Association of progranulin polymorphism rs5848 with neurodegenerative diseases: a meta-analysis

Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis

(2013) A. Cannon et al.   NEUROLOGY

Association between GRN rs5848 Polymorphism and Parkinson′s Disease in Taiwanese Population

(2013) Kuo-Hsuan Chang et al.   PLoS One

Progranulin Mutations as Risk Factors for Alzheimer Disease

(2013) David C. Perry et al.   JAMA Neurology

Progranulin: An emerging target for FTLD therapies

(2012) Jennifer Gass et al.   BRAIN RESEARCH

Towards Unveiling the Genetics of Neurodegenerative Diseases

(2012) Christina Lill et al.   SEMINARS IN NEUROLOGY

Potential Mechanisms of Progranulin-deficient FTLD

(2011) Michael Emmerson Ward et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

rs5848 Variant of Progranulin Gene Is a Risk of Alzheimer’s Disease in the Taiwanese Population

(2011) Ming-Jen Lee et al.   Neurodegenerative Diseases

Common Variant inGRNIs a Genetic Risk Factor for Hippocampal Sclerosis in the Elderly

(2010) Dennis W. Dickson et al.   Neurodegenerative Diseases

The granulin gene family: from cancer to dementia

(2009) Andrew Bateman et al.   BIOESSAYS

Rethinking ALS: The FUS about TDP-43

(2009) Clotilde Lagier-Tourenne et al.   CELL

GRN3′UTR+78 C>T is not associated with risk for Parkinson’s disease

(2009) B. Jasinska-Myga et al.   EUROPEAN JOURNAL OF NEUROLOGY

Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models

(2009) Sandra Pereson et al.   JOURNAL OF PATHOLOGY

No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort

(2009) Roberto Del Bo et al.   NEUROBIOLOGY OF AGING

No association of PGRN 3′UTR rs5848 in frontotemporal lobar degeneration

(2009) Sara Rollinson et al.   NEUROBIOLOGY OF AGING

The heritability and genetics of frontotemporal lobar degeneration

(2009) J. D. Rohrer et al.   NEUROLOGY

Variation at GRN 3′-UTR rs5848 Is Not Associated with a Risk of Frontotemporal Lobar Degeneration in Dutch Population

(2009) Javier Simón-Sánchez et al.   PLoS One

An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population

(2008) Jayashree Viswanathan et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

(2008) Rosa Rademakers et al.   HUMAN MOLECULAR GENETICS

Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease

(2008) Anne Rovelet-Lecrux et al.   NEUROBIOLOGY OF DISEASE

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

(2008) N. Brouwers et al.   NEUROLOGY

Progranulin variability has no major role in Parkinson disease genetic etiology

(2008) K. Nuytemans et al.   NEUROLOGY

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

(2008) K. Sleegers et al.   NEUROLOGY

Loss of progranulin function in frontotemporal lobar degeneration

(2008) Marc Cruts et al.   TRENDS IN GENETICS

Genetic studies of GRN and IFT74 in amyotrophic lateral sclerosis

(2007) Shangxi Xiao et al.   NEUROBIOLOGY OF AGING