Torthaí cuardaigh - Sali M.K. Farhan
- 1 - 20 toradh as 21 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion de réir Rossella Spataro, Maria Kousi, Sali M.K. Farhan, Jason R. Willer, Jay P. Ross, Patrick A. Dion, Guy A. Rouleau, Mark J. Daly, Benjamin M. Neale, Vincenzo La Bella, Nicholas Katsanis
Foilsithe / Cruthaithe 2019Artigo -
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Enhancing Variant of Uncertain Significance (VUS) Interpretation in Neurogenetics: Collaborative Experiences from a Tertiary Care Centre de réir Kayla Horowitz, Nellie H. Fotopoulos, Alana J. Mistry, J. A. Simó, Miranda Medeiros, Isabela Dall’Oglio Bucco, Mia Ginsberg, Emily Dwosh, Roberta La Piana, Guy A. Rouleau, Allison A. Dilliott, Sali M.K. Farhan
Foilsithe / Cruthaithe 2024Pré-impressão -
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Enhancing variant of uncertain significance (VUS) interpretation in neurogenetics: collaborative experiences from a tertiary care centre de réir Kayla Horowitz, Nellie H. Fotopoulos, Alana J. Mistry, J. A. Simó, Miranda Medeiros, Isabela Dall’Oglio Bucco, Mia Ginsberg, Emily Dwosh, Roberta La Piana, Guy A. Rouleau, Allison A. Dilliott, Sali M.K. Farhan
Foilsithe / Cruthaithe 2024Artigo -
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Modulation of neuronal resilience during aging by Hsp70/Hsp90/STI1 chaperone system de réir Rachel E. Lackie, Abdul Razzaq, Sali M.K. Farhan, Gilli Moshitzky, Flávio H. Beraldo, Marilene H. Lopes, Andrzej Maciejewski, Robert Gros, Jue Fan, Wing‐Yiu Choy, David Greenberg, Vilma R. Martins, Martin L. Duennwald, Hermona Soreq, Marco A. M. Prado, Marco A. M. Prado
Foilsithe / Cruthaithe 2018Pré-impressão -
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A hypomorphic Stip1 allele reveals the requirement for chaperone networks in mouse development and aging de réir Rachel E. Lackie, Marilene H. Lopes, Sali M.K. Farhan, Abdul Razzaq, Gilli Moshitzky, Mariana Brandão Prado, Flávio H. Beraldo, Andrzej Maciejewski, Robert Gros, Jue Fan, Wing‐Yiu Choy, David Greenberg, Vilma R. Martins, Martin L. Duennwald, Hermona Soreq, Vânia F. Prado, Marco A. M. Prado
Foilsithe / Cruthaithe 2018Pré-impressão -
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Modulation of hippocampal neuronal resilience during aging by the Hsp70/Hsp90 co‐chaperone STI1 de réir Rachel E. Lackie, Abdul Razzaq, Sali M.K. Farhan, Lily R. Qiu, Gilli Moshitzky, Flávio H. Beraldo, Marilene H. Lopes, Andrzej Maciejewski, Robert Gros, Jue Fan, Wing‐Yiu Choy, David Greenberg, Vilma R. Martins, Martin L. Duennwald, Jason P. Lerch, Hermona Soreq, Vânia F. Prado, Marco A. M. Prado
Foilsithe / Cruthaithe 2019Artigo -
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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease de réir Allison A. Dilliott, Sali M.K. Farhan, Mahdi Ghani, Christine Sato, Eric Liang, Ming Zhang, Adam D. McIntyre, Henian Cao, Lemuel Racacho, John F. Robinson, Michael J. Strong, Mario Masellis, Dennis E. Bulman, Ekaterina Rogaeva, Anthony E. Lang, Maria Carmela Tartaglia, Elizabeth Finger, Lorne Zinman, John Turnbull, Morris Freedman, Rick Swartz, Sandra E. Black, Robert A. Hegele
Foilsithe / Cruthaithe 2018Artigo -
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The Neurodegenerative Disease Knowledge Portal de réir Allison A. Dilliott, Maria C. Costanzo, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Bradford Casey, Quy Hoang, Hirotaka Iwaki, Dongkeun Jang, Jonggeol Jeffrey Kim, Hampton L. Leonard, Kristin Levine, Mary B. Makarious, Trang Thi Huyen Nguyen, Guy A. Rouleau, Andrew Singleton, Patrick Smadbeck, Justin Solle, Dan Vitale, Mike A. Nalls, Jason Flannick, Noël P. Burtt, Sali M.K. Farhan
Foilsithe / Cruthaithe 2025Revisão -
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The Ontario Neurodegenerative Disease Research Initiative (ONDRI) de réir Sali M.K. Farhan, Robert Bartha, Sandra E. Black, Dale Corbett, Elizabeth Finger, Morris Freedman, Barry Greenberg, David A. Grimes, Robert A. Hegele, Chris Hudson, Peter Kleinstiver, Anthony E. Lang, Mario Masellis, William E. McIlroy, Paula McLaughlin, Manuel Montero‐Odasso, David G. Munoz, Douglas P. Munoz, Stephen C. Strother, Richard H. Swartz, Sean Symons, Maria Carmela Tartaglia, Lorne Zinman, Michael J. Strong
Foilsithe / Cruthaithe 2016Artigo -
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Targeting Tau Mitigates Mitochondrial Fragmentation and Oxidative Stress in Amyotrophic Lateral Sclerosis de réir Tiziana Petrozziello, Evan A. Bordt, Alexandra N. Mills, Spencer E. Kim, Ellen Sapp, Benjamin A. Devlin, Abigail A. Obeng-Marnu, Sali M.K. Farhan, Ana C. Amaral, Simon Dujardin, Patrick M. Dooley, Christopher M. Henstridge, Derek H. Oakley, Andreas Neueder, Bradley T. Hyman, Tara L. Spires‐Jones, Staci D. Bilbo, Khashayar Vakili, Merit Cudkowicz, James Berry, Marian DiFiglia, M. Catarina Silva, Stephen J. Haggarty, Ghazaleh Sadri‐Vakili
Foilsithe / Cruthaithe 2021Artigo -
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An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2 de réir Koen C. Demaegd, Aoife Kernan, Johnathan Cooper‐Knock, Joke J.F.A. van Vugt, Calum Harvey, Tobias Moll, David O’Brien, Sarah Gornall, Luke Drury, Sali M.K. Farhan, Patrick A. Dion, Guy A. Rouleau, Andrea Western, Paul J. Parsons, Bruce McLean, Michael Benatar, Leonard H. van den Berg, Philip Van Damme, Jan Willem Dankbaar, Jeroen Hendrikse, Wouter Koole, Charlotte de Bie, Esther Hobson, Jan H. Veldink, Bart van de Warrenburg, R. Jeroen Pasterkamp, Wouter van Rheenen, Janine Kirby, Pamela J. Shaw, Michael A. van Es
Foilsithe / Cruthaithe 2025Artigo -
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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein de réir Sali M.K. Farhan, Daniel P. Howrigan, Liam Abbott, Joseph R. Klim, Simon Topp, Andrea Byrnes, Claire Churchhouse, Hemali Phatnani, Bradley Smith, Evadnie Rampersaud, Gang Wu, Joanne Wuu, Aleksey Shatunov, Alfredo Iacoangeli, Ahmad Al Khleifat, Daniel A. Mordes, Sulagna Ghosh, Kevin Eggan, Rosa Rademakers, Jacob L. McCauley, Rebecca Schüle, Stephan Züchner, Michael Benatar, J. Paul Taylor, Michael A. Nalls, Marc Gotkine, Pamela J. Shaw, Karen Morrison, Ammar Al‐Chalabi, Bryan J. Traynor, Christopher E. Shaw, David B. Goldstein, Matthew B. Harms, Mark J. Daly, Benjamin M. Neale
Foilsithe / Cruthaithe 2019Artigo -
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Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implications de réir Alfredo Iacoangeli, Allison A. Dilliott, Ahmad Al Khleifat, Peter M. Andersen, A. Nazlı Başak, Johnathan Cooper‐Knock, Philippe Corcia, Philippe Couratier, Mamede de Carvalho, Vivian E. Drory, Jonathan D. Glass, Marc Gotkine, Yosef M Lerner, Orla Hardiman, John E. Landers, Russell L. McLaughlin, Jesús S. Mora Pardina, Karen Morrison, Susana Pinto, Mónica Povedano, Christopher E. Shaw, Pamela J. Shaw, Vincenzo Silani, Nicola Ticozzi, Philip Van Damme, Leonard H. van den Berg, Patrick Vourc’h, Markus Weber, Jan H. Veldink, Richard Dobson, Guy A. Rouleau, Ammar Al‐Chalabi, Sali M.K. Farhan
Foilsithe / Cruthaithe 2025Artigo -
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Clinical testing panels for ALS: global distribution, consistency, and challenges de réir Allison A. Dilliott, Ahmad Al Nasser, Marwa Elnageeb, Jennifer A. Fifita, Lyndal Henden, Ingrid M. Keseler, Steven Lenz, Heather Marriott, Emily P. McCann, Maysen Mesaros, Sarah Opie-Martin, Emma Owens, Brooke Palus, Justyne Ross, Zhanjun Wang, Hannah L. White, Ammar Al‐Chalabi, Peter M. Andersen, Michael Benatar, Ian P. Blair, Johnathan Cooper‐Knock, Luke Drury, Elizabeth A. Harrington, Jeannine M. Heckmann, John E. Landers, Cristiane Araújo Martins Moreno, Melissa Nel, Evadnie Rampersaud, Jennifer Roggenbuck, Guy A. Rouleau, Bryan J. Traynor, Marka van Blitterswijk, Wouter van Rheenen, Jan H. Veldink, Jochen H. Weishaupt, Matthew Harms, Sali M.K. Farhan
Foilsithe / Cruthaithe 2022Pré-impressão -
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Clinical testing panels for ALS: global distribution, consistency, and challenges de réir Allison A. Dilliott, Ahmad Al Nasser, Marwa Elnagheeb, Jennifer A. Fifita, Lyndal Henden, Ingrid M. Keseler, Steven Lenz, Heather Marriott, Emily P. McCann, Maysen Mesaros, Sarah Opie-Martin, Emma Owens, Brooke Palus, Justyne Ross, Zhanjun Wang, Hannah L. White, Ammar Al‐Chalabi, Peter M. Andersen, Michael Benatar, Ian P. Blair, Johnathan Cooper‐Knock, Elizabeth A. Harrington, Jeannine M. Heckmann, John E. Landers, Cristiane Araújo Martins Moreno, Melissa Nel, Evadnie Rampersaud, Jennifer Roggenbuck, Guy A. Rouleau, Bryan J. Traynor, Marka van Blitterswijk, Wouter van Rheenen, Jan H. Veldink, Jochen H. Weishaupt, Luke Drury, Matthew B. Harms, Sali M.K. Farhan
Foilsithe / Cruthaithe 2023Revisão -
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Human genetics and neuropathology suggest a link between miR-218 and amyotrophic lateral sclerosis pathophysiology de réir Irit Reichenstein, Chen Eitan, Sandra Díaz-García, Guy Haim, Iddo Magen, Aviad Siany, Mariah L. Hoye, Natali Rivkin, Tsviya Olender, Beáta Tóth, 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 Araújo Martins Moreno, Giancarlo Costaguta, Kristel R. van Eijk, Hemali Phatnani, Ammar Al‐Chalabi, A. Nazlı Başak, Leonard H. van den Berg, Orla Hardiman, John E. Landers, Jesús S. Mora, Karen Morrison, Pamela J. Shaw, Jan H. Veldink, Samuel L. Pfaff, Ofer Yizhar, Christina Groß, Robert H. Brown, John Ravits, Matthew Harms, Timothy M. Miller, Eran Hornstein
Foilsithe / Cruthaithe 2019Artigo -
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Association of plasma biomarkers with cognition, cognitive decline, and daily function across and within neurodegenerative diseases: Results from the Ontario Neurodegenerative Dise... de réir Erlan Sanchez, Tim Wilkinson, Gillian Coughlan, Saira Saeed Mirza, Andrée‐Ann Baril, Joel Ramirez, Malcolm A. Binns, Sandra E. Black, Michael Borrie, Allison A. Dilliott, Roger A. Dixon, Dar Dowlatshahi, Sali M.K. Farhan, Elizabeth Finger, Corinne E. Fischer, Andrew Frank, Morris Freedman, Rafaella A. Gonçalves, David A. Grimes, Ayman Hassan, Robert A. Hegele, Sanjeev Kumar, Anthony E. Lang, Connie Marras, Paula McLaughlin, J. B. Orange, Stephen Pasternak, Bruce G. Pollock, Tarek K. Rajji, Angela Roberts, John F. Robinson, Ekaterina Rogaeva, Demetrios J. Sahlas, Gustavo Saposnik, Michael J. Strong, Richard H. Swartz, David F. Tang‐Wai, Maria Carmela Tartaglia, Angela K. Troyer, Hlin Kvartsberg, Henrik Zetterberg, Douglas P. Munoz, Mario Masellis
Foilsithe / Cruthaithe 2023Artigo -
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Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3′UTR protect against ALS de réir 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 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 H. Veldink, Johnathan Cooper‐Knock, Kevin P. Kenna, Philip Van Damme, Leonard H. van den Berg, Eran Hornstein, Eran Hornstein
Foilsithe / Cruthaithe 2022Artigo -
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Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis de réir Sai Zhang, Johnathan Cooper‐Knock, Annika K. Weimer, Minyi Shi, Tobias Moll, Jack N.G. Marshall, Calum Harvey, Helia Ghahremani Nezhad, John Franklin, Cleide Dos Santos Souza, Ke Ning, Cheng Wang, Jingjing Li, Allison A. Dilliott, Sali M.K. Farhan, Eran Elhaik, Iris-Stefania Pasniceanu, Matthew R. Livesey, Chen Eitan, Eran Hornstein, Kevin P. Kenna, Jan H. Veldink, Laura Ferraiuolo, Pamela J. Shaw, M Snyder, Ian P. Blair, Naomi R. Wray, Matthew C. Kiernan, Miguel Mitne‐Neto, Adriano Chió, Ruben J. Cauchi, Wim Robberecht, Philip Van Damme, Philippe Corcia, 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, Mònica 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
Foilsithe / Cruthaithe 2022Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Disease
Medicine
Biology
Pathology
Genetics
Amyotrophic lateral sclerosis
Gene
Internal medicine
Neuroscience
Neurodegeneration
Cell biology
Dementia
Frontotemporal dementia
Bioinformatics
Genetic testing
Heat shock protein
Chaperone (clinical)
Cognition
Computational biology
Environmental health
Exome sequencing
Hsp90
Population
Psychology
SOD1
Allele
C9orf72
Cognitive decline
Computer science
Economic growth