Back to Authors

Younkin, Steve

A5042216535 | I2801572250

Mayo Clinic

Jacksonville College

Citations 7

P4‐126: Cognitive Performance Correlates with Resting State Connectivity and is Effected by APOE Status

Alzheimer's & Dementia | October 26, 2010 | Volume: 6 | Issue: 4S_Part_21 | Pages: No page available

10.1016/j.jalz.2010.08.185

P4‐054: First Multicenter Qualification of an Assay (INNO‐BIA Plasma Aß Forms Assay) for Measurement of ß‐amyloid Proteins as Part of US‐ADNI Efforts for Biomarker Qualification

Alzheimer's & Dementia | October 26, 2010 | Volume: 6 | Issue: 4S_Part_20 | Pages: No page available

10.1016/j.jalz.2010.08.114

IC‐P‐062: Cognitive Performance Correlates with Resting State Connectivity and is Effected by APOE Status

Alzheimer's & Dementia | July 11, 2010 | Volume: 6 | Issue: 4S_Part_1 | Pages: No page available

10.1016/j.jalz.2010.05.077

P4‐124: An examination of previously reported Alzheimer candidate genes within a large genome‐wide association dataset

Alzheimer's & Dementia | June 25, 2009 | Volume: 5 | Issue: 4S_Part_15 | Pages: No page available

10.1016/j.jalz.2009.04.792

P4‐121: Genome‐wide association study of Alzheimer's with psychotic symptoms

Alzheimer's & Dementia | June 25, 2009 | Volume: 5 | Issue: 4S_Part_15 | Pages: No page available

10.1016/j.jalz.2009.04.789

A worldwide multicentre comparison of assays for cerebrospinal fluid biomarkers in Alzheimer's disease

Annals of Clinical Biochemistry: International Journal of Laboratory Medicine | April 23, 2009 | Volume: 46 | Issue: 3 | Pages: 235-240

10.1258/acb.2009.008232 | PMID 19342441

Background Different cerebrospinal fluid (CSF) amyloid-beta 1–42 (A β 1–42 ), total Tau (Tau) and Tau phosphorylated at threonine 181 (P-Tau) levels are reported, but currently there is a lack of quality control programmes. The aim of this study was to compare the measurements of these CSF biomarkers, between and within centres. Methods Three CSF-pool samples were distributed to 13 laboratories in 2004 and the same samples were again distributed to 18 laboratories in 2008. In 2004 six laboratories measured A β 1–42 , Tau and P-Tau and seven laboratories measured one or two of these marker(s) by enzyme-linked immunosorbent assays (ELISAs). In 2008, 12 laboratories measured all three markers, three laboratories measured one or two marker(s) by ELISAs and three laboratories measured the markers by Luminex. Results In 2004, the ELISA intercentre coefficients of variance (interCV) were 31%, 21% and 13% for A β 1–42 , Tau and P-Tau, respectively. These were 37%, 16% and 15%, respectively, in 2008. When we restricted the analysis to the Innotest ® ( N = 13) for A β 1–42 , lower interCV were calculated (22%). The centres that participated in both years ( N = 9) showed interCVs of 21%, 15% and 9% and intra-centre coefficients (intraCV) of variance of 25%,18% and 7% in 2008. Conclusions The highest variability was found for A β 1–42 . The variabilities for Tau and P-Tau were lower in both years. The centres that participated in both years showed a high intraCV comparable to their interCV, indicating that there is not only a high variation between but also within centres. Besides a uniform standardization of (pre)analytical procedures, the same assay should be used to decrease the inter/intracentre variation.
P4‐167: Investigation of mitochondrial DNA damage in late‐onset Alzheimer's disease

Alzheimer's & Dementia | July 24, 2008 | Volume: 4 | Issue: 4S_Part_22 | Pages: No page available

10.1016/j.jalz.2008.05.2234