Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Surya P. Rednam"'
Autor:
Owen R. Hirschi, Stephanie A. Felker, Surya P. Rednam, Kelly L. Vallance, D. Williams Parsons, Angshumoy Roy, Gregory M. Cooper, Sharon E. Plon
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101850- (2024)
Purpose: Clinical variant analysis pipelines likely have poor sensitivity to the effects on splicing from variants beyond 10 to 20 bases of exon-intron boundaries. Here, we demonstrate the value of SpliceAI to inform curation of rare variants previou
Externí odkaz:
https://doaj.org/article/b1e1261f7f7d4684992f0aa6000961d8
Publikováno v:
Therapeutic Advances in Endocrinology and Metabolism, Vol 9 (2018)
Individuals with PTEN Hamartoma Tumor Syndrome (PHTS) are at greatly increased risk for developing well-differentiated thyroid cancer. Specific circumstances in which total thyroidectomies should be considered have not been defined. A 14-year-old mac
Externí odkaz:
https://doaj.org/article/868561155dc44c7fbc4abdf7567d2e9c
Autor:
Suzanne P. MacFarland, Luke Maese, Surya P. Rednam, Junne Kamihara, Melissa R. Perrino, Kim E. Nichols, Garrett M. Brodeur, Joshua D. Schiffman, Sharon E. Plon, Lisa R. Diller, David Malkin, Christopher C. Porter, Anita Villani
Publikováno v:
Cancer Prevention Research. 15:645-652
Germline pathogenic variants in cancer susceptibility genes are identified in up to 18% of all children with cancer. Because pediatric cancer predisposition syndromes (CPS) themselves are rare and underrecognized, there are limited data to guide the
Autor:
Jonathan D. Wasserman, Joshua D. Schiffman, Stephan D. Voss, Anita Villani, Gail E. Tomlinson, Lisa J. States, Katherine L. Nathanson, Wendy K. Kohlmann, Junne Kamihara, Katherine A. Janeway, Harriet Druker, Ayelet Erez, Surya P. Rednam
Exposures to avoid prior to metanephrine testing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ab7ac29eef799721567ec45d6beffe5
https://doi.org/10.1158/1078-0432.22463313.v1
https://doi.org/10.1158/1078-0432.22463313.v1
Autor:
Jonathan D. Wasserman, Joshua D. Schiffman, Stephan D. Voss, Anita Villani, Gail E. Tomlinson, Lisa J. States, Katherine L. Nathanson, Wendy K. Kohlmann, Junne Kamihara, Katherine A. Janeway, Harriet Druker, Ayelet Erez, Surya P. Rednam
Von Hippel–Lindau disease (vHL) is a hereditary tumor predisposition syndrome that places affected individuals at risk for multiple tumors, which are predominantly benign and generally occur in the central nervous system or abdomen. Although the ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2be5c9e35d1118f8700fcd8ce03da9cc
https://doi.org/10.1158/1078-0432.c.6525366
https://doi.org/10.1158/1078-0432.c.6525366
Autor:
Stephen F. Kralik, M. Fatih Okcu, Patricia Baxter, Guillermo Aldave Orzaiz, Fatema Malbari, Murali Chintagumpala, Alexis C. Wood, Holly Lindsay, Surya P. Rednam, Jack Su, Frank Y. Lin, William E. Whitehead, Nucharin Supakul, Adam S. Levy, Robert C. Dauser, Arnold C. Paulino
Publikováno v:
Pediatric Blood & Cancer. 68
BACKGROUND Patients with chiasmatic-hypothalamic low-grade glioma (CHLGG) have frequent MRIs with gadolinium-based contrast agents (GBCA) for disease monitoring. Cumulative gadolinium deposition in the brains of children is a potential concern. The p
Autor:
Vidal M. Arroyo, Murali Chintagumpala, M. Fatih Okcu, Philip J. Lupo, Surya P. Rednam, Austin L. Brown, Michael E. Scheurer, Jeffrey C. Murray
Publikováno v:
Cancer Epidemiology. 59:71-74
Introduction Methylation-derived neutrophil-to-lymphocyte ratio (mdNLR) has been identified as a potential prognostic biomarker of outcomes in various cancers. We evaluated the prognostic value of blood-derived mdNLR within a retrospective cohort of
Updates on progress in cancer screening for children with hereditary cancer predisposition syndromes
Autor:
Surya P. Rednam
Publikováno v:
Current Opinion in Pediatrics. 31:41-47
PURPOSE OF REVIEW A significant proportion of pediatric cancer occurs in children with hereditary cancer predisposition syndromes. Their survival may be significantly improved and/or late effects diminished through screening for their greatly elevate
Autor:
Katherine A. Schneider, Rose B. McGee, Maria Isabel Achatz, Laurence Brugières, Kris Ann P. Schultz, Surya P. Rednam, Junne Kamihara, Jonathan D. Wasserman, William D. Foulkes, Harriet Druker, Lisa Diller, Leslie Doros
Publikováno v:
Clinical Cancer Research. 23:e76-e82
PTEN hamartoma tumor syndrome (PHTS), DICER1 syndrome, and hereditary leiomyomatosis and renal cell cancer (HLRCC) syndrome are pleiotropic tumor predisposition syndromes that include benign and malignant neoplasms affecting adults and children. PHTS
Publikováno v:
Gastrointestinal Endoscopy. 91:AB502-AB503