The <scp><i>ZFHX3</i> GGC</scp> Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder
Zhongbo Chen(Institute of Human Genetics), Henry Houlden(Queen Mary University of London), John Hardy(UK Dementia Research Institute), Pilar Álvarez Jerez(National Institute on Aging), Per Svenningsson(Karolinska Institutet), Daniel Nilsson(Karolinska University Hospital), Mina Ryten(Guy's Hospital), Martin Paucar(Karolinska University Hospital), Kylie Montgomery(New England Biolabs (United States)), Martin Engvall(Linköping University), Claire Anderson(Great Ormond Street Hospital), Louis J. Ptáček(University of California, San Francisco), Katherine D. Mathews(University of Iowa), Jasmaine Lee(Queen Mary University of London), Hannah Macpherson(University College London), Emil K. Gustavsson(University of British Columbia), Cornelis Blauwendraat(National Institute of Neurological Disorders and Stroke), Ying‐Hui Fu(University of California, San Francisco), Andrew B. Singleton(National Institutes of Health), José Miguel Laffita‐Mesa(Karolinska Institutet), Anna Wedell(Karolinska University Hospital), Inger Nennesmo(Karolinska University Hospital), Arianna Tucci(Queen Mary University of London), Annarita Scardamaglia(Queen Mary University of London)
Cited by 5
Related Papers
Mild cognitive impairment – beyond controversies, towards a consensus: report of the International Working Group on Mild Cognitive Impairment
|Journal of Internal Medicine|2004|5k
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
|Nature Genetics|2009|3.4k
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk
|Nature Genetics|2019|2.5k
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
|Nature Genetics|2011|2.1k