Rothstein JH - Search Results

1

Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates.

Sieh W, Choi Y, Chapman NH, Craig UK, Steinbart EJ, Rothstein JH, Oyanagi K, Garruto RM, Bird TD, Galasko DR, Schellenberg GD, Wijsman EM. Sieh W, et al. Among authors: rothstein jh. Hum Mol Genet. 2009 Oct 1;18(19):3725-38. doi: 10.1093/hmg/ddp300. Epub 2009 Jun 30. Hum Mol Genet. 2009. PMID: 19567404 Free PMC article.

2

Approaches to mapping genetically correlated complex traits.

George AW, Basu S, Li N, Rothstein JH, Sieberts SK, Stewart W, Wijsman EM, Thompson EA. George AW, et al. Among authors: rothstein jh. BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S71. doi: 10.1186/1471-2156-4-S1-S71. BMC Genet. 2003. PMID: 14975139 Free PMC article.

3

Genomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.

Igo RP Jr, Chapman NH, Berninger VW, Matsushita M, Brkanac Z, Rothstein JH, Holzman T, Nielsen K, Raskind WH, Wijsman EM. Igo RP Jr, et al. Among authors: rothstein jh. Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):15-27. doi: 10.1002/ajmg.b.30245. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16331673 Free PMC article.

4

Comparison of marker types and map assumptions using Markov chain Monte Carlo-based linkage analysis of COGA data.

Sieh W, Basu S, Fu AQ, Rothstein JH, Scheet PA, Stewart WC, Sung YJ, Thompson EA, Wijsman EM. Sieh W, et al. Among authors: rothstein jh. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S11. doi: 10.1186/1471-2156-6-S1-S11. BMC Genet. 2005. PMID: 16451566 Free PMC article.

5

Evidence for multiple loci from a genome scan of autism kindreds.

Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM. Schellenberg GD, et al. Mol Psychiatry. 2006 Nov;11(11):1049-60, 979. doi: 10.1038/sj.mp.4001874. Epub 2006 Aug 1. Mol Psychiatry. 2006. PMID: 16880825 Free article.

6

Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees.

Wijsman EM, Rothstein JH, Thompson EA. Wijsman EM, et al. Among authors: rothstein jh. Am J Hum Genet. 2006 Nov;79(5):846-58. doi: 10.1086/508472. Epub 2006 Sep 20. Am J Hum Genet. 2006. PMID: 17033961 Free PMC article.

7

Comparison of multipoint linkage analyses for quantitative traits in the CEPH data: parametric LOD scores, variance components LOD scores, and Bayes factors.

Sung YJ, Di Y, Fu AQ, Rothstein JH, Sieh W, Tong L, Thompson EA, Wijsman EM. Sung YJ, et al. Among authors: rothstein jh. BMC Proc. 2007;1 Suppl 1(Suppl 1):S93. doi: 10.1186/1753-6561-1-s1-s93. Epub 2007 Dec 18. BMC Proc. 2007. PMID: 18466597 Free PMC article.

8

Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.

Wijsman EM, Rothstein JH, Igo RP Jr, Brunzell JD, Motulsky AG, Jarvik GP. Wijsman EM, et al. Among authors: rothstein jh. Hum Genet. 2010 Jun;127(6):705-19. doi: 10.1007/s00439-010-0819-2. Epub 2010 Apr 11. Hum Genet. 2010. PMID: 20383777 Free PMC article.

9

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.

Chapman NH, Estes A, Munson J, Bernier R, Webb SJ, Rothstein JH, Minshew NJ, Dawson G, Schellenberg GD, Wijsman EM. Chapman NH, et al. Among authors: rothstein jh. Hum Genet. 2011 Jan;129(1):59-70. doi: 10.1007/s00439-010-0899-z. Epub 2010 Oct 21. Hum Genet. 2011. PMID: 20963441 Free PMC article.

10

Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE.

Wijsman EM, Pankratz ND, Choi Y, Rothstein JH, Faber KM, Cheng R, Lee JH, Bird TD, Bennett DA, Diaz-Arrastia R, Goate AM, Farlow M, Ghetti B, Sweet RA, Foroud TM, Mayeux R; NIA-LOAD/NCRAD Family Study Group. Wijsman EM, et al. Among authors: rothstein jh. PLoS Genet. 2011 Feb;7(2):e1001308. doi: 10.1371/journal.pgen.1001308. Epub 2011 Feb 17. PLoS Genet. 2011. PMID: 21379329 Free PMC article.

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