Inferring Causal Relationships Between Risk Factors and Outcomes from Genome-Wide Association Study Data von Burgess, Stephen, Foley, Christopher N, Zuber, Verena

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A robust and efficient method for Mendelian randomization with hundreds of genetic variants von Burgess, Stephen, Foley, Christopher N, Allara, Elias, Staley, James R, Howson, Joanna M. M.

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A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits von Foley, Christopher N., Staley, James R., Breen, Philip G., Sun, Benjamin B., Kirk, Paul D. W., Burgess, Stephen, Howson, Joanna M. M.

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Systematic discovery of gene-environment interactions underlying the human plasma proteome in UK Biobank von Hillary, Robert F., Gadd, Danni A., Kuncheva, Zhana, Mangelis, Tasos, Lin, Tinchi, Ferber, Kyle, McLaughlin, Helen, Runz, Heiko, Marioni, Riccardo E., Foley, Christopher N., Sun, Benjamin B.

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Newton versus the machine: solving the chaotic three-body problem using deep neural networks von Breen, Philip G, Foley, Christopher N, Boekholt, Tjarda, Zwart, Simon Portegies

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MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized data von Broadbent, Jim R., Foley, Christopher N., Grant, Andrew J., Mason, Amy M., Staley, James R., Burgess, Stephen

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Factorial Mendelian randomization: using genetic variants to assess interactions von Rees, Jessica M B, Foley, Christopher N, Burgess, Stephen

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Shared mechanisms between coronary heart disease and depression: findings from a large UK general population-based cohort von Khandaker, Golam M., Zuber, Verena, Rees, Jessica M. B., Carvalho, Livia, Mason, Amy M., Foley, Christopher N., Gkatzionis, Apostolos, Jones, Peter B., Burgess, Stephen

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Modal-based estimation via heterogeneity-penalized weighting: model averaging for consistent and efficient estimation in Mendelian randomization when a plurality of candidate instr... von Burgess, Stephen, Zuber, Verena, Gkatzionis, Apostolos, Foley, Christopher N

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MR-Clust: clustering of genetic variants in Mendelian randomization with similar causal estimates von Foley, Christopher N, Mason, Amy M, Kirk, Paul D W, Burgess, Stephen

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Genetic associations of protein-coding variants in human disease von Sun, Benjamin B., Kurki, Mitja I., Foley, Christopher N., Mechakra, Asma, Chen, Chia-Yen, Marshall, Eric, Wilk, Jemma B., Chahine, Mohamed, Chevalier, Philippe, Christé, Georges, Palotie, Aarno, Daly, Mark J., Runz, Heiko

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Genetically Predicted Glucose-Dependent Insulinotropic Polypeptide (GIP) Levels and Cardiovascular Disease Risk Are Driven by Distinct Causal Variants in the GIPR Region von Bowker, Nicholas, Hansford, Robert, Burgess, Stephen, Foley, Christopher N., Auyeung, Victoria P. W., Erzurumluoglu, A. Mesut, Stewart, Isobel D., Wheeler, Eleanor, Pietzner, Maik, Gribble, Fiona, Reimann, Frank, Bhatnagar, Pallav, Coghlan, Matthew P., Wareham, Nicholas J., Langenberg, Claudia

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Genetic Determinants of Lipids and Cardiovascular Disease Outcomes: A Wide-Angled Mendelian Randomization Investigation von Allara, Elias, Morani, Gabriele, Carter, Paul, Gkatzionis, Apostolos, Zuber, Verena, Foley, Christopher N, Rees, Jessica M B, Mason, Amy M, Bell, Steven, Gill, Dipender, Lindström, Sara, Butterworth, Adam S, Di Angelantonio, Emanuele, Peters, James, Burgess, Stephen

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Correction: Shared mechanisms between coronary heart disease and depression: findings from a large UK general population-based cohort von Khandaker, Golam M., Zuber, Verena, Rees, Jessica M. B., Carvalho, Livia, Mason, Amy M., Foley, Christopher N., Gkatzionis, Apostolos, Jones, Peter B., Burgess, Stephen

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Blood protein assessment of leading incident diseases and mortality in the UK Biobank von Gadd, Danni A, Hillary, Robert F, Kuncheva, Zhana, Mangelis, Tasos, Cheng, Yipeng, Dissanayake, Manju, Admanit, Romi, Gagnon, Jake, Lin, Tinchi, Ferber, Kyle L, Runz, Heiko, Foley, Christopher N, Marioni, Riccardo E, Sun, Benjamin B

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Modal-based estimation via heterogeneity-penalized weighting: model averaging for consistent and efficient estimation in Mendelian randomization when a plurality of candidate instr... von Burgess, Stephen, Zuber, Verena, Gkatzionis, Apostolos, Foley, Christopher N

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MendelianRandomization v0.5.0: updates to an R package for performing Mendelian randomization analyses using summarized data von Broadbent, Jim R, Foley, Christopher N, Grant, Andrew J, Mason, Amy M, Staley, James R, Burgess, Stephen

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Shared mechanisms between coronary heart disease and depression: findings from a large UK general population-based cohort (vol 25, 1477, 2020) von Khandaker, Golam M., Zuber, Verena, Rees, Jessica M. B., Carvalho, Livia, Mason, Amy M., Foley, Christopher N., Gkatzionis, Apostolos, Jones, Peter B., Burgess, Stephend

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Genetic map of regional sulcal morphology in the human brain from UK biobank data von Sun, Benjamin B., Loomis, Stephanie J., Pizzagalli, Fabrizio, Shatokhina, Natalia, Painter, Jodie N., Foley, Christopher N., Jensen, Megan E., McLaren, Donald G., Chintapalli, Sai Spandana, Zhu, Alyssa H., Dixon, Daniel, Islam, Tasfiya, Ba Gari, Iyad, Runz, Heiko, Medland, Sarah E., Thompson, Paul M., Jahanshad, Neda, Whelan, Christopher D.

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FinnGen provides genetic insights from a well-phenotyped isolated population (vol 613, pg 508, 2023) von Kurki, MI, Karjalainen, J, Palta, P, Sipila, TP, Kristiansson, K, Donner, KM, Reeve, MP, Laivuori, H, Aavikko, M, Kaunisto, MA

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