52. ClinGen Pediatric Cancer Taskforce initiatives to advance pediatric clinical interpretations through expert curation
Saliba, Jason, Corson, Laura B., Lever, Jake, Golem, Shivani, Satgunaseelan, Laveniya, Meredith, David M., Grisdale, Cameron J., Krysiak, Kilannin, Evans, Mark G., Luo, Minjie, Sukhanova, Madina, Mathew, Mariam T., Seifi, Morteza, Williams, Heather E., Yap, Kai Lee, Akesson, Lauren, Kanagal-Shamanna, Rashmi, Ji, Jianling, Fakim, Yasmina Jaufeerally, Danos, Arpad, Akkari, Yassmine, Parsons, D. Williams, Schriml, Lynn, Wagner, Alex H., Griffith, Obi L., Griffith, Malachi, Roy, Angshumoy, Raca, Gordana
Published in Cancer genetics (01.11.2023)
Published in Cancer genetics (01.11.2023)
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Journal Article
Abstract 4877: Transcriptome sequencing of pediatric hepatocellular carcinoma reveals genomic events involving APC and TERT
Haines, Katherine, Roy, Angshumoy, Sarabia, Stephen, Wang, Linghua, Sumazin, Pavel, Covington, Kyle, Doddapaneni, Harsha, Hampton, Oliver, Muzny, Donna M., Lopez-Terrada, Dolores, Wheeler, David A., Plon, Sharon E., Parsons, D. Williams
Published in Cancer research (Chicago, Ill.) (01.07.2017)
Published in Cancer research (Chicago, Ill.) (01.07.2017)
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Journal Article
50 Years Ago in T he J ournal of P ediatrics
Heikamp, Emily B., MD, PhD, MSc, Parsons, D. Williams, MD, PhD, Plon, Sharon E., MD, PhD
Published in The Journal of pediatrics (2016)
Published in The Journal of pediatrics (2016)
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Journal Article
Pediatric Oncology Enters the Era of Precision Medicine
Seibel, Nita L, Janeway, Katherine, Allen, Carl E, Chi, Susan N, Cho, Y Jae, Glade Bender, Julia L, Kim, AeRang, Laetsch, Theodore W, Irwin, Meredith S, Takebe, Naoko, Tricoli, James V, Parsons, D. Williams
Published in Current problems in cancer (01.05.2017)
Published in Current problems in cancer (01.05.2017)
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Journal Article
Abstract 4031: Mutant isocitrate dehydrogenase 1 (IDH1) inhibitor synergistically prolongs animal survival with standard therapies in patient-derived IDH1 mutant glioma xenograft mouse models
Kogiso, Mari, Qi, Lin, Zhang, Huiyuan, Braun, Frank K., Du, Yuchen, Huang, Yulun, Lindsay, Holly, Zhao, Sibo, Injac, Sarah G. G., Liu, Zhen, Baxter, Patricia A., Su, Jack M., Perlaky, Laszlo, Parsons, D. Williams, Chintagumpala, Murali, Adesina, Adekunle, Wang, Jialiang, Song, Yongcheng, Li, Xiao-Nan
Published in Cancer research (Chicago, Ill.) (01.07.2017)
Published in Cancer research (Chicago, Ill.) (01.07.2017)
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Journal Article
Abstract A33: Discovery of chimeric transcripts involving APC and TERT in pediatric HCC by RNA sequencing
Haines, Katherine, Roy, Angshumoy, Wang, Linghua, Sumazin, Pavel, Covington, Kyle R., Muzny, Donna M., Kumar, Vijetha, Doddapaneni, Harsha, Chao, Hsu, Wheeler, David A., Tomlinson, Gail, Parsons, D. Williams, Plon, Sharon E., Lopez-Terrada, Dolores
Published in Cancer research (Chicago, Ill.) (01.03.2016)
Published in Cancer research (Chicago, Ill.) (01.03.2016)
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Journal Article
TBIO-20. CLINICAL TUMOR WHOLE EXOME SEQUENCING FOR PEDIATRIC NEURO-ONCOLOGY PATIENTS – RESULTS FROM THE BAYLOR ADVANCING SEQUENCING IN CHILDHOOD CANCER CARE (BASIC3) CLINICAL SEQUENCING STUDY
Lin, Frank, Potter, Samara, Ting, Michelle, Chandramohan, Raghu, Kakkar, Nipun, Wang, Tao, Raesz-Martinez, Robin, Scollon, Sarah, Bergstrom, Katie, Lopez-Terrada, Dolores, Adesina, Adekunle, Mohila, Carrie, Whitehead, William, Ramamurthy, Uma, Hilsenbeck, Susan, Wheeler, David, Berg, Stacey, Chintagumpala, Murali, Eng, Christine, Gibbs, Richard, Roy, Angshumoy, Plon, Sharon, Williams Parsons, D
Published in Neuro-oncology (Charlottesville, Va.) (22.06.2018)
Published in Neuro-oncology (Charlottesville, Va.) (22.06.2018)
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Journal Article
Portero versus portador: Spanish interpretation of genomic terminology during whole exome sequencing results disclosure
Gutierrez, Amanda M, Robinson, Jill O, Statham, Emily E, Scollon, Sarah, Bergstrom, Katie L, Slashinski, Melody J, Parsons, Donald W, Plon, Sharon E, McGuire, Amy L, Street, Richard L
Published in Personalized medicine (01.11.2017)
Published in Personalized medicine (01.11.2017)
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Journal Article
Sodium ion channel mutations in glioblastoma patients correlate with shorter survival
Joshi, Avadhut D, Parsons, D Williams, Velculescu, Victor E, Riggins, Gregory J
Published in Molecular cancer (11.02.2011)
Published in Molecular cancer (11.02.2011)
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Journal Article
GE-06IDENTIFICATION OF TARGETABLE MUTATIONS IN RARE PEDIATRIC BRAIN TUMORS BY CLINICAL WHOLE EXOME SEQUENCING
Lin, Frank Y., Bavle, Abhishek, Wheeler, David, Gibbs, Richard, Lam, Sandi, Su, Jack, Chintagumpala, Murali, Adesina, Adekunle, Roy, Angshumoy, Plon, Sharon E., Parsons, D. Williams
Published in Neuro-oncology (Charlottesville, Va.) (21.04.2015)
Published in Neuro-oncology (Charlottesville, Va.) (21.04.2015)
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Journal Article
Abstract 04: Impact of whole exome sequencing results on clinical decision making for pediatric solid tumor patients in the hypothetical scenario of tumor relapse: A survey of pediatric oncologists
Bavle, Abhishek, Wang, Tao, Lin, Frank Y., Roy, Angshumoy, Kerstein, Robin A., Scollon, Sarah, Bergstrom, Katie, Gutierrez, Stephanie, Ramamurthy, Uma, Yang, Yaping, Eng, Christine M., Gibbs, Richard A., Chintagumpala, Murali M., Hilsenbeck, Susan G., Plon, Sharon E., Berg, Stacey L., Parsons, D. Williams
Published in Clinical cancer research (01.01.2016)
Published in Clinical cancer research (01.01.2016)
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Journal Article
When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority
Brothers, Kyle B., MD, PhD, Holm, Ingrid A., MD, MPH, Childerhose, Janet E., PhD, Antommaria, Armand H.M., MD, PhD, Bernhardt, Barbara A., MS, CGC, Clayton, Ellen Wright, MD, JD, Gelb, Bruce D., MD, Joffe, Steven, MD, MPH, Lynch, John A., PhD, McCormick, Jennifer B., PhD, McCullough, Laurence B., PhD, Parsons, D. Williams, MD, PhD, Sundaresan, Agnes S., MD, Wolf, Wendy A., PhD, Yu, Joon-Ho, MPH, PhD, Wilfond, Benjamin S., MD
Published in The Journal of pediatrics (01.01.2016)
Published in The Journal of pediatrics (01.01.2016)
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Journal Article
Current state of pediatric sarcoma biology and opportunities for future discovery: A report from the sarcoma translational research workshop
Hingorani, Pooja, Janeway, Katherine, Crompton, Brian D, Kadoch, Cigall, Mackall, Crystal L, Khan, Javed, Shern, Jack F, Schiffman, Joshua, Mirabello, Lisa, Savage, Sharon A, Ladanyi, Marc, Meltzer, Paul, Bult, Carol J, Adamson, Peter C, Lupo, Philip J, Mody, Rajen, DuBois, Steven G, Parsons, D. Williams, Khanna, Chand, Lau, Ching, Hawkins, Douglas S, Randall, R. Lor, Smith, Malcolm, Sorensen, Poul H, Plon, Sharon E, Skapek, Stephen X, Lessnick, Stephen, Gorlick, Richard, Reed, Damon R
Published in Cancer genetics (01.05.2016)
Published in Cancer genetics (01.05.2016)
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Journal Article
Abstract IA16: Evaluating the implementation and utility of clinical tumor exome sequencing in the pediatric oncology clinic: Early results of the BASIC3 study
Parsons, D. Williams, Roy, Angshumoy, Monzon, Federico A., López-Terrada, Dolores H., Chintagumpala, Murali M., Berg, Stacey L., Hilsenbeck, Susan G., Wang, Tao, Kerstein, Robin A., Scollon, Sarah, Bergstrom, Katie, Street, Richard L., McCullough, Laurence B., McGuire, Amy L., Ramamurthy, Uma, Wheeler, David A., Eng, Christine M., Yang, Yaping, Reid, Jeff G., Muzny, Donna M., Gibbs, Richard A., Plon, Sharon E.
Published in Cancer research (Chicago, Ill.) (15.10.2014)
Published in Cancer research (Chicago, Ill.) (15.10.2014)
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Journal Article
What’s in an exome? Diversity of diagnostic and incidental findings revealed by clinical tumor and germline sequencing of 100 children with solid tumors
Parsons, D. Williams, Roy, Angshumoy, Monzon, Federico A., Yang, Yaping, López-Terrada, Dolores H., Chintagumpala, Murali M., Berg, Stacey L., Nuchtern, Jed G, Hilsenbeck, Susan G., Wang, Tao, Kerstein, Robin A., Scollon, Sarah, Bergstrom, Katie, Ramamurthy, Uma, Reid, Jeff G., Muzny, Donna M., Wheeler, David A., Eng, Christine M., Gibbs, Richard A., Plon, Sharon E.
Published in Journal of clinical oncology (20.05.2014)
Published in Journal of clinical oncology (20.05.2014)
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Journal Article
Abstract 4592: Exome sequencing of hepatoblastoma reveals recurrent mutations in NFE2L2
Trevino, Lisa R., Wheeler, David A., Finegold, Milton J., Chintagumpala, Murali, Patel, Kayuri U., Sarabia, Stephen F., Comerford, Sarah A., Hammer, Robert E., Rakheja, Dinesh, Meyers, Rebecka L., Chen, Yidong, Pollock, Bradley H., Tomlinson, Gail E., López-Terrada, Dolores H., Parsons, D. Williams
Published in Cancer research (Chicago, Ill.) (15.04.2013)
Published in Cancer research (Chicago, Ill.) (15.04.2013)
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Journal Article
ASSESSING THE UTILITY OF CLINICAL TUMOR SEQUENCING IN THE PEDIATRIC NEURO-ONCOLOGY CLINIC
Parsons, D. W., Roy, A., Monzon, F. A., Lopez-Terrada, D. H., Chintagumpala, M. M., Berg, S. L., Hilsenbeck, S. G., Wang, T., Adesina, A. M., Li, X.-N., Kerstein, R. A., Scollon, S., Bergstrom, K., Street, R. L., McCullough, L. B., McGuire, A. L., Ramamurthy, U., Wheeler, D. A., Eng, C. M., Yang, Y., Reid, J. G., Muzny, D. M., Gibbs, R. A., Plon, S. E.
Published in Neuro-oncology (Charlottesville, Va.) (01.07.2014)
Published in Neuro-oncology (Charlottesville, Va.) (01.07.2014)
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Journal Article
HG-48INTEGRATED SEQUENCING OF PEDIATRIC PILOCYTIC ASTROCYTOMA WITH ANAPLASIA REVEALS MOLECULAR FEATURES OF BOTH LOW AND HIGH-GRADE GLIAL TUMORS
Lin, Frank Y., Ramos, Enrique, Reuther, Jacquelyn, Bavle, Abhishek, Hampton, Oliver, Barsan, Valentin V., Wheeler, David A., Lam, Sandi K., Paulino, Arnold, Su, Jack M., Chintagumpala, Murali M., Plon, Sharon E., Roy, Angshumoy, Adesina, Adekunle M., Parsons, D. Williams
Published in Neuro-oncology (Charlottesville, Va.) (01.06.2016)
Published in Neuro-oncology (Charlottesville, Va.) (01.06.2016)
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Journal Article
Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for Pathogenicity
Hirschi, Owen R, Felker, Stephanie A, Rednam, Surya P, Vallance, Kelly L, Parsons, D Williams, Roy, Angshumoy, Cooper, Gregory M, Plon, Sharon E
Published in medRxiv : the preprint server for health sciences (01.11.2023)
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Published in medRxiv : the preprint server for health sciences (01.11.2023)
Journal Article
An 11 Base Pair Duplication in Exon 6 of the SMN Gene Produces a Type I Spinal Muscular Atrophy (SMA) Phenotype: Further Evidence For SMN as the Primary SMA-Determining Gene
Parsons, D. Williams, McAndrew, Patricia E., Monani, Umrao R., Mendell, Jerry R., Burghes, Arthur H. M., Prior, Thomas W.
Published in Human molecular genetics (01.11.1996)
Published in Human molecular genetics (01.11.1996)
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