Duncan Sproul

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Topics

Dna Methylation

Circulating Tumor

Top Venues

Nature communications

Nature genetics

Cancer research

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

Publications

Francesca Taglini, Ioannis Kafetzopoulos, Willow Rolls, Kamila Irena Musialik, Heng Yang Lee, Yujie Zhang, Mattia Marenda, Lyndsay Kerr, Hannah Finan, Cristina Rubio-Ramon, Philippe Gautier, Hannah Wapenaar, Dhananjay Kumar, Hazel Davidson-Smith, Jimi C Wills, Laura C Murphy, Ann Wheeler, Marcus D Wilson, Duncan Sproul
DNMT3B PWWP mutations cause hypermethylation of heterochromatin. EMBO reports (2024)
Francesca Taglini, Ioannis Kafetzopoulos, Willow Rolls, Kamila Irena Musialik, Heng Yang Lee, Yujie Zhang, Mattia Marenda, Lyndsay Kerr, Hannah Finan, Cristina Rubio-Ramon, Philippe Gautier, Hannah Wapenaar, Dhananjay Kumar, Hazel Davidson-Smith, Jimi C Wills, Laura C Murphy, Ann Wheeler, Marcus D Wilson, Duncan Sproul
DNMT3B PWWP mutations cause hypermethylation of heterochromatin. EMBO reports (2024)
Francesca Taglini, Ioannis Kafetzopoulos, Willow Rolls, Kamila Irena Musialik, Heng Yang Lee, Yujie Zhang, Mattia Marenda, Lyndsay Kerr, Hannah Finan, Cristina Rubio-Ramon, Philippe Gautier, Hannah Wapenaar, Dhananjay Kumar, Hazel Davidson-Smith, Jimi C Wills, Laura C Murphy, Ann Wheeler, Marcus D Wilson, Duncan Sproul
DNMT3B PWWP mutations cause hypermethylation of heterochromatin. EMBO reports 25 (3) (2024)
Francesca Taglini, Ioannis Kafetzopoulos, Willow Rolls, Kamila Irena Musialik, Heng Yang Lee, Yujie Zhang, Mattia Marenda, Lyndsay Kerr, Hannah Finan, Cristina Rubio-Ramon, Philippe Gautier, Hannah Wapenaar, Dhananjay Kumar, Hazel Davidson-Smith, Jimi C Wills, Laura C Murphy, Ann Wheeler, Marcus D Wilson, Duncan Sproul
DNMT3B PWWP mutations cause hypermethylation of heterochromatin. EMBO reports (2024)
Francesca Taglini, Ioannis Kafetzopoulos, Willow Rolls, Kamila Irena Musialik, Heng Yang Lee, Yujie Zhang, Mattia Marenda, Lyndsay Kerr, Hannah Finan, Cristina Rubio-Ramon, Philippe Gautier, Hannah Wapenaar, Dhananjay Kumar, Hazel Davidson-Smith, Jimi C Wills, Laura C Murphy, Ann Wheeler, Marcus D Wilson, Duncan Sproul
DNMT3B PWWP mutations cause hypermethylation of heterochromatin. EMBO reports 25 (3) (2024)
Francesca Taglini, Ioannis Kafetzopoulos, Willow Rolls, Kamila Irena Musialik, Heng Yang Lee, Yujie Zhang, Mattia Marenda, Lyndsay Kerr, Hannah Finan, Cristina Rubio-Ramon, Philippe Gautier, Hannah Wapenaar, Dhananjay Kumar, Hazel Davidson-Smith, Jimi C Wills, Laura C Murphy, Ann Wheeler, Marcus D Wilson, Duncan Sproul
DNMT3B PWWP mutations cause hypermethylation of heterochromatin. EMBO reports 25 (3) (2024)
Lyndsay Kerr, Ioannis Kafetzopoulos, Ramon Grima, Duncan Sproul
Genome-wide single-molecule analysis of long-read DNA methylation reveals heterogeneous patterns at heterochromatin that reflect nucleosome organisation. PLoS genetics 19 (10) (2023)
Jonathan Higham, Lyndsay Kerr, Qian Zhang, Rosie M Walker, Sarah E Harris, David M Howard, Emma L Hawkins, Anca-Larisa Sandu, J Douglas Steele, Gordon D Waiter, Alison D Murray, Kathryn L Evans, Andrew M McIntosh, Peter M Visscher, Ian J Deary, Simon R Cox, Duncan Sproul
Local CpG density affects the trajectory and variance of age-associated DNA methylation changes. Genome biology 23 (1) (2022)
Nicholas T Younger, Mollie L Wilson, Anabel Martinez Lyons, Edward J Jarman, Alison M Meynert, Graeme R Grimes, Konstantinos Gournopanos, Scott H Waddell, Peter A Tennant, David H Wilson, Rachel V Guest, Stephen J Wigmore, Juan Carlos Acosta, Timothy James Kendall, Martin S Taylor, Duncan Sproul, Pleasantine Mill, Luke Boulter
In Vivo Modeling of Patient Genetic Heterogeneity Identifies New Ways to Target Cholangiocarcinoma. Cancer research 82 (8) (2022)
Roza H Ali Masalmeh, Francesca Taglini, Cristina Rubio-Ramon, Kamila I Musialik, Jonathan Higham, Hazel Davidson-Smith, Ioannis Kafetzopoulos, Kamila P Pawlicka, Hannah M Finan, Richard Clark, Jimi Wills, Andrew J Finch, Lee Murphy, Duncan Sproul
De novo DNA methyltransferase activity in colorectal cancer is directed towards H3K36me3 marked CpG islands. Nature communications 12 (1) (2021)
Hemalvi Patani, Michael D Rushton, Jonathan Higham, Saul A Teijeiro, David Oxley, Pedro Rodriguez Cutillas, Duncan Sproul, Gabriella Ficz
Transition to naïve human pluripotency mirrors pan-cancer DNA hypermethylation. Nature communications 11 (1) (2020)
Carolina Uggenti, Alice Lepelley, Marine Depp, Andrew P Badrock, Mathieu P Rodero, Marie-Thérèse El-Daher, Gillian I Rice, Somdutta Dhir, Ann P Wheeler, Ashish Dhir, Waad Albawardi, Marie-Louise Frémond, Luis Seabra, Jennifer Doig, Natalie Blair, Maria José Martin-Niclos, Erika Della Mina, Alejandro Rubio-Roldán, Jose Luis García-Pérez, Duncan Sproul, Jan Rehwinkel, Jonny Hertzog, Anne Boland-Auge, Robert Olaso, Jean François Deleuze, Julien Baruteau, Karine Brochard, Jonathan Buckley, Vanessa Cavallera, Cristina Cereda, Liesbeth M H De Waele, Angus Dobbie, Diane Doummar, Frances Elmslie, Margarete Koch-Hogrebe, Ram Kumar, Kate Lamb, John H Livingston, Anirban Majumdar, Charles Marques Lorenço, Simona Orcesi, Sylviane Peudenier, Kevin Rostasy, Caroline A Salmon, Christiaan Scott, Davide Tonduti, Guy Touati, Marialuisa Valente, Hélio van der Linden, Hilde Van Esch, Marie Vermelle, Kate Webb, Andrew P Jackson, Martin A M Reijns, Nick Gilbert, Yanick J Crow
cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing. Nature genetics 52 (12) (2020)
Yanni Zeng, Carmen Amador, Charley Xia, Riccardo Marioni, Duncan Sproul, Rosie M Walker, Stewart W Morris, Andrew Bretherick, Oriol Canela-Xandri, Thibaud S Boutin, David W Clark, Archie I Campbell, Konrad Rawlik, Caroline Hayward, Reka Nagy, Albert Tenesa, David J Porteous, James F Wilson, Ian J Deary, Kathryn L Evans, Andrew M McIntosh, Pau Navarro, Christopher S Haley
Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation. Nature communications 10 (1) (2019)
Yanni Zeng, Carmen Amador, Charley Xia, Riccardo Marioni, Duncan Sproul, Rosie M Walker, Stewart W Morris, Andrew Bretherick, Oriol Canela-Xandri, Thibaud S Boutin, David W Clark, Archie I Campbell, Konrad Rawlik, Caroline Hayward, Reka Nagy, Albert Tenesa, David J Porteous, James F Wilson, Ian J Deary, Kathryn L Evans, Andrew M McIntosh, Pau Navarro, Christopher S Haley
Parent of origin genetic effects on methylation in humans are common and influence complex trait variation. Nature communications 10 (1) (2019)
Patricia Heyn, Clare V Logan, Adeline Fluteau, Rachel C Challis, Tatsiana Auchynnikava, Carol-Anne Martin, Joseph A Marsh, Francesca Taglini, Fiona Kilanowski, David A Parry, Valerie Cormier-Daire, Chin-To Fong, Kate Gibson, Vivian Hwa, Lourdes Ibáñez, Stephen P Robertson, Giorgia Sebastiani, Juri Rappsilber, Robin C Allshire, Martin A M Reijns, Andrew Dauber, Duncan Sproul, Andrew P Jackson
Gain-of-function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions. Nature genetics 51 (1) (2018)