نتائج البحث - Allison A. Dilliott
- يعرض 1 - 12 نتائج من 12
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Enhancing Variant of Uncertain Significance (VUS) Interpretation in Neurogenetics: Collaborative Experiences from a Tertiary Care Centre حسب 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
منشور في 2024Pré-impressão -
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Enhancing variant of uncertain significance (VUS) interpretation in neurogenetics: collaborative experiences from a tertiary care centre حسب 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
منشور في 2024Artigo -
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Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically حسب Jian Wang, Jacqueline S. Dron, Matthew R. Ban, John F. Robinson, Adam D. McIntyre, Maher Alazzam, Pei Zhao, Allison A. Dilliott, Henian Cao, Murray W. Huff, David Rhainds, Cécile Low‐Kam, Marie‐Pierre Dubé, Guillaume Lettre, Jean‐Claude Tardif, Robert A. Hegele
منشور في 2016Artigo -
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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease حسب 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
منشور في 2018Artigo -
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The Neurodegenerative Disease Knowledge Portal حسب 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
منشور في 2025Revisão -
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Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implications حسب 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
منشور في 2025Artigo -
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Clinical testing panels for ALS: global distribution, consistency, and challenges حسب 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
منشور في 2022Pré-impressão -
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Clinical testing panels for ALS: global distribution, consistency, and challenges حسب 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
منشور في 2023Revisão -
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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... حسب 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
منشور في 2023Artigo -
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Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis حسب 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
منشور في 2022Artigo -
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Cognitive correlates of antisaccade behaviour across multiple neurodegenerative diseases حسب Heidi C. Riek, Donald C. Brien, Brian C. Coe, Jeff Huang, Julia E. Perkins, Rachel Yep, Paula McLaughlin, J. B. Orange, Alicia Peltsch, Angela Roberts, Malcolm A. Binns, Wendy Lou, Agessandro Abrahão, Stephen R. Arnott, Derek Beaton, Sandra E. Black, Dar Dowlatshahi, Elizabeth Finger, Corinne E. Fischer, Andrew Frank, David A. Grimes, Sanjeev Kumar, Anthony E. Lang, Jane M. Lawrence‐Dewar, Jennifer Mandzia, Connie Marras, Mario Masellis, Stephen Pasternak, Bruce G. Pollock, Tarek K. Rajji, Demetrios J. Sahlas, Gustavo Saposnik, Dallas Seitz, Christen Shoesmith, Thomas Steeves, Stephen C. Strother, Kelly M. Sunderland, Richard H. Swartz, Brian Tan, David F. Tang‐Wai, Maria Carmela Tartaglia, John Turnbull, Lorne Zinman, Douglas P. Munoz, Sabrina Adamo, Robert Bartha, Courtney Berezuk, Alanna Black, Michael Borrie, Susan E. Bronskill, Dennis E. Bulman, Leanne K. Casaubon, Ben Cornish, Sherif Defrawy, Allison A. Dilliott, Roger A. Dixon, Sali M.K. Farhan, Frederico Faria, Julia Fraser, Morris Freedman, Mahdi Ghani, Barry Greenberg, Hassan Haddad, Ayman Hassan, Wendy Hatch, Rob Hegele, Melissa F. Holmes, Chris Hudson, Mandar Jog, Peter Kleinstiver, Donna Kwan, Elena Leontieva, Brian Levine, Efrem D. Mandelcorn, Ed Margolin, Bill McIlroy, Manuel Montero‐Odasso, David G. Munoz, Nuwan D. Nanayakkara, Miracle Ozzoude, Joel Ramirez, Natalie Rashkovan, John F. Robinson, Ekaterina Rogaeva, Yanina Sarquis Adamson, Christopher J.M. Scott, Michael J. Strong, Sujeevini Sujanthan, Sean Symons, Athena Theyers, Angela K. Troyer, Karen Van Ooteghem, John Woulfe, Mojdeh Zamyadi
منشور في 2023Artigo
أدوات البحث:
موضوعات ذات صلة
Medicine
Disease
Biology
Internal medicine
Pathology
Genetics
Amyotrophic lateral sclerosis
Bioinformatics
Genetic testing
Neuroscience
Computational biology
Dementia
Frontotemporal dementia
Gene
Cognition
Cognitive decline
Computer science
Economic growth
Economics
Environmental health
Family medicine
Gene expression
Genetic counseling
Genome
Genomics
Health care
Multidisciplinary approach
Neurogenetics
Population
Psychiatry