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List of works by Peter Heutink

A Genome-Wide Search for Genes Involved in Type 2 Diabetes in a Recently Genetically Isolated Population From the Netherlands

article

A common polymorphism in the ABCB1 gene is associated with side effects of PGP-dependent antidepressants in a large naturalistic Dutch cohort.

scientific article

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

scientific article published on April 1, 1992

A new locus for postaxial polydactyly type A/B on chromosome 7q21–q34 ⬇️

scientific article published on 01 May 2003

A new polymorphic probe on chromosome 22: NB17 (D22S181) ⬇️

scientific article published on February 11, 1991

A new polymorphic probe on chromosome 22: NB84 (D22S183) ⬇️

scientific article published on February 11, 1991

A new polymorphic probe on chromosome 22q: NB129 (D22S193) ⬇️

scientific article published on February 11, 1991

A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p

scientific article published on 16 October 2007

A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family

scientific article published on 3 March 2016

A promoter-level mammalian expression atlas

scientific article

An atlas of human long non-coding RNAs with accurate 5' ends.

scientific article

An integrated expression atlas of miRNAs and their promoters in human and mouse.

scientific article

Analysis of variation in the melanocortin-4 receptor gene (mc4r) in golden retriever dogs

scientific article published on 7 September 2010

Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases

scientific article published on 04 January 2019

Brachydactyly and short stature in a kindred with early-onset parkinsonism

scientific article published on 01 September 2004

Brain-specific noncoding RNAs are likely to originate in repeats and may play a role in up-regulating genes in cis.

scientific article published on 30 June 2014

C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers.

scientific article

CAGE-defined promoter regions of the genes implicated in Rett Syndrome.

scientific article published on 24 December 2014

Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1

scientific article published on 01 June 2015

Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36

Common variants underlying cognitive ability: further evidence for association between the SNAP-25 gene and cognition using a family-based study in two independent Dutch cohorts

article

Deep learning-based cell composition analysis from tissue expression profiles

scientific article published on 22 July 2020

Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome ⬇️

scientific article

Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease

scientific article published on 17 September 2018

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

scientific article published on 18 June 2015

Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia.

scientific article published on 25 March 2013

FANTOM5 CAGE profiles of human and mouse samples

scientific article published on 29 August 2017

Familial aggregation of parkinsonism in progressive supranuclear palsy.

scientific article

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia

scientific article published on 01 January 2020

Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts

scientific article published on 09 July 2019

Genetic study on Tourette syndrome in The Netherlands

scientific article published on January 1, 1992

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

scientific article published on 09 February 2019

Genome-wide association study of Tourette's syndrome

scientific article

Genome-wide association study of obsessive-compulsive disorder.

scientific article

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

scientific article published on 10 September 2019

HPCA confirmed as a genetic cause of DYT2-like dystonia phenotype

scientific article published on 25 August 2018

Joint reanalysis of 29 correlated SNPs supports the role of PCLO/Piccolo as a causal risk factor for major depressive disorder

scientific article published on 01 July 2009

Linkage and Tourette syndrome ⬇️

scientific article published on January 12, 1991

Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset

scientific article published on 01 February 2002

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

scientific article published in April 2003

MAPT-Related Disorders

scientific article published on 26 October 2010

Medical image. Post mortem diagnosis of severe sepsis

scientific article published on 23 September 2011

Melanocortin-4 Receptor Gene Mutations in a Dutch Cohort of Obese Children

article

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.

scientific article

Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohort.

scientific article

Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly.

scientific article

Neurodegeneration: new road leads back to the synapse.

scientific article

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

scientific article

Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms

scientific article published on 07 April 2019

Population and genomic lessons from genetic analysis of two Indian populations.

scientific article published in July 2014

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

scientific article

Publisher Correction: Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease

scientific article published on 01 January 2019

Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's disease. ⬇️

scientific article published on 28 July 2016

Regional differences in gene expression and promoter usage in aged human brains.

scientific article

Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease.

scientific article published in March 2018

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy ⬇️

scientific article published on February 1, 1998

Somatic retrotransposition alters the genetic landscape of the human brain

scientific article (publication date: 30 October 2011)

Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25.

scientific article published on 28 July 2012

Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options.

scientific article

The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence

scientific article

Trehalose improves human fibroblast deficits in a new CHIP-mutation related ataxia.

scientific article

Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population.

scientific article

[Parkinson's disease(s): recent insight into genetic factors]

scientific article published on 01 July 2007

β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's disease.

scientific article

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