Contribution of rare and common coding variants to haematological malignancies in the UK biobank

被引:0
|
作者
Zoller, Bengt [1 ,3 ]
Manderstedt, Eric [1 ]
Lind-Hallden, Christina [2 ]
Hallden, Christer [2 ]
机构
[1] Lund Univ & Reg Skane, Ctr Primary Hlth Care Res, Dept Clin Sci, Malmo, Sweden
[2] Kristianstad Univ, Dept Environm Sci & Biosci, Kristianstad, Sweden
[3] Skane Univ Hosp, Ctr Primary Hlth Care Res, CRC, Bldg 28,Floor 11,Jan Waldenstroms Gata 35, S-20502 Malmo, Sweden
来源
LEUKEMIA RESEARCH REPORTS | 2023年 / 19卷
基金
瑞典研究理事会;
关键词
Genetics; Hematologic neoplasms; Mutation; Whole exome sequencing;
D O I
10.1016/j.lrr.2023.100362
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页数:3
相关论文
共 50 条
  • [1] ASSOCIATION OF RARE CODING VARIANTS WITH GENERALISED COGNITION IN UK BIOBANK
    Fenner, Eilidh
    Walters, James
    Rees, Elliott
    [J]. EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2022, 63 : E94 - E95
  • [2] Contribution of rare genetic variants to heart failure and cardiomyopathy in the UK Biobank
    Zoller, Bengt
    Manderstedt, Eric
    Lind-Hallden, Christina
    Hallden, Christer
    [J]. ESC HEART FAILURE, 2023, 10 (05): : 3234 - 3235
  • [3] Interactive Effects of Common and Rare Genetic Variants on Psychopathology in the UK Biobank
    Mollon, Josephine
    Schultz, Laura
    Knowles, Emma
    Huguet, Guillaume
    Saci, Zohra
    Louis, Martineau Jean
    Douard, Elise
    Mathias, Samuel
    Rodrigue, Amanda
    Jacquemont, Sebastien
    Almasy, Laura
    Glahn, David
    [J]. BIOLOGICAL PSYCHIATRY, 2022, 91 (09) : S80 - S80
  • [4] The contribution of rare and common genetic variants to risk of prostate cancer and second primary cancer after prostate in the UK Biobank
    Beebe-Dimmer, Jennifer Lynn
    Snyder, Nathan
    Schwartz, Ann G.
    Wei, Jun
    Shi, Zhuqing
    Tran, Huy
    Zheng, Lily
    Shevach, Jeffrey
    Cooney, Kathleen A.
    Xu, Jianfeng
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2024, 42 (16)
  • [5] The impact of rare coding variants in schizophrenia associated genes on cognition within the UK Biobank
    Fenner, Eilidh
    Walters, James
    Rees, Elliott
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 487 - 488
  • [6] Damaging rare coding variants in constrained genes are associated with reduced generalised intelligence in the UK Biobank
    Fenner, Eilidh
    Walters, James
    Rees, Elliott
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 59 - 60
  • [7] Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants
    Curtis, David
    [J]. HUMAN HEREDITY, 2024, 89 (01) : 1 - 7
  • [8] Contribution of Rare Coding Variants to Complex Trait Heritability
    Pathan, Nazia
    Khan, Mohammad
    Deng, Wei Q.
    Chong, Michael
    Di Scipio, Matteo
    Mao, Shihong
    Morton, Rob
    Pigeyre, Marie
    Lali, Ricky
    Pare, Guillaume
    [J]. GENETIC EPIDEMIOLOGY, 2022, 46 (07) : 523 - 523
  • [9] Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia
    Curtis, David
    [J]. JOURNAL OF MEDICAL GENETICS, 2022, 59 (06) : 597 - 604
  • [10] The relative contribution of common and rare genetic variants to ADHD
    J Martin
    M C O'Donovan
    A Thapar
    K Langley
    N Williams
    [J]. Translational Psychiatry, 2015, 5 : e506 - e506