Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2004 | 1 |
2005 | 1 |
2007 | 2 |
2010 | 1 |
2011 | 1 |
2014 | 1 |
2024 | 0 |
Search Results
7 results
Results by year
Filters applied: . Clear all
Page 1
Symptom onset in autosomal dominant Alzheimer disease: a systematic review and meta-analysis.
Neurology. 2014 Jul 15;83(3):253-60. doi: 10.1212/WNL.0000000000000596. Epub 2014 Jun 13.
Neurology. 2014.
PMID: 24928124
Free PMC article.
Review.
APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation.
Wijsman EM, Daw EW, Yu X, Steinbart EJ, Nochlin D, Bird TD, Schellenberg GD.
Wijsman EM, et al.
Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):14-20. doi: 10.1002/ajmg.b.30087.
Am J Med Genet B Neuropsychiatr Genet. 2005.
PMID: 15389756
Item in Clipboard
A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2.
Kay DM, Stevens CF, Hamza TH, Montimurro JS, Zabetian CP, Factor SA, Samii A, Griffith A, Roberts JW, Molho ES, Higgins DS, Gancher S, Moses L, Zareparsi S, Poorkaj P, Bird T, Nutt J, Schellenberg GD, Payami H.
Kay DM, et al.
Neurology. 2010 Sep 28;75(13):1189-94. doi: 10.1212/WNL.0b013e3181f4d832.
Neurology. 2010.
PMID: 20876472
Free PMC article.
Item in Clipboard
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Höglinger GU, Melhem NM, Dickson DW, Sleiman PM, Wang LS, Klei L, Rademakers R, de Silva R, Litvan I, Riley DE, van Swieten JC, Heutink P, Wszolek ZK, Uitti RJ, Vandrovcova J, Hurtig HI, Gross RG, Maetzler W, Goldwurm S, Tolosa E, Borroni B, Pastor P; PSP Genetics Study Group; Cantwell LB, Han MR, Dillman A, van der Brug MP, Gibbs JR, Cookson MR, Hernandez DG, Singleton AB, Farrer MJ, Yu CE, Golbe LI, Revesz T, Hardy J, Lees AJ, Devlin B, Hakonarson H, Müller U, Schellenberg GD.
Höglinger GU, et al.
Nat Genet. 2011 Jun 19;43(7):699-705. doi: 10.1038/ng.859.
Nat Genet. 2011.
PMID: 21685912
Free PMC article.
Item in Clipboard
Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease.
Sieh W, Yu CE, Bird TD, Schellenberg GD, Wijsman EM.
Sieh W, et al.
Hum Hered. 2007;63(1):26-34. doi: 10.1159/000098459. Epub 2007 Jan 11.
Hum Hered. 2007.
PMID: 17215579
Item in Clipboard
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2.
Wijsman EM, Daw EW, Yu CE, Payami H, Steinbart EJ, Nochlin D, Conlon EM, Bird TD, Schellenberg GD.
Wijsman EM, et al.
Am J Hum Genet. 2004 Sep;75(3):398-409. doi: 10.1086/423393. Epub 2004 Jul 8.
Am J Hum Genet. 2004.
PMID: 15248153
Free PMC article.
Item in Clipboard
Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data.
Wijsman EM, Sung YJ, Buil A, Atkinson E, Bastone L, Christensen GB, Diao G, Feng T, Franceschini N, Huang S, Kan D, Kerner B, Lantieri F, Lee E, Papachristou C, Paterson A, Rangrej J, Wang S, Xing C, Zhu X.
Wijsman EM, et al.
Genet Epidemiol. 2007;31 Suppl 1:S75-85. doi: 10.1002/gepi.20283.
Genet Epidemiol. 2007.
PMID: 18046772
Item in Clipboard
Cite
Cite