Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome

Karen Hsiao, Harry F. Baker, Tim Crow, +6

Nature

Creutzfeldt-jakob DiseaseGenetic DisorderGeneticsPathogenesisProtein Genetics +7

INCREASED DOPAMINE-RECEPTOR SENSITIVITY IN SCHIZOPHRENIA

F. Owen, Timothy J. Crow, Mark Poulter, +3

The Lancet

PsychiatryPsychotic DisorderSchizophreniaNeuropharmacologySocial Sciences +5

Balancing Selection at the Prion Protein Gene Consistent with Prehistoric Kurulike Epidemics

Simon Mead, Michael P. H. Stumpf, Jerome Whitfield, +8

Science

Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

Jon Beck, Mark Poulter, Davina J. Hensman Moss, +24

The American Journal of Human Genetics

Neurodegenerative DiseasesGenetic DisorderGeneticsMultiple Neurodegenerative SyndromesDegenerative Disease +5

Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

O Nöel Gill, Y. I. Spencer, Angela Richard-Loendt, +14

BMJ

Prion dementia without characteristic pathology

John Collinge, F. Owen, Mark Poulter, +7

The Lancet

Alzheimer's DiseaseCreutzfeldt-jakob DiseasePrion DementiaDementiaPrion Disease +6

Lactase Haplotype Diversity in the Old World

Edward J. Hollox, Mark Poulter, Marek Zvarík, +5

The American Journal of Human Genetics

Lactase Haplotype DiversityHaplotype DeterminationMolecular EcologyMedicineGenetics +6

<i>C9orf72</i> expansions are the most common genetic cause of Huntington disease phenocopies

Davina J. Hensman Moss, Mark Poulter, Jon Beck, +12

Neurology

A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure

Simon Mead, Jerome Whitfield, Mark Poulter, +11

New England Journal of Medicine

INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION: 2. CLINICAL AND PATHOLOGICAL FEATURES

John Collinge, Jeremy M. Brown, John Hardy, +17

Brain