Incidental findings in clinical exome sequencing

被引：0
|
作者：
Yntema, H. G. [1 ]
van der Schoot, V. [2 ]
Haer-Wigman, L. [1 ]
Oerlemans, A. J. M. [3 ]
van Koolwijk, M. [1 ]
Tammer, F. [1 ]
Arens, Y. [2 ]
Brunner, H. G. [1 ,2 ]
Vissers, L. E. L. M. [1 ]
Feenstra, I. [1 ]
机构：
[1] Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands
[2] Maastricht Univ, Med Ctr, Dept Clin Genet, Maastricht, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Sci Ctr Qual Healthcare, Nijmegen, Netherlands
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27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：
P24.05B
引用
收藏
页码：1811 / 1812
页数：2
相关论文
共 50 条
  • [41] An incidental finding in prenatal exome sequencing-A case study and review of the clinical and ethical considerations
    Rudd, Ignatius
    Gill, Gulvir
    Buckley, Michael
    Downie, Lilian
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2023, 191 (12) : 2856 - 2859
  • [42] Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing
    Yang, Yaping
    Muzny, Donna M.
    Xia, Fan
    Niu, Zhiyv
    Person, Richard
    Ding, Yan
    Ward, Patricia
    Braxton, Alicia
    Wang, Min
    Buhay, Christian
    Veeraraghavan, Narayanan
    Hawes, Alicia
    Chiang, Theodore
    Leduc, Magalie
    Beuten, Joke
    Zhang, Jing
    He, Weimin
    Scull, Jennifer
    Willis, Alecia
    Landsverk, Megan
    Craigen, William J.
    Bekheirnia, Mir Reza
    Stray-Pedersen, Asbjorg
    Liu, Pengfei
    Wen, Shu
    Alcaraz, Wendy
    Cui, Hong
    Walkiewicz, Magdalena
    Reid, Jeffrey
    Bainbridge, Matthew
    Patel, Ankita
    Boerwinkle, Eric
    Beaudet, Arthur L.
    Lupski, James R.
    Plon, Sharon E.
    Gibbs, Richard A.
    Eng, Christine M.
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2014, 312 (18): : 1870 - 1879
  • [43] Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing
    不详
    OBSTETRICAL & GYNECOLOGICAL SURVEY, 2015, 70 (03) : 164 - 167
  • [44] Pharmacogenomic findings from clinical whole exome sequencing of diagnostic odyssey patients
    Cousin, Margot A.
    Matey, Eric T.
    Blackburn, Patrick R.
    Boczek, Nicole J.
    McAllister, Tammy M.
    Kruisselbrink, Teresa M.
    Babovic-Vuksanovic, Dusica
    Lazaridis, Konstantinos N.
    Klee, Eric W.
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2017, 5 (03): : 269 - 279
  • [45] The impact of reporting incidental findings from exome and whole-genome sequencing: predicted frequencies based on modeling
    Ding, Lucy-Enid
    Burnett, Leslie
    Chesher, Douglas
    GENETICS IN MEDICINE, 2015, 17 (03) : 197 - 204
  • [46] Frequency of Medically Actionable Incidental Findings from Exome Sequencing Data of Deemed Healthy Individuals from India
    Bhanushali, Aparna
    Kulkarni, Smita
    Shah, Sanchi
    Prabha, Anu
    Pradhan, Ashlesha
    Chatterjee, Anirvan
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2024, 26 (06): : S1 - S2
  • [47] Oncologists' and cancer patients' views on whole-exome sequencing and incidental findings: results from the CanSeq study
    Gray, Stacy W.
    Park, Elyse R.
    Najita, Julie
    Martins, Yolanda
    Traeger, Lara
    Bair, Elizabeth
    Gagne, Joshua
    Garber, Judy
    Janne, Pasi A.
    Lindeman, Neal
    Lowenstein, Carol
    Oliver, Nelly
    Sholl, Lynette
    Van Allen, Eliezer M.
    Wagle, Nikhil
    Wood, Sam
    Garraway, Levi
    Joffe, Steven
    GENETICS IN MEDICINE, 2016, 18 (10) : 1011 - 1019
  • [48] Exome Sequencing in Clinical Hepatology
    Vilarinho, Silvia
    Mistry, Pramod K.
    HEPATOLOGY, 2019, 70 (06) : 2185 - 2192
  • [49] Exome Sequencing and Clinical Diagnosis
    Friedman, Jan M.
    Jones, Kenneth Lyons
    Carey, John C.
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2020, 324 (07): : 627 - 628
  • [50] Exome sequencing findings in children with annular pancreas
    Pitsava, Georgia
    Pankratz, Nathan
    Lane, John
    Yang, Wei
    Rigler, Shannon
    Shaw, Gary M.
    Mills, James L.
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2023,
12345