Jan Herman Veldink (Jan H Veldink, Jan Veldink)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 86

Top Venues

Nature genetics

Nature communications

Journal of neurology, neurosurgery, and psychiatry

Neurology

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)
Gizem Taş, Timo Westerdijk, Eric Postma, null null, Jan Herman Veldink, Alexander Schönhuth, Marleen Balvert
Computing linkage disequilibrium aware genome embeddings using autoencoders. Bioinformatics (Oxford, England) 40 (6) (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)
Gizem Taş, Timo Westerdijk, Eric Postma, null null, Jan Herman Veldink, Alexander Schönhuth, Marleen Balvert
Computing linkage disequilibrium aware genome embeddings using autoencoders. Bioinformatics (Oxford, England) 40 (6) (2024)
Annebelle Michielsen, Kevin van Veenhuijzen, Mark R Janse van Mantgem, Michael A van Es, Jan Herman Veldink, Ruben P A van Eijk, Leonard H van den Berg, Henk-Jan Westeneng
Association Between Hypothalamic Volume and Metabolism, Cognition, and Behavior in Patients With Amyotrophic Lateral Sclerosis. Neurology 103 (2) (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)
Annebelle Michielsen, Kevin van Veenhuijzen, Mark R Janse van Mantgem, Michael A van Es, Jan Herman Veldink, Ruben P A van Eijk, Leonard H van den Berg, Henk-Jan Westeneng
Association Between Hypothalamic Volume and Metabolism, Cognition, and Behavior in Patients With Amyotrophic Lateral Sclerosis. Neurology 103 (2) (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)
Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, Olubunmi Abel, Keith Mayl, Puja R Mehta, Aleksey Shatunov, Isabella Fogh, Harry Bowles, Naomi Limbachiya, Thomas P Spargo, Ahmad Al Khleifat, Kelly Louise Williams, Jennifer Jockel-Balsarotti, Taha Bali, Wade K Self, Lyndal Henden, Garth A Nicholson, Nicola Ticozzi, Diane McKenna-Yasek, Lu Tang, Dame Pamela J Shaw, Adriano Chio, Albert Ludolph, Jochen H Weishaupt, John E Landers, Jonathan D Glass, Jesus S Mora, Wim Robberecht, Philip Van Damme, Russell Lewis McLaughlin, Orla Hardiman, Leonard van den Berg, Jan Herman Veldink, Phillippe Corcia, Zorica Stevic, Nailah Siddique, Vincenzo Silani, Ian P Blair, Dong-Sheng Fan, Florence Esselin, Elisa de la Cruz, William Camu, Nazli A Basak, Teepu Siddique, Timothy Miller, Robert H Brown, Ammar Al Chalabi, Christopher E Shaw
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration. Nature communications 15 (1) (2024)
Renata Vieira de Sá, Emma Sudria-Lopez, Marta Cañizares Luna, Oliver Harschnitz, Dianne M A van den Heuvel, Sandra Kling, Danielle Vonk, Henk-Jan Westeneng, Henk Karst, Lauri Bloemenkamp, Suzy Varderidou-Minasian, Domino K Schlegel, Mayte Mars, Mark H Broekhoven, Nicky C H van Kronenburg, Youri Adolfs, Vamshidhar R Vangoor, Rianne de Jongh, Tijana Ljubikj, Lianne Peeters, Sabine Seeler, Enric Mocholi, Onur Basak, David Gordon, Fabrizio Giuliani, Tessa Verhoeff, Giel Korsten, Teresa Calafat Pla, Morten T Venø, Jørgen Kjems, Kevin Talbot, Michael A Van Es, Jan Herman Veldink, Leonard H van den Berg, Pavol Zelina, Ronald Jeroen Pasterkamp
ATAXIN-2 intermediate-length polyglutamine expansions elicit ALS-associated metabolic and immune phenotypes. Nature communications 15 (1) (2024)
Gizem Taş, Timo Westerdijk, Eric Postma, null null, Jan Herman Veldink, Alexander Schönhuth, Marleen Balvert
Computing linkage disequilibrium aware genome embeddings using autoencoders. Bioinformatics (Oxford, England) 40 (6) (2024)
Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, Olubunmi Abel, Keith Mayl, Puja R Mehta, Aleksey Shatunov, Isabella Fogh, Harry Bowles, Naomi Limbachiya, Thomas P Spargo, Ahmad Al Khleifat, Kelly Louise Williams, Jennifer Jockel-Balsarotti, Taha Bali, Wade K Self, Lyndal Henden, Garth A Nicholson, Nicola Ticozzi, Diane McKenna-Yasek, Lu Tang, Dame Pamela J Shaw, Adriano Chio, Albert Ludolph, Jochen H Weishaupt, John E Landers, Jonathan D Glass, Jesus S Mora, Wim Robberecht, Philip Van Damme, Russell Lewis McLaughlin, Orla Hardiman, Leonard van den Berg, Jan Herman Veldink, Phillippe Corcia, Zorica Stevic, Nailah Siddique, Vincenzo Silani, Ian P Blair, Dong-Sheng Fan, Florence Esselin, Elisa de la Cruz, William Camu, Nazli A Basak, Teepu Siddique, Timothy Miller, Robert H Brown, Ammar Al Chalabi, Christopher E Shaw
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration. Nature communications 15 (1) (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)
Salim Megat, Natalia Mora, Jason Sanogo, Olga Roman, Alberto Catanese, Najwa Ouali Alami, Axel Freischmidt, Xhuljana Mingaj, Hortense De Calbiac, François Muratet, Sylvie Dirrig-Grosch, Stéphane Dieterle, Nick Van Bakel, Kathrin Müller, Kirsten Sieverding, Jochen Weishaupt, Peter Munch Andersen, Markus Weber, Christoph Neuwirth, Markus Margelisch, Andreas Sommacal, Kristel R Van Eijk, Jan Herman Veldink, null null, Géraldine Lautrette, Philippe Couratier, Agnès Camuzat, Isabelle Le Ber, Maurizio Grassano, Adriano Chio, Tobias M Böckers, Albert C Ludolph, Francesco Roselli, Deniz Yilmazer-Hanke, Stéphanie Millecamps, Edor Kabashi, Erik Storkebaum, Chantal Sellier, Luc Dupuis
Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Nature communications 14 (1) (2023)
Iris F Van Wijk, Ruben P A van Eijk, Loes Van Boxmeer, Henk-Jan Westeneng, Michael A Van Es, Wouter Van Rheenen, Leonard H Van Den Berg, Marinus J C Eijkemans, Jan Herman Veldink
Assessment of risk of ALS conferred by the GGGGCC hexanucleotide repeat expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion. Amyotrophic lateral sclerosis & frontotemporal degeneration (2023)
Mark K Bakker, Jos P Kanning, Gad Abraham, Amy E Martinsen, Bendik Slagsvold Winsvold, John-Anker Zwart, Romain Bourcier, Tomonobu Sawada, Masaru Koido, Yoichiro Kamatani, Sandrine Morel, Phillippe Amouyel, Stephanie Debette, Philippe Bijlenga, Takiy-Eddine Berrandou, Santhi K Ganesh, Nabila Bouatia-Naji, Gregory T Jones, Matthew J Bown, Gabriel J E Rinkel, Jan Herman Veldink, Ynte M Ruigrok, null null
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity. Stroke (2023)
Niek de Klein, Ellen A 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 E Marshall, Maria I Zavodszky, Wouter Van Rheenen, Mark K Bakker, Jan Herman Veldink, Tom R Gaunt, Heiko Runz, Lude H Franke, Harm-Jan Westra
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases. Nature genetics 55 (3) (2023)
Mark K Bakker, Jos P Kanning, Gad Abraham, Amy E Martinsen, Bendik Slagsvold Winsvold, John-Anker Zwart, Romain Bourcier, Tomonobu Sawada, Masaru Koido, Yoichiro Kamatani, Sandrine Morel, Phillippe Amouyel, Stephanie Debette, Philippe Bijlenga, Takiy-Eddine Berrandou, Santhi K Ganesh, Nabila Bouatia-Naji, Gregory T Jones, Matthew J Bown, Gabriel J E Rinkel, Jan Herman Veldink, Ynte M Ruigrok, null null
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity. Stroke 54 (3) (2023)
Niek de Klein, Ellen A 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 E Marshall, Maria I Zavodszky, Wouter Van Rheenen, Mark K Bakker, Jan Herman Veldink, Tom R Gaunt, Heiko Runz, Lude H Franke, Harm-Jan Westra
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases. Nature genetics 55 (3) (2023)
Bharati Jadhav, Paras Garg, Joke J F A van Vugt, Kristina Ibanez Garikano, Delia Gagliardi, William Lee, Alejandro Martin-Trujillo, Scott L Gies, Mafalda Barbosa, Miten Jain, Henry Houlden, Benedict Paten, null null, null null, Jan Herman Veldink, Arianna Tucci, Andrew J Sharp
A GCC repeat expansion in AFF3 is a significant cause of intellectual disability. medRxiv : the preprint server for health sciences (2023)
Niek de Klein, Ellen A 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 E Marshall, Maria I Zavodszky, Wouter Van Rheenen, Mark K Bakker, Jan Herman Veldink, Tom R Gaunt, Heiko Runz, Lude H Franke, Harm-Jan Westra
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases. Nature genetics (2023)
Niek de Klein, Ellen A 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 E Marshall, Maria I Zavodszky, Wouter Van Rheenen, Mark K Bakker, Jan Herman Veldink, Tom R Gaunt, Heiko Runz, Lude H Franke, Harm-Jan Westra
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases. Nature genetics 55 (3) (2023)
Salim Megat, Natalia Mora, Jason Sanogo, Olga Roman, Alberto Catanese, Najwa Ouali Alami, Axel Freischmidt, Xhuljana Mingaj, Hortense De Calbiac, François Muratet, Sylvie Dirrig-Grosch, Stéphane Dieterle, Nick Van Bakel, Kathrin Müller, Kirsten Sieverding, Jochen Weishaupt, Peter Munch Andersen, Markus Weber, Christoph Neuwirth, Markus Margelisch, Andreas Sommacal, Kristel R Van Eijk, Jan Herman Veldink, null null, Géraldine Lautrette, Philippe Couratier, Agnès Camuzat, Isabelle Le Ber, Maurizio Grassano, Adriano Chio, Tobias M Böckers, Albert C Ludolph, Francesco Roselli, Deniz Yilmazer-Hanke, Stéphanie Millecamps, Edor Kabashi, Erik Storkebaum, Chantal Sellier, Luc Dupuis
Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Nature communications 14 (1) (2023)
Mandy L Ballinger, Swetansu Pattnaik, Piyushkumar A Mundra, Milita Zaheed, Emma M Rath, Peter Priestley, Jonathan Baber, Isabelle L Ray-Coquard, Nicholas Isambert, Sylvain Causeret, Winette T A van der Graaf, Ajay Puri, Florence Duffaud, Axel Le Cesne, Beatrice Seddon, Coonoor Chandrasekar, Joshua D Schiffman, Andrew S Brohl, Paul A James, Jean-Emmanuel Kurtz, Nicolas Penel, Ola Myklebost, Leonardo A Meza-Zepeda, Hilda Pickett, Maya Kansara, Nicola Waddell, Olga Kondrashova, John V Pearson, Andrew P Barbour, Sherly X Li, Tuong Linh Nguyen, Diane Fatkin, Robert M Graham, Eleni Giannoulatou, Melissa Jane Green, Warren Kaplan, Shyamsundar Ravishankar, Joseph Copty, Joseph E Powell, Edwin Cuppen, Kristel van Eijk, Jan Herman Veldink, Jin-Hee Ahn, Jeong Eun Kim, Robert Lor Randall, Katherine M Tucker, Ian R Judson, Rajiv Sarin, Thomas E Ludwig, French Exome Consortium, Jean François Deleuze, null null, Michelle Haber, Glenn M Marshall, Murray J Cairns, Jean Yves Blay, null null, David M Thomas, Martin Tattersall, Susan Neuhaus, Craig Lewis, Kathy Tucker, Richard Carey-Smith, David Wood, Sandro Porceddu, Ian Dickinson, Heather Thorne, Paul James, Isabelle Ray-Coquard, Jean-Yves Blay, Philippe Cassier, Axel Le Cesne, Florence Duffaud, Nicolas Penel, Nicolas Isambert, Jean-Emmanuel Kurtz, Ajay Puri, Rajiv Sarin, Jin-Hee Ahn, Jeong Eun Kim, Iain Ward, Ian Judson, Winette van der Graaf, Beatrice Seddon, Coonoor Chandrasekar, Rory Rickar, Ivo Hennig, Joshua Schiffman, R Lor Randall, Audrey Silvestri, Anaiis Zaratzian, Michael Tayao, Kelly Walwyn, Eveline Niedermayr, Denia Mang, Richard Clark, Tina Thorpe, Jessica MacDonald, Kim Riddell, Jasmine Mar, Vicki Fennelly, Allison Wicht, Belinda Zielony, Emma Galligan, Genna Glavich, Johanna Stoeckert, Lynda Williams, Lana Djandjgava, Iwona Buettner, Carla Osinki, Sonya Stephens, Muriel Rogasik, Laure Bouclier, Magali Girodet, Amandine Charreton, Yohan Fayet, Saniya Crasto, Bhanupriya Sandupatla, Yeon Yoon, Noda Je, Liz Thompson, Trent Fowler, Bella Johnson, Galina Petrikova, Thomas Hambridge, Angela Hutchins, Diego Bottero, Deborah Scanlon, Jo Stokes-Denson, Emmanuelle Génin, Dominique Campion, Jean-François Dartigues, Jean-François Deleuze, Jean-Charles Lambert, Richard Redon, Thomas Ludwig, Benjamin Grenier-Boley, Sébastien Letort, Pierre Lindenbaum, Vincent Meyer, Olivier Quenez, Christian Dina, Céline Bellenguez, Camille Charbonnier Le Clézio, Joanna Giemza, Stéphanie Chatel, Claude Férec, Hervé Le Marec, Luc Letenneur, Gaël Nicolas, Karen Rouault
Heritable defects in telomere and mitotic function selectively predispose to sarcomas. Science (New York, N.Y.) 379 (6629) (2023)
Salim Megat, Natalia Mora, Jason Sanogo, Olga Roman, Alberto Catanese, Najwa Ouali Alami, Axel Freischmidt, Xhuljana Mingaj, Hortense De Calbiac, François Muratet, Sylvie Dirrig-Grosch, Stéphane Dieterle, Nick Van Bakel, Kathrin Müller, Kirsten Sieverding, Jochen Weishaupt, Peter Munch Andersen, Markus Weber, Christoph Neuwirth, Markus Margelisch, Andreas Sommacal, Kristel R Van Eijk, Jan Herman Veldink, null null, Géraldine Lautrette, Philippe Couratier, Agnès Camuzat, Isabelle Le Ber, Maurizio Grassano, Adriano Chio, Tobias M Böckers, Albert C Ludolph, Francesco Roselli, Deniz Yilmazer-Hanke, Stéphanie Millecamps, Edor Kabashi, Erik Storkebaum, Chantal Sellier, Luc Dupuis
Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Nature communications 14 (1) (2023)
Salim Megat, Natalia Mora, Jason Sanogo, Olga Roman, Alberto Catanese, Najwa Ouali Alami, Axel Freischmidt, Xhuljana Mingaj, Hortense De Calbiac, François Muratet, Sylvie Dirrig-Grosch, Stéphane Dieterle, Nick Van Bakel, Kathrin Müller, Kirsten Sieverding, Jochen Weishaupt, Peter Munch Andersen, Markus Weber, Christoph Neuwirth, Markus Margelisch, Andreas Sommacal, Kristel R Van Eijk, Jan Herman Veldink, null null, Géraldine Lautrette, Philippe Couratier, Agnès Camuzat, Isabelle Le Ber, Maurizio Grassano, Adriano Chio, Tobias M Böckers, Albert C Ludolph, Francesco Roselli, Deniz Yilmazer-Hanke, Stéphanie Millecamps, Edor Kabashi, Erik Storkebaum, Chantal Sellier, Luc Dupuis
Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Nature communications 14 (1) (2023)
Mark K Bakker, Jos P Kanning, Gad Abraham, Amy E Martinsen, Bendik Slagsvold Winsvold, John-Anker Zwart, Romain Bourcier, Tomonobu Sawada, Masaru Koido, Yoichiro Kamatani, Sandrine Morel, Phillippe Amouyel, Stephanie Debette, Philippe Bijlenga, Takiy-Eddine Berrandou, Santhi K Ganesh, Nabila Bouatia-Naji, Gregory T Jones, Matthew J Bown, Gabriel J E Rinkel, Jan Herman Veldink, Ynte M Ruigrok, null null
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity. Stroke 54 (3) (2023)
Mark K Bakker, Jos P Kanning, Gad Abraham, Amy E Martinsen, Bendik Slagsvold Winsvold, John-Anker Zwart, Romain Bourcier, Tomonobu Sawada, Masaru Koido, Yoichiro Kamatani, Sandrine Morel, Phillippe Amouyel, Stephanie Debette, Philippe Bijlenga, Takiy-Eddine Berrandou, Santhi K Ganesh, Nabila Bouatia-Naji, Gregory T Jones, Matthew J Bown, Gabriel J E Rinkel, Jan Herman Veldink, Ynte M Ruigrok, null null
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity. Stroke 54 (3) (2023)
Koen F Dekkers, Roderick C Slieker, Andreea Ioan-Facsinay, Maarten van Iterson, null null, Mohammad Arfan Ikram, Marleen M J van Greevenbroek, Jan Herman Veldink, Lude H Franke, Dorret I Boomsma, Pieternella Eline Slagboom, Johan Wouter Jukema, Bastiaan T Heijmans
Lipid-induced transcriptomic changes in blood link to lipid metabolism and allergic response. Nature communications 14 (1) (2023)
Adriaan D de Jongh, Ruben P A van Eijk, Leonhard A Bakker, Tommy M Bunte, Anita Beelen, Conny van der Meijden, Michael A van Es, Johanna M A Visser-Meily, Esther T Kruitwagen, Jan Herman Veldink, Leonard H van den Berg
Development of a Rasch-Built Amyotrophic Lateral Sclerosis Impairment Multidomain Scale to Measure Disease Progression in ALS. Neurology (2023)
Niek de Klein, Ellen A 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 E Marshall, Maria I Zavodszky, Wouter Van Rheenen, Mark K Bakker, Jan Herman Veldink, Tom R Gaunt, Heiko Runz, Lude H Franke, Harm-Jan Westra
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases. Nature genetics 55 (3) (2023)
Koen F Dekkers, Roderick C Slieker, Andreea Ioan-Facsinay, Maarten van Iterson, null null, Mohammad Arfan Ikram, Marleen M J van Greevenbroek, Jan Herman Veldink, Lude H Franke, Dorret I Boomsma, Pieternella Eline Slagboom, Johan Wouter Jukema, Bastiaan T Heijmans
Lipid-induced transcriptomic changes in blood link to lipid metabolism and allergic response. Nature communications 14 (1) (2023)
Koen F Dekkers, Roderick C Slieker, Andreea Ioan-Facsinay, Maarten van Iterson, null null, Mohammad Arfan Ikram, Marleen M J van Greevenbroek, Jan Herman Veldink, Lude H Franke, Dorret I Boomsma, Pieternella Eline Slagboom, Johan Wouter Jukema, Bastiaan T Heijmans
Lipid-induced transcriptomic changes in blood link to lipid metabolism and allergic response. Nature communications 14 (1) (2023)
Eva M J de Boer, Koen C Demaegd, Charlotte I de Bie, Jan Herman Veldink, Leonard H Van Den Berg, Michael A Van Es
Familial motor neuron disease: co-occurrence of PLS and ALS (-FTD). Amyotrophic lateral sclerosis & frontotemporal degeneration (2023)
Niek de Klein, Ellen A 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 E Marshall, Maria I Zavodszky, Wouter Van Rheenen, Mark K Bakker, Jan Herman Veldink, Tom R Gaunt, Heiko Runz, Lude H Franke, Harm-Jan Westra
Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases. Nature genetics (2023)
Koen F Dekkers, Roderick C Slieker, Andreea Ioan-Facsinay, Maarten van Iterson, null null, Mohammad Arfan Ikram, Marleen M J van Greevenbroek, Jan Herman Veldink, Lude H Franke, Dorret I Boomsma, Pieternella Eline Slagboom, Johan Wouter Jukema, Bastiaan T Heijmans
Lipid-induced transcriptomic changes in blood link to lipid metabolism and allergic response. Nature communications 14 (1) (2023)
Sean W Willemse, Peter Harley, Ruben P A van Eijk, Koen C Demaegd, Pavol Zelina, R Jeroen Pasterkamp, Philip Van Damme, Caroline Ingre, Wouter van Rheenen, Jan Herman Veldink, Matthew C Kiernan, Ammar Al Chalabi, Leonard H van den Berg, Pietro Fratta, Michael A van Es
UNC13A in amyotrophic lateral sclerosis: from genetic association to therapeutic target. Journal of neurology, neurosurgery, and psychiatry (2023)
Mark K Bakker, Jos P Kanning, Gad Abraham, Amy E Martinsen, Bendik Slagsvold Winsvold, John-Anker Zwart, Romain Bourcier, Tomonobu Sawada, Masaru Koido, Yoichiro Kamatani, Sandrine Morel, Phillippe Amouyel, Stephanie Debette, Philippe Bijlenga, Takiy-Eddine Berrandou, Santhi K Ganesh, Nabila Bouatia-Naji, Gregory T Jones, Matthew J Bown, Gabriel J E Rinkel, Jan Herman Veldink, Ynte M Ruigrok, null null
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity. Stroke (2023)
Mandy L Ballinger, Swetansu Pattnaik, Piyushkumar A Mundra, Milita Zaheed, Emma M Rath, Peter Priestley, Jonathan Baber, Isabelle L Ray-Coquard, Nicholas Isambert, Sylvain Causeret, Winette T A van der Graaf, Ajay Puri, Florence Duffaud, Axel Le Cesne, Beatrice Seddon, Coonoor Chandrasekar, Joshua D Schiffman, Andrew S Brohl, Paul A James, Jean-Emmanuel Kurtz, Nicolas Penel, Ola Myklebost, Leonardo A Meza-Zepeda, Hilda Pickett, Maya Kansara, Nicola Waddell, Olga Kondrashova, John V Pearson, Andrew P Barbour, Sherly X Li, Tuong Linh Nguyen, Diane Fatkin, Robert M Graham, Eleni Giannoulatou, Melissa Jane Green, Warren Kaplan, Shyamsundar Ravishankar, Joseph Copty, Joseph E Powell, Edwin Cuppen, Kristel van Eijk, Jan Herman Veldink, Jin-Hee Ahn, Jeong Eun Kim, Robert Lor Randall, Katherine M Tucker, Ian R Judson, Rajiv Sarin, Thomas E Ludwig, French Exome Consortium, Jean François Deleuze, null null, Michelle Haber, Glenn M Marshall, Murray J Cairns, Jean Yves Blay, null null, David M Thomas, Martin Tattersall, Susan Neuhaus, Craig Lewis, Kathy Tucker, Richard Carey-Smith, David Wood, Sandro Porceddu, Ian Dickinson, Heather Thorne, Paul James, Isabelle Ray-Coquard, Jean-Yves Blay, Philippe Cassier, Axel Le Cesne, Florence Duffaud, Nicolas Penel, Nicolas Isambert, Jean-Emmanuel Kurtz, Ajay Puri, Rajiv Sarin, Jin-Hee Ahn, Jeong Eun Kim, Iain Ward, Ian Judson, Winette van der Graaf, Beatrice Seddon, Coonoor Chandrasekar, Rory Rickar, Ivo Hennig, Joshua Schiffman, R Lor Randall, Audrey Silvestri, Anaiis Zaratzian, Michael Tayao, Kelly Walwyn, Eveline Niedermayr, Denia Mang, Richard Clark, Tina Thorpe, Jessica MacDonald, Kim Riddell, Jasmine Mar, Vicki Fennelly, Allison Wicht, Belinda Zielony, Emma Galligan, Genna Glavich, Johanna Stoeckert, Lynda Williams, Lana Djandjgava, Iwona Buettner, Carla Osinki, Sonya Stephens, Muriel Rogasik, Laure Bouclier, Magali Girodet, Amandine Charreton, Yohan Fayet, Saniya Crasto, Bhanupriya Sandupatla, Yeon Yoon, Noda Je, Liz Thompson, Trent Fowler, Bella Johnson, Galina Petrikova, Thomas Hambridge, Angela Hutchins, Diego Bottero, Deborah Scanlon, Jo Stokes-Denson, Emmanuelle Génin, Dominique Campion, Jean-François Dartigues, Jean-François Deleuze, Jean-Charles Lambert, Richard Redon, Thomas Ludwig, Benjamin Grenier-Boley, Sébastien Letort, Pierre Lindenbaum, Vincent Meyer, Olivier Quenez, Christian Dina, Céline Bellenguez, Camille Charbonnier Le Clézio, Joanna Giemza, Stéphanie Chatel, Claude Férec, Hervé Le Marec, Luc Letenneur, Gaël Nicolas, Karen Rouault
Heritable defects in telomere and mitotic function selectively predispose to sarcomas. Science (New York, N.Y.) 379 (6629) (2023)
Sean W Willemse, Peter Harley, Ruben P A van Eijk, Koen C Demaegd, Pavol Zelina, R Jeroen Pasterkamp, Philip Van Damme, Caroline Ingre, Wouter van Rheenen, Jan Herman Veldink, Matthew C Kiernan, Ammar Al Chalabi, Leonard H van den Berg, Pietro Fratta, Michael A van Es
UNC13A in amyotrophic lateral sclerosis: from genetic association to therapeutic target. Journal of neurology, neurosurgery, and psychiatry (2023)
Mandy L Ballinger, Swetansu Pattnaik, Piyushkumar A Mundra, Milita Zaheed, Emma M Rath, Peter Priestley, Jonathan Baber, Isabelle L Ray-Coquard, Nicholas Isambert, Sylvain Causeret, Winette T A van der Graaf, Ajay Puri, Florence Duffaud, Axel Le Cesne, Beatrice Seddon, Coonoor Chandrasekar, Joshua D Schiffman, Andrew S Brohl, Paul A James, Jean-Emmanuel Kurtz, Nicolas Penel, Ola Myklebost, Leonardo A Meza-Zepeda, Hilda Pickett, Maya Kansara, Nicola Waddell, Olga Kondrashova, John V Pearson, Andrew P Barbour, Sherly X Li, Tuong Linh Nguyen, Diane Fatkin, Robert M Graham, Eleni Giannoulatou, Melissa Jane Green, Warren Kaplan, Shyamsundar Ravishankar, Joseph Copty, Joseph E Powell, Edwin Cuppen, Kristel van Eijk, Jan Herman Veldink, Jin-Hee Ahn, Jeong Eun Kim, Robert Lor Randall, Katherine M Tucker, Ian R Judson, Rajiv Sarin, Thomas E Ludwig, French Exome Consortium, Jean François Deleuze, null null, Michelle Haber, Glenn M Marshall, Murray J Cairns, Jean Yves Blay, null null, David M Thomas, Martin Tattersall, Susan Neuhaus, Craig Lewis, Kathy Tucker, Richard Carey-Smith, David Wood, Sandro Porceddu, Ian Dickinson, Heather Thorne, Paul James, Isabelle Ray-Coquard, Jean-Yves Blay, Philippe Cassier, Axel Le Cesne, Florence Duffaud, Nicolas Penel, Nicolas Isambert, Jean-Emmanuel Kurtz, Ajay Puri, Rajiv Sarin, Jin-Hee Ahn, Jeong Eun Kim, Iain Ward, Ian Judson, Winette van der Graaf, Beatrice Seddon, Coonoor Chandrasekar, Rory Rickar, Ivo Hennig, Joshua Schiffman, R Lor Randall, Audrey Silvestri, Anaiis Zaratzian, Michael Tayao, Kelly Walwyn, Eveline Niedermayr, Denia Mang, Richard Clark, Tina Thorpe, Jessica MacDonald, Kim Riddell, Jasmine Mar, Vicki Fennelly, Allison Wicht, Belinda Zielony, Emma Galligan, Genna Glavich, Johanna Stoeckert, Lynda Williams, Lana Djandjgava, Iwona Buettner, Carla Osinki, Sonya Stephens, Muriel Rogasik, Laure Bouclier, Magali Girodet, Amandine Charreton, Yohan Fayet, Saniya Crasto, Bhanupriya Sandupatla, Yeon Yoon, Noda Je, Liz Thompson, Trent Fowler, Bella Johnson, Galina Petrikova, Thomas Hambridge, Angela Hutchins, Diego Bottero, Deborah Scanlon, Jo Stokes-Denson, Emmanuelle Génin, Dominique Campion, Jean-François Dartigues, Jean-François Deleuze, Jean-Charles Lambert, Richard Redon, Thomas Ludwig, Benjamin Grenier-Boley, Sébastien Letort, Pierre Lindenbaum, Vincent Meyer, Olivier Quenez, Christian Dina, Céline Bellenguez, Camille Charbonnier Le Clézio, Joanna Giemza, Stéphanie Chatel, Claude Férec, Hervé Le Marec, Luc Letenneur, Gaël Nicolas, Karen Rouault
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Sean W Willemse, Peter Harley, Ruben P A van Eijk, Koen C Demaegd, Pavol Zelina, R Jeroen Pasterkamp, Philip Van Damme, Caroline Ingre, Wouter van Rheenen, Jan Herman Veldink, Matthew C Kiernan, Ammar Al Chalabi, Leonard H van den Berg, Pietro Fratta, Michael A van Es
UNC13A in amyotrophic lateral sclerosis: from genetic association to therapeutic target. Journal of neurology, neurosurgery, and psychiatry (2023)
Mark K Bakker, Jos P Kanning, Gad Abraham, Amy E Martinsen, Bendik Slagsvold Winsvold, John-Anker Zwart, Romain Bourcier, Tomonobu Sawada, Masaru Koido, Yoichiro Kamatani, Sandrine Morel, Phillippe Amouyel, Stephanie Debette, Philippe Bijlenga, Takiy-Eddine Berrandou, Santhi K Ganesh, Nabila Bouatia-Naji, Gregory T Jones, Matthew J Bown, Gabriel J E Rinkel, Jan Herman Veldink, Ynte M Ruigrok, null null
Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity. Stroke (2023)
Salim Megat, Natalia Mora, Jason Sanogo, Olga Roman, Alberto Catanese, Najwa Ouali Alami, Axel Freischmidt, Xhuljana Mingaj, Hortense De Calbiac, François Muratet, Sylvie Dirrig-Grosch, Stéphane Dieterle, Nick Van Bakel, Kathrin Müller, Kirsten Sieverding, Jochen Weishaupt, Peter Munch Andersen, Markus Weber, Christoph Neuwirth, Markus Margelisch, Andreas Sommacal, Kristel R Van Eijk, Jan Herman Veldink, null null, Géraldine Lautrette, Philippe Couratier, Agnès Camuzat, Isabelle Le Ber, Maurizio Grassano, Adriano Chio, Tobias M Böckers, Albert C Ludolph, Francesco Roselli, Deniz Yilmazer-Hanke, Stéphanie Millecamps, Edor Kabashi, Erik Storkebaum, Chantal Sellier, Luc Dupuis
Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Nature communications 14 (1) (2023)
Mandy L Ballinger, Swetansu Pattnaik, Piyushkumar A Mundra, Milita Zaheed, Emma M Rath, Peter Priestley, Jonathan Baber, Isabelle L Ray-Coquard, Nicholas Isambert, Sylvain Causeret, Winette T A van der Graaf, Ajay Puri, Florence Duffaud, Axel Le Cesne, Beatrice Seddon, Coonoor Chandrasekar, Joshua D Schiffman, Andrew S Brohl, Paul A James, Jean-Emmanuel Kurtz, Nicolas Penel, Ola Myklebost, Leonardo A Meza-Zepeda, Hilda Pickett, Maya Kansara, Nicola Waddell, Olga Kondrashova, John V Pearson, Andrew P Barbour, Sherly X Li, Tuong Linh Nguyen, Diane Fatkin, Robert M Graham, Eleni Giannoulatou, Melissa Jane Green, Warren Kaplan, Shyamsundar Ravishankar, Joseph Copty, Joseph E Powell, Edwin Cuppen, Kristel van Eijk, Jan Herman Veldink, Jin-Hee Ahn, Jeong Eun Kim, Robert Lor Randall, Katherine M Tucker, Ian R Judson, Rajiv Sarin, Thomas E Ludwig, French Exome Consortium, Jean François Deleuze, null null, Michelle Haber, Glenn M Marshall, Murray J Cairns, Jean Yves Blay, null null, David M Thomas, Martin Tattersall, Susan Neuhaus, Craig Lewis, Kathy Tucker, Richard Carey-Smith, David Wood, Sandro Porceddu, Ian Dickinson, Heather Thorne, Paul James, Isabelle Ray-Coquard, Jean-Yves Blay, Philippe Cassier, Axel Le Cesne, Florence Duffaud, Nicolas Penel, Nicolas Isambert, Jean-Emmanuel Kurtz, Ajay Puri, Rajiv Sarin, Jin-Hee Ahn, Jeong Eun Kim, Iain Ward, Ian Judson, Winette van der Graaf, Beatrice Seddon, Coonoor Chandrasekar, Rory Rickar, Ivo Hennig, Joshua Schiffman, R Lor Randall, Audrey Silvestri, Anaiis Zaratzian, Michael Tayao, Kelly Walwyn, Eveline Niedermayr, Denia Mang, Richard Clark, Tina Thorpe, Jessica MacDonald, Kim Riddell, Jasmine Mar, Vicki Fennelly, Allison Wicht, Belinda Zielony, Emma Galligan, Genna Glavich, Johanna Stoeckert, Lynda Williams, Lana Djandjgava, Iwona Buettner, Carla Osinki, Sonya Stephens, Muriel Rogasik, Laure Bouclier, Magali Girodet, Amandine Charreton, Yohan Fayet, Saniya Crasto, Bhanupriya Sandupatla, Yeon Yoon, Noda Je, Liz Thompson, Trent Fowler, Bella Johnson, Galina Petrikova, Thomas Hambridge, Angela Hutchins, Diego Bottero, Deborah Scanlon, Jo Stokes-Denson, Emmanuelle Génin, Dominique Campion, Jean-François Dartigues, Jean-François Deleuze, Jean-Charles Lambert, Richard Redon, Thomas Ludwig, Benjamin Grenier-Boley, Sébastien Letort, Pierre Lindenbaum, Vincent Meyer, Olivier Quenez, Christian Dina, Céline Bellenguez, Camille Charbonnier Le Clézio, Joanna Giemza, Stéphanie Chatel, Claude Férec, Hervé Le Marec, Luc Letenneur, Gaël Nicolas, Karen Rouault
Heritable defects in telomere and mitotic function selectively predispose to sarcomas. Science (New York, N.Y.) 379 (6629) (2023)
Eva M J de Boer, Balint S de Vries, Maartje Pennings, Erik-Jan Kamsteeg, Jan Herman Veldink, Leonard H Van Den Berg, Michael A Van Es
Genetic characterization of primary lateral sclerosis. Journal of neurology (2023)
Bharati Jadhav, Paras Garg, Joke J F A van Vugt, Kristina Ibanez Garikano, Delia Gagliardi, William Lee, Alejandro Martin-Trujillo, Scott L Gies, Mafalda Barbosa, Miten Jain, Henry Houlden, Benedict Paten, null null, null null, Jan Herman Veldink, Arianna Tucci, Andrew J Sharp
A GCC repeat expansion in AFF3 is a significant cause of intellectual disability. medRxiv : the preprint server for health sciences (2023)
Kevin van Veenhuijzen, Henk-Jan Westeneng, Harold H G Tan, Abram D Nitert, Hannelore K van der Burgh, Isabel Gosselt, Michael A Van Es, Tanja C W Nijboer, Jan Herman Veldink, Leonard H Van Den Berg
Longitudinal Effects of Asymptomatic C9orf72 Carriership on Brain Morphology. Annals of neurology (2022)
Chen Eitan, Aviad Siany, Elad Barkan, Tsviya Olender, Kristel R van Eijk, Matthieu Moisse, Sali M K Farhan, Yehuda M Danino, Eran Yanowski, Hagai Marmor-Kollet, Natalia Rivkin, Nancy Sarah Yacovzada, Shu-Ting Hung, Johnathan Cooper-Knock, Chien-Hsiung Yu, Cynthia Louis, Seth L Masters, Kevin P Kenna, Rick A A van der Spek, William Sproviero, Ahmad Al Khleifat, Alfredo Iacoangeli, Aleksey Shatunov, Ashley R Jones, Yael Elbaz-Alon, Yahel Cohen, Elik Chapnik, Daphna Rothschild, Omer Weissbrod, Gilad Beck, Elena Ainbinder, Shifra Ben-Dor, Sebastian Werneburg, Dorothy P Schafer, Robert H Brown, Pamela J Shaw, Philip Van Damme, Leonard H van den Berg, Hemali Phatnani, Eran Segal, Justin K Ichida, Ammar Al Chalabi, Jan Herman Veldink, null null, null null, Eran Hornstein
Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3'UTR protect against ALS. Nature neuroscience 25 (4) (2022)
Rachel M Brouwer, Marieke Klein, Katrina L Grasby, Hugo G Schnack, Neda Jahanshad, Jalmar Teeuw, Sophia I Thomopoulos, Emma Sprooten, Carol E Franz, Nitin Gogtay, William S Kremen, Matthew S Panizzon, Loes M Olde Loohuis, Christopher D Whelan, Moji Aghajani, Clara Alloza, Dag Alnaes, Eric Artiges, Rosa Ayesa-Arriola, Gareth J Barker, Mark E Bastin, Elisabet Blok, Erlend Bøen, Isabella A Breukelaar, Joanna K Bright, Elizabeth E L Buimer, Robin Bülow, Dara M Cannon, Simone Ciufolini, Nicolas A Crossley, Christienne G Damatac, Paola Dazzan, Casper L de Mol, Sonja M C de Zwarte, Sylvane Desrivieres, Covadonga Martinez Diaz-Caneja, Nhat Trung Doan, Katharina Dohm, Juliane Hilde Fröhner, Janik Goltermann, Antoine Grigis, Dominik Grotegerd, Laura K M Han, Mathew A Harris, Catharina A Hartman, Sarah J Heany, Walter Heindel, Dirk J Heslenfeld, Sarah Hohmann, Bernd Ittermann, Philip R Jansen, Joost Janssen, Tianye Jia, Jiyang Jiang, Christiane Jockwitz, Temmuz Karali, Daniel Keeser, Martijn G J C Koevoets, Rhoshel K Lenroot, Berend Malchow, René C W Mandl, Vicente Medel, Susanne Meinert, Catherine A Morgan, Thomas W Mühleisen, Leila Nabulsi, Nils Opel, Víctor Ortiz-García de la Foz, Bronwyn J Overs, Marie-Laure Paillère Martinot, Ronny Redlich, Tiago Reis Marques, Jonathan Repple, Gloria Roberts, Gennady V Roshchupkin, Nikita Setiaman, Elena Shumskaya, Frederike Stein, Gustavo Sudre, Shun Takahashi, Anbupalam Thalamuthu, Diana Tordesillas-Gutiérrez, Aad van der Lugt, Neeltje E M van Haren, Joanna Marguerite Wardlaw, Wei Wen, Henk-Jan Westeneng, Katharina Wittfeld, Alyssa H Zhu, Andre Zugman, Nicola J Armstrong, Gaia Bonfiglio, Janita Bralten, Shareefa Dalvie, Gail Davies, Marta Di Forti, Linda Ding, Gary Donohoe, Andreas J Forstner, Javier Gonzalez-Peñas, Joao P O F T Guimaraes, Georg Homuth, Jouke- Jan Hottenga, Maria J Knol, John B J Kwok, Stephanie Le Hellard, Karen A Mather, Yuri Milaneschi, Derek W Morris, Markus Maria Nöthen, Sergi Papiol, Marcella D C Rietschel, Marcos Leite Santoro, Vidar M Steen, Jason L Stein, Fabian Streit, Rick M Tankard, Alexander Teumer, Dennis van 't Ent, Dennis van der Meer, Kristel R van Eijk, Evangelos Vassos, Javier Váquez-Bourgon, Stephanie-H Witt, null null, Hieab H H Adams, Ingrid Agartz, David Ames, Katrin Amunts, Ole Andreas Andreassen, Celso Arango, Tobias Banaschewski, Bernhard T Baune, Sintia Nogueira Belangero, Arun L W Bokde, Dorret I Boomsma, Rodrigo A Bressan, Henry Brodaty, Jan K Buitelaar, Wiepke Cahn, Svenja Caspers, Sven Cichon, Benedicto Crespo-Facorro, Simon R Cox, Udo Dannlowski, Torbjørn Elvsåshagen, Thomas Espeseth, Peter G Falkai, Simon E Fisher, Herta Flor, Janice M Fullerton, Hugh Garavan, Penny A Gowland, Hans Jörgen Grabe, Tim Hahn, Andreas Heinz, Manon H J Hillegers, Jacqueline Hoare, Pieter J Hoekstra, Mohammad Arfan Ikram, Andrea Parolin Jackowski, Andreas Jansen, Erik G Jönsson, Rene S Kahn, Tilo Kircher, Mayuresh S Korgaonkar, Axel Krug, Herve Lemaitre, Ulrik F Malt, Jean-Luc Martinot, Colm McDonald, Philip B Mitchell, Ryan L Muetzel, Robin M Murray, Frauke Nees, Igor Nenadić, Jaap Oosterlaan, Roel A Ophoff, Pedro M Pan, Brenda W J H Penninx, Luise Poustka, Perminder Singh Sachdev, Giovanni A Salum, Peter R Schofield, Gunter Schumann, Philip Shaw, Kang Sim, Michael N Smolka, Dan J Stein, Julian N Trollor, Leonard H van den Berg, Jan Herman Veldink, Henrik Walter, Lars Tjelta Westlye, Robert Whelan, Tonya White, Margaret J Wright, Sarah E Medland, Barbara Franke, Paul M Thompson, Hilleke E Hulshoff Pol
Genetic variants associated with longitudinal changes in brain structure across the lifespan. Nature neuroscience 25 (4) (2022)
Mark K Bakker, Suze Cobyte, Frederic A M Hennekam, Gabriel J E Rinkel, Jan Herman Veldink, Ynte M Ruigrok
Genome-wide linkage analysis combined with genome sequencing in large families with intracranial aneurysms. European journal of human genetics : EJHG 30 (7) (2022)
Julien Barc, Rafik Tadros, Charlotte Glinge, David Y Chiang, Mariam Jouni, Floriane Simonet, Sean Joseph Jurgens, Manon Baudic, Michele Nicastro, Franck Potet, Joost A Offerhaus, Roddy Walsh, Seung Hoan Choi, Arjan C Houweling, Yuka Mizusawa, Soraya Anys, Damien Minois, Marine Arnaud, Josselin Duchateau, Yanushi D Wijeyeratne, Alison Muir, Michael Papadakis, Silvia Castelletti, Margherita Torchio, Cristina Gil Ortuño, Javier Lacunza, Daniela Francesca Giachino, Natascia Cerrato, Raphaël P Martins, Òscar 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 K Rowe, Claire Federspiel, Sophie Le Page, Leslie Placide, Antoine Milhem, Hector Barajas-Martinez, Britt-Maria Beckmann, Ingrid P Krapels, Johannes Steinfurt, Bo Gregers Winkel, Reza Jabbari, Moore B Shoemaker, Bas J Boukens, Doris Škorić-Milosavljević, Hennie Bikker, Federico Manevy, Peter Lichtner, Marta Ribasés, Thomas Meitinger, Martina Müller-Nuraysid, null null, Jan Herman Veldink, Leonard H van den Berg, Philip Van Damme, Daniele Cusi, Chiara Lanzani, Sidwell Rigade, Eric Charpentier, Estelle Baron, Stéphanie Bonnaud, Simon Lecointe, Audrey Donnart, Hervé Le Marec, Stéphanie Chatel, Matilde Karakachoff, Stephane Bezieau, Barry London, Jacob Tfelt-Hansen, Dan Roden, Katja E Odening, Marina Cerrone, Larry A Chinitz, Paul G Volders, Maarten P van den Berg, Gabriel Laurent, Laurence Faivre, Charles Antzelevitch, Stefan Kääb, Alain Al Arnaout, Jean-Marc Dupuis, Jean-Luc Pasquie, Olivier Billon, Jason D Roberts, Laurence Jesel, Martin Borggrefe, Pier D Lambiase, Jacques Mansourati, Bart Loeys, Antoine Leenhardt, Pascale Guicheney, Philippe Maury, Eric Schulze-Bahr, Tomas Robyns, Jeroen Breckpot, Dominique Babuty, Silvia G Priori, Carlo Napolitano, null null, Carlos De Asmundis, Pedro Brugada, Ramon Brugada, Elena Arbelo, Josep Brugada, Philippe Mabo, Nathalie Behar, Carla Giustetto, Maria Sabater Molina, Juan R Gimeno, Can Hasdemir, Peter J Schwartz, Lia Crotti, Pascal P McKeown, Sanjay Sharma, Elijah R Behr, Michel Haissaguerre, Frédéric Sacher, Caroline Rooryck, Hanno L Tan, Carol A Remme, Pieter G Postema, Mario Delmar, Patrick T Ellinor, Steven A Lubitz, Jean-Baptiste Gourraud, Michael W T Tanck, Alfred L George, Calum A MacRae, Maged M Costantine, Christian Dina, Vincent Probst, Arthur A Wilde, Jean-Jacques Schott, Richard Redon, Connie R Bezzina
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature genetics 54 (3) (2022)
Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, Olubunmi Abel, Keith Mayl, Puja R Mehta, Aleksey Shatunov, Isabella Fogh, Harry Bowles, Naomi Limbachiya, Thomas P Spargo, Ahmad Al Khleifat, Kelly Louise Williams, Jennifer Jockel-Balsarotti, Taha Bali, Wade K Self, Lyndal Henden, Garth A Nicholson, Nicola Ticozzi, Diane McKenna-Yasek, Lu Tang, Dame Pamela J Shaw, Adriano Chio, Albert Ludolph, Jochen H Weishaupt, John E Landers, Jonathan D Glass, Jesus S Mora, Wim Robberecht, Philip Van Damme, Russell Lewis McLaughlin, Orla Hardiman, Leonard van den Berg, Jan Herman Veldink, Phillippe Corcia, Zorica Stevic, Nailah Siddique, Vincenzo Silani, Ian P Blair, Dong-Sheng Fan, Florence Esselin, Elisa de la Cruz, William Camu, Nazli A Basak, Teepu Siddique, Timothy Miller, Robert H Brown, Ammar Al Chalabi, Christopher E Shaw
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration. Nature communications 13 (1) (2022)
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)
Mark R Janse van Mantgem, Wouter Van Rheenen, Anemone V Hackeng, Michael A van Es, Jan Herman Veldink, Leonard H van den Berg, Ruben P A van Eijk
Association Between Serum Lipids and Survival in Patients With Amyotrophic Lateral Sclerosis: A Meta-analysis and Population-Based Study. Neurology (2022)
Thomas Jaworek, Huichun Xu, Brady J Gaynor, John W Cole, Kristiina Rannikmae, Tara M Stanne, Liisa Tomppo, Vida Abedi, Phillippe Amouyel, Nicole D Armstrong, John Richard Attia, Steven Bell, Oscar R Benavente, Giorgio B Boncoraglio, Adam S Butterworth, null null, Jara Cárcel-Márquez, Zhengming Chen, Michael Chong, Cruchaga Carlos, Andrea N Edginton, John Danesh, Stephanie Debette, David J Duggan, Jon Peter Durda, Gunnar Engstrom, Chris Enzinger, Jessica D Faul, Natalie S Fecteau, Israel Fernandez-Cadenas, Christian Gieger, Anne-Katrin Giese, Raji P Grewal, Ulrike Grittner, Aki Samuli Havulinna, Laura Heitsch, Marc C Hochberg, Elizabeth Holliday, Jie Hu, Andreea Ilinca, null null, Marguerite R Irvin, Rebecca D Jackson, Mina A Jacob, Raquel Rabionet Janssen, Jordi Jiménez-Conde, Julie A Johnson, Yoichiro Kamatani, Sharon L Kardia, Masaru Koido, Michiaki Kubo, Leslie Lange, Jin-Moo Lee, Robin Lemmens, Christopher R Levi, Jiang Li, Liming Li, Kuang Lin, Haley Lopez, Sothear Luke, Jane Maguire, Patrick F McArdle, Caitrin W McDonough, James F Meschia, Tiina Metso, Martina Müller-Nuraysid, Timothy D O'Connor, Martin O'Donnell, Leema R Peddareddygari, Joanna Pera, James A Perry, Annette Peters, Jukka Putaala, Debashree Ray, Kathyrn M Rexrode, Marta Ribases, Jonathan Rosand, Peter M Rothwell, Tatjana Rundek, Kathleen A Ryan, Ralph L Sacco, Veikko V Salomaa, Cristina Sánchez-Mora, Reinhold Schmidt, Pankaj Sharma, Agnieszka Slowik, Jennifer A Smith, Nicholas L Smith, Sylvia Wassertheil-Smoller, Martin Soederholm, O C Stine, Strbian Daniel, Cathie L M Sudlow, Turgut Tatlisumak, Chikashi C Terao, Vincent N Thijs, Nuria P Torres-Aguila, David-Alexandre Tregouet, Anil Man Tuladhar, Jan Herman Veldink, Robin G Walters, David R Weir, Daniel Woo, Bradford B Worrall, Charles C Hong, Owen Ross, Ramin Zand, Frank-Erik de Leeuw, Arne G Lindgren, Guillaume Paré, Christopher D Anderson, Hugh Stephen Markus, Christina Jern, Rainer Malik, Martin Dichgans, Braxton D Mitchell, Steven J Kittner, null null
Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke. Neurology (2022)
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Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis. NPJ genomic medicine 7 (1) (2022)
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Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. Circulation research (2021)
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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature genetics 53 (12) (2021)
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Altered perivascular fibroblast activity precedes ALS disease onset. Nature medicine 27 (4) (2021)
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Adriaan D de Jongh, Ruben P A van Eijk, Susan M Peters, Michael A van Es, Anja M C Horemans, Anneke J van der Kooi, Nicol C Voermans, Roel C H Vermeulen, Jan Herman Veldink, Leonard H van den Berg
Incidence, Prevalence and Geographical Clustering of Motor Neuron Disease in the Netherlands. Neurology (2021)
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Distinctive pattern of temporal atrophy in patients with frontotemporal dementia and the I383V variant in TARDBP. Journal of neurology, neurosurgery, and psychiatry 92 (7) (2021)
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Genetic analysis of ALS cases in the isolated island population of Malta. European journal of human genetics : EJHG 29 (4) (2021)
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Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology. Science translational medicine 11 (523) (2020)
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The genetic architecture of the human cerebral cortex. Science (New York, N.Y.) 367 (6484) (2020)
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The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public. Amyotrophic lateral sclerosis & frontotemporal degeneration 20 (5-6) (2020)
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Prognostic value of weight loss in patients with amyotrophic lateral sclerosis: a population-based study. Journal of neurology, neurosurgery, and psychiatry 91 (8) (2020)
Ross P Byrne, Wouter Van Rheenen, null null, Leonard H van den Berg, Jan Herman Veldink, Russell Lewis McLaughlin
Dutch population structure across space, time and GWAS design. Nature communications 11 (1) (2020)
Mark K Bakker, Rick A A van der Spek, Wouter Van Rheenen, Sandrine Morel, Romain Bourcier, Isabel Charlotte Hostettler, Varinder S Alg, Kristel R van Eijk, Masaru Koido, Masato Akiyama, Chikashi C Terao, Koichi Matsuda, Robin G Walters, Kuang Lin, Liming Li, Iona Y Millwood, Zhengming Chen, Guy A Rouleau, Sirui Zhou, Kristiina Rannikmäe, Cathie L M Sudlow, Henry Houlden, Leonard H van den Berg, Christian Dina, Olivier Naggara, Jean-Christophe Gentric, Eimad Shotar, Francisco Macian, Hubert Desal, Bendik Slagsvold Winsvold, Sigrid Børte, Marianne Bakke Johnsen, Ben Michael 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, Olivier Martin, null null, null null, null null, null null, null null, null null, null null, Gregory T Jones, Matthew J Bown, Nerissa U Ko, Helen Kim, Jonathan R I Coleman, Gerome Breen, Jonathan G Zaroff, Catharina J M Klijn, Rainer Malik, Martin Dichgans, Muralidharan Sargurupremraj, Turgut Tatlisumak, Phillippe Amouyel, Stephanie Debette, Gabriel J E Rinkel, Bradford B Worrall, Joanna Pera, Agnieszka Slowik, Emília I Gaál-Paavola, Mika Niemelä, Juha E Jääskeläinen, Mikael von Und Zu Fraunberg, Antti E Lindgren, Joseph P Broderick, David John Werring, Daniel Woo, Richard Redon, Philippe Bijlenga, Yoichiro Kamatani, Jan Herman Veldink, Ynte M Ruigrok
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Nature genetics 52 (12) (2020)
Anne E Visser, Fabrizio D'Ovidio, Susan Peters, Roel Ch Vermeulen, Ettore Beghi, Adriano Chio, Jan Herman Veldink, Giancarlo Logroscino, Orla Hardiman, Leonard H van den Berg, null null
Multicentre, population-based, case-control study of particulates, combustion products and amyotrophic lateral sclerosis risk. Journal of neurology, neurosurgery, and psychiatry 90 (8) (2019)
David W Clark, Yukinori Okada, Kristjan Helgi Swerford Moore, Dan Mason, Nicola Pirastu, Antonietta Robino, Hannele Mattsson, Catriona L K Barnes, Kuang Lin, Jing Hua Zhao, Patrick Deelen, Rebecca Rohde, Claudia Schurmann, Xiuqing Guo, Franco Giulianini, Weihua Zhang, Carolina Medina-Gomez, Robert Karlsson, Yanchun Bao, Traci M Bartz, Clemens Baumbach, Ginevra Biino, Matthew J Bixley, Marco Brumat, Jin Fang Chai, Tanguy Corre, Diana L Cousminer, Annelot M Dekker, David A Eccles, Kristel R van Eijk, Christian Fuchsberger, He Gao, Marine Germain, Scott D Gordon, Hugoline G de Haan, Sarah E Harris, Edith Hofer, Alicia Huerta-Chagoya, Catherine Igartua, Iris E Jansen, Yucheng Jia, Tim Kacprowski, Torgny Karlsson, Marcus Edi Kleber, Shengchao Alfred Li, Ruifang Li-Gao, Anubha Mahajan, Koichi Matsuda, Karina Meidtner, Weihua Meng, May E Montasser, Peter J van der Most, Matthias Munz, Teresa Nutile, Teemu Palviainen, Gauri Prasad, Rashmi B Prasad, Tallapragada Divya Sri Priyanka, Federica Rizzi, Mirna Andelic, Bishwa R Sapkota, Daniel Shriner, Line Skotte, Melissa C Smart, Albert Vernon Smith, Ashley van der Spek, Cassandra N Spracklen, Rona Juliette Strawbridge, Salman M Tajuddin, Stella Trompet, Constance Turman, Niek Verweij, Clara Viberti, Lihua Wang, Helen R Warren, Robyn E Wootton, Lisa R Yanek, Jie Yao, Noha A Yousri, Wei Zhao, Adebowale A Adeyemo, Saima Afaq, Carlos Alberto Aguilar-Salinas, Masato Akiyama, Matthew L Albert, Matthew A Allison, Maris Alver, Tin Aung, Fereidoun Azizi, Amy R Bentley, Heiner Boeing, Eric Boerwinkle, Judith B Borja, Gert J de Borst, Erwin P Bottinger, Linda Broer, Harry Campbell, Stephen J Chanock, Miao-Li Chee, Guanjie Chen, Yii-Der I Chen, Zhengming Chen, Yen-Feng Chiu, Massimiliano Cocca, Francis S Collins, Maria Pina Concas, Janie Corley, Giovanni Cugliari, Rob M van Dam, Anna Damulina, Maryam S Daneshpour, Felix R Day, Graciela E Delgado, Klodian Dhana, Alexander S F Doney, Marcus Dörr, Ayo P Doumatey, Nduna Dzimiri, S Sunna Ebenesersdóttir, Joshua Elliott, Paul Elliott, Ralf Ewert, Janine F Felix, Krista Fischer, Barry I Freedman, Giorgia Girotto, Anuj Goel, Martin Gögele, Mark O Goodarzi, Mariaelisa Graff, Einat Granot-Hershkovitz, Francine Grodstein, Simonetta Guarrera, Daníel F Guðbjartsson, Kamran Guity, Bjarni Gunnarsson, Yu Guo, Saskia P Hagenaars, Christopher A Haiman, Avner Halevy, Tamara B Harris, Mehdi Hedayati, David A van Heel, Makoto Hirata, Imo Höfer, Chao Agnes Hsiung, Jinyan Huang, Yi-Jen Hung, Mohammad Arfan Ikram, Anuradha Jagadeesan, Pekka Jousilahti, Yoichiro Kamatani, Masahiro Kanai, Nicola D Kerrison, Thorsten Kessler, Kay-Tee Khaw, Chiea Chuen Khor, Dominique P V de Kleijn, Woon-Puay Koh, Ivana Kolčić, Peter Kraft, Bernhard K Krämer, Zoltán Kutalik, Johanna Kuusisto, Claudia Langenberg, Lenore J Launer, Deborah A Lawlor, I-Te Lee, Wen-Jane Lee, Markus M Lerch, Liming Li, Jian-Jun Liu, Marie Loh, Stephanie J London, Stephanie Loomis, Yingchang Lu, Jian'an Luan, Reedik Mägi, Ani W Manichaikul, Paolo Manunta, Gísli Másson, Nana Matoba, Winnie Xue Mei, Christa Meisinger, Thomas Meitinger, Massimo Mezzavilla, Lili A Milani, Iona Y Millwood, Yukihide Momozawa, Amy Moore, Pierre-Emmanuel Morange, Hortensia Moreno-Macías, Trevor A Mori, Alanna C Morrison, Taulant Muka, Yoshinori Murakami, Alison D Murray, Renée de Mutsert, Josyf C Mychaleckyi, Mike A Nalls, Matthias Nauck, Matthew J Neville, Ilja Maria Nolte, Ken K Ong, Lorena Orozco, Sandosh Padmanabhan, Gunnar Pálsson, James S Pankow, Cristian Pattaro, Alison Pattie, Ozren Polasek, Neil Poulter, Peter P Pramstaller, Lluis Quintana-Murci, Katri Räikkönen, Sarju Ralhan, Dabeeru C Rao, Wouter Van Rheenen, Stephen S Rich, Paul M Ridker, Cornelius A Rietveld, Antonietta Robino, Frank J A van Rooij, Daniela Ruggiero, Yasaman Saba, Sabanayagam Charumathi, Maria Sabater-Lleal, Cinzia Felicita Sala, Veikko V Salomaa, Kevin Sandow, Helena Schmidt, Laura J Scott, William R Scott, Bahareh Sedaghati-Khayat, Bengt Sennblad, Jessica van Setten, Peter J Sever, Wayne H-H Sheu, Yuan Shi, Smeeta Shrestha, Sharvari Rahul Shukla, Jon K Sigurdsson, Timo Tonis Sikka, Jai Rup Singh, Blair Hamilton Smith, Alena Stančáková Yaluri, Alice V Stanton, John M Starr, Lilja Stefansdottir, Leon M Straker, Patrick Sulem, Gardar Sveinbjornsson, Morris A Swertz, Adele M Taylor, Kent D Taylor, Natalie Terzikhan, Yih-Chung Tham, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Annika Tillander, Russell P Tracy, Teresa Tusié-Luna, Joanna Tzoulaki, Simona Vaccargiu, Jagadish Vangipurapu, Jan Herman Veldink, Veronique Vitart, Linus Völker, Eero Vuoksimaa, Salma M Wakil, Melanie Waldenberger, Gurpreet Singh Wander, Ya-Xing Wang, Nicholas J Wareham, Sarah D Wild, Chittaranjan S Yajnik, Woon-Puay Koh, Lingyao Zeng, Liang Zhang, Jie Zhou, Najaf Amin, Folkert W. Asselbergs, Stephan J L Bakker, Diane M Becker, Benjamin Lehne, David A Bennett, Leonard H van den Berg, Sonja I Berndt, Dwaipayan Bharadwaj, Lawrence F Bielak, Murielle Bochud, Michael Boehnke, Claude Bouchard, Jonathan P Bradfield, Jennifer A Brody, Archie I Campbell, Shai Carmi, Mark J Caulfield, David Cesarini, John C Chambers, Giriraj Ratan Chandak, Ching-Yu Cheng, Marina Ciullo, Marilyn Cornelis, Daniele Cusi, George Davey Smith, Ian J Deary, Rajkumar Dorajoo, Cornelia M van Duijn, David Ellinghaus, Jeanette Erdmann, Johan G Eriksson, Evangelos Evangelou, Michele K Evans, Jessica D Faul, Bjarke Feenstra, Mary F Feitosa, Sylvain Foisy, Andre Franke, Yechiel Friedlander, Paolo Gasparini, Christian Gieger, Clicerio Gonzalez, Philippe Goyette, Struan F A Grant, Lyn R Griffiths, Leif C Groop, Vilmundur G Gudnason, Ulf Gyllensten, Hakon Hakonarson, Anders Hamsten, Pim van der Harst, Chew-Kiat Heng, Andrew A Hicks, Hagit Hochner, Heikki Huikuri, Steven C Hunt, Vincent W V Jaddoe, Philip Lawrence De Jager, Magnus Johannesson, Åsa Johansson, Jost Bruno Jonas, Johan Wouter Jukema, Juhani Junttila, Jaakko A Kaprio, Sharon L R Kardia, Fredrik Karpe, Meena Kumari, Markku Laakso, Sander W van der Laan, Jari M T Lahti, Matthias Laudes, Rodney A Lea, Wolfgang Lieb, Thomas Lumley, Nicholas G Martin, Winfried März, Giuseppe Matullo, Mark I McCarthy, Sarah E Medland, Tony Raymond Merriman, Andres Metspalu, Brian F Meyer, Karen L Mohlke, Grant W Montgomery, Dennis Mook-Kanamori, Patricia B Munroe, Kari E North, Dale R Nyholt, Jeffery R O'connell, Carole Ober, Albertine J Oldehinkel, Walter Palmas, Colin Neil Alexander Palmer, Gerard G Pasterkamp, Etienne Patin, Craig E Pennell, Louis Perusse, Patricia A Peyser, Mario Pirastu, Tinca J C Polderman, David J Porteous, Danielle Posthuma, Bruce M Psaty, John D Rioux, Fernando Rivadeneira, Charles N Rotimi, Jerome I Rotter, Igor Rudan, Hester M Den Ruijter, Dharambir K Sanghera, Naveed Sattar, Reinhold Schmidt, Matthias B Schulze, Heribert Schunkert, Robert A Scott, Alan R Shuldiner, Xueling S Sim, Neil Small, Jennifer A Smith, Nona Sotoodehnia, E-Shyong Tai, Alexander Teumer, Nicholas John Timpson, Daniela Toniolo, David-Alexandre Tregouet, Tiinamaija Tuomi, Peter Vollenweider, Carol A Wang, David R Weir, John B Whitfield, Cisca Wijmenga, Tien-Yin Wong, John Wright, Jingyun Yang, Lei Yu, Babette S Zemel, Alan B Zonderman, Markus Perola, Patrik K E Magnusson, Andre G Uitterlinden, Jaspal S Kooner, Daniel I Chasman, Ruth J F Loos, Nora Franceschini, Lude H Franke, Christopher S Haley, Caroline Hayward, Robin G Walters, John R B Perry, Tōnu Esko, Agnar Helgason, Kari Stefansson, Peter K Joshi, Michiaki Kubo, James F Wilson
Associations of autozygosity with a broad range of human phenotypes. Nature communications 10 (1) (2019)
Susan Peters, Anne E Visser, Fabrizio D'Ovidio, Jelle Vlaanderen, Lützen Portengen, Ettore Beghi, Adriano Chio, Giancarlo Logroscino, Orla Hardiman, Elisabetta Pupillo, Jan Herman Veldink, Roel Vermeulen, Leonard H van den Berg, null null
Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR. Journal of neurology, neurosurgery, and psychiatry 91 (1) (2019)
Jurjen J Luykx, Fabrizio Giuliani, Giuliano Giuliani, Jan Herman Veldink
Coding and Non-Coding RNA Abnormalities in Bipolar Disorder. Genes 10 (11) (2019)
Iris J Broce, Celeste M Karch, Natalie Wen, Chun C Fan, Yunpeng Wang, Chin Hong Tan, Naomi Kouri, Owen A Ross, Günter U Höglinger, Ulrich Muller, John Hardy, null null, Parastoo Momeni, Christopher P Hess, William P Dillon, Zachary A Miller, Luke W Bonham, Gil D Rabinovici, Howard J Rosen, Gerard D Schellenberg, Andre Franke, Tom H Karlsen, Jan Herman Veldink, Raffaele Ferrari, Jennifer S Yokoyama, Bruce L Miller, Ole A Andreassen, Anders M Dale, Rahul S Desikan, Leo P Sugrue
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies. PLoS medicine 15 (1) (2018)
Jan Herman Veldink
What does age at onset in ALS tell us about the genetic basis of the disease? Journal of neurology, neurosurgery, and psychiatry 90 (3) (2018)
Rick A A van der Spek, Wouter van Rheenen, Sara L Pulit, Kevin P Kenna, Nicola Ticozzi, Maarten Kooyman, Russell L Mclaughlin, Matthieu Moisse, Kristel R van Eijk, Joke J F A van Vugt, Alfredo Iacoangeli, Peter Andersen, A Nazli Basak, Ian Blair, Mamede de Carvalho, Adriano Chio, Philippe Corcia, Phillipe Couratier, Vivian E Drory, Jonathan D Glass, Orla Hardiman, Jesús S Mora, Karen E Morrison, Miguel Mitne-Neto, Wim Robberecht, Dame Pamela J Shaw, Monica P Panadés, Philip van Damme, Vincenzo Silani, Marc Gotkine, Markus Weber, Michael A van Es, John E Landers, Ammar Al Chalabi, Leonard H van den Berg, Jan Herman Veldink, null null
Reconsidering the causality of TIA1 mutations in ALS. Amyotrophic lateral sclerosis & frontotemporal degeneration 19 (1-2) (2017)

Jan Herman Veldink.css-eqlu8i{font-size:small;padding-left:4px;} (Jan H Veldink, Jan Veldink)

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Jan Herman Veldink (Jan H Veldink, Jan Veldink)