Gene-based rare variant analysis of whole-exome sequencing in relation to eosinophil counts

被引：0
|
作者：
Hoglund, J. R. [1 ]
Ek, W. E. [1 ]
Karlsson, T. [1 ]
Johansson, A. [1 ]
机构：
[1] Uppsala Univ, Uppsala, Sweden
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2020年 / 28卷 / SUPPL 1期
基金：
瑞典研究理事会;
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：
P19.034.B
引用
收藏
页码：712 / 713
页数：2
相关论文
共 50 条
  • [31] Whole-Exome Sequencing Enables the Diagnosis of Variant-Type Xeroderma Pigmentosum
    Fang, Xiaokai
    Sun, Yonghu
    FRONTIERS IN GENETICS, 2019, 10
  • [32] Improved Variant Calling Accuracy by Merging Replicates in Whole-Exome Sequencing Studies
    Zhang, Yanfeng
    Li, Bingshan
    Li, Chun
    Cai, Qiuyin
    Zheng, Wei
    Long, Jirong
    BIOMED RESEARCH INTERNATIONAL, 2014, 2014
  • [33] Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traits
    Kucukali, Fahri
    Neumann, Alexander
    Van Dongen, Jasper
    De Pooter, Tim
    Joris, Geert
    De Rijk, Peter
    Ohlei, Olena
    Dobricic, Valerija
    Bos, Isabelle
    Vos, Stephanie J. B.
    Engelborghs, Sebastiaan
    De Roeck, Ellen
    Vandenberghe, Rik
    Gabel, Silvy
    Meersmans, Karen
    Tsolaki, Magda
    Verhey, Frans
    Martinez-Lage, Pablo
    Tainta, Mikel
    Frisoni, Giovanni
    Blin, Oliver
    Richardson, Jill C.
    Bordet, Regis
    Scheltens, Philip
    Popp, Julius
    Peyratout, Gwendoline
    Johannsen, Peter
    Frolich, Lutz
    Freund-Levi, Yvonne
    Streffer, Johannes
    Lovestone, Simon
    Legido-Quigley, Cristina
    Ten Kate, Mara
    Barkhof, Frederik
    Zetterberg, Henrik
    Bertram, Lars
    Strazisar, Mojca
    Visser, Pieter Jelle
    Van Broeckhoven, Christine
    Sleegers, Kristel
    ALZHEIMERS & DEMENTIA, 2022, : 2317 - 2331
  • [34] Whole-exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis
    Razmara, Ehsan
    Azimi, Homeyra
    Bitaraf, Amirreza
    Daneshmand, Mohammad Ali
    Galehdari, Mohammad
    Dokhanchi, Maryam
    Esmaeilzadeh-Gharehdaghi, Elika
    Garshasbi, Masoud
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (03):
  • [35] Whole-Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans
    Gourh, Pravitt
    Remmers, Elaine F.
    Boyden, Steven E.
    Alexander, Theresa
    Morgan, Nadia D.
    Shah, Ami A.
    Mayes, Maureen D.
    Doumatey, Ayo
    Bentley, Amy R.
    Shriner, Daniel
    Domsic, Robyn T.
    Medsger, Thomas A.
    Steen, Virginia D.
    Ramos, Paula S.
    Silver, Richard M.
    Korman, Benjamin
    Varga, John
    Schiopu, Elena
    Khanna, Dinesh
    Hsu, Vivien
    Gordon, Jessica K.
    Saketkoo, Lesley Ann
    Gladue, Heather
    Kron, Brynn
    Criswell, Lindsey A.
    Derk, Chris T.
    Bridges, S. Louis
    Shanmugam, Victoria K.
    Kolstad, Kathleen D.
    Chung, Lorinda
    Jan, Reem
    Bernstein, Elana J.
    Goldberg, Avram
    Trojanowski, Marcin
    Kafaja, Suzanne
    Maksimowicz-McKinnon, Kathleen M.
    Mullikin, James C.
    Adeyemo, Adebowale
    Rotimi, Charles
    Boin, Francesco
    Kastner, Daniel L.
    Wigley, Fredrick M.
    ARTHRITIS & RHEUMATOLOGY, 2018, 70 (10) : 1654 - 1660
  • [36] RARE VARIANT ASSOCIATION STUDY OF OBSESSIVE-COMPULSIVE DISORDER BY WHOLE-EXOME SEQUENCING AND UNIFIED MIXED-EFFECT MODEL ANALYSIS
    Domenech, Laura
    Rabionet, Raquel
    Escaramis, Georgia
    Real, Eva
    Trujillano, Daniel
    Bosio, Mattia
    Ossowski, Stephan
    Carracedo, Angel
    Alonso, Pino
    Estivill, Xavier
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2017, 27 : S175 - S175
  • [37] Unsolved challenges in pediatric whole-exome sequencing: A literature analysis
    Bertier, Gabrielle
    Senecal, Karine
    Borry, Pascal
    Vears, Danya F.
    CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES, 2017, 54 (02) : 134 - 142
  • [38] Can whole-exome sequencing data be used for linkage analysis?
    Steven Gazal
    Simon Gosset
    Edgard Verdura
    Françoise Bergametti
    Stéphanie Guey
    Marie-Claude Babron
    Elisabeth Tournier-Lasserve
    European Journal of Human Genetics, 2016, 24 : 581 - 586
  • [39] Clinical application of whole-exome sequencing analysis in childhood epilepsy
    Gavaz, Meral
    Aslan, Elif S.
    Tekes, Selahattin
    JOURNAL OF NEUROGENETICS, 2024, 38 (04) : 187 - 194
  • [40] Can whole-exome sequencing data be used for linkage analysis?
    Gazal, Steven
    Gosset, Simon
    Verdura, Edgard
    Bergametti, Francoise
    Guey, Stephanie
    Babron, Marie-Claude
    Tournier-Lasserve, Elisabeth
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2016, 24 (04) : 581 - 586
12345