S. Rednam

发表

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

D. Parsons, S. Plon, Angshumoy Roy, 2019, Cold Spring Harbor molecular case studies.

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

T. Druley, R. Hennekam, S. Plon, 2017, Clinical Cancer Research.

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

Michael F. Wangler, E. Zackai, David T. Miller, 2018, Genetics in Medicine.

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

C. Lau, A. Adesina, M. Okcu, 2013, Pediatric blood & cancer.

Considerations for total thyroidectomy in an adolescent with PTEN mutation

S. Rednam, M. Brandt, M. Tosur, 2018, Therapeutic advances in endocrinology and metabolism.

USP11 negatively regulates TNFalpha-induced NF-kappaB activation by targeting on IkappaBalpha.

J. Qin, Songbin Fu, Xiongbin Lu, 2010, Cellular signalling.

Respiratory syncytial virus augments production of fibroblast growth factor basic in vitro: Implications for a possible mechanism of prolonged wheezing after infection

S. Rednam, A. Dosanjh, M. Martín, 2003, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

PTEN, DICER1, FH, and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood

W. Foulkes, L. Diller, K. Schneider, 2017, Clinical Cancer Research.

Gliomas in the context of Li-Fraumeni syndrome: An international cohort.

D. Evans, T. Slavin, J. Schiffman, 2019, Journal of Clinical Oncology.

Germ-line and somatic DICER1 mutations in pineoblastoma

J. Lupski, S. Jhangiani, W. Foulkes, 2014, Acta Neuropathologica.

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.

Ali H. Palejwala, C. Koh, A. Jea, 2017, Journal of neurosurgery. Pediatrics.

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

Austin L. Brown, J. Murray, M. Chintagumpala, 2019, Cancer epidemiology.

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

Austin L. Brown, J. Murray, C. Lau, 2017, Neuro-oncology.

Epidemiology of childhood brain tumors

M. Chintagumpala, P. Lupo, S. Rednam, 2018 .

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

Juliane Hoyer, Bernt Popp, André Reis, 2017, American journal of human genetics.

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

A. Pappo, J. Hicks, S. Rednam, 2011, Journal of pediatric hematology/oncology.

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

K. Nathanson, J. Schiffman, G. Tomlinson, 2017, Clinical Cancer Research.

Abdominal undifferentiated small round cell tumor with unique translocation (X;19)(q13;q13.3)

A. Bertuch, J. Yustein, K. Eldin, 2010, Pediatric blood & cancer.

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

S. Rednam, 2019, Current opinion in pediatrics.

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

Austin L. Brown, C. Lau, M. Okcu, 2015, Cancer medicine.

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

David M. Thomas, R. Eeles, L. Strong, 2017, JAMA oncology.

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

K. Nathanson, K. Pajtler, J. Schiffman, 2017, Clinical Cancer Research.

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

Austin L. Brown, J. Murray, C. Lau, 2016, Cancer epidemiology.

Gadolinium is not necessary for surveillance MR imaging in children with chiasmatic‐hypothalamic low‐grade glioma

W. Whitehead, M. Chintagumpala, A. Levy, 2021, Pediatric blood & cancer.

Guidelines for surveillance of patients with von Hippel‐Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance

A. Tirosh, S. Pruthi, A. Daniels, 2023, Cancer.

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

Katie Wusik, S. Rednam, I. Iacobas, 2020, Pediatric blood & cancer.

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

Michael F. Wangler, David T. Miller, B. Korf, 2018, Genetics in Medicine.

Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotypeâ€“phenotype correlation

Michael F. Wangler, David T. Miller, B. Korf, 2019 .

Collaboration to Promote Research and Improve Clinical Care in the Evolving Field of Childhood Cancer Predisposition.

S. Plon, J. Schiffman, L. Diller, 2022, Cancer Prevention Research.

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

K. Nathanson, J. Schiffman, G. Tomlinson, 2017, Clinical Cancer Research.