Sara Rollinson |
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration. |
2011 |
0 |
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Winnie C Pao |
Hippocampal Sclerosis in the Elderly: Genetic and Pathologic Findings, Some Mimicking AlzheimerDisease Clinically |
2011 |
0 |
10.1097/WAD.0b013e31820f8f50 |
Ging-Yuek R Hsiung |
rs5848 polymorphism and serum progranulin level. |
2011 |
0 |
 |
Daniela Galimberti |
GRN variability contributes to sporadic frontotemporal lobar degeneration. |
2010 |
3 |
10.3233/JAD-2010-1225 |
Dennis W Dickson |
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly. |
2010 |
0 |
10.1159/000289231 |
Jayashree Viswanathan |
An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population. |
2009 |
5 |
10.1002/ajmg.b.30889 |
B Jasinska-Myga |
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease. |
2009 |
5 |
10.1111/j.1468-1331.2009.02621.x |
B Jasinska-Myga |
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease. |
2009 |
4 |
- |
Mikko Hiltunen1 Anna Kämäläinen1, Jayashree Viswanathan1, Teemu Natunen1, Seppo Helisalmi1, Tarja Kauppinen1, Maria Pikkarainen1, Juha-Pekka Pursiheimo2, Irina Alafuzoff3, Miia Kivipelto1, 4, 5, Annakaisa Haapasalo1, Hilkka Soininen1, 6, Sanna-Kaisa Herukka1, 6 |
GRN Variant rs5848 Reduces Plasma and Brain Levels of Granulin in Alzheimer's Disease Patients |
2012 |
1 |
 |
Rosa Rademakers |
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia. |
2008 |
49 |
10.1093/hmg/ddn257 |
Sara Rollinson |
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration. |
2011 |
5 |
10.1016/j.neurobiolaging.2009.04.009 |
Javier Simón-Sánchez |
Variation at GRN 3′-UTR rs5848 Is Not Associated with a Risk of Frontotemporal Lobar Degeneration in Dutch Population |
2009 |
0 |
10.1371/journal.pone.0007494 |
Maria Neuner |
Progranulin Gene Variability and Plasma Levels in Bipolar Disorder and Schizophrenia |
2012 |
1 |
10.1371/journal.pone.0032164 |
Rosa Rademakers |
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia |
2008 |
0 |
10.1093/hmg/ddn257 |
Kuo-Hsuan Chang |
Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population. |
2013 |
1 |
10.1371/journal.pone.0054448 |
Caroline Racine |
Sporadic corticobasal syndrome due to FTLD-TDP |
2010 |
12 |
10.1007/s00401-009-0605-1 |
Daniela Galimberti |
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia. |
2012 |
0 |
10.1371/journal.pone.0032164 |
Ming-Jen Lee |
Robinson Annulation |
2011 |
0 |
10.1159/000322538 |
Sara Rollinson |
No association of PGRN 3'UTR rs5848 in frontotemporal lobar degeneration |
2011 |
5 |
10.1016/j.neurobiolaging.2009.04.009 |
Stuart M Pickering-Brown |
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 |
1 |
- |
Jayashree Viswanathan |
An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population. |
2009 |
0 |
 |
Kuo Hsuan Chang |
Association between GRN rs5848 Polymorphism and Parkinson′s Disease in Taiwanese Population |
2013 |
2 |
10.1371/journal.pone.0054448 |
Ming-Jen Lee |
rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population. |
2011 |
0 |
 |
Ming-Jen Lee |
rs5848 Variant of Progranulin Gene Is a Risk of Alzheimer's Disease in the Taiwanese Population. |
2011 |
0 |
10.1159/000322538 |
M C Tartaglia |
Sporadic corticobasal syndrome due to FTLD-TDP |
2010 |
0 |
10.1007/s00401-009-0605-1 |
Ming-Jen Lee |
Robinson Annulation |
2011 |
2 |
10.1159/000322538 |
Javier Simón-Sánchez |
Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population. |
2009 |
8 |
10.1371/journal.pone.0007494 |
Ging-Yuek R Hsiung |
rs5848 polymorphism and serum progranulin level. |
2011 |
15 |
10.1016/j.jns.2010.10.009 |
Ming-Jen Lee |
rs5848 variant of progranulin gene is a risk of Alzheimer's disease in the Taiwanese population. |
2011 |
10 |
000322538 [pii]\r10.1159/000322538 |
Ging Yuek R Hsiung |
Rs5848 polymorphism and serum progranulin level |
2011 |
16 |
10.1016/j.jns.2010.10.009 |
Daniela Galimberti |
GRN variability contributes to sporadic frontotemporal lobar degeneration. |
2010 |
0 |
 |
Dennis W Dickson |
Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly. |
2010 |
11 |
10.1159/000289231 |