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Papers authored by Nicholas Timpson

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2015 Shane Mccarthy, Peter N. Taylor, Saeed Al Turki, Eleonora Porcu, Shelby Chew, Maria Soler Artigas, Purdey J. Campbell, Michela Traglia, Suzanne J. Brown, Benjamin H. Mullin, Scott G. Wilson, Saeed Al Turki, Hashem A. Shihab, Carl Anderson, Richard Anney and 218 other authors

Whole-genome sequence-based analysis of thyroid function

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Qing Li, Robert Wojciechowski, Claire L. Simpson, Pirro G. Hysi, Virginie J. M. Verhoeven, René Höhn, Veronique Vitart, Alex W. Hewitt, Konrad Oexle, Kari-Matti Mäkelä, Stuart MacGregor, Mario Pirastu, Qiao Fan, Ching-Yu Cheng, Beate St Pourcain and 33 other authors

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error

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Daniel A. King, Wendy D. Jones, Yanick J. Crow, Anna F. Dominiczak, Nicola A. Foster, Tom R. Gaunt, Jade Harris, Stephen W. Hellens, Tessa Homfray, Josie Innes, Elizabeth A. Jones, Shelagh Joss, Abhijit Kulkarni, Sahar Mansour, Andrew D. Morris and 14 other authors

Mosaic structural variation in children with developmental disorders

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S. Burgess, N. J. Timpson

ORCID

, S. Ebrahim, G. Davey Smith

Mendelian randomization 10 years on: where are we now and where are we going?

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A. van Vlieg, Ashley van der Spek, Peter J. van der Most, Sander W. van der Laan, Astrid van Hylckama Vlieg, Jessica van Setten, Pim van der Harst, Cornelia M. van Duijn, Peter K. Joshi

ORCID

, Wei Zhao, Chen Yd, Anne U. Jackson, Albert V. Smith

ORCID

, Chen Y.-.I, Palmas Wr and 534 other authors

Directional dominance on stature and cognition in diverse human populations

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Laura J. Corbin

ORCID

, Nicholas J. Timpson

ORCID

Using inactivating mutations to provide insight into drug action

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S. M. van den Berg, Marleen de Moor, Stéphanie M. Berg, H. de Wit, C. M. van Duijn, Marleen H. M. Moor, C. J. H. Verweij, Karin J. H. Verweij, Robert F. Krueger, Michelle Luciano, A. A. Vasquez, Alejandro Arias Vasquez, Lindsay K. Matteson, Jaime Derringer, Tõnu Esko and 112 other authors

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

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W. M. Monique Verschuren, B. Thorand, Dr Daniel I. Swerdlow, David Preiss, Karoline B. Kuchenbaecker, Michael V. Holmes, Jorgen E. L. Engmann, Tina Shah, H.-E. Wichmann, Reecha Sofat, Stefan Stender, Anke Maitland van H. Zee, Paul C. D. Johnson, Robert A. Scott, Maarten Leusink and 135 other authors

HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials

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2014 Rebecca C. Richmond, Andrew J. Simpkin, Geoff Woodward, Tom R. Gaunt

ORCID

, Oliver Lyttleton, Wendy L. McArdle, Susan M. Ring, Andrew D. A. C. Smith, Nicholas J. Timpson

ORCID

, Kate Tilling, George Davey Smith, George Davey Smith, Caroline L. Relton

Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC)

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Beate St Pourcain

ORCID

, C. M. A. Haworth, O. S. P. Davis, Kai Wang, Nicholas J. Timpson

ORCID

, David M. Evans, John P. Kemp, Angelica Ronald, Tom Price

ORCID

, Emma Meaburn, Susan M. Ring, Jean Golding, Hakon Hakonarson, R. Plomin

ORCID

, George Davey Smith and 1 other authors

Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence

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Jonathan Flint, Nicholas Timpson

ORCID

, Marcus Munafo

Assessing the utility of intermediate phenotypes for genetic mapping of psychiatric disease

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Anette Varbo, Marianne Benn, George Davey Smith, Nicholas J. Timpson

ORCID

, Anne Tybjaerg-Hansen, Børge G. Nordestgaard

Remnant Cholesterol, Low-Density Lipoprotein Cholesterol, and Blood Pressure as Mediators From Obesity to Ischemic Heart Disease

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Kaitlin H. Wade

ORCID

, Nita G. Forouhi, Derek G. Cook, Paul Johnson, Alex McConnachie, Richard W. Morris, Santiago Rodriguez, Zheng Ye, Shah Ebrahim, Sandosh Padmanabhan, Graham Watt, K. Richard Bruckdorfer, Nick J. Wareham, Peter H. Whincup, Stephen Chanock and 4 other authors

Variation in the SLC23A1 gene does not influence cardiometabolic outcomes to the extent expected given its association with l-ascorbic acid

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Aaron Leong, Waheed Rehman, Zari Dastani, Celia Greenwood, Nicholas Timpson

ORCID

, Lisa Langsetmo, Claudie Berger, Lei Fu, Betty Y. L. Wong, Suneil Malik, Rainer Malik, David A. Hanley, David E. C. Cole, David Goltzman, J. Brent Richards and 2 other authors

The Causal Effect of Vitamin D Binding Protein (DBP) Levels on Calcemic and Cardiometabolic Diseases: A Mendelian Randomization Study

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Ralf J. P. van der Valk, Eskil Kreiner-Moller, Marjolein N. Kooijman, Mònica Guxens, Evangelia Stergiakouli, Annika Saaf, A. Sï¿½ï¿½f, Jonathan P. Bradfield, M. Geoffrey Hayes, Frank Geller, A. Korner, Annika Sääf, Diana L. Cousminer, Antje Koerner, Elisabeth Thiering and 126 other authors

A novel common variant in DCST2 is associated with length in early life and height in adulthood

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Fend Zhang, Pingbo Zhang, Hou-Feng Zheng, Nicholas J. Timpson

ORCID

, Klaudia Walter, Josine L. Min, J. Brent Richards, Ioanna Tachmazidou, Saeed Al Turki, Carl Anderson, Giovanni Malerba, Richard Anney, Dinu Antony, Maria Soler Artigas, Muhammad Ayub and 192 other authors

A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans

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Cornelius A. Rietveld, Tõnu Esko

ORCID

, Gail Davies, Tune H. Pers, Patrick Turley, Beben Benyamin, Christopher F. Chabris, Valur Emilsson, Andrew D. Johnson, James J. Lee, Christiaan de Leeuw, Christiaan de Leeuw, Riccardo E. Marioni, Sarah E. Medland, Michael B. Miller and 46 other authors

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

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Evangelia Stergiakouli, Romy Gaillard, Jeremy M. Tavaré, Nina Balthasar, Ruth J. Loos, Hendrik R. Taal, David M. Evans, Fernando Rivadeneira, Beate St Pourcain, André G. Uitterlinden, John P. Kemp, Albert Hofman, Susan M. Ring, Tim J. Cole, Vincent W. V. Jaddoe and 2 other authors

Genome-wide association study of height-adjusted BMI in childhood identifies functional variant inADCY3

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Mary E. Ward, George McMahon, Beate St Pourcain

ORCID

, David M. Evans, Cornelius A. Rietveld, Daniel J. Benjamin, Philipp D. Koellinger, David Cesarini, George Davey Smith, Social Science Genetic Association Consortium, Nicholas J. Timpson

ORCID

, Consortium The Social Science Genetic Association

Genetic Variation Associated with Differential Educational Attainment in Adults Has Anticipated Associations with School Performance in Children

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Jennifer L. Bolton, Caroline Hayward, Nese Direk, John G. Lewis, Geoffrey L. Hammond, Lesley A. Hill, Anna Anderson, Jennifer Huffman, James F. Wilson, Harry Campbell, Igor Rudan, Alan Wright, Nicholas Hastie, Sarah H. Wild, Fleur P. Velders and 47 other authors

Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin

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