Christopher D. Heinen

Affiliations: 
University of Connecticut, Storrs, CT, United States 
Area:
Philosophy of Science, Biochemistry, Oncology, Molecular Biology
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"Christopher Heinen"
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Publications

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Pelletier D, Rath A, Sabbaghian N, et al. (2023) Functional and phenotypic consequences of an unusual inversion in MSH2. Familial Cancer
Madden-Hennessey K, Gupta D, Radecki AA, et al. (2022) Loss of mismatch repair promotes a direct selective advantage in human stem cells. Stem Cell Reports. 17: 2661-2673
Rath A, Radecki AA, Rahman K, et al. (2022) A calibrated cell-based functional assay to aid classification of MLH1 DNA mismatch repair gene variants. Human Mutation
Brnich SE, Abou Tayoun AN, Couch FJ, et al. (2019) Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework. Genome Medicine. 12: 3
Taghbalout A, Du M, Jillette N, et al. (2019) Enhanced CRISPR-based DNA demethylation by Casilio-ME-mediated RNA-guided coupling of methylcytosine oxidation and DNA repair pathways. Nature Communications. 10: 4296
Rath A, Mishra A, Ferreira VD, et al. (2019) Functional Interrogation of Lynch Syndrome Associated MSH2 Missense Variants via CRISPR-Cas9 Gene Editing in Human Embryonic Stem Cells. Human Mutation
Gupta D, Heinen CD. (2019) The mismatch repair-dependent DNA damage response: Mechanisms and implications. Dna Repair. 78: 60-69
Gupta D, Lin B, Cowan A, et al. (2018) ATR-Chk1 activation mitigates replication stress caused by mismatch repair-dependent processing of DNA damage. Proceedings of the National Academy of Sciences of the United States of America
Lin B, Yang Q, Rath A, et al. (2017) Abstract 1411: Differential mismatch repair-dependent damage responses in subpopulations of cells from human intestinal organoids Cancer Research. 77: 1411-1411
Klapacz J, Pottenger LH, Engelward BP, et al. (2016) Contributions of DNA repair and damage response pathways to the non-linear genotoxic responses of alkylating agents. Mutation Research. Reviews in Mutation Research. 767: 77-91
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