Edinburgh CRF



Publications

AuthorsTitlePublicationPublication DateVolumeIssuePages
Adele M. Taylora, Stuart J. Ritchiea, b, Ian J. Deary
Associations of intelligence across the life course with optimism and pessimism in older ageIntelligence
3/2017



Stuart J. Ritchiea, b, , , Elliot M. Tucker-Drobc, Simon R. Coxa, b, Janie Corleya, Dominika Dykierta, b, Paul Redmonda, Alison Pattiea, Adele M. Taylora, Ruth Sibbetta, b, d, John M. Starra, b, d, Ian J. Dearya, b
Predictors of ageing-related decline across multiple cognitive functionsIntelligence
8/2016
59

115-126
Stuart J. Ritchiea, b, , , Elliot M. Tucker-Drobc, Simon R. Coxa, b, Janie Corleya, Dominika Dykierta, b, Paul Redmonda, Alison Pattiea, Adele M. Taylora, Ruth Sibbetta, b, d, John M. Starra, b, d, Ian J. Deary
Predictors of age-related decline across multiple cognitive functionsIntelligence
11/2016
59

115-126
Okbay, A., 110 authors, Deary, I. J., 68 authors, Cesarini, D.
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analysesNature Genetics
6/2016
48

624-633
Arden et al
The association between intelligence and lifespan is mostly genetic. International Journal of Epidemiology
3/2016
45
2
576-7
Cheng et al
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1. Scientific Reports
12/2015
5

17369
Fallon et al
Randomized Double-Blind Trial of Pregabalin Versus Placebo in Conjunction With Palliative Radiotherapy for Cancer-Induced Bone Pain. J Clin Oncol.
2015



Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, et al.
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.Nature genetics
12/2015
48
2
134-43
Harris et al
Polygenic risk of ischemic stroke is associated with cognitive ability. Neurology
2015



Rahbari R, Wuster A, Lindsay SJ, Hardwick RJ, Alexandrov LB, Al Turki S, et al.
Timing, rates and spectra of human germline mutation.Nature genetics
12/2015
48
2
126-33
Soler Artigas M1, Wain LV1, Miller S2, Kheirallah AK2, Huffman JE3, Ntalla I1, Shrine N1, Obeidat M4, Trochet H3,5, McArdle WL6, Alves AC7, Hui J8,9,10,11, Zhao JH12, Joshi PK13, Teumer A14,15, Albrecht E16, Imboden M17,18, Rawal R16,19,20, Lopez LM21,22, Marten J3, Enroth S23, Surakka I24,25, Polasek O13,26, Lyytikäinen LP27,28, Granell R6, Hysi PG29, Flexeder C30, Mahajan A31, Beilby J8,9,11, Bossé Y32, Brandsma CA33, Campbell H13, Gieger C16,19,20, Gläser S34, González JR35,36,37, Grallert H19, Hammond CJ29, Harris SE21,38, Hartikainen AL39, Heliövaara M25, Henderson J6, Hocking L5,40, Horikoshi M31,41, Hutri-Kähönen N42,43, Ingelsson E31,44,45, Johansson Å23,46, Kemp JP6,47,48, Kolcic I26, Kumar A17,18,31,49, Lind L50, Melén E51, Musk AW8,52,53, Navarro P3, Nickle DC54, Padmanabhan S5,55, Raitakari OT56,57, Ried JS16, Ripatti S24,58,59, Schulz H30,60, Scott RA12, Sin DD4,61, Starr JM21,62; UK BiLEVE, Viñuela A29, Völzke H14, Wild SH13, Wright AF3, Zemunik T63, Jarvis DL64,65, Spector TD29, Evans DM6,47,48, Lehtimäki T27,28, Vitart V3, Kähönen M66, Gyllensten U23, Rudan I13,67, Deary IJ21,22, Karrasch S30,68,69, Probst-Hensch NM17,18, Heinrich J30,60,70, Stubbe B34, Wilson JF3,13, Wareham NJ12, James AL8,71,53, Morris AP31,72,73, Jarvelin MR7,74,75,76, Hayward C5, Sayers I2, Strachan DP77, Hall IP2, Tobin MD1,78
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputationNat Commun
12/2015
4
6

Williams SR, Hsu FC, Keene KL, Chen WM, Nelson S, Southerland AM, et al.
Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.Neurology
12/2015
86
4
351-9
Wendy Johnson, , Caroline E. Brett, Catherine Calvin, Ian J. Deary
Childhood characteristics and participation in Scottish Mental Survey 1947 6-Day Sample Follow-ups: Implications for participation in aging studiesIntelligence
12/2015
54

70-79
Briffa et al
Multi-Scale Genomic, Transcriptomic and Proteomic Analysis of Colorectal Cancer Cell Lines to Identify Novel Biomarkers. PLoS One.
12/2015
10
12
e0144708
de Vries PS, Chasman DI, Sabater-Lleal M, Chen MH, Huffman JE, Steri M, et al.
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.Human molecular genetics
11/2015
25
2
358-70
Andrews PJ, Sinclair HL, Rodriguez A, Harris BA, Battison CG, Rhodes JK, et al.
Hypothermia for Intracranial Hypertension after Traumatic Brain Injury.The New England journal of medicine
10/2015



Cleyen et al
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study. Lancet
1/2016
387
10014
156-67
Gabriel et al
Epigenetic landscape correlates with genetic subtype but does not predict outcome in childhood acute lymphoblastic leukemia. Epigenetics
2015
10
8
717-726
Garbacz WG, Huang JT, Higgins LG, Wahli W, Palmer CN
PPARα Is Required for PPARδ Action in Regulation of Body Weight and Hepatic Steatosis in Mice.PPAR research
10/2015
2015

927057
Hausenloy DJ, Candilio L, Evans R, Ariti C, Jenkins DP, Kolvekar S, et al.
Remote Ischemic Preconditioning and Outcomes of Cardiac Surgery.The New England Journal of Medicine
10/2015
373
15
1408-17
Rushton et al
Methylation quantitative trait locus analysis of osteoarthritis links epigenetics with genetic risk. Hum Mol Genet.
2015
24
25
7432-7444
Timofeeva MN1, Kinnersley B2, Farrington SM1, Whiffin N2, Palles C3, Svinti V1, Lloyd A2, Gorman M3, Ooi LY1, Hosking F2, Barclay E3, Zgaga L1, Dobbins S2, Martin L3, Theodoratou E1,4, Broderick P2, Tenesa A5,6, Smillie C1, Grimes G6, Hayward C6, Campbell A6,7, Porteous D6,7, Deary IJ8, Harris SE6,8, Northwood EL9, Barrett JH9, Smith G10, Wolf R10, Forman D11, Morreau H12, Ruano D12, Tops C13, Wijnen J14, Schrumpf M12, Boot A12, Vasen HF15, Hes FJ13, van Wezel T12, Franke A16, Lieb W17, Schafmayer C18, Hampe J19, Buch S19, Propping P20, Hemminki K21,22, Försti A21,22, Westers H23, Hofstra R23,24, Pinheiro M25, Pinto C25, Teixeira M25, Ruiz-Ponte C26, Fernández-Rozadilla C26,3, Carracedo A26, Castells A27, Castellví-Bel S27, Campbell H1,4, Bishop DT9, Tomlinson IP3, Dunlop MG1, Houlston RS2.
Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal CancerScientific Reports
11/2015
10
5

Traylor et al
Differences in Common Genetic Predisposition to Ischemic Stroke by Age and Sex. Stroke
2015
46
11
3042-3047
Vilhjálmsson et al
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores. Am J Hum Genet.
2015
97
4
576-592
Winkler et al
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS Genet
10/2015
1
11

Cunningham S, Rodriguez A, Adams T, Boyd KA, Butcher I, Enderby B, et al.
Oxygen saturation targets in infants with bronchiolitis (BIDS): a double-blind, randomised, equivalence trial.Lancet (London, England)
9/2015
386
9998
1041-8
Day et al
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat Genet.
2015
47
11
1294-1303
Gharib et al
Integrative pathway genomics of lung function and airflow obstruction. Hum Mol Genet.
2015
24
23
6836-6848
Holmes et al
Utility of Whole-Genome Sequencing of Escherichia coli O157 for Outbreak Detection and Epidemiological Surveillance. Journal of Clinical Microbiology.
9/2015
53
11
3565-73
Howrigan DP, Simonson MA, Davies G, Harris SE, Tenesa A, Starr JM, et al.
Genome-wide autozygosity is associated with lower general cognitive ability.Molecular psychiatry
9/2015



Kato N, Loh M, Takeuchi F, Verweij N, Wang X, Zhang W, et al.
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.Nature genetics
9/2015
47
11
1282-93
Obeidat et al
Molecular mechanisms underlying variations in lung function: a systems genetics analysis. Lancet Respir Med.
2015
3
10
782-795
van den Berg et al
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behav Genet.
2015



Chalmers et al
No Strong Relationship Between Components of the Lectin Pathway of Complement and Susceptibility to Pulmonary Tuberculosis. Inflammation.
8/2015
38
4
1731-1737
Lunetta et al
Rare coding variants and X-linked loci associated with age at menarche. Nat Commun.
2015
6


Quinn et al
Association between cognition and gene polymorphisms involved in thrombosis and haemostasis. Age (Dordr).
2015



Alton EW, Armstrong DK, Ashby D, Bayfield KJ, Bilton D, Bloomfield EV, et al.
Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial.The Lancet. Respiratory medicine
7/2015
3
9
684-91
Hanscombe et al
Genetic Factors Influencing Coagulation Factor XIII B-Subunit Contribute to Risk of Ischemic Stroke. Stroke
2015
46
8
2069-2074
Joshi et al
Directional dominance on stature and cognition in diverse human populations. Nature
2015
523
7561
459-462
Liu et al
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. Nature Genetics
2015
47
9
979-986
Clarke et al
Major depressive disorder and current psychological distress moderate the effect of polygenic risk for obesity on body mass index. Translational Psychiatry.
6/2015
5

e592
Koussounadis A1, Langdon SP2, Um IH3, Harrison DJ3, Smith VA1
Relationship between differentially expressed mRNA and mRNA-protein correlations in a xenograft model systemScientific Reports
6/2015
8
5

Luciano et al
Current versus lifetime depression, APOE variation, and their interaction on cognitive performance in younger and older adults. Psychosomatic Medicine
2015
77
5
480-492
Shah S, Bonder MJ, Marioni RE, Zhu Z, McRae AF, Zhernakova A, et al.
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations.American journal of human genetics
6/2015
97
1
75-85
Al-Tassan et al
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer. Scientific Report
5/2015
5

10442
Deary et al
Predicting and retrodicting intelligence between childhood and old age in the 6-Day Sample of the Scottish Mental Survey 1947. Intelligence
2015
50

one-9
Rutten-Jacobs et al
Common NOTCH3 Variants and Cerebral Small-Vessel Disease. Stroke
2015
46
6
1482-1487
Stewart GD, O'Mahony FC, Laird A, Eory L, Lubbock AL, Mackay A, et al.
Sunitinib Treatment Exacerbates Intratumoral Heterogeneity in Metastatic Renal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research
5/2015
21
18
4212-23
Thomson et al
DNA immunoprecipitation semiconductor sequencing (DIP-SC-seq) as a rapid method to generate genome wide epigenetic signatures Nature Scientific Reports
2015
5
9778
one-9
Trampush JW, Lencz T, Knowles E, Davies G, Guha S, Pe'er I, et al.
Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
5/2015
168B
5
363-73
Bielicki et al
Cytokine gene polymorphisms in obstructive sleep apnoea/hypopnoea syndrome. Sleep Medicine
6/2015
16
6
792-795
Clarke et al
Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort. Addict Biol
4/2015



Cook PC1, Owen H2, Deaton AM3, Borger JG2, Brown SL1, Clouaire T3, Jones GR1, Jones LH2, Lundie RJ2, Marley AK2, Morrison VL4, Phythian-Adams AT1, Wachter E3, Webb LM1, Sutherland TE2, Thomas GD2, Grainger JR1, Selfridge J3, McKenzie AN5, Allen JE2, Fagerholm SC4, Maizels RM2, Ivens AC2, Bird A3, MacDonald AS1
A dominant role for the methyl-CpG-binding protein Mbd2 in controlling Th2 induction by dendritic cellsNat Commun
4/2015
24
6

Hansell et al
Genetic basis of a cognitive complexity metric. PLoS One
2015
10
4
e0123886
Rushton MD, Young DA, Loughlin J, Reynard LN
Differential DNA methylation and expression of inflammatory and zinc transporter genes defines subgroups of osteoarthritic hip patients.Annals of the rheumatic diseases
4/2015
74
9
1778-82
Anblagan D, Bastin ME, Sparrow S, Piyasena C, Pataky R, Moore EJ, et al.
Tract shape modeling detects changes associated with preterm birth and neuroprotective treatment effects.NeuroImage. Clinical
3/2015
8

51-8
Bérénos C, Ellis PA, Pilkington JG, Lee SH, Gratten J, Pemberton JM
Heterogeneity of genetic architecture of body size traits in a free-living population.Molecular ecology
3/2015
24
8
1810-30
Clarke TK, Lupton MK, Fernandez-Pujals AM, Starr J, Davies G, Cox S, et al.
Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population.Molecular psychiatry
3/2015



Henderson P, Kennedy NA, Van Limbergen JE, Cameron FL, Satsangi J, Russell RK, et al.
Serum C-reactive protein and CRP genotype in pediatric inflammatory bowel disease: influence on phenotype, natural history, and response to therapy.Inflammatory bowel diseases
3/2015
21
3
596-605
Huffman JE, Albrecht E, Teumer A, Mangino M, Kapur K, Johnson T, et al.
Modulation of genetic associations with serum urate levels by body-mass-index in humans.PloS one
3/2015
10
3
e0119752
Kochunov P, Jahanshad N, Marcus D, Winkler A, Sprooten E, Nichols TE, et al.
Heritability of fractional anisotropy in human white matter: a comparison of Human Connectome Project and ENIGMA-DTI data.NeuroImage
3/2015
111

300-11
Kranc KR, Oliveira DV, Armesilla-Diaz A, Pacheco-Leyva I, Catarina Matias A, Luisa Escapa A, et al.
Acute loss of Cited2 impairs Nanog expression and decreases self-renewal of mouse embryonic stem cells.Stem cells (Dayton, Ohio)
3/2015
33
3
699-712
López-Knowles et al
Integrative analyses identify modulators of response to neoadjuvant aromatase inhibitors in patients with early breast cancer. Breast Cancer Res.
2015
17

35
Luciano M, Svinti V, Campbell A, Marioni RE, Hayward C, Wright AF, et al.
Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.Twin research and human genetics : the official journal of the International Society for Twin Studies
3/2015
18
2
117-25
Miyake M1, Yamashiro K2, Tabara Y3, Suda K2, Morooka S2, Nakanishi H2, Khor CC4, Chen P5, Qiao F5, Nakata I1, Akagi-Kurashige Y1, Gotoh N3, Tsujikawa A2, Meguro A6, Kusuhara S7, Polasek O8, Hayward C9, Wright AF9, Campbell H10, Richardson AJ11, Schache M11, Takeuchi M12, Mackey DA13, Hewitt AW11, Cuellar G14, Shi Y15, Huang L15, Yang Z16, Leung KH17, Kao PY18, Yap MK18, Yip SP17, Moriyama M19, Ohno-Matsui K19, Mizuki N6, MacGregor S14, Vitart V9, Aung T20, Saw SM21, Tai ES22, Wong TY23, Cheng CY24, Baird PN11, Yamada R3, Matsuda F3; Nagahama Study Group, Yoshimura N2
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopiaNat Commun
3/2015
31
6

van Leeuwen EM, Karssen LC, Deelen J, Isaacs A, Medina-Gomez C, Mbarek H, et al.
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels.Nature communications
2015
6

6065
van Leeuwen et al
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. Nat Commun.
2015
6

6065
Byrne EM, , Raheja UK, Stephens SH, Heath AC, Madden PA, et al.
Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder.The Journal of clinical psychiatry
2/2015
76
2
128-34
Davies G, Armstrong N, Bis JC, Bressler J, Chouraki V, Giddaluru S, et al.
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).Molecular psychiatry
2/2015
20
2
183-92
Fallon MT, Storey DJ, Krishan A, Weir CJ, Mitchell R, Fleetwood-Walker SM, et al.
Cancer treatment-related neuropathic pain: proof of concept study with menthol-a TRPM8 agonist.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
2/2015
23
9
2769-77
Locke AE, Kahali B, Berndt SI, Justice AE, Pers TH, Day FR, et al.
Genetic studies of body mass index yield new insights for obesity biology.Nature
2/2015
518
7538
197-206
Murray JE, van der Burg M, IJspeert H, Carroll P, Wu Q, Ochi T, et al.
Mutations in the NHEJ component XRCC4 cause primordial dwarfism.American journal of human genetics
2/2015
96
3
412-24
Nestor CE, Ottaviano R, Reinhardt D, Cruickshanks HA, Mjoseng HK, McPherson RC, et al.
Rapid reprogramming of epigenetic and transcriptional profiles in mammalian culture systems.Genome biology
2/2015
16

11
Nüesch et al
New genetic loci link adipose and insulin biology to body fat distribution. Int J Epidemiol.
2015



Rannikmäe K, Davies G, Thomson PA, Bevan S, Devan WJ, Falcone GJ, et al.
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease.Neurology
2/2015
84
9
918-26
Shungin D, Winkler TW, Croteau-Chonka DC, Ferreira T, Locke AE, Mägi R, et al.
New genetic loci link adipose and insulin biology to body fat distribution.Nature
2/2015
518
7538
187-96
Vallet M, Soares DC, Wani S, Sophocleous A, Warner J, Salter DM, et al.
Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone.Human molecular genetics
2/2015
24
11
3286-95
Verhaaren BF, Debette S, Bis JC, Smith JA, Ikram MK, Adams HH, et al.
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.Circulation. Cardiovascular genetics
2/2015
8
2
398-409
Hibar DP, Stein JL, Renteria ME, Arias-Vasquez A, Desrivières S, Jahanshad N, et al.
Common genetic variants influence human subcortical brain structures.Nature
1/2015
520
7546
224-9
Holliday EG, Traylor M, Malik R, Bevan S, Falcone G, Hopewell JC, et al.
Genetic overlap between diagnostic subtypes of ischemic stroke.Stroke; a journal of cerebral circulation
1/2015
46
3
615-9
King et al
Mosaic structural variation in children with developmental disorders. Hum Mol Genet
2015
24
10
2733-2745
Lopez LM, Hill WD, Harris SE, Valdes Hernandez M, Munoz Maniega S, Bastin ME, et al.
Genes from a translational analysis support a multifactorial nature of white matter hyperintensities.Stroke; a journal of cerebral circulation
1/2015
46
2
341-7
Maier R, Moser G, Chen GB, Ripke S, , Coryell W, et al.
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder.American journal of human genetics
1/2015
96
2
283-94
Marioni RE, Shah S, McRae AF, Chen BH, Colicino E, Harris SE, et al.
DNA methylation age of blood predicts all-cause mortality in later life.Genome biology
1/2015
16

25
Marioni RE, Shah S, McRae AF, Ritchie SJ, Muniz-Terrera G, Harris SE, et al.
The epigenetic clock is correlated with physical and cognitive fitness in the Lothian Birth Cohort 1936.International journal of epidemiology
1/2015



Mõttus R, Luciano M, Sarr JM, McCarthy MI, Deary IJ
Childhood Cognitive Ability Moderates Later-Life Manifestation of Type 2 Diabetes Genetic Risk.Health psychology : official journal of the Division of Health Psychology, American Psychological Association
1/2015



Network and Pathway Analysis Subgroup of Psychiatric Genomics Consortium
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. Nat Neurosci.
2015
18
2
199-209
Pers TH, Karjalainen JM, Chan Y, Westra HJ, Wood AR, Yang J, et al.
Biological interpretation of genome-wide association studies using predicted gene functions.Nature communications
2015
6

5890
Walker RM, Rybka J, Anderson SM, Torrance HS, Boxall R, Sussmann JE, et al.
Preliminary investigation of miRNA expression in individuals at high familial risk of bipolar disorder.Journal of psychiatric research
1/2015
62

48-55
Wessel J, Chu AY, Willems SM, Wang S, Yaghootkar H, Brody JA, et al.
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.Nature communications
2015
6

5897

Large-scale discovery of novel genetic causes of developmental disorders.Nature
12/2014
519
7542
223-8
Adib-Samii P, Devan W, Traylor M, Lanfranconi S, Zhang CR, Cloonan L, et al.
Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke.Stroke; a journal of cerebral circulation
12/2014
46
2
348-53
Baumert J, Huang J, McKnight B, Sabater-Lleal M, Steri M, Chu AY, et al.
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
12/2014
9
12
e111156
Bihlmeyer NA, Brody JA, Smith AV, Lunetta KL, Nalls M, Smith JA, et al.
Genetic diversity is a predictor of mortality in humans.BMC genetics
12/2014
15

159
Talmud PJ, Cooper JA, Morris RW, Dudbridge F, Shah T, Engmann J, et al.
Sixty-five common genetic variants and prediction of type 2 diabetes.Diabetes
12/2014



Taylor AE, Morris RW, Fluharty ME, Bjorngaard JH, Åsvold BO, Gabrielsen ME, et al.
Stratification by smoking status reveals an association of CHRNA5-A3-B4 genotype with body mass index in never smokers.PLoS genetics
12/2014
10
12
e1004799
Wright et al
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data. Lancet
2015
385
9975
1305-1314
Buck AH, Coakley G, Simbari F, McSorley HJ, Quintana JF, Le Bihan T, et al.
Exosomes secreted by nematode parasites transfer small RNAs to mammalian cells and modulate innate immunity.Nature communications
2014
5

5488
Debette et al
Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium. Biol Psychiatry
2015



Debette S, Ibrahim Verbaas CA, Bressler J, Schuur M, Smith A, Bis JC, et al.
Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium.Biological psychiatry
11/2014
77
8
749-63
Li Q, Wojciechowski R, Simpson CL, Hysi PG, Verhoeven VJ, Ikram MK, et al.
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.Human genetics
11/2014
134
2
131-46
Michailidou Z, Morton NM, Moreno Navarrete JM, West CC, Stewart KJ, Fernández-Real JM, et al.
Adipocyte pseudohypoxia suppresses lipolysis and facilitates benign adipose tissue expansion.Diabetes
11/2014
64
3
733-45
Sava GP, Speedy HE, Di Bernardo MC, Dyer MJ, Holroyd A, Sunter NJ, et al.
Common variation at 12q24.13 (OAS3) influences chronic lymphocytic leukemia risk.Leukemia
11/2014
29
3
748-51
Whalley HC, Hall L, Romaniuk L, Macdonald A, Lawrie SM, Sussmann JE, et al.
Impact of cross-disorder polygenic risk on frontal brain activation with specific effect of schizophrenia risk.Schizophrenia research
11/2014
161
2-3
484-9
Adams AT, Kennedy NA, Hansen R, Ventham NT, OʼLeary KR, Drummond HE, et al.
Two-stage genome-wide methylation profiling in childhood-onset Crohn's Disease implicates epigenetic alterations at the VMP1/MIR21 and HLA loci.Inflammatory bowel diseases
10/2014
20
10
1784-93
Holliday EG, Traylor M, Malik R, Bevan S, Maguire J, Koblar SA, et al.
Polygenic overlap between kidney function and large artery atherosclerotic stroke.Stroke; a journal of cerebral circulation
10/2014
45
12
3508-13
Rahmioglu N, Macgregor S, Drong AW, Hedman ÅK, Harris HR, Randall JC, et al.
Genome-wide enrichment analysis between endometriosis and obesity-related traits reveals novel susceptibility loci.Human molecular genetics
10/2014
24
4
1185-99
Taylor AE, Fluharty ME, Bjørngaard JH, Gabrielsen ME, Skorpen F, Marioni RE, et al.
Investigating the possible causal association of smoking with depression and anxiety using Mendelian randomisation meta-analysis: the CARTA consortium.BMJ open
2014
4
10
e006141
Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, et al.
Defining the role of common variation in the genomic and biological architecture of adult human height.Nature genetics
10/2014
46
11
1173-86
Khulan B, Manning JR, Dunbar DR, Seckl JR, Raikkonen K, Eriksson JG, et al.
Epigenomic profiling of men exposed to early-life stress reveals DNA methylation differences in association with current mental state.Translational psychiatry
2014
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The PDE4B gene confers sex-specific protection against schizophrenia Psychiatric Genetics
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A study into the association between retinal vascular network geometry and cognitive ability in an elderly population Investigative Opthalmology and Visual Science
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