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Abstract A023 Establishment of the consortium for childhood cancer predisposition and the childhood cancer predisposition study

Christopher C. Porter, Garrett M. Brodeur, Lisa Diller, Chloe Edgerton, Junne Kamihara, Wendy Kohlmann, Suzanne P. MacFarland, Luke Maese, David Malkin, Kim E. Nichols, Melissa R. Perrino, Sharon E. Plon, Surya Rednam, Anita Villani

Cancer Res (2024) 84 (17_Supplement): A023.

https://doi.org/10.1158/1538-7445.PEDIATRIC24-A023

Published: 05 September 2024

View articletitled, Abstract A023 Establishment of the consortium for childhood cancer predisposition and the childhood cancer predisposition study

Journal Articles

Abstract 5610: Investigating the role of BRCA2 in the development of pediatric rhabdomyosarcoma

P. Adam Weinstein, Ryan Zabriskie, Cem Ozdemir, Kyle M. Miller, Olga Medina-Martinez, Jason D. Heaney, Aniko Sabo, Philip J. Lupo, Sharon E. Plon

Cancer Res (2024) 84 (6_Supplement): 5610.

https://doi.org/10.1158/1538-7445.AM2024-5610

Published: 22 March 2024

View articletitled, Abstract 5610: Investigating the role of BRCA2 in the development of pediatric rhabdomyosarcoma

Journal Articles

Abstract 6376: Establishment of the Consortium for Childhood Cancer Predisposition and the Childhood Cancer Predisposition Study

Anita Villani, Garrett M. Brodeur, Lisa R. Diller, Chloe Edgerton, Junne Kamihara, Wendy Kohlmann, Suzanne P. MacFarland, Luke Maese, David Malkin, Kim E. Nichols, Melissa R. Perrino, Sharon E. Plon, Surya Rednam, Christopher C. Porter

Cancer Res (2024) 84 (6_Supplement): 6376.

https://doi.org/10.1158/1538-7445.AM2024-6376

Published: 22 March 2024

View articletitled, Abstract 6376: Establishment of the Consortium for Childhood Cancer Predisposition and the Childhood Cancer Predisposition Study

Journal Articles

Abstract 6370: Evaluating the risk of carcinomas among children with congenital anomalies: A population-based study of 21 million births

Jeremy M. Schraw, Tania A. Desrosiers, Tiffany M. Chambers, Michael E. Scheurer, Charles J. Shumate, Wendy N. Nembhard, Mahsa M. Yazdy, Eirini Nestoridi, Amanda E. Janitz, Jean Paul Tanner, Russell S. Kirby, Jason L. Salemi, Chad D. Huff, Sharon E. Plon, Philip J. Lupo

Cancer Res (2024) 84 (6_Supplement): 6370.

https://doi.org/10.1158/1538-7445.AM2024-6370

Published: 22 March 2024

View articletitled, Abstract 6370: Evaluating the risk of carcinomas among children with congenital anomalies: A population-based study of 21 million births

Journal Articles

Abstract 1192: The Clinical Genome Resource (ClinGen) somatic cancer clinical domain working group

Cancer Res (2022) 82 (12_Supplement): 1192.

https://doi.org/10.1158/1538-7445.AM2022-1192

Published: 15 June 2022

View articletitled, Abstract 1192: The Clinical Genome Resource (ClinGen) somatic cancer clinical domain working group

Journal Articles

Abstract 1998: A population-based assessment of cancer risk in children with recurrent multiple congenital anomalies

Alexander Renwick, Jeremy M. Schraw, Tania A. Desrosiers, Amanda E. Janitz, Michael E. Scheurer, Mark A. Canfield, Peter H. Langlois, Angela E. Scheuerle, Sharon E. Plon, Philip J. Lupo

Cancer Res (2022) 82 (12_Supplement): 1998.

https://doi.org/10.1158/1538-7445.AM2022-1998

Published: 15 June 2022

View articletitled, Abstract 1998: A population-based assessment of cancer risk in children with recurrent multiple congenital anomalies

Journal Articles

Abstract 631: Germline cancer predisposition results from the National Cancer Institute - Children's Oncology Group (NCI-COG) Pediatric MATCH Trial

Cancer Res (2021) 81 (13_Supplement): 631.

https://doi.org/10.1158/1538-7445.AM2021-631

Published: 01 July 2021

View articletitled, Abstract 631: Germline cancer predisposition results from the National Cancer Institute - Children's Oncology Group (NCI-COG) Pediatric MATCH Trial

Journal Articles

Abstract PR03: Sex ratio disparities and the risk of childhood cancer: Evaluating the mediating effect of birth defects among 15,000 childhood cancer cases

Erin L. Marcotte, Jeremy M. Schraw, Tania A. Desrosiers, Wendy N. Nembhard, Peter H. Langlois, Mark A. Canfield, Robert E. Meyer, Sharon E. Plon, Philip Lupo

Cancer Res (2020) 80 (14_Supplement): PR03.

https://doi.org/10.1158/1538-7445.PEDCA19-PR03

Published: 15 July 2020

View articletitled, Abstract PR03: Sex ratio disparities and the risk of childhood cancer: Evaluating the mediating effect of birth defects among 15,000 childhood cancer cases

Journal Articles

Abstract 5054: Are co-occurring structural birth defects associated with risk of acute lymphoblastic leukemia among children with Down syndrome

Jeremy M. Schraw, Tiffany M. Chambers, John P. Woodhouse, Peter H. Langlois, Mark A. Canfield, Angela E. Scheuerle, Michael E. Scheurer, Sharon E. Plon, Karen R. Rabin, Philip J. Lupo

Cancer Res (2019) 79 (13_Supplement): 5054.

https://doi.org/10.1158/1538-7445.AM2019-5054

Published: 01 July 2019

View articletitled, Abstract 5054: Are co-occurring structural birth defects associated with risk of acute lymphoblastic leukemia among children with Down syndrome

Journal Articles

Abstract LB-161: A population-based assessment of cancer risk among children with non-chromosomal birth defects in 10 million live births

Jeremy M. Schraw, Tania A. Desrosiers, Wendy N. Nembhard, Glenn Copeland, Robert E. Meyer, Austin L. Brown, Tiffany M. Chambers, Heather E. Danysh, Saumya Sisoudiya, Chunqiao Luo, Amir Mian, Michael E. Scheurer, Sharon E. Plon, Philip J. Lupo

Cancer Res (2018) 78 (13_Supplement): LB-161.

https://doi.org/10.1158/1538-7445.AM2018-LB-161

Published: 01 July 2018

View articletitled, Abstract LB-161: A population-based assessment of cancer risk among children with non-chromosomal birth defects in 10 million live births

Journal Articles

Abstract 4877: Transcriptome sequencing of pediatric hepatocellular carcinoma reveals genomic events involving APC and TERT

Katherine Haines, Angshumoy Roy, Stephen Sarabia, Linghua Wang, Pavel Sumazin, Kyle Covington, Harsha Doddapaneni, Oliver Hampton, Donna M. Muzny, Dolores Lopez-Terrada, David A. Wheeler, Sharon E. Plon, D. Williams Parsons

Cancer Res (2017) 77 (13_Supplement): 4877.

https://doi.org/10.1158/1538-7445.AM2017-4877

Published: 01 July 2017

View articletitled, Abstract 4877: Transcriptome sequencing of pediatric hepatocellular carcinoma reveals genomic events involving APC and TERT

Journal Articles

Abstract A33: Discovery of chimeric transcripts involving APC and TERT in pediatric HCC by RNA sequencing

Katherine Haines, Angshumoy Roy, Linghua Wang, Pavel Sumazin, Kyle R. Covington, Donna M. Muzny, Vijetha Kumar, Harsha Doddapaneni, Hsu Chao, David A. Wheeler, Gail Tomlinson, D. Williams Parsons, Sharon E. Plon, Dolores Lopez-Terrada

Cancer Res (2016) 76 (5_Supplement): A33.

https://doi.org/10.1158/1538-7445.PEDCA15-A33

Published: 04 April 2016

View articletitled, Abstract A33: Discovery of chimeric transcripts involving APC and TERT in pediatric HCC by RNA sequencing

Journal Articles

Abstract 2741: The risk of cancer among children with birth defects

Philip J. Lupo, Michael E. Scheurer, Sharon E. Plon, Logan E. Spector, Beth A. Mueller

Cancer Res (2015) 75 (15_Supplement): 2741.

https://doi.org/10.1158/1538-7445.AM2015-2741

Published: 01 August 2015

View articletitled, Abstract 2741: The risk of cancer among children with birth defects

Journal Articles

Abstract 3301: Uncovering novel radiation sensitivity syndromes through exome sequencing

Deborah I. Ritter, Andrea K. Petersen, Katherine M. Haines, Ryan C. Zabriskie, David A. Wheeler, Sharon E. Plon

Cancer Res (2015) 75 (15_Supplement): 3301.

https://doi.org/10.1158/1538-7445.AM2015-3301

Published: 01 August 2015

View articletitled, Abstract 3301: Uncovering novel radiation sensitivity syndromes through exome sequencing

Journal Articles

Abstract 4856: ITD Assembler: An algorithm for internal tandem duplication discovery from short-read sequencing data

Oliver A. Hampton, Navin Rustagi, Jie Li, Liu Xi, Richard A. Gibbs, Sharon E. Plon, Marek Kimmel, David A. Wheeler

Cancer Res (2015) 75 (15_Supplement): 4856.

https://doi.org/10.1158/1538-7445.AM2015-4856

Published: 01 August 2015

View articletitled, Abstract 4856: ITD Assembler: An algorithm for internal tandem duplication discovery from short-read sequencing data

Journal Articles

Abstract 11: Evaluating cancer susceptibility mutations and incidental findings from whole exome sequencing of sequentially diagnosed pediatric solid and brain tumor patients: Early results of the BASIC3 study

Sharon E. Plon, Sarah Scollon, Katie Bergstrom, Robin A. Kerstein, Murali Chintagumpala, Stacey L. Berg, Susan G. Hilsenbeck, Tao Wang, Surya Rednam, David Wheeler, Laurence McCullough, Richard Street, Amy L. McGuire, Reid G. Jeffrey, Donna M. Muzny, Christine M. Eng, Yaping Yang, Richard A. Gibbs, Donald W. Parsons

Cancer Res (2014) 74 (23_Supplement): 11.

https://doi.org/10.1158/1538-7445.CANSUSC14-11

Published: 12 December 2014

View articletitled, Abstract 11: Evaluating cancer susceptibility mutations and incidental findings from whole exome sequencing of sequentially diagnosed pediatric solid and brain tumor patients: Early results of the BASIC3 study

Journal Articles

Abstract IA16: Evaluating the implementation and utility of clinical tumor exome sequencing in the pediatric oncology clinic: Early results of the BASIC3 study

Cancer Res (2014) 74 (20_Supplement): IA16.

https://doi.org/10.1158/1538-7445.PEDCAN-IA16

Published: 09 October 2014

View articletitled, Abstract IA16: Evaluating the implementation and utility of clinical tumor exome sequencing in the pediatric oncology clinic: Early results of the BASIC3 study

Journal Articles

Abstract A8: Functional analysis of genomic variants identified through whole exome sequencing of pediatric lymphocytic leukemia kindreds

Jason Saliba, Ryan Zabriskie, Bradford Powell, Stephanie Hicks, Marek Kimmel, Hannah Cheung, Deborah Ritter, Donna M. Muzny, Jeffrey G. Reid, David A. Wheeler, Richard A. Gibbs, Sharon E. Plon

Cancer Res (2014) 74 (20_Supplement): A8.

https://doi.org/10.1158/1538-7445.PEDCAN-A8

Published: 09 October 2014

View articletitled, Abstract A8: Functional analysis of genomic variants identified through whole exome sequencing of pediatric lymphocytic leukemia kindreds

Journal Articles

Abstract 1296: Family history of cancer and rhabdomyosarcoma in children: a report from the Children's Oncology Group

Philip J. Lupo, Heather E. Danysh, Sharon E. Plon, David Malkin, Simone Hettmer, Douglas S. Hawkins, Stephen X. Skapek, Logan G. Spector, Karin Papworth, Beatrice Melin, Erik B. Erhardt, Seymour Grufferman

Cancer Res (2014) 74 (19_Supplement): 1296.

https://doi.org/10.1158/1538-7445.AM2014-1296

Published: 01 October 2014

View articletitled, Abstract 1296: Family history of cancer and rhabdomyosarcoma in children: a report from the Children's Oncology Group

Journal Articles

Abstract 5169: Diagnostic yield of clinical tumor and germline exome sequencing for newly diagnosed children with solid tumors

Cancer Res (2014) 74 (19_Supplement): 5169.

https://doi.org/10.1158/1538-7445.AM2014-5169

Published: 01 October 2014

View articletitled, Abstract 5169: Diagnostic yield of clinical tumor and germline exome sequencing for newly diagnosed children with solid tumors

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Abstract A023 Establishment of the consortium for childhood cancer predisposition and the childhood cancer predisposition study

Abstract 5610: Investigating the role of BRCA2 in the development of pediatric rhabdomyosarcoma

Abstract 6376: Establishment of the Consortium for Childhood Cancer Predisposition and the Childhood Cancer Predisposition Study

Abstract 6370: Evaluating the risk of carcinomas among children with congenital anomalies: A population-based study of 21 million births

Abstract 1192: The Clinical Genome Resource (ClinGen) somatic cancer clinical domain working group

Abstract 1998: A population-based assessment of cancer risk in children with recurrent multiple congenital anomalies

Abstract 631: Germline cancer predisposition results from the National Cancer Institute - Children's Oncology Group (NCI-COG) Pediatric MATCH Trial

Abstract PR03: Sex ratio disparities and the risk of childhood cancer: Evaluating the mediating effect of birth defects among 15,000 childhood cancer cases

Abstract 5054: Are co-occurring structural birth defects associated with risk of acute lymphoblastic leukemia among children with Down syndrome

Abstract LB-161: A population-based assessment of cancer risk among children with non-chromosomal birth defects in 10 million live births

Abstract 4877: Transcriptome sequencing of pediatric hepatocellular carcinoma reveals genomic events involving APC and TERT

Abstract A33: Discovery of chimeric transcripts involving APC and TERT in pediatric HCC by RNA sequencing

Abstract 2741: The risk of cancer among children with birth defects

Abstract 3301: Uncovering novel radiation sensitivity syndromes through exome sequencing

Abstract 4856: ITD Assembler: An algorithm for internal tandem duplication discovery from short-read sequencing data

Abstract 11: Evaluating cancer susceptibility mutations and incidental findings from whole exome sequencing of sequentially diagnosed pediatric solid and brain tumor patients: Early results of the BASIC3 study

Abstract IA16: Evaluating the implementation and utility of clinical tumor exome sequencing in the pediatric oncology clinic: Early results of the BASIC3 study

Abstract A8: Functional analysis of genomic variants identified through whole exome sequencing of pediatric lymphocytic leukemia kindreds

Abstract 1296: Family history of cancer and rhabdomyosarcoma in children: a report from the Children's Oncology Group

Abstract 5169: Diagnostic yield of clinical tumor and germline exome sequencing for newly diagnosed children with solid tumors

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