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Achieving high-sensitivity for clinical applications using augmented exome sequencing.
Genome Med. 2015 Jul 16;7(1):71. doi: 10.1186/s13073-015-0197-4. eCollection 2015.
Genome Med. 2015.
PMID: 26269718
Free PMC article.
Variant priorization and analysis incorporating problematic regions of the genome.
Patwardhan A, Clark M, Morgan A, Chervitz S, Pratt M, Bartha G, Chandratillake G, Garcia S, Leng N, Chen R.
Patwardhan A, et al. Among authors: chandratillake g.
Pac Symp Biocomput. 2014:277-87.
Pac Symp Biocomput. 2014.
PMID: 24297554
Free article.
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Exome sequencing in 32 patients with anophthalmia/microphthalmia and developmental eye defects.
Slavotinek AM, Garcia ST, Chandratillake G, Bardakjian T, Ullah E, Wu D, Umeda K, Lao R, Tang PL, Wan E, Madireddy L, Lyalina S, Mendelsohn BA, Dugan S, Tirch J, Tischler R, Harris J, Clark MJ, Chervitz S, Patwardhan A, West JM, Ursell P, de Alba Campomanes A, Schneider A, Kwok PY, Baranzini S, Chen RO.
Slavotinek AM, et al. Among authors: chandratillake g.
Clin Genet. 2015 Nov;88(5):468-73. doi: 10.1111/cge.12543. Epub 2015 Jan 6.
Clin Genet. 2015.
PMID: 25457163
Free PMC article.
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Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing.
Shoemaker LD, Clark MJ, Patwardhan A, Chandratillake G, Garcia S, Chen R, Morgan AA, Leng N, Kirk S, Chen R, Cook DJ, Snyder M, Steinberg GK.
Shoemaker LD, et al. Among authors: chandratillake g.
G3 (Bethesda). 2015 Nov 3;6(1):41-9. doi: 10.1534/g3.115.020321.
G3 (Bethesda). 2015.
PMID: 26530418
Free PMC article.
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Recommendations for designing genetic test reports to be understood by patients and non-specialists.
Farmer GD, Gray H, Chandratillake G, Raymond FL, Freeman ALJ.
Farmer GD, et al. Among authors: chandratillake g.
Eur J Hum Genet. 2020 Jul;28(7):885-895. doi: 10.1038/s41431-020-0579-y. Epub 2020 Feb 5.
Eur J Hum Genet. 2020.
PMID: 32024982
Free PMC article.
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Correction: Creating genetic reports that are understood by nonspecialists: a case study.
Recchia G, Chiappi A, Chandratillake G, Raymond L, Freeman ALJ.
Recchia G, et al. Among authors: chandratillake g.
Genet Med. 2020 Jan;22(1):240-241. doi: 10.1038/s41436-019-0663-2.
Genet Med. 2020.
PMID: 31548640
Free PMC article.
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Creating genetic reports that are understood by nonspecialists: a case study.
Recchia G, Chiappi A, Chandratillake G, Raymond L, Freeman ALJ.
Recchia G, et al. Among authors: chandratillake g.
Genet Med. 2020 Feb;22(2):353-361. doi: 10.1038/s41436-019-0649-0. Epub 2019 Sep 11.
Genet Med. 2020.
PMID: 31506646
Free PMC article.
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