Keren Jacqueline Carss (Keren J Carss, Keren Carss)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 6

Top Topics

Genome Wide Association

Affordable Care Act

Cross Sectional

Coronary Artery

Top Venues

Circulation. Genomic and precision medicine

Nature reviews. Drug discovery

Nature genetics

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

Publications

Oliver S Burren, Ryan S Dhindsa, Sri V V Deevi, Sean Wen, Abhishek Nag, Jonathan Mitchell, Fengyuan Hu, Douglas P Loesch, Katherine R Smith, Neetu Razdan, Henric Olsson, Adam Platt, Dimitrios Michael Vitsios, Qiang Wu, null null, Veryan Codd, Christopher P Nelson, Nilesh J Samani, Ruth E March, Sebastian Wasilewski, Keren Jacqueline Carss, Margarete Fabre, Quanli Wang, Menelas N Pangalos, Slavé Petrovski
Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences. Nature genetics (2024)
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)
Luca Stefanucci, Janine H Collins, Matthew Christopher Sims, Iñigo Barrio-Hernandez, Luanluan Sun, Oliver S Burren, Livia Perfetto, Isobel Bender, Tiffany J Callahan, Kathryn Fleming, Jose Antonio Guerrero, Henning Hermjakob, Maria Jesus Martin, James David Stephenson, Kalpana Panneerselvam, Slavé Petrovski, Pablo Porras, Peter Nick Robinson, Quanli Wang, Xavier Watkins, Mattia Frontini, Roman A Laskowski, Pedro Beltrao, Emanuele Di Angelantonio, Keith Gomez, Michael A Laffan, Willem Hendrik Ouwehand, Andrew D Mumford, Kathleen Freson, Keren Jacqueline Carss, Kate Downes, Nicholas S Gleadall, Karyn Megy, Elspeth A Bruford, Dragana Vuckovic
The effects of pathogenic variants for inherited hemostasis disorders in 140,214 UK Biobank participants. Blood (2023)
Kimberley M Reid, Robert V V Spaull, Smrithi Salian, Katy Barwick, Esther Meyer, Juan Zhen, Hiromi Hirata, Diba Sheipouri, Hind Benkerroum, Kathleen M Gorman, Apostolos Papandreou, Michael A Simpson, Yoshinobu Hirano, Irene Farabella, Andriy Kryshtafovych, Detelina Grozeva, Keren Jacqueline Carss, Martin Smith, Hardev Pall, Peter Lunt, Susanna De Gressi, Erik-Jan Kamsteeg, Tobias B Haack, Lucinda J Carr, Rita Guerreiro, Jose Bras, Eamonn R Maher, Richard H Scott, Robert J Vandenberg, F Lucy Raymond, Wui K Chong, Sniya Valsa Sudhakar, Kshitij Mankad, Maarten E A Reith, Philippe M Campeau, Robert J Harvey, Manju A Kurian
MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia. Movement disorders : official journal of the Movement Disorder Society 37 (10) (2022)
Ingrid S Tarr, Stephanie E Hesselson, Siiri E Iismaa, Emma M Rath, Steven Monger, Michael Troup, Ketan Mishra, Claire M Y Wong, Pei-Chen Hsu, Keerat Junday, David T Humphreys, David Adlam, Thomas R Webb, Ania A Baranowska, Stephen E Hamby, Keren Jacqueline Carss, Nilesh J Samani, Monique Bax, Lucy McGrath-Cadell, Jason C Kovacic, Sally L Dunwoodie, Diane Fatkin, David W M Muller, Robert M Graham, Eleni Giannoulatou
Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing. Circulation. Genomic and precision medicine 15 (4) (2022)
Keren Jacqueline Carss, Aimee M Deaton, Alberto Del Rio-Espinola, Dorothée Diogo, Mark Fielden, Diptee A Kulkarni, Jonathan Moggs, Peter Newham, Matthew R Nelson, Frank D Sistare, Lucas D Ward, Jing Yuan
Using human genetics to improve safety assessment of therapeutics. Nature reviews. Drug discovery (2022)