Integrating common and rare genetic variants to predict cancer risks in diverse populations

被引：0
|
作者：
Elmas, Abdulkadir
Kittrell, Hannah
Huang, Kuan-lin
机构：
来源：
CANCER RESEARCH | 2023年 / 83卷 / 07期
关键词：
D O I：
10.1158/1538-7445.AM2023-1980
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
1980
引用
收藏
页数：2
相关论文
共 50 条
  • [1] Integrating common and rare genetic variation in diverse human populations
    Altshuler, David M.
    Gibbs, Richard A.
    Peltonen, Leena
    Dermitzakis, Emmanouil
    Schaffner, Stephen F.
    Yu, Fuli
    Bonnen, Penelope E.
    de Bakker, Paul I. W.
    Deloukas, Panos
    Gabriel, Stacey B.
    Gwilliam, Rhian
    Hunt, Sarah
    Inouye, Michael
    Jia, Xiaoming
    Palotie, Aarno
    Parkin, Melissa
    Whittaker, Pamela
    Chang, Kyle
    Hawes, Alicia
    Lewis, Lora R.
    Ren, Yanru
    Wheeler, David
    Muzny, Donna Marie
    Barnes, Chris
    Darvishi, Katayoon
    Hurles, Matthew
    Korn, Joshua M.
    Kristiansson, Kati
    Lee, Charles
    McCarroll, Steven A.
    Nemesh, James
    Keinan, Alon
    Montgomery, Stephen B.
    Pollack, Samuela
    Price, Alkes L.
    Soranzo, Nicole
    Gonzaga-Jauregui, Claudia
    Anttila, Verneri
    Brodeur, Wendy
    Daly, Mark J.
    Leslie, Stephen
    McVean, Gil
    Moutsianas, Loukas
    Nguyen, Huy
    Zhang, Qingrun
    Ghori, Mohammed J. R.
    McGinnis, Ralph
    McLaren, William
    Takeuchi, Fumihiko
    Grossman, Sharon R.
    NATURE, 2010, 467 (7311) : 52 - 58
  • [2] Integrating common and rare genetic variation in diverse human populations
    Nature, 2010, 467 : 52 - 58
  • [3] Integrating both common and rare variants to predict bone mineral density and fracture
    Gai, Sirui
    Qian, Yu
    Zhang, Zhenlin
    Zheng, Hou-Feng
    JOURNAL OF BONE AND MINERAL RESEARCH, 2024, 39 (03) : 193 - 194
  • [4] Revisiting the Relative Contribution of Common and Rare Genetic Variants to Attention-Deficit/ Hyperactivity Disorder Among Diverse Populations
    Dai, Yulin
    Fernandes, Brisa S.
    Zhao, Zhongming
    BIOLOGICAL PSYCHIATRY, 2024, 95 (09) : 822 - 824
  • [5] Rare Germline Genetic Variants and the Risks of Epithelial Ovarian Cancer
    Pavanello, Marina
    Chan, Isaac H. Y.
    Ariff, Amir
    Pharoah, Paul D. P.
    Gayther, Simon A.
    Ramus, Susan J.
    CANCERS, 2020, 12 (10) : 1 - 23
  • [6] Both common and rare genetic variants of ABCG2 are risks for gout
    Higashino, T.
    Takada, T.
    Nakaoka, H.
    Toyoda, Y.
    Stiburkova, B.
    Miyata, H.
    Ikebuchi, Y.
    Nakashima, H.
    Shimizu, S.
    Kawaguchi, M.
    Sakiyama, M.
    Nakayama, A.
    Akashi, A.
    Tanahashi, Y.
    Kawamura, Y.
    Nakamura, T.
    Wakai, K.
    Okada, R.
    Yamamoto, K.
    Hosomichi, K.
    Hosoya, T.
    Ichida, K.
    Ooyama, H.
    Suzuki, H.
    Inoue, I.
    Merriman, T. R.
    Shinomiya, N.
    Matsuo, H.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 645 - 646
  • [7] Integrating genetic and genomic information into effective cancer care in diverse populations
    Fashoyin-Aje, L.
    Sanghavi, K.
    Bjornard, K.
    Bodurtha, J.
    ANNALS OF ONCOLOGY, 2013, 24 : 48 - 54
  • [8] Discovery of common and rare genetic risk variants for colorectal cancer
    Jeroen R. Huyghe
    Stephanie A. Bien
    Tabitha A. Harrison
    Hyun Min Kang
    Sai Chen
    Stephanie L. Schmit
    David V. Conti
    Conghui Qu
    Jihyoun Jeon
    Christopher K. Edlund
    Peyton Greenside
    Michael Wainberg
    Fredrick R. Schumacher
    Joshua D. Smith
    David M. Levine
    Sarah C. Nelson
    Nasa A. Sinnott-Armstrong
    Demetrius Albanes
    M. Henar Alonso
    Kristin Anderson
    Coral Arnau-Collell
    Volker Arndt
    Christina Bamia
    Barbara L. Banbury
    John A. Baron
    Sonja I. Berndt
    Stéphane Bézieau
    D. Timothy Bishop
    Juergen Boehm
    Heiner Boeing
    Hermann Brenner
    Stefanie Brezina
    Stephan Buch
    Daniel D. Buchanan
    Andrea Burnett-Hartman
    Katja Butterbach
    Bette J. Caan
    Peter T. Campbell
    Christopher S. Carlson
    Sergi Castellví-Bel
    Andrew T. Chan
    Jenny Chang-Claude
    Stephen J. Chanock
    Maria-Dolores Chirlaque
    Sang Hee Cho
    Charles M. Connolly
    Amanda J. Cross
    Katarina Cuk
    Keith R. Curtis
    Albert de la Chapelle
    Nature Genetics, 2019, 51 : 76 - 87
  • [9] Discovery of common and rare genetic risk variants for colorectal cancer
    Huyghe, Jeroen R.
    Bien, Stephanie A.
    Harrison, Tabitha A.
    Kang, Hyun Min
    Chen, Sai
    Schmit, Stephanie L.
    Conti, David V.
    Qu, Conghui
    Jeon, Jihyoun
    Edlund, Christopher K.
    Greenside, Peyton
    Wainberg, Michael
    Schumacher, Fredrick R.
    Smith, Joshua D.
    Levine, David M.
    Nelson, Sarah C.
    Sinnott-Armstrong, Nasa A.
    Albanes, Demetrius
    Alonso, M. Henar
    Anderson, Kristin
    Arnau-Collell, Coral
    Arndt, Volker
    Bamia, Christina
    Banbury, Barbara L.
    Baron, John A.
    Berndt, Sonja I.
    Bezieau, Stephane
    Bishop, D. Timothy
    Boehm, Juergen
    Boeing, Heiner
    Brenner, Hermann
    Brezina, Stefanie
    Buch, Stephan
    Buchanan, Daniel D.
    Burnett-Hartman, Andrea
    Butterbach, Katja
    Caan, Bette J.
    Campbell, Peter T.
    Carlson, Christopher S.
    Castellvi-Bel, Sergi
    Chan, Andrew T.
    Chang-Claude, Jenny
    Chanock, Stephen J.
    Chirlaque, Maria-Dolores
    Cho, Sang Hee
    Connolly, Charles M.
    Cross, Amanda J.
    Cuk, Katarina
    Curtis, Keith R.
    de la Chapelle, Albert
    NATURE GENETICS, 2019, 51 (01) : 76 - +
  • [10] Multiple rare variants in immune genes predict common respiratory infections burden in isolated populations
    Gelemanovic, A.
    Relja, A.
    Hayward, C.
    Koli, I.
    Polasek, O.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 322 - 322
12345