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James R. Broach
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Journal Articles

Abstract 2953: Subtype-specific and structure variation induced 3D genome alteration in acute myeloid leukemia

Jie Xu, Fan Song, Baozhen Zhang, Huijue Lyu, Mikoto Kobayashi, Ziyu Zhao, Ye Hou, Xiaotao Wang, Yu Luan, Bei Jia, Lena Stasiak, Qixuan Wang, Qi Jin, Qiushi Jin, Yihao Fu, Ross C. Hardison, Sinisa Dovat, Leonidas C. Platanias, Yue Yang, Tomoko Yamada, Aaron D. Viny, Ross L. Levine, David F. Claxton, James R. Broach, Hong Zheng, Feng Yue
Journal: Cancer Research
Cancer Res (2022) 82 (12_Supplement): 2953.
https://doi.org/10.1158/1538-7445.AM2022-2953
Published: 15 June 2022
View articletitled, Abstract 2953: Subtype-specific and structure variation induced 3D genome alteration in acute myeloid leukemia
Journal Articles

Genetic Variants Implicate Dual Oxidase-2 in Familial and Sporadic Nonmedullary Thyroid Cancer

Darrin V. Bann, Qunyan Jin, Kathryn E. Sheldon, Kenneth R. Houser, Lan Nguyen, Joshua I. Warrick, Maria J. Baker, James R. Broach, Glenn S. Gerhard, David Goldenberg
Journal: Cancer Research
Cancer Res (2019) 79 (21): 5490–5499.
https://doi.org/10.1158/0008-5472.CAN-19-0721
Published: 01 November 2019
View articletitled, Genetic Variants Implicate Dual Oxidase-2 in Familial and Sporadic Nonmedullary Thyroid Cancer
Open the PDF for Genetic Variants Implicate Dual Oxidase-2 in Familial and Sporadic Nonmedullary Thyroid Cancer in another window
Includes: Supplementary data
Journal Articles

Abstract 1708: An integrated framework for genome analysis reveals numerous previously unrecognizable structural variants in leukemia patients’ samples

James R. Broach, Jie Xu, Emily Schleicher, Christopher Pool, Max Hennessy, Kathryn Sheldon, Charyguly Annageldiyev, Arati Sharma, Yuanyuan Chang, Alex Hastie, Barbara Miller, David Goldenberg, David Claxton, George-Lucian Moldovan, Feng Yue
Journal: Cancer Research
Cancer Res (2019) 79 (13_Supplement): 1708.
https://doi.org/10.1158/1538-7445.AM2019-1708
Published: 01 July 2019
View articletitled, Abstract 1708: An integrated framework for genome analysis reveals numerous previously unrecognizable structural variants in leukemia patients’ samples