Works by Mead, Simon

Results: 109

Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer’s disease.
Published in:
PLoS ONE, 2019, v. 14, n. 7, p. 1, doi. 10.1371/journal.pone.0218111
By:
- Baker, Emily;
- Sims, Rebecca;
- Leonenko, Ganna;
- Frizzati, Aura;
- Harwood, Janet C.;
- Grozeva, Detelina;
- null, null;
- Morgan, Kevin;
- Passmore, Peter;
- Holmes, Clive;
- Powell, John;
- Brayne, Carol;
- Gill, Michael;
- Mead, Simon;
- Bossù, Paola;
- Spalletta, Gianfranco;
- Goate, Alison M.;
- Cruchaga, Carlos;
- Maier, Wolfgang;
- Heun, Reinhard
Publication type:
Article
Recent US Case of Variant Creutzfeldt-Jakob Disease-Global Implications.
Published in:
2015
By:
- Maheshwari, Atul;
- Fischer, Michael;
- Gambetti, Pierluigi;
- Parker, Alicia;
- Ram, Aarthi;
- Soto, Claudio;
- Concha-Marambio, Luis;
- Cohen, Yvonne;
- Belay, Ermias D;
- Maddox, Ryan A;
- Mead, Simon;
- Goodman, Clay;
- Kass, Joseph S;
- Schonberger, Lawrence B;
- Hussein, Haitham M
Publication type:
journal article
Recent US Case of Variant Creutzfeldt-Jakob Disease--Global Implications.
Published in:
2015
By:
- Maheshwari, Atul;
- Fischer, Michael;
- Gambetti, Pierluigi;
- Parker, Alicia;
- Ram, Aarthi;
- Soto, Claudio;
- Concha-Marambio, Luis;
- Cohen, Yvonne;
- Belay, Ermias D.;
- Maddox, Ryan A.;
- Mead, Simon;
- Goodman, Clay;
- Kass, Joseph S.;
- Schonberger, Lawrence B.;
- Hussein, Haitham M.
Publication type:
Case Study
Familial Creutzfeldt-Jakob disease in an Indian kindred.
Published in:
Annals of Indian Academy of Neurology, 2019, v. 22, n. 4, p. 458, doi. 10.4103/aian.AIAN_214_19
By:
- Katrak, Sarosh;
- Pauranik, Apoorva;
- Desai, Shrinivas;
- Mead, Simon;
- Beck, Jon;
- Brandner, Sebastian;
- Collinge, John
Publication type:
Article
PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit.
Published in:
Human Mutation, 2010, v. 31, n. 7, p. E1551, doi. 10.1002/humu.21281
By:
- Beck, Jon A.;
- Poulter, Mark;
- Campbell, Tracy A.;
- Adamson, Gary;
- Uphill, James B.;
- Guerreiro, Rita;
- Jackson, Graham S.;
- Stevens, James C.;
- Manji, Hadi;
- Collinge, John;
- Mead, Simon
Publication type:
Article
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platforms.
Published in:
2008
By:
- Mead, Simon;
- Poulter, Mark;
- Beck, John;
- Uphill, James;
- Jones, Chris;
- Ang, Cheng Eng;
- Mein, Charles A.;
- Collinge, John
Publication type:
Other
Erratum: Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy.
Published in:
2015
By:
- Jaunmuktane, Zane;
- Mead, Simon;
- Ellis, Matthew;
- Wadsworth, Jonathan D. F.;
- Nicoll, Andrew J.;
- Kenny, Joanna;
- Launchbury, Francesca;
- Linehan, Jacqueline;
- Richard-Loendt, Angela;
- Walker, A. Sarah;
- Rudge, Peter;
- Collinge, John;
- Brandner, Sebastian
Publication type:
Correction Notice
Evidence for human transmission of amyloid-β pathology and cerebral amyloid angiopathy.
Published in:
Nature, 2015, v. 525, n. 7568, p. 247, doi. 10.1038/nature15369
By:
- Jaunmuktane, Zane;
- Mead, Simon;
- Ellis, Matthew;
- Wadsworth, Jonathan D. F.;
- Nicoll, Andrew J.;
- Kenny, Joanna;
- Launchbury, Francesca;
- Linehan, Jacqueline;
- Richard-Loendt, Angela;
- Walker, A. Sarah;
- Rudge, Peter;
- Collinge, John;
- Brandner, Sebastian
Publication type:
Article
A naturally occurring variant of the human prion protein completely prevents prion disease.
Published in:
Nature, 2015, v. 522, n. 7557, p. 478, doi. 10.1038/nature14510
By:
- Asante, Emmanuel A.;
- Smidak, Michelle;
- Grimshaw, Andrew;
- Houghton, Richard;
- Tomlinson, Andrew;
- Jeelani, Asif;
- Jakubcova, Tatiana;
- Hamdan, Shyma;
- Richard-Londt, Angela;
- Linehan, Jacqueline M.;
- Brandner, Sebastian;
- Alpers, Michael;
- Whitfield, Jerome;
- Mead, Simon;
- Wadsworth, Jonathan D. F.;
- Collinge, John
Publication type:
Article
NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression.
Published in:
Cells (2073-4409), 2021, v. 10, n. 12, p. 3514, doi. 10.3390/cells10123514
By:
- Mengel, David;
- Mok, Tze How;
- Nihat, Akin;
- Liu, Wen;
- Rissman, Robert A.;
- Galasko, Douglas;
- Zetterberg, Henrik;
- Mead, Simon;
- Collinge, John;
- Walsh, Dominic M.
Publication type:
Article
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Published in:
Human Molecular Genetics, 2012, v. 21, n. 8, p. 1897, doi. 10.1093/hmg/ddr607
By:
- Mead, Simon;
- Uphill, James;
- Beck, John;
- Poulter, Mark;
- Campbell, Tracy;
- Lowe, Jessica;
- Adamson, Gary;
- Hummerich, Holger;
- Klopp, Norman;
- Rückert, Ina-Maria;
- Wichmann, H-Erich;
- Azazi, Dhoyazan;
- Plagnol, Vincent;
- Pako, Wandagi H.;
- Whitfield, Jerome;
- Alpers, Michael P.;
- Whittaker, John;
- Balding, David J.;
- Zerr, Inga;
- Kretzschmar, Hans
Publication type:
Article
Longitudinal measurement of serum neurofilament light in presymptomatic familial Alzheimer's disease.
Published in:
Alzheimer's Research & Therapy, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13195-019-0472-5
By:
- Weston, Philip S. J.;
- Poole, Teresa;
- O'Connor, Antoinette;
- Heslegrave, Amanda;
- Ryan, Natalie S.;
- Liang, Yuying;
- Druyeh, Ronald;
- Mead, Simon;
- Blennow, Kaj;
- Schott, Jonathan M.;
- Frost, Chris;
- Zetterberg, Henrik;
- Fox, Nick C.
Publication type:
Article
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion.
Published in:
2021
By:
- Brennecke, Nicholas;
- Cali, Ignazio;
- Mok, Tze How;
- Speedy, Helen;
- Hosszu, Laszlo L. P.;
- Stehmann, Christiane;
- Cracco, Laura;
- Puoti, Gianfranco;
- Prior, Thomas W.;
- Cohen, Mark L.;
- Collins, Steven J.;
- Mead, Simon;
- Appleby, Brian S.
Publication type:
Case Study
P.183: Multi-parameter MRI analysis in the national prion monitoring cohort.
Published in:
Prion, 2014, v. 8, p. 111
By:
- Porter, Marie-Claire;
- De Vita, Enrico;
- Simpson, Ivor;
- Ourselin, Sebastien;
- Lowe, Jessica;
- Franko, Edit;
- Bjurstrom, Nina;
- Rudge, Peter;
- Mead, Simon;
- Collinge, John;
- Thornton, John;
- Hyare, Harpreet
Publication type:
Article
P.70: In-vitro screen of prion disease susceptibility genes using the scrapie cell assay.
Published in:
Prion, 2014, v. 8, p. 56
By:
- Brown, Craig A.;
- Schmidt, Christian;
- Poulter, Mark;
- Hummerich, Holger;
- Klöhn, Peter-Christian;
- Jat, Parmjit;
- Mead, Simon;
- Collinge, John;
- Lloyd, Sarah E.
Publication type:
Article
Invited.21: Stratified medicine approach in sporadic Creutzfeldt-Jakob disease greatly increases power in simulated clinical trials.
Published in:
Prion, 2014, v. 8, p. 10
By:
- Mead, Simon;
- Burnell, Matthew;
- Lowe, Jessica;
- Lukic, Ana;
- Porter, Marie-Claire;
- Thompson, Andrew;
- Carswell, Christopher;
- Kaski, Diego;
- Kenny, Janna;
- Bjurgsrom, Nina;
- Gorham, Michele;
- Druyeh, Ron;
- Wadsworth, Jonathan;
- Brandner, Sebastian;
- Hyare, Harpreet;
- Walker, A. Sarah;
- Rudge, Peter;
- Collinge, John
Publication type:
Article
Genome wide association studies and prion disease.
Published in:
Prion, 2011, v. 5, n. 3, p. 154, doi. 10.4161/pri.5.3.16892
By:
- Lukic, Ana;
- Mead, Simon
Publication type:
Article
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patient.
Published in:
PLoS Pathogens, 2025, v. 21, n. 2, p. 1, doi. 10.1371/journal.ppat.1012904
By:
- Zhang, Fuquan;
- Joiner, Susan;
- Linehan, Jacqueline M.;
- Pintilii, Florin;
- Nazari, Tamsin;
- Argentina, Fabio;
- Preston, Connor;
- Taema, Maged;
- Cunningham, Thomas J.;
- Asante, Emmanuel A.;
- Mok, Tzehow;
- Mead, Simon;
- Brandner, Sebastian;
- Collinge, John;
- Wadsworth, Jonathan D.F.
Publication type:
Article
Video Rating in Neurodegenerative Disease Clinical Trials: The Experience of PRION-1.
Published in:
Dementia & Geriatric Cognitive Disorders Extra, 2012, v. 2, n. 1, p. 286, doi. 10.1159/000339730
By:
- Carswell, Christopher;
- Rañopa, Michael;
- Pal, Suvankar;
- MacFarlane, Rebecca;
- Siddique, Durre;
- Thomas, Dafydd;
- Webb, Tom;
- Wroe, Steve;
- Walker, Sarah;
- Darbyshire, Janet;
- Collinge, John;
- Mead, Simon;
- Rudge, Peter
Publication type:
Article
Profiles of white matter tract pathology in frontotemporal dementia.
Published in:
Human Brain Mapping, 2014, v. 35, n. 8, p. 4163, doi. 10.1002/hbm.22468
By:
- Mahoney, Colin J.;
- Ridgway, Gerard R.;
- Malone, Ian B.;
- Downey, Laura E.;
- Beck, Jonathan;
- Kinnunen, Kirsi M.;
- Schmitz, Nicole;
- Golden, Hannah L.;
- Rohrer, Jonathan D.;
- Schott, Jonathan M.;
- Rossor, Martin N.;
- Ourselin, Sebastien;
- Mead, Simon;
- Fox, Nick C.;
- Warren, Jason D.
Publication type:
Article
Early onset cerebral amyloid angiopathy following childhood exposure to cadaveric dura.
Published in:
2019
By:
- Banerjee, Gargi;
- Adams, Matthew E.;
- Jaunmuktane, Zane;
- Alistair Lammie, G.;
- Turner, Ben;
- Wani, Mushtaq;
- Sawhney, Inder M. S.;
- Houlden, Henry;
- Mead, Simon;
- Brandner, Sebastian;
- Werring, David J.
Publication type:
journal article
Comment on validation of diagnostic criteria for variant Creutzfeldt-Jakob disease.
Published in:
Annals of Neurology, 2011, v. 69, n. 1, p. 212, doi. 10.1002/ana.22273
By:
- Lukic, Ana;
- Mead, Simon;
- Rudge, Peter;
- Collinge, John
Publication type:
Article
Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes.
Published in:
2006
By:
- Rohrer JD;
- Mead S;
- Omar R;
- Poulter M;
- Warren JD;
- Collinge J;
- Rossor MN;
- Rohrer, Jonathan D;
- Mead, Simon;
- Omar, Rohani;
- Poulter, Mark;
- Warren, Jason D;
- Collinge, John;
- Rossor, Martin N
Publication type:
Letter
Prion disease masquerading as Alzheimer's disease
Published in:
2011
By:
- Thompson, Andrew;
- Mahoney, Colin;
- Ryan, Natalie;
- Bajaj, Nin;
- Lukic, Ana;
- Carswell, Chris;
- Hyare, Harpreet;
- Gopalakrishnan, Gosala;
- Mummery, Cath;
- Collinge, John;
- Rudge, Peter;
- Fox, Nick;
- Mead, Simon
Publication type:
Abstract
White matter lesions in familial Alzheimer's disease: evidence for influence of mutation position on amyloid angiopathy?
Published in:
2011
By:
- Ryan, Natalie;
- Biessels, Geert-Jan;
- Bastos-Leite, Antonio;
- Mead, Simon;
- Rossor, Martin;
- Fox, Nick
Publication type:
Abstract
Prion
Published in:
2011
By:
- Mead, Simon
Publication type:
Abstract
Duplications of APP—but not PRNP—are a significant cause of early-onset dementia in a large UK referral series
Published in:
2009
By:
- Ryan, Natalie;
- McNaughton, Daniel;
- Knight, Will;
- Guerreiro, Rita;
- Poulter, Mark;
- Nicholl, David;
- Hardy, John;
- Rossor, Martin;
- Collinge, John;
- Mead, Simon
Publication type:
Abstract
P2-211: Genome-wide association study identifies genetic risk factors for variant Creutzfeldt-Jakob disease
Published in:
2008
By:
- Mead, Simon;
- Poulter, Mark;
- Uphill, James;
- Beck, John;
- Webb, Thomas;
- Campbell, Tracy;
- Adamson, Gary;
- Molonou, Eleni;
- Hummerich, Holger;
- Verzilli, Claudio;
- Whittaker, John;
- Collinge, John
Publication type:
Abstract
Gene expression and epigenetic markers of prion diseases.
Published in:
Cell & Tissue Research, 2023, v. 392, n. 1, p. 285, doi. 10.1007/s00441-022-03603-2
By:
- Viré, Emmanuelle A.;
- Mead, Simon
Publication type:
Article
A stop-codon mutation in the BRI gene associated with familial British dementia.
Published in:
Nature, 1999, v. 399, n. 6738, p. 776, doi. 10.1038/21637
By:
- Vidal, Ruben;
- Frangione, Blas;
- Rostango, Agueda;
- Mead, Simon;
- Revesz, Tamas;
- Plant, Gordon;
- Ghiso, Jorge
Publication type:
Article
Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine.
Published in:
JAMA Neurology, 2016, v. 73, n. 12, p. 1454, doi. 10.1001/jamaneurol.2016.3733
By:
- Luk, Connie;
- Jones, Samantha;
- Thomas, Claire;
- Fox, Nick C.;
- Mok, Tze H.;
- Mead, Simon;
- Collinge, John;
- Jackson, Graham S.
Publication type:
Article
Use of Diffusion-Weighted Magnetic Resonance Imaging in Sporadic Creutzfeldt-Jakob Disease.
Published in:
JAMA Neurology, 2016, v. 73, n. 9, p. 1153, doi. 10.1001/jamaneurol.2016.2381
By:
- Vitali, Paolo;
- Pan, Marina;
- Caverzasi, Eduardo;
- Eisenmenger, Laura;
- Mead, Simon;
- Hyare, Harpreet
Publication type:
Article
Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease.
Published in:
JAMA Neurology, 2016, v. 73, n. 4, p. 447, doi. 10.1001/jamaneurol.2015.4885
By:
- Mead, Simon;
- Burnell, Matthew;
- Lowe, Jessica;
- Thompson, Andrew;
- Lukic, Ana;
- Porter, Marie-Claire;
- Carswell, Christopher;
- Kaski, Diego;
- Kenny, Janna;
- Mok, Tze How;
- Bjurstrom, Nina;
- Franko, Edit;
- Gorham, Michele;
- Druyeh, Ronald;
- Wadsworth, Jonathan D. F.;
- Jaunmuktane, Zane;
- Brandner, Sebastian;
- Hyare, Harpreet;
- Rudge, Peter;
- Sarah Walker, A.
Publication type:
Article
Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation.
Published in:
JAMA Neurology, 2016, v. 73, n. 1, p. 76, doi. 10.1001/jamaneurol.2015.3159
By:
- Eisenmenger, Laura;
- Porter, Marie-Claire;
- Carswell, Christopher J.;
- Thompson, Andrew;
- Mead, Simon;
- Rudge, Peter;
- Collinge, John;
- Brandner, Sebastian;
- Jäger, Hans R.;
- Hyare, Harpreet
Publication type:
Article
Blood Test for Variant Creutzfeldt-Jakob Disease.
Published in:
JAMA Neurology, 2014, v. 71, n. 8, p. 1054, doi. 10.1001/jamaneurol.2014.944
By:
- Bennett, Peter;
- Jackson, Graham S.;
- Burk-Rafel, Jesse;
- Mead, Simon;
- Collinge, John
Publication type:
Article
Population Screening for Variant Creutzfeldt-Jakob Disease Using a Novel Blood Test.
Published in:
JAMA Neurology, 2014, v. 71, n. 4, p. 421, doi. 10.1001/jamaneurol.2013.6001
By:
- Jackson, Graham S.;
- Burk-Rafel, Jesse;
- Edgeworth, Julie Ann;
- Sicilia, Anita;
- Abdilahi, Sabah;
- Korteweg, Justine;
- Mackey, Jonathan;
- Thomas, Claire;
- Wang, Guosu;
- Schott, Jonathan M.;
- Mummery, Catherine;
- Chinnery, Patrick F.;
- Mead, Simon;
- Collinge, John
Publication type:
Article
Variant Creutzfeldt-Jakob Disease With Extremely Low Lymphoreticular Deposition of Prion Protein.
Published in:
JAMA Neurology, 2014, v. 71, n. 3, p. 340, doi. 10.1001/jamaneurol.2013.5378
By:
- Mead, Simon;
- Wadsworth, Jonathan D. F.;
- Porter, Marie-Claire;
- Linehan, Jacqueline M.;
- Pietkiewicz, Wojciech;
- Jackson, Graham S.;
- Brandner, Sebastian;
- Collinge, John
Publication type:
Article
Creutzfeldt-Jakob Disease.
Published in:
JAMA Neurology, 2013, v. 70, n. 12, p. 1588, doi. 10.1001/jamaneurol.2013.4412
By:
- Benninger, Felix F.;
- Steiner, Israel;
- Angus-Leppan, Heather;
- Rudge, Peter;
- Mead, Simon;
- Collinge, John;
- Vincent, Angela
Publication type:
Article
Autoantibodies in Sporadic Creutzfeldt-Jakob Disease.
Published in:
JAMA Neurology, 2013, v. 70, n. 7, p. 919, doi. 10.1001/jamaneurol.2013.2077
By:
- Angus-Leppan, Heather;
- Rudge, Peter;
- Mead, Simon;
- Collinge, John;
- Vincent, Angela
Publication type:
Article
Prion protein gene mutation detection using long-read Nanopore sequencing.
Published in:
Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-12130-7
By:
- Kroll, François;
- Dimitriadis, Athanasios;
- Campbell, Tracy;
- Darwent, Lee;
- Collinge, John;
- Mead, Simon;
- Vire, Emmanuelle
Publication type:
Article
Predictive testing for inherited prion disease: report of 22 years experience.
Published in:
European Journal of Human Genetics, 2014, v. 22, n. 12, p. 1351, doi. 10.1038/ejhg.2014.42
By:
- Owen, Jane;
- Beck, Jon;
- Campbell, Tracy;
- Adamson, Gary;
- Gorham, Michele;
- Thompson, Andrew;
- Smithson, Sarah;
- Rosser, Elizabeth;
- Rudge, Peter;
- Collinge, John;
- Mead, Simon
Publication type:
Article
Academic neurology in the UK: a plea to turn away from the precipice.
Published in:
Brain: A Journal of Neurology, 2024, v. 147, n. 7, p. 2270, doi. 10.1093/brain/awae151
By:
- Devine, Helen;
- Jabbari, Edwin;
- Scott, James;
- Mehta, Arpan R;
- Dobson, Ruth;
- Mead, Simon
Publication type:
Article
Clinical considerations in early-onset cerebral amyloid angiopathy.
Published in:
Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 3991, doi. 10.1093/brain/awad193
By:
- Banerjee, Gargi;
- Collinge, John;
- Fox, Nick C;
- Lashley, Tammaryn;
- Mead, Simon;
- Schott, Jonathan M;
- Werring, David J;
- Ryan, Natalie S
Publication type:
Article
Plasma amyloid-β ratios in autosomal dominant Alzheimer's disease: the influence of genotype.
Published in:
2021
By:
- O'Connor, Antoinette;
- Pannee, Josef;
- Poole, Teresa;
- Arber, Charles;
- Portelius, Erik;
- Swift, Imogen J;
- Heslegrave, Amanda J;
- Abel, Emily;
- Willumsen, Nanet;
- Rice, Helen;
- Weston, Philip S J;
- Ryan, Natalie S;
- Polke, James M;
- Nicholas, Jennifer M;
- Mead, Simon;
- Wray, Selina;
- Chávez-Gutiérrez, Lucía;
- Frost, Chris;
- Blennow, Kaj;
- Zetterberg, Henrik
Publication type:
journal article
Cognitive decline heralds onset of symptomatic inherited prion disease.
Published in:
2021
By:
- Mole, Joseph;
- Mead, Simon;
- Rudge, Peter;
- Nihat, Akin;
- Mok, Tzehow;
- Collinge, John;
- Caine, Diana
Publication type:
journal article
Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease.
Published in:
2019
By:
- Rudge, Peter;
- Jaunmuktane, Zane;
- Hyare, Harpreet;
- Ellis, Matthew;
- Koltzenburg, Martin;
- Collinge, John;
- Brandner, Sebastian;
- Mead, Simon
Publication type:
journal article
HECTD2 Is Associated with Susceptibility to Mouse and Human Prion Disease.
Published in:
PLoS Genetics, 2009, v. 5, n. 2, p. 1, doi. 10.1371/journal.pgen.1000383
By:
- Lloyd, Sarah E.;
- Maytham, Emma G.;
- Pota, Hirva;
- Grizenkova, Julia;
- Molou, Eleni;
- Uphill, James;
- Hummerich, Holger;
- Whitfield, Jerome;
- Alpers, Michael P.;
- Mead, Simon;
- Collinge, John
Publication type:
Article
DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt–Jakob disease.
Published in:
Acta Neuropathologica, 2022, v. 144, n. 4, p. 785, doi. 10.1007/s00401-022-02481-w
By:
- Guntoro, Fernando;
- Viré, Emmanuelle;
- Giordani, Chiara;
- Darwent, Lee;
- Hummerich, Holger;
- Linehan, Jacqueline;
- Sinka, Katy;
- Jaunmuktane, Zane;
- Brandner, Sebastian;
- Collinge, John;
- Mead, Simon
Publication type:
Article
Alzheimer's disease neuropathological change three decades after iatrogenic amyloid-β transmission.
Published in:
Acta Neuropathologica, 2021, v. 142, n. 1, p. 211, doi. 10.1007/s00401-021-02326-y
By:
- Jaunmuktane, Zane;
- Banerjee, Gargi;
- Paine, Simon;
- Parry-Jones, Adrian;
- Rudge, Peter;
- Grieve, Joan;
- Toma, Ahmed K.;
- Farmer, Simon F.;
- Mead, Simon;
- Houlden, Henry;
- Werring, David J.;
- Brandner, Sebastian
Publication type:
Article
Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt–Jakob disease.
Published in:
Acta Neuropathologica, 2020, v. 140, n. 6, p. 863, doi. 10.1007/s00401-020-02224-9
By:
- Dabin, Luke C.;
- Guntoro, Fernando;
- Campbell, Tracy;
- Bélicard, Tony;
- Smith, Adam R.;
- Smith, Rebecca G.;
- Raybould, Rachel;
- Schott, Jonathan M.;
- Lunnon, Katie;
- Sarkies, Peter;
- Collinge, John;
- Mead, Simon;
- Viré, Emmanuelle
Publication type:
Article