Browsing Universitätsbibliographie by Author "Heutink, Peter"

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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

Simón-Sánchez, Javier; Gasser, Thomas; Heutink, Peter (2019)
A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family

Giri, Anamika; Hauser, Ann-Kathrin; Heutink, Peter; Gasser, Thomas; Simón-Sánchez, Javier; Lohmann, Ebba (2016)
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia

Rizzu, Patrizia; Heutink, Peter (2017)
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance

Jansen, Iris Elisabeth; Sharma, Manu; Gasser, Thomas; Heutink, Peter (2016)
An atlas of human long non-coding RNAs with accurate 5 ' ends

Heutink, Peter (2017)
An integrated expression atlas of miRNAs and their promoters in human and mouse

Heutink, Peter; Rizzu, Patrizia (2017)
Analysis of shared heritability in common disorders of the brain

Lerche, Holger; Becker, Felicitas; Gasser, Thomas; Heutink, Peter; Sharma, Manu; Freilinger, Tobias Maximilian (2018)
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases

Heutink, Peter; Rizzu, Patrizia (2019)
beta(2)-Adrenoreceptor is a regulator of the alpha-synuclein gene driving risk of Parkinson's disease

Rizzu, Patrizia; Heutink, Peter (2017)
Brain-specific noncoding RNAs are likely to originate in repeats and may play a role in up-regulating genes in cis

Francescatto, Margherita; Heutink, Peter (2014)
C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriers

Rizzu, Patrizia; Blauwendraat, Cornelis; Heetveld, Sasja; Lynes, Emily M.; Castillo-Lizardo, Melissa; Dhingra, Ashutosh; Pyz, Elwira; Hobert, Markus Alexander; Synofzik, Matthis Benjamin; Simón-Sánchez, Javier; Francescatto, Margherita; Heutink, Peter (2016)
C9orf72; abnormal RNA expression is the key

Heutink, Peter; Lynes, Emily M. (2014)
CAGE-defined promoter regions of the genes implicated in Rett Syndrome

Heutink, Peter (2014)
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia

Wilke, Carlo; Deuschle, Christian; Hobert, Markus Alexander; Jansen, Iris Elisabeth; Heutink, Peter; Gasser, Thomas; Maetzler, Walter; Blauwendraat, Cornelis; Metzger, Florian G.; Synofzik, Matthis Benjamin (2017)
Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe

Blauwendraat, Cornelis; Francescatto, Margherita; Jansen, Iris Elisabeth; Simón-Sánchez, Javier; Rizzu, Patrizia; Heutink, Peter (2016)
Data Descriptor: FANTOM5 CAGE profiles of human and mouse samples

Heutink, Peter; Rizzu, Patrizia (2017)
Deep learning-based cell composition analysis from tissue expression profiles

Menden, Kevin; Dalmia, Anupriya; Heutink, Peter; Bonn, Stefan (2020)
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

Simón-Sánchez, Javier; Heutink, Peter; Brockmann, Kathrin; Schulte, Claudia; Gasser, Thomas (2016)
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome

Rizzu, Patrizia; Heutink, Peter (2015)
DGEclust: differential expression analysis of clustered count data

Francescatto, Margherita; Heutink, Peter (2015)

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