McCarroll SA - Search Results

1

Copy number variation in schizophrenia in Sweden.

Szatkiewicz JP, O'Dushlaine C, Chen G, Chambert K, Moran JL, Neale BM, Fromer M, Ruderfer D, Akterin S, Bergen SE, Kähler A, Magnusson PK, Kim Y, Crowley JJ, Rees E, Kirov G, O'Donovan MC, Owen MJ, Walters J, Scolnick E, Sklar P, Purcell S, Hultman CM, McCarroll SA, Sullivan PF. Szatkiewicz JP, et al. Among authors: mccarroll sa. Mol Psychiatry. 2014 Jul;19(7):762-73. doi: 10.1038/mp.2014.40. Epub 2014 Apr 29. Mol Psychiatry. 2014. PMID: 24776740 Free PMC article.

2

Evaluation of common variants in the six known maturity-onset diabetes of the young (MODY) genes for association with type 2 diabetes.

Winckler W, Weedon MN, Graham RR, McCarroll SA, Purcell S, Almgren P, Tuomi T, Gaudet D, Boström KB, Walker M, Hitman G, Hattersley AT, McCarthy MI, Ardlie KG, Hirschhorn JN, Daly MJ, Frayling TM, Groop L, Altshuler D. Winckler W, et al. Among authors: mccarroll sa. Diabetes. 2007 Mar;56(3):685-93. doi: 10.2337/db06-0202. Diabetes. 2007. PMID: 17327436

3

Copy-number variation and association studies of human disease.

McCarroll SA, Altshuler DM. McCarroll SA, et al. Nat Genet. 2007 Jul;39(7 Suppl):S37-42. doi: 10.1038/ng2080. Nat Genet. 2007. PMID: 17597780 Review.

4

Rare chromosomal deletions and duplications increase risk of schizophrenia.

International Schizophrenia Consortium. International Schizophrenia Consortium. Nature. 2008 Sep 11;455(7210):237-41. doi: 10.1038/nature07239. Epub 2008 Jul 30. Nature. 2008. PMID: 18668038 Free PMC article.

5

Integrated detection and population-genetic analysis of SNPs and copy number variation.

McCarroll SA, Kuruvilla FG, Korn JM, Cawley S, Nemesh J, Wysoker A, Shapero MH, de Bakker PI, Maller JB, Kirby A, Elliott AL, Parkin M, Hubbell E, Webster T, Mei R, Veitch J, Collins PJ, Handsaker R, Lincoln S, Nizzari M, Blume J, Jones KW, Rava R, Daly MJ, Gabriel SB, Altshuler D. McCarroll SA, et al. Nat Genet. 2008 Oct;40(10):1166-74. doi: 10.1038/ng.238. Epub 2008 Sep 7. Nat Genet. 2008. PMID: 18776908

6

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.

Korn JM, Kuruvilla FG, McCarroll SA, Wysoker A, Nemesh J, Cawley S, Hubbell E, Veitch J, Collins PJ, Darvishi K, Lee C, Nizzari MM, Gabriel SB, Purcell S, Daly MJ, Altshuler D. Korn JM, et al. Among authors: mccarroll sa. Nat Genet. 2008 Oct;40(10):1253-60. doi: 10.1038/ng.237. Epub 2008 Sep 7. Nat Genet. 2008. PMID: 18776909 Free PMC article.

7

Extending genome-wide association studies to copy-number variation.

McCarroll SA. McCarroll SA. Hum Mol Genet. 2008 Oct 15;17(R2):R135-42. doi: 10.1093/hmg/ddn282. Hum Mol Genet. 2008. PMID: 18852202 Review.

8

A genome-wide linkage and association scan reveals novel loci for autism.

Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium; Daly MJ, Chakravarti A. Weiss LA, et al. Nature. 2009 Oct 8;461(7265):802-8. doi: 10.1038/nature08490. Nature. 2009. PMID: 19812673 Free PMC article.

9

Copy number variation and human genome maps.

McCarroll SA. McCarroll SA. Nat Genet. 2010 May;42(5):365-6. doi: 10.1038/ng0510-365. Nat Genet. 2010. PMID: 20428091

10

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.

Raychaudhuri S, Korn JM, McCarroll SA; International Schizophrenia Consortium; Altshuler D, Sklar P, Purcell S, Daly MJ. Raychaudhuri S, et al. Among authors: mccarroll sa. PLoS Genet. 2010 Sep 9;6(9):e1001097. doi: 10.1371/journal.pgen.1001097. PLoS Genet. 2010. PMID: 20838587 Free PMC article.

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