CharisEngMDPhD

PubMed

• 32 citations
  PTEN in Hereditary and Sporadic Cancer.
  Joanne Ngeow, Charis Eng
  Cold Spring Harbor Perspectives in Medicine. 2020-04-01
• 104 citations
  De Novo Mutation of GDNF, Ligand for the RET/GDNFR-α Receptor Complex, in Hirschsprung Disease
  Stacey Ivanchuk, Shirley M. Myers, Charis Eng, Lois M. Mulligan
  Human Molecular Genetics. 1996-12-01
• 11 citations
  Genomic structure and chromosomal localization of the human GDNFR -α gene
  Charis Eng, Shirley M. Myers, Michael D Kogon, Michele Sanicola, C Hession
  Oncogene. 1998-02-05

Journal Articles

• KLLN-Mediated DNA Damage-Induced Apoptosis Is Associated with Regulation of p53 Phosphorylation and Acetylation in Breast Cancer Cells  
  Charis Eng, MD, Nature

Books/Book Chapters

• Practical Handbook of Human Cancer Genetics 
  Foulkes WR, Hodgson SV, Eng C, Maher ERSpringerEdition 4th,2013
• Practical Handbook of Human Cancer Genetics 
  Foulkes WR, Hodgson SV, Eng C, Maher ERSpringerEdition 4th,2013
• WHO Classification of Tumours of the Digestive System 
  Chapter: Cowden syndrome 
  Eng C, Eng Ca, Burt RWEditors: Bostman FT, Carneiro F, Hruban RH, Theise ND.IARC Press, Lyon, FranceEdition 4th,2010
• Genetic Syndromes and Management 
  Chapter: PTEN hamartoma tumor syndrome 
  Edelman E, Eng CEditors: Cassidy S, Allanson JE.Wiley-Blackwell, New YorkEdition 3rd,2010
• A Clinical Approach to Endocrine and Metabolic Diseases 
  Chapter: Management of paraganglioma 
  Neumann HPH, Eng CEditors: Ladenson PW.The Endocrine Society, Chevy Case, MD2010
• A Guide to Cancer Genetics in Clinical Practice 
  Chapter: Hamartomatous polyposis syndromes 
  Leach BH, Kalady M, Eng CEditors: Clark S.tfm Publishing Ltd, Shrewsbury, UK2009
• Pediatric Endocrinology 
  Chapter: Pheochromocytoma and the multiple endocrine neoplasia syndromes 
  Chernausek SD, Eng C.Editors: Sperling M.Saunders ElsevierEdition 3rd,2008
• Hereditary Breast Cancer 
  Chapter: PTEN and Cowden syndrome 
  Zbuk KM, Stein J, Eng CEditors: Isaacs C, Rebbeck TM.Informa Healthcare, New York2007
• WHO Classification of Tumours. Pathology and Genetics of Tumours of Skin 
  Chapter: Cowden syndrome 
  Kazakov DV, Burg G, Eng CEditors: Weedon D, LeBoit P, Burg G, Sarasin A.IARC Press, Lyon, France2005
• WHO Classification of Tumours. Pathology and Genetics of Tumours of Endocrine Organs 
  Chapter: Parathyroid adenoma 
  Grimelius L, DeLellis RA, Bondeson L, Akerstom G, Arnold A, Franssila KO, Hendy GN, Dupuy D, Eng CEditors: DeLellis R, Lloyd R, Heitz PU, Eng C.IARC Press, Lyon, France2004
• WHO Classification of Tumours. Pathology and Genetics of Tumours of Endocrine Organs 
  Chapter: Follicular carcinoma (Thyroid) 
  Sobrinho-Simoes M, Asa SL, Kroli TG, Nikiforov Y, DeLellis RA, Farid P, Kitamura Y, Noguchi SU, Eng C, Harach HR, Williams ED, Schneider AB, Fagin JA, Ghossein RA, Maz...Editors: DeLellis R, Lloyd R, Heitz PU, Eng C.IARC Press, Lyon, France2004
• Genetic Predisposition to Cancer 
  Chapter: Multiple endocrine neoplasia type 2 
  Eng C, Ponder BAJEditors: Eeles RA, Easton DF, Ponder BAJ, Eng C.Edward Arnold, Ltd, LondonEdition 2nd,2004
• Familial Breast and Ovarian Cancer 
  Chapter: Cowden syndrome and related disorders 
  Eng CEditors: Morrison P, Hodgson SV, Haites N.Cambridge University Press, Cambridge2002
• Genetic Disorders of Endocrine Neoplasia 
  Chapter: Hereditary endocrine neoplasias: fundamental insights and the practice of clinical cancer genetics 
  Dahia PLM, Eng CEditors: Dahia PLM, Eng C.Karger, Basel2001
• Molecular Genetics of Cancer 
  Chapter: Multiple endocrine neoplasia type 2 
  Eng CEditors: Cowell JK.BIOS Scientific Publishers Ltd, Oxford2001
• WHO Classification of Tumours. Pathology and Genetics of Digestive Tract Tumours 
  Chapter: Cowden syndrome 
  Eng C, Burt R, Talbot ICEditors: Hamilton S, Aaltonen L.IARC Press, Lyon, France2000
• Multiple Primary Cancers 
  Chapter: Dominant genes and phacomatoses associated with multiple primary cancers 
  Eng C, Maher EREditors: Neugut AI, Robinson E, Meadows AT.Lippincott, Williams and Wilkins, Philadelphia1999
• The Genetic Basis of Human Cancer 
  Chapter: Cowden syndrome 
  Eng C, Parsons REditors: Vogelstein B, Kinzler KW.McGraw Hill and Co., New York1998
• Clinical Endocrinology 
  Chapter: Multiple endocrine neoplasia type 2 and medullary carcinoma of the thyroid 
  Eng C, Ponder BAJEditors: Grossman A.Blackwell Science, OxfordEdition 2nd,1998
• Hormonal Hypertension 
  Chapter: Multiple endocrine neoplasia type 2 
  Neumann HPH, Eng C, Bender BUEditors: Sznjderman M, Januszewicz W, Januszwicz A.Wydawnictwo Naukowe, Warsaw1997
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Abstracts/Posters

• Limitations in the patient’s right not-to-know genetic test results: case report and discussion
  Cook R, Nardini M, Sharp RR, Eng C, Proc Natl Soc Genet Counsel, 1/1/2013
• CDH1 family and dynamics
  Polk J, Makar V, Walsh M, Eng C, Proc Natl Soc Genet Counsel, 1/1/2013
• Implementation of tumor testing for Lynch syndrome in endometrial cancers at a large academic medical center
  Moline J, Mahdi H, Yang B, Biscotti C, Roma AA, Heald B, Rose PG, Michener C, Eng C, Proc Natl Soc Genet Counsel, 1/1/2013
• Health information technology in clinical genetic counseling
  Doerr M, Seller Fecteau H, Eng C, Proc Natl Soc Genet Counsel, 1/1/2013
• Second primary malignancies in PTEN hamartoma tumor syndrome
  Ngeow J, Mester JL, Barnholtz-Sloan J, Eng C, J Clin Oncol, 1/1/2013
• Risk for endometrial carcinoma, ovarian tumors and other gynecologic diagnoses in women with Cowden syndrome and germline PTEN mutation
  Mester JL, Escobar P, Roma A, Eng C, Soc Gynecol Oncol, 1/1/2012
• PTEN germline mutations in patients first tested for other hereditary cancer syndromes: Would use of risk assessment tools have reduced healthcare costs?
  Mester JL, Moore RA, Eng C, J Clin Oncol, 1/1/2012
• Implementation of institutional MSI and IHC testing for Lynch syndrome diagnosis: Cleveland Clinic experience
  Heald B, Plesec T, Liu X, Moline J, Burke CA, Kalady MF, Church J, Eng C, Proc Natl Soc Genet Counsel, 1/1/2012
• Implementation of institutional MSI and IHC testing for Lynch syndrome diagnosis: Cleveland Clinic experience
  Heald B, Plesec T, Liu X, Moline J, Burke CA, Kalady MF, Church J, Eng C, CGA/ISHC, 1/1/2012
• Approach to systematic screening of endometrial cancers for Lynch syndrome: the Cleveland Clinic experience
  Moline J, Biscotti C, Drake R, Eng C, Proc Natl Soc Genet Counsel, 1/1/2011
• Comparison of neoplastic phenotypes in Cowden/Cowden-like syndrome characterized by germline SDHx variants, PTEN mutations versus KLLN epimutations
  Ni Y, Tan MH, Bennett K, Mester J, Chen J, Moline J, Orloff M, Eng C, Am Soc Hum Genet/Intl Congr Hum Genet, 1/1/2011
• Germline SDHC whole-gene deletion in a patient with malignant extraadrenal pheochromoctyoma: Reconsideration of clinical testing strategy
  Moline J, Chen JL, Eng C, Am Soc Hum Genet, 1/1/2010
• Comparison of family health history to personal genomic screening for risk assessment of colon cancer
  Leach BH, Eng C, Collaborative Group of the Americas on Inherited Colorectal Cancer Syndromes, 1/1/2010
• PTEN association with mTOR pathway activation and outcomes in bladder cancer
  Orloff M, Elson P, Yan YR, Eng C, Hansel DE, Proc Am Assoc Cancer Res, 1/1/2010
• SDHx as novel susceptibility genes for Cowden and Cowden-like syndromes
  Ni Y, Orloff MS, Eng C, HHMI Molecular Medicine Scientific Retreat, 1/1/2010
• Activator protein 2 alpha-targeted methylation and silencing of relevant genes in head and neck squamous cell cancer (HNSCC) pathogenesis
  Bennett KL, Eng C, Proc Am Assoc Cancer Res, 1/1/2009
• Children and young adults with germline PTEN mutations: phenotypic description and key features to early diagnosis
  Mester J, Heald Leach B, Orloff MS, Eng C, Am Soc Hum Genet, 1/1/2009
• Genomic counseling in the setting of an institutional initiative for direct-to-consumer personal genomic testing
  Edelman EE, Sharp RR, Eng C, Am Soc Hum Genet, 1/1/2009
• Children and young adults with germline PTEN mutations: phenotypic description and key features to early diagnosis
  Mester J, Heald B, Orloff MS, Eng C, Proc Natl Soc Genet Counsel, 1/1/2009
• Gastrointestinal polyps and PTEN mutations: an underacknowledged diagnostic criterion
  Heald Leach B, Burke C, Eng C, Am Soc Hum Genet, 1/1/2009
• Clinical and molecular analyses of PTEN promoter variant –1084 C>T in 22 families with PTEN hamartoma tumor syndrome
  Edelman E, Eng C, Am Soc Hum Genet, 1/1/2008
• Common and cancer type-specific loss-of-heterozygosity (LOH) in the tumor stroma and epithelium of 3 carcinoma types associated with clinical outcome
  Orloff M, Xu Y, Zhang L, Eng C, Am Soc Hum Genet, 1/1/2008
• An association between hereditary colon cancer and sarcoma? A report of 2 families with mismatch repair mutations and rare presentation of rhabdomyosarcoma
  Heald B, Edelman E, Eng C, Proc Natl Soc Genet Counsel, 1/1/2008
• Adult-onset congenital erythropoietic porphyria: an extra challenge in the diagnosis of porphyria
  Gustafson S, Lichtin A, Astrin K, Eng C, Am Soc Hum Genet, 1/1/2007
• Micro-RNAs: Negative regulators of PTEN and modifiers of Cowden syndrome
  Pezzolesi MG, Waite KA, Eng C, Am Soc Hum Genet, 1/1/2007
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