Breast cancer risk and clinical implications for germline PTEN mutation carriers
Ngeow, Joanne, Sesock, Kaitlin, Eng, Charis
Published in Breast cancer research and treatment (01.08.2017)
Published in Breast cancer research and treatment (01.08.2017)
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Journal Article
Clinical Implications for Germline PTEN Spectrum Disorders
Ngeow, Joanne, Sesock, Kaitlin, Eng, Charis
Published in Endocrinology and metabolism clinics of North America (01.06.2017)
Published in Endocrinology and metabolism clinics of North America (01.06.2017)
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Journal Article
Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations
Yehia, Lamis, Ni, Ying, Sesock, Kaitlin, Niazi, Farshad, Fletcher, Benjamin, Chen, Hannah Jin Lian, LaFramboise, Thomas, Eng, Charis
Published in PLoS genetics (23.04.2018)
Published in PLoS genetics (23.04.2018)
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The c.1364C>A (p.A455E) Mutation in the CFTR Pseudogene Results in an Incorrectly Assigned Carrier Status by a Commonly Used Screening Platform
Deeb, Kristin K, Metcalf, James D, Sesock, Kaitlin M, Shen, Junqing, Wensel, Christine A, Rippel, Larisa I, Smith, Michelle, Chapman, Mark S, Zhang, Shulin
Published in The Journal of molecular diagnostics : JMD (01.07.2015)
Published in The Journal of molecular diagnostics : JMD (01.07.2015)
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Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome
Chen, Hannah Jinlian, Romigh, Todd, Sesock, Kaitlin, Eng, Charis
Published in Human mutation (01.10.2017)
Published in Human mutation (01.10.2017)
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Journal Article
Gene‐specific criteria for PTEN variant curation: Recommendations from the ClinGen PTEN Expert Panel
Mester, Jessica L., Ghosh, Rajarshi, Pesaran, Tina, Huether, Robert, Karam, Rachid, Hruska, Kathleen S., Costa, Helio A., Lachlan, Katherine, Ngeow, Joanne, Barnholtz‐Sloan, Jill, Sesock, Kaitlin, Hernandez, Felicia, Zhang, Liying, Milko, Laura, Plon, Sharon E., Hegde, Madhuri, Eng, Charis
Published in Human mutation (01.11.2018)
Published in Human mutation (01.11.2018)
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Journal Article
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome: CHEN et al
Chen, Hannah Jinlian, Romigh, Todd, Sesock, Kaitlin, Eng, Charis
Published in Human mutation (01.10.2017)
Published in Human mutation (01.10.2017)
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