1 - 25 of 98 results for author:"Schellenberg G.D." in Literature citations
Results Customize
› Repeat search in UniProtKB (20)
| Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. Alzheimer Disease Genetics Consortium JAMA 309:1483-1492(2013) · Mapped (5) |
| APOE epsilon4 increases risk for dementia in pure synucleinopathies. Tsuang D., Leverenz J.B., Lopez O.L., Hamilton R.L., Bennett D.A., Schneider J.A., Buchman A.S., Larson E.B., Crane P.K., Kaye J.A. et al. JAMA Neurol 70:223-228(2013) · Mapped (5) |
| Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Alzheimer's Disease Genetics Consortium Nat. Genet. 44:1349-1354(2012) · Mapped (25) |
| Comprehensive search for Alzheimer disease susceptibility loci in the APOE region. Alzheimer's Disease Genetics Consortium Arch. Neurol. 69:1270-1279(2012) · Mapped (5) |
| Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets. ARRA Autism Sequencing Consortium Am. J. Hum. Genet. 90:1002-1013(2012) · Mapped (8) |
| Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory. Barral S., Bird T., Goate A., Farlow M.R., Diaz-Arrastia R., Bennett D.A., Graff-Radford N., Boeve B.F., Sweet R.A., Stern Y. et al. Neurology 78:1464-1471(2012) · Mapped (20) |
| Patterns and rates of exonic de novo mutations in autism spectrum disorders. Neale B.M., Kou Y., Liu L., Ma'ayan A., Samocha K.E., Sabo A., Lin C.F., Stevens C., Wang L.S., Makarov V. et al. Nature 485:242-245(2012) · Mapped (3) |
| Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. PD GWAS Consortium Ann. Neurol. 71:370-384(2012) · Mapped (1) |
| Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Chromosome 9-ALS/FTD Consortium Lancet Neurol 11:323-330(2012) · Mapped (2) |
| Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families. NIA-LOAD/NCRAD Family Study Consortium PLoS ONE 7:e31039-e31039(2012) · Mapped (13) |
| Genome-wide association study of Alzheimer's disease with psychotic symptoms. GERAD Consortium Mol. Psychiatry 17:1316-1327(2012) · Mapped (4) |
| Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Hoglinger G.U., Melhem N.M., Dickson D.W., Sleiman P.M., Wang L.S., Klei L., Rademakers R., de Silva R., Litvan I., Riley D.E. et al. Nat. Genet. 43:699-705(2011) · Mapped (6) |
| ABCB1 genotype and CSF beta-amyloid in Alzheimer disease. Kohen R., Shofer J.B., Korvatska O., Petrie E.C., Wang L.Y., Schellenberg G.D., Peskind E.R., Wilkinson C.W. J Geriatr Psychiatry Neurol 24:63-66(2011) · Mapped (9) |
| Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Naj A.C., Jun G., Beecham G.W., Wang L.S., Vardarajan B.N., Buros J., Gallins P.J., Buxbaum J.D., Jarvik G.P., Crane P.K. et al. Nat. Genet. 43:436-441(2011) · Mapped (14) |
| Mutations in the TSGA14 gene in families with autism spectrum disorders. Korvatska O., Estes A., Munson J., Dawson G., Bekris L.M., Kohen R., Yu C.E., Schellenberg G.D., Raskind W.H. Am. J. Med. Genet. B Neuropsychiatr. Genet. 156:303-311(2011) · UniProtKB (1) |
| Amyloid precursor protein (APP) processing genes and cerebrospinal fluid APP cleavage product levels in Alzheimer's disease. Bekris L.M., Galloway N.M., Millard S., Lockhart D., Li G., Galasko D.R., Farlow M.R., Clark C.M., Quinn J.F., Kaye J.A. et al. Neurobiol. Aging 32:556.e13-23(2011) · Mapped (3) |
| Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study. Han M.R., Schellenberg G.D., Wang L.S. BMC Neurol 10:90-90(2010) · Mapped (20) |
| A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2. Kay D.M., Stevens C.F., Hamza T.H., Montimurro J.S., Zabetian C.P., Factor S.A., Samii A., Griffith A., Roberts J.W., Molho E.S. et al. Neurology 75:1189-1194(2010) · Mapped (33) |
| Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. Noor A., Whibley A., Marshall C.R., Gianakopoulos P.J., Piton A., Carson A.R., Orlic-Milacic M., Lionel A.C., Sato D., Pinto D. et al. Sci. Transl. Med. 2:49RA68-49RA68(2010) · UniProtKB (2) · Mapped (2) |
| Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. Alzheimer's Disease Genetics Consortium Arch. Neurol. 67:1473-1484(2010) · Mapped (38) |
| A genome-wide scan for common alleles affecting risk for autism. Anney R., Klei L., Pinto D., Regan R., Conroy J., Magalhaes T.R., Correia C., Abrahams B.S., Sykes N., Pagnamenta A.T. et al. Hum. Mol. Genet. 19:4072-4082(2010) · Mapped (14) |
| Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice. Melrose H.L., Dachsel J.C., Behrouz B., Lincoln S.J., Yue M., Hinkle K.M., Kent C.B., Korvatska E., Taylor J.P., Witten L. et al. Neurobiol. Dis. 40:503-517(2010) · Mapped (4) |
| Age-varying association between statin use and incident Alzheimer's disease. Li G., Shofer J.B., Rhew I.C., Kukull W.A., Peskind E.R., McCormick W., Bowen J.D., Schellenberg G.D., Crane P.K., Breitner J.C. et al. J Am Geriatr Soc 58:1311-1317(2010) · Mapped (5) |
| Functional impact of global rare copy number variation in autism spectrum disorders. Pinto D., Pagnamenta A.T., Klei L., Anney R., Merico D., Regan R., Conroy J., Magalhaes T.R., Correia C., Abrahams B.S. et al. Nature 466:368-372(2010) · Mapped (7) |
| APOE genotype is associated with oral herpetic lesions but not genital or oral herpes simplex virus shedding. Koelle D.M., Magaret A., Warren T., Schellenberg G.D., Wald A. Sex Transm Infect 86:202-206(2010) · Mapped (5) |