Paul J Hop

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 10

Top Topics

Dna Methylation

Amyotrophic Lateral Sclerosis

Quality Control

Top Venues

Nature genetics

NAR genomics and bioinformatics

Science translational medicine

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

Publications

Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Maarten Kooyman, null Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I Soto-Beasley, null null, Zbigniew K Wszolek, Ryan J Uitti, Ioannis Ugo Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A Ross, Jan Herman Veldink, Tatiana M Foroud, Kevin P Kenna, John E Landers
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease. Nature genetics 56 (7) (2024)
Paul J Hop, Ramona A J Zwamborn, Eilis J Hannon, Gemma L Shireby, Marta F Nabais, Emma M Walker, Wouter Van Rheenen, Joke J F A van Vugt, Annelot M Dekker, Henk-Jan Westeneng, Gijs H P Tazelaar, Kristel R van Eijk, Matthieu Moisse, Denis Baird, Ahmad Al Khleifat, Alfredo Iacoangeli, Nicola Ticozzi, Antonia Ratti, Johnathan Cooper-Knock, Karen E Morrison, Dame Pamela J Shaw, Ayse Nazli Basak, Adriano Chio, Andrea Calvo, Cristina Moglia, Antonio Canosa, Maura Brunetti, Maurizio Grassano, Marc Gotkine, Yossef Lerner, Michal Zabari, Patrick Vourc'h, Philippe Corcia, Philippe Couratier, Jesus S Mora, Teresa Salas, Patrick Dion, Jay P Ross, Robert David Henderson, Susan Mathers, Pamela A McCombe, Merrilee Needham, Garth Nicholson, Dominic B Rowe, Roger Pamphlett, Karen A Mather, Perminder Singh Sachdev, Sarah Furlong, Fleur C Garton, Anjali K Henders, Tian Lin, Shyuan T Ngo, Frederik J Steyn, Leanne Wallace, Kelly Louise Williams, null null, null null, Miguel Mitne Neto, Ruben J Cauchi, Ian P Blair, Matthew C Kiernan, Vivian Drory, Monica Povedano, Mamede de Carvalho, Susana Pinto, Markus Weber, Guy A Rouleau, Vincenzo Silani, John E Landers, Christopher E Shaw, Peter Munch Andersen, Allan F McRae, Michael A van Es, R Jeroen Pasterkamp, Naomi R Wray, Russell Lewis McLaughlin, Orla Hardiman, Kevin P Kenna, Ellen A Tsai, Heiko Runz, Ammar Al Chalabi, Leonard H van den Berg, Philip Van Damme, Jonathan S Mill, Jan Herman Veldink
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS. Science translational medicine 14 (633) (2022)
Paul J Hop, René Luijk, Lucia Daxinger, Maarten van Iterson, Koen F Dekkers, Rick Jansen, null null, Joyce B J van Meurs, Peter A C 't Hoen, M Arfan Ikram, Marleen M J van Greevenbroek, Dorret I Boomsma, P Eline Slagboom, Jan H Veldink, Erik W van Zwet, Bastiaan T Heijmans
Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference. Genome biology 21 (1) (2020)
Paul J Hop, Ramona A J Zwamborn, Eilis J Hannon, Annelot M Dekker, Kristel R van Eijk, Emma M Walker, Alfredo Iacoangeli, Ashley R Jones, Aleksey Shatunov, Ahmad Al Khleifat, Sarah Opie-Martin, Christopher E Shaw, Karen E Morrison, Pamela J Shaw, Russell Lewis McLaughlin, Orla Hardiman, Ammar Al-Chalabi, Leonard H Van Den Berg, Jonathan Mill, Jan H Veldink
Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies. NAR genomics and bioinformatics 2 (4) (2020)