Jan H. Veldink

Active 1998–2026

221
Papers
36,442
Citations
103
h-index
207
i10-index

Citations

Citations per year for Jan H. Veldink1951: 3 citations1967: 1 citations1977: 1 citations1996: 2 citations1999: 1 citations2000: 2 citations2001: 2 citations2002: 7 citations2003: 12 citations2004: 16 citations2005: 18 citations2006: 30 citations2007: 36 citations2008: 34 citations2009: 93 citations2010: 88 citations2011: 187 citations2012: 253 citations2013: 314 citations2014: 350 citations2015: 381 citations2016: 476 citations2017: 585 citations2018: 550 citations2019: 1,414 citations2020: 1,737 citations2021: 1,744 citations2022: 1,546 citations2023: 1,193 citations2024: 1,745 citations2025: 799 citations2026: 41 citations1952–1966: no citations, so these years are not shown1968–1976: no citations, so these years are not shown1978–1995: no citations, so these years are not shown1997–1998: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,673 citing papers, 18.5% of this breakdownUnited Kingdom: 2,555 citing papers, 10.1% of this breakdownChina: 1,529 citing papers, 6.1% of this breakdownGermany: 1,504 citing papers, 6% of this breakdownNetherlands: 1,468 citing papers, 5.8% of this breakdownItaly: 1,172 citing papers, 4.6% of this breakdownAustralia: 1,130 citing papers, 4.5% of this breakdownCanada: 1,056 citing papers, 4.2% of this breakdownFrance: 849 citing papers, 3.4% of this breakdownSweden: 810 citing papers, 3.2% of this breakdownSpain: 694 citing papers, 2.7% of this breakdownSwitzerland: 505 citing papers, 2% of this breakdown
0%18.5%Other 28.9%

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

All papers

Open in search
  1. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  2. A reference panel of 64,976 haplotypes for genotype imputation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  3. Amyotrophic lateral sclerosis

    Authors: , , , , , , - The Lancet 2017 cited by 1,264

  4. Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases

    Authors: , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2023 cited by 254

  5. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  6. Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  7. Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  8. Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  9. Multiple common variants for celiac disease influencing immune gene expression

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  10. Detection of long repeat expansions from PCR-free whole-genome sequence data

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  11. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  12. Identification of context-dependent expression quantitative trait loci in whole blood

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  13. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  14. Systematic identification of trans eQTLs as putative drivers of known disease associations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  15. Disease variants alter transcription factor levels and methylation of their binding sites

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  16. Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - The Lancet Neurology 2014 cited by 425

  17. Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  18. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Philippe Couratier, Orla Hardiman, Russell McLaughin, Marc Gotkine, Vivian E. Drory, Nicola Ticozzi, Vincenzo Silani, Jan H. Veldink, Leonard H. van den Berg, Mamede de Carvalho, Jesús S. Mora Pardina, Mónica Povedano, Peter M. Andersen, Markus Weber, Nazlı Başak, Ammar Al‐Chalabi, Christopher E. Shaw, Pamela J. Shaw, Karen Morrison, John E. Landers, Jonathan D. Glass, Jan H. Veldink, Laura Ferraiuolo, Pamela J. Shaw, M Snyder - Neuron 2022 cited by 122

  19. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Frank Baas, Anneke J. van der Kooi, Marianne de Visser, Anneloor L.M.A. ten Asbroek, Peter C. Sapp, Diane McKenna‐Yasek, Meraida Polak, Seneshaw Asress, José Luís Muñoz-Blanco, Tim M. Strom, Thomas Meitinger, Karen Morrison, Giuseppe Lauria, Kelly L. Williams, P. Nigel Leigh, Garth A. Nicholson, Ian P. Blair, Claire S. Leblond, Patrick A. Dion, Guy A. Rouleau, Hardev Pall, Pamela J. Shaw, Martin R. Turner, Kevin Talbot, Franco Taroni, Khrista Boylan, Marka van Blitterswijk, Rosa Rademakers, Jesús Esteban‐Pérez, Alberto García‐Redondo, Phillip Van Damme, Wim Robberecht, Adriano Chiò, Cinzia Gellera, Carsten Drepper, Michael Sendtner, Antonia Ratti, Jonathan D. Glass, Jesús S. Mora, Nazlı Başak, Orla Hardiman, Albert C. Ludolph, Peter M. Andersen, Jochen H. Weishaupt, Robert H. Brown, Ammar Al‐Chalabi, Vincenzo Silani, Christopher E. Shaw, Leonard H. van den Berg, Jan H. Veldink, John E. Landers - Nature Genetics 2016 cited by 294

  20. The multistep hypothesis of ALS revisited

    Authors: , , , , , , , , , , , , , , , , , , , , - Neurology 2018 cited by 216

  21. Genetic and environmental influences interact with age and sex in shaping the human methylome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marijn Verkerk, Ruud van der Breggen, Jeroen van Rooij, Nico Lakenberg, Hailiang Mei, Jan Bot, Dasha V. Zhernakova, Peter van’t Hof, Patrick Deelen, Irene Nooren, Matthijs Moed, Martijn Vermaat, René Luijk, Marc Jan Bonder, Freerk van Dijk, Michiel van Galen, Wibowo Arindrarto, Szymon M. Kiełbasa, Morris A. Swertz, Erik W. van Zwet, Aaron Isaacs, Lude Franke, H. Eka D. Suchiman, Rick Jansen, Joyce B. J. van Meurs, Bastiaan T. Heijmans, P. Eline Slagboom, Dorret I. Boomsma - Nature Communications 2016 cited by 435

  22. Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ian P. Blair, Jonathan D. Glass, Orla Hardiman, Winston Hide, Pamela J. Shaw, Jesus S. Mora, Karen E. Morrison, Naomi R. Wray - European Journal of Human Genetics 2018 cited by 198

  23. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Shaun Purcell, Sven Cichon, Markus M. Nöthen, H‐Erich Wichmann, Stefan Schreiber, Sita H. Vermeulen, Lambertus A. Kiemeney, John H. J. Wokke, Simon Cronin, Russell L. McLaughlin, Orla Hardiman, Katsumi Fumoto, R. Jeroen Pasterkamp, Vincent Meininger, Judith Melki, P. Nigel Leigh, Christopher E. Shaw, John E. Landers, Ammar Al‐Chalabi, Robert H. Brown, Wim Robberecht, Peter M. Andersen, Roel A. Ophoff, Leonard H. van den Berg - Nature Genetics 2009 cited by 404

  24. Genetic variability in sporadic amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Leonard H. van den Berg, Ammar Al‐Chalabi, Jan H. Veldink, Philip Van Damme - Brain 2023 cited by 86