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Katerina S. Kucera, Ph.D. - Publications

Affiliations: 
2011 Genetics and Genomics Duke University, Durham, NC 
Area:
Genetics, Women's Studies
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5/15 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2012 Reddy TE, Gertz J, Pauli F, Kucera KS, Varley KE, Newberry KM, Marinov GK, Mortazavi A, Williams BA, Song L, Crawford GE, Wold B, Willard HF, Myers RM. Effects of sequence variation on differential allelic transcription factor occupancy and gene expression. Genome Research. 22: 860-9. PMID 22300769 DOI: 10.1101/Gr.131201.111  0.56
2011 Gertz J, Varley KE, Reddy TE, Bowling KM, Pauli F, Parker SL, Kucera KS, Willard HF, Myers RM. Analysis of DNA methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation. Plos Genetics. 7: e1002228. PMID 21852959 DOI: 10.1371/Journal.Pgen.1002228  0.509
2011 Kucera KS, Reddy TE, Pauli F, Gertz J, Logan JE, Myers RM, Willard HF. Allele-specific distribution of RNA polymerase II on female X chromosomes. Human Molecular Genetics. 20: 3964-73. PMID 21791549 DOI: 10.1093/Hmg/Ddr315  0.506
2010 McDaniell R, Lee BK, Song L, Liu Z, Boyle AP, Erdos MR, Scott LJ, Morken MA, Kucera KS, Battenhouse A, Keefe D, Collins FS, Willard HF, Lieb JD, Furey TS, et al. Heritable individual-specific and allele-specific chromatin signatures in humans. Science (New York, N.Y.). 328: 235-9. PMID 20299549 DOI: 10.1126/Science.1184655  0.546
2006 Murphy SK, Nolan CM, Huang Z, Kucera KS, Freking BA, Smith TP, Leymaster KA, Weidman JR, Jirtle RL. Callipyge mutation affects gene expression in cis: a potential role for chromatin structure. Genome Research. 16: 340-6. PMID 16415109 DOI: 10.1101/Gr.4389306  0.416
Low-probability matches (unlikely to be authored by this person)
2018 Tilot AK, Kucera KS, Vino A, Asher JE, Baron-Cohen S, Fisher SE. Rare variants in axonogenesis genes connect three families with sound-color synesthesia. Proceedings of the National Academy of Sciences of the United States of America. PMID 29507195 DOI: 10.1073/Pnas.1715492115  0.268
2005 Zhang J, Bao S, Furumai R, Kucera KS, Ali A, Dean NM, Wang XF. Protein phosphatase 5 is required for ATR-mediated checkpoint activation. Molecular and Cellular Biology. 25: 9910-9. PMID 16260606 DOI: 10.1128/Mcb.25.22.9910-9919.2005  0.25
2019 Uddén J, Hultén A, Bendtz K, Mineroff Z, Kucera KS, Vino A, Fedorenko E, Hagoort P, Fisher SE. Towards robust functional neuroimaging genetics of cognition. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 31570534 DOI: 10.1523/Jneurosci.0888-19.2019  0.248
2019 Tilot AK, Vino A, Kucera KS, Carmichael DA, van den Heuvel L, den Hoed J, Sidoroff-Dorso AV, Campbell A, Porteous DJ, St Pourcain B, van Leeuwen TM, Ward J, Rouw R, Simner J, Fisher SE. Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 374: 20190026. PMID 31630655 DOI: 10.1098/Rstb.2019.0026  0.247
2020 Tilot AK, Vino A, Kucera KS, Carmichael DA, van den Heuvel L, den Hoed J, Sidoroff-Dorso AV, Campbell A, Porteous DJ, St Pourcain B, van Leeuwen TM, Ward J, Rouw R, Simner J, Fisher SE. Correction to 'Investigating genetic links between grapheme-colour synaesthesia and neuropsychiatric traits'. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 375: 20190746. PMID 32075566 DOI: 10.1098/Rstb.2019.0746  0.154
2021 Kucera KS, Taylor JL, Robles VR, Clinard K, Migliore B, Boyea BL, Okoniewski KC, Duparc M, Rehder CW, Shone SM, Fan Z, Raspa M, Peay HL, Wheeler AC, Powell CM, et al. A Voluntary Statewide Newborn Screening Pilot for Spinal Muscular Atrophy: Results from Early Check. International Journal of Neonatal Screening. 7. PMID 33801060 DOI: 10.3390/ijns7010020  0.049
2023 Kim JH, Robles V, Weimer KED, Gehtland LM, Kucera KS. Improved Dried Blood Spot PCR Assay for Universal Congenital Cytomegalovirus Screening in Newborns. Microbiology Spectrum. e0404122. PMID 36939327 DOI: 10.1128/spectrum.04041-22  0.049
2023 Dantonio P, Tavakoli NP, Migliore B, McCown E, Lim T, Park S, Caggana M, Kucera KS, Phan H, Street N, Petritis K, Vogt RF. Multi-Laboratory Evaluation of Prototype Dried Blood Spot Quality Control Materials for Creatine Kinase-MM Newborn Screening Assays. International Journal of Neonatal Screening. 9. PMID 36975851 DOI: 10.3390/ijns9010013  0.048
2022 Migliore BA, Zhou L, Duparc M, Robles VR, Rehder CW, Peay HL, Kucera KS. Evaluation of the GSP Creatine Kinase-MM Assay and Assessment of CK-MM Stability in Newborn, Patient, and Contrived Dried Blood Spots for Newborn Screening for Duchenne Muscular Dystrophy. International Journal of Neonatal Screening. 8. PMID 35225934 DOI: 10.3390/ijns8010012  0.018
2023 Kucera KS, Boyea BL, Migliore B, Potter SN, Robles VR, Kutsa O, Cope H, Okoniewski KC, Wheeler A, Rehder CW, Smith EC, Peay HL. Two Years of Newborn Screening for Duchenne Muscular Dystrophy as a Part of the Statewide Early Check Research Program in North Carolina. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101009. PMID 37864479 DOI: 10.1016/j.gim.2023.101009  0.014
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