Works by Mead, Simon

Results: 111

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

The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's disease.

Published in:

Journal of Neurogenetics, 2025, v. 39, n. 1, p. 16, doi. 10.1080/01677063.2024.2440395

By:

Holm-Mercer, Leah;
Coysh, Thomas;
Mok, Tze How;
Rudge, Peter;
Reisz, Zita;
Troakes, Claire;
Al-Sarraj, Safa;
Campbell, Tracy;
Hosszu, Laszlo L.P.;
Bieschke, Jan;
Zhang, Fuquan;
Wadsworth, Jonathan D.F.;
Smith, Colin;
Jenkinson, Jenna;
Rittman, Timothy;
Brandner, Sebastian;
Jaunmuktane, Zane;
Collinge, John;
Mead, Simon

Publication type:

Article

The cognitive profile of prion disease: a prospective clinical and imaging study.

Published in:

Annals of Clinical & Translational Neurology, 2015, v. 2, n. 5, p. 548, doi. 10.1002/acn3.195

By:

Caine, Diana;
Tinelli, Renata J.;
Hyare, Harpreet;
De Vita, Enrico;
Lowe, Jessica;
Lukic, Ana;
Thompson, Andrew;
Porter, Marie‐Claire;
Cipolotti, Lisa;
Rudge, Peter;
Collinge, John;
Mead, Simon

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

Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations.

Published in:

Neuropathology & Applied Neurobiology, 2015, v. 41, n. 7, p. 858, doi. 10.1111/nan.12250

By:

Lashley, Tammaryn;
Rohrer, Jonathan D.;
Mead, Simon;
Revesz, Tamas

Publication type:

Article

A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia.

Published in:

Neuropathology & Applied Neurobiology, 2014, v. 40, n. 4, p. 502, doi. 10.1111/nan.12100

By:

Lashley, Tammaryn;
Rohrer, Jonathan D.;
Mahoney, Colin;
Gordon, Elizabeth;
Beck, Jon;
Mead, Simon;
Warren, Jason;
Rossor, Martin;
Revesz, Tamas

Publication type:

Article

Prion disease genetics.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 3, p. 273, doi. 10.1038/sj.ejhg.5201544

By:

Mead, Simon

Publication type:

Article

A common single-nucleotide variant in T is strongly associated with chordoma.

Published in:

Nature Genetics, 2012, v. 44, n. 11, p. 1185, doi. 10.1038/ng.2419

By:

Pillay, Nischalan;
Plagnol, Vincent;
Tarpey, Patrick S;
Lobo, Samira B;
Presneau, Nadège;
Szuhai, Karoly;
Halai, Dina;
Berisha, Fitim;
Cannon, Stephen R;
Mead, Simon;
Kasperaviciute, Dalia;
Palmen, Jutta;
Talmud, Philippa J;
Kindblom, Lars-Gunnar;
Amary, M Fernanda;
Tirabosco, Roberto;
Flanagan, Adrienne M

Publication type:

Article

Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS.

Published in:

PLoS Biology, 2020, v. 18, n. 6, p. 1, doi. 10.1371/journal.pbio.3000725

By:

Asante, Emmanuel A.;
Linehan, Jacqueline M.;
Tomlinson, Andrew;
Jakubcova, Tatiana;
Hamdan, Shyma;
Grimshaw, Andrew;
Smidak, Michelle;
Jeelani, Asif;
Nihat, Akin;
Mead, Simon;
Brandner, Sebastian;
Wadsworth, Jonathan D. F.;
Collinge, John

Publication type:

Article

The C9ORF72 expansion mutation: gene structure, phenotypic and diagnostic issues.

Published in:

Acta Neuropathologica, 2014, v. 127, n. 3, p. 319, doi. 10.1007/s00401-014-1253-7

By:

Woollacott, Ione;
Mead, Simon

Publication type:

Article

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.

Published in:

Acta Neuropathologica, 2013, v. 126, n. 3, p. 401, doi. 10.1007/s00401-013-1147-0

By:

Fratta, Pietro;
Poulter, Mark;
Lashley, Tammaryn;
Rohrer, Jonathan;
Polke, James;
Beck, Jon;
Ryan, Natalie;
Hensman, Davina;
Mizielinska, Sarah;
Waite, Adrian;
Lai, Mang-Ching;
Gendron, Tania;
Petrucelli, Leonard;
Fisher, Elizabeth;
Revesz, Tamas;
Warren, Jason;
Collinge, John;
Isaacs, Adrian;
Mead, Simon

Publication type:

Article

Tau, prions and Aβ: the triad of neurodegeneration.

Published in:

Acta Neuropathologica, 2011, v. 121, n. 1, p. 5, doi. 10.1007/s00401-010-0691-0

By:

Reiniger, Lilla;
Lukic, Ana;
Linehan, Jacqueline;
Rudge, Peter;
Collinge, John;
Mead, Simon;
Brandner, Sebastian

Publication type:

Article

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

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

Genetic Variability in CLU and Its Association with Alzheimer's Disease.

Published in:

PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009510

By:

Guerreiro, Rita J.;
Beck, John;
Gibbs, J. Raphael;
Santana, Isabel;
Rossor, Martin N.;
Schott, Jonathan M.;
Nalls, Michael A.;
Ribeiro, Helena;
Santiago, Beatriz;
Fox, Nick C.;
Oliveira, Catarina;
Collinge, John;
Mead, Simon;
Singleton, Andrew;
Hardy, John

Publication type:

Article

Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease.

Published in:

2021

By:

Hassan, Ahamad;
Campbell, Tracy;
Darwent, Lee;
Odd, Hans;
Green, Alison;
Collinge, John;
Mead, Simon

Publication type:

journal article

Novel regulators of PrP<sup>C</sup> biosynthesis revealed by genome-wide RNA interference.

Published in:

PLoS Pathogens, 2021, v. 17, n. 10, p. 1, doi. 10.1371/journal.ppat.1010013

By:

Heinzer, Daniel;
Avar, Merve;
Pease, Daniel Patrick;
Dhingra, Ashutosh;
Yin, Jiang-An;
Schaper, Elke;
Doğançay, Berre;
Emmenegger, Marc;
Spinelli, Anna;
Maggi, Kevin;
Chincisan, Andra;
Mead, Simon;
Hornemann, Simone;
Heutink, Peter;
Aguzzi, Adriano

Publication type:

Article

Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease.

Published in:

Brain Communications, 2022, v. 4, n. 4, p. 1, doi. 10.1093/braincomms/fcac201

By:

Nihat, Akın;
Ranson, Janice M.;
Harris, Dominique;
McNiven, Kirsty;
TzeHow Mok;
Rudge, Peter;
Collinge, John;
Llewellyn, David J.;
Mead, Simon

Publication type:

Article

In vitro screen of prion disease susceptibility genes using the scrapie cell assay.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 19, p. 5102, doi. 10.1093/hmg/ddu233

By:

Brown, Craig A.;
Schmidt, Christian;
Poulter, Mark;
Hummerich, Holger;
Klöhn, Peter-C.;
Jat, Parmjit;
Mead, Simon;
Collinge, John;
Lloyd, Sarah E.

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

CHCHD10 Pro34Ser is not a highly penetrant pathogenic variant for amyotrophic lateral sclerosis and frontotemporal dementia.

Published in:

2016

By:

Abdelkarim, Samir;
Morgan, Sarah;
Plagno, Vincent;
Lu, Ching-Hua;
Adamson, Gary;
Howard, Robin;
Malaspina, Andrea;
Orrell, Richard;
Sharma, Nikhil;
Sidle, Katie;
Clarke, Jan;
Fox, Nick C.;
Rossor, Martin N.;
Warren, Jason D.;
Clark, Camilla N.;
Rohrer, Jonathan D.;
Fisher, Elizabeth M. C.;
Mead, Simon;
Pittman, Alan;
Fratta, Pietro

Publication type:

Letter

Common polygenic variation enhances risk prediction for Alzheimer's disease.

Published in:

2015

By:

Escott-Price, Valentina;
Sims, Rebecca;
Bannister, Christian;
Harold, Denise;
Vronskaya, Maria;
Majounie, Elisa;
Badarinarayan, Nandini;
Morgan, Kevin;
Passmore, Peter;
Holmes, Clive;
Powell, John;
Brayne, Carol;
Gill, Michael;
Mead, Simon;
Goate, Alison;
Cruchaga, Carlos;
Lambert, Jean-Charles;
van Duijn, Cornelia;
Maier, Wolfgang;
Ramirez, Alfredo

Publication type:

journal article

Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years.

Published in:

2015

By:

Rudge, Peter;
Jaunmuktane, Zane;
Adlard, Peter;
Bjurstrom, Nina;
Caine, Diana;
Lowe, Jessica;
Norsworthy, Penny;
Hummerich, Holger;
Druyeh, Ron;
Wadsworth, Jonathan D. F.;
Brandner, Sebastian;
Hyare, Harpreet;
Mead, Simon;
Collinge, John

Publication type:

journal article

The Medical Research Council Prion Disease Rating Scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies.

Published in:

Brain: A Journal of Neurology, 2013, v. 136, n. 4, p. 1116, doi. 10.1093/brain/awt048

By:

Thompson, Andrew G.B.;
Lowe, Jessica;
Fox, Zoe;
Lukic, Ana;
Porter, Marie-Claire;
Ford, Liz;
Gorham, Michele;
Gopalakrishnan, Gosala S.;
Rudge, Peter;
Walker, A. Sarah;
Collinge, John;
Mead, Simon

Publication type:

Article

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features.

Published in:

Brain: A Journal of Neurology, 2012, v. 135, n. 3, p. 736, doi. 10.1093/brain/awr361

By:

Mahoney, Colin J.;
Beck, Jon;
Rohrer, Jonathan D.;
Lashley, Tammaryn;
Mok, Kin;
Shakespeare, Tim;
Yeatman, Tom;
Warrington, Elizabeth K.;
Schott, Jonathan M.;
Fox, Nick C.;
Rossor, Martin N.;
Hardy, John;
Collinge, John;
Revesz, Tamas;
Mead, Simon;
Warren, Jason D.

Publication type:

Article

Prion protein gene M232R variation is probably an uncommon polymorphism rather than a pathogenic mutation.

Published in:

Brain: A Journal of Neurology, 2012, v. 135, n. 2, p. e209, doi. 10.1093/brain/awr294

By:

Beck, Jon;
Collinge, John;
Mead, Simon

Publication type:

Article

Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.

Published in:

Brain: A Journal of Neurology, 2011, v. 134, n. 9, p. 2565, doi. 10.1093/brain/awr198

By:

Rohrer, Jonathan D.;
Lashley, Tammaryn;
Schott, Jonathan M.;
Warren, Jane E.;
Mead, Simon;
Isaacs, Adrian M.;
Beck, Jonathan;
Hardy, John;
de Silva, Rohan;
Warrington, Elizabeth;
Troakes, Claire;
Al-Sarraj, Safa;
King, Andrew;
Borroni, Barbara;
Clarkson, Matthew J.;
Ourselin, Sebastien;
Holton, Janice L.;
Fox, Nick C.;
Revesz, Tamas;
Rossor, Martin N.

Publication type:

Article

Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors.

Published in:

Brain: A Journal of Neurology, 2011, v. 134, n. 6, p. 1829, doi. 10.1093/brain/awr079

By:

Kaski, Diego N.;
Pennington, Catherine;
Beck, Jon;
Poulter, Mark;
Uphill, James;
Bishop, Matthew T.;
Linehan, Jaqueline M.;
O’Malley, Catherine;
Wadsworth, Jonathan D. F.;
Joiner, Susan;
Knight, Richard S. G.;
Ironside, James W.;
Brandner, Sebastian;
Collinge, John;
Mead, Simon

Publication type:

Article

Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseases.

Published in:

Brain: A Journal of Neurology, 2010, v. 133, n. 10, p. 3058, doi. 10.1093/brain/awq243

By:

Siddique, Durrenajaf;
Hyare, Harpreet;
Wroe, Stephen;
Webb, Thomas;
Macfarlane, Rebecca;
Rudge, Peter;
Collinge, John;
Powell, Caroline;
Brandner, Sebastian;
Po-Wah So;
Walker, Sarah;
Mead, Simon;
Yousry, Tarek;
Thornton, John S.

Publication type:

Article

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.

Published in:

Brain: A Journal of Neurology, 2008, v. 131, n. 3, p. 706, doi. 10.1093/brain/awm320

By:

Jonathan Beck;
Jonathan D. Rohrer;
Tracy Campbell;
Adrian Isaacs;
Karen E. Morrison;
Emily F. Goodall;
Elizabeth K. Warrington;
John Stevens;
Tamas Revesz;
Janice Holton;
Safa Al-Sarraj;
Andrew King;
Rachael Scahill;
Jason D. Warren;
Nick C. Fox;
Martin N. Rossor;
John Collinge;
Simon Mead

Publication type:

Article

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

Published in:

2006

By:

Mead S;
Poulter M;
Beck J;
Webb TE;
Campbell TA;
Linehan JM;
Desbruslais M;
Joiner S;
Wadsworth JD;
King A;
Lantos P;
Collinge J;
Mead, Simon;
Poulter, Mark;
Beck, Jon;
Webb, Thomas E F;
Campbell, Tracy A;
Linehan, Jacqueline M;
Desbruslais, Melanie;
Joiner, Susan

Publication type:

journal article

Inherited prion disease with six octapeptide repeat insertional mutation—molecular analysis of phenotypic heterogeneity.

Published in:

Brain: A Journal of Neurology, 2006, v. 129, n. 9, p. 2297, doi. 10.1093/brain/awl226

By:

Simon Mead;
Mark Poulter;
Jon Beck;
Thomas E. F. Webb;
Tracy A. Campbell;
Jacqueline M. Linehan;
Melanie Desbruslais;
Susan Joiner;
Jonathan D. F. Wadsworth;
Andrew King;
Peter Lantos;
John Collinge

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

The differential genetic architecture between posterior cortical atrophy and amnestic Alzheimer's disease: Genetics/atypical and other dementias.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.038851

By:

Scelsi, Marzia Antonella;
Napolioni, Valerio;
Mead, Simon;
Crutch, Sebastian J.;
Schott, Jonathan M.;
Greicius, Michael D.;
Altmann, Andre

Publication type:

Article

P4‐240: STOP‐GAIN VARIANT IN MICROGLIA‐EXPRESSED GENE GMIP IS ASSOCIATED WITH EARLY‐ONSET ALZHEIMER'S DISEASE.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1534, doi. 10.1016/j.jalz.2018.07.061

By:

Khan, Raiyan R.;
Altmann, Andre;
Napolioni, Valerio;
Kim, Yongha;
Guerreiro, Rita;
Bras, Jose T.;
Carmona, Susana;
Pereira, Miguel;
Santana, Isabel;
Hardy, John;
Mead, Simon;
Cruchaga, Carlos;
Fernandez, Maria Victoria;
Holstege, Henne;
Van der Flier, Wiesje M.;
Hulsman, Marc;
Van der Lee, Sven J.;
Chen, Yuning;
Bis, Joshua C.;
Launer, Lenore J.

Publication type:

Article