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ClinGen Allele Registry links information about genetic variants.
Hum Mutat. 2018 Nov;39(11):1690-1701. doi: 10.1002/humu.23637.
Hum Mutat. 2018.
PMID: 30311374
Free PMC article.
ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants.
Patel RY, Shah N, Jackson AR, Ghosh R, Pawliczek P, Paithankar S, Baker A, Riehle K, Chen H, Milosavljevic S, Bizon C, Rynearson S, Nelson T, Jarvik GP, Rehm HL, Harrison SM, Azzariti D, Powell B, Babb L, Plon SE, Milosavljevic A; ClinGen Resource.
Patel RY, et al. Among authors: pawliczek p.
Genome Med. 2017 Jan 12;9(1):3. doi: 10.1186/s13073-016-0391-z.
Genome Med. 2017.
PMID: 28081714
Free PMC article.
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ClinGen advancing genomic data-sharing standards as a GA4GH driver project.
Dolman L, Page A, Babb L, Freimuth RR, Arachchi H, Bizon C, Brush M, Fiume M, Haendel M, Hansen DP, Milosavljevic A, Patel RY, Pawliczek P, Yates AD, Rehm HL.
Dolman L, et al. Among authors: pawliczek p.
Hum Mutat. 2018 Nov;39(11):1686-1689. doi: 10.1002/humu.23625.
Hum Mutat. 2018.
PMID: 30311379
Free PMC article.
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Allele-specific epigenome maps reveal sequence-dependent stochastic switching at regulatory loci.
Onuchic V, Lurie E, Carrero I, Pawliczek P, Patel RY, Rozowsky J, Galeev T, Huang Z, Altshuler RC, Zhang Z, Harris RA, Coarfa C, Ashmore L, Bertol JW, Fakhouri WD, Yu F, Kellis M, Gerstein M, Milosavljevic A.
Onuchic V, et al. Among authors: pawliczek p.
Science. 2018 Sep 28;361(6409):eaar3146. doi: 10.1126/science.aar3146. Epub 2018 Aug 23.
Science. 2018.
PMID: 30139913
Free PMC article.
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Parallel deconvolution of large 3D images obtained by confocal laser scanning microscopy.
Pawliczek P, Romanowska-Pawliczek A, Soltys Z.
Pawliczek P, et al.
Microsc Res Tech. 2010 Mar;73(3):187-94. doi: 10.1002/jemt.20773.
Microsc Res Tech. 2010.
PMID: 19725070
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