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Abstract PS8-04: Clinical and pathological characteristics and screening outcome for secondary cancers in breast cancer patients with li-fraumeni syndrome attending the MD anderson li-fraumeni education and early detection program clinic

Aydah Al-Awadhi, Nour Abuhadra, Diane D Liu, Angelica M Gutierrez Barrera, Jessica Corredor, Louise C Strong, Banu K Arun

Cancer Res (2021) 81 (4_Supplement): PS8-04.

DOI: https://doi.org/10.1158/1538-7445.SABCS20-PS8-04

Published: 15 February 2021

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Journal Articles

Penetrance of Different Cancer Types in Families with Li-Fraumeni Syndrome: A Validation Study Using Multicenter Cohorts

Seung Jun Shin, Elissa B. Dodd-Eaton, Gang Peng, Jasmina Bojadzieva, Jingxiao Chen, Christopher I. Amos, Megan N. Frone, Payal P. Khincha, Phuong L. Mai, Sharon A. Savage, Mandy L. Ballinger, David M. Thomas, Ying Yuan, Louise C. Strong, Wenyi Wang

Cancer Res (2020) 80 (2): 354–360.

DOI: https://doi.org/10.1158/0008-5472.CAN-19-0728

Published: 15 January 2020

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Journal Articles

Penetrance Estimates Over Time to First and Second Primary Cancer Diagnosis in Families with Li-Fraumeni Syndrome: A Single Institution Perspective

Seung Jun Shin, Elissa B. Dodd-Eaton, Fan Gao, Jasmina Bojadzieva, Jingxiao Chen, Xianhua Kong, Christopher I. Amos, Jing Ning, Louise C. Strong, Wenyi Wang

Cancer Res (2020) 80 (2): 347–353.

DOI: https://doi.org/10.1158/0008-5472.CAN-19-0725

Published: 15 January 2020

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Includes: Supplementary data

Journal Articles

Abstract 2406: A general probabilistic algorithm to predict de novo mutations in familial diseases as demonstrated in Li-Fraumeni Syndrome

Xuedong Pan, Fan Gao, Elissa B. Dodd, Jasmina Bojadzieva, Phuong L. Mai, Valen E. Johnson, Kristin Zelley, Kim E. Nichols, Judy E. Garber, Sharon A. Savage, Louise C. Strong, Wenyi Wang

Cancer Res (2019) 79 (13_Supplement): 2406.

DOI: https://doi.org/10.1158/1538-7445.AM2019-2406

Published: 01 July 2019

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Journal Articles

Abstract 2434: Characterizing age-of-onset of multiple primary cancers and specific cancer types in families with Li-Fraumeni syndrome

Seung Jun Shin, Elissa Dodd, Gang Peng, Jasmina Bojadzieva, Jingxiao Chen, Jing Ning, Phuong L. Mai, Sharon A. Savage, Mandy L. Ballinger, David M. Thomas, Ying Yuan, Louise C. Strong, Wenyi Wang

Cancer Res (2019) 79 (13_Supplement): 2434.

DOI: https://doi.org/10.1158/1538-7445.AM2019-2434

Published: 01 July 2019

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Journal Articles

Abstract 3587: Intratumoral divergence of copy number alterations in NSCLC

Yasminka A. Jakubek, Smruthy Sivakumar, Louise C. Strong, Humam Kadara, Paul Scheet

Cancer Res (2017) 77 (13_Supplement): 3587.

DOI: https://doi.org/10.1158/1538-7445.AM2017-3587

Published: 01 July 2017

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Journal Articles

Recommended Guidelines for Validation, Quality Control, and Reporting of TP53 Variants in Clinical Practice

Cancer Res (2017) 77 (6): 1250–1260.

DOI: https://doi.org/10.1158/0008-5472.CAN-16-2179

Published: 14 March 2017

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Includes: Supplementary data

Journal Articles

Abstract 2691: Genome-wide association study identifies two susceptibility loci that modify radiation-related risk for breast cancer after childhood cancer: A report from the Childhood Cancer Survivor Study and St. Jude Lifetime Cohort

Lindsay M. Morton, Joshua N. Sampson, Gregory T. Armstrong, Ting-Huei Chen, Melissa Hudson, Eric Karlins, Casey L. Dagnall, Shenchao Li, Carmen L. Wilson, Kumar Srivastava, Wei Liu, Guolian Kang, Kevin Oeffinger, Tara O. Henderson, Chaya S. Moskowitz, Todd M. Gibson, Diana M. Merino, Jeannette R. Wong, Sue Hammond, Joseph P. Neglia, Lucie M. Turcotte, Jeremy Miller, Laura Bowen, William A. Wheeler, Wendy M. Leisenring, John A. Whitton, Laurie Burdette, Belynda D. Hicks, Mitchell J. Machiela, Aurelie Vogt, Zhaoming Wang, Meredith Yeager, Geoffrey Neale, Matthew Lear, Louise C. Strong, Yutaka Yasui, Marilyn Stovall, Rita E. Weathers, Susan A. Smith, Rebecca Howell, Stella M. Davies, Gretchen A. Radloff, Amy Berrington de González, Peter D. Inskip, Preetha Rajaraman, Joseph F. Fraumeni, Smita Bhatia, Stephen J. Chanock, Margaret A. Tucker, Leslie L. Robison

Cancer Res (2016) 76 (14_Supplement): 2691.

DOI: https://doi.org/10.1158/1538-7445.AM2016-2691

Published: 15 July 2016

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Journal Articles

Abstract 5092: Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma

Kenan Onel, Timothy Best, Andrew D. Skol, Dalin Li, Tomas Kirchhoff, Yutaka Yasui, Smita Bhatia, Louise C. Strong, Susan M. Domchek, Katherine L. Nathanson, Olufunmilayo Olopade, Thomas M. Mack, David V. Conti, Kenneth Offit, Wendy Cozen, Leslie L. Robison

Cancer Res (2011) 71 (8_Supplement): 5092.

DOI: https://doi.org/10.1158/1538-7445.AM2011-5092

Published: 15 April 2011

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Journal Articles

Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis

Deborah W. Neklason, Richard A. Kerber, David B. Nilson, Hoda Anton-Culver, Ann G. Schwartz, Constance A. Griffin, Jan T. Lowery, Joellen M. Schildkraut, James P. Evans, Gail E. Tomlinson, Louise C. Strong, Alexander R. Miller, Jill E. Stopfer, Dianne M. Finkelstein, Prakash M. Nadkarni, Carol H. Kasten, Geraldine P. Mineau, Randall W. Burt

Cancer Res (2008) 68 (21): 8993–8997.

DOI: https://doi.org/10.1158/0008-5472.CAN-08-1376

Published: 30 October 2008

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Includes: Supplementary data

Journal Articles

Joint Effects of Germ-Line p53 Mutation and Sex on Cancer Risk in Li-Fraumeni Syndrome

Chih-Chieh Wu, Sanjay Shete, Christopher I. Amos, Louise C. Strong

Cancer Res (2006) 66 (16): 8287–8292.

DOI: https://doi.org/10.1158/0008-5472.CAN-05-4247

Published: 15 August 2006

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Journal Articles

Genetic Mapping of a Third Li-Fraumeni Syndrome Predisposition Locus to Human Chromosome 1q23

Linda L. Bachinski, Shodimu-Emmanuel Olufemi, Xiaojun Zhou, Chih-Chieh Wu, Linwah Yip, Sanjay Shete, Guillermina Lozano, Christopher I. Amos, Louise C. Strong, Ralf Krahe

Cancer Res (2005) 65 (2): 427–431.

DOI: https://doi.org/10.1158/0008-5472.427.65.2

Published: 03 February 2005

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Journal Articles

High Frequency Loss of Heterozygosity in von Hippel-Lindau (VHL)-associated and Sporadic Pancreatic Islet Cell Tumors: Evidence for a Stepwise Mechanism for Malignant Conversion in VHL Tumorigenesis

Steven T. Lott, Dawn S. Chandler, Steven A. Curley, Carolyn J. Foster, Adel El-Naggar, Marsha Frazier, Louise C. Strong, Mercedes Lovell, Ann McNeill Killary

Cancer Res (2002) 62 (7): 1952–1955.

Published: 01 April 2002

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Journal Articles

Renal Failure in the Denys-Drash and Wilms’ Tumor-Aniridia Syndromes

Norman E. Breslow, Janice R. Takashima, Michael L. Ritchey, Louise C. Strong, Daniel M. Green

Cancer Res (2000) 60 (15): 4030–4032.

Published: 01 August 2000

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Journal Articles

Linkage of Familial Wilms' Tumor Predisposition to Chromosome 19 and a Two-Locus Model for the Etiology of Familial Tumors

J. Matthew McDonald, Edwin C. Douglass, Ross Fisher, Clementina F. Geiser, Carl E. Krill, Louise C. Strong, David Virshup, Vicki Huff

Cancer Res (1998) 58 (7): 1387–1390.

Published: 01 April 1998

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Journal Articles

Localization of a Novel Tumor Suppressor Locus on Human Chromosome 3q Important in Osteosarcoma Tumorigenesis

Russell P. Kruzelock, Edwin C. Murphy, Louise C. Strong, Susan L. Naylor, Marc F. Hansen

Cancer Res (1997) 57 (1): 106–109.

Published: 01 January 1997

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Journal Articles

Nonlinkage of 16q Markers to Familial Predisposition to Wilms' Tumor

Vicki Huff, Anthony E. Reeve, Mark Leppert, Louise C. Strong, Edwin C. Douglass, Clementina F. Geiser, Frederick P. Li, Anna Meadows, David F. Callen, Gilbert Lenoir, Grady F. Saunders

Cancer Res (1992) 52 (21): 6117–6120.

Published: 01 November 1992

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Journal Articles

A Germ Line Mutation in Exon 5 of the p53 Gene in an Extended Cancer Family

John C. Law, Louise C. Strong, Abirami Chidambaram, Robert E. Ferrell

Cancer Res (1991) 51 (23_Part_1): 6385–6387.

Published: 12 January 1991

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Journal Articles

Spontaneous Abnormalities in Normal Fibroblasts from Patients with Li-Fraumeni Cancer Syndrome: Aneuploidy and Immortalization

Farideh Z. Bischoff, Sun O. Yim, Sen Pathak, Grace Grant, Michael J. Siciliano, B. C. Giovanella, Louise C. Strong, Michael A. Tainsky

Cancer Res (1990) 50 (24): 7979–7984.

Published: 01 December 1990

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Journal Articles

Radiation Sensitivity of Cell Strains from Families with Genetic Disorders Predisposing to Radiation-induced Cancer

John B. Little, Warren W. Nichols, Philip Troilo, Hatsumi Nagasawa, Louise C. Strong

Cancer Res (1989) 49 (17): 4705–4714.

Published: 01 September 1989

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NARROW

Abstract PS8-04: Clinical and pathological characteristics and screening outcome for secondary cancers in breast cancer patients with li-fraumeni syndrome attending the MD anderson li-fraumeni education and early detection program clinic

Penetrance of Different Cancer Types in Families with Li-Fraumeni Syndrome: A Validation Study Using Multicenter Cohorts

Penetrance Estimates Over Time to First and Second Primary Cancer Diagnosis in Families with Li-Fraumeni Syndrome: A Single Institution Perspective

Abstract 2406: A general probabilistic algorithm to predict de novo mutations in familial diseases as demonstrated in Li-Fraumeni Syndrome

Abstract 2434: Characterizing age-of-onset of multiple primary cancers and specific cancer types in families with Li-Fraumeni syndrome

Abstract 3587: Intratumoral divergence of copy number alterations in NSCLC

Recommended Guidelines for Validation, Quality Control, and Reporting of TP53 Variants in Clinical Practice

Abstract 2691: Genome-wide association study identifies two susceptibility loci that modify radiation-related risk for breast cancer after childhood cancer: A report from the Childhood Cancer Survivor Study and St. Jude Lifetime Cohort

Abstract 5092: Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma

Common Familial Colorectal Cancer Linked to Chromosome 7q31: A Genome-Wide Analysis

Joint Effects of Germ-Line p53 Mutation and Sex on Cancer Risk in Li-Fraumeni Syndrome

Genetic Mapping of a Third Li-Fraumeni Syndrome Predisposition Locus to Human Chromosome 1q23

High Frequency Loss of Heterozygosity in von Hippel-Lindau (VHL)-associated and Sporadic Pancreatic Islet Cell Tumors: Evidence for a Stepwise Mechanism for Malignant Conversion in VHL Tumorigenesis

Renal Failure in the Denys-Drash and Wilms’ Tumor-Aniridia Syndromes

Linkage of Familial Wilms' Tumor Predisposition to Chromosome 19 and a Two-Locus Model for the Etiology of Familial Tumors

Localization of a Novel Tumor Suppressor Locus on Human Chromosome 3q Important in Osteosarcoma Tumorigenesis

Nonlinkage of 16q Markers to Familial Predisposition to Wilms' Tumor

A Germ Line Mutation in Exon 5 of the p53 Gene in an Extended Cancer Family

Spontaneous Abnormalities in Normal Fibroblasts from Patients with Li-Fraumeni Cancer Syndrome: Aneuploidy and Immortalization

Radiation Sensitivity of Cell Strains from Families with Genetic Disorders Predisposing to Radiation-induced Cancer

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