Andrew R Harper (Andrew Harper)

Scopus Author ID ResearcherID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 25

Top Topics

Congenital Heart Disease

Left Ventricular

Genome Wide Association Study

Hypertrophic Cardiomyopathy

Top Venues

Circulation. Genomic and precision medicine

Nature communications

Science advances

Nature genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Lawrence Middleton, Ioannis Melas, Chirag Vasavda, Arwa Bin Raies, Benedek Rozemberczki, Ryan S Dhindsa, Justin S Dhindsa, Blake Weido, Quanli Wang, Andrew R Harper, Gavin Edwards, Slavé Petrovski, Dimitrios Michael Vitsios
Phenome-wide identification of therapeutic genetic targets, leveraging knowledge graphs, graph neural networks, and UK Biobank data. Science advances 10 (19) (2024)
Lawrence Middleton, Ioannis Melas, Chirag Vasavda, Arwa Bin Raies, Benedek Rozemberczki, Ryan S Dhindsa, Justin S Dhindsa, Blake Weido, Quanli Wang, Andrew R Harper, Gavin Edwards, Slavé Petrovski, Dimitrios Michael Vitsios
Phenome-wide identification of therapeutic genetic targets, leveraging knowledge graphs, graph neural networks, and UK Biobank data. Science advances 10 (19) (2024)
Manik Garg, Marcin Karpinski, Dorota Matelska, Lawrence Middleton, Oliver S Burren, Fengyuan Hu, Eleanor Wheeler, Katherine R Smith, Margarete A Fabre, Jonathan Mitchell, Amanda O'Neill, Euan A Ashley, Andrew R Harper, Quanli Wang, Ryan S Dhindsa, Slavé Petrovski, Dimitrios Michael Vitsios
Disease prediction with multi-omics and biomarkers empowers case-control genetic discoveries in the UK Biobank. Nature genetics 56 (9) (2024)
Lawrence Middleton, Ioannis Melas, Chirag Vasavda, Arwa Bin Raies, Benedek Rozemberczki, Ryan S Dhindsa, Justin S Dhindsa, Blake Weido, Quanli Wang, Andrew R Harper, Gavin Edwards, Slavé Petrovski, Dimitrios Michael Vitsios
Phenome-wide identification of therapeutic genetic targets, leveraging knowledge graphs, graph neural networks, and UK Biobank data. Science advances 10 (19) (2024)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 16 (1) (2023)
Ryan S Dhindsa, Oliver S Burren, Benjamin B Sun, Bram P Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Andreas Bender, Ventzislava A Hristova, Katherine R Smith, Keren Jacqueline Carss, Sebastian Wasilewski, Andrew R Harper, Dirk S Paul, Margarete A Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, null null, Dimitrios Michael Vitsios, Euan A Ashley, Christopher D Whelan, Menelas N Pangalos, Quanli Wang, Slavé Petrovski
Rare variant associations with plasma protein levels in the UK Biobank. Nature (2023)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine (2023)
William J Young, Jeffrey Haessler, Jan-Walter Benjamins, Linda Repetto, Jie Yao, Aaron Isaacs, Andrew R Harper, Julia Ramírez, Sophie Garnier, Stefan van Duijvenboden, Antoine R Baldassari, Maria Pina Concas, ThuyVy Duong, Luisa Foco, Jonas L Isaksen, Hao Mei, Raymond Noordam, Casia Nursyifa, Anne Richmond, Meddly L Santolalla, Colleen M Sitlani, Negin Soroush, Sébastien Thériault, Stella Trompet, Stefanie Aeschbacher, Fariba Ahmadizar, Alvaro Alonso, Jennifer A Brody, Archie I Campbell, Adolfo Correa, Dawood Darbar, Antonio De Luca, Jean François Deleuze, Christina Ellervik, Christian Fuchsberger, Anuj Goel, Christopher Grace, Xiuqing Guo, Torben Hansen, Susan R Heckbert, Rebecca D Jackson, Jan A Kors, Maria Fernanda Lima-Costa, Allan Linneberg, Peter W Macfarlane, Alanna C Morrison, Pau Navarro, David J Porteous, Peter Paul Pramstaller, Alexander P Reiner, Lorenz Risch, Ulrich Schotten, Xia Shen, Gianfranco Sinagra, Elsayed Z Soliman, Monika Stoll, Eduardo Tarazona-Santos, Andrew Tinker, Katerina Trajanoska, Eric Villard, Helen R Warren, Eric A Whitsel, Kerri L Wiggins, Dan E Arking, Christy L Avery, David Conen, Giorgia Girotto, Niels Grarup, Caroline Hayward, Johan Wouter Jukema, Dennis O Mook-Kanamori, Morten Salling Olesen, Sandosh Padmanabhan, Bruce M Psaty, Cristian Pattaro, Antonio Luiz Pinho Ribeiro, Jerome I Rotter, Bruno H Stricker, Pim van der Harst, Cornelia M Van Duijn, Niek Verweij, James G Wilson, Michele Orini, Philippe Charron, Hugh C Watkins, Charles Kooperberg, Henry J Lin, James F Wilson, Jørgen Kim Kanters, Nona Sotoodehnia, Borbala Mifsud, Pier D Lambiase, Larisa G Tereshchenko, Patricia B Munroe
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Nature communications 14 (1) (2023)
William J Young, Jeffrey Haessler, Jan-Walter Benjamins, Linda Repetto, Jie Yao, Aaron Isaacs, Andrew R Harper, Julia Ramírez, Sophie Garnier, Stefan van Duijvenboden, Antoine R Baldassari, Maria Pina Concas, ThuyVy Duong, Luisa Foco, Jonas L Isaksen, Hao Mei, Raymond Noordam, Casia Nursyifa, Anne Richmond, Meddly L Santolalla, Colleen M Sitlani, Negin Soroush, Sébastien Thériault, Stella Trompet, Stefanie Aeschbacher, Fariba Ahmadizar, Alvaro Alonso, Jennifer A Brody, Archie I Campbell, Adolfo Correa, Dawood Darbar, Antonio De Luca, Jean François Deleuze, Christina Ellervik, Christian Fuchsberger, Anuj Goel, Christopher Grace, Xiuqing Guo, Torben Hansen, Susan R Heckbert, Rebecca D Jackson, Jan A Kors, Maria Fernanda Lima-Costa, Allan Linneberg, Peter W Macfarlane, Alanna C Morrison, Pau Navarro, David J Porteous, Peter Paul Pramstaller, Alexander P Reiner, Lorenz Risch, Ulrich Schotten, Xia Shen, Gianfranco Sinagra, Elsayed Z Soliman, Monika Stoll, Eduardo Tarazona-Santos, Andrew Tinker, Katerina Trajanoska, Eric Villard, Helen R Warren, Eric A Whitsel, Kerri L Wiggins, Dan E Arking, Christy L Avery, David Conen, Giorgia Girotto, Niels Grarup, Caroline Hayward, Johan Wouter Jukema, Dennis O Mook-Kanamori, Morten Salling Olesen, Sandosh Padmanabhan, Bruce M Psaty, Cristian Pattaro, Antonio Luiz Pinho Ribeiro, Jerome I Rotter, Bruno H Stricker, Pim van der Harst, Cornelia M Van Duijn, Niek Verweij, James G Wilson, Michele Orini, Philippe Charron, Hugh C Watkins, Charles Kooperberg, Henry J Lin, James F Wilson, Jørgen Kim Kanters, Nona Sotoodehnia, Borbala Mifsud, Pier D Lambiase, Larisa G Tereshchenko, Patricia B Munroe
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Nature communications 14 (1) (2023)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 16 (1) (2023)
Mengyao Yu, Andrew R Harper, Matthew Aguirre, Maureen Pittman, Catherine Tcheandjieu, Dulguun Amgalan, Christopher Grace, Anuj Goel, Martin Farrall, Ke Xiao, Jesse Engreitz, Katherine S Pollard, Hugh C Watkins, James R Priest
Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine (2023)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine (2023)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 16 (1) (2023)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 16 (1) (2023)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 16 (1) (2023)
William J Young, Jeffrey Haessler, Jan-Walter Benjamins, Linda Repetto, Jie Yao, Aaron Isaacs, Andrew R Harper, Julia Ramírez, Sophie Garnier, Stefan van Duijvenboden, Antoine R Baldassari, Maria Pina Concas, ThuyVy Duong, Luisa Foco, Jonas L Isaksen, Hao Mei, Raymond Noordam, Casia Nursyifa, Anne Richmond, Meddly L Santolalla, Colleen M Sitlani, Negin Soroush, Sébastien Thériault, Stella Trompet, Stefanie Aeschbacher, Fariba Ahmadizar, Alvaro Alonso, Jennifer A Brody, Archie I Campbell, Adolfo Correa, Dawood Darbar, Antonio De Luca, Jean François Deleuze, Christina Ellervik, Christian Fuchsberger, Anuj Goel, Christopher Grace, Xiuqing Guo, Torben Hansen, Susan R Heckbert, Rebecca D Jackson, Jan A Kors, Maria Fernanda Lima-Costa, Allan Linneberg, Peter W Macfarlane, Alanna C Morrison, Pau Navarro, David J Porteous, Peter Paul Pramstaller, Alexander P Reiner, Lorenz Risch, Ulrich Schotten, Xia Shen, Gianfranco Sinagra, Elsayed Z Soliman, Monika Stoll, Eduardo Tarazona-Santos, Andrew Tinker, Katerina Trajanoska, Eric Villard, Helen R Warren, Eric A Whitsel, Kerri L Wiggins, Dan E Arking, Christy L Avery, David Conen, Giorgia Girotto, Niels Grarup, Caroline Hayward, Johan Wouter Jukema, Dennis O Mook-Kanamori, Morten Salling Olesen, Sandosh Padmanabhan, Bruce M Psaty, Cristian Pattaro, Antonio Luiz Pinho Ribeiro, Jerome I Rotter, Bruno H Stricker, Pim van der Harst, Cornelia M Van Duijn, Niek Verweij, James G Wilson, Michele Orini, Philippe Charron, Hugh C Watkins, Charles Kooperberg, Henry J Lin, James F Wilson, Jørgen Kim Kanters, Nona Sotoodehnia, Borbala Mifsud, Pier D Lambiase, Larisa G Tereshchenko, Patricia B Munroe
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Nature communications 14 (1) (2023)
William J Young, Jeffrey Haessler, Jan-Walter Benjamins, Linda Repetto, Jie Yao, Aaron Isaacs, Andrew R Harper, Julia Ramírez, Sophie Garnier, Stefan van Duijvenboden, Antoine R Baldassari, Maria Pina Concas, ThuyVy Duong, Luisa Foco, Jonas L Isaksen, Hao Mei, Raymond Noordam, Casia Nursyifa, Anne Richmond, Meddly L Santolalla, Colleen M Sitlani, Negin Soroush, Sébastien Thériault, Stella Trompet, Stefanie Aeschbacher, Fariba Ahmadizar, Alvaro Alonso, Jennifer A Brody, Archie I Campbell, Adolfo Correa, Dawood Darbar, Antonio De Luca, Jean François Deleuze, Christina Ellervik, Christian Fuchsberger, Anuj Goel, Christopher Grace, Xiuqing Guo, Torben Hansen, Susan R Heckbert, Rebecca D Jackson, Jan A Kors, Maria Fernanda Lima-Costa, Allan Linneberg, Peter W Macfarlane, Alanna C Morrison, Pau Navarro, David J Porteous, Peter Paul Pramstaller, Alexander P Reiner, Lorenz Risch, Ulrich Schotten, Xia Shen, Gianfranco Sinagra, Elsayed Z Soliman, Monika Stoll, Eduardo Tarazona-Santos, Andrew Tinker, Katerina Trajanoska, Eric Villard, Helen R Warren, Eric A Whitsel, Kerri L Wiggins, Dan E Arking, Christy L Avery, David Conen, Giorgia Girotto, Niels Grarup, Caroline Hayward, Johan Wouter Jukema, Dennis O Mook-Kanamori, Morten Salling Olesen, Sandosh Padmanabhan, Bruce M Psaty, Cristian Pattaro, Antonio Luiz Pinho Ribeiro, Jerome I Rotter, Bruno H Stricker, Pim van der Harst, Cornelia M Van Duijn, Niek Verweij, James G Wilson, Michele Orini, Philippe Charron, Hugh C Watkins, Charles Kooperberg, Henry J Lin, James F Wilson, Jørgen Kim Kanters, Nona Sotoodehnia, Borbala Mifsud, Pier D Lambiase, Larisa G Tereshchenko, Patricia B Munroe
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Nature communications 14 (1) (2023)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 16 (1) (2023)
Nay Aung, Luis Rocha Lopes, Stefan van Duijvenboden, Andrew R Harper, Anuj Goel, Christopher Grace, Carolyn Y Ho, William S Weintraub, Christopher M Kramer, Stefan Neubauer, Hugh C Watkins, Steffen Erhard Petersen, Patricia B Munroe
Genome-Wide Analysis of Left Ventricular Maximum Wall Thickness in the UK Biobank Cohort Reveals a Shared Genetic Background With Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 16 (1) (2023)
Andrew R Harper, Anuj Goel, Christopher Grace, Kate L Thomson, Steffen Erhard Petersen, Xiao Xu, Adam Waring, Elizabeth Ormondroyd, Christopher M Kramer, Carolyn Y Ho, Stefan Neubauer, null null, Rafik Tadros, James Simon Ware, Connie R Bezzina, Martin Farrall, Hugh C Watkins
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity. Nature genetics 53 (2) (2021)
Rafik Tadros, Catherine Francis, Xiao Xu, Alexa M C Vermeer, Andrew R Harper, Roy Huurman, Ken Kelu Bisabu, Roddy Walsh, Edgar T Hoorntje, Wouter P Te Rijdt, Rachel J Buchan, Hannah G van Velzen, Marjon A van Slegtenhorst, Jentien M Vermeulen, Joost Allard Offerhaus, Wenjia Bai, Antonio de Marvao, Najim Lahrouchi, Leander Beekman, Jacco C Karper, Jan Herman Veldink, Elham Kayvanpour, Antonis Pantazis, A John Baksi, Nicola Whiffin, Francesco Mazzarotto, Geraldine Sloane, Hideaki Suzuki, Deborah Schneider-Luftman, Paul Elliott, Pascale Richard, Flavie Ader, Eric Villard, Peter Lichtner, Thomas Meitinger, Michael W T Tanck, van J Peter Tintelen, Andrew Thain, David McCarty, Robert A Hegele, Jason D Roberts, Julie Amyot, Marie-Pierre Dubé, Julia Cadrin-Tourigny, Geneviève Giraldeau, Philippe L L'Allier, Patrick Garceau, Jean-Claude Tardif, S Matthijs Boekholdt, R Thomas Lumbers, Folkert W. Asselbergs, Paul J R Barton, Stuart A Cook, Sanjay K Prasad, Declan P O'Regan, Jolanda van der Velden, Karin J H Verweij, Mario Talajic, Guillaume Lettre, Yigal M Pinto, Benjamin Meder, Philippe Charron, Rudolf A de Boer, Imke Christiaans, Michelle Michels, Arthur A M Wilde, Hugh C Watkins, Paul M Matthews, James Simon Ware, Connie R Bezzina
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Nature genetics 53 (2) (2021)
Quanli Wang, Ryan S Dhindsa, Keren Carss, Andrew R Harper, Abhishek Nag, Ioanna Tachmazidou, Dimitrios Vitsios, Sri V V Deevi, Alex Mackay, Daniel Muthas, Michael Hühn, Susan Monkley, Henric Olsson, null null, Sebastian Wasilewski, Katherine R Smith, Ruth March, Adam Platt, Carolina Haefliger, Slavé Petrovski
Rare variant contribution to human disease in 281,104 UK Biobank exomes. Nature 597 (7877) (2021)
Adam Waring, Andrew R Harper, Silvia Salatino, Christopher Kramer, Stefan Neubauer, Kate Thomson, Hugh Watkins, Martin Farrall
Data-driven modelling of mutational hotspots and in silico predictors in hypertrophic cardiomyopathy. Journal of medical genetics 58 (8) (2020)
Elizabeth Ormondroyd, Andrew R Harper, Kate L Thomson, Michael P Mackley, Jennifer Martin, Christopher J Penkett, Silvia Salatino, Hannah Stark, Jonathan Stephens, Hugh C Watkins
Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes. European journal of human genetics : EJHG 28 (11) (2020)
David Steven Crossland, Katrijn Jansen, Gareth Parry, Andrew R Harper, Gianluigi Perri, Alison Davidson, Fabrizio De Rita, Antony Hermuzi, Mohamed Nassar, Neil Seller, Guy A MacGowan, Asif Hasan, John J O'Sullivan, Louise Coats
Outcome following heart transplant assessment in adults with congenital heart disease. Heart (British Cardiac Society) 105 (22) (2019)