Frontotemporal Dementia: From Mendelian Genetics Towards Genome Wide Association Studies
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Frontotemporal Dementia: From Mendelian Genetics Towards Genome Wide Association Studies
Authors
Keywords
-
Journal
JOURNAL OF MOLECULAR NEUROSCIENCE
Volume 45, Issue 3, Pages 500-515
Publisher
Springer Nature
Online
2011-09-07
DOI
10.1007/s12031-011-9635-y
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Valosin-Containing Protein Gene Mutations: Cellular Phenotypes Relevant to Neurodegeneration
- (2011) Karen S. Poksay et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
- (2011) Adam C Naj et al. NATURE GENETICS
- Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
- (2011) Paul Hollingworth et al. NATURE GENETICS
- The Many Faces of Tau
- (2011) Meaghan Morris et al. NEURON
- The Growth Factor Progranulin Binds to TNF Receptors and Is Therapeutic Against Inflammatory Arthritis in Mice
- (2011) W. Tang et al. SCIENCE
- Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis
- (2010) Ryan Vass et al. ACTA NEUROPATHOLOGICA
- Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma
- (2010) Minerva M. Carrasquillo et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Monte Carlo Simulations of Tau Proteins: Effect of Phosphorylation
- (2010) Y.S. Jho et al. BIOPHYSICAL JOURNAL
- Disentangling the Role of the Tau Gene Locus in Sporadic Tauopathies
- (2010) J. Vandrovcova et al. Current Alzheimer Research
- Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy
- (2010) J. S. Ju et al. HUMAN MOLECULAR GENETICS
- Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations
- (2010) Hazel Urwin et al. HUMAN MOLECULAR GENETICS
- Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures
- (2010) Gernot Kleinberger et al. JOURNAL OF NEUROCHEMISTRY
- CHMP2B mutations are rare in French families with frontotemporal lobar degeneration
- (2010) Mustapha Ghanim et al. JOURNAL OF NEUROLOGY
- Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review
- (2010) H. Seelaar et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- A map of human genome variation from population-scale sequencing
- (2010) Richard M. Durbin et al. NATURE
- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
- (2010) Vivianna M Van Deerlin et al. NATURE GENETICS
- Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations
- (2010) Jonathan D. Rohrer et al. NEUROIMAGE
- TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers
- (2010) N. Finch et al. NEUROLOGY
- Sortilin-Mediated Endocytosis Determines Levels of the Frontotemporal Dementia Protein, Progranulin
- (2010) Fenghua Hu et al. NEURON
- Towards a complete resolution of the genetic architecture of disease
- (2010) Andrew B. Singleton et al. TRENDS IN GENETICS
- Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
- (2009) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Serum biomarker for progranulin-associated frontotemporal lobar degeneration
- (2009) Kristel Sleegers et al. ANNALS OF NEUROLOGY
- The role of CHMP2B in frontotemporal dementia
- (2009) Hazel Urwin et al. BIOCHEMICAL SOCIETY TRANSACTIONS
- Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
- (2009) N. Finch et al. BRAIN
- Neurobiology of cognitive disorders
- (2009) Alexander Kurz et al. CURRENT OPINION IN PSYCHIATRY
- No Evidence of PGRN or MAPT Gene Dosage Alterations in a Collection of Patients with Frontotemporal Lobar Degeneration
- (2009) Lena Skoglund et al. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
- Partial deletion of theMAPTgene: A novel mechanism of FTDP-17
- (2009) Anne Rovelet-Lecrux et al. HUMAN MUTATION
- VCPMutations Causing Frontotemporal Lobar Degeneration Disrupt Localization of TDP-43 and Induce Cell Death
- (2009) Michael A. Gitcho et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- 17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction
- (2009) B Grisart et al. JOURNAL OF MEDICAL GENETICS
- Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin
- (2009) Dorothee Dormann et al. JOURNAL OF NEUROCHEMISTRY
- Hereditary Inclusion Body Myopathy-Linked p97/VCP Mutations in the NH2 Domain and the D1 Ring Modulate p97/VCP ATPase Activity and D2 Ring Conformation
- (2009) D. Halawani et al. MOLECULAR AND CELLULAR BIOLOGY
- Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
- (2009) Jean-Charles Lambert et al. NATURE GENETICS
- Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
- (2009) Denise Harold et al. NATURE GENETICS
- The heritability and genetics of frontotemporal lobar degeneration
- (2009) J. D. Rohrer et al. NEUROLOGY
- Valosin-containing protein disease: Inclusion body myopathy with Paget’s disease of the bone and fronto-temporal dementia
- (2009) Conrad C. Weihl et al. NEUROMUSCULAR DISORDERS
- Genomewide Association Studies and Human Disease
- (2009) John Hardy et al. NEW ENGLAND JOURNAL OF MEDICINE
- Genetic screen identifies serpin5 as a regulator of the toll pathway and CHMP2B toxicity associated with frontotemporal dementia
- (2009) S. T. Ahmad et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
- (2008) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Gene expression study on peripheral blood identifies progranulin mutations
- (2008) Giovanni Coppola et al. ANNALS OF NEUROLOGY
- Argyrophilic grain disease
- (2008) I. Ferrer et al. BRAIN
- Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
- (2008) Stuart M. Pickering-Brown et al. BRAIN
- Granulin mutations associated with frontotemporal lobar degeneration and related disorders: An update
- (2008) I. Gijselinck et al. HUMAN MUTATION
- Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia
- (2008) Odity Mukherjee et al. HUMAN MUTATION
- Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia
- (2008) John C van Swieten et al. LANCET NEUROLOGY
- Evolutionary toggling of the MAPT 17q21.31 inversion region
- (2008) Michael C Zody et al. NATURE GENETICS
- Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease
- (2008) Anne Rovelet-Lecrux et al. NEUROBIOLOGY OF DISEASE
- Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide
- (2008) Luisa Benussi et al. NEUROBIOLOGY OF DISEASE
- Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
- (2008) R. Ghidoni et al. NEUROLOGY
- Adapting Proteostasis for Disease Intervention
- (2008) William E. Balch et al. SCIENCE
- Loss of progranulin function in frontotemporal lobar degeneration
- (2008) Marc Cruts et al. TRENDS IN GENETICS
- A novel deletion in progranulin gene is associated with FTDP-17 and CBS
- (2006) Luisa Benussi et al. NEUROBIOLOGY OF AGING
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search