Similar articles for PMID: 26084464

Year	Number of Results
2004	1
2005	2
2006	3
2008	1
2009	3
2010	2
2011	2
2012	1
2013	3
2014	5
2015	11
2016	7
2017	5
2018	5
2019	9
2020	4
2021	4
2022	6
2024	0

1

Massively parallel quantification of the regulatory effects of noncoding genetic variation in a human cohort.

Vockley CM, Guo C, Majoros WH, Nodzenski M, Scholtens DM, Hayes MG, Lowe WL Jr, Reddy TE. Vockley CM, et al. Genome Res. 2015 Aug;25(8):1206-14. doi: 10.1101/gr.190090.115. Epub 2015 Jun 17. Genome Res. 2015. PMID: 26084464 Free PMC article.

2

Rare and common regulatory variation in population-scale sequenced human genomes.

Montgomery SB, Lappalainen T, Gutierrez-Arcelus M, Dermitzakis ET. Montgomery SB, et al. PLoS Genet. 2011 Jul;7(7):e1002144. doi: 10.1371/journal.pgen.1002144. Epub 2011 Jul 21. PLoS Genet. 2011. PMID: 21811411 Free PMC article.

3

Meta-analysis of massively parallel reporter assays enables prediction of regulatory function across cell types.

Kreimer A, Yan Z, Ahituv N, Yosef N. Kreimer A, et al. Hum Mutat. 2019 Sep;40(9):1299-1313. doi: 10.1002/humu.23820. Epub 2019 Jun 18. Hum Mutat. 2019. PMID: 31131957 Free PMC article.

4

A composite of multiple signals distinguishes causal variants in regions of positive selection.

Grossman SR, Shlyakhter I, Karlsson EK, Byrne EH, Morales S, Frieden G, Hostetter E, Angelino E, Garber M, Zuk O, Lander ES, Schaffner SF, Sabeti PC. Grossman SR, et al. Science. 2010 Feb 12;327(5967):883-6. doi: 10.1126/science.1183863. Epub 2010 Jan 7. Science. 2010. PMID: 20056855

5

Deciphering regulatory DNA sequences and noncoding genetic variants using neural network models of massively parallel reporter assays.

Movva R, Greenside P, Marinov GK, Nair S, Shrikumar A, Kundaje A. Movva R, et al. PLoS One. 2019 Jun 17;14(6):e0218073. doi: 10.1371/journal.pone.0218073. eCollection 2019. PLoS One. 2019. PMID: 31206543 Free PMC article.

6

Genomic approaches for understanding the genetics of complex disease.

Lowe WL Jr, Reddy TE. Lowe WL Jr, et al. Genome Res. 2015 Oct;25(10):1432-41. doi: 10.1101/gr.190603.115. Genome Res. 2015. PMID: 26430153 Free PMC article.

7

Construction of an integrative regulatory element and variation map of the murine Tst locus.

Beltram J, Morton NM, Kunej T, Horvat S. Beltram J, et al. BMC Genet. 2016 Jun 11;17(1):77. doi: 10.1186/s12863-016-0381-6. BMC Genet. 2016. PMID: 27287690 Free PMC article.

8

Multiple causal variants underlie genetic associations in humans.

Abell NS, DeGorter MK, Gloudemans MJ, Greenwald E, Smith KS, He Z, Montgomery SB. Abell NS, et al. Science. 2022 Mar 18;375(6586):1247-1254. doi: 10.1126/science.abj5117. Epub 2022 Mar 17. Science. 2022. PMID: 35298243 Free PMC article.

9

Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.

Li MJ, Yan B, Sham PC, Wang J. Li MJ, et al. Brief Bioinform. 2015 May;16(3):393-412. doi: 10.1093/bib/bbu018. Epub 2014 Jun 10. Brief Bioinform. 2015. PMID: 24916300 Review.

10

A method to predict the impact of regulatory variants from DNA sequence.

Lee D, Gorkin DU, Baker M, Strober BJ, Asoni AL, McCallion AS, Beer MA. Lee D, et al. Nat Genet. 2015 Aug;47(8):955-61. doi: 10.1038/ng.3331. Epub 2015 Jun 15. Nat Genet. 2015. PMID: 26075791 Free PMC article.

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