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Peter Heutink

Showing results (31-40 of 240) with videos related to

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Plos One|August 29, 2009
Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathwaysIraad F Bronner, Zoltán Bochdanovits, Patrizia Rizzu, et al.
Plos One|October 23, 2009
Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch populationJavier Simón-Sánchez, Harro Seelaar, Zoltán Bochdanovits, et al.
BMC Medical Genetics|July 20, 2010
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 a case-control studyMarieke E Teeuw, Lidewij Henneman, Zoltan Bochdanovits, et al.
Alzheimer Disease and Associated Disorders|February 23, 2012
Extended kindred with recessive late-onset Alzheimer disease maps to locus 8p22-p21.2: a genome-wide linkage analysisManuel Baron, Estrella Gomez-Tortosa, Zoltan Bochdanovits, et al.
BMC Medical Genetics|November 13, 2007
Exploring the functional role of the CHRM2 gene in human cognition: results from a dense genotyping and brain expression studyFlorencia M Gosso, Eco J C de Geus, Tinca J C Polderman, et al.
European Journal of Human Genetics : EJHG|April 3, 2008
Catechol O-methyl transferase and dopamine D2 receptor gene polymorphisms: evidence of positive heterosis and gene-gene interaction on working memory functioningM Florencia Gosso, Eco J C de Geus, Tinca J C Polderman, et al.
Genomics|June 18, 2003
CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorderAnnemieke J M H Verkerk, Carol A Mathews, Marijke Joosse, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|January 2, 2007
Attention problems and attention-deficit/hyperactivity disorder in discordant and concordant monozygotic twins: evidence of environmental mediatorsHanne Lehn, Eske M Derks, James J Hudziak, et al.
American Journal of Medical Genetics|September 5, 2002
Another family with nonspecific X-linked mental retardation (MRX78) maps to Xp11.4-p11.23Bert B A de Vries, Guido J Breedveld, Wouter H Deelen, et al.
Human Molecular Genetics|September 4, 2003
The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexesMaria G Macedo, Burcu Anar, Iraad F Bronner, et al.
Pageof 24

Showing results (31-40 of 240) with videos related to

Sort By:
Pageof 24
Plos One|August 29, 2009
Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathwaysIraad F Bronner, Zoltán Bochdanovits, Patrizia Rizzu, et al.
Plos One|October 23, 2009
Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch populationJavier Simón-Sánchez, Harro Seelaar, Zoltán Bochdanovits, et al.
BMC Medical Genetics|July 20, 2010
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 a case-control studyMarieke E Teeuw, Lidewij Henneman, Zoltan Bochdanovits, et al.
Alzheimer Disease and Associated Disorders|February 23, 2012
Extended kindred with recessive late-onset Alzheimer disease maps to locus 8p22-p21.2: a genome-wide linkage analysisManuel Baron, Estrella Gomez-Tortosa, Zoltan Bochdanovits, et al.
BMC Medical Genetics|November 13, 2007
Exploring the functional role of the CHRM2 gene in human cognition: results from a dense genotyping and brain expression studyFlorencia M Gosso, Eco J C de Geus, Tinca J C Polderman, et al.
European Journal of Human Genetics : EJHG|April 3, 2008
Catechol O-methyl transferase and dopamine D2 receptor gene polymorphisms: evidence of positive heterosis and gene-gene interaction on working memory functioningM Florencia Gosso, Eco J C de Geus, Tinca J C Polderman, et al.
Genomics|June 18, 2003
CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorderAnnemieke J M H Verkerk, Carol A Mathews, Marijke Joosse, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|January 2, 2007
Attention problems and attention-deficit/hyperactivity disorder in discordant and concordant monozygotic twins: evidence of environmental mediatorsHanne Lehn, Eske M Derks, James J Hudziak, et al.
American Journal of Medical Genetics|September 5, 2002
Another family with nonspecific X-linked mental retardation (MRX78) maps to Xp11.4-p11.23Bert B A de Vries, Guido J Breedveld, Wouter H Deelen, et al.
Human Molecular Genetics|September 4, 2003
The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexesMaria G Macedo, Burcu Anar, Iraad F Bronner, et al.
Pageof 24