Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

被引：0
|
作者：
Yu An
Wenyuan Duan
Guoying Huang
Xiaoli Chen
Li Li
Chenxia Nie
Jia Hou
Yonghao Gui
Yiming Wu
Feng Zhang
Yiping Shen
Bailin Wu
Hongyan Wang
机构：
[1] Institutes of Biomedical Sciences and Children’s Hospital,The State Key Laboratory of Genetic Engineering, Ministry of Education (MOE) Key Laboratory of Contemporary Anthropology, and Collaborative Innovation Center of Genetics and Development, School of L
[2] Fudan University,Children’s Hospital
[3] Fudan University,Department of Biology
[4] Jinan Military General Hospital,Department of Laboratory Medicine
[5] Fudan University,undefined
[6] Capital Institute of Pediatrics,undefined
[7] Changzhi MedicalCollege,undefined
[8] Children’s Hospital Boston,undefined
[9] Harvard Medical School,undefined
[10] School of Life Sciences,undefined
[11] Obstetrics & Gynecology Hospital,undefined
[12] Institute of Reproduction & Development,undefined
[13] Fudan University,undefined
来源：
BMC Medical Genomics | / 9卷
关键词：
Ventricular septal defect; aCGH; Congenital heart defect; Copy number variants;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 50 条
  • [31] Genome-wide copy number analysis in pediatric glioblastoma multiforme
    Giunti, Laura
    Pantaleo, Marilena
    Sardi, Iacopo
    Provenzano, Aldesia
    Magi, Alberto
    Cardellicchio, Stefania
    Castiglione, Francesca
    Tattini, Lorenzo
    Novara, Francesca
    Buccoliero, Anna Maria
    de Martino, Maurizio
    Genitori, Lorenzo
    Zuffardi, Orsetta
    Giglio, Sabrina
    AMERICAN JOURNAL OF CANCER RESEARCH, 2014, 4 (03): : 293 - 303
  • [32] Genome-wide Association Analysis Based on Copy Number Variations
    Sun Yu-Lin
    Liu Fei
    Zhao Xiao-Hang
    PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, 2009, 36 (08) : 968 - 977
  • [33] Genome-wide copy number analysis in primary breast cancer
    Ueno, Takayuki
    Emi, Mitsuru
    Sato, Hidenori
    Ito, Noriko
    Muta, Mariko
    Kuroi, Katsumasa
    Toi, Masakazu
    EXPERT OPINION ON THERAPEUTIC TARGETS, 2012, 16 : S31 - S35
  • [34] A genome-wide analysis of the role of Copy Number Variants in asthma
    Rogers, A.
    Darvishi, K.
    Chu, J. -H.
    Ionita-Laza, I.
    Klanderman, B. J.
    Lee, C.
    Raby, B.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2010, 181
  • [35] Genome-wide analysis of DNA copy number variations in osteosarcoma
    Gokgoz, Nalan
    Wunder, Jay S.
    Andrulis, Irene L.
    CANCER RESEARCH, 2012, 72
  • [36] GENOME-WIDE ANALYSIS OF COPY NUMBER VARIATION IN A SOUTH AFRICAN XHOSA POPULATION AFFECTED BY SCHIZOPHRENIA
    Majara, Lerato
    Van der Merwe, Celia
    Mufford, Mary-Anne
    Chimusa, Emile
    Stein, Dan
    Ramesar, Raj
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2019, 29 : 1325 - 1326
  • [37] Systematic assessment of copy number variant detection via genome-wide SNP genotyping
    Cooper, Gregory M.
    Zerr, Troy
    Kidd, Jeffrey M.
    Eichler, Evan E.
    Nickerson, Deborah A.
    NATURE GENETICS, 2008, 40 (10) : 1199 - 1203
  • [38] Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array
    Anna-Maja Molin
    Jonas Berglund
    Matthew T Webster
    Kerstin Lindblad-Toh
    BMC Genomics, 15
  • [39] Systematic assessment of copy number variant detection via genome-wide SNP genotyping
    Gregory M Cooper
    Troy Zerr
    Jeffrey M Kidd
    Evan E Eichler
    Deborah A Nickerson
    Nature Genetics, 2008, 40 : 1199 - 1203
  • [40] Genome-wide copy number variant discovery in dogs using the CanineHD genotyping array
    Molin, Anna-Maja
    Berglund, Jonas
    Webster, Matthew T.
    Lindblad-Toh, Kerstin
    BMC GENOMICS, 2014, 15
12345