (2015) Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF. Blood, 126(11), e19-e29. (doi:10.1182/blood-2015-02-624551) (PMID:26105150) (PMCID:PMC4566813)

Jiao, H., Arner, P., Gerdhem, P., Strawbridge, R. J. , Näslund, E., Thorell, A., Hamsten, A., Kere, J. and Dahlman, I. (2015) Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity. European Journal of Human Genetics, 23(9), pp. 1216-1222. (doi:10.1038/ejhg.2014.255) (PMID:25406998) (PMCID:PMC4538196)

Persson, J. et al. (2015) Sex‐specific effects of adiponectin on carotid intima‐media thickness and incident cardiovascular disease. Journal of the American Heart Association, 4(8), e001853. (doi:10.1161/JAHA.115.001853) (PMID:26276317) (PMCID:PMC4599454)

Joshi, P. K. et al. (2015) Directional dominance on stature and cognition in diverse human populations. Nature, 523(7561), pp. 459-462. (doi:10.1038/nature14618) (PMID:26131930)

Moreno Velásquez, I. et al. (2015) Duffy antigen receptor genetic variant and the association with Interleukin 8 levels. Cytokine, 72(2), pp. 178-184. (doi:10.1016/j.cyto.2014.12.019) (PMID:25647274)

den Hoed, M. et al. (2015) GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb. Atherosclerosis, 239(2), pp. 304-310. (doi:10.1016/j.atherosclerosis.2015.01.032) (PMID:25682028)

Zimmermann, E. et al. (2015) Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults. Obesity Reviews, 16(4), pp. 327-340. (doi:10.1111/obr.12263)

Gigante, B. et al. (2015) Analysis of the role of interleukin 6 receptor haplotypes in the regulation of circulating levels of inflammatory biomarkers and risk of coronary heart disease. PLoS ONE, 10(3), e0119980. (doi:10.1371/journal.pone.0119980) (PMID:25781951) (PMCID:PMC4364007)

Silveira, A. et al. (2015) Plasma IL-5 concentration and subclinical carotid atherosclerosis. Atherosclerosis, 239(1), pp. 125-130. (doi:10.1016/j.atherosclerosis.2014.12.046) (PMID:25587992) (PMCID:PMC4340644)

Shungin, D. et al. (2015) New genetic loci link adipose and insulin biology to body fat distribution. Nature, 518(7538), pp. 187-196. (doi:10.1038/nature14132) (PMID:25673412) (PMCID:PMC4338562)

Bruzelius, M., Bottai, M., Sabater-Lleal, M., Strawbridge, R.J. , Bergendal, A., Silveira, A., Sundström, A., Kieler, H., Hamsten, A. and Odeberg, J. (2015) Predicting venous thrombosis in women using a combination of genetic markers and clinical risk factors. Journal of Thrombosis and Haemostasis, 13(2), pp. 219-227. (doi:10.1111/jth.12808) (PMID:25472531)

Wessel, J. et al. (2015) Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nature Communications, 6, 5897. (doi:10.1038/ncomms6897) (PMID:25631608) (PMCID:PMC4311266)

Locke, A. E. et al. (2015) Genetic studies of body mass index yield new insights for obesity biology. Nature, 518(7538), pp. 197-206. (doi:10.1038/nature14177) (PMID:25673413) (PMCID:PMC4382211)

Strodthoff, D. et al. (2015) Toll-like receptor 3 influences glucose homeostasis and β-cell insulin secretion. Diabetes, 64(10), pp. 3425-3438. (doi:10.2337/db14-0838) (PMID:25918231)

2014

Gigante, B. et al. (2014) Low levels of IgM antibodies against phosphorylcholine are associated with fast carotid intima media thickness progression and cardiovascular risk in men. Atherosclerosis, 236(2), pp. 394-399. (doi:10.1016/j.atherosclerosis.2014.07.030) (PMID:25150937)

Bruzelius, M. et al. (2014) Influence of coronary artery disease-associated genetic variants on risk of venous thromboembolism. Thrombosis Research, 134(2), pp. 426-432. (doi:10.1016/j.thromres.2014.03.054) (PMID:24745723)

Strawbridge, R. J. et al. (2014) A serum 25-hydroxyvitamin D concentration-associated genetic variant in DHCR7 interacts with type 2 diabetes status to influence subclinical atherosclerosis (measured by carotid intima–media thickness). Diabetologia, 57(6), pp. 1159-1172. (doi:10.1007/s00125-014-3215-y) (PMID:24663808)

Mahajan, A. et al. (2014) Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics, 46(3), pp. 234-244. (doi:10.1038/ng.2897) (PMID:24509480) (PMCID:PMC3969612)

McLeod, O. et al. (2014) Plasma autoantibodies against apolipoprotein B-100 peptide 210 in subclinical atherosclerosis. Atherosclerosis, 232(1), pp. 242-248. (doi:10.1016/j.atherosclerosis.2013.11.041) (PMID:24401246)

Baumert, J. et al. (2014) No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects. PLoS ONE, 9(12), e111156. (doi:10.1371/journal.pone.0111156) (PMID:25551457) (PMCID:PMC4281156)

Wood, A. R. et al. (2014) Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, 46(11), pp. 1173-1186. (doi:10.1038/ng.3097)

2013

Deleskog, A. et al. (2013) Serum 25-hydroxyvitamin D concentration in subclinical carotid atheroscleros. Arteriosclerosis, Thrombosis, and Vascular Biology, 33(11), pp. 2633-2638. (doi:10.1161/ATVBAHA.113.301593) (PMID:24072691)

Do, R. et al. (2013) Common variants associated with plasma triglycerides and risk for coronary artery disease. Nature Genetics, 45(11), pp. 1345-1352. (doi:10.1038/ng.2795) (PMID:24097064) (PMCID:PMC3904346)

Willer, C. J. et al. (2013) Discovery and refinement of loci associated with lipid levels. Nature Genetics, 45(11), pp. 1274-1283. (doi:10.1038/ng.2797) (PMID:24097068) (PMCID:PMC3838666)

Scott, R.A. et al. (2013) Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. Nature Genetics, 44(9), pp. 991-1005. (doi:10.1038/ng.2385)

Paramel, G. V., Folkersen, L., Strawbridge, R. J. , Elmabsout, A. A., Särndahl, E., Lundman, P., Jansson, J.-H., Hansson, G. K., Sirsjö, A. and Fransén, K. (2013) CARD8 gene encoding a protein of innate immunity is expressed in human atherosclerosis and associated with markers of inflammation. Clinical Science, 125(8), pp. 401-407. (doi:10.1042/CS20120572) (PMID:23611467)

Randall, J. C. et al. (2013) Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits. PLoS Genetics, 9(6), e1003500. (doi:10.1371/journal.pgen.1003500) (PMID:23754948) (PMCID:PMC3674993)

Berndt, S. I. et al. (2013) Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics, 45(5), pp. 501-512. (doi:10.1038/ng.2606) (PMID:23563607) (PMCID:PMC3973018)

Harrison, S. C. et al. (2013) A gene-centric study of common carotid artery remodelling. Atherosclerosis, 226(2), pp. 440-446. (doi:10.1016/j.atherosclerosis.2012.11.002) (PMID:23246012) (PMCID:PMC3573227)

Shah, S. et al. (2013) Causal relevance of blood lipid fractions in the development of carotid atherosclerosis: mendelian randomization analysis. Circulation: Cardiovascular Genetics, 6(1), pp. 63-72. (doi:10.1161/CIRCGENETICS.112.963140) (PMID:23275344)

Sabater-Lleal, M. et al. (2013) Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. Circulation, 128(12), pp. 1310-1324. (doi:10.1161/CIRCULATIONAHA.113.002251)

2012

Huang, J. et al. (2012) Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood, 120(24), pp. 4873-4881. (doi:10.1182/blood-2012-06-436188) (PMID:22990020) (PMCID:PMC3520624)

Gertow, K. et al. (2012) Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk. Circulation: Cardiovascular Genetics, 5(6), pp. 656-665. (doi:10.1161/CIRCGENETICS.112.963660) (PMID:2315247)

Morris, A. P. et al. (2012) Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nature Genetics, 44(9), pp. 981-990. (doi:10.1038/ng.2383) (PMID:22885922) (PMCID:PMC3442244)

Helgadottir, A. et al. (2012) Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism. Journal of the American College of Cardiology, 60(8), pp. 722-729. (doi:10.1016/j.jacc.2012.01.078) (PMID:22898070)

Manning, A.K. et al. (2012) A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nature Genetics, 44, pp. 659-669. (doi:10.1038/ng.2274)

2011

Strawbridge, R.J. et al. (2011) Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. Diabetes, 60(10), pp. 2624-2634. (doi:10.2337/db11-0415)

The IBC 50K CAD Consortium, and Strawbridge, R. (2011) Large-scale gene-centric analysis identifies novel variants for coronary artery disease. PLoS Genetics, 7(9), e1002260. (doi:10.1371/journal.pgen.1002260) (PMID:21966275) (PMCID:PMC3178591)

Peden, J. F. et al. (2011) A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nature Genetics, 43(4), pp. 339-344. (doi:10.1038/ng.782) (PMID:21378988)

Sandling, J. K. et al. (2011) A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE. European Journal of Human Genetics, 19(4), pp. 479-484. (doi:10.1038/ejhg.2010.197) (PMID:21179067) (PMCID:PMC3060320)

2010

Soranzo, N. et al. (2010) Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways. Diabetes, 59(12), pp. 3229-3239. (doi:10.2337/db10-0502) (PMID:20858683) (PMCID:PMC2992787)

Heid, I. M. et al. (2010) Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics, 42(11), pp. 949-960. (doi:10.1038/ng.685) (PMID:20935629) (PMCID:PMC3000924)

2008

Strawbridge, R. J. , Nister, M., Brismar, K., Li, C. and Lindström, S. (2008) Influence of MUC1 genetic variation on prostate cancer risk and survival. European Journal of Human Genetics, 16(12), pp. 1521-1525. (doi:10.1038/ejhg.2008.131) (PMID:18628787)

Strawbridge, R. J. , Nistér, M., Brismar, K., Grönberg, H. and Li, C. (2008) MUC1 as a putative prognostic marker for prostate cancer. Biomarker Insights, 3, pp. 303-315. (PMID:19578514) (PMCID:PMC2688377)

2007

Strawbridge, R.J. , Kärvestedt, L., Li, C., Efendic, S., Östenson, C.G., Gu, H.F. and Brismar, K. (2007) GHR exon 3 polymorphism: Association with type 2 diabetes mellitus and metabolic disorder. Growth Hormone and IGF Research, 17(5), pp. 392-398. (doi:10.1016/j.ghir.2007.04.005) (PMID:17537658)

This list was generated on Sat Aug 17 20:54:56 2019 BST.
Jump to: Articles
Number of items: 82.

Articles

Ward, J. et al. (2019) The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function. Molecular Psychiatry, (doi:10.1038/s41380-019-0439-8) (PMID:31168069) (Early Online Publication)

Lyall, D. M. et al. (2019) Assessing for interaction between APOE ε4, sex and lifestyle on cognitive abilities. Neurology, 92, e2691-e2698. (doi:10.1212/WNL.0000000000007551) (PMID:31028125) (PMCID:PMC6556094)

Johnston, K. J.A., Adams, M. J., Nicholl, B. I. , Ward, J., Strawbridge, R. , Ferguson, A., McIntosh, A., Bailey, M. E.S. and Smith, D. J. (2019) Genome-wide association study of multisite chronic pain in UK Biobank. PLoS Genetics, 15(6), e1008164. (doi:10.1371/journal.pgen.1008164) (PMID:31194737)

Morris, J. et al. (2019) Genetic variation in CADM2 as a link between psychological traits and obesity. Scientific Reports, 9, 7339. (doi:10.1038/s41598-019-43861-9) (PMID:31089183) (PMCID:PMC6517397)

Lyall, D. M. et al. (2019) Association between APOE e4 and white matter hyperintensity volume, but not total brain volume or white matter integrity. Brain Imaging and Behavior, (doi:10.1007/s11682-019-00069-9) (PMID:30903549) (Early Online Publication)

Strawbridge, R. J. et al. (2019) Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide. EBioMedicine, 41, pp. 517-525. (doi:10.1016/j.ebiom.2019.02.005) (PMID:30745170) (PMCID:PMC6442001)

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This list was generated on Sat Aug 17 20:54:56 2019 BST.