Jan H. Veldink
Active 1998–2026
- 221
- Papers
- 36,442
- Citations
- 103
- h-index
- 207
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1%
- Broad Institute0.7%
- King's College London0.6%
- University College London0.6%
- Massachusetts General Hospital0.6%
- Inserm0.6%
- Other95.9%
Fields
- Medicine49.9%
- Biochemistry, Genetics and Molecular Biology37.2%
- Neuroscience7%
- Immunology and Microbiology2.5%
- Psychology0.7%
- Environmental Science0.6%
- Other2.1%
Topics
- Amyotrophic Lateral Sclerosis Research9.6%
- Genetic Associations and Epidemiology6.9%
- Neurogenetic and Muscular Disorders Research4.8%
- Epigenetics and DNA Methylation3.3%
- Parkinson's Disease Mechanisms and Treatments2.5%
- Genetic Neurodegenerative Diseases2.4%
- Other70.5%
Coauthors
- Leonard H. van den Berg132
- Michael A. van Es50
- Wouter van Rheenen39
- Philip Van Damme28
- Henk‐Jan Westeneng27
- Ammar Al‐Chalabi26
- Adriano Chiò25
- Lude Franke25
- Orla Hardiman25
- Pamela J. Shaw20
- Patrick Deelen20
- Alfredo Iacoangeli19
- John H. J. Wokke19
- Marianne de Visser19
- Aleksey Shatunov18
- Christopher E. Shaw17
- Helenius J. Schelhaas17
- Joke J.F.A. van Vugt17
- Kristel R. van Eijk17
- Rick Jansen17
- Ahmad Al Khleifat16
- Anneke J. van der Kooi16
- Cisca Wijmenga16
- Dorret I. Boomsma16
All papers
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Authors: Urmo Võsa, Annique Claringbould, Harm-Jan Westra, Marc Jan Bonder, Patrick Deelen, Biao Zeng, Holger Kirsten, Ashis Saha, Roman Kreuzhuber, Seyhan Yazar, Harm Brugge, Roy Oelen, Dylan H. de Vries, Monique G.P. van der Wijst, Silva Kasela, Natalia Pervjakova, Isabel Alves, Marie-Julie Favé, Mawussé Agbessi, Mark Christiansen, Rick Jansen, Ilkka Seppälä, Tong Lin, Alexander Teumer, Katharina Schramm, Gibran Hemani, Joost Verlouw, Hanieh Yaghootkar, Reyhan Sönmez Flitman, Andrew Brown, Viktorija Kukushkina, Anette Kalnapenkis, Sina Rüeger, Eleonora Porcu, Jaanika Kronberg, Johannes Kettunen, Bernett Lee, Futao Zhang, Ting Qi, José Alquicira-Hernández, Wibowo Arindrarto, Frank Beutner, Peter A.C. ’t Hoen, Joyce B. J. van Meurs, Jenny van Dongen, Maarten van Iterson, Morris A. Swertz, Marc Jan Bonder, Julia Dmitrieva, Mahmoud Elansary, Benjamin P. Fairfax, Michel Georges, Bastiaan T. Heijmans, Alex W. Hewitt, Mika Kähönen, Yungil Kim, Julian C. Knight, Péter Kovács, Knut Krohn, Shuang� Li, Markus Loeffler, Urko M. Marigorta, Hailang Mei, Yukihide Momozawa, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Jonathan K. Pritchard, Olli T. Raitakari, Olaf Rötzschke, P. Eline Slagboom, Coen D.A. Stehouwer, Michael Stümvoll, Patrick Sullivan, Peter A.C. ’t Hoen, Joachim Thiery, Anke Tönjes, Jenny van Dongen, Maarten van Iterson, Jan H. Veldink, Uwe Völker, Robert Warmerdam, Cisca Wijmenga, Morris A. Swertz, Anand Kumar Andiappan, Grant W. Montgomery, Samuli Ripatti, Markus Perola, Zoltán Kutalik, Emmanouil T. Dermitzakis, Sven Bergmann, Timothy M. Frayling, Joyce B. J. van Meurs, Holger Prokisch, Habibul Ahsan, Brandon L. Pierce, Terho Lehtimäki, Dorret I. Boomsma, Bruce M. Psaty and 14 more - Nature Genetics 2021 cited by 2,182
- A reference panel of 64,976 haplotypes for genotype imputation
Authors: Richard Durbin, Klaudia Walter, Yang Luo, Shane McCarthy, Nicole Soranzo, Jeffrey C. Barrett, Eleftheria Zeggini, Arthur Gilly, Carl A. Anderson, Sayantan Das, Sayantan Das, Christian Fuchsberger, Hyun Min Kang, Sai Chen, Sai Chen, Michael Boehnke, Gonçalo Abecasis, Warren Kretzschmar, Sayantan Das, Mark I McCarthy, Hyun Min Kang, Sai Chen, Andrew R Wood, Michael Boehnke, Timothy Frayling, Anubha Mahajan, Warren W. Kretzschmar, Petr Danecek, Kevin Sharp, Olivier Delaneau, Andrew R. Wood, Marcus A. Tuke, Timothy M. Frayling, Alexander Teumer, Matthias Nauck, Alexander Teumer, Petr Danecek, Kevin Sharp, Veikko Salomaa, Andrea Angius, Fabio Busonero, Francesco Cucca, Carlo Sidore, Josine L. Min, Nicholas J. Timpson, George Davey Smith, Laura J. Corbin, Seppo Koskinen, Veikko Salomaa, Scott Vrieze, Scott Vrieze, Cristen J. Willer, He Zhang, Jan H. Veldink, Wouter van Rheenen, Leonard H. van den Berg, Annelot M. Dekker, Tabitha A. Harrison, Charles Kooperberg, Ulrike Peters, Ulrike Peters, Michele T. Pato, Carlos N. Pato, Cornelia M. van Duijn, Matthew G. Sampson, Christopher E. Gillies, Nicola Pirastu, Ilaria Gandin, Massimiliano Cocca, Paolo Gasparini, Massimo Mezzavilla, Massimo Mezzavilla, Paolo Gasparini, Daniela Toniolo, Michela Traglia, Cinzia Sala, Dorrett Boomsma, Kari Branham, Gerome Breen, Gerome Breen, Chad M. Brummett, Ross M. Fraser, James F. Wilson, Harry Campbell, Andrew T. Chan, Andrew T. Chan, Cristen J. Willer, Matthias Kretzler, Sai Chen, Cristen J. Willer, Matthias Kretzler, Sai Chen, Emily Y. Chew, Francis S. Collins, George Dedoussis, Aliki‐Eleni Farmaki, Marcus Dörr, Matthias Nauck, Uwe Völker, Marcus Dörr and 11 more - Nature Genetics 2016 cited by 3,273
- Amyotrophic lateral sclerosis
Authors: Michael A. van Es, Orla Hardiman, Adriano Chiò, Ammar Al‐Chalabi, R. Jeroen Pasterkamp, Jan H. Veldink, Leonard H. van den Berg - The Lancet 2017 cited by 1,264
- Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases
Authors: Niek de Klein, Ellen Tsai, Martijn Vochteloo, Denis Baird, Yunfeng Huang, Chia‐Yen Chen, Sipko van Dam, Roy Oelen, Patrick Deelen, Olivier B. Bakker, Omar El Garwany, Zhengyu Ouyang, Eric Marshall, Maria I. Zavodszky, Wouter van Rheenen, Mark K. Bakker, Jan H. Veldink, Tom R. Gaunt, Heiko Runz, Lude Franke, Harm-Jan Westra - Nature Genetics 2023 cited by 254
- Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Authors: Elizabeth T. Cirulli, Brittany N. Lasseigne, Slavé Petrovski, Peter C. Sapp, Patrick A. Dion, Claire S. Leblond, Julien Couthouis, Yifan Lu, Quanli Wang, Brian J. Krueger, Zhong Ren, Jonathan Keebler, Yujun Han, Shawn Levy, Braden Boone, Jack R. Wimbish, Lindsay L. Waite, Angela L. Jones, John P. Carulli, Kelly L. Williams, John F. Staropoli, Winnie Xin, Alessandra Chesi, Alya R. Raphael, Diane McKenna‐Yasek, Janet Cady, J.M.B.V. de Jong, Kevin P. Kenna, Bradley Smith, Simon Topp, Jack W. Miller, Soragia Athina Gkazi, Ammar Al‐Chalabi, Leonard H. van den Berg, Jan H. Veldink, Vincenzo Silani, Nicola Ticozzi, Christopher E. Shaw, Robert H. Baloh, Stanley H. Appel, Ericka Simpson, Clotilde Lagier‐Tourenne, Stefan M. Pulst, Summer Gibson, John Q. Trojanowski, Lauren Elman, Leo McCluskey, Murray Grossman, Neil A. Shneider, Wendy K. Chung, John Ravits, Jonathan D. Glass, Katherine B. Sims, Vivianna M. Van Deerlin, Tom Maniatis, Sebastian Hayes, Alban Ordureau, Sharan Swarup, John E. Landers, Frank Baas, Andrew S. Allen, Richard Bedlack, J. Wade Harper, Aaron D. Gitler, Guy A. Rouleau, Robert H. Brown, Matthew B. Harms, Gregory M. Cooper, Tim Harris, R Myers, David B. Goldstein - Science 2015 cited by 992
- Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
Authors: Henk-Jan Westeneng, Thomas P. A. Debray, Anne E Visser, Ruben P. A. van Eijk, James Rooney, Andrea Calvo, Sarah Martin, Christopher McDermott, Alexander G. Thompson, Susana Pinto, Xenia Kobeleva, Angela Rosenbohm, Beatrice Stubendorff, Helma Sommer, Bas Middelkoop, Annelot M. Dekker, Joke J.F.A. van Vugt, Wouter van Rheenen, Alice Vajda, Mark Heverin, Mbombe Kazoka, Hannah Hollinger, Marta Gromicho, Sonja Körner, Thomas Ringer, Annekathrin Rödiger, A. Gunkel, Christopher E. Shaw, Annelien L. Bredenoord, Michael A. van Es, Philippe Corcia, Philippe Couratier, Markus Weber, Julian Großkreutz, Albert C. Ludolph, Susanne Petri, Mamede de Carvalho, Philip Van Damme, Kevin Talbot, Martin R. Turner, Pamela J. Shaw, Ammar Al‐Chalabi, Adriano Chiò, Orla Hardiman, Karel G.M. Moons, Jan H. Veldink, Leonard H. van den Berg - The Lancet Neurology 2018 cited by 517
- Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Authors: Rafik Tadros, Catherine Francis, Xiao Yun Xu, Alexa M.C. Vermeer, Andrew R. Harper, Roy Huurman, Ken Kelu Bisabu, Roddy Walsh, Edgar T. Hoorntje, Wouter P. te Rijdt, Rachel Buchan, Hannah G. van Velzen, Marjon A. van Slegtenhorst, Jentien M. Vermeulen, Joost A. Offerhaus, Wenjia Bai, Antonio de Marvao, Najim Lahrouchi, Leander Beekman, Jacco C. Karper, Jan H. 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, J. Peter van 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 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 Watkins, Paul M. Matthews, James S. Ware, Connie R. Bezzina - Nature Genetics 2021 cited by 292
- Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Authors: HUNT All-In Stroke, Mark K. Bakker, China Kadoorie Biobank Collaborative Group, The ICAN Study Group, CADISP Group, Genetics and Observational Subarachnoid Haemorrhage (GOSH) Study investigators, Rick A. A. van der Spek, Wouter van Rheenen, Sandrine Morel, Romain Bourcier, Isabel C. Hostettler, Varinder S. Alg, Kristel R. van Eijk, Masaru Koido, Masato Akiyama, Chikashi Terao, Koichi Matsuda, Robin Walters, Kuang Lin, Liming Li, Iona Y. Millwood, Zhengming Chen, Guy A. Rouleau, Sirui Zhou, Kristiina Rannikmäe, Cathie Sudlow, Henry Houlden, Leonard H. van den Berg, Christian Dina, Olivier Naggara, Jean‐Christophe Gentric, Eimad Shotar, François Eugène, Hubert Desal, Bendik S. Winsvold, Sigrid Børte, Marianne Bakke Johnsen, Ben Brumpton, Marie Søfteland Sandvei, Cristen J. Willer, Kristian Hveem, John‐Anker Zwart, W. M. Monique Verschuren, Christoph M. Friedrich, Sven Hirsch, Sabine Schilling, Jérôme Dauvillier, O. Martin, Gregory T. Jones, Matthew J. Bown, Nerissa Ko, Helen Kim, Jonathan R. I. Coleman, Gerome Breen, Jonathan G. Zaroff, Catharina J.M. Klijn, Rainer Malik, Martin Dichgans, Muralidharan Sargurupremraj, Turgut Tatlisumak, Philippe Amouyel, Stéphanie Debette, Gabriël J.E. Rinkel, Bradford B. Worrall, Joanna Pera, Agnieszka Słowik, Emília Gaál‐Paavola, Mika Niemelä, Juha E. Jääskeläinen, Mikael von und zu Fraunberg, Antti Lindgren, Joseph Broderick, David J. Werring, Daniel Woo, Richard Redon, Philippe Bijlenga, Yoichiro Kamatani, Jan H. Veldink, Ynte M. Ruigrok - Nature Genetics 2020 cited by 346
- Multiple common variants for celiac disease influencing immune gene expression
Authors: P Dubois, Gosia Trynka, Lude Franke, Karen A. Hunt, Jihane Romanos, Alessandra Curtotti, Alexandra Zhernakova, Graham Heap, Róza Ádány, Arpo Aromaa, Maria Teresa Bardella, Leonard H. van den Berg, Nicholas Bockett, Emilio G. de la Concha, Bárbara Dema, Rudolf S.N. Fehrmann, Miguel Fernández‐Arquero, Szilvia Fiatal, Elvira Grandone, Peter M. Green, Harry J.M. Groen, Rhian Gwilliam, Roderick H.J. Houwen, Sarah Hunt, Katri Kaukinen, Dermot Kelleher, Ilma R. Korponay‐Szabó, Kalle Kurppa, Padraic MacMathúna, Markku Mäki, Maria Cristina Mazzilli, Owen T McCann, M. Luisa Mearin, Charles A. Mein, Muddassar M. Mirza, Vanisha Mistry, Barbara Mora, Katherine I. Morley, Chris J. Mulder, Joseph A. Murray, Concepción Núñez, Elvira Oosterom, Roel A. Ophoff, Isabel Polanco, Leena Peltonen, Mathieu Platteel, Anna Rybak, Veikko Salomaa, Joachim J. Schweizer, Maria Pia Sperandeo, Greetje J. Tack, Graham Turner, Jan H. Veldink, Wieke H.M. Verbeek, Rinse K. Weersma, Victorien M. Wolters, Elena Urcelay, Božena Cukrowská, Luigi Greco, Susan L. Neuhausen, Ross McManus, Donatella Barisani, Panos Deloukas, Jeffrey C. Barrett, Päivi Saavalainen, Cisca Wijmenga, David A. van Heel - Nature Genetics 2010 cited by 1,052
- Detection of long repeat expansions from PCR-free whole-genome sequence data
Authors: Egor Dolzhenko, Joke J.F.A. van Vugt, Richard J. Shaw, Mitchell A. Bekritsky, Marka van Blitterswijk, Giuseppe Narzisi, Subramanian S. Ajay, Vani Rajan, Bryan R. Lajoie, Nathan Johnson, Zoya Kingsbury, Sean Humphray, Raymond D. Schellevis, William J. Brands, Matt Baker, Rosa Rademakers, Maarten Kooyman, Gijs H.P. Tazelaar, Michael A. van Es, Russell L. McLaughlin, William Sproviero, Aleksey Shatunov, Ashley Jones, Ahmad Al Khleifat, Alan Pittman, Sarah Morgan, Orla Hardiman, Ammar Al‐Chalabi, Christopher E. Shaw, Bradley Smith, Edmund Jin Rui Neo, Karen Morrison, Pamela J. Shaw, Catherine Reeves, Lara Winterkorn, Nancy S. Wexler, David E. Housman, Christopher Ng, Alina Li, Ryan J. Taft, Leonard H. van den Berg, David Bentley, Jan H. Veldink, Michael A. Eberle - Genome Research 2017 cited by 437
- Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
Authors: Eleonora Porcu, Sina Rüeger, Kaido Lepik, Mawussé Agbessi, Habibul Ahsan, Isabel Alves, Anand Kumar Andiappan, Wibowo Arindrarto, Philip Awadalla, Alexis Battle, Frank Beutner, Marc Jan Bonder, Dorret I. Boomsma, Mark Christiansen, Annique Claringbould, Patrick Deelen, Tõnu Esko, Marie-Julie Favé, Lude Franke, Timothy M. Frayling, Sina A. Gharib, Gregory Gibson, Bastiaan T. Heijmans, Gibran Hemani, Rick Jansen, Mika Kähönen, Anette Kalnapenkis, Silva Kasela, Johannes Kettunen, Yungil Kim, Holger Kirsten, Péter Kovács, Knut Krohn, Jaanika Kronberg-Guzman, Viktorija Kukushkina, Bernett Lee, Terho Lehtimäki, Markus Loeffler, Urko M. Marigorta, Hailang Mei, Lili Milani, Grant W. Montgomery, Martina Müller‐Nurasyid, Matthias Nauck, Michel G. Nivard, Brenda W.J.H. Penninx, Markus Perola, Natalia Pervjakova, Brandon L. Pierce, Joseph E. Powell, Holger Prokisch, Bruce M. Psaty, Olli T. Raitakari, Samuli Ripatti, Olaf Rötzschke, Ashis Saha, Markus Scholz, Katharina Schramm, Ilkka Seppälä, P. Eline Slagboom, Coen D.A. Stehouwer, Michael Stümvoll, Patrick Sullivan, Peter A.C. ’t Hoen, Alexander Teumer, Joachim Thiery, Tong Lin, Anke Tönjes, Jenny van Dongen, Maarten van Iterson, Joyce B. J. van Meurs, Jan H. Veldink, Joost Verlouw, Peter M. Visscher, Uwe Völker, Urmo Võsa, Harm-Jan Westra, Cisca Wijmenga, Hanieh Yaghootkar, Jian Yang, Biao Zeng, Futao Zhang, Wibowo Arindrarto, Marian Beekman, Dorret I. Boomsma, Jan Bot, Joris Deelen, Patrick Deelen, Lude Franke, Bastiaan T. Heijmans, Peter A.C. ’t Hoen, Bert A. Hofman, Jouke J. Hottenga, Aaron Isaacs, Marc Jan Bonder, P. Mila Jhamai, Rick Jansen, Szymon M. Kiełbasa, Nico Lakenberg, René Luijk and 35 more - Nature Communications 2019 cited by 347
- Identification of context-dependent expression quantitative trait loci in whole blood
Authors: Daria V. Zhernakova, Patrick Deelen, Martijn Vermaat, Maarten van Iterson, Michiel van Galen, Wibowo Arindrarto, Peter van ‘t Hof, Hailiang Mei, Freerk van Dijk, Harm-Jan Westra, Marc Jan Bonder, Jeroen van Rooij, Marijn Verkerk, P. Mila Jhamai, Matthijs Moed, Szymon M. Kiełbasa, Jan Bot, Irene Nooren, René Pool, Jenny van Dongen, Jouke Hottenga, Coen D.A. Stehouwer, Carla Kallen, Casper G. Schalkwijk, Alexandra Zhernakova, Yang Li, Ettje F. Tigchelaar, Niek de Klein, Marian Beekman, Joris Deelen, Diana van Heemst, Leonard H. van den Berg, Albert Hofman, André G. Uitterlinden, Marleen M. J. van Greevenbroek, Jan H. Veldink, Dorret I. Boomsma, Cornelia M. van Duijn, Cisca Wijmenga, P. Eline Slagboom, Morris A. Swertz, Aaron Isaacs, Joyce B. J. van Meurs, Rick Jansen, Bastiaan T. Heijmans, Peter A.C. ’t Hoen, Lude Franke - Nature Genetics 2016 cited by 516
- Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
Authors: Julien Barc, Rafik Tadros, Charlotte Glinge, David Y. Chiang, Mariam Jouni, Floriane Simonet, Sean J. Jurgens, Manon Baudic, Michele Nicastro, F Potet, Joost A. Offerhaus, Roddy Walsh, Seung Hoan Choi, Arie O. Verkerk, Yuka Mizusawa, Soraya Anys, Damien Minois, Marine Arnaud, Josselin Duchâteau, Yanushi D. Wijeyeratne, Alison Muir, Michael Papadakis, Silvia Castelletti, Margherita Torchio, Cristina Gil, Javier Lacunza, Daniela Giachino, Natascia Cerrato, Raphaël P. Martins, Óscar Campuzano, Sonia Van Dooren, Aurélie Thollet, Florence Kyndt, Andrea Mazzanti, Nicolas Clémenty, Arnaud Bisson, Anniek Corveleyn, Birgit Stallmeyer, Sven Dittmann, Johan Saenen, Antoine Noël, Shohreh Honarbakhsh, Boris Rudic, Halim Marzak, Matthew Rowe, Claire Federspiel, Sophie Le Page, Leslie Placide, Antoine Milhem, Héctor Barajas-Martínez, Britt Maria Beckmann, Ingrid P.C. Krapels, Johannes Steinfurt, Bo Gregers Winkel, Reza Jabbari, M. Benjamin Shoemaker, Bas J. Boukens, Doris Škorić‐Milosavljević, Hennie Bikker, Federico Manevy, Peter Lichtner, Marta Ribasés, Thomas Meitinger, Martina Müller‐Nurasyid, KORA-Study Group, Konstantin Strauch, Annette Peters, Holger Schulz, Lars Schwettmann, Reiner Leidl, Margit Heier, Jan H. Veldink, Leonard H. van den Berg, Philip Van Damme, Daniele Cusi, Chiara Lanzani, Sidwell Rigade, Éric Charpentier, Estelle Baron, Stéphanie Bonnaud, Simon Lecointe, Audrey Donnart, Hervé Le Marec, Stéphanie Chatel, Matilde Karakachoff, Stéphane Bezieau, Barry London, Jacob Tfelt‐Hansen, Dan M. Roden, Katja E. Odening, Marina Cerrone, Larry A. Chinitz, Paul G.A. Volders, Maarten P. van den Berg, Gabriel Laurent, Laurence Faivre, Charles Antzelevitch, Stefan Kääb, Alain Al Arnaout, Jean‐Marc Dupuis and 57 more - Nature Genetics 2022 cited by 142
- Systematic identification of trans eQTLs as putative drivers of known disease associations
Authors: Harm-Jan Westra, Marjolein J. Peters, Tōnu Esko, Hanieh Yaghootkar, Claudia Schurmann, Johannes Kettunen, Mark Christiansen, Benjamin P. Fairfax, Katharina Schramm, Joseph E. Powell, Alexandra Zhernakova, Daria V. Zhernakova, Jan H. Veldink, Leonard H. van den Berg, Juha Karjalainen, Sebo Withoff, André G. Uitterlinden, Albert Hofman, Fernando Rivadeneira, Peter A.C. ’t Hoen, Eva Reinmaa, Krista Fischer, Mari Nelis, Lili Milani, David Melzer, Luigi Ferrucci, Andrew Singleton, Dena Hernández, Michael A. Nalls, Georg Homuth, Matthias Nauck, Dörte Radke, Uwe Völker, Markus Perola, Veikko Salomaa, Jennifer A. Brody, Astrid M. Suchy‐Dicey, Sina A. Gharib, Daniel A. Enquobahrie, Thomas Lumley, Grant W. Montgomery, Seiko Makino, Holger Prokisch, Christian Herder, Michael Roden, Harald Grallert, Thomas Meitinger, Konstantin Strauch, Yang Li, Ritsert C. Jansen, Peter M. Visscher, Julian C. Knight, Bruce M. Psaty, Samuli Ripatti, Alexander Teumer, Timothy M. Frayling, Andres Metspalu, Joyce B. J. van Meurs, Lude Franke - Nature Genetics 2013 cited by 1,769
- Disease variants alter transcription factor levels and methylation of their binding sites
Authors: Marc Jan Bonder, René Luijk, Daria V. Zhernakova, Matthijs Moed, Patrick Deelen, Martijn Vermaat, Maarten van Iterson, Freerk van Dijk, Michiel van Galen, Jan Bot, Roderick C. Slieker, P. Mila Jhamai, Michaël Verbiest, H. Eka D. Suchiman, Marijn Verkerk, Ruud van der Breggen, Jeroen van Rooij, Nico Lakenberg, Wibowo Arindrarto, Szymon M. Kiełbasa, Iris H. Jonkers, Peter van ‘t Hof, Irene Nooren, Marian Beekman, Joris Deelen, Diana van Heemst, Alexandra Zhernakova, Ettje F. Tigchelaar, Morris A. Swertz, Albert Hofman, André G. Uitterlinden, René Pool, Jenny van Dongen, Jouke‐Jan Hottenga, Coen D.A. Stehouwer, Carla Kallen, Casper G. Schalkwijk, Leonard H. van den Berg, Erik W. van Zwet, Hailiang Mei, Yang Li, Mathieu Lemire, Thomas J. Hudson, P. Eline Slagboom, Cisca Wijmenga, Jan H. Veldink, Marleen M. J. van Greevenbroek, Cornelia M. van Duijn, Dorret I. Boomsma, Aaron Isaacs, Rick Jansen, Joyce B. J. van Meurs, Peter A.C. ’t Hoen, Lude Franke, Bastiaan T. Heijmans - Nature Genetics 2016 cited by 564
- Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study
Authors: Ammar Al‐Chalabi, Andrea Calvo, Adriano Chiò, Shuna Colville, Cathy Ellis, Orla Hardiman, Mark Heverin, Robin Howard, Mark Huisman, Noa Keren, P. Nigel Leigh, Letizia Mazzini, Gabriele Mora, Richard W. Orrell, James Rooney, Kirsten M. Scott, William J. Scotton, Meinie Seelen, Christopher E. Shaw, Katie Sidle, Robert Swingler, Miho Tsuda, Jan H. Veldink, Anne E Visser, Leonard H. van den Berg, Neil Pearce - The Lancet Neurology 2014 cited by 425
- Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS
Authors: Paul J. Hop, Ramona A.J. Zwamborn, Eilís Hannon, Gemma Shireby, Marta F. Nabais, Emma 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 Morrison, Pamela J. Shaw, A. Nazlı Başak, Adriano Chiò, Andrea Calvo, Cristina Moglia, Antonio Canosa, Maura Brunetti, Maurizio Grassano, Marc Gotkine, Yossef Lerner, Michal Zabari, Patrick Vourc’h, Philippe Corcia, P. Couratier, Jesús S. Mora Pardina, Teresa Salas, Patrick A. Dion, Jay P. Ross, Robert D. Henderson, Susan Mathers, Pamela A. McCombe, Merrilee Needham, Garth Nicholson, Dominic B. Rowe, Roger Pamphlett, Karen A. Mather, Perminder S. Sachdev, Sarah Furlong, Fleur C. Garton, Anjali K. Henders, Tian Lin, Shyuan T. Ngo, Frederik J. Steyn, Leanne Wallace, Kelly L. Williams, Miguel Mitne Neto, Ruben J. Cauchi, Ian P. Blair, Matthew C. Kiernan, Vivian Drory, Mónica Povedano, Mamede de Carvalho, Susana Pinto, Markus Weber, Guy A. Rouleau, Vincenzo Silani, John E. Landers, Christopher E. Shaw, Peter M. Andersen, Allan F. McRae, Michael A. van Es, R. Jeroen Pasterkamp, Naomi R. Wray, Russell L. McLaughlin, Orla Hardiman, Kevin P. Kenna, Ellen Tsai, Heiko Runz, Ammar Al‐Chalabi, Leonard H. van den Berg, Philip Van Damme, Jonathan Mill, Jan H. Veldink, Bastiaan T. Heijmans, Peter A.C. t Hoen, Joyce van Meurs, Rick Jansen, Lude Franke, Dorret I. Boomsma, René Pool, Jenny van Dongen, Joukje J. Hottenga, Marleen M. J. van Greevenbroek, Coen D.A. Stehouwer, Carla Kallen, Casper G. Schalkwijk, Cisca Wijmenga, Lude Franke, Sasha Zhernakova, Ettje F. Tigchelaar and 54 more - Science Translational Medicine 2022 cited by 93
- Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
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