Churchill J - Search Results

1

Methylation of the candidate biomarker TCF21 is very frequent across a spectrum of early-stage nonsmall cell lung cancers.

Richards KL, Zhang B, Sun M, Dong W, Churchill J, Bachinski LL, Wilson CD, Baggerly KA, Yin G, Hayes DN, Wistuba II, Krahe R. Richards KL, et al. Among authors: churchill j. Cancer. 2011 Feb 1;117(3):606-17. doi: 10.1002/cncr.25472. Epub 2010 Oct 13. Cancer. 2011. PMID: 20945327 Free PMC article.

2

Exome-based mapping and variant prioritization for inherited Mendelian disorders.

Koboldt DC, Larson DE, Sullivan LS, Bowne SJ, Steinberg KM, Churchill JD, Buhr AC, Nutter N, Pierce EA, Blanton SH, Weinstock GM, Wilson RK, Daiger SP. Koboldt DC, et al. Among authors: churchill jd. Am J Hum Genet. 2014 Mar 6;94(3):373-84. doi: 10.1016/j.ajhg.2014.01.016. Epub 2014 Feb 20. Am J Hum Genet. 2014. PMID: 24560519 Free PMC article.

3

Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa.

Churchill JD, Bowne SJ, Sullivan LS, Lewis RA, Wheaton DK, Birch DG, Branham KE, Heckenlively JR, Daiger SP. Churchill JD, et al. Invest Ophthalmol Vis Sci. 2013 Feb 19;54(2):1411-6. doi: 10.1167/iovs.12-11541. Invest Ophthalmol Vis Sci. 2013. PMID: 23372056 Free PMC article.

4

Characterization of genetic sequence variation of 58 STR loci in four major population groups.

Novroski NMM, King JL, Churchill JD, Seah LH, Budowle B. Novroski NMM, et al. Forensic Sci Int Genet. 2016 Nov;25:214-226. doi: 10.1016/j.fsigen.2016.09.007. Epub 2016 Sep 28. Forensic Sci Int Genet. 2016. PMID: 27697609

5

Massively parallel sequencing of 68 insertion/deletion markers identifies novel microhaplotypes for utility in human identity testing.

Wendt FR, Warshauer DH, Zeng X, Churchill JD, Novroski NMM, Song B, King JL, LaRue BL, Budowle B. Wendt FR, et al. Forensic Sci Int Genet. 2016 Nov;25:198-209. doi: 10.1016/j.fsigen.2016.09.005. Epub 2016 Sep 20. Forensic Sci Int Genet. 2016. PMID: 27685342

6

More comprehensive forensic genetic marker analyses for accurate human remains identification using massively parallel DNA sequencing.

Ambers AD, Churchill JD, King JL, Stoljarova M, Gill-King H, Assidi M, Abu-Elmagd M, Buhmeida A, Al-Qahtani M, Budowle B. Ambers AD, et al. BMC Genomics. 2016 Oct 17;17(Suppl 9):750. doi: 10.1186/s12864-016-3087-2. BMC Genomics. 2016. PMID: 27766958 Free PMC article.

7

Genetic analysis of the Yavapai Native Americans from West-Central Arizona using the Illumina MiSeq FGx™ forensic genomics system.

Wendt FR, Churchill JD, Novroski NMM, King JL, Ng J, Oldt RF, McCulloh KL, Weise JA, Smith DG, Kanthaswamy S, Budowle B. Wendt FR, et al. Among authors: churchill jd. Forensic Sci Int Genet. 2016 Sep;24:18-23. doi: 10.1016/j.fsigen.2016.05.008. Epub 2016 May 17. Forensic Sci Int Genet. 2016. PMID: 27243782

8

Flanking region variation of ForenSeq™ DNA Signature Prep Kit STR and SNP loci in Yavapai Native Americans.

Wendt FR, King JL, Novroski NMM, Churchill JD, Ng J, Oldt RF, McCulloh KL, Weise JA, Smith DG, Kanthaswamy S, Budowle B. Wendt FR, et al. Among authors: churchill jd. Forensic Sci Int Genet. 2017 May;28:146-154. doi: 10.1016/j.fsigen.2017.02.014. Epub 2017 Feb 27. Forensic Sci Int Genet. 2017. PMID: 28273507

9

Evaluation of the Illumina(®) Beta Version ForenSeq™ DNA Signature Prep Kit for use in genetic profiling.

Churchill JD, Schmedes SE, King JL, Budowle B. Churchill JD, et al. Forensic Sci Int Genet. 2016 Jan;20:20-29. doi: 10.1016/j.fsigen.2015.09.009. Epub 2015 Sep 21. Forensic Sci Int Genet. 2016. PMID: 26433485

10

Population and performance analyses of four major populations with Illumina's FGx Forensic Genomics System.

Churchill JD, Novroski NMM, King JL, Seah LH, Budowle B. Churchill JD, et al. Forensic Sci Int Genet. 2017 Sep;30:81-92. doi: 10.1016/j.fsigen.2017.06.004. Epub 2017 Jun 17. Forensic Sci Int Genet. 2017. PMID: 28651097

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