Lodewijk A. Sandkuijl, M.D. (July 31, 1953–December 4, 2002)

Por Freimer, Nelson B., Heutink, Peter, Wijmenga, Cisca
Publicado em 2003

High Content Screening in Neurodegenerative Diseases

Por Jain, Shushant, van Kesteren, Ronald E., Heutink, Peter
Publicado em 2012

DGEclust: differential expression analysis of clustered count data

Por Vavoulis, Dimitrios V, Francescatto, Margherita, Heutink, Peter, Gough, Julian
Publicado no Genome Biol (2015)

Genome-Wide Prediction of Functional Gene-Gene Interactions Inferred from Patterns of Genetic Differentiation in Mice and Men

Por Bochdanovits, Zoltán, Sondervan, David, Perillous, Sophie, van Beijsterveldt, Toos, Boomsma, Dorret, Heutink, Peter
Publicado em 2008

Rhizosphere Acidification by Iron Deficient Bean Plants: The Role of Trace Amounts of Divalent Metal Ions: A Study on Roots of Intact Plants with the Use of (11)C- and (31)P-NMR

Por Bienfait, H. Frits, Lubberding, Henk J., Heutink, Peter, Lindner, L., Visser, Jacques, Kaptein, Rob, Dijkstra, Klaas
Publicado em 1989

Accurate prediction of a minimal region around a genetic association signal that contains the causal variant

Por Bochdanovits, Zoltán, Simón-Sánchez, Javier, Jonker, Marianne, Hoogendijk, Witte J, van der Vaart, Aad, Heutink, Peter
Publicado em 2014

Molecular Analysis of Mutant and Wild-Type Tau Deposited in the Brain Affected by the FTDP-17 R406W Mutation

Por Miyasaka, Tomohiro, Morishima-Kawashima, Maho, Ravid, Rivka, Heutink, Peter, van Swieten, John C., Nagashima, Kazuo, Ihara, Yasuo
Publicado em 2001

Exploring the functional role of the CHRM2 gene in human cognition: results from a dense genotyping and brain expression study

Por Gosso, Florencia M, de Geus, Eco JC, Polderman, Tinca JC, Boomsma, Dorret I, Posthuma, Danielle, Heutink, Peter
Publicado em 2007

Comprehensive mRNA Expression Profiling Distinguishes Tauopathies and Identifies Shared Molecular Pathways

Por Bronner, Iraad F., Bochdanovits, Zoltán, Rizzu, Patrizia, Kamphorst, Wouter, Ravid, Rivka, van Swieten, John C., Heutink, Peter
Publicado em 2009

Variation at GRN 3′-UTR rs5848 Is Not Associated with a Risk of Frontotemporal Lobar Degeneration in Dutch Population

Por Simón-Sánchez, Javier, Seelaar, Harro, Bochdanovits, Zoltán, Deeg, Dorly J. H., van Swieten, John C., Heutink, Peter
Publicado em 2009

Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of...

Por Teeuw, Marieke E, Henneman, Lidewij, Bochdanovits, Zoltan, Heutink, Peter, Kuik, Dirk J, Cornel, Martina C, ten Kate, Leo P
Publicado em 2010

Profiling transcription initiation in human aged brain using deep-CAGE

Por Francescatto, Margherita, Pardo, Luba, Rizzu, Patrizia, Vitezic, Morana, Simón-Sánchez, Javier, Takahashi, Hazuki, Daub, Carsten, Carninci, Piero, Heutink, Peter
Publicado em 2011

Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report

Por Bettencourt, Conceição, Santos, Cristina, Coutinho, Paula, Rizzu, Patrizia, Vasconcelos, João, Kay, Teresa, Cymbron, Teresa, Raposo, Mafalda, Heutink, Peter, Lima, Manuela
Publicado em 2011

Benign Hereditary Chorea of Early Onset Maps to Chromosome 14q

Por de Vries, Bert B. A., Arts, Willem F. M., Breedveld, Guido J., Hoogeboom, Jeannette J. M., Niermeijer, Martinus F., Heutink, Peter
Publicado em 2000

Global similarity with local differences in linkage disequilibrium between the Dutch and HapMap–CEU populations

Por Pardo, Luba, Bochdanovits, Zoltán, de Geus, Eco, Hottenga, Jouke J, Sullivan, Patrick, Posthuma, Danielle, Penninx, Brenda W J H, Boomsma, Dorret, Heutink, Peter
Publicado em 2009

Investigation of a Patient with a Partial Trisomy 16q Including the Fat mass and Obesity Associated gene (FTO): Fine Mapping and FTO Gene Expression Study

Por van den Berg, Linda, Delemarre-van de Waal, Henriette, Han, Joan C., Ylstra, Bauke, Eijk, Paul, Nesterova, Maria, Heutink, Peter, Stratakis, Constantine A.
Publicado em 2010

The Primary Erythermalgia–Susceptibility Gene Is Located on Chromosome 2q31-32

Por Drenth, Joost P. H., Finley, Wayne H., Breedveld, Guido J., Testers, Leon, Michiels, Jan J., Guillet, G., Taieb, Alain, Kirby, R. Lee, Heutink, Peter
Publicado em 2001

Evidence for Immune Response, Axonal Dysfunction and Reduced Endocytosis in the Substantia Nigra in Early Stage Parkinson’s Disease

Por Dijkstra, Anke A., Ingrassia, Angela, de Menezes, Renee X., van Kesteren, Ronald E., Rozemuller, Annemieke J. M., Heutink, Peter, van de Berg, Wilma D. J.
Publicado no PLoS One (2015)

PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism

Por Giri, Anamika, Guven, Gamze, Hanagasi, Hasmet, Hauser, Ann-Kathrin, Erginul-Unaltuna, Nihan, Bilgic, Basar, Gurvit, Hakan, Heutink, Peter, Gasser, Thomas, Lohmann, Ebba, Simón-Sánchez, Javier
Publicado no Tremor Other Hyperkinet Mov (N Y) (2016)

Dissecting the genetic make-up of North-East Sardinia using a large set of haploid and autosomal markers

Por Pardo, Luba M, Piras, Giovanna, Asproni, Rosanna, van der Gaag, Kristiaan J, Gabbas, Attilio, Ruiz-Linares, Andres, de Knijff, Peter, Monne, Maria, Rizzu, Patrizia, Heutink, Peter
Publicado em 2012