Peter Heutink
Peter Heutink
Verified email at - Homepage
Cited by
Cited by
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron 72 (2), 257-268, 2011
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
M Hutton, CL Lendon, P Rizzu, M Baker, S Froelich, H Houlden, ...
Nature 393 (6686), 702-705, 1998
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
V Bonifati, P Rizzu, MJ Van Baren, O Schaap, GJ Breedveld, E Krieger, ...
science 299 (5604), 256-259, 2003
An atlas of active enhancers across human cell types and tissues
R Andersson, C Gebhard, I Miguel-Escalada, I Hoof, J Bornholdt, M Boyd, ...
Nature 507 (7493), 455-461, 2014
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
KA McAllister, KM Grogg, DW Johnson, CJ Gallione, MA Baldwin, ...
Nature genetics 8 (4), 345-351, 1994
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
A promoter-level mammalian expression atlas
Fantom Consortium
Nature 507 (7493), 462, 2014
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
International Parkinson Disease Genomics Consortium
The Lancet 377 (9766), 641-649, 2011
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
B Brais, JP Bouchard, YG Xie, DL Rochefort, N Chrétien, F Tomé, ...
Nature genetics 18 (2), 164-167, 1998
An atlas of human long non-coding RNAs with accurate 5′ ends
CC Hon, JA Ramilowski, J Harshbarger, N Bertin, OJL Rackham, J Gough, ...
Nature 543 (7644), 199-204, 2017
Somatic retrotransposition alters the genetic landscape of the human brain
JK Baillie, MW Barnett, KR Upton, DJ Gerhardt, TA Richmond, F De Sapio, ...
Nature 479 (7374), 534-537, 2011
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers
CF Lippa, JE Duda, M Grossman, HI Hurtig, D Aarsland, BF Boeve, ...
Neurology 68 (11), 812-819, 2007
Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population‐based study
SM Rosso, LD Kaat, T Baks, M Joosse, I De Koning, Y Pijnenburg, ...
Brain 126 (9), 2016-2022, 2003
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis
OT Njajou, N Vaessen, M Joosse, B Berghuis, JWF van Dongen, ...
Nature genetics 28 (3), 213-214, 2001
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
CM Lill, JT Roehr, MB McQueen, FK Kavvoura, S Bagade, BMM Schjeide, ...
PLoS genetics 8 (3), e1002548, 2012
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly
LA Lettice, T Horikoshi, SJH Heaney, MJ van Baren, HC van der Linde, ...
Proceedings of the national academy of sciences 99 (11), 7548-7553, 2002
Role of COL4A1 in small-vessel disease and hemorrhagic stroke
DB Gould, FC Phalan, SE Van Mil, JP Sundberg, K Vahedi, P Massin, ...
New England Journal of Medicine 354 (14), 1489-1496, 2006
The system can't perform the operation now. Try again later.
Articles 1–20