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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2010 | 2 |
2011 | 1 |
2013 | 1 |
2014 | 2 |
2024 | 0 |
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Page 1
Robust regression analysis of copy number variation data based on a univariate score.
PLoS One. 2014 Feb 7;9(2):e86272. doi: 10.1371/journal.pone.0086272. eCollection 2014.
PLoS One. 2014.
PMID: 24516529
Free PMC article.
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia.
Mulle JG, Pulver AE, McGrath JA, Wolyniec PS, Dodd AF, Cutler DJ, Sebat J, Malhotra D, Nestadt G, Conrad DF, Hurles M, Barnes CP, Ikeda M, Iwata N, Levinson DF, Gejman PV, Sanders AR, Duan J, Mitchell AA, Peter I, Sklar P, O'Dushlaine CT, Grozeva D, O'Donovan MC, Owen MJ, Hultman CM, Kähler AK, Sullivan PF; Molecular Genetics of Schizophrenia Consortium; Kirov G, Warren ST.
Mulle JG, et al.
Biol Psychiatry. 2014 Mar 1;75(5):371-7. doi: 10.1016/j.biopsych.2013.05.040. Epub 2013 Jul 17.
Biol Psychiatry. 2014.
PMID: 23871472
Free PMC article.
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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, Collinson MN, Beal SJ, Ackley T, Pickering DL, Golden DM, Aston E, Whitby H, Shetty S, Rossi MR, Rudd MK, South ST, Brothman AR, Sanger WG, Iyer RK, Crolla JA, Thorland EC, Aradhya S, Ledbetter DH, Martin CL.
Kaminsky EB, et al.
Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9.
Genet Med. 2011.
PMID: 21844811
Free PMC article.
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Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population.
Bray SM, Mulle JG, Dodd AF, Pulver AE, Wooding S, Warren ST.
Bray SM, et al.
Proc Natl Acad Sci U S A. 2010 Sep 14;107(37):16222-7. doi: 10.1073/pnas.1004381107. Epub 2010 Aug 26.
Proc Natl Acad Sci U S A. 2010.
PMID: 20798349
Free PMC article.
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Microdeletions of 3q29 confer high risk for schizophrenia.
Mulle JG, Dodd AF, McGrath JA, Wolyniec PS, Mitchell AA, Shetty AC, Sobreira NL, Valle D, Rudd MK, Satten G, Cutler DJ, Pulver AE, Warren ST.
Mulle JG, et al.
Am J Hum Genet. 2010 Aug 13;87(2):229-36. doi: 10.1016/j.ajhg.2010.07.013.
Am J Hum Genet. 2010.
PMID: 20691406
Free PMC article.
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