-Charis Eng Researcher Activity Profile

Research Author Detailed Information 

Charis Eng Publication Rate By Year

Charis Eng has published 2 paper(s) in 2003, 1 paper(s) in 2005, 2 paper(s) in 2006, 22 paper(s) in 2007, 6 paper(s) in 2008, for a total of 33 research publications in total.

Charis C Eng Author Information

LAST NAME: eng

FIRST NAME: charis

INITIALS: C

AFFILIATION:

Papers

Charis Eng's Publication Record

1. BMP2 exposure results in decreased PTEN protein degradation and increased PTEN levels. Year Published: 2003
Clinical Cancer Genetics Program, Comprehensive Cancer Center, Division of Human Genetics, Department of Internal Medicine, The Ohio State University, Columbus, OH, 43210, USA.
2. Gastroesophageal reflux symptoms in patients with adenocarcinoma of the esophagus or cardia. Year Published: 2006
Division of Gastroenterology, University Hospitals of Cleveland and Ireland Cancer Center, Cleveland, Ohio 44106, USA. Amitabh.chak@case.edu
3. Mapping geographic zones of cancer risk with epigenetic biomarkers in normal breast tissue. Year Published: 2006
Department of Hematology and Oncology, Comprehensive Cancer Center, College of Medicine and Public Health, The Ohio State University, Columbus, Ohio 43210, USA, and Department of Pathology, Addenbrooks' Hospital, Cambridge, UK.
4. Pilot study of rosiglitazone therapy in women with breast cancer: effects of short-term therapy on tumor tissue and serum markers. Year Published: 2007
Division of Surgical Oncology, Department of Surgery, The Ohio State University, Columbus, Ohio, USA. lisa.yee@osumc.edu
5. Essential role for nuclear PTEN in maintaining chromosomal integrity. Year Published: 2007
Department of Radiation Oncology, College of Physicians and Surgeons, Columbia University, 630 West 168th Street, New York, NY 10032, USA.
6. Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data. Year Published: 2007
Mathematical Biosciences Institute, The Ohio State University, 231 W, 18th Avenue, Columbus, OH 43210, USA. zailong.wang@yahoo.com <zailong.wang@yahoo.com>
7. Cowden syndrome. Year Published: 2007
Center for Personalized Genetic Healthcare, Genomic Medicine Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
8. Genomic instability within tumor stroma and clinicopathological characteristics of sporadic primary invasive breast carcinoma. Year Published: 2007
Genomic Medicine Institute, Lerner Research Institute and Taussig Cancer Center, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
9. Tumor suppressor activity of CCAAT/enhancer binding protein alpha is epigenetically down-regulated in head and neck squamous cell carcinoma. Year Published: 2007
Department of Molecular Genetics, The Comprehensive Cancer Center, Ohio State University, Columbus, Ohio, USA.
10. Consortium approach to identifying genes for Barrett's esophagus and esophageal adenocarcinoma. Year Published: 2007
Department of Epidemiology and Biostatistics, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
11. A novel PTEN mutation in Cowden syndrome is associated with a mixed degenerative-erosive arthritic process: potential molecular pathogenic mechanisms. Year Published: 2007
Department of Internal Medicine, The Ohio State University Medical Center, 1581 Dodd Drive, Columbus, OH 43210, USA. joseph.pinzone@osumc.edu
12. Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1. Year Published: 2007
Department of Neurology, University Medical Center Freiburg, Germany.
13. Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers. Year Published: 2007
Centre for Research in Women's Health, Women's College Hospital, University of Toronto, Room 750, 790 Bay Street, 7th Floor, Toronto, ON M5G 1N8, Canada.
14. Evidence of MEN-2 in the original description of classic pheochromocytoma. Year Published: 2007
Department of Nephrology, University of Freiburg Medical Center, Freiburg im Breisgau, Germany. hartmut.neumann@uniklinik-freiburg.de
15. Familial adenomatous polyposis in a patient with unexplained mental retardation. Year Published: 2007
Center for Personalized Genetic Healthcare, Genomic Medicine Institute and the Taussig Cancer Center, Cleveland, OH 44195, USA.
16. Cowden syndrome. Year Published: 2007
Center for Personalized Genetic Healthcare, Genomic Medicine Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
17. Loss of expression of protein kinase a regulatory subunit 1alpha in pigmented epithelioid melanocytoma but not in melanoma or other melanocytic lesions. Year Published: 2007
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. dr.zembowicz@DermatopathologyConsultations.com
18. Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. Year Published: 2007
1Department of Genetics, Biology and Biochemistry, University of Torino, Turin, Italy.
19. Loss of expression of protein kinase a regulatory subunit 1alpha in pigmented epithelioid melanocytoma but not in melanoma or other melanocytic lesions. Year Published: 2007
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. dr.zembowicz@DermatopathologyConsultations.com
20. Breast-cancer stromal cells with TP53 mutations and nodal metastases. Year Published: 2007
Genomic Medicine Institute, Cleveland Clinic Foundation, Cleveland 44195, USA.
21. Breast-cancer stromal cells with TP53 mutations and nodal metastases. Year Published: 2007
Genomic Medicine Institute, Cleveland Clinic Foundation, Cleveland 44195, USA.
22. Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers. Year Published: 2007
Centre for Research in Women's Health, Women's College Hospital, University of Toronto, Room 750, 790 Bay Street, 7th Floor, Toronto, ON M5G 1N8, Canada.
23. Caveolin-1 and caveolin-2,together with three bone morphogenetic protein-related genes, may encode novel tumor suppressors down-regulated in sporadic follicular thyroid carcinogenesis. Year Published: 2003
Department of Molecular Virology, Immunology, and Medical Genetics, The Ohio State University, Columbus, Ohio 43210, USA.
24. Genetic classification of benign and malignant thyroid follicular neoplasia based on a three-gene combination. Year Published: 2005
Clinical Cancer Genetics Program, Department of Internal Medicine, The Ohio State University, Columbus, Ohio 43210, USA.
25. Familial adenomatous polyposis in a patient with unexplained mental retardation. Year Published: 2007
Center for Personalized Genetic Healthcare, Genomic Medicine Institute and the Taussig Cancer Center, Cleveland, OH 44195, USA.
26. Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. Year Published: 2007
Department of Genetics, Biology and Biochemistry, University of Torino, Turin, Italy.
27. Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation. Year Published: 2008
Department of Hypertension at the Institute of Cardiology, Warsaw, Poland.
28. The nuclear affairs of PTEN. Year Published: 2008
Genomic Medicine Institute, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
29. Direct evidence for epithelial-mesenchymal transitions in breast cancer. Year Published: 2008
Department of Molecular Genetics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.
30. Direct evidence for epithelial-mesenchymal transitions in breast cancer. Year Published: 2008
Department of Molecular Genetics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.
31. Clinical and molecular genetics of patients with the Carney-Stratakis syndrome and germline mutations of the genes coding for the succinate dehydrogenase subunits SDHB, SDHC, and SDHD. Year Published: 2007
Department of Genetics, Biology and Biochemistry, University of Torino, Turin, Italy.
32. Frequency of germline genomic homozygosity associated with cancer cases. Year Published: 2008
Genomic Medicine Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
33. Frequency of germline genomic homozygosity associated with cancer cases. Year Published: 2008
Genomic Medicine Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.