Publications by authors named "Surya Rednam"

22Publications

Impact of vascular anomalies on the PTEN phenotype in children and young adults.

Authors:
Arun Gurunathan Kiersten Ricci Ionela Iacobas Surya P Rednam Katie Wusik Lin Fei Adrienne M Hammilll

Pediatr Blood Cancer 2020 06 20;67(6):e28258. Epub 2020 Mar 20.

Division of Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

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June 2020

Germline mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency.

Authors:
Holly Lindsay Sarah Scollon Jacquelyn Reuther Horatiu Voicu Surya P Rednam Frank Y Lin Kevin E Fisher Murali Chintagumpala Adekunle M Adesina D Will Parsons Sharon E Plon Angshumoy Roy

Cold Spring Harb Mol Case Stud 2019 10 23;5(5). Epub 2019 Oct 23.

Department of Pediatrics, Division of Hematology-Oncology, Baylor College of Medicine, Houston, Texas 77030, USA.

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October 2019

Pilot study of DNA methylation-derived neutrophil-to-lymphocyte ratio and survival in pediatric medulloblastoma.

Authors:
Vidal M Arroyo Philip J Lupo Michael E Scheurer Surya P Rednam Jeffrey Murray M Fatih Okcu Murali M Chintagumpala Austin L Brown

Cancer Epidemiol 2019 04 29;59:71-74. Epub 2019 Jan 29.

Baylor College of Medicine, One Baylor Plaza, Houston, TX, USA; Texas Children's Cancer and Hematology Centers, Houston, TX, USA. Electronic address:

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April 2019

Updates on progress in cancer screening for children with hereditary cancer predisposition syndromes.

Authors:
Surya P Rednam

Curr Opin Pediatr 2019 02;31(1):41-47

Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas, USA.

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February 2019

Correction: 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.

Authors:
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 Bird Maria A Blazo Leah W Burke Ashley Cannon Felicity Collins Colette DeFilippo Ellen Denayer Maria C Digilio Shelley K Dills Laura Dosa Robert S Greenwood Cristin Griffis Punita Gupta Rachel K Hachen Concepción Hernández-Chico Sandra Janssens Kristi J Jones Justin T Jordan Peter Kannu Bruce R Korf Andrea M Lewis Robert H Listernick Fortunato Lonardo Maurice J Mahoney Mayra Martinez Ojeda Marie T McDonald Carey McDougall Nancy Mendelsohn David T Miller Mari Mori Rianne Oostenbrink Sebastién Perreault Mary Ella Pierpont Carmelo Piscopo Dinel A Pond Linda M Randolph Katherine A Rauen Surya Rednam S Lane Rutledge Veronica Saletti G Bradley Schaefer Elizabeth K Schorry Daryl A Scott Andrea Shugar Elizabeth Siqveland Lois J Starr Ashraf Syed Pamela L Trapane Nicole J Ullrich Emily G Wakefield Laurence E Walsh Michael F Wangler Elaine Zackai Kathleen B M Claes Katharina Wimmer Rick van Minkelen Alessandro De Luca Yolanda Martin Eric Legius Ludwine M Messiaen

Genet Med 2019 03;21(3):764-765

Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.

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March 2019

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.

Authors:
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 Bird Maria A Blazo Leah W Burke Ashley Cannon Felicity Collins Colette DeFilippo Ellen Denayer Maria C Digilio Shelley K Dills Laura Dosa Robert S Greenwood Cristin Griffis Punita Gupta Rachel K Hachen Concepción Hernández-Chico Sandra Janssens Kristi J Jones Justin T Jordan Peter Kannu Bruce R Korf Andrea M Lewis Robert H Listernick Fortunato Lonardo Maurice J Mahoney Mayra Martinez Ojeda Marie T McDonald Carey McDougall Nancy Mendelsohn David T Miller Mari Mori Rianne Oostenbrink Sebastién Perreault Mary Ella Pierpont Carmelo Piscopo Dinel A Pond Linda M Randolph Katherine A Rauen Surya Rednam S Lane Rutledge Veronica Saletti G Bradley Schaefer Elizabeth K Schorry Daryl A Scott Andrea Shugar Elizabeth Siqveland Lois J Starr Ashraf Syed Pamela L Trapane Nicole J Ullrich Emily G Wakefield Laurence E Walsh Michael F Wangler Elaine Zackai Kathleen B M Claes Katharina Wimmer Rick van Minkelen Alessandro De Luca Yolanda Martin Eric Legius Ludwine M Messiaen

Genet Med 2019 04 7;21(4):867-876. Epub 2018 Sep 7.

Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.

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April 2019

Considerations for total thyroidectomy in an adolescent with mutation.

Authors:
Mustafa Tosur Mary L Brandt Ioanna D Athanassaki Surya P Rednam

Ther Adv Endocrinol Metab 2018 Sep 4;9(9):299-301. Epub 2018 Jul 4.

Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.

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September 2018

Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features.

Authors:
Paweł Stankiewicz Tahir N Khan Przemyslaw Szafranski Leah Slattery Haley Streff Francesco Vetrini Jonathan A Bernstein Chester W Brown Jill A Rosenfeld Surya Rednam Sarah Scollon Katie L Bergstrom Donald W Parsons Sharon E Plon Marta W Vieira Caio R D C Quaio Wagner A R Baratela Johanna C Acosta Guio Ruth Armstrong Sarju G Mehta Patrick Rump Rolph Pfundt Raymond Lewandowski Erica M Fernandes Deepali N Shinde Sha Tang Juliane Hoyer Christiane Zweier André Reis Carlos A Bacino Rui Xiao Amy M Breman Janice L Smith Nicholas Katsanis Bret Bostwick Bernt Popp Erica E Davis Yaping Yang

Am J Hum Genet 2017 Oct 21;101(4):503-515. Epub 2017 Sep 21.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Baylor Genetics, Houston, TX 77021, USA. Electronic address:

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October 2017

Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis.

Authors:
Mandy L Ballinger Ana Best Phuong L Mai Payal P Khincha Jennifer T Loud June A Peters Maria Isabel Achatz Rubens Chojniak Alexandre Balieiro da Costa Karina Miranda Santiago Judy Garber Allison F O'Neill Rosalind A Eeles D Gareth Evans Eveline Bleiker Gabe S Sonke Marielle Ruijs Claudette Loo Joshua Schiffman Anne Naumer Wendy Kohlmann Louise C Strong Jasmina Bojadzieva David Malkin Surya P Rednam Elena M Stoffel Erika Koeppe Jeffrey N Weitzel Thomas P Slavin Bita Nehoray Mark Robson Michael Walsh Lorenzo Manelli Anita Villani David M Thomas Sharon A Savage

JAMA Oncol 2017 12;3(12):1634-1639

Biostatistics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland

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December 2017

Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.

Authors:
Jonathan D Wasserman Gail E Tomlinson Harriet Druker Junne Kamihara Wendy K Kohlmann Christian P Kratz Katherine L Nathanson Kristian W Pajtler Andreu Parareda Surya P Rednam Lisa J States Anita Villani Michael F Walsh Kristin Zelley Joshua D Schiffman

Clin Cancer Res 2017 07;23(13):e123-e132

Department of Pediatrics and Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah.

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July 2017

Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma.

Authors:
Jennifer M Kalish Leslie Doros Lee J Helman Raoul C Hennekam Roland P Kuiper Saskia M Maas Eamonn R Maher Kim E Nichols Sharon E Plon Christopher C Porter Surya Rednam Kris Ann P Schultz Lisa J States Gail E Tomlinson Kristin Zelley Todd E Druley

Clin Cancer Res 2017 07;23(13):e115-e122

Division of Pediatric Hematology and Oncology, Washington University, St. Louis, Missouri.

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July 2017

, and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.

Authors:
Kris Ann P Schultz Surya P Rednam Junne Kamihara Leslie Doros Maria Isabel Achatz Jonathan D Wasserman Lisa R Diller Laurence Brugières Harriet Druker Katherine A Schneider Rose B McGee William D Foulkes

Clin Cancer Res 2017 Jun;23(12):e76-e82

Department of Human Genetics and Research Institute, McGill University Health Centre, McGill University, Montreal, Québec, Canada.

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June 2017

Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.

Authors:
Surya P Rednam Ayelet Erez Harriet Druker Katherine A Janeway Junne Kamihara Wendy K Kohlmann Katherine L Nathanson Lisa J States Gail E Tomlinson Anita Villani Stephan D Voss Joshua D Schiffman Jonathan D Wasserman

Clin Cancer Res 2017 Jun;23(12):e68-e75

Division of Endocrinology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

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June 2017

DNA methylation of a novel PAK4 locus influences ototoxicity susceptibility following cisplatin and radiation therapy for pediatric embryonal tumors.

Authors:
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 Michael E Scheurer

Neuro Oncol 2017 Oct;19(10):1372-1379

Department of Pediatrics Hematology-Oncology Section, Baylor College of Medicine, Houston, Texas; Department of Internal Medicine, Baylor College of Medicine, Houston, Texas; Department of Hematology & Oncology, Cook Children's Medical Center, Fort Worth, Texas.

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October 2017

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-year follow-up.

Authors:
Ali H Palejwala Jared S Fridley Krystal Garcia Sanjeev A Vasudevan David Khechoyan Surya Rednam Chester J Koh Andrew Jea

J Neurosurg Pediatr 2017 Jan 30;19(1):102-107. Epub 2016 Sep 30.

Neuro-Spine Program, Division of Pediatric Neurosurgery.

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January 2017

Exploratory analysis of ERCC2 DNA methylation in survival among pediatric medulloblastoma patients.

Authors:
Emilyn Banfield Austin L Brown Erin C Peckham Surya P Rednam Jeffrey Murray M Fatih Okcu Laura E Mitchell Murali M Chintagumpala Ching C Lau Michael E Scheurer Philip J Lupo

Cancer Epidemiol 2016 10 5;44:161-166. Epub 2016 Sep 5.

Baylor College of Medicine, One Baylor Plaza, Houston, TX, USA; Texas Children's Cancer and Hematology Centers, Houston, TX, USA. Electronic address:

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October 2016

SOD2 genetic variant associated with treatment-related ototoxicity in cisplatin-treated pediatric medulloblastoma.

Authors:
Austin L Brown Philip J Lupo Mehmet Fatih Okcu Ching C Lau Surya Rednam Michael E Scheurer

Cancer Med 2015 Nov 24;4(11):1679-86. Epub 2015 Sep 24.

Section of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.

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November 2015

Germ-line and somatic DICER1 mutations in pineoblastoma.

Authors:
Leanne de Kock Nelly Sabbaghian Harriet Druker Evan Weber Nancy Hamel Suzanne Miller Catherine S Choong Nicholas G Gottardo Ursula R Kees Surya P Rednam Liselotte P van Hest Marjolijn C Jongmans Shalini Jhangiani James R Lupski Margaret Zacharin Dorothée Bouron-Dal Soglio Annie Huang John R Priest Arie Perry Sabine Mueller Steffen Albrecht David Malkin Richard G Grundy William D Foulkes

Acta Neuropathol 2014 Oct 15;128(4):583-95. Epub 2014 Jul 15.

Department of Human Genetics, McGill University, Montreal, QC, Canada.

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October 2014

Glutathione S-transferase P1 single nucleotide polymorphism predicts permanent ototoxicity in children with medulloblastoma.

Authors:
Surya Rednam Michael E Scheurer Adekunle Adesina Ching C Lau Mehmet Fatih Okcu

Pediatr Blood Cancer 2013 Apr 12;60(4):593-8. Epub 2012 Oct 12.

Section of Hematology-Oncology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.

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April 2013

Metastatic squamous cell carcinoma of the oropharynx in a child with a mutation in the Connexin 26 gene.

Authors:
Surya Rednam John Hicks Moise L Levy Alberto S Pappo

J Pediatr Hematol Oncol 2011 Jul;33(5):387-9

Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

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July 2011