Whole genome sequencing to define the germline-somatic interaction in young-onset lung cancer

被引：0

作者：

LoPiccolo, J. ^{[1
]}

Collins, R. ^{[2
]}

Koeller, D. R. ^{[3
]}

Pollaci, A. C. ^{[3
]}

Voligny, E. ^{[1
]}

Nguyen, T. ^{[1
]}

Pangilinan, A. J. ^{[1
]}

Wang, X. ^{[4
]}

Su, L. ^{[4
]}

Lin, J. ^{[5
]}

Garber, J. E. ^{[3
]}

Christiani, D. C. ^{[4
]}

Gusev, S. ^{[2
]}

Janne, P. A. ^{[1
]}

机构：

[1] Dana Farber Canc Inst, Lowe Ctr Thorac Oncol, Boston, MA USA

[2] Dana Farber Canc Inst, Div Populat Sci, Boston, MA USA

[3] Dana Farber Canc Inst, Ctr Canc Genet & Prevent, Boston, MA USA

[4] Harvard TH Chan Sch Publ Hlth, Environm Hlth, Boston, MA USA

[5] MGH, Thorac Oncol Dept, Boston, MA USA

来源：

ANNALS OF ONCOLOGY | 2023年 / 34卷

关键词：

D O I：

10.1016/j.annonc.2023.09.1321

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

2294P

引用

页码：S1174 / S1174

页数：1

共 50 条

[31] Somatic mutations in young-onset colorectal cancer unrelated to hereditary syndromes: A comparative study using high-depth targeted exome sequencing.
You, Y. Nancy
Chang, Kyle
Chen, Ken
Mehdizadeh, Amir
Cuddy, Amanda
Lieu, Christopher Hanyoung
Shaw, Kenna Rael
Sanchez, Eduardo Vilar
Eng, Cathy
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (03)
[32] A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing
Alioto, Tyler S.
Buchhalter, Ivo
Derdak, Sophia
Hutter, Barbara
Eldridge, Matthew D.
Hovig, Eivind
Heisler, Lawrence E.
Beck, Timothy A.
Simpson, Jared T.
Tonon, Laurie
Sertier, Anne-Sophie
Patch, Ann-Marie
Jaeger, Natalie
Ginsbach, Philip
Drews, Ruben
Paramasivam, Nagarajan
Kabbe, Rolf
Chotewutmontri, Sasithorn
Diessl, Nicolle
Previti, Christopher
Schmidt, Sabine
Brors, Benedikt
Feuerbach, Lars
Heinold, Michael
Groebner, Susanne
Korshunov, Andrey
Tarpey, Patrick S.
Butler, Adam P.
Hinton, Jonathan
Jones, David
Menzies, Andrew
Raine, Keiran
Shepherd, Rebecca
Stebbings, Lucy
Teague, Jon W.
Ribeca, Paolo
Giner, Francesc Castro
Beltran, Sergi
Raineri, Emanuele
Dabad, Marc
Heath, Simon C.
Gut, Marta
Denroche, Robert E.
Harding, Nicholas J.
Yamaguchi, Takafumi N.
Fujimoto, Akihiro
Nakagawa, Hidewaki
Quesada, Ctor
Valdes-Mas, Rafael
Nakken, Sigve
NATURE COMMUNICATIONS, 2015, 6
[33] A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing
Tyler S. Alioto
Ivo Buchhalter
Sophia Derdak
Barbara Hutter
Matthew D. Eldridge
Eivind Hovig
Lawrence E. Heisler
Timothy A. Beck
Jared T. Simpson
Laurie Tonon
Anne-Sophie Sertier
Ann-Marie Patch
Natalie Jäger
Philip Ginsbach
Ruben Drews
Nagarajan Paramasivam
Rolf Kabbe
Sasithorn Chotewutmontri
Nicolle Diessl
Christopher Previti
Sabine Schmidt
Benedikt Brors
Lars Feuerbach
Michael Heinold
Susanne Gröbner
Andrey Korshunov
Patrick S. Tarpey
Adam P. Butler
Jonathan Hinton
David Jones
Andrew Menzies
Keiran Raine
Rebecca Shepherd
Lucy Stebbings
Jon W. Teague
Paolo Ribeca
Francesc Castro Giner
Sergi Beltran
Emanuele Raineri
Marc Dabad
Simon C. Heath
Marta Gut
Robert E. Denroche
Nicholas J. Harding
Takafumi N. Yamaguchi
Akihiro Fujimoto
Hidewaki Nakagawa
Víctor Quesada
Rafael Valdés-Mas
Sigve Nakken
Nature Communications, 6
[34] Young-onset kidney tumors: Clinico-pathological features and subset examination of their genome-wide somatic mutations
Malouf, Gabriel G.
Su, Xiaoping
Mouawad, Roger
Comperat, Eva
Roupret, Morgan
Cussenot, Olivier
Spano, Jean-Philippe
Khayat, David
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15)
[35] Whole-genome sequencing of East Asian lung cancers reveals new germline pathogenic variants
Mukherjee, Semanti
Carrot-Zhang, Jian
CANCER CELL, 2022, 40 (10) : 1081 - 1083
[36] Whole genome and transcriptome sequencing of lung cancer: Options for personalized cancer treatment.
Chooback, Negar
Ho, Cheryl
Shen, Yaoqing
Tsang, Erica S.
Zhao, Yongjun
Mungall, Andrew J.
Moore, Richard
Lim, Howard John
Renouf, Daniel John
Gelmon, Karen A.
Yip, Stephen
Jones, Steven
Laskin, Janessa J.
Marra, Marco
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
[37] Young cancer patient perspectives on undertaking whole genome sequencing: A qualitative study
Best, Megan
Bartley, Nicole
Jacobs, Chris
Juraskova, Ilona
Newson, Ainsley
Savard, Jacqueline
Meiser, Bettina
Ballinger, Mandy
Thomas, David
Biesecker, Barbara
Butow, Phyllis
ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2018, 14 : 144 - 144
[38] Whole genome sequencing of Malaysian colorectal cancer patients reveals specific druggable somatic mutations
Mohd Yunos, Ryia Illani
Ab Mutalib, Nurul-Syakima
Khoo, Jia-shiun
Saidin, Sazuita
Ishak, Muhiddin
Syafruddin, Saiful Effendi
Tieng, Francis Yew Fu
Md Yusof, Najwa Farhah
Abd Razak, Mohd Ridhwan
Mahamad Nadzir, Norshahidah
Abu, Nadiah
Rose, Isa Md
Sagap, Ismail
Mazlan, Luqman
Jamal, Rahman
FRONTIERS IN MOLECULAR BIOSCIENCES, 2023, 9
[39] Assigning clinical meaning to somatic and germline whole exome sequencing data to guide cancer precision medicine.
Ghazani, Arezou A.
Oliver, Nelly
St Pierre, Joseph P.
Garofalo, Andrea
Sholl, Lynette M.
Lindeman, Neal Ian
Garber, Judy Ellen
Joffe, Steven
Janne, Pasi A.
Gray, Stacy W.
Garraway, Levi A.
Van Allen, Eliezer Mendel
Wagle, Nikhil
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (15)
[40] The most frequent germline pathogenic variants in Russian patients with breast cancer: whole genome sequencing results
Makarova, Maria
Nemtsova, Marina
Byakhova, Maria
Danishevich, Anastasia
Chernevskiy, Denis
Sagaidak, Olesya
Vorontsova, Maria
Belenikin, Maxim
Krinitsina, Anastasia
Antonenko, Aleksey
Semenova, Anna
Bodunova, Natalia
Khatkov, Igor
Galkin, Vsevolod
EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 919 - 919

← 1 2 3 4 5 →