The role of rare variants in male-pattern hair loss: Analysis of whole-exome sequencing data in the UK Biobank

被引：0
|
作者：
Henne, Sabrina [1 ,2 ]
Sivalingam, Sugirthan [3 ,4 ,5 ]
Hochfeld, Lara [1 ,2 ]
Maj, Carlo [3 ]
Borisov, Oleg [3 ]
Buness, Andreas [3 ,4 ,5 ]
Noethen, Markus M. [1 ,2 ]
Krawitz, Peter [3 ]
Heilmann-Heimbach, Stefanie [1 ,2 ]
机构：
[1] Univ Bonn, Inst Human Genet, Sch Med, Bonn, Germany
[2] Univ Hosp Bonn, Bonn, Germany
[3] Univ Bonn, Inst Genom Stat & Bioinformat, Bonn, Germany
[4] Univ Bonn, Dept Med Biometry Informat & Epidemiol, Bonn, Germany
[5] Univ Bonn, Core Unit Bioinformat Data Anal, Bonn, Germany
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
EP05.049
引用
收藏
页码：136 / 136
页数：1
相关论文
共 50 条
  • [1] The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
    Henne, S. K.
    Aldisi, R.
    Sivalingam, S.
    Hochfeld, L. M.
    Maj, C.
    Borisov, O.
    Nothen, M. M.
    Krawitz, P. M.
    Heilmann-Heimbach, S.
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2022, 142 (12) : S232 - S232
  • [2] Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
    Sabrina Katrin Henne
    Rana Aldisi
    Sugirthan Sivalingam
    Lara Maleen Hochfeld
    Oleg Borisov
    Peter Michael Krawitz
    Carlo Maj
    Markus Maria Nöthen
    Stefanie Heilmann-Heimbach
    [J]. Nature Communications, 14 (1)
  • [3] Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
    Henne, Sabrina Katrin
    Aldisi, Rana
    Sivalingam, Sugirthan
    Hochfeld, Lara Maleen
    Borisov, Oleg
    Krawitz, Peter Michael
    Maj, Carlo
    Noethen, Markus Maria
    Heilmann-Heimbach, Stefanie
    [J]. NATURE COMMUNICATIONS, 2023, 14 (01)
  • [4] Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank
    Hofmeister, Robin J.
    Ribeiro, Diogo M.
    Rubinacci, Simone
    Delaneau, Olivier
    [J]. NATURE GENETICS, 2023, 55 (07) : 1243 - +
  • [5] Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank
    Robin J. Hofmeister
    Diogo M. Ribeiro
    Simone Rubinacci
    Olivier Delaneau
    [J]. Nature Genetics, 2023, 55 : 1243 - 1249
  • [6] Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression
    Tian, Ruoyu
    Ge, Tian
    Kweon, Hyeokmoon
    Rocha, Daniel B.
    Lam, Max
    Liu, Jimmy Z.
    Singh, Kritika
    Levey, Daniel F.
    Gelernter, Joel
    Stein, Murray B.
    Tsai, Ellen A.
    Huang, Hailiang
    Chabris, Christopher F.
    Lencz, Todd
    Runz, Heiko
    Chen, Chia-Yen
    [J]. NATURE COMMUNICATIONS, 2024, 15 (01)
  • [7] Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression
    Ruoyu Tian
    Tian Ge
    Hyeokmoon Kweon
    Daniel B. Rocha
    Max Lam
    Jimmy Z. Liu
    Kritika Singh
    Daniel F. Levey
    Joel Gelernter
    Murray B. Stein
    Ellen A. Tsai
    Hailiang Huang
    Christopher F. Chabris
    Todd Lencz
    Heiko Runz
    Chia-Yen Chen
    [J]. Nature Communications, 15
  • [8] ASSOCIATION OF RARE MONOGENIC VARIANTS WITH DIAGNOSIS OF BPH USING WHOLE EXOME SEQUENCING IN THE UK BIOBANK
    Judge, Clark
    Nusbaum, David
    Wei, Jun
    Shi, Zhuqing
    Rifkin, Andrew
    Zheng, S. Lilly
    Helfand, Brian
    Glaser, Alexander
    Xu, Jianfeng
    [J]. JOURNAL OF UROLOGY, 2023, 209 : E322 - E322
  • [9] Rare variant associations and novel loci for eosinophil count - a UK Biobank whole-exome sequencing study
    Hoglund, Julia
    Hadizadeh, Fatemeh
    Ek, Weronica
    Karlsson, Torgny
    Johansson, Asa
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 695 - 696
  • [10] Whole-exome Sequencing Identifies Rare Variants and Genes Associated with Glaucoma
    Chiariglione, Marion
    Arch, Alexander J.
    Gao, XIaoyi R.
    [J]. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2023, 64 (08)
12345