PROJECT MINE ALS SEQUENCING CONSORTIUM
Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes.
Megat S, Mora N, Sanogo J, Roman O, Catanese A, Alami N, Freischmidt A, Mingaj X, De Calbiac H, Muratet F, Dirrig-Grosch S, Dieterle S, Van Bakel N, Müller K, Sieverding K, Weishaupt J, Andersen P, Weber M, Neuwirth C, Margelisch M, Sommacal A, van Eijk K, Veldink J, PROJECT MINE ALS SEQUENCING CONSORTIUM, Lautrette G, Couratier P, Camuzat A, Le Ber I, Grassano M, Chio A, Boeckers T, Ludolph A, Roselli F, Yilmazer-Hanke D, Millecamps S, Kabashi E, Storkebaum E, Sellier C, Dupuis L. Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Nat Commun 2023; 14:8026.
04.12.2023Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes.
04.12.2023Nat Commun 2023; 14:8026
Megat Salim, Mora Natalia, Sanogo Jason, Roman Olga, Catanese Alberto, Alami Najwa Ouali, Freischmidt Axel, Mingaj Xhuljana, De Calbiac Hortense, Muratet François, Dirrig-Grosch Sylvie, Dieterle Stéphane, Van Bakel Nick, Müller Kathrin, Sieverding Kirsten, Weishaupt Jochen H, Andersen Peter Munch, Weber Markus, Neuwirth Christoph, Margelisch Markus, Sommacal Andreas, van Eijk Kristel R, Veldink Jan H, PROJECT MINE ALS SEQUENCING CONSORTIUM, Lautrette Géraldine, Couratier Philippe, Camuzat Agnès, Le Ber Isabelle, Grassano Maurizio, Chio Adriano, Boeckers Tobias, Ludolph Albert C., Roselli Francesco, Yilmazer-Hanke Deniz, Millecamps Stéphanie, Kabashi Edor, Storkebaum Erik, Sellier Chantal, Dupuis Luc
Integrative genetic analysis illuminates ALS heritability and identifies risk genes.
Megat S, Mora N, Sanogo J, Roman O, Catanese A, Alami N, Freischmidt A, Mingaj X, De Calbiac H, Muratet F, Dirrig-Grosch S, Dieterle S, Van Bakel N, Müller K, Sieverding K, Weishaupt J, Andersen P, Weber M, Neuwirth C, Margelisch M, Sommacal A, van Eijk K, Veldink J, PROJECT MINE ALS SEQUENCING CONSORTIUM, Lautrette G, Couratier P, Camuzat A, Le Ber I, Grassano M, Chio A, Boeckers T, Ludolph A, Roselli F, Yilmazer-Hanke D, Millecamps S, Kabashi E, Storkebaum E, Sellier C, Dupuis L. Integrative genetic analysis illuminates ALS heritability and identifies risk genes. Nat Commun 2023; 14:342.
20.01.2023Integrative genetic analysis illuminates ALS heritability and identifies risk genes.
20.01.2023Nat Commun 2023; 14:342
Megat Salim, Mora Natalia, Sanogo Jason, Roman Olga, Catanese Alberto, Alami Najwa Ouali, Freischmidt Axel, Mingaj Xhuljana, De Calbiac Hortense, Muratet François, Dirrig-Grosch Sylvie, Dieterle Stéphane, Van Bakel Nick, Müller Kathrin, Sieverding Kirsten, Weishaupt Jochen H, Andersen Peter Munch, Weber Markus, Neuwirth Christoph, Margelisch Markus, Sommacal Andreas, van Eijk Kristel R, Veldink Jan H, PROJECT MINE ALS SEQUENCING CONSORTIUM, Lautrette Géraldine, Couratier Philippe, Camuzat Agnès, Le Ber Isabelle, Grassano Maurizio, Chio Adriano, Boeckers Tobias, Ludolph Albert C., Roselli Francesco, Yilmazer-Hanke Deniz, Millecamps Stéphanie, Kabashi Edor, Storkebaum Erik, Sellier Chantal, Dupuis Luc
The impact of age on genetic testing decisions in amyotrophic lateral sclerosis.
Mehta P, Iacoangeli A, Opie-Martin S, Farei-Campagna J, Al Khleifat A, Bredin A, Ossher L, Andersen P, Hardiman O, Mehta A, Fratta P, Talbot K, PROJECT MINE ALS SEQUENCING CONSORTIUM, Al-Chalabi A. The impact of age on genetic testing decisions in amyotrophic lateral sclerosis. Brain 2022; 145:4440-4447.
19.12.2022The impact of age on genetic testing decisions in amyotrophic lateral sclerosis.
19.12.2022Brain 2022; 145:4440-4447
Mehta Puja R, Iacoangeli Alfredo, Opie-Martin Sarah, Farei-Campagna Jan Marino, Al Khleifat Ahmad, Bredin Andrea, Ossher Lynn, Andersen Peter Munch, Hardiman Orla, Mehta Arpan R, Fratta Pietro, Talbot Kevin, PROJECT MINE ALS SEQUENCING CONSORTIUM, Al-Chalabi Ammar
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis.
Zhang S, Cooper-Knock J, Weimer A, Shi M, Moll T, Marshall J, Harvey C, Nezhad H, Franklin J, Souza C, Ning K, Wang C, Li J, Dilliott A, Farhan S, Elhaik E, Pasniceanu I, Livesey M, Eitan C, Hornstein E, Kenna K, PROJECT MINE ALS SEQUENCING CONSORTIUM, Veldink J, Ferraiuolo L, Openshaw P, Snyder M. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis. Neuron 2022; 110:992-1008.e11.
18.01.2022Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis.
18.01.2022Neuron 2022; 110:992-1008.e11
Zhang Sai, Cooper-Knock Johnathan, Weimer Annika K, Shi Minyi, Moll Tobias, Marshall Jack N G, Harvey Calum, Nezhad Helia Ghahremani, Franklin John, Souza Cleide Dos Santos, Ning Kaida, Wang Cheng, Li Jingjing, Dilliott Allison A, Farhan Sali, Elhaik Eran, Pasniceanu Iris, Livesey Matthew R, Eitan Chen, Hornstein Eran, Kenna Kevin P, PROJECT MINE ALS SEQUENCING CONSORTIUM, Veldink Jan H, Ferraiuolo Laura, Openshaw Peter J M, Snyder Michael P
repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization.
Tazelaar G, Boeynaems S, De Decker M, Farei-Campagna J, Kool L, Goedee H, McLaughlin R, Sproviero W, Iacoangeli A, Moisse M, Jacquemyn M, Daelemans D, Dekker A, Van Der Spek R, Westeneng H, Kenna K, Assialioui A, Da Silva N, PROJECT MINE ALS SEQUENCING CONSORTIUM, Povedano M, Mora J, Hardiman O, Salachas F, Millecamps S, Vourc'h P, Corcia P, Couratier P, Morrison K, Openshaw P, Shaw C, Pasterkamp R, Landers J, Van Den Bosch L, Robberecht W, Al-Chalabi A, van den Berg L, Van Damme P, Veldink J, van Es M. repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization. Brain Commun 2020; 2:fcaa064.
19.05.2020repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization.
19.05.2020Brain Commun 2020; 2:fcaa064
Tazelaar Gijs H P, Boeynaems Steven, De Decker Mathias, Farei-Campagna Jan Marino, Kool Lindy, Goedee H Stephan, McLaughlin Russell L, Sproviero William, Iacoangeli Alfredo, Moisse Matthieu, Jacquemyn Maarten, Daelemans Dirk, Dekker Annelot M, Van Der Spek Rick A, Westeneng Henk-Jan, Kenna Kevin P, Assialioui Abdelilah, Da Silva Nica, PROJECT MINE ALS SEQUENCING CONSORTIUM, Povedano Monica, Mora Jesus S, Hardiman Orla, Salachas François, Millecamps Stéphanie, Vourc'h Patrick, Corcia Philippe, Couratier Philippe, Morrison Karen E, Openshaw Peter J M, Shaw Christopher E, Pasterkamp R Jeroen, Landers John E, Van Den Bosch Ludo, Robberecht Wim, Al-Chalabi Ammar, van den Berg Leonard H, Van Damme Philip, Veldink Jan H, van Es Michael A
Reconsidering the causality of TIA1 mutations in ALS
Van Der Spek R, Hardiman O, Mora J, Morrison K, Mitne-Neto M, Robberecht W, Shaw P, Panadés M, Van Damme P, Silani V, Gotkine M, Weber M, van Es M, Landers J, Al-Chalabi A, van den Berg L, Veldink J, Glass J, Drory V, van Rheenen W, Pulit S, Kenna K, Ticozzi N, Kooyman M, McLaughlin R, Moisse M, van Eijk K, Van Vugt J, Andersen P, Nazli Basak A, Blair I, de Carvalho M, Chio A, Corcia P, Couratier P, PROJECT MINE ALS SEQUENCING CONSORTIUM. Reconsidering the causality of TIA1 mutations in ALS. Amyotroph Lateral Scler Frontotemporal Degener 2017:1-3.
13.12.2017Reconsidering the causality of TIA1 mutations in ALS
13.12.2017Amyotroph Lateral Scler Frontotemporal Degener 2017:1-3
Van Der Spek Rick A, Hardiman Orla, Mora Jesus S, Morrison Karen E, Mitne-Neto Miguel, Robberecht Wim, Shaw Pamela J, Panadés Monica P, Van Damme Philip, Silani Vincenzo, Gotkine Marc, Weber Markus, van Es Michael A, Landers John E, Al-Chalabi Ammar, van den Berg Leonard H, Veldink Jan H, Glass Jonathan D, Drory Vivian E, van Rheenen Wouter, Pulit Sara L, Kenna Kevin P, Ticozzi Nicola, Kooyman Maarten, McLaughlin Russell L, Moisse Matthieu, van Eijk Kristel R, Van Vugt Joke J F A, Andersen Peter, Nazli Basak A, Blair Ian, de Carvalho Mamede, Chio Adriano, Corcia Philippe, Couratier Phillipe, PROJECT MINE ALS SEQUENCING CONSORTIUM
Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype
Cooper-Knock J, Kirby J, McDermott C, Hautbergue G, Ince P, PROJECT MINE ALS SEQUENCING CONSORTIUM, Kazoka M, Walsh T, Higginbottom A, Heath P, Wyles M, Niedermoser I, Robins H, Shaw P. Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype. Front Mol Neurosci 2017; 10:370.
09.11.2017Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype
09.11.2017Front Mol Neurosci 2017; 10:370
Cooper-Knock Johnathan, Kirby Janine, McDermott Christopher J, Hautbergue Guillaume M, Ince Paul G, PROJECT MINE ALS SEQUENCING CONSORTIUM, Kazoka Mbombe, Walsh Theresa, Higginbottom Adrian, Heath Paul R, Wyles Matthew, Niedermoser Isabell, Robins Henry, Shaw Pamela J