SURYAREDNAMSURYA REDNAM0.000000000000000.000000000000003909REDNAM, SURYAAssociate Professorprns:coAuthorOfcoauthor ofFaculty Rankprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasFacultyRankhas faculty rankprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:mainImagephotoprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:physicalNeighborOfphysical neighborprns:positionInDepartmentposition in departmentprns:positionInDivisionposition in divisionprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:similarTosimilar toprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierAddressvivo:address1address line 1vivo:addressCitycityvivo:addressPostalCodepostal codevivo:addressStatestate or provincevivo:authorInAuthorshipselected publicationsvivo:authorRankauthor rank in publicationAuthorshipDepartmentDivisionvivo:hasResearchArearesearch areasvivo:hrJobTitleHR job titleInformation Resourcevivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcevivo:mailingAddressmailing addressvivo:orcidIdORCID idvivo:personInPositionpositionsPositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonAuthorship 922911Endocrine Neoplasia & HDRadiation OncologyMD AndersonCAMILOJIMENEZCAMILO JIMENEZ9385JIMENEZ, CAMILOAssociate ProfessorARNOLD DELA CRUZPAULINOARNOLD DELA CRUZ PAULINO9923PAULINO, ARNOLD DELA CRUZProfessorMUSTAFATOSURMUSTAFA TOSUR10176TOSUR, MUSTAFAAssociate Professor26400460Brown AL, Lupo PJ, Okcu MF, Lau CC, Rednam S, Scheurer MECancer medicineSOD2 genetic variant associated with treatment-related ototoxicity in cisplatin-treated pediatric medulloblastoma. Cancer Med. 2015 Nov; 4(11):1679-86.Cancer Med2015-09-24T00:00:002015SOD2 genetic variant associated with treatment-related ototoxicity in cisplatin-treated pediatric medulloblastoma.Authorship 298218514675469Dosanjh A, Rednam S, Martin MPediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and ImmunologyRespiratory syncytial virus augments production of fibroblast growth factor basic in vitro: implications for a possible mechanism of prolonged wheezing after infection. Pediatr Allergy Immunol. 2003 Dec; 14(6):437-40.Pediatr Allergy Immunol2003-12-01T00:00:002003Respiratory syncytial virus augments production of fibroblast growth factor basic in vitro: implications for a possible mechanism of prolonged wheezing after infection.74Professor10Assistant Professor14Associate Professor6Adjunct ProfessorMedicine-Epidemiology & Populat Sci6701 FANNINHouston, 77030TXALEXANDRASTEVENSALEXANDRA STEVENS0.000000000000000.000000000000005162STEVENS, ALEXANDRAAssociate Professor19874889Sun W, Tan X, Shi Y, Xu G, Mao R, Gu X, Fan Y, Yu Y, Burlingame S, Zhang H, Rednam SP, Lu X, Zhang T, Fu S, Cao G, Qin J, Yang JCellular signallingUSP11 negatively regulates TNFalpha-induced NF-kappaB activation by targeting on IkappaBalpha. Cell Signal. 2010 Mar; 22(3):386-94.Cell Signal2010-03-01T00:00:002010USP11 negatively regulates TNFalpha-induced NF-kappaB activation by targeting on IkappaBalpha.Authorship 328105427607585Banfield E, Brown AL, Peckham EC, Rednam SP, Murray J, Okcu MF, Mitchell LE, Chintagumpala MM, Lau CC, Scheurer ME, Lupo PJCancer epidemiologyExploratory analysis of ERCC2 DNA methylation in survival among pediatric medulloblastoma patients. Cancer Epidemiol. 2016 10; 44:161-166.Cancer Epidemiol2016-09-05T00:00:002016Exploratory analysis of ERCC2 DNA methylation in survival among pediatric medulloblastoma patients.Authorship 653500627689246Palejwala AH, Fridley JS, Garcia K, Vasudevan SA, Khechoyan D, Rednam S, Koh CJ, Jea AJournal of neurosurgery. PediatricsHemisacrectomy 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. J Neurosurg Pediatr. 2017 Jan; 19(1):102-107.J Neurosurg Pediatr2016-09-30T00:00:002016Hemisacrectomy 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.20162687Yustein JT, Rednam S, Bertuch AA, Goss JA, Brandt ML, Eldin K, Lu X, Hicks JPediatric blood & cancerAbdominal undifferentiated small round cell tumor with unique translocation (X;19)(q13;q13.3). Pediatr Blood Cancer. 2010 Jul 01; 54(7):1041-4.Pediatr Blood Cancer2010-07-01T00:00:002010Abdominal undifferentiated small round cell tumor with unique translocation (X;19)(q13;q13.3).20829717Rednam S, Hicks J, Levy ML, Pappo ASJournal of pediatric hematology/oncologyMetastatic squamous cell carcinoma of the oropharynx in a child with a mutation in the Connexin 26 gene. J Pediatr Hematol Oncol. 2011 Jul; 33(5):387-9.J Pediatr Hematol Oncol2011-07-01T00:00:002011Metastatic squamous cell carcinoma of the oropharynx in a child with a mutation in the Connexin 26 gene.28444219Brown AL, Foster KL, Lupo PJ, Peckham-Gregory EC, Murray JC, Okcu MF, Lau CC, Rednam SP, Chintagumpala M, Scheurer MENeuro-oncologyDNA methylation of a novel PAK4 locus influences ototoxicity susceptibility following cisplatin and radiation therapy for pediatric embryonal tumors. Neuro Oncol. 2017 Oct 01; 19(10):1372-1379.Neuro Oncol2017-10-01T00:00:002017DNA methylation of a novel PAK4 locus influences ototoxicity susceptibility following cisplatin and radiation therapy for pediatric embryonal tumors.Authorship 1022121Authorship 10350311Authorship 8728371Authorship 872921228620007Rednam SP, Erez A, Druker H, Janeway KA, Kamihara J, Kohlmann WK, Nathanson KL, States LJ, Tomlinson GE, Villani A, Voss SD, Schiffman JD, Wasserman JDClinical cancer research : an official journal of the American Association for Cancer ResearchVon Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood. Clin Cancer Res. 2017 Jun 15; 23(12):e68-e75.Clin Cancer Res2017-06-15T00:00:002017Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.28620008Schultz KAP, Rednam SP, Kamihara J, Doros L, Achatz MI, Wasserman JD, Diller LR, Brugi?res L, Druker H, Schneider KA, McGee RB, Foulkes WDClinical cancer research : an official journal of the American Association for Cancer ResearchPTEN, DICER1, FH, and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood. Clin Cancer Res. 2017 Jun 15; 23(12):e76-e82.Clin Cancer Res2017-06-15T00:00:002017PTEN, DICER1, FH, and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.Authorship 87467910Authorship 874680928674120Kalish JM, Doros L, Helman LJ, Hennekam RC, Kuiper RP, Maas SM, Maher ER, Nichols KE, Plon SE, Porter CC, Rednam S, Schultz KAP, States LJ, Tomlinson GE, Zelley K, Druley TEClinical cancer research : an official journal of the American Association for Cancer ResearchSurveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma. Clin Cancer Res. 2017 07 01; 23(13):e115-e122.Clin Cancer Res2017-07-01T00:00:002017Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma.28674121Wasserman JD, Tomlinson GE, Druker H, Kamihara J, Kohlmann WK, Kratz CP, Nathanson KL, Pajtler KW, Parareda A, Rednam SP, States LJ, Villani A, Walsh MF, Zelley K, Schiffman JDClinical cancer research : an official journal of the American Association for Cancer ResearchMultiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood. Clin Cancer Res. 2017 07 01; 23(13):e123-e132.Clin Cancer Res2017-07-01T00:00:002017Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.Authorship 8763983628772291Ballinger ML, Best A, Mai PL, Khincha PP, Loud JT, Peters JA, Achatz MI, Chojniak R, Balieiro da Costa A, Santiago KM, Garber J, O'Neill AF, Eeles RA, Evans DG, Bleiker E, Sonke GS, Ruijs M, Loo C, Schiffman J, Naumer A, Kohlmann W, Strong LC, Bojadzieva J, Malkin D, Rednam SP, Stoffel EM, Koeppe E, Weitzel JN, Slavin TP, Nehoray B, Robson M, Walsh M, Manelli L, Villani A, Thomas DM, Savage SAJAMA oncologyBaseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis. JAMA Oncol. 2017 12 01; 3(12):1634-1639.JAMA Oncol2017-12-01T00:00:002017Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis.23065688Rednam S, Scheurer ME, Adesina A, Lau CC, Okcu MFPediatric blood & cancerGlutathione S-transferase P1 single nucleotide polymorphism predicts permanent ototoxicity in children with medulloblastoma. Pediatr Blood Cancer. 2013 Apr; 60(4):593-8.Pediatr Blood Cancer2012-10-12T00:00:002012Glutathione S-transferase P1 single nucleotide polymorphism predicts permanent ototoxicity in children with medulloblastoma.Authorship 8789658Authorship 8794551028942966Stankiewicz P, Khan TN, Szafranski P, Slattery L, Streff H, Vetrini F, Bernstein JA, Brown CW, Rosenfeld JA, Rednam S, Scollon S, Bergstrom KL, Parsons DW, Plon SE, Vieira MW, Quaio CRDC, Baratela WAR, Acosta Guio JC, Armstrong R, Mehta SG, Rump P, Pfundt R, Lewandowski R, Fernandes EM, Shinde DN, Tang S, Hoyer J, Zweier C, Reis A, Bacino CA, Xiao R, Breman AM, Smith JL, Deciphering Developmental Disorders Study, Katsanis N, Bostwick B, Popp B, Davis EE, Yang YAmerican journal of human geneticsHaploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features. Am J Hum Genet. 2017 Oct 05; 101(4):503-515.Am J Hum Genet2017-09-21T00:00:002017Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features.CHRISAMOSCHRIS AMOS13498AMOS, CHRISProfessortrue1ProfessorProfessortrue1ProfessorProfessortrue1Associate ProfessorAssociate Professortrue1ProfessorProfessorD055088Procedures46812660.550653Early Detection of CancerD009386Disorders1282210.823017Neoplastic Syndromes, HereditaryD006623Disorders571150.900493von Hippel-Lindau Disease30703618Arroyo VM, Lupo PJ, Scheurer ME, Rednam SP, Murray J, Okcu MF, Chintagumpala MM, Brown ALCancer epidemiologyPilot study of DNA methylation-derived neutrophil-to-lymphocyte ratio and survival in pediatric medulloblastoma. Cancer Epidemiol. 2019 04; 59:71-74.Cancer Epidemiol2019-01-29T00:00:002019Pilot study of DNA methylation-derived neutrophil-to-lymphocyte ratio and survival in pediatric medulloblastoma.Authorship 93026945Authorship 9309234Authorship 9350421Authorship 93801045Authorship 939468430275510Koczkowska M, Callens T, Gomes A, Sharp A, Chen Y, Hicks AD, Aylsworth AS, Azizi AA, Basel DG, Bellus G, Bird LM, Blazo MA, Burke LW, Cannon A, Collins F, DeFilippo C, Denayer E, Digilio MC, Dills SK, Dosa L, Greenwood RS, Griffis C, Gupta P, Hachen RK, Hern?ndez-Chico C, Janssens S, Jones KJ, Jordan JT, Kannu P, Korf BR, Lewis AM, Listernick RH, Lonardo F, Mahoney MJ, Ojeda MM, McDonald MT, McDougall C, Mendelsohn N, Miller DT, Mori M, Oostenbrink R, Perreault S, Pierpont ME, Piscopo C, Pond DA, Randolph LM, Rauen KA, Rednam S, Rutledge SL, Saletti V, Schaefer GB, Schorry EK, Scott DA, Shugar A, Siqveland E, Starr LJ, Syed A, Trapane PL, Ullrich NJ, Wakefield EG, Walsh LE, Wangler MF, Zackai E, Claes KBM, Wimmer K, van Minkelen R, De Luca A, Martin Y, Legius E, Messiaen LMGenetics in medicine : official journal of the American College of Medical GeneticsCorrection: 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. Genet Med. 2019 03; 21(3):764-765.Genet Med2019-03-01T00:00:002019Correction: 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.30190611Koczkowska M, Callens T, Gomes A, Sharp A, Chen Y, Hicks AD, Aylsworth AS, Azizi AA, Basel DG, Bellus G, Bird LM, Blazo MA, Burke LW, Cannon A, Collins F, DeFilippo C, Denayer E, Digilio MC, Dills SK, Dosa L, Greenwood RS, Griffis C, Gupta P, Hachen RK, Hern?ndez-Chico C, Janssens S, Jones KJ, Jordan JT, Kannu P, Korf BR, Lewis AM, Listernick RH, Lonardo F, Mahoney MJ, Ojeda MM, McDonald MT, McDougall C, Mendelsohn N, Miller DT, Mori M, Oostenbrink R, Perreault S, Pierpont ME, Piscopo C, Pond DA, Randolph LM, Rauen KA, Rednam S, Rutledge SL, Saletti V, Schaefer GB, Schorry EK, Scott DA, Shugar A, Siqveland E, Starr LJ, Syed A, Trapane PL, Ullrich NJ, Wakefield EG, Walsh LE, Wangler MF, Zackai E, Claes KBM, Wimmer K, van Minkelen R, De Luca A, Martin Y, Legius E, Messiaen LMGenetics in medicine : official journal of the American College of Medical GeneticsExpanding 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. Genet Med. 2019 04; 21(4):867-876.Genet Med2018-09-07T00:00:002018Expanding 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.30181857Tosur M, Brandt ML, Athanassaki ID, Rednam SPTherapeutic advances in endocrinology and metabolismConsiderations for total thyroidectomy in an adolescent with PTEN mutation. Ther Adv Endocrinol Metab. 2018 Sep; 9(9):299-301.Ther Adv Endocrinol Metab2018-07-04T00:00:002018Considerations for total thyroidectomy in an adolescent with PTEN mutation.30531401Rednam SPCurrent opinion in pediatricsUpdates on progress in cancer screening for children with hereditary cancer predisposition syndromes. Curr Opin Pediatr. 2019 02; 31(1):41-47.Curr Opin Pediatr2019-02-01T00:00:002019Updates on progress in cancer screening for children with hereditary cancer predisposition syndromes.D002528Disorders1604310.694909Cerebellar NeoplasmsD008527Disorders1705380.66767MedulloblastomaDepartment of MedicineDepartment of PediatricsMedicine-Athero & LipoproteinsPediatrics-Endocrinology/MetabolismPediatrics-OncologyBaylor College of MedicineMICHAELSCHEURERMICHAEL SCHEURER0.000000000000000.000000000000001350SCHEURER, MICHAEL0000-0002-8379-6088ProfessorMEHMETOKCUMEHMET OKCU0.000000000000000.00000000000000438OKCU, MEHMETProfessorERICBOERWINKLEERIC BOERWINKLE0.000000000000000.000000000000002653BOERWINKLE, ERICAdjunct ProfessorMURALICHINTAGUMPALAMURALI CHINTAGUMPALA0.000000000000000.000000000000003240CHINTAGUMPALA, MURALIProfessorLISABOUCHIER-HAYESLISA BOUCHIER-HAYES0.000000000000000.000000000000003984BOUCHIER-HAYES, LISAAssociate ProfessorMOSTAFAGABERMOSTAFA GABER0.000000000000000.000000000000001569GABER, MOSTAFAProfessorMICHELEREDELLMICHELE REDELL0.000000000000000.000000000000002094REDELL, MICHELEAssociate Professor0.856080.00673584182research areas0.672330.023568743coauthor of21.47793.9011460similar to1128selected publicationsPHILIPLUPOPHILIP LUPO29.70508570000000-95.401808700000004333LUPO, PHILIP0000-0003-0978-5863ProfessorCARLALLENCARL ALLEN0.000000000000000.00000000000000909ALLEN, CARL0000-0002-6625-739XProfessorAuthorship 957396531624068Lindsay H, Scollon S, Reuther J, Voicu H, Rednam SP, Lin FY, Fisher KE, Chintagumpala M, Adesina AM, Parsons DW, Plon SE, Roy ACold Spring Harbor molecular case studiesGermline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency. Cold Spring Harb Mol Case Stud. 2019 10; 5(5).Cold Spring Harb Mol Case Stud2019-10-23T00:00:002019Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency.Authorship 979515432196895Gurunathan A, Ricci K, Iacobas I, Rednam SP, Wusik K, Fei L, Hammilll AMPediatric blood & cancerImpact of vascular anomalies on the PTEN phenotype in children and young adults. Pediatr Blood Cancer. 2020 06; 67(6):e28258.Pediatr Blood Cancer2020-03-20T00:00:002020Impact of vascular anomalies on the PTEN phenotype in children and young adults.true1Adjunct ProfessorAdjunct Professortrue1ProfessorProfessorAuthorship 113460234133064Malbari F, Chintagumpala MM, Wood AC, Levy AS, Su JM, Okcu MF, Lin FY, Lindsay H, Rednam SP, Baxter PA, Paulino AC, Orzaiz GA, Whitehead WE, Dauser R, Supakul N, Kralik SFPediatric blood & cancerGadolinium is not necessary for surveillance MR imaging in children with chiasmatic-hypothalamic low-grade glioma. Pediatr Blood Cancer. 2021 10; 68(10):e29178.Pediatr Blood Cancer2021-06-16T00:00:002021Gadolinium is not necessary for surveillance MR imaging in children with chiasmatic-hypothalamic low-grade glioma.Authorship 10212639true1Associate ProfessorAssociate Professortrue1ProfessorProfessortrue1ProfessorProfessortrue1Assistant ProfessorAssistant ProfessorPediatric-Oncology EPItrue1ProfessorProfessorAuthorship 1056044336001348MacFarland SP, Maese L, Rednam SP, Kamihara J, Perrino MR, Nichols KE, Brodeur GM, Schiffman JD, Plon SE, Diller LR, Malkin D, Porter CC, Villani ACancer prevention research (Philadelphia, Pa.)Collaboration to Promote Research and Improve Clinical Care in the Evolving Field of Childhood Cancer Predisposition. Cancer Prev Res (Phila). 2022 10 04; 15(10):645-652.Cancer Prev Res (Phila)2022-10-04T00:00:002022Collaboration to Promote Research and Improve Clinical Care in the Evolving Field of Childhood Cancer Predisposition.Authorship 1073516937337409Daniels AB, Tirosh A, Huntoon K, Mehta GU, Spiess PE, Friedman DL, Waguespack SG, Kilkelly JE, Rednam S, Pruthi S, Jonasch EA, Baum L, Chahoud J, International VHL Surveillance Guidelines ConsortiumCancerGuidelines for surveillance of patients with von Hippel-Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance. Cancer. 2023 10 01; 129(19):2927-2940.Cancer2023-06-19T00:00:002023Guidelines for surveillance of patients with von Hippel-Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance.true1Associate ProfessorAssociate ProfessorAuthorship 1080518437788149Connolly GK, Harris RD, Shumate C, Rednam SP, Canfield MA, Plon SE, Nguyen J, Schraw JM, Lupo PJCancerPediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population-based assessment in seven million children. Cancer. 2024 02 01; 130(3):467-475.Cancer2023-10-03T00:00:002023Pediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population-based assessment in seven million children.true1Associate ProfessorAssociate Professortrue1Associate ProfessorAssociate ProfessorAuthorship 1084163337961416Hirschi OR, Felker SA, Rednam SP, Vallance KL, Parsons DW, Roy A, Cooper GM, Plon SEmedRxiv : the preprint server for health sciencesCombined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for Pathogenicity. medRxiv. 2023 Nov 01.medRxiv2023-11-01T00:00:002023Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for Pathogenicity.true1Associate ProfessorAssociate Professortrue1ProfessorProfessorAUSTINBROWNAUSTIN BROWN7357BROWN, AUSTINAssistant ProfessorAuthorship 619162Authorship 1509121025022261de Kock L, Sabbaghian N, Druker H, Weber E, Hamel N, Miller S, Choong CS, Gottardo NG, Kees UR, Rednam SP, van Hest LP, Jongmans MC, Jhangiani S, Lupski JR, Zacharin M, Bouron-Dal Soglio D, Huang A, Priest JR, Perry A, Mueller S, Albrecht S, Malkin D, Grundy RG, Foulkes WDActa neuropathologicaGerm-line and somatic DICER1 mutations in pineoblastoma. Acta Neuropathol. 2014 Oct; 128(4):583-95.Acta Neuropathol2014-07-15T00:00:002014Germ-line and somatic DICER1 mutations in pineoblastoma.