Heather J Cordell (Heather Cordell)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 37

Top Venues

Nature genetics

Circulation. Genomic and precision medicine

Nature communications

PLoS genetics

Newcastle University

University of Oxford (MSC)

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

Affiliation History

Newcastle University

United Kingdom

Professor of Statistical Genetics :: Institute of Genetic Medicine

University of Cambridge

United Kingdom

Wellcome Senior Research Fellow :: Medical Genetics

University of Cambridge

United Kingdom

Wellcome/JDRF Career Development Fellow :: Medical Genetics

University of Cambridge

United Kingdom

Postdoctoral Research Associate :: Medical Genetics

Case Western Reserve University

United States

Postdoctoral Research Associate :: Epidemiology and Biostatistics

Education History

University of Oxford

United Kingdom

MSC :: Statistics

Publications

Ana Topf, Dan Cox, Irina T Zaharieva, Valeria Di Leo, Jaakko Sarparanta, Per Harald Jonson, Ian M Sealy, Andrei Smolnikov, Richard J White, Anna Vihola, Marco Savarese, Munise Merteroglu, Neha Wali, Kristen M Laricchia, Cristina Venturini, Bas Vroling, Sarah L Stenton, Beryl B Cummings, Elizabeth Harris, Chiara Marini-Bettolo, Jordi Diaz-Manera, Matt Henderson, Rita Barresi, Jennifer Duff, Eleina M England, Jane Patrick, Sundos Al-Husayni, Valerie Biancalana, Alan H Beggs, Istvan Bodi, Shobhana Bommireddipalli, Carsten G Bonnemann, Anita Cairns, Mei-Ting Chiew, Kristl G Claeys, Sandra T Cooper, Mark R Davis, Sandra Donkervoort, Corrie E Erasmus, Mahmoud R Fassad, Casie A Genetti, Carla Grosmann, Heinz Jungbluth, Erik-Jan Kamsteeg, Xavière Lornage, Wolfgang N Löscher, Edoardo Malfatti, Adnan Manzur, Pilar Martí, Tiziana E Mongini, Nuria Muelas, Atsuko Nishikawa, Anne H O'Donnell-Luria, Narumi Ogonuki, Gina L O'Grady, Emily O'Heir, Stéphanie Paquay, Rahul Phadke, Beth A Pletcher, Norma B Romero, Meyke Schouten, Snehal Shah, Izelle Smuts, Yves Sznajer, Giorgio Tasca, Robert W Taylor, Allysa Tuite, Peter Van den Bergh, Grace VanNoy, Nicol C Voermans, Julia V Wanschitz, Elizabeth Wraige, Kimihiko Yoshimura, Emily C Oates, Osamu Nakagawa, Ichizo Nishino, Jocelyn Laporte, Juan Jesus Vilchez, Daniel G MacArthur, Anna Sarkozy, Heather J Cordell, Bjarne Udd, Elisabeth M Busch-Nentwich, Francesco Muntoni, Volker Straub
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy. Nature genetics 56 (3) (2024)
Ana Topf, Dan Cox, Irina T Zaharieva, Valeria Di Leo, Jaakko Sarparanta, Per Harald Jonson, Ian M Sealy, Andrei Smolnikov, Richard J White, Anna Vihola, Marco Savarese, Munise Merteroglu, Neha Wali, Kristen M Laricchia, Cristina Venturini, Bas Vroling, Sarah L Stenton, Beryl B Cummings, Elizabeth Harris, Chiara Marini-Bettolo, Jordi Diaz-Manera, Matt Henderson, Rita Barresi, Jennifer Duff, Eleina M England, Jane Patrick, Sundos Al-Husayni, Valerie Biancalana, Alan H Beggs, Istvan Bodi, Shobhana Bommireddipalli, Carsten G Bonnemann, Anita Cairns, Mei-Ting Chiew, Kristl G Claeys, Sandra T Cooper, Mark R Davis, Sandra Donkervoort, Corrie E Erasmus, Mahmoud R Fassad, Casie A Genetti, Carla Grosmann, Heinz Jungbluth, Erik-Jan Kamsteeg, Xavière Lornage, Wolfgang N Löscher, Edoardo Malfatti, Adnan Manzur, Pilar Martí, Tiziana E Mongini, Nuria Muelas, Atsuko Nishikawa, Anne H O'Donnell-Luria, Narumi Ogonuki, Gina L O'Grady, Emily O'Heir, Stéphanie Paquay, Rahul Phadke, Beth A Pletcher, Norma B Romero, Meyke Schouten, Snehal Shah, Izelle Smuts, Yves Sznajer, Giorgio Tasca, Robert W Taylor, Allysa Tuite, Peter Van den Bergh, Grace VanNoy, Nicol C Voermans, Julia V Wanschitz, Elizabeth Wraige, Kimihiko Yoshimura, Emily C Oates, Osamu Nakagawa, Ichizo Nishino, Jocelyn Laporte, Juan Jesus Vilchez, Daniel G MacArthur, Anna Sarkozy, Heather J Cordell, Bjarne Udd, Elisabeth M Busch-Nentwich, Francesco Muntoni, Volker Straub
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy. Nature genetics (2024)
Ana Topf, Dan Cox, Irina T Zaharieva, Valeria Di Leo, Jaakko Sarparanta, Per Harald Jonson, Ian M Sealy, Andrei Smolnikov, Richard J White, Anna Vihola, Marco Savarese, Munise Merteroglu, Neha Wali, Kristen M Laricchia, Cristina Venturini, Bas Vroling, Sarah L Stenton, Beryl B Cummings, Elizabeth Harris, Chiara Marini-Bettolo, Jordi Diaz-Manera, Matt Henderson, Rita Barresi, Jennifer Duff, Eleina M England, Jane Patrick, Sundos Al-Husayni, Valerie Biancalana, Alan H Beggs, Istvan Bodi, Shobhana Bommireddipalli, Carsten G Bonnemann, Anita Cairns, Mei-Ting Chiew, Kristl G Claeys, Sandra T Cooper, Mark R Davis, Sandra Donkervoort, Corrie E Erasmus, Mahmoud R Fassad, Casie A Genetti, Carla Grosmann, Heinz Jungbluth, Erik-Jan Kamsteeg, Xavière Lornage, Wolfgang N Löscher, Edoardo Malfatti, Adnan Manzur, Pilar Martí, Tiziana E Mongini, Nuria Muelas, Atsuko Nishikawa, Anne H O'Donnell-Luria, Narumi Ogonuki, Gina L O'Grady, Emily O'Heir, Stéphanie Paquay, Rahul Phadke, Beth A Pletcher, Norma B Romero, Meyke Schouten, Snehal Shah, Izelle Smuts, Yves Sznajer, Giorgio Tasca, Robert W Taylor, Allysa Tuite, Peter Van den Bergh, Grace VanNoy, Nicol C Voermans, Julia V Wanschitz, Elizabeth Wraige, Kimihiko Yoshimura, Emily C Oates, Osamu Nakagawa, Ichizo Nishino, Jocelyn Laporte, Juan Jesus Vilchez, Daniel G MacArthur, Anna Sarkozy, Heather J Cordell, Bjarne Udd, Elisabeth M Busch-Nentwich, Francesco Muntoni, Volker Straub
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy. Nature genetics 56 (3) (2024)
Ana Topf, Dan Cox, Irina T Zaharieva, Valeria Di Leo, Jaakko Sarparanta, Per Harald Jonson, Ian M Sealy, Andrei Smolnikov, Richard J White, Anna Vihola, Marco Savarese, Munise Merteroglu, Neha Wali, Kristen M Laricchia, Cristina Venturini, Bas Vroling, Sarah L Stenton, Beryl B Cummings, Elizabeth Harris, Chiara Marini-Bettolo, Jordi Diaz-Manera, Matt Henderson, Rita Barresi, Jennifer Duff, Eleina M England, Jane Patrick, Sundos Al-Husayni, Valerie Biancalana, Alan H Beggs, Istvan Bodi, Shobhana Bommireddipalli, Carsten G Bonnemann, Anita Cairns, Mei-Ting Chiew, Kristl G Claeys, Sandra T Cooper, Mark R Davis, Sandra Donkervoort, Corrie E Erasmus, Mahmoud R Fassad, Casie A Genetti, Carla Grosmann, Heinz Jungbluth, Erik-Jan Kamsteeg, Xavière Lornage, Wolfgang N Löscher, Edoardo Malfatti, Adnan Manzur, Pilar Martí, Tiziana E Mongini, Nuria Muelas, Atsuko Nishikawa, Anne H O'Donnell-Luria, Narumi Ogonuki, Gina L O'Grady, Emily O'Heir, Stéphanie Paquay, Rahul Phadke, Beth A Pletcher, Norma B Romero, Meyke Schouten, Snehal Shah, Izelle Smuts, Yves Sznajer, Giorgio Tasca, Robert W Taylor, Allysa Tuite, Peter Van den Bergh, Grace VanNoy, Nicol C Voermans, Julia V Wanschitz, Elizabeth Wraige, Kimihiko Yoshimura, Emily C Oates, Osamu Nakagawa, Ichizo Nishino, Jocelyn Laporte, Juan Jesus Vilchez, Daniel G MacArthur, Anna Sarkozy, Heather J Cordell, Bjarne Udd, Elisabeth M Busch-Nentwich, Francesco Muntoni, Volker Straub
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy. Nature genetics 56 (3) (2024)
Ana Topf, Dan Cox, Irina T Zaharieva, Valeria Di Leo, Jaakko Sarparanta, Per Harald Jonson, Ian M Sealy, Andrei Smolnikov, Richard J White, Anna Vihola, Marco Savarese, Munise Merteroglu, Neha Wali, Kristen M Laricchia, Cristina Venturini, Bas Vroling, Sarah L Stenton, Beryl B Cummings, Elizabeth Harris, Chiara Marini-Bettolo, Jordi Diaz-Manera, Matt Henderson, Rita Barresi, Jennifer Duff, Eleina M England, Jane Patrick, Sundos Al-Husayni, Valerie Biancalana, Alan H Beggs, Istvan Bodi, Shobhana Bommireddipalli, Carsten G Bonnemann, Anita Cairns, Mei-Ting Chiew, Kristl G Claeys, Sandra T Cooper, Mark R Davis, Sandra Donkervoort, Corrie E Erasmus, Mahmoud R Fassad, Casie A Genetti, Carla Grosmann, Heinz Jungbluth, Erik-Jan Kamsteeg, Xavière Lornage, Wolfgang N Löscher, Edoardo Malfatti, Adnan Manzur, Pilar Martí, Tiziana E Mongini, Nuria Muelas, Atsuko Nishikawa, Anne H O'Donnell-Luria, Narumi Ogonuki, Gina L O'Grady, Emily O'Heir, Stéphanie Paquay, Rahul Phadke, Beth A Pletcher, Norma B Romero, Meyke Schouten, Snehal Shah, Izelle Smuts, Yves Sznajer, Giorgio Tasca, Robert W Taylor, Allysa Tuite, Peter Van den Bergh, Grace VanNoy, Nicol C Voermans, Julia V Wanschitz, Elizabeth Wraige, Kimihiko Yoshimura, Emily C Oates, Osamu Nakagawa, Ichizo Nishino, Jocelyn Laporte, Juan Jesus Vilchez, Daniel G MacArthur, Anna Sarkozy, Heather J Cordell, Bjarne Udd, Elisabeth M Busch-Nentwich, Francesco Muntoni, Volker Straub
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy. Nature genetics 56 (3) (2024)
Ana Topf, Dan Cox, Irina T Zaharieva, Valeria Di Leo, Jaakko Sarparanta, Per Harald Jonson, Ian M Sealy, Andrei Smolnikov, Richard J White, Anna Vihola, Marco Savarese, Munise Merteroglu, Neha Wali, Kristen M Laricchia, Cristina Venturini, Bas Vroling, Sarah L Stenton, Beryl B Cummings, Elizabeth Harris, Chiara Marini-Bettolo, Jordi Diaz-Manera, Matt Henderson, Rita Barresi, Jennifer Duff, Eleina M England, Jane Patrick, Sundos Al-Husayni, Valerie Biancalana, Alan H Beggs, Istvan Bodi, Shobhana Bommireddipalli, Carsten G Bonnemann, Anita Cairns, Mei-Ting Chiew, Kristl G Claeys, Sandra T Cooper, Mark R Davis, Sandra Donkervoort, Corrie E Erasmus, Mahmoud R Fassad, Casie A Genetti, Carla Grosmann, Heinz Jungbluth, Erik-Jan Kamsteeg, Xavière Lornage, Wolfgang N Löscher, Edoardo Malfatti, Adnan Manzur, Pilar Martí, Tiziana E Mongini, Nuria Muelas, Atsuko Nishikawa, Anne H O'Donnell-Luria, Narumi Ogonuki, Gina L O'Grady, Emily O'Heir, Stéphanie Paquay, Rahul Phadke, Beth A Pletcher, Norma B Romero, Meyke Schouten, Snehal Shah, Izelle Smuts, Yves Sznajer, Giorgio Tasca, Robert W Taylor, Allysa Tuite, Peter Van den Bergh, Grace VanNoy, Nicol C Voermans, Julia V Wanschitz, Elizabeth Wraige, Kimihiko Yoshimura, Emily C Oates, Osamu Nakagawa, Ichizo Nishino, Jocelyn Laporte, Juan Jesus Vilchez, Daniel G MacArthur, Anna Sarkozy, Heather J Cordell, Bjarne Udd, Elisabeth M Busch-Nentwich, Francesco Muntoni, Volker Straub
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy. Nature genetics 56 (3) (2024)
Ana Topf, Dan Cox, Irina T Zaharieva, Valeria Di Leo, Jaakko Sarparanta, Per Harald Jonson, Ian M Sealy, Andrei Smolnikov, Richard J White, Anna Vihola, Marco Savarese, Munise Merteroglu, Neha Wali, Kristen M Laricchia, Cristina Venturini, Bas Vroling, Sarah L Stenton, Beryl B Cummings, Elizabeth Harris, Chiara Marini-Bettolo, Jordi Diaz-Manera, Matt Henderson, Rita Barresi, Jennifer Duff, Eleina M England, Jane Patrick, Sundos Al-Husayni, Valerie Biancalana, Alan H Beggs, Istvan Bodi, Shobhana Bommireddipalli, Carsten G Bonnemann, Anita Cairns, Mei-Ting Chiew, Kristl G Claeys, Sandra T Cooper, Mark R Davis, Sandra Donkervoort, Corrie E Erasmus, Mahmoud R Fassad, Casie A Genetti, Carla Grosmann, Heinz Jungbluth, Erik-Jan Kamsteeg, Xavière Lornage, Wolfgang N Löscher, Edoardo Malfatti, Adnan Manzur, Pilar Martí, Tiziana E Mongini, Nuria Muelas, Atsuko Nishikawa, Anne H O'Donnell-Luria, Narumi Ogonuki, Gina L O'Grady, Emily O'Heir, Stéphanie Paquay, Rahul Phadke, Beth A Pletcher, Norma B Romero, Meyke Schouten, Snehal Shah, Izelle Smuts, Yves Sznajer, Giorgio Tasca, Robert W Taylor, Allysa Tuite, Peter Van den Bergh, Grace VanNoy, Nicol C Voermans, Julia V Wanschitz, Elizabeth Wraige, Kimihiko Yoshimura, Emily C Oates, Osamu Nakagawa, Ichizo Nishino, Jocelyn Laporte, Juan Jesus Vilchez, Daniel G MacArthur, Anna Sarkozy, Heather J Cordell, Bjarne Udd, Elisabeth M Busch-Nentwich, Francesco Muntoni, Volker Straub
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy. Nature genetics 56 (3) (2024)
Victoria L Mulcahy, Evaggelia Liaskou, Jose-Ezequiel Martin, Prasanti Kotagiri, Jonathan Badrock, Rebecca L Jones, Simon M Rushbrook, Stephen D Ryder, Douglas Thorburn, Simon D Taylor-Robinson, Graeme Clark, Heather J Cordell, Richard N Sandford, David E J Jones, Gideon M Hirschfield, George F Mells
Regulation of immune responses in primary biliary cholangitis: a transcriptomic analysis of peripheral immune cells. Hepatology communications 7 (4) (2023)
Younghun Han, Jinyoung Byun, Catherine Zhu, Ryan Sun, Julia Y Roh, Heather J Cordell, Hyun-Sung Lee, Vikram R Shaw, Sung Wook Kang, Javad Razjouyan, Matthew A Cooley, Manal M Hassan, Katherine A Siminovitch, Trine Folseraas, David Ellinghaus, Annika Bergquist, Simon M Rushbrook, Andre Franke, Tom Hemming Karlsen, Konstantinos N Lazaridis, null null, Katherine A McGlynn, Lewis Rowland Roberts, Christopher Ian Amos
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis. Nature communications 14 (1) (2023)
Younghun Han, Jinyoung Byun, Catherine Zhu, Ryan Sun, Julia Y Roh, Heather J Cordell, Hyun-Sung Lee, Vikram R Shaw, Sung Wook Kang, Javad Razjouyan, Matthew A Cooley, Manal M Hassan, Katherine A Siminovitch, Trine Folseraas, David Ellinghaus, Annika Bergquist, Simon M Rushbrook, Andre Franke, Tom Hemming Karlsen, Konstantinos N Lazaridis, null null, Katherine A McGlynn, Lewis Rowland Roberts, Christopher Ian Amos
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis. Nature communications 14 (1) (2023)
Mengyao Yu, Matthew Aguirre, Meiwen Jia, Ketrin Gjoni, Aldo Cordova-Palomera, Chad Munger, Dulguun Amgalan, X Rosa Ma, Alexandre da Costa Pereira, Catherine Tcheandjieu, Christine E Seidman, Jonathan G Seidman, Martin Tristani-Firouzi, Wendy K Chung, Elizabeth Goldmuntz, Deepak Srivastava, Ruth J F Loos, Nathalie Chami, Heather J Cordell, Martina Dreßen, Bertram Mueller-Myhsok, Harald Lahm, Markus Krane, Katherine S Pollard, Jesse M Engreitz, Sarah A Gagliano Taliun, Bruce D Gelb, James R Priest
Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes. Circulation. Genomic and precision medicine (2023)
Younghun Han, Jinyoung Byun, Catherine Zhu, Ryan Sun, Julia Y Roh, Heather J Cordell, Hyun-Sung Lee, Vikram R Shaw, Sung Wook Kang, Javad Razjouyan, Matthew A Cooley, Manal M Hassan, Katherine A Siminovitch, Trine Folseraas, David Ellinghaus, Annika Bergquist, Simon M Rushbrook, Andre Franke, Tom Hemming Karlsen, Konstantinos N Lazaridis, null null, Katherine A McGlynn, Lewis Rowland Roberts, Christopher Ian Amos
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis. Nature communications 14 (1) (2023)
Nikolaos Tzoumas, David Kavanagh, Heather J Cordell, Andrew J Lotery, Praveen J Patel, David H W Steel
Rare complement factor I variants associated with reduced macular thickness and age-related macular degeneration in the UK Biobank. Human molecular genetics 31 (16) (2022)
Marijana Vujkovic, Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J Cordell, Jing He, Yevgeniy Gindin, Chuhan Chung, Robert P Myers, Carolin V Schneider, Joseph Park, Kyung Min Lee, Marina Serper, Rotonya M Carr, David E Kaplan, Mary E Haas, Matthew T MacLean, Walter R Witschey, Xiang Zhu, Catherine Tcheandjieu, Rachel L Kember, Henry R Kranzler, Anurag Verma, Ayush Giri, Derek M Klarin, Yan V Sun, Jie Huang, Jennifer E Huffman, Kate Townsend Creasy, Nicholas J Hand, Ching-Ti Liu, Michelle T Long, Jie Yao, Matthew J Budoff, Jingyi Tan, Xiaohui Li, Henry J Lin, Yii-Der Ida Chen, Kent D Taylor, Ruey-Kang Chang, Ronald M Krauss, Silvia Vilarinho, Joseph Brancale, Jonas B Nielsen, Adam E Locke, Marcus B Jones, Niek Verweij, Aris Baras, K Rajender Reddy, Brent A Neuschwander-Tetri, Jeffrey B Schwimmer, Arun J Sanyal, Naga Chalasani, Kathleen A Ryan, Braxton D Mitchell, Dipender Gill, Andrew D Wells, Elisabetta Manduchi, Yedidya Saiman, Nadim Mahmud, Donald R Miller, Peter D Reaven, Lawrence S Phillips, Sumitra Muralidhar, Scott L Duvall, Jennifer S Lee, Themistocles L Assimes, Saiju Pyarajan, Kelly Cho, Todd L Edwards, Scott M Damrauer, Peter W Wilson, J Michael Gaziano, Christopher J O'Donnell, Amit V Khera, Struan F A Grant, Christopher D Brown, Philip S Tsao, Danish Saleheen, Luca A Lotta, Lisa Bastarache, Quentin M Anstee, Ann K Daly, James B Meigs, Jerome I Rotter, Julie A Lynch, null null, null null, null null, null null, Daniel James Rader, Benjamin F Voight, Kyong-Mi Chang
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Nature genetics 54 (6) (2022)
Tafadzwa Machipisa, Chishala Chishala, Gasnat Shaboodien, Liesl J Zühlke, Babu Muhamed, Shahiemah Pandie, Jantina de Vries, Nakita Laing, Alexia Joachim, Rezeen Daniels, Mpiko Ntsekhe, Christopher T Hugo-Hamman, Bernard Gitura, Stephen Ogendo, Peter S Lwabi, Emmy Okello, Albertino Damasceno, Celia Novela, Ana Olga Mocumbi, Geoffrey Madeira, John Musuku, Agnes Mtaja, Ahmed ElSayed, Huda H M Alhassan, Fidelia Bode-Thomas, Christopher S Yilgwan, Ganiyu Amusa, Esin Nkereuwem, Nicola Mulder, Rajkumar Ramesar, Maia Lesosky, Heather J Cordell, Michael Chong, Bernard D Keavney, Guillaume Paré, Mark M Engel, null null
Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†. Circulation. Genomic and precision medicine (2022)
Richard Howey, Heather J Cordell
Confirmation of the superior performance of the causal Graphical Analysis Using Genetics (cGAUGE) pipeline in comparison to various competing alternatives. Wellcome open research 7 (2022)
Tafadzwa Machipisa, Chishala Chishala, Gasnat Shaboodien, Liesl J Zühlke, Babu Muhamed, Shahiemah Pandie, Jantina de Vries, Nakita Laing, Alexia Joachim, Rezeen Daniels, Mpiko Ntsekhe, Christopher T Hugo-Hamman, Bernard Gitura, Stephen Ogendo, Peter S Lwabi, Emmy Okello, Albertino Damasceno, Celia Novela, Ana Olga Mocumbi, Geoffrey Madeira, John Musuku, Agnes Mtaja, Ahmed ElSayed, Huda H M Alhassan, Fidelia Bode-Thomas, Christopher S Yilgwan, Ganiyu Amusa, Esin Nkereuwem, Nicola Mulder, Rajkumar Ramesar, Maia Lesosky, Heather J Cordell, Michael Chong, Bernard D Keavney, Guillaume Paré, Mark M Engel, null null
Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†. Circulation. Genomic and precision medicine (2022)
James J Fryett, Andrew P Morris, Heather J Cordell
Investigating the prediction of CpG methylation levels from SNP genotype data to help elucidate relationships between methylation, gene expression and complex traits. Genetic epidemiology 46 (8) (2022)
Laura A Devlin, Janice Coles, Claire L Jackson, Miguel Barroso-Gil, Ben Green, Woolf T Walker, N Simon Thomas, James Thompson, Simon A Rock, Ruxandra Neatu, Laura Powell, Elisa Molinari, null null, Ian J Wilson, Heather J Cordell, Eric Olinger, Colin G Miles, John Andrew Sayer, Gabrielle Wheway, Jane S A Lucas
Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome. Clinical genetics (2022)
Wei-Yu Lin, Sarah E Fordham, Eric Hungate, Nicola J Sunter, Claire Elstob, Yaobo Xu, Catherine Park, Anne Quante, Konstantin Strauch, Christian Gieger, Andrew Skol, Thahira Rahman, Lara Sucheston-Campbell, Junke Wang, Theresa Hahn, Alyssa I Clay-Gilmour, Gail L Jones, Helen J Marr, Graham H Jackson, Tobias Menne, Matthew Collin, Adam Ivey, Robert K Hills, Alan K Burnett, Nigel H Russell, Jude Fitzgibbon, Richard A Larson, Michelle M Le Beau, Wendy Stock, Olaf Heidenreich, Abrar Alharbi, David John Allsup, Richard S Houlston, Jean Norden, Anne M Dickinson, Elisabeth Douglas, Beverley Clare Lendrem, Ann K Daly, Louise Palm, Kim Piechocki, Sally Jeffries, Martin Bornhäuser, Christoph Röllig, Heidi Altmann, Leo Ruhnke, Desiree Kunadt, Lisa Wagenführ, Heather J Cordell, Rebecca Darlay, Mette K Andersen, Maria C Fontana, Giovanni Martinelli, Giovanni Marconi, Miguel Angel Sanz, José Cervera, Inés Gómez-Seguí, Thomas Cluzeau, Chimène Moreilhon, Sophie Raynaud, Heinz Sill, Maria Teresa Teresa Voso, Francesco Lo-Coco, Hervé Dombret, Meyling H Cheok, Claude Preudhomme, Rosemary E Gale, David Linch, Julia Gaal-Wesinger, Andras Masszi, Daniel Nowak, Wolf-Karsten Hofmann, Amanda Gilkes, Kimmo Porkka, Jelena D Milosevic Feenstra, Robert Kralovics, David Grimwade, Manja Meggendorfer, Torsten Haferlach, Szilvia Krizsán, Csaba Bödör, Friedrich Stölzel, Kenan Onel, James M Allan
Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Nature communications 13 (1) (2022)
Tafadzwa Machipisa, Chishala Chishala, Gasnat Shaboodien, Liesl J Zühlke, Babu Muhamed, Shahiemah Pandie, Jantina de Vries, Nakita Laing, Alexia Joachim, Rezeen Daniels, Mpiko Ntsekhe, Christopher T Hugo-Hamman, Bernard Gitura, Stephen Ogendo, Peter S Lwabi, Emmy Okello, Albertino Damasceno, Celia Novela, Ana Olga Mocumbi, Geoffrey Madeira, John Musuku, Agnes Mtaja, Ahmed ElSayed, Huda H M Alhassan, Fidelia Bode-Thomas, Christopher S Yilgwan, Ganiyu Amusa, Esin Nkereuwem, Nicola Mulder, Rajkumar Ramesar, Maia Lesosky, Heather J Cordell, Michael Chong, Bernard D Keavney, Guillaume Paré, Mark M Engel, null null
Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†. Circulation. Genomic and precision medicine 16 (1) (2022)
Tafadzwa Machipisa, Chishala Chishala, Gasnat Shaboodien, Liesl J Zühlke, Babu Muhamed, Shahiemah Pandie, Jantina de Vries, Nakita Laing, Alexia Joachim, Rezeen Daniels, Mpiko Ntsekhe, Christopher T Hugo-Hamman, Bernard Gitura, Stephen Ogendo, Peter S Lwabi, Emmy Okello, Albertino Damasceno, Celia Novela, Ana Olga Mocumbi, Geoffrey Madeira, John Musuku, Agnes Mtaja, Ahmed ElSayed, Huda H M Alhassan, Fidelia Bode-Thomas, Christopher S Yilgwan, Ganiyu Amusa, Esin Nkereuwem, Nicola Mulder, Rajkumar Ramesar, Maia Lesosky, Heather J Cordell, Michael Chong, Bernard D Keavney, Guillaume Paré, Mark M Engel, null null
Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†. Circulation. Genomic and precision medicine 16 (1) (2022)
Tafadzwa Machipisa, Chishala Chishala, Gasnat Shaboodien, Liesl J Zühlke, Babu Muhamed, Shahiemah Pandie, Jantina de Vries, Nakita Laing, Alexia Joachim, Rezeen Daniels, Mpiko Ntsekhe, Christopher T Hugo-Hamman, Bernard Gitura, Stephen Ogendo, Peter S Lwabi, Emmy Okello, Albertino Damasceno, Celia Novela, Ana Olga Mocumbi, Geoffrey Madeira, John Musuku, Agnes Mtaja, Ahmed ElSayed, Huda H M Alhassan, Fidelia Bode-Thomas, Christopher S Yilgwan, Ganiyu Amusa, Esin Nkereuwem, Nicola Mulder, Rajkumar Ramesar, Maia Lesosky, Heather J Cordell, Michael Chong, Bernard D Keavney, Guillaume Paré, Mark M Engel, null null
Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†. Circulation. Genomic and precision medicine 16 (1) (2022)
Tafadzwa Machipisa, Chishala Chishala, Gasnat Shaboodien, Liesl J Zühlke, Babu Muhamed, Shahiemah Pandie, Jantina de Vries, Nakita Laing, Alexia Joachim, Rezeen Daniels, Mpiko Ntsekhe, Christopher T Hugo-Hamman, Bernard Gitura, Stephen Ogendo, Peter S Lwabi, Emmy Okello, Albertino Damasceno, Celia Novela, Ana Olga Mocumbi, Geoffrey Madeira, John Musuku, Agnes Mtaja, Ahmed ElSayed, Huda H M Alhassan, Fidelia Bode-Thomas, Christopher S Yilgwan, Ganiyu Amusa, Esin Nkereuwem, Nicola Mulder, Rajkumar Ramesar, Maia Lesosky, Heather J Cordell, Michael Chong, Bernard D Keavney, Guillaume Paré, Mark M Engel, null null
Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†. Circulation. Genomic and precision medicine 16 (1) (2022)
Richard Howey, Alexander D Clark, Najib Naamane, Louise N Reynard, Arthur G Pratt, Heather J Cordell
A Bayesian network approach incorporating imputation of missing data enables exploratory analysis of complex causal biological relationships. PLoS genetics 17 (9) (2021)
Wei-Yu Lin, Sarah E Fordham, Eric Hungate, Nicola J Sunter, Claire Elstob, Yaobo Xu, Catherine Park, Anne Quante, Konstantin Strauch, Christian Gieger, Andrew Skol, Thahira Rahman, Lara Sucheston-Campbell, Junke Wang, Theresa Hahn, Alyssa I Clay-Gilmour, Gail L Jones, Helen J Marr, Graham H Jackson, Tobias Menne, Matthew Collin, Adam Ivey, Robert K Hills, Alan K Burnett, Nigel H Russell, Jude Fitzgibbon, Richard A Larson, Michelle M Le Beau, Wendy Stock, Olaf Heidenreich, Abrar Alharbi, David John Allsup, Richard S Houlston, Jean Norden, Anne M Dickinson, Elisabeth Douglas, Beverley Clare Lendrem, Ann K Daly, Louise Palm, Kim Piechocki, Sally Jeffries, Martin Bornhäuser, Christoph Röllig, Heidi Altmann, Leo Ruhnke, Desiree Kunadt, Lisa Wagenführ, Heather J Cordell, Rebecca Darlay, Mette K Andersen, Maria C Fontana, Giovanni Martinelli, Giovanni Marconi, Miguel Angel Sanz, José Cervera, Inés Gómez-Seguí, Thomas Cluzeau, Chimène Moreilhon, Sophie Raynaud, Heinz Sill, Maria Teresa Teresa Voso, Francesco Lo-Coco, Hervé Dombret, Meyling H Cheok, Claude Preudhomme, Rosemary E Gale, David Linch, Julia Gaal-Wesinger, Andras Masszi, Daniel Nowak, Wolf-Karsten Hofmann, Amanda Gilkes, Kimmo Porkka, Jelena D Milosevic Feenstra, Robert Kralovics, David Grimwade, Manja Meggendorfer, Torsten Haferlach, Szilvia Krizsán, Csaba Bödör, Friedrich Stölzel, Kenan Onel, James M Allan
Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Nature communications 12 (1) (2021)
Joris Deelen, Daniel S Evans, Dan E Arking, Niccolo' Tesi, Marianne Nygaard, Xiaomin Liu, Mary K Wojczynski, Mary L Biggs, Ashley van der Spek, Gil Atzmon, Erin B Ware, Chloé Sarnowski, Albert V Smith, Ilkka Seppälä, Heather J Cordell, Janina Dose, Najaf Amin, Alice M Arnold, Kristin L Ayers, Nir Barzilai, Elizabeth J Becker, Marian Beekman, Hélène Blanché, Kaare Christensen, Lene Christiansen, Joanna C Collerton, Sarah Cubaynes, Steven R Cummings, Karen Davies, Birgit Debrabant, Jean-François Deleuze, Rachel Duncan, Jessica D Faul, Claudio Franceschi, Pilar Galan, Vilmundur G Gudnason, Tamara B Harris, Martijn Huisman, Mikko A Hurme, Carol Jagger, Iris Jansen, Marja Jylhä, Mika Kähönen, David Karasik, Sharon L R Kardia, Andrew Kingston, Thomas B L Kirkwood, Lenore J Launer, Terho Lehtimäki, Wolfgang Lieb, Leo-Pekka Lyytikäinen, Carmen Martín-Ruiz, Junxia Min, Almut Nebel, Anne B Newman, Chao Nie, Ellen A Nohr, Eric S Orwoll, Thomas T Perls, Michael A Province, Bruce M Psaty, Olli T Raitakari, Marcel J T Reinders, Jean Marie Robine, Jerome I Rotter, Paola Sebastiani, Jennifer A Smith, Thorkild I A Sørensen, Kent D Taylor, Andre G Uitterlinden, Wiesje van der Flier, Sven J Van der Lee, Cornelia M van Duijn, Diana van Heemst, James W Vaupel, David R Weir, Kenny Ye, Yi Zeng, Wanlin Zheng, Henne Holstege, Douglas P Kiel, Kathryn L Lunetta, P Eline Slagboom, Joanne M Murabito
Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes. Nature communications 12 (1) (2021)
Nardeen Eldafashi, Rebecca Darlay, Ruchi Shukla, Misti Vanette McCain, Robyn Watson, Yang Lin Liu, Nikki McStraw, Moustafa Fathy, Michael Atef Fawzy, Marco Y W Zaki, Ann K Daly, João P Maurício, Alastair D Burt, Beate Haugk, Heather J Cordell, Cristiana Bianco, Jean-François Dufour, Luca Vittorio Valenti, Quentin Mark Anstee, Helen L Reeves
A PDCD1 Role in the Genetic Predisposition to NAFLD-HCC? Cancers 13 (6) (2021)
Naushin H Waseem, Sancy Low, Amna Z Shah, Deepa Avisetti, Pia Ostergaard, Michael Simpson, Katarzyna A Niemiec, Belen Martin-Martin, Hebah Aldehlawi, Saima Usman, Pak Sang Lee, Anthony P Khawaja, Jonathan B Ruddle, Ameet Shah, Ege Ozkan, Alexander C Day, Yuzhen Jiang, Geoff Swinfield, Ananth Viswanathan, Giovanna Alfano, Christina Chakarova, Heather J Cordell, David F Garway-Heath, Peng T Khaw, Shomi S Bhattacharya, Ahmad Waseem, Paul J Foster
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma. PLoS genetics 16 (4) (2020)
Svetlana Cherlin, Myles J Lewis, Darren Plant, Nisha Nair, Katriona Goldmann, Evan Tzanis, Michael R Barnes, Paul McKeigue, Jennifer H Barrett, Costantino Pitzalis, Anne Barton, null null, Heather J Cordell
Investigation of genetically regulated gene expression and response to treatment in rheumatoid arthritis highlights an association between IL18RAP expression and treatment response. Annals of the rheumatic diseases 79 (11) (2020)
Richard Howey, So-Youn Shin, Caroline Relton, George Davey Smith, Heather J Cordell
Bayesian network analysis incorporating genetic anchors complements conventional Mendelian randomization approaches for exploratory analysis of causal relationships in complex data. PLoS genetics 16 (3) (2020)
Joris Deelen, Daniel S Evans, Dan E Arking, Niccolo' Tesi, Marianne Nygaard, Xiaomin Liu, Mary K Wojczynski, Mary L Biggs, Ashley van der Spek, Gil Atzmon, Erin B Ware, Chloé Sarnowski, Albert V Smith, Ilkka Seppälä, Heather J Cordell, Janina Dose, Najaf Amin, Alice M Arnold, Kristin L Ayers, Nir Barzilai, Elizabeth J Becker, Marian Beekman, Hélène Blanché, Kaare Christensen, Lene Christiansen, Joanna C Collerton, Sarah Cubaynes, Steven R Cummings, Karen Davies, Birgit Debrabant, Jean-François Deleuze, Rachel Duncan, Jessica D Faul, Claudio Franceschi, Pilar Galan, Vilmundur G Gudnason, Tamara B Harris, Martijn Huisman, Mikko A Hurme, Carol Jagger, Iris Jansen, Marja Jylhä, Mika Kähönen, David Karasik, Sharon L R Kardia, Andrew Kingston, Thomas B L Kirkwood, Lenore J Launer, Terho Lehtimäki, Wolfgang Lieb, Leo-Pekka Lyytikäinen, Carmen Martín-Ruiz, Junxia Min, Almut Nebel, Anne B Newman, Chao Nie, Ellen A Nohr, Eric S Orwoll, Thomas T Perls, Michael A Province, Bruce M Psaty, Olli T Raitakari, Marcel J T Reinders, Jean Marie Robine, Jerome I Rotter, Paola Sebastiani, Jennifer A Smith, Thorkild I A Sørensen, Kent D Taylor, Andre G Uitterlinden, Wiesje van der Flier, Sven J Van der Lee, Cornelia M van Duijn, Diana van Heemst, James W Vaupel, David R Weir, Kenny Ye, Yi Zeng, Wanlin Zheng, Henne Holstege, Douglas P Kiel, Kathryn L Lunetta, P Eline Slagboom, Joanne M Murabito
A meta-analysis of genome-wide association studies identifies multiple longevity genes. Nature communications 10 (1) (2019)
Giorgio Sirugo, Scott M Williams, Sarah A Tishkoff, Heather J Cordell, Jonathan Marchini, Gregory S Barsh, Gregory P Copenhaver
The Plight of Muntaser Ibrahim. PLoS genetics 15 (3) (2019)
Svetlana Cherlin, Darren Plant, John C Taylor, Marco Colombo, Athina Spiliopoulou, Evan Tzanis, Ann W Morgan, Michael R Barnes, Paul McKeigue, Jennifer H Barrett, Costantino Pitzalis, Anne Barton, Matura Consortium, Heather J Cordell
Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP data. Genetic epidemiology 42 (8) (2018)
Rebecca Darlay, Kristin L Ayers, George F Mells, Lynsey S Hall, Jimmy Z Liu, Mohamed A Almarri, Graeme J Alexander, David E Jones, Richard N Sandford, Carl A Anderson, Heather J Cordell
Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis. PLoS genetics 14 (12) (2018)
Richard Howey, Heather J Cordell
Further investigations of the W-test for pairwise epistasis testing. Wellcome open research 2 (2017)
Holly F Ainsworth, So-Youn Shin, Heather J Cordell
A comparison of methods for inferring causal relationships between genotype and phenotype using additional biological measurements. Genetic epidemiology 41 (7) (2017)

Heather J Cordell.css-eqlu8i{font-size:small;padding-left:4px;} (Heather Cordell)

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Heather J Cordell (Heather Cordell)