Anders Paetau mostly deals with Pathology, Genetics, Mitochondrial DNA, Mutation and Mitochondrial disease. His Pathology research is multidisciplinary, incorporating perspectives in Inflammation and Stroke. His study involves Compound heterozygosity, Haplotype, C9orf72, C9orf72 Protein and DNA Repeat Expansion, a branch of Genetics.
The various areas that Anders Paetau examines in his Mitochondrial DNA study include Ataxia and Biopsy. His study in Mutation is interdisciplinary in nature, drawing from both Gene duplication, Hypertrophic cardiomyopathy, Idiopathic dilated cardiomyopathy and Polymerase chain reaction. His Mitochondrial disease study combines topics in areas such as Molecular biology, Respiratory chain, TRNA aminoacylation, Cytochrome c oxidase and Genetically modified mouse.
The scientist’s investigation covers issues in Pathology, Genetics, Internal medicine, Dementia and Molecular biology. His Pathology research focuses on Immunohistochemistry, Myopathy, Cerebral amyloid angiopathy, Neuropathology and Disease. His is involved in several facets of Genetics study, as is seen by his studies on Mitochondrial DNA, Compound heterozygosity, Mutation, Mitochondrial disease and Exome sequencing.
Mitochondrial DNA and Respiratory chain are frequently intertwined in his study. His Internal medicine study combines topics from a wide range of disciplines, such as Gastroenterology and Endocrinology. Anders Paetau focuses mostly in the field of Molecular biology, narrowing it down to topics relating to Glial fibrillary acidic protein and, in certain cases, Intermediate filament.
Anders Paetau mainly investigates Pathology, Genetics, Internal medicine, Dementia and Neuropathology. His Pathology research is multidisciplinary, incorporating elements of Encephalopathy and Hyperintensity. Mutation, Compound heterozygosity, Exon, Exome sequencing and Respiratory chain are the primary areas of interest in his Genetics study.
His Compound heterozygosity research includes elements of Muscle biopsy, Neurofilament and Missense mutation. His study explores the link between Internal medicine and topics such as Endocrinology that cross with problems in Mutation, Alpha and Single Center. His Neuropathology research integrates issues from Autopsy, Framingham Risk Score, Cerebral amyloid angiopathy and Single-nucleotide polymorphism.
His main research concerns Pathology, Genetics, Neuropathology, Mitochondrial myopathy and Immunology. Pathology and Hippocampal sclerosis are two areas of study in which Anders Paetau engages in interdisciplinary research. His work on Genetics deals in particular with Respiratory chain, Allele frequency, Allele, Compound heterozygosity and Mutation.
Anders Paetau focuses mostly in the field of Allele frequency, narrowing it down to matters related to Exome sequencing and, in some cases, Missense mutation. His Neuropathology study deals with Encephalopathy intersecting with Cell type and Astrocyte. Anders Paetau has included themes like Biochemistry of Alzheimer's disease, P3 peptide, Amyloid precursor protein, Disease and Exon in his Immunology study.
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Alan E. Renton;Elisa Majounie;Adrian James Waite;Javier Simón-Sánchez;Javier Simón-Sánchez.
Neuron (2011)
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
Tomlinson Ip;Alam Na;Rowan Aj;Barclay E.
Nature Genetics (2002)
Remodeling of Saccular Cerebral Artery Aneurysm Wall Is Associated With Rupture Histological Analysis of 24 Unruptured and 42 Ruptured Cases
Juhana Frösen;Anna Piippo;Anders Paetau;Marko Kangasniemi.
Stroke (2004)
A novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology
Petra Pasanen;Liisa Myllykangas;Maija Siitonen;Anna Raunio.
Neurobiology of Aging (2014)
Senile systemic amyloidosis affects 25% of the very aged and associates with genetic variation in alpha2-macroglobulin and tau: a population-based autopsy study
Maarit Tanskanen;Terhi Peuralinna;Tuomo Polvikoski;Irma-Leena Notkola.
Annals of Medicine (2008)
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1
Richard Crook;Auli Verkkoniemi;Jordi Perez-Tur;Nitin Mehta.
Nature Medicine (1998)
Saccular intracranial aneurysm: pathology and mechanisms
Juhana Frösen;Riikka Tulamo;Anders Paetau;Elisa Laaksamo.
Acta Neuropathologica (2012)
FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study.
Anu Suomalainen;Anu Suomalainen;Jenni M Elo;Kirsi H Pietiläinen;Anna H Hakonen.
Lancet Neurology (2011)
Adverse long-term effects of brain radiotherapy in adult low-grade glioma patients.
O. Surma-aho;M. Niemelä;J. Vilkki;M. Kouri.
Neurology (2001)
Mutant mitochondrial helicase Twinkle causes multiple mtDNA deletions and a late-onset mitochondrial disease in mice
Henna Tyynismaa;Katja Peltola Mjosund;Sjoerd Wanrooij;Ilse Lappalainen.
Proceedings of the National Academy of Sciences of the United States of America (2005)
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