MtDNA deletions discriminate affected from unaffected LRRK2 mutation carriersOuzren, Nassima; Delcambre, Sylvie; Ghelfi, Jenny; Seibler, Philip; Farrer, Matthew J.; König, Inke R.; Aasly, Jan O.; Trinh, Joanne; Klein, Christine; Grünewald, Anne · Annals of Neurology · 2019

PARK11 is not linked with Parkinson's disease in European familiesPrestel, Jürgen; Sharma, Manu; Leitner, Petra; Zimprich, Alexander; Vaughan, Jenny R; Dürr, Alexandra; Bonifati, Vincenzo; De Michele, Giuseppe; Hanagasi, Hasmet A; Farrer, Matthew · 2004

Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs diseaseLincoln, Sarah; Vaughan, Jenny; Wood, Nick; Baker, Matt; Adamson, Jennifer; Gwinn-Hardy, Katrina; Lynch, Tim; Hardy, John; Farrer, Matt · NeuroReport · 1999

Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's diseaseMaria Martinez; Alexis Brice; Jenny R. Vaughan; Alexander Zimprich; Monique M.B. Breteler; Giuseppe Meco; Alessandro Filla; Matthew J. Farrer; Christine Bétard; Andrew Singleton; John Hardy; Giuseppe De Michele; Vincenzo Bonifati; Ben A. Oostra; Thomas Gasser; Nick W. Wood; Alexandra Dürr · 2005

Caspase-8, association with Alzheimer’s Disease and functional analysis of rare variantsRehker, Jan; Rodhe, Johanna; Nesbitt, Ryan R.; Boyle, Evan A.; Martin, Beth K.; Lord, Jenny; Karaca, Ilker; Naj, Adam; Jessen, Frank; Helisalmi, Seppo; Soininen, Hilkka; Hiltunen, Mikko; Ramirez, Alfredo; Scherer, Martin; Farrer, Lindsay A.; Haines, Jonathan L.; Pericak-Vance, Margaret A.; Raskind, Wendy H.; Cruchaga, Carlos; Schellenberg, Gerard D.; Joseph, Bertrand; Brkanac, Zoran; Lakshmana, Madepalli K. · PLOS ONE · 2017

Missense variant in TREML2 protects against Alzheimer's diseaseBenitez, Bruno A.; Jin, Sheng Chih; Guerreiro, Rita; Graham, Rob; Lord, Jenny; Harold, Denise; Sims, Rebecca; Lambert, Jean-Charles; Gibbs, J. Raphael; Bras, Jose; Sassi, Celeste; Harari, Oscar; Bertelsen, Sarah; Lupton, Michelle K.; Powell, John; Bellenguez, Celine; Brown, Kristelle; Medway, Christopher; Haddick, Patrick CG.; van der Brug, Marcel P.; Bhangale, Tushar; Ortmann, Ward; Behrens, Tim; Mayeux, Richard; Pericak-Vance, Margaret A.; Farrer, Lindsay A.; Schellenberg, Gerard D.; Haines, Jonathan L.; Turton, Jim; Braae, Anne; Barber, Imelda; Fagan, Anne M.; Holtzman, David M.; Morris, John C.; Williams, Julie; Kauwe, John S.K.; Amouyel, Philippe; Morgan, Kevin; Singleton, Andy; Hardy, John; Goate, Alison M.; Cruchaga, Carlos · Neurobiology of Aging · 2014

The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB.Sanjay Harhangi; Matthew J. Farrer; Sarah Lincoln; Vincenzo Bonifati; Giuseppe Meco; Giuseppe De Michele; Alexis Brice; Alexandra Dürr; Maria Martinez; Thomas Gasser; Benjamin Bereznai; Jenny R. Vaughan; Nicholas W. Wood; John Hardy; Ben A. Oostra; Monique M.B. Breteler · 1999