SUMO modification regulates BLM and RAD51 interaction at damaged replication forks
Ouyang, Karen J, Woo, Leslie L, Zhu, Jianmei, Huo, Dezheng, Matunis, Michael J, Ellis, Nathan A
Published in PLoS biology (01.12.2009)
Published in PLoS biology (01.12.2009)
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Spectrum of splicing variants in disease genes and the ability of RNA analysis to reduce uncertainty in clinical interpretation
Truty, Rebecca, Ouyang, Karen, Rojahn, Susan, Garcia, Sarah, Colavin, Alexandre, Hamlington, Barbara, Freivogel, Mary, Nussbaum, Robert L., Nykamp, Keith, Aradhya, Swaroop
Published in American journal of human genetics (01.04.2021)
Published in American journal of human genetics (01.04.2021)
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Journal Article
BLM SUMOylation regulates ssDNA accumulation at stalled replication forks
Ouyang, Karen J, Yagle, Mary K, Matunis, Michael J, Ellis, Nathan A
Published in Frontiers in genetics (2013)
Published in Frontiers in genetics (2013)
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Journal Article
SNP Array Analysis Detects Genomic Alterations Associated with High-Risk Disease in Neuroblastoma
Ouyang, Karen J, Morales, Andres, Raca, Gordana, Cohn, Susan L
Published in Cancer genetics (01.07.2012)
Published in Cancer genetics (01.07.2012)
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Journal Article
High Resolution Genomic Profiling of Metastatic Testicular Teratomas
Ouyang, Karen J, Drendel, Holli, Szymanska, Jadwiga, Cummings, Oscar, Einhorn, Lawrence, Vance, Gail H
Published in Cancer genetics (01.05.2013)
Published in Cancer genetics (01.05.2013)
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Journal Article
The DNA-binding domain of CaNdt80p is required to activate CDR1 involved in drug resistance in Candida albicans
Wang, Jang-Shiun, Yang, Yun-Liang, Wu, Chin-Jung, Ouyang, Karen J, Tseng, Kuo-Yun, Chen, Chia-Geun, Wang, Hsin, Lo, Hsiu-Jung
Published in Journal of medical microbiology (01.10.2006)
Published in Journal of medical microbiology (01.10.2006)
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18 Tracking Uncertainty in Germline Genetic Testing for Inborn Errors of Immunity: Sources, Attributes, and Resolution of Variants of Uncertain Significance in Over 44,000 Individuals
Ting, Yi-Lee, Chen, Elaine, Facio, Flavia, Hatchell, Kathryn, Aguilar, Sienna, Ouyang, Karen, Aradhya, Swaroop, Johnson, Britt
Published in Clinical immunology (Orlando, Fla.) (01.05.2024)
Published in Clinical immunology (Orlando, Fla.) (01.05.2024)
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PO-01-182 TRACKING UNCERTAINTY IN GERMLINE GENETIC TESTING FOR ARRHYTHMIAS: SOURCES, ATTRIBUTES, AND RESOLUTION OF VARIANTS OF UNCERTAIN SIGNIFICANCE IN OVER 9,000 INDIVIDUALS
Ting, Yi-Lee, Chen, Elaine, Facio, Flavia M., Hatchell, Kathryn E., Aguilar, Sienna, Ouyang, Karen, Aradhya, Swaroop, Johnson, Britt
Published in Heart rhythm (01.05.2024)
Published in Heart rhythm (01.05.2024)
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Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk
O’Leary, Erin, Iacoboni, Daniela, Holle, Jennifer, Michalski, Scott T., Esplin, Edward D., Yang, Shan, Ouyang, Karen
Published in Annals of surgical oncology (01.10.2017)
Published in Annals of surgical oncology (01.10.2017)
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Journal Article
Systematic use of phenotype evidence in clinical genetic testing reduces the frequency of variants of uncertain significance
Johnson, Britt, Ouyang, Karen, Frank, Lauren, Truty, Rebecca, Rojahn, Susan, Morales, Ana, Aradhya, Swaroop, Nykamp, Keith
Published in American journal of medical genetics. Part A (01.09.2022)
Published in American journal of medical genetics. Part A (01.09.2022)
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Li‐Fraumeni versus Pseudo‐Li‐Fraumeni Syndrome: Key Insights for Interpreting Next‐Generation Sequencing Reports in Patients with Suspected Cancer Predisposition Syndromes
Sorscher, Steven, Desnoyers, Rodwige, Ouyang, Karen, Ramkissoon, Shakti
Published in The oncologist (Dayton, Ohio) (01.09.2017)
Published in The oncologist (Dayton, Ohio) (01.09.2017)
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Journal Article
FH Variant Pathogenicity Promotes Purine Salvage Pathway Dependence in Kidney Cancer
Wilde, Blake R, Chakraborty, Nishma, Matulionis, Nedas, Hernandez, Stephanie, Ueno, Daiki, Gee, Michayla E, Esplin, Edward D, Ouyang, Karen, Nykamp, Keith, Shuch, Brian, Christofk, Heather R
Published in Cancer discovery (06.09.2023)
Published in Cancer discovery (06.09.2023)
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Patterns of mosaicism for sequence and copy-number variants discovered through clinical deep sequencing of disease-related genes in one million individuals
Truty, Rebecca, Rojahn, Susan, Ouyang, Karen, Kautzer, Curtis, Kennemer, Michael, Pineda-Alvarez, Daniel, Johnson, Britt, Stafford, Amanda, Basel-Salmon, Lina, Saitta, Sulagna, Slavotinek, Anne, Chandrasekharappa, Settara C., Suarez, Carlos Jose, Burnett, Leslie, Nussbaum, Robert L., Aradhya, Swaroop
Published in American journal of human genetics (06.04.2023)
Published in American journal of human genetics (06.04.2023)
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Journal Article
Fumarate hydratase variant prevalence and manifestations among individuals receiving germline testing
Lu, Eric, Hatchell, Kathryn E., Nielsen, Sarah M., Esplin, Edward D., Ouyang, Karen, Nykamp, Keith, Zavoshi, Shirin, Li, Shantao, Zhang, Liying, Wilde, Blake R., Christofk, Heather R., Boutros, Paul C., Shuch, Brian
Published in Cancer (15.02.2022)
Published in Cancer (15.02.2022)
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Journal Article
Fumarate Hydratase Variants and Their Association With Paraganglioma/Pheochromocytoma
Zavoshi, Shirin, Lu, Eric, Boutros, Paul C., Zhang, Liying, Harari, Avital, Hatchell, Kathryn E., Nielsen, Sarah M., Esplin, Edward D., Ouyang, Karen, Nykamp, Keith, Wilde, Blake, Christofk, Heather, Shuch, Brian
Published in Urology (Ridgewood, N.J.) (01.06.2023)
Published in Urology (Ridgewood, N.J.) (01.06.2023)
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Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing
Chen, Elaine, Facio, Flavia M., Aradhya, Kerry W., Rojahn, Susan, Hatchell, Kathryn E., Aguilar, Sienna, Ouyang, Karen, Saitta, Sulagna, Hanson-Kwan, Andrea K., Capurro, Nicole Nakousi, Takamine, Eriko, Jamuar, Saumya Shekhar, McKnight, Dianalee, Johnson, Britt, Aradhya, Swaroop
Published in JAMA network open (25.10.2023)
Published in JAMA network open (25.10.2023)
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