Peter Heutink
Peter Heutink
Verified email at dzne.de - Homepage
TitleCited byYear
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, 1998
32171998
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
27332011
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
25352003
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, 1994
14501994
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, 2014
12872014
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, 2014
9232014
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
B Brais, JP Bouchard, YG Xie, DL Rochefort, N Chrétien, FMS Tomé, ...
Nature genetics 18 (2), 164, 1998
7611998
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
7252012
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
7102011
A promoter-level mammalian expression atlas
ARR Forrest, H Kawaji, M Rehli, JK Baillie, MJL De Hoon, V Haberle, ...
Nature 507 (7493), 462, 2014
6612014
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, 2011
5662011
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, 2001
5172001
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
5152007
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
5152003
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
4682002
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
4362012
High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands
P Rizzu, JC Van Swieten, M Joosse, M Hasegawa, M Stevens, A Tibben, ...
The American Journal of Human Genetics 64 (2), 414-421, 1999
4281999
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36
CM Van Duijn, MCJ Dekker, V Bonifati, RJ Galjaard, ...
The American Journal of Human Genetics 69 (3), 629-634, 2001
4202001
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
4132006
Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly
DB Gould, FC Phalan, GJ Breedveld, SE van Mil, RS Smith, JC Schimenti, ...
Science 308 (5725), 1167-1171, 2005
4112005
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