Sarah Tabrizi (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sarah Tabrizi" in English language version.

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52nih.gov

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acmedsci.ac.uk

"Fellow - Academy of Medical Sciences". www.acmedsci.ac.uk.

aopgbi.org

"Programme and Speakers - AoPGBI". Retrieved 24 June 2022.

bbc.co.uk

Gallagher, James (11 December 2017). "Huntington's breakthrough may stop disease". bbc.co.uk.

doi.org

Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Deriziotis, Pelagia; André, Ralph; Smith, David M; Goold, Rob; Kinghorn, Kerri J; Kristiansen, Mark; Nathan, James A; Rosenzweig, Rina; Krutauz, Dasha; Glickman, Michael H; Collinge, John; Goldberg, Alfred L; Tabrizi, Sarah J (8 July 2011). "Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry". The EMBO Journal. 30 (15): 3065–3077. doi:10.1038/emboj.2011.224. PMC 3160194. PMID 21743439.
Kristiansen, Mark; Messenger, Marcus J.; Klöhn, Peter-Christian; Brandner, Sebastian; Wadsworth, Jonathan D. F.; Collinge, John; Tabrizi, Sarah J. (18 November 2005). "Disease-related Prion Protein Forms Aggresomes in Neuronal Cells Leading to Caspase Activation and Apoptosis". Journal of Biological Chemistry. 280 (46): 38851–38861. doi:10.1074/jbc.M506600200. PMID 16157591.
Kristiansen, Mark; Deriziotis, Pelagia; Dimcheff, Derek E.; Jackson, Graham S.; Ovaa, Huib; Naumann, Heike; Clarke, Anthony R.; van Leeuwen, Fijs W.B.; Menéndez-Benito, Victoria; Dantuma, Nico P.; Portis, John L.; Collinge, John; Tabrizi, Sarah J. (April 2007). "Disease-Associated Prion Protein Oligomers Inhibit the 26S Proteasome". Molecular Cell. 26 (2): 175–188. doi:10.1016/j.molcel.2007.04.001. hdl:11858/00-001M-0000-0012-2650-5. PMID 17466621.
Goold, R.; Rabbanian, S.; Sutton, L.; Andre, R.; Arora, P.; Moonga, J.; Clarke, A.R.; Schiavo, G.; Jat, P.; Collinge, J.; Tabrizi, S.J. (19 April 2011). "Rapid cell-surface prion protein conversion revealed using a novel cell system". Nature Communications. 2 (1): 281–. Bibcode:2011NatCo...2..281G. doi:10.1038/ncomms1282. PMC 3104518. PMID 21505437.
McKinnon, Chris; Goold, Rob; Andre, Ralph; Devoy, Anny; Ortega, Zaira; Moonga, Julie; Linehan, Jacqueline M.; Brandner, Sebastian; Lucas, José J.; Collinge, John; Tabrizi, Sarah J. (8 December 2015). "Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin–proteasome system". Acta Neuropathologica. 131 (3): 411–425. doi:10.1007/s00401-015-1508-y. PMC 4752964. PMID 26646779.
Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Mohammadi, Dara (July 2015). "Fast-forwarding treatment for neurodegenerative disorders". The Lancet Neurology. 14 (7): 687–688. doi:10.1016/S1474-4422(15)00110-6. PMID 26067120.
Deriziotis, Pelagia; André, Ralph; Smith, David M; Goold, Rob; Kinghorn, Kerri J; Kristiansen, Mark; Nathan, James A; Rosenzweig, Rina; Krutauz, Dasha; Glickman, Michael H; Collinge, John (8 July 2011). "Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry". The EMBO Journal. 30 (15): 3065–3077. doi:10.1038/emboj.2011.224. ISSN 0261-4189. PMC 3160194. PMID 21743439.
Kristiansen, Mark; Deriziotis, Pelagia; Dimcheff, Derek E.; Jackson, Graham S.; Ovaa, Huib; Naumann, Heike; Clarke, Anthony R.; van Leeuwen, Fijs W.B.; Menéndez-Benito, Victoria; Dantuma, Nico P.; Portis, John L. (April 2007). "Disease-Associated Prion Protein Oligomers Inhibit the 26S Proteasome". Molecular Cell. 26 (2): 175–188. doi:10.1016/j.molcel.2007.04.001. hdl:11858/00-001M-0000-0012-2650-5. PMID 17466621.
Kristiansen, Mark; Messenger, Marcus J.; Klöhn, Peter-Christian; Brandner, Sebastian; Wadsworth, Jonathan D. F.; Collinge, John; Tabrizi, Sarah J. (18 November 2005). "Disease-related Prion Protein Forms Aggresomes in Neuronal Cells Leading to Caspase Activation and Apoptosis". Journal of Biological Chemistry. 280 (46): 38851–38861. doi:10.1074/jbc.M506600200. ISSN 0021-9258. PMID 16157591.
Björkqvist, Maria; Wild, Edward J; Thiele, Jenny; Silvestroni, Aurelio; Andre, Ralph; Lahiri, Nayana; Raibon, Elsa; Lee, Richard V; Benn, Caroline L; Soulet, Denis; Magnusson, Anna; Woodman, Ben; Landles, Christian; Pouladi, Mahmoud A; Hayden, Michael R; Khalili-Shirazi, Azadeh; Lowdell, Mark W; Brundin, Patrik; Bates, Gillian P; Leavitt, Blair R; Möller, Thomas; Tabrizi, Sarah J (2008). "A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease". The Journal of Experimental Medicine. 205 (8): 1869–77. doi:10.1084/jem.20080178. PMC 2525598. PMID 18625748.
Weiss, Andreas; Träger, Ulrike; Wild, Edward J; Grueninger, Stephan; Farmer, Ruth; Landles, Christian; Scahill, Rachael I; Lahiri, Nayana; Haider, Salman; MacDonald, Douglas; Frost, Chris; Bates, Gillian P; Bilbe, Graeme; Kuhn, Rainer; Andre, Ralph; Tabrizi, Sarah J (2012). "Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression". Journal of Clinical Investigation. 122 (10): 3731–6. doi:10.1172/jci64565. PMC 3461928. PMID 22996692.
Tabrizi, Sarah J; Langbehn, Douglas R; Leavitt, Blair R; Roos, Raymund AC; Durr, Alexandra; Craufurd, David; Kennard, Christopher; Hicks, Stephen L; Fox, Nick C; Scahill, Rachael I; Borowsky, Beth; Tobin, Allan J; Rosas, H Diana; Johnson, Hans; Reilmann, Ralf; Landwehrmeyer, Bernhard; Stout, Julie C (2009). "Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: Cross-sectional analysis of baseline data". The Lancet Neurology. 8 (9): 791–801. doi:10.1016/s1474-4422(09)70170-x. PMC 3725974. PMID 19646924.
Tabrizi, Sarah J; Scahill, Rachael I; Durr, Alexandra; Roos, Raymund AC; Leavitt, Blair R; Jones, Rebecca; Landwehrmeyer, G Bernhard; Fox, Nick C; Johnson, Hans; Hicks, Stephen L; Kennard, Christopher; Craufurd, David; Frost, Chris; Langbehn, Douglas R; Reilmann, Ralf; Stout, Julie C; TRACK-HD Investigators (2011). "Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: The 12-month longitudinal analysis". The Lancet Neurology. 10 (1): 31–42. doi:10.1016/s1474-4422(10)70276-3. PMID 21130037. S2CID 2602096.
Tabrizi, Sarah J; Reilmann, Ralf; Roos, Raymund AC; Durr, Alexandra; Leavitt, Blair; Owen, Gail; Jones, Rebecca; Johnson, Hans; Craufurd, David; Hicks, Stephen L; Kennard, Christopher; Landwehrmeyer, Bernhard; Stout, Julie C; Borowsky, Beth; Scahill, Rachael I; Frost, Chris; Langbehn, Douglas R; TRACK-HD investigators (2012). "Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: Analysis of 24 month observational data". The Lancet Neurology. 11 (1): 42–53. doi:10.1016/s1474-4422(11)70263-0. PMID 22137354. S2CID 34929053.
Tabrizi, Sarah J; Scahill, Rachael I; Owen, Gail; Durr, Alexandra; Leavitt, Blair R; Roos, Raymund A; Borowsky, Beth; Landwehrmeyer, Bernhard; Frost, Chris; Johnson, Hans; Craufurd, David; Reilmann, Ralf; Stout, Julie C; Langbehn, Douglas R (2013). "Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: Analysis of 36-month observational data". The Lancet Neurology. 12 (7): 637–49. doi:10.1016/s1474-4422(13)70088-7. PMID 23664844. S2CID 12204298.
Klöppel, Stefan; Gregory, Sarah; Scheller, Elisa; Minkova, Lora; Razi, Adeel; Durr, Alexandra; Roos, Raymund A.C; Leavitt, Blair R; Papoutsi, Marina; Landwehrmeyer, G. Bernhard; Reilmann, Ralf; Borowsky, Beth; Johnson, Hans; Mills, James A; Owen, Gail; Stout, Julie; Scahill, Rachael I; Long, Jeffrey D; Rees, Geraint; Tabrizi, Sarah J (2015). "Compensation in Preclinical Huntington's Disease: Evidence from the Track-On HD Study". eBioMedicine. 2 (10): 1420–9. doi:10.1016/j.ebiom.2015.08.002. PMC 4634199. PMID 26629536.
Gregory, Sarah; Long, Jeffrey D; Klöppel, Stefan; Razi, Adeel; Scheller, Elisa; Minkova, Lora; Papoutsi, Marina; Mills, James A; Durr, Alexandra; Leavitt, Blair R; Roos, Raymund A. C; Stout, Julie C; Scahill, Rachael I; Langbehn, Douglas R; Tabrizi, Sarah J; Rees, Geraint (2017). "Operationalizing compensation over time in neurodegenerative disease". Brain. 140 (4): 1158–1165. doi:10.1093/brain/awx022. PMC 5382953. PMID 28334888.
Gregory, Sarah; Long, Jeffrey D; Klöppel, Stefan; Razi, Adeel; Scheller, Elisa; Minkova, Lora; Johnson, Eileanoir B; Durr, Alexandra; Roos, Raymund A C; Leavitt, Blair R; Mills, James A; Stout, Julie C; Scahill, Rachael I; Tabrizi, Sarah J; Rees, Geraint; Coleman, A; Decolongon, J; Fan, M; Koren, T; Leavitt, B; Durr, A; Jauffret, C; Justo, D; Lehericy, S; Nigaud, K; Valabrègue, R; Roos, R; Hart, E P 't; Schoonderbeek, A; et al. (2018). "Testing a longitudinal compensation model in premanifest Huntington's disease". Brain. 141 (7): 2156–2166. doi:10.1093/brain/awy122. PMC 6022638. PMID 29788038.
Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/s0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Arney, Kat (2018). "Improved metrics for Huntington's disease trials". Nature. 557 (7707): S46–S47. Bibcode:2018Natur.557S..46A. doi:10.1038/d41586-018-05179-w. PMID 29844554. S2CID 256768548.
Moss, Davina J Hensman; Pardiñas, Antonio F; Langbehn, Douglas; Lo, Kitty; Leavitt, Blair R; Roos, Raymund; Durr, Alexandra; Mead, Simon; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J; Coleman, A; Santos, R Dar; Decolongon, J; Sturrock, A; Bardinet, E; Ret, C Jauff; Justo, D; Lehericy, S; Marelli, C; Nigaud, K; Valabrègue, R; Van Den Bogaard, SJA; Dumas, E M; Van Der Grond, J; t'Hart, EP; Jurgens, C; Witjes-Ane, M-N; Arran, N; et al. (2017). "Identification of genetic variants associated with Huntington's disease progression: A genome-wide association study" (PDF). The Lancet Neurology. 16 (9): 701–711. doi:10.1016/s1474-4422(17)30161-8. PMID 28642124. S2CID 588163.
Flower, Michael; Lomeikaite, Vilija; Ciosi, Marc; Cumming, Sarah; Morales, Fernando; Lo, Kitty; Hensman Moss, Davina; Jones, Lesley; Holmans, Peter; Monckton, Darren G.; Tabrizi, Sarah J. (1 July 2019). "MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1". Brain. 142 (7): 1876–1886. doi:10.1093/brain/awz115. ISSN 0006-8950. PMC 6598626. PMID 31216018.
Tabrizi, Sarah J.; Estevez-Fraga, Carlos; van Roon-Mom, Willeke M. C.; Flower, Michael D.; Scahill, Rachael I.; Wild, Edward J.; Muñoz-Sanjuan, Ignacio; Sampaio, Cristina; Rosser, Anne E.; Leavitt, Blair R. (July 2022). "Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities". The Lancet. Neurology. 21 (7): 645–658. doi:10.1016/S1474-4422(22)00121-1. ISSN 1474-4465. PMC 7613206. PMID 35716694.
Goold, Robert; Flower, Michael; Moss, Davina Hensman; Medway, Chris; Wood-Kaczmar, Alison; Andre, Ralph; Farshim, Pamela; Bates, Gill P; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J (15 February 2019). "FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat". Human Molecular Genetics. 28 (4): 650–661. doi:10.1093/hmg/ddy375. ISSN 0964-6906. PMC 6360275. PMID 30358836.
Goold, Robert; Hamilton, Joseph; Menneteau, Thomas; Flower, Michael; Bunting, Emma L.; Aldous, Sarah G.; Porro, Antonio; Vicente, José R.; Allen, Nicholas D.; Wilkinson, Hilary; Bates, Gillian P.; Sartori, Alessandro A.; Thalassinos, Konstantinos; Balmus, Gabriel; Tabrizi, Sarah J. (August 2021). "FAN1 controls mismatch repair complex assembly via MLH1 retention to stabilize CAG repeat expansion in Huntington's disease". Cell Reports. 36 (9): 109649. doi:10.1016/j.celrep.2021.109649. PMC 8424649. PMID 34469738.
Tabrizi, Sarah J.; Flower, Michael D.; Ross, Christopher A.; Wild, Edward J. (October 2020). "Huntington disease: new insights into molecular pathogenesis and therapeutic opportunities". Nature Reviews Neurology. 16 (10): 529–546. doi:10.1038/s41582-020-0389-4. ISSN 1759-4758. PMID 32796930. S2CID 221129777.
Drew, Liam (2018). "How the gene behind Huntington's disease could be neutralized". Nature. 557 (7707): S39–S41. Bibcode:2018Natur.557S..39D. doi:10.1038/d41586-018-05176-z. PMID 29844556. S2CID 256768090.
Tabrizi, Sarah J.; Leavitt, Blair R.; Landwehrmeyer, G. Bernhard; Wild, Edward J.; Saft, Carsten; Barker, Roger A.; Blair, Nick F.; Craufurd, David; Priller, Josef (6 May 2019). "Targeting Huntingtin Expression in Patients with Huntington's Disease" (PDF). New England Journal of Medicine. 380 (24): 2307–2316. doi:10.1056/NEJMoa1900907. ISSN 0028-4793. PMID 31059641.
Leavitt, Blair R.; Tabrizi, Sarah J. (27 March 2020). "Antisense oligonucleotides for neurodegeneration". Science. 367 (6485): 1428–1429. Bibcode:2020Sci...367.1428L. doi:10.1126/science.aba4624. ISSN 0036-8075. PMID 32217715. S2CID 214671177.
Tabrizi, Sarah J; Estevez-Fraga, Carlos; van Roon-Mom, Willeke M C; Flower, Michael D; Scahill, Rachael I; Wild, Edward J; Muñoz-Sanjuan, Ignacio; Sampaio, Cristina; Rosser, Anne E; Leavitt, Blair R (July 2022). "Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities". The Lancet Neurology. 21 (7): 645–658. doi:10.1016/S1474-4422(22)00121-1. PMC 7613206. PMID 35716694.
Scahill, Rachael I; Zeun, Paul; Osborne-Crowley, Katherine; Johnson, Eileanoir B; Gregory, Sarah; Parker, Christopher; Lowe, Jessica; Nair, Akshay; O'Callaghan, Claire; Langley, Christelle; Papoutsi, Marina (June 2020). "Biological and clinical characteristics of gene carriers far from predicted onset in the Huntington's disease Young Adult Study (HD-YAS): a cross-sectional analysis". The Lancet Neurology. 19 (6): 502–512. doi:10.1016/S1474-4422(20)30143-5. PMC 7254065. PMID 32470422.
Tabrizi, Sarah J.; Schobel, Scott; Gantman, Emily C.; Mansbach, Alexandra; Borowsky, Beth; Konstantinova, Pavlina; Mestre, Tiago A.; Panagoulias, Jennifer; Ross, Christopher A.; Zauderer, Maurice; Mullin, Ariana P.; Romero, Klaus; Sivakumaran, Sudhir; Turner, Emily C.; Long, Jeffrey D. (July 2022). "A biological classification of Huntington's disease: the Integrated Staging System". The Lancet. Neurology. 21 (7): 632–644. doi:10.1016/S1474-4422(22)00120-X. ISSN 1474-4465. PMID 35716693. S2CID 249682267.
Shetty, Priya (2 June 2012). "Sarah Tabrizi: tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. ISSN 0140-6736. PMID 22656876. S2CID 40222846.
Burton, Adrian (2018). "Sarah Tabrizi: Timed to perfection". The Lancet Neurology. 17 (2): 117. doi:10.1016/s1474-4422(17)30303-4. PMID 28916420.

ed.ac.uk

pure.ed.ac.uk

Tabrizi, Sarah J.; Leavitt, Blair R.; Landwehrmeyer, G. Bernhard; Wild, Edward J.; Saft, Carsten; Barker, Roger A.; Blair, Nick F.; Craufurd, David; Priller, Josef (6 May 2019). "Targeting Huntingtin Expression in Patients with Huntington's Disease" (PDF). New England Journal of Medicine. 380 (24): 2307–2316. doi:10.1056/NEJMoa1900907. ISSN 0028-4793. PMID 31059641.

google.co.uk

scholar.google.co.uk

"Sarah J Tabrizi - Google Scholar Citations". scholar.google.co.uk.

handle.net

hdl.handle.net

Kristiansen, Mark; Deriziotis, Pelagia; Dimcheff, Derek E.; Jackson, Graham S.; Ovaa, Huib; Naumann, Heike; Clarke, Anthony R.; van Leeuwen, Fijs W.B.; Menéndez-Benito, Victoria; Dantuma, Nico P.; Portis, John L.; Collinge, John; Tabrizi, Sarah J. (April 2007). "Disease-Associated Prion Protein Oligomers Inhibit the 26S Proteasome". Molecular Cell. 26 (2): 175–188. doi:10.1016/j.molcel.2007.04.001. hdl:11858/00-001M-0000-0012-2650-5. PMID 17466621.
Kristiansen, Mark; Deriziotis, Pelagia; Dimcheff, Derek E.; Jackson, Graham S.; Ovaa, Huib; Naumann, Heike; Clarke, Anthony R.; van Leeuwen, Fijs W.B.; Menéndez-Benito, Victoria; Dantuma, Nico P.; Portis, John L. (April 2007). "Disease-Associated Prion Protein Oligomers Inhibit the 26S Proteasome". Molecular Cell. 26 (2): 175–188. doi:10.1016/j.molcel.2007.04.001. hdl:11858/00-001M-0000-0012-2650-5. PMID 17466621.

harvard.edu

ui.adsabs.harvard.edu

Goold, R.; Rabbanian, S.; Sutton, L.; Andre, R.; Arora, P.; Moonga, J.; Clarke, A.R.; Schiavo, G.; Jat, P.; Collinge, J.; Tabrizi, S.J. (19 April 2011). "Rapid cell-surface prion protein conversion revealed using a novel cell system". Nature Communications. 2 (1): 281–. Bibcode:2011NatCo...2..281G. doi:10.1038/ncomms1282. PMC 3104518. PMID 21505437.
Arney, Kat (2018). "Improved metrics for Huntington's disease trials". Nature. 557 (7707): S46–S47. Bibcode:2018Natur.557S..46A. doi:10.1038/d41586-018-05179-w. PMID 29844554. S2CID 256768548.
Drew, Liam (2018). "How the gene behind Huntington's disease could be neutralized". Nature. 557 (7707): S39–S41. Bibcode:2018Natur.557S..39D. doi:10.1038/d41586-018-05176-z. PMID 29844556. S2CID 256768090.
Leavitt, Blair R.; Tabrizi, Sarah J. (27 March 2020). "Antisense oligonucleotides for neurodegeneration". Science. 367 (6485): 1428–1429. Bibcode:2020Sci...367.1428L. doi:10.1126/science.aba4624. ISSN 0036-8075. PMID 32217715. S2CID 214671177.

iospress.nl

"Journal of Huntington's Disease". www.iospress.nl. Retrieved 13 June 2016.

itv.com

"Study provides 'vital insights' into best time to treat Huntington's disease". ITV News. 26 May 2020. Retrieved 30 November 2020.

jbc.org

Kristiansen, Mark; Messenger, Marcus J.; Klöhn, Peter-Christian; Brandner, Sebastian; Wadsworth, Jonathan D. F.; Collinge, John; Tabrizi, Sarah J. (18 November 2005). "Disease-related Prion Protein Forms Aggresomes in Neuronal Cells Leading to Caspase Activation and Apoptosis". Journal of Biological Chemistry. 280 (46): 38851–38861. doi:10.1074/jbc.M506600200. ISSN 0021-9258. PMID 16157591.

nature.com

Tabrizi, Sarah J.; Flower, Michael D.; Ross, Christopher A.; Wild, Edward J. (October 2020). "Huntington disease: new insights into molecular pathogenesis and therapeutic opportunities". Nature Reviews Neurology. 16 (10): 529–546. doi:10.1038/s41582-020-0389-4. ISSN 1759-4758. PMID 32796930. S2CID 221129777.

nih.gov

pubmed.ncbi.nlm.nih.gov

Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Deriziotis, Pelagia; André, Ralph; Smith, David M; Goold, Rob; Kinghorn, Kerri J; Kristiansen, Mark; Nathan, James A; Rosenzweig, Rina; Krutauz, Dasha; Glickman, Michael H; Collinge, John; Goldberg, Alfred L; Tabrizi, Sarah J (8 July 2011). "Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry". The EMBO Journal. 30 (15): 3065–3077. doi:10.1038/emboj.2011.224. PMC 3160194. PMID 21743439.
Kristiansen, Mark; Messenger, Marcus J.; Klöhn, Peter-Christian; Brandner, Sebastian; Wadsworth, Jonathan D. F.; Collinge, John; Tabrizi, Sarah J. (18 November 2005). "Disease-related Prion Protein Forms Aggresomes in Neuronal Cells Leading to Caspase Activation and Apoptosis". Journal of Biological Chemistry. 280 (46): 38851–38861. doi:10.1074/jbc.M506600200. PMID 16157591.
Kristiansen, Mark; Deriziotis, Pelagia; Dimcheff, Derek E.; Jackson, Graham S.; Ovaa, Huib; Naumann, Heike; Clarke, Anthony R.; van Leeuwen, Fijs W.B.; Menéndez-Benito, Victoria; Dantuma, Nico P.; Portis, John L.; Collinge, John; Tabrizi, Sarah J. (April 2007). "Disease-Associated Prion Protein Oligomers Inhibit the 26S Proteasome". Molecular Cell. 26 (2): 175–188. doi:10.1016/j.molcel.2007.04.001. hdl:11858/00-001M-0000-0012-2650-5. PMID 17466621.
Goold, R.; Rabbanian, S.; Sutton, L.; Andre, R.; Arora, P.; Moonga, J.; Clarke, A.R.; Schiavo, G.; Jat, P.; Collinge, J.; Tabrizi, S.J. (19 April 2011). "Rapid cell-surface prion protein conversion revealed using a novel cell system". Nature Communications. 2 (1): 281–. Bibcode:2011NatCo...2..281G. doi:10.1038/ncomms1282. PMC 3104518. PMID 21505437.
McKinnon, Chris; Goold, Rob; Andre, Ralph; Devoy, Anny; Ortega, Zaira; Moonga, Julie; Linehan, Jacqueline M.; Brandner, Sebastian; Lucas, José J.; Collinge, John; Tabrizi, Sarah J. (8 December 2015). "Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin–proteasome system". Acta Neuropathologica. 131 (3): 411–425. doi:10.1007/s00401-015-1508-y. PMC 4752964. PMID 26646779.
Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Mohammadi, Dara (July 2015). "Fast-forwarding treatment for neurodegenerative disorders". The Lancet Neurology. 14 (7): 687–688. doi:10.1016/S1474-4422(15)00110-6. PMID 26067120.
Deriziotis, Pelagia; André, Ralph; Smith, David M; Goold, Rob; Kinghorn, Kerri J; Kristiansen, Mark; Nathan, James A; Rosenzweig, Rina; Krutauz, Dasha; Glickman, Michael H; Collinge, John (8 July 2011). "Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry". The EMBO Journal. 30 (15): 3065–3077. doi:10.1038/emboj.2011.224. ISSN 0261-4189. PMC 3160194. PMID 21743439.
Kristiansen, Mark; Deriziotis, Pelagia; Dimcheff, Derek E.; Jackson, Graham S.; Ovaa, Huib; Naumann, Heike; Clarke, Anthony R.; van Leeuwen, Fijs W.B.; Menéndez-Benito, Victoria; Dantuma, Nico P.; Portis, John L. (April 2007). "Disease-Associated Prion Protein Oligomers Inhibit the 26S Proteasome". Molecular Cell. 26 (2): 175–188. doi:10.1016/j.molcel.2007.04.001. hdl:11858/00-001M-0000-0012-2650-5. PMID 17466621.
Kristiansen, Mark; Messenger, Marcus J.; Klöhn, Peter-Christian; Brandner, Sebastian; Wadsworth, Jonathan D. F.; Collinge, John; Tabrizi, Sarah J. (18 November 2005). "Disease-related Prion Protein Forms Aggresomes in Neuronal Cells Leading to Caspase Activation and Apoptosis". Journal of Biological Chemistry. 280 (46): 38851–38861. doi:10.1074/jbc.M506600200. ISSN 0021-9258. PMID 16157591.
Björkqvist, Maria; Wild, Edward J; Thiele, Jenny; Silvestroni, Aurelio; Andre, Ralph; Lahiri, Nayana; Raibon, Elsa; Lee, Richard V; Benn, Caroline L; Soulet, Denis; Magnusson, Anna; Woodman, Ben; Landles, Christian; Pouladi, Mahmoud A; Hayden, Michael R; Khalili-Shirazi, Azadeh; Lowdell, Mark W; Brundin, Patrik; Bates, Gillian P; Leavitt, Blair R; Möller, Thomas; Tabrizi, Sarah J (2008). "A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease". The Journal of Experimental Medicine. 205 (8): 1869–77. doi:10.1084/jem.20080178. PMC 2525598. PMID 18625748.
Weiss, Andreas; Träger, Ulrike; Wild, Edward J; Grueninger, Stephan; Farmer, Ruth; Landles, Christian; Scahill, Rachael I; Lahiri, Nayana; Haider, Salman; MacDonald, Douglas; Frost, Chris; Bates, Gillian P; Bilbe, Graeme; Kuhn, Rainer; Andre, Ralph; Tabrizi, Sarah J (2012). "Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression". Journal of Clinical Investigation. 122 (10): 3731–6. doi:10.1172/jci64565. PMC 3461928. PMID 22996692.
Tabrizi, Sarah J; Langbehn, Douglas R; Leavitt, Blair R; Roos, Raymund AC; Durr, Alexandra; Craufurd, David; Kennard, Christopher; Hicks, Stephen L; Fox, Nick C; Scahill, Rachael I; Borowsky, Beth; Tobin, Allan J; Rosas, H Diana; Johnson, Hans; Reilmann, Ralf; Landwehrmeyer, Bernhard; Stout, Julie C (2009). "Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: Cross-sectional analysis of baseline data". The Lancet Neurology. 8 (9): 791–801. doi:10.1016/s1474-4422(09)70170-x. PMC 3725974. PMID 19646924.
Tabrizi, Sarah J; Scahill, Rachael I; Durr, Alexandra; Roos, Raymund AC; Leavitt, Blair R; Jones, Rebecca; Landwehrmeyer, G Bernhard; Fox, Nick C; Johnson, Hans; Hicks, Stephen L; Kennard, Christopher; Craufurd, David; Frost, Chris; Langbehn, Douglas R; Reilmann, Ralf; Stout, Julie C; TRACK-HD Investigators (2011). "Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: The 12-month longitudinal analysis". The Lancet Neurology. 10 (1): 31–42. doi:10.1016/s1474-4422(10)70276-3. PMID 21130037. S2CID 2602096.
Tabrizi, Sarah J; Reilmann, Ralf; Roos, Raymund AC; Durr, Alexandra; Leavitt, Blair; Owen, Gail; Jones, Rebecca; Johnson, Hans; Craufurd, David; Hicks, Stephen L; Kennard, Christopher; Landwehrmeyer, Bernhard; Stout, Julie C; Borowsky, Beth; Scahill, Rachael I; Frost, Chris; Langbehn, Douglas R; TRACK-HD investigators (2012). "Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: Analysis of 24 month observational data". The Lancet Neurology. 11 (1): 42–53. doi:10.1016/s1474-4422(11)70263-0. PMID 22137354. S2CID 34929053.
Tabrizi, Sarah J; Scahill, Rachael I; Owen, Gail; Durr, Alexandra; Leavitt, Blair R; Roos, Raymund A; Borowsky, Beth; Landwehrmeyer, Bernhard; Frost, Chris; Johnson, Hans; Craufurd, David; Reilmann, Ralf; Stout, Julie C; Langbehn, Douglas R (2013). "Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: Analysis of 36-month observational data". The Lancet Neurology. 12 (7): 637–49. doi:10.1016/s1474-4422(13)70088-7. PMID 23664844. S2CID 12204298.
Klöppel, Stefan; Gregory, Sarah; Scheller, Elisa; Minkova, Lora; Razi, Adeel; Durr, Alexandra; Roos, Raymund A.C; Leavitt, Blair R; Papoutsi, Marina; Landwehrmeyer, G. Bernhard; Reilmann, Ralf; Borowsky, Beth; Johnson, Hans; Mills, James A; Owen, Gail; Stout, Julie; Scahill, Rachael I; Long, Jeffrey D; Rees, Geraint; Tabrizi, Sarah J (2015). "Compensation in Preclinical Huntington's Disease: Evidence from the Track-On HD Study". eBioMedicine. 2 (10): 1420–9. doi:10.1016/j.ebiom.2015.08.002. PMC 4634199. PMID 26629536.
Gregory, Sarah; Long, Jeffrey D; Klöppel, Stefan; Razi, Adeel; Scheller, Elisa; Minkova, Lora; Papoutsi, Marina; Mills, James A; Durr, Alexandra; Leavitt, Blair R; Roos, Raymund A. C; Stout, Julie C; Scahill, Rachael I; Langbehn, Douglas R; Tabrizi, Sarah J; Rees, Geraint (2017). "Operationalizing compensation over time in neurodegenerative disease". Brain. 140 (4): 1158–1165. doi:10.1093/brain/awx022. PMC 5382953. PMID 28334888.
Gregory, Sarah; Long, Jeffrey D; Klöppel, Stefan; Razi, Adeel; Scheller, Elisa; Minkova, Lora; Johnson, Eileanoir B; Durr, Alexandra; Roos, Raymund A C; Leavitt, Blair R; Mills, James A; Stout, Julie C; Scahill, Rachael I; Tabrizi, Sarah J; Rees, Geraint; Coleman, A; Decolongon, J; Fan, M; Koren, T; Leavitt, B; Durr, A; Jauffret, C; Justo, D; Lehericy, S; Nigaud, K; Valabrègue, R; Roos, R; Hart, E P 't; Schoonderbeek, A; et al. (2018). "Testing a longitudinal compensation model in premanifest Huntington's disease". Brain. 141 (7): 2156–2166. doi:10.1093/brain/awy122. PMC 6022638. PMID 29788038.
Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/s0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Arney, Kat (2018). "Improved metrics for Huntington's disease trials". Nature. 557 (7707): S46–S47. Bibcode:2018Natur.557S..46A. doi:10.1038/d41586-018-05179-w. PMID 29844554. S2CID 256768548.
Moss, Davina J Hensman; Pardiñas, Antonio F; Langbehn, Douglas; Lo, Kitty; Leavitt, Blair R; Roos, Raymund; Durr, Alexandra; Mead, Simon; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J; Coleman, A; Santos, R Dar; Decolongon, J; Sturrock, A; Bardinet, E; Ret, C Jauff; Justo, D; Lehericy, S; Marelli, C; Nigaud, K; Valabrègue, R; Van Den Bogaard, SJA; Dumas, E M; Van Der Grond, J; t'Hart, EP; Jurgens, C; Witjes-Ane, M-N; Arran, N; et al. (2017). "Identification of genetic variants associated with Huntington's disease progression: A genome-wide association study" (PDF). The Lancet Neurology. 16 (9): 701–711. doi:10.1016/s1474-4422(17)30161-8. PMID 28642124. S2CID 588163.
Flower, Michael; Lomeikaite, Vilija; Ciosi, Marc; Cumming, Sarah; Morales, Fernando; Lo, Kitty; Hensman Moss, Davina; Jones, Lesley; Holmans, Peter; Monckton, Darren G.; Tabrizi, Sarah J. (1 July 2019). "MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1". Brain. 142 (7): 1876–1886. doi:10.1093/brain/awz115. ISSN 0006-8950. PMC 6598626. PMID 31216018.
Tabrizi, Sarah J.; Estevez-Fraga, Carlos; van Roon-Mom, Willeke M. C.; Flower, Michael D.; Scahill, Rachael I.; Wild, Edward J.; Muñoz-Sanjuan, Ignacio; Sampaio, Cristina; Rosser, Anne E.; Leavitt, Blair R. (July 2022). "Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities". The Lancet. Neurology. 21 (7): 645–658. doi:10.1016/S1474-4422(22)00121-1. ISSN 1474-4465. PMC 7613206. PMID 35716694.
Goold, Robert; Flower, Michael; Moss, Davina Hensman; Medway, Chris; Wood-Kaczmar, Alison; Andre, Ralph; Farshim, Pamela; Bates, Gill P; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J (15 February 2019). "FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat". Human Molecular Genetics. 28 (4): 650–661. doi:10.1093/hmg/ddy375. ISSN 0964-6906. PMC 6360275. PMID 30358836.
Goold, Robert; Hamilton, Joseph; Menneteau, Thomas; Flower, Michael; Bunting, Emma L.; Aldous, Sarah G.; Porro, Antonio; Vicente, José R.; Allen, Nicholas D.; Wilkinson, Hilary; Bates, Gillian P.; Sartori, Alessandro A.; Thalassinos, Konstantinos; Balmus, Gabriel; Tabrizi, Sarah J. (August 2021). "FAN1 controls mismatch repair complex assembly via MLH1 retention to stabilize CAG repeat expansion in Huntington's disease". Cell Reports. 36 (9): 109649. doi:10.1016/j.celrep.2021.109649. PMC 8424649. PMID 34469738.
Tabrizi, Sarah J.; Flower, Michael D.; Ross, Christopher A.; Wild, Edward J. (October 2020). "Huntington disease: new insights into molecular pathogenesis and therapeutic opportunities". Nature Reviews Neurology. 16 (10): 529–546. doi:10.1038/s41582-020-0389-4. ISSN 1759-4758. PMID 32796930. S2CID 221129777.
Drew, Liam (2018). "How the gene behind Huntington's disease could be neutralized". Nature. 557 (7707): S39–S41. Bibcode:2018Natur.557S..39D. doi:10.1038/d41586-018-05176-z. PMID 29844556. S2CID 256768090.
Tabrizi, Sarah J.; Leavitt, Blair R.; Landwehrmeyer, G. Bernhard; Wild, Edward J.; Saft, Carsten; Barker, Roger A.; Blair, Nick F.; Craufurd, David; Priller, Josef (6 May 2019). "Targeting Huntingtin Expression in Patients with Huntington's Disease" (PDF). New England Journal of Medicine. 380 (24): 2307–2316. doi:10.1056/NEJMoa1900907. ISSN 0028-4793. PMID 31059641.
Leavitt, Blair R.; Tabrizi, Sarah J. (27 March 2020). "Antisense oligonucleotides for neurodegeneration". Science. 367 (6485): 1428–1429. Bibcode:2020Sci...367.1428L. doi:10.1126/science.aba4624. ISSN 0036-8075. PMID 32217715. S2CID 214671177.
Tabrizi, Sarah J; Estevez-Fraga, Carlos; van Roon-Mom, Willeke M C; Flower, Michael D; Scahill, Rachael I; Wild, Edward J; Muñoz-Sanjuan, Ignacio; Sampaio, Cristina; Rosser, Anne E; Leavitt, Blair R (July 2022). "Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities". The Lancet Neurology. 21 (7): 645–658. doi:10.1016/S1474-4422(22)00121-1. PMC 7613206. PMID 35716694.
Scahill, Rachael I; Zeun, Paul; Osborne-Crowley, Katherine; Johnson, Eileanoir B; Gregory, Sarah; Parker, Christopher; Lowe, Jessica; Nair, Akshay; O'Callaghan, Claire; Langley, Christelle; Papoutsi, Marina (June 2020). "Biological and clinical characteristics of gene carriers far from predicted onset in the Huntington's disease Young Adult Study (HD-YAS): a cross-sectional analysis". The Lancet Neurology. 19 (6): 502–512. doi:10.1016/S1474-4422(20)30143-5. PMC 7254065. PMID 32470422.
Tabrizi, Sarah J.; Schobel, Scott; Gantman, Emily C.; Mansbach, Alexandra; Borowsky, Beth; Konstantinova, Pavlina; Mestre, Tiago A.; Panagoulias, Jennifer; Ross, Christopher A.; Zauderer, Maurice; Mullin, Ariana P.; Romero, Klaus; Sivakumaran, Sudhir; Turner, Emily C.; Long, Jeffrey D. (July 2022). "A biological classification of Huntington's disease: the Integrated Staging System". The Lancet. Neurology. 21 (7): 632–644. doi:10.1016/S1474-4422(22)00120-X. ISSN 1474-4465. PMID 35716693. S2CID 249682267.
Shetty, Priya (2 June 2012). "Sarah Tabrizi: tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. ISSN 0140-6736. PMID 22656876. S2CID 40222846.
Burton, Adrian (2018). "Sarah Tabrizi: Timed to perfection". The Lancet Neurology. 17 (2): 117. doi:10.1016/s1474-4422(17)30303-4. PMID 28916420.

ncbi.nlm.nih.gov

Deriziotis, Pelagia; André, Ralph; Smith, David M; Goold, Rob; Kinghorn, Kerri J; Kristiansen, Mark; Nathan, James A; Rosenzweig, Rina; Krutauz, Dasha; Glickman, Michael H; Collinge, John; Goldberg, Alfred L; Tabrizi, Sarah J (8 July 2011). "Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry". The EMBO Journal. 30 (15): 3065–3077. doi:10.1038/emboj.2011.224. PMC 3160194. PMID 21743439.
Goold, R.; Rabbanian, S.; Sutton, L.; Andre, R.; Arora, P.; Moonga, J.; Clarke, A.R.; Schiavo, G.; Jat, P.; Collinge, J.; Tabrizi, S.J. (19 April 2011). "Rapid cell-surface prion protein conversion revealed using a novel cell system". Nature Communications. 2 (1): 281–. Bibcode:2011NatCo...2..281G. doi:10.1038/ncomms1282. PMC 3104518. PMID 21505437.
McKinnon, Chris; Goold, Rob; Andre, Ralph; Devoy, Anny; Ortega, Zaira; Moonga, Julie; Linehan, Jacqueline M.; Brandner, Sebastian; Lucas, José J.; Collinge, John; Tabrizi, Sarah J. (8 December 2015). "Prion-mediated neurodegeneration is associated with early impairment of the ubiquitin–proteasome system". Acta Neuropathologica. 131 (3): 411–425. doi:10.1007/s00401-015-1508-y. PMC 4752964. PMID 26646779.
Deriziotis, Pelagia; André, Ralph; Smith, David M; Goold, Rob; Kinghorn, Kerri J; Kristiansen, Mark; Nathan, James A; Rosenzweig, Rina; Krutauz, Dasha; Glickman, Michael H; Collinge, John (8 July 2011). "Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry". The EMBO Journal. 30 (15): 3065–3077. doi:10.1038/emboj.2011.224. ISSN 0261-4189. PMC 3160194. PMID 21743439.
Björkqvist, Maria; Wild, Edward J; Thiele, Jenny; Silvestroni, Aurelio; Andre, Ralph; Lahiri, Nayana; Raibon, Elsa; Lee, Richard V; Benn, Caroline L; Soulet, Denis; Magnusson, Anna; Woodman, Ben; Landles, Christian; Pouladi, Mahmoud A; Hayden, Michael R; Khalili-Shirazi, Azadeh; Lowdell, Mark W; Brundin, Patrik; Bates, Gillian P; Leavitt, Blair R; Möller, Thomas; Tabrizi, Sarah J (2008). "A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease". The Journal of Experimental Medicine. 205 (8): 1869–77. doi:10.1084/jem.20080178. PMC 2525598. PMID 18625748.
Weiss, Andreas; Träger, Ulrike; Wild, Edward J; Grueninger, Stephan; Farmer, Ruth; Landles, Christian; Scahill, Rachael I; Lahiri, Nayana; Haider, Salman; MacDonald, Douglas; Frost, Chris; Bates, Gillian P; Bilbe, Graeme; Kuhn, Rainer; Andre, Ralph; Tabrizi, Sarah J (2012). "Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression". Journal of Clinical Investigation. 122 (10): 3731–6. doi:10.1172/jci64565. PMC 3461928. PMID 22996692.
Tabrizi, Sarah J; Langbehn, Douglas R; Leavitt, Blair R; Roos, Raymund AC; Durr, Alexandra; Craufurd, David; Kennard, Christopher; Hicks, Stephen L; Fox, Nick C; Scahill, Rachael I; Borowsky, Beth; Tobin, Allan J; Rosas, H Diana; Johnson, Hans; Reilmann, Ralf; Landwehrmeyer, Bernhard; Stout, Julie C (2009). "Biological and clinical manifestations of Huntington's disease in the longitudinal TRACK-HD study: Cross-sectional analysis of baseline data". The Lancet Neurology. 8 (9): 791–801. doi:10.1016/s1474-4422(09)70170-x. PMC 3725974. PMID 19646924.
Klöppel, Stefan; Gregory, Sarah; Scheller, Elisa; Minkova, Lora; Razi, Adeel; Durr, Alexandra; Roos, Raymund A.C; Leavitt, Blair R; Papoutsi, Marina; Landwehrmeyer, G. Bernhard; Reilmann, Ralf; Borowsky, Beth; Johnson, Hans; Mills, James A; Owen, Gail; Stout, Julie; Scahill, Rachael I; Long, Jeffrey D; Rees, Geraint; Tabrizi, Sarah J (2015). "Compensation in Preclinical Huntington's Disease: Evidence from the Track-On HD Study". eBioMedicine. 2 (10): 1420–9. doi:10.1016/j.ebiom.2015.08.002. PMC 4634199. PMID 26629536.
Gregory, Sarah; Long, Jeffrey D; Klöppel, Stefan; Razi, Adeel; Scheller, Elisa; Minkova, Lora; Papoutsi, Marina; Mills, James A; Durr, Alexandra; Leavitt, Blair R; Roos, Raymund A. C; Stout, Julie C; Scahill, Rachael I; Langbehn, Douglas R; Tabrizi, Sarah J; Rees, Geraint (2017). "Operationalizing compensation over time in neurodegenerative disease". Brain. 140 (4): 1158–1165. doi:10.1093/brain/awx022. PMC 5382953. PMID 28334888.
Gregory, Sarah; Long, Jeffrey D; Klöppel, Stefan; Razi, Adeel; Scheller, Elisa; Minkova, Lora; Johnson, Eileanoir B; Durr, Alexandra; Roos, Raymund A C; Leavitt, Blair R; Mills, James A; Stout, Julie C; Scahill, Rachael I; Tabrizi, Sarah J; Rees, Geraint; Coleman, A; Decolongon, J; Fan, M; Koren, T; Leavitt, B; Durr, A; Jauffret, C; Justo, D; Lehericy, S; Nigaud, K; Valabrègue, R; Roos, R; Hart, E P 't; Schoonderbeek, A; et al. (2018). "Testing a longitudinal compensation model in premanifest Huntington's disease". Brain. 141 (7): 2156–2166. doi:10.1093/brain/awy122. PMC 6022638. PMID 29788038.
Flower, Michael; Lomeikaite, Vilija; Ciosi, Marc; Cumming, Sarah; Morales, Fernando; Lo, Kitty; Hensman Moss, Davina; Jones, Lesley; Holmans, Peter; Monckton, Darren G.; Tabrizi, Sarah J. (1 July 2019). "MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1". Brain. 142 (7): 1876–1886. doi:10.1093/brain/awz115. ISSN 0006-8950. PMC 6598626. PMID 31216018.
Tabrizi, Sarah J.; Estevez-Fraga, Carlos; van Roon-Mom, Willeke M. C.; Flower, Michael D.; Scahill, Rachael I.; Wild, Edward J.; Muñoz-Sanjuan, Ignacio; Sampaio, Cristina; Rosser, Anne E.; Leavitt, Blair R. (July 2022). "Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities". The Lancet. Neurology. 21 (7): 645–658. doi:10.1016/S1474-4422(22)00121-1. ISSN 1474-4465. PMC 7613206. PMID 35716694.
Goold, Robert; Flower, Michael; Moss, Davina Hensman; Medway, Chris; Wood-Kaczmar, Alison; Andre, Ralph; Farshim, Pamela; Bates, Gill P; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J (15 February 2019). "FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat". Human Molecular Genetics. 28 (4): 650–661. doi:10.1093/hmg/ddy375. ISSN 0964-6906. PMC 6360275. PMID 30358836.
Goold, Robert; Hamilton, Joseph; Menneteau, Thomas; Flower, Michael; Bunting, Emma L.; Aldous, Sarah G.; Porro, Antonio; Vicente, José R.; Allen, Nicholas D.; Wilkinson, Hilary; Bates, Gillian P.; Sartori, Alessandro A.; Thalassinos, Konstantinos; Balmus, Gabriel; Tabrizi, Sarah J. (August 2021). "FAN1 controls mismatch repair complex assembly via MLH1 retention to stabilize CAG repeat expansion in Huntington's disease". Cell Reports. 36 (9): 109649. doi:10.1016/j.celrep.2021.109649. PMC 8424649. PMID 34469738.
Tabrizi, Sarah J; Estevez-Fraga, Carlos; van Roon-Mom, Willeke M C; Flower, Michael D; Scahill, Rachael I; Wild, Edward J; Muñoz-Sanjuan, Ignacio; Sampaio, Cristina; Rosser, Anne E; Leavitt, Blair R (July 2022). "Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities". The Lancet Neurology. 21 (7): 645–658. doi:10.1016/S1474-4422(22)00121-1. PMC 7613206. PMID 35716694.
Scahill, Rachael I; Zeun, Paul; Osborne-Crowley, Katherine; Johnson, Eileanoir B; Gregory, Sarah; Parker, Christopher; Lowe, Jessica; Nair, Akshay; O'Callaghan, Claire; Langley, Christelle; Papoutsi, Marina (June 2020). "Biological and clinical characteristics of gene carriers far from predicted onset in the Huntington's disease Young Adult Study (HD-YAS): a cross-sectional analysis". The Lancet Neurology. 19 (6): 502–512. doi:10.1016/S1474-4422(20)30143-5. PMC 7254065. PMID 32470422.

oup.com

academic.oup.com

Goold, Robert; Flower, Michael; Moss, Davina Hensman; Medway, Chris; Wood-Kaczmar, Alison; Andre, Ralph; Farshim, Pamela; Bates, Gill P; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J (15 February 2019). "FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat". Human Molecular Genetics. 28 (4): 650–661. doi:10.1093/hmg/ddy375. ISSN 0964-6906. PMC 6360275. PMID 30358836.

royalsociety.org

https://royalsociety.org/news/2024/05/new-fellows-2024/

science.org

Leavitt, Blair R.; Tabrizi, Sarah J. (27 March 2020). "Antisense oligonucleotides for neurodegeneration". Science. 367 (6485): 1428–1429. Bibcode:2020Sci...367.1428L. doi:10.1126/science.aba4624. ISSN 0036-8075. PMID 32217715. S2CID 214671177.

semanticscholar.org

api.semanticscholar.org

Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Tabrizi, Sarah J; Scahill, Rachael I; Durr, Alexandra; Roos, Raymund AC; Leavitt, Blair R; Jones, Rebecca; Landwehrmeyer, G Bernhard; Fox, Nick C; Johnson, Hans; Hicks, Stephen L; Kennard, Christopher; Craufurd, David; Frost, Chris; Langbehn, Douglas R; Reilmann, Ralf; Stout, Julie C; TRACK-HD Investigators (2011). "Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: The 12-month longitudinal analysis". The Lancet Neurology. 10 (1): 31–42. doi:10.1016/s1474-4422(10)70276-3. PMID 21130037. S2CID 2602096.
Tabrizi, Sarah J; Reilmann, Ralf; Roos, Raymund AC; Durr, Alexandra; Leavitt, Blair; Owen, Gail; Jones, Rebecca; Johnson, Hans; Craufurd, David; Hicks, Stephen L; Kennard, Christopher; Landwehrmeyer, Bernhard; Stout, Julie C; Borowsky, Beth; Scahill, Rachael I; Frost, Chris; Langbehn, Douglas R; TRACK-HD investigators (2012). "Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: Analysis of 24 month observational data". The Lancet Neurology. 11 (1): 42–53. doi:10.1016/s1474-4422(11)70263-0. PMID 22137354. S2CID 34929053.
Tabrizi, Sarah J; Scahill, Rachael I; Owen, Gail; Durr, Alexandra; Leavitt, Blair R; Roos, Raymund A; Borowsky, Beth; Landwehrmeyer, Bernhard; Frost, Chris; Johnson, Hans; Craufurd, David; Reilmann, Ralf; Stout, Julie C; Langbehn, Douglas R (2013). "Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: Analysis of 36-month observational data". The Lancet Neurology. 12 (7): 637–49. doi:10.1016/s1474-4422(13)70088-7. PMID 23664844. S2CID 12204298.
Shetty, Priya (2012). "Sarah Tabrizi: Tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/s0140-6736(12)60884-8. PMID 22656876. S2CID 40222846.
Arney, Kat (2018). "Improved metrics for Huntington's disease trials". Nature. 557 (7707): S46–S47. Bibcode:2018Natur.557S..46A. doi:10.1038/d41586-018-05179-w. PMID 29844554. S2CID 256768548.
Moss, Davina J Hensman; Pardiñas, Antonio F; Langbehn, Douglas; Lo, Kitty; Leavitt, Blair R; Roos, Raymund; Durr, Alexandra; Mead, Simon; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J; Coleman, A; Santos, R Dar; Decolongon, J; Sturrock, A; Bardinet, E; Ret, C Jauff; Justo, D; Lehericy, S; Marelli, C; Nigaud, K; Valabrègue, R; Van Den Bogaard, SJA; Dumas, E M; Van Der Grond, J; t'Hart, EP; Jurgens, C; Witjes-Ane, M-N; Arran, N; et al. (2017). "Identification of genetic variants associated with Huntington's disease progression: A genome-wide association study" (PDF). The Lancet Neurology. 16 (9): 701–711. doi:10.1016/s1474-4422(17)30161-8. PMID 28642124. S2CID 588163.
Tabrizi, Sarah J.; Flower, Michael D.; Ross, Christopher A.; Wild, Edward J. (October 2020). "Huntington disease: new insights into molecular pathogenesis and therapeutic opportunities". Nature Reviews Neurology. 16 (10): 529–546. doi:10.1038/s41582-020-0389-4. ISSN 1759-4758. PMID 32796930. S2CID 221129777.
Drew, Liam (2018). "How the gene behind Huntington's disease could be neutralized". Nature. 557 (7707): S39–S41. Bibcode:2018Natur.557S..39D. doi:10.1038/d41586-018-05176-z. PMID 29844556. S2CID 256768090.
Leavitt, Blair R.; Tabrizi, Sarah J. (27 March 2020). "Antisense oligonucleotides for neurodegeneration". Science. 367 (6485): 1428–1429. Bibcode:2020Sci...367.1428L. doi:10.1126/science.aba4624. ISSN 0036-8075. PMID 32217715. S2CID 214671177.
Tabrizi, Sarah J.; Schobel, Scott; Gantman, Emily C.; Mansbach, Alexandra; Borowsky, Beth; Konstantinova, Pavlina; Mestre, Tiago A.; Panagoulias, Jennifer; Ross, Christopher A.; Zauderer, Maurice; Mullin, Ariana P.; Romero, Klaus; Sivakumaran, Sudhir; Turner, Emily C.; Long, Jeffrey D. (July 2022). "A biological classification of Huntington's disease: the Integrated Staging System". The Lancet. Neurology. 21 (7): 632–644. doi:10.1016/S1474-4422(22)00120-X. ISSN 1474-4465. PMID 35716693. S2CID 249682267.
Shetty, Priya (2 June 2012). "Sarah Tabrizi: tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. ISSN 0140-6736. PMID 22656876. S2CID 40222846.

theguardian.com

Devlin, Hannah (11 December 2017). "Excitement as trial shows Huntington's drug could slow progress of disease". guardian.com.

thelancet.com

Shetty, Priya (2 June 2012). "Sarah Tabrizi: tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. ISSN 0140-6736. PMID 22656876. S2CID 40222846.

ucl.ac.uk

"Department of Neurodegenerative Disease". UCL Institute of Neurology. 2 August 2018.
"The UCL Huntington's Disease Centre opens". 2 March 2017.
"Full Results from Huntingtin Lowering Antisense Oligonucleotides Trial now published". UCL Queen Square Institute of Neurology. 7 May 2019.
UCL (5 June 2023). "Professor Sarah Tabrizi receives the 2023 Arvid Carlsson Award". UCL Queen Square Institute of Neurology. Retrieved 5 June 2023.
UCL (28 June 2022). "Professor Sarah Tabrizi receives 2022 Osler Medal and HDSA 2022 Research Award". UCL Queen Square Institute of Neurology. Retrieved 20 July 2022.
UCL (5 November 2019). "Co-Heads of Department awarded Alexander Morison medal in successive years". UCL Queen Square Institute of Neurology. Retrieved 6 November 2019.
UCL (31 October 2019). "Professor Sarah Tabrizi receives Yahr award at World Congress of Neurology 2019". UCL Queen Square Institute of Neurology. Retrieved 6 November 2019.
"Professor Sarah Tabrizi, UCL Queen Square Institute of Neurology, receives the 2018 Cotzias Award". UCL News. 16 November 2018.
Tabrizi, Sarah (19 October 2018). "The NHS at 70 years". ucl.ac.uk.
"UCL News". ucl.ac.uk. 9 November 2017.

iris.ucl.ac.uk

"Iris View Profile". IRIS - UCL. Retrieved 5 May 2016.
"Professor Sarah J Tabrizi". UCL Iris.

hdresearch.ucl.ac.uk

"UCL Huntington's Disease Research". hdresearch.ucl.ac.uk.

discovery.ucl.ac.uk

Moss, Davina J Hensman; Pardiñas, Antonio F; Langbehn, Douglas; Lo, Kitty; Leavitt, Blair R; Roos, Raymund; Durr, Alexandra; Mead, Simon; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J; Coleman, A; Santos, R Dar; Decolongon, J; Sturrock, A; Bardinet, E; Ret, C Jauff; Justo, D; Lehericy, S; Marelli, C; Nigaud, K; Valabrègue, R; Van Den Bogaard, SJA; Dumas, E M; Van Der Grond, J; t'Hart, EP; Jurgens, C; Witjes-Ane, M-N; Arran, N; et al. (2017). "Identification of genetic variants associated with Huntington's disease progression: A genome-wide association study" (PDF). The Lancet Neurology. 16 (9): 701–711. doi:10.1016/s1474-4422(17)30161-8. PMID 28642124. S2CID 588163.

uclh.nhs.uk

"Prof Sarah Tabrizi". www.uclh.nhs.uk. Archived from the original on 31 August 2022. Retrieved 5 May 2016.

ukri.org

"MRC announces Millennium Medal winners and Impact Prize finalists". www.ukri.org. 8 December 2022. Retrieved 13 December 2022.

ukwhoswho.com

"Who's Who 2016 - Tabrizi, Prof. Sarah Joanna". Who's Who 2016. Retrieved 6 May 2016.

web.archive.org

"Prof Sarah Tabrizi". www.uclh.nhs.uk. Archived from the original on 31 August 2022. Retrieved 5 May 2016.

wellcome.ac.uk

"Governance - Wellcome". wellcome.ac.uk.

worldcat.org

Deriziotis, Pelagia; André, Ralph; Smith, David M; Goold, Rob; Kinghorn, Kerri J; Kristiansen, Mark; Nathan, James A; Rosenzweig, Rina; Krutauz, Dasha; Glickman, Michael H; Collinge, John (8 July 2011). "Misfolded PrP impairs the UPS by interaction with the 20S proteasome and inhibition of substrate entry". The EMBO Journal. 30 (15): 3065–3077. doi:10.1038/emboj.2011.224. ISSN 0261-4189. PMC 3160194. PMID 21743439.
Kristiansen, Mark; Messenger, Marcus J.; Klöhn, Peter-Christian; Brandner, Sebastian; Wadsworth, Jonathan D. F.; Collinge, John; Tabrizi, Sarah J. (18 November 2005). "Disease-related Prion Protein Forms Aggresomes in Neuronal Cells Leading to Caspase Activation and Apoptosis". Journal of Biological Chemistry. 280 (46): 38851–38861. doi:10.1074/jbc.M506600200. ISSN 0021-9258. PMID 16157591.
Flower, Michael; Lomeikaite, Vilija; Ciosi, Marc; Cumming, Sarah; Morales, Fernando; Lo, Kitty; Hensman Moss, Davina; Jones, Lesley; Holmans, Peter; Monckton, Darren G.; Tabrizi, Sarah J. (1 July 2019). "MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1". Brain. 142 (7): 1876–1886. doi:10.1093/brain/awz115. ISSN 0006-8950. PMC 6598626. PMID 31216018.
Tabrizi, Sarah J.; Estevez-Fraga, Carlos; van Roon-Mom, Willeke M. C.; Flower, Michael D.; Scahill, Rachael I.; Wild, Edward J.; Muñoz-Sanjuan, Ignacio; Sampaio, Cristina; Rosser, Anne E.; Leavitt, Blair R. (July 2022). "Potential disease-modifying therapies for Huntington's disease: lessons learned and future opportunities". The Lancet. Neurology. 21 (7): 645–658. doi:10.1016/S1474-4422(22)00121-1. ISSN 1474-4465. PMC 7613206. PMID 35716694.
Goold, Robert; Flower, Michael; Moss, Davina Hensman; Medway, Chris; Wood-Kaczmar, Alison; Andre, Ralph; Farshim, Pamela; Bates, Gill P; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J (15 February 2019). "FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat". Human Molecular Genetics. 28 (4): 650–661. doi:10.1093/hmg/ddy375. ISSN 0964-6906. PMC 6360275. PMID 30358836.
Tabrizi, Sarah J.; Flower, Michael D.; Ross, Christopher A.; Wild, Edward J. (October 2020). "Huntington disease: new insights into molecular pathogenesis and therapeutic opportunities". Nature Reviews Neurology. 16 (10): 529–546. doi:10.1038/s41582-020-0389-4. ISSN 1759-4758. PMID 32796930. S2CID 221129777.
Tabrizi, Sarah J.; Leavitt, Blair R.; Landwehrmeyer, G. Bernhard; Wild, Edward J.; Saft, Carsten; Barker, Roger A.; Blair, Nick F.; Craufurd, David; Priller, Josef (6 May 2019). "Targeting Huntingtin Expression in Patients with Huntington's Disease" (PDF). New England Journal of Medicine. 380 (24): 2307–2316. doi:10.1056/NEJMoa1900907. ISSN 0028-4793. PMID 31059641.
Leavitt, Blair R.; Tabrizi, Sarah J. (27 March 2020). "Antisense oligonucleotides for neurodegeneration". Science. 367 (6485): 1428–1429. Bibcode:2020Sci...367.1428L. doi:10.1126/science.aba4624. ISSN 0036-8075. PMID 32217715. S2CID 214671177.
Tabrizi, Sarah J.; Schobel, Scott; Gantman, Emily C.; Mansbach, Alexandra; Borowsky, Beth; Konstantinova, Pavlina; Mestre, Tiago A.; Panagoulias, Jennifer; Ross, Christopher A.; Zauderer, Maurice; Mullin, Ariana P.; Romero, Klaus; Sivakumaran, Sudhir; Turner, Emily C.; Long, Jeffrey D. (July 2022). "A biological classification of Huntington's disease: the Integrated Staging System". The Lancet. Neurology. 21 (7): 632–644. doi:10.1016/S1474-4422(22)00120-X. ISSN 1474-4465. PMID 35716693. S2CID 249682267.
Shetty, Priya (2 June 2012). "Sarah Tabrizi: tracking Huntington's disease". The Lancet. 379 (9831): 2043. doi:10.1016/S0140-6736(12)60884-8. ISSN 0140-6736. PMID 22656876. S2CID 40222846.

zeitgeistminds.com

Tabrizi, Sarah (May 2016). "The Human Revolution". zeitgeistminds.com.