SuryaRednamMD

PubMed

• Update on cancer predisposition syndromes and surveillance guidelines for childhood brain tumors.
  Jordan R Hansford, Anirban Das, Rose B McGee, Yoshiko Nakano, Jack Brzezinski, Sarah R Scollon, Surya P Rednam, Jaclyn Schienda, Orli Michaeli, Sun Young Kim, Mary-Lou...> ;Clinical Cancer Research. 2024 Apr 4
• Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for Pathogenicity.
  Owen R Hirschi, Stephanie A Felker, Surya P Rednam, Kelly L Vallance, D Williams Parsons, Angshumoy Roy, Gregory M Cooper, Sharon E Plon> ;Medrxiv. 2023 Nov 1
• Pediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population-based assessment in seven million children.
  Gillean K Connolly, Rachel D Harris, Charles Shumate, Surya P Rednam, Mark A Canfield, Sharon E Plon, Joanne Nguyen, Jeremy M Schraw, Philip J Lupo> ;Cancer. 2024 Feb 1
• 4 citations
  Guidelines for surveillance of patients with von Hippel-Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance.
  Anthony B Daniels, Amit Tirosh, Kristin Huntoon, Gautam U Mehta, Philippe E Spiess, Debra L Friedman, Steven G Waguespack, Jill E Kilkelly, Surya Rednam, Sumit Pruthi,...> ;Cancer. 2023 Oct 1
• 1 citations
  Collaboration to Promote Research and Improve Clinical Care in the Evolving Field of Childhood Cancer Predisposition.
  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...> ;Cancer Prevention Research. 2022 Oct 4
• 5 citations
  Gadolinium is not necessary for surveillance MR imaging in children with chiasmatic-hypothalamic low-grade glioma.
  Fatema Malbari, Murali Chintagumpala, Alexis C. Wood, Adam S. Levy, Jack Su, M. Fatih Okcu, Frank Y. Lin, Holly Lindsay, Surya P. Rednam, Patricia Baxter, Arnold C. Pa...> ;Pediatric Blood & Cancer. 2021 Jun 16
• 4 citations
  Impact of vascular anomalies on the PTEN phenotype in children and young adults.
  Arun Gurunathan, Kiersten W. Ricci, Ionela Iacobas, Surya P. Rednam, Katie Wusik, Lin Fei, Adrienne M. Hammilll> ;Pediatric Blood & Cancer. 2020 Mar 20
• 19 citations
  Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency.
  Holly Lindsay, Sarah Scollon, Jacquelyn Reuther, Horatiu Voicu, Surya P. Rednam, Frank Y. Lin, Kevin E. Fisher, Murali Chintagumpala, Adekunle M. Adesina, D. Will Pars...> ;Cold Spring Harbor Molecular Case Studies. 2019 Oct 23
• 20 citations
  Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.
  Magdalena Koczkowska, Tom Callens, Alicia Gomes, Angela Sharp, Yunjia Chen, Alesha D Hicks, Arthur S Aylsworth, Amedeo A Azizi, Donald G Basel, Gary Bellus, Lynne M Bi...> ;Genetics in Medicine. 2019 Apr 1
• 6 citations
  Pilot study of DNA methylation-derived neutrophil-to-lymphocyte ratio and survival in pediatric medulloblastoma.
  Vidal M. Arroyo, Philip J. Lupo, Michael E. Scheurer, Surya P. Rednam, Jeffrey C. Murray, M. Fatih Okcu, Murali Chintagumpala, Austin L. Brown> ;Cancer Epidemiology. 2019 Apr 1
• 7 citations
  Updates on progress in cancer screening for children with hereditary cancer predisposition syndromes.
  Surya P. Rednam> ;Current Opinion in Pediatrics. 2019 Feb 1
• 4 citations
  Considerations for total thyroidectomy in an adolescent with PTEN mutation
  Mustafa Tosur, Mary L. Brandt, Ioanna D. Athanassaki, Surya P. Rednam> ;Therapeutic Advances in Endocrinology and Metabolism. 2018 Jul 4
• Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlat...
  Magdalena Koczkowska, Tom Callens, Alicia Gomes, Angela Sharp, Yunjia Chen, Alesha D. Hicks, Arthur S. Aylsworth, Amedeo A. Azizi, Donald Basel, Gary Bellus, Lynne M. ...> ;Genetics in Medicine. 2018 Jan 1
• 118 citations
  Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis.
  Mandy L. Ballinger, Ana F. Best, Phuong L. Mai, Payal P. Khincha, Jennifer T. Loud, June A. Peters, Maria Isabel Achatz, Rubens Chojniak, Alexandre Balieiro da Costa, ...> ;JAMA Oncology. 2017 Dec 1
• 51 citations
  Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features
  Pawel Stankiewicz, Tahir N. Khan, Przemyslaw Szafranski, Leah Slattery, Haley Streff, Francesco Vetrini, Jonathan A. Bernstein, Chester W. Brown, Jill A. Rosenfeld, Su...> ;American Journal of Human Genetics. 2017 Oct 5
• 6 citations
  DNA methylation of a novel PAK4 locus influences ototoxicity susceptibility following cisplatin and radiation therapy for pediatric embryonal tumors
  Austin L. Brown, Kayla L. Foster, Philip J. Lupo, Erin C. Peckham-Gregory, Jeffrey C. Murray, M. Fatih Okcu, Ching C. Lau, Surya P. Rednam, Murali Chintagumpala, Micha...> ;Neuro-Oncology. 2017 Oct 1
• 112 citations
  Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma
  Jennifer M. Kalish, Leslie Doros, Lee J. Helman, Raoul C.M. Hennekam, Roland P. Kuiper, Saskia M. Maas, Eamonn R. Maher, Kim E. Nichols, Sharon E. Plon, Christopher C....> ;Clinical Cancer Research. 2017 Jul 1
• 33 citations
  Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood
  Jonathan D. Wasserman, Gail E. Tomlinson, Harriet Druker, Junne Kamihara, Wendy Kohlmann, Christian P. Kratz, Katherine L. Nathanson, Kristian W. Pajtler, Andreu Parar...> ;Clinical Cancer Research. 2017 Jul 1
• 138 citations
  Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.
  Surya P. Rednam, Ayelet Erez, Harriet Druker, Katherine A. Janeway, Junne Kamihara, Wendy Kohlmann, Katherine L. Nathanson, Lisa J. States, Gail E. Tomlinson, Anita Vi...> ;Clinical Cancer Research. 2017 Jun 15
• 98 citations
  PTEN, DICER1, FH, and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.
  Kris Ann P. Schultz, Surya P. Rednam, Junne Kamihara, Leslie Doros, Maria Isabel Achatz, Jonathan D. Wasserman, Lisa Diller, Laurence Brugières, Harriet Druker, Kather...> ;Clinical Cancer Research. 2017 Jun 15
• 2 citations
  Hemisacrectomy with preservation of the contralateral sacral nerve roots and sacroiliac joint for pelvic neurofibrosarcoma in a 7-year-old child: case report with 2-ye...
  Ali H. Palejwala, Jared Fridley, Krystal Garcia, Sanjeev A. Vasudevan, David Y. Khechoyan, Surya Rednam, Chester J. Koh, Andrew Jea> ;Journal of Neurosurgery. Pediatrics. 2017 Jan 1
• 1 citations
  Exploratory analysis of ERCC2 DNA methylation in survival among pediatric medulloblastoma patients
  Emilyn Banfield, Austin L. Brown, Erin C. Peckham, Surya P. Rednam, Jeffrey C. Murray, M. Fatih Okcu, Laura E. Mitchell, Murali Chintagumpala, Ching C. Lau, Michael E....> ;Cancer Epidemiology. 2016 Oct 1
• 32 citations
  SOD2 genetic variant associated with treatment-related ototoxicity in cisplatin-treated pediatric medulloblastoma.
  Austin L. Brown, Philip J. Lupo, Mehmet Fatih Okcu, Ching C. Lau, Surya P. Rednam, Michael E. Scheurer> ;Cancer Medicine. 2015 Nov 1
• 45 citations
  Glutathione S-Transferase P1 Single Nucleotide Polymorphism Predicts Permanent Ototoxicity in Children with Medulloblastoma
  Surya P. Rednam, Mph Michael E. Scheurer PhD, Adekunle M. Adesina, Ching C. Lau, Mph Mehmet Fatih Okcu Md> ;Pediatric Blood & Cancer. 2013 Apr 1
• 7 citations
  Metastatic squamous cell carcinoma of the oropharynx in a child with a mutation in the Connexin 26 gene.
  Surya P. Rednam, John Hicks, Moise L. Levy, Alberto S. Pappo> ;Journal of Pediatric Hematology/oncology. 2011 Jul 1
• Join now to see all