John E Landers

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 23

Top Venues

Nature genetics

Nature communications

Science translational medicine

Science advances

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

Publications

Salome Funes, Jonathan Jung, Del Hayden Gadd, Michelle Mosqueda, Jianjun Zhong, null Shankaracharya, Matthew Unger, Karly Stallworth, Debra Cameron, Melissa S Rotunno, Pepper Dawes, Megan E Fowler-Magaw, Pamela J Keagle, Justin A McDonough, Sivakumar Boopathy, Miguel Sena-Esteves, Jeffrey A Nickerson, Cathleen M Lutz, William C Skarnes, Elaine T Lim, Dorothy P Schafer, Francesca Massi, John E Landers, Daryl A Bosco
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia. 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 (2024)
Salome Funes, Jonathan Jung, Del Hayden Gadd, Michelle Mosqueda, Jianjun Zhong, null Shankaracharya, Matthew Unger, Karly Stallworth, Debra Cameron, Melissa S Rotunno, Pepper Dawes, Megan E Fowler-Magaw, Pamela J Keagle, Justin A McDonough, Sivakumar Boopathy, Miguel Sena-Esteves, Jeffrey A Nickerson, Cathleen M Lutz, William C Skarnes, Elaine T Lim, Dorothy P Schafer, Francesca Massi, John E Landers, Daryl A Bosco
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia. 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)
Salome Funes, Jonathan Jung, Del Hayden Gadd, Michelle Mosqueda, Jianjun Zhong, null Shankaracharya, Matthew Unger, Karly Stallworth, Debra Cameron, Melissa S Rotunno, Pepper Dawes, Megan E Fowler-Magaw, Pamela J Keagle, Justin A McDonough, Sivakumar Boopathy, Miguel Sena-Esteves, Jeffrey A Nickerson, Cathleen M Lutz, William C Skarnes, Elaine T Lim, Dorothy P Schafer, Francesca Massi, John E Landers, Daryl A Bosco
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia. 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)
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)
Salome Funes, Jonathan Jung, Del Hayden Gadd, Michelle Mosqueda, Jianjun Zhong, null Shankaracharya, Matthew Unger, Karly Stallworth, Debra Cameron, Melissa S Rotunno, Pepper Dawes, Megan E Fowler-Magaw, Pamela J Keagle, Justin A McDonough, Sivakumar Boopathy, Miguel Sena-Esteves, Jeffrey A Nickerson, Cathleen M Lutz, William C Skarnes, Elaine T Lim, Dorothy P Schafer, Francesca Massi, John E Landers, Daryl A Bosco
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia. 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)
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)
Salome Funes, Jonathan Jung, Del Hayden Gadd, Michelle Mosqueda, Jianjun Zhong, null Shankaracharya, Matthew Unger, Karly Stallworth, Debra Cameron, Melissa S Rotunno, Pepper Dawes, Megan E Fowler-Magaw, Pamela J Keagle, Justin A McDonough, Sivakumar Boopathy, Miguel Sena-Esteves, Jeffrey A Nickerson, Cathleen M Lutz, William C Skarnes, Elaine T Lim, Dorothy P Schafer, Francesca Massi, John E Landers, Daryl A Bosco
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microglia. Nature communications 15 (1) (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)
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)
Jacob R Mann, Elizabeth D McKenna, Darilang Mawrie, Vasileios Papakis, Francesco Alessandrini, Eric N Anderson, Ryan Mayers, Hannah E Ball, Evan Kaspi, Katherine Lubinski, Desiree M Baron, Liana Tellez, John E Landers, Udai Bhan Pandey, Evangelos Kiskinis
Loss of function of the ALS-associated NEK1 kinase disrupts microtubule homeostasis and nuclear import. Science advances 9 (33) (2023)
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)
Ahmad Al Khleifat, Alfredo Iacoangeli, Joke J F A van Vugt, Harry Bowles, Matthieu Moisse, Ramona A J Zwamborn, Rick A A van der Spek, Aleksey Shatunov, Johnathan Cooper-Knock, Simon Topp, Ross P Byrne, Cinzia Gellera, Victoria López, Ashley R Jones, Sarah Opie-Martin, Atay Vural, Yolanda Campos, Wouter Van Rheenen, Brendan Kenna, Kristel R Van Eijk, Kevin Kenna, Markus Weber, Bradley Smith, Isabella Fogh, Vincenzo Silani, Karen E Morrison, Richard James Butler Dobson, Michael A Van Es, Russell Lewis McLaughlin, Patrick Vourc'h, Adriano Chio, Philippe Corcia, Mamede de Carvalho, Marc Gotkine, Monica P Panades, Jesus S Mora, Pamela J Shaw, John E Landers, Jonathan D Glass, Christopher E Shaw, Nazli Basak, Orla Hardiman, Wim Robberecht, Philip Van Damme, Leonard H van den Berg, Jan Herman Veldink, Ammar Al Chalabi
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis. NPJ genomic medicine 7 (1) (2022)
Matthieu Moisse, Ramona A J Zwamborn, Joke J F A van Vugt, Rick A A van der Spek, Wouter Van Rheenen, Brendan Kenna, Kristel Van Eijk, Kevin Kenna, Philippe Corcia, Philippe Couratier, Patrick Vourc'h, Orla Hardiman, Russell Lewis McLaughlin, Marc Gotkine, Vivian Drory, Nicola Ticozzi, Vincenzo Silani, Mamede de Carvalho, Jesus S Mora, Monica Povedano, Peter Munch Andersen, Markus Weber, Ayse Nazli Basak, Xiao Chen, Michael A Eberle, Ammar Al Chalabi, Chris Shaw, Dame Pamela J Shaw, Karen E Morrison, John E Landers, Jonathan D Glass, Wim Robberecht, Michael A Van Es, Leonard H Van Den Berg, Jan Herman Veldink, Philip Van Damme, null null
The Effect of SMN Gene Dosage on ALS Risk and Disease Severity. Annals of neurology 89 (4) (2021)
Sara Saez-Atienzar, Sara Bandres-Ciga, Rebekah G Langston, Jonggeol J Kim, Shing Wan Choi, Regina Hertfelder Reynolds, null null, null null, Yevgeniya Abramzon, Ramita Dewan, Sarah Ahmed, John E Landers, Ruth Chia, Mina Ryten, Mark R Cookson, Michael A Nalls, Adriano Chio, Bryan J Traynor
Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types. Science advances 7 (3) (2021)
Wouter Van Rheenen, Rick A A van der Spek, Mark K Bakker, Joke J F A van Vugt, Paul J Hop, Ramona A J Zwamborn, Niek de Klein, Harm-Jan Westra, Olivier B Bakker, Patrick Deelen, Gemma Shireby, Eilis J Hannon, Matthieu Moisse, Denis Baird, Restuadi Restuadi, Egor Dolzhenko, Annelot M Dekker, Klara Gawor, Henk-Jan Westeneng, Gijs H P Tazelaar, Kristel R van Eijk, Maarten Kooyman, Ross P Byrne, Mark Doherty, Mark Heverin, Ahmad Al Khleifat, Alfredo Iacoangeli, Aleksey Shatunov, Nicola Ticozzi, Johnathan Cooper-Knock, Bradley N Smith, Marta Gromicho, Siddharthan Chandran, Suvankar Pal, Karen E Morrison, Pamela J Shaw, John Hardy, Richard W Orrell, Michael Sendtner, Thomas Meyer, Nazli Başak, Anneke J van der Kooi, Antonia Ratti, Isabella Fogh, Cinzia Gellera, Giuseppe Lauria, Stefania Corti, Cristina Cereda, Daisy Sproviero, Sandra D'Alfonso, Gianni Sorarù, Gabriele Siciliano, Massimiliano Filosto, Alessandro Padovani, Adriano Chiò, Andrea Calvo, Cristina Moglia, Maura Brunetti, Antonio Canosa, Maurizio Grassano, Ettore Beghi, Elisabetta Pupillo, Giancarlo Logroscino, Beatrice Nefussy, Alma Osmanovic, Angelica Nordin, Yossef Lerner, Michal Zabari, Marc Gotkine, Robert H Baloh, Shaughn Bell, Patrick Vourc'h, Philippe Corcia, Philippe Couratier, Stéphanie Millecamps, Vincent Meininger, François Salachas, Jesus S Mora Pardina, Abdelilah Assialioui, Ricardo Rojas-García, Patrick A Dion, Jay P Ross, Albert C Ludolph, Jochen H Weishaupt, David Brenner, Axel Freischmidt, Gilbert Bensimon, Alexis Brice, Alexandra Durr, Christine A M Payan, Safa Saker-Delye, Nicholas W Wood, Simon D Topp, Rosa Rademakers, Lukas Tittmann, Wolfgang Lieb, Andre Franke, Stephan Ripke, Alice Braun, Julia Kraft, David C Whiteman, Catherine M Olsen, Andre G Uitterlinden, Albert Hofman, Marcella D C Rietschel, Sven Cichon, Markus Maria Nöthen, Phillippe Amouyel, null null, null null, null null, null null, Bryan J Traynor, Andrew B Singleton, Miguel Mitne Neto, Ruben J Cauchi, Roel A Ophoff, Martina Wiedau-Pazos, Catherine Lomen-Hoerth, Vivanna M Van Deerlin, Julian Grosskreutz, Annekathrin Roediger, Nayana Gaur, Alexander Jörk, Tabea Barthel, Erik Theele, Benjamin Ilse, Beatrice Stubendorff, Otto W Witte, Robert Steinbach, Christian A Hübner, Caroline Graff, Lev Brylev, Vera Fominykh, Vera Demeshonok, Anastasia Ataulina, Boris Rogelj, Blaz Koritnik, Janez Zidar, Metka Ravnik-Glavač, Damjan Glavač, Zorica Stević, Vivian Drory, Monica Povedano, Ian P Blair, Matthew C Kiernan, Beben Benyamin, Robert D Henderson, Sarah Furlong, Susan Mathers, Pamela A McCombe, Merrilee Needham, Shyuan T Ngo, Garth A Nicholson, Roger Pamphlett, Dominic B Rowe, Frederik J Steyn, Kelly Louise Williams, Karen A Mather, Perminder Singh Sachdev, Anjali K Henders, Leanne Wallace, Mamede de Carvalho, Susana Pinto, Susanne Petri, Markus Weber, Guy A Rouleau, Vincenzo Silani, Charles J Curtis, Gerome D Breen, Jonathan D Glass, Robert H Brown, John E Landers, Christopher E Shaw, Peter Munch Andersen, Ewout Joan Nicolaas Groen, Michael A Van Es, Ronald Jeroen Pasterkamp, Dongsheng Fan, Fleur C Garton, Allan F McRae, George Davey Smith, Tom R Gaunt, Michael A Eberle, Jonathan S Mill, Russell Lewis McLaughlin, Orla Hardiman, Kevin P Kenna, Naomi R Wray, Ellen A Tsai, Heiko Runz, Lude H Franke, Ammar Al Chalabi, Philip Van Damme, Leonard H van den Berg, Jan Herman Veldink
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)
Irit Reichenstein, Chen Eitan, Sandra Diaz-Garcia, Guy Haim, Iddo Magen, Aviad Siany, Mariah L Hoye, Natali Rivkin, Tsviya Olender, Beata Toth, Revital Ravid, Amitai D Mandelbaum, Eran Yanowski, Jing Liang, Jeffrey K Rymer, Rivka Levy, Gilad Beck, Elena Ainbinder, Sali M K Farhan, Kimberly A Lennox, Nicole M Bode, Mark A Behlke, Thomas Möller, Smita Saxena, Cristiane de Araújo Martins Moreno, Giancarlo Costaguta, Kristel R van Eijk, Hemali Phatnani, Ammar Al Chalabi, A Nazli Başak, Leonard H van den Berg, Orla Hardiman, John E Landers, Jesus S Mora, Karen E Morrison, Dame Pamela J Shaw, Jan Herman Veldink, Samuel L Pfaff, Ofer Yizhar, Christina Gross, Robert H Brown, John M Ravits, Matthew B Harms, Timothy M Miller, Eran Hornstein
Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology. Science translational medicine 11 (523) (2020)
Bradley N Smith, Simon D Topp, Claudia Fallini, Hideki Shibata, Han-Jou Chen, Claire Troakes, Andrew King, Nicola Ticozzi, Kevin P Kenna, Athina Soragia-Gkazi, Jack W Miller, Akane Sato, Diana Marques Dias, Maryangel Jeon, Caroline Vance, Chun Hao Wong, Martina de Majo, Wejdan Kattuah, Jacqueline C Mitchell, Emma L Scotter, Nicholas W Parkin, Peter C Sapp, Matthew Nolan, Peter J Nestor, Michael Simpson, Michael Weale, Monkel Lek, Frank Baas, J M Vianney de Jong, Anneloor L M A Ten Asbroek, Alberto Garcia Redondo, Jesús Esteban-Pérez, Cinzia Tiloca, Federico Verde, Stefano Duga, P Nigel Leigh, Hardev Pall, Karen E Morrison, Ammar Al-Chalabi, Christopher E Shaw, Janine Kirby, Matthew C Kiernan, Kevin Talbot, Orla Hardiman, Jonathan D Glass, Jacqueline S de Belleroche, Masatoshi Maki, Stephen E Moss, Christopher Miller, Cinzia Gellera, Antonia Ratti, Safa Al-Sarraj, Robert H Brown, Vincenzo Silani, John E Landers, Christopher E Shaw
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis. Science translational medicine 9 (388) (2018)

John E Landers.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

John E Landers