Younkin SG - Search Results

1

A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts.

Younkin SG, Scharpf RB, Schwender H, Parker MM, Scott AF, Marazita ML, Beaty TH, Ruczinski I. Younkin SG, et al. Birth Defects Res A Clin Mol Teratol. 2015 Apr;103(4):276-83. doi: 10.1002/bdra.23362. Epub 2015 Mar 16. Birth Defects Res A Clin Mol Teratol. 2015. PMID: 25776870 Free PMC article.

2

Fast detection of de novo copy number variants from SNP arrays for case-parent trios.

Scharpf RB, Beaty TH, Schwender H, Younkin SG, Scott AF, Ruczinski I. Scharpf RB, et al. Among authors: younkin sg. BMC Bioinformatics. 2012 Dec 12;13:330. doi: 10.1186/1471-2105-13-330. BMC Bioinformatics. 2012. PMID: 23234608 Free PMC article.

3

A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk.

Younkin SG, Scharpf RB, Schwender H, Parker MM, Scott AF, Marazita ML, Beaty TH, Ruczinski I. Younkin SG, et al. BMC Genet. 2014 Feb 14;15:24. doi: 10.1186/1471-2156-15-24. BMC Genet. 2014. PMID: 24528994 Free PMC article.

4

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.

Bureau A, Younkin SG, Parker MM, Bailey-Wilson JE, Marazita ML, Murray JC, Mangold E, Albacha-Hejazi H, Beaty TH, Ruczinski I. Bureau A, et al. Among authors: younkin sg. Bioinformatics. 2014 Aug 1;30(15):2189-96. doi: 10.1093/bioinformatics/btu198. Epub 2014 Apr 16. Bioinformatics. 2014. PMID: 24740360 Free PMC article.

5

On multi-marker tests for association in case-control studies.

Taub MA, Schwender HR, Younkin SG, Louis TA, Ruczinski I. Taub MA, et al. Among authors: younkin sg. Front Genet. 2013 Dec 16;4:252. doi: 10.3389/fgene.2013.00252. eCollection 2013. Front Genet. 2013. PMID: 24379823 Free PMC article.

6

Detecting disease variants in case-parent trio studies using the bioconductor software package trio.

Schwender H, Li Q, Neumann C, Taub MA, Younkin SG, Berger P, Scharpf RB, Beaty TH, Ruczinski I. Schwender H, et al. Among authors: younkin sg. Genet Epidemiol. 2014 Sep;38(6):516-22. doi: 10.1002/gepi.21836. Epub 2014 Jul 21. Genet Epidemiol. 2014. PMID: 25048299 Free PMC article.

7

Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studies.

Neumann C, Taub MA, Younkin SG, Beaty TH, Ruczinski I, Schwender H. Neumann C, et al. Among authors: younkin sg. Biom J. 2014 Nov;56(6):1076-92. doi: 10.1002/bimj.201300148. Epub 2014 Aug 14. Biom J. 2014. PMID: 25123830 Free PMC article.

8

Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection.

Zhang Q, Zeng X, Younkin S, Kawli T, Snyder MP, Keleş S. Zhang Q, et al. BMC Bioinformatics. 2016 Feb 24;17:96. doi: 10.1186/s12859-016-0957-1. BMC Bioinformatics. 2016. PMID: 26908256 Free PMC article.

9

Amyloid-β predominant Alzheimer's disease neuropathologic change.

Kovacs GG, Katsumata Y, Wu X, Aung KZ, Fardo DW, Forrest SL; Alzheimer's Disease Genetics Consortium; Nelson PT. Kovacs GG, et al. Brain. 2024 Oct 17:awae325. doi: 10.1093/brain/awae325. Online ahead of print. Brain. 2024. PMID: 39417691

10

Whole genome-wide sequence analysis of long-lived families (Long-Life Family Study) identifies MTUS2 gene associated with late-onset Alzheimer's disease.

Xicota L, Cosentino S, Vardarajan B, Mayeux R, Perls TT, Andersen SL, Zmuda JM, Thyagarajan B, Yashin A, Wojczynski MK, Krinsky-McHale S, Handen BL, Christian BT, Head E, Mapstone ME, Schupf N, Lee JH, Barral S; Long‐Life Family Study (LLFS); Alzheimer's Disease Genetic Consortium (ADGC); Alzheimer's Biomarkers Consortium‐Down Syndrome (ABC‐DS). Xicota L, et al. Alzheimers Dement. 2024 Apr;20(4):2670-2679. doi: 10.1002/alz.13718. Epub 2024 Feb 21. Alzheimers Dement. 2024. PMID: 38380866 Free PMC article.

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