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Mancuso N, Gayther S, Gusev A, Zheng W, Penney KL; PRACTICAL consortium, Kote-Jarai Z, Eeles R, Freedman M, Haiman C, Pasaniuc B. Author Correction: Large-scale transcriptome-wide association study identifies new prostate cancer risk regions. Nat Commun. 2019 Jan 8;10(1):171. Doi: 10.1038/s41467-018-08108-7. Erratum for: Nat Commun. 2018 Oct 4;9(1):4079. PMID: 30622272; PMCID: PMC6325152.

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Major M, Freund MK, Burch KS, Mancuso N, Ng M, Furniss D, Pasaniuc B, Ophoff RA. Integrative analysis of Dupuytren’s disease identifies novel risk locus and reveals a shared genetic etiology with BMI. Genet Epidemiol. 2019 Sep;43(6):629-645. Doi: 10.1002/gepi.22209. Epub 2019 May 13. PMID: 31087417; PMCID: PMC6699495.

Hou K, Burch KS, Majumdar A, Shi H, Mancuso N, Wu Y, Sankararaman S, Pasaniuc B. Accurate estimation of SNP-heritability from biobank-scale data irrespective of genetic architecture. Nat Genet. 2019 Aug;51(8):1244-1251. Doi: 10.1038/s41588-019-0465-0. Epub 2019 Jul 29. PMID: 31358995; PMCID: PMC6686906.

Walker RL, Ramaswami G, Hartl C, Mancuso N, Gandal MJ, de la Torre-Ubieta L, Pasaniuc B, Stein JL, Geschwind DH. Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms. Cell. 2019 Oct 17;179(3):750-771.e22. doi: 10.1016/j.cell.2019.09.021. PMID: 31626773. PMCID in progress

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Brown R, Kichaev G, Mancuso N, Boocock J, Pasaniuc B. Enhanced methods to detect haplotypic effects on gene expression. Bioinformatics. 2017 Aug 1;33(15):2307-2313. Doi: 10.1093/bioinformatics/btx142. PMID: 28369161; PMCID: PMC5860109.

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Rosen EY, Wexler EM, Versano R, Coppola G, Gao F, Winden KD, Oldham MC, Martens LH, Zhou P, Farese RV Jr, Geschwind DH. Functional genomic analyses identify pathways dysregulated by progranulin deficiency, implicating Wnt signaling. Neuron. 2011 Sep 22;71(6):1030-42. Doi: 10.1016/j.neuron.2011.07.021. Epub 2011 Sep 21. PMID: 21943601; PMCID: PMC3633414.

Joshi AA, Leporé N, Joshi SH, Lee AD, Barysheva M, Stein JL, McMahon KL, Johnson K, de Zubicaray GI, Martin NG, Wright MJ, Toga AW, Thompson PM. The contribution of genes to cortical thickness and volume. Neuroreport. 2011 Feb 16;22(3):101-5. Doi: 10.1097/WNR.0b013e3283424c84. PMID: 21233781; PMCID: PMC3079384.

Hibar DP, Stein JL, Kohannim O, Jahanshad N, Saykin AJ, Shen L, Kim S, Pankratz N, Foroud T, Huentelman MJ, Potkin SG, Jack CR Jr, Weiner MW, Toga AW, Thompson PM; Alzheimer’s Disease Neuroimaging Initiative. Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects. Neuroimage. 2011 Jun 15;56(4):1875-91. Doi: 10.1016/j.neuroimage.2011.03.077. Epub 2011 Apr 8. PMID: 21497199; PMCID: PMC3366726.

Marenco S, Stein JL, Savostyanova AA, Sambataro F, Tan HY, Goldman AL, Verchinski BA, Barnett AS, Dickinson D, Apud JA, Callicott JH, Meyer-Lindenberg A, Weinberger DR. Investigation of anatomical thalamo-cortical connectivity and FMRI activation in schizophrenia. Neuropsychopharmacology. 2012 Jan;37(2):499-507. Doi: 10.1038/npp.2011.215. Epub 2011 Sep 28. PMID: 21956440; PMCID: PMC3242311.

Hibar DP, Kohannim O, Stein JL, Chiang MC, Thompson PM. Multilocus genetic analysis of brain images. Front Genet. 2011 Oct 21;2:73. Doi: 10.3389/fgene.2011.00073. PMID: 22303368; PMCID: PMC3268626.

Kochunov P, Glahn DC, Nichols TE, Winkler AM, Hong EL, Holcomb HH, Stein JL, Thompson PM, Curran JE, Carless MA, Olvera RL, Johnson MP, Cole SA, Kochunov V, Kent J, Blangero J. Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain. Front Neurosci. 2011 Oct 19;5:120. Doi: 10.3389/fnins.2011.00120. PMID: 22028680; PMCID: PMC3199541.

Vounou M, Janousova E, Wolz R, Stein JL, Thompson PM, Rueckert D, Montana G; Alzheimer’s Disease Neuroimaging Initiative. Sparse reduced-rank regression detects genetic associations with voxel-wise longitudinal phenotypes in Alzheimer’s disease. Neuroimage. 2012 Mar;60(1):700-16. Doi: 10.1016/j.neuroimage.2011.12.029. Epub 2011 Dec 22. PMID: 22209813; PMCID: PMC3551466.

J Jahanshad N, Kohannim O, Hibar DP, Stein JL, McMahon KL, de Zubicaray GI, Medland SE, Montgomery GW, Whitfield JB, Martin NG, Wright MJ, Toga AW, Thompson PM. Brain structure in healthy adults is related to serum transferrin and the H63D polymorphism in the HFE gene. Proc Natl Acad Sci U S A. 2012 Apr 3;109(14):E851-9. Doi: 10.1073/pnas.1105543109. Epub 2012 Jan 9. PMID: 22232660; PMCID: PMC3325658.

Braskie MN, Jahanshad N, Stein JL, Barysheva M, Johnson K, McMahon KL, de Zubicaray GI, Martin NG, Wright MJ, Ringman JM, Toga AW, Thompson PM. Relationship of a variant in the NTRK1 gene to white matter microstructure in young adults. J Neurosci. 2012 Apr 25;32(17):5964-72. Doi: 10.1523/JNEUROSCI.5561-11.2012. PMID: 22539856; PMCID: PMC3393752.

Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, Murtha RC, Choi M, Overton JD, Bjornson RD, Carriero NJ, Meyer KA, Bilguvar K, Mane SM, Sestan N, Lifton RP, Günel M, Roeder K, Geschwind DH, Devlin B, State MW. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 2012 Apr 4;485(7397):237-41. Doi: 10.1038/nature10945. PMID: 22495306; PMCID: PMC3667984.

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