Concepedia

Trio Sequencing

Trio Sequencing is a genomic sequencing approach that belongs to the class of family-based genetic analysis methods, distinguished by the simultaneous whole-exome or whole-genome sequencing of both biological parents and their affected offspring to identify de novo, inherited, and rare genetic variants underlying disorders such as Autism Spectrum Disorder and rare diseases.

199

Publications

11.1K

Citations

2.6K

Authors

852

Institutions

Publications per year

2017–2026

163

Variants

Trio-based Sequencing

Parents

Publications

199

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

Hane Lee, Joshua L. Deignan, Naghmeh Dorrani et al. · JAMA · 2014 · 981 citations · Full text

, , +17

Use of Exome Sequencing for Infants in Intensive Care Units

Linyan Meng, Mohan Pammi, Anirudh Saronwala et al. · JAMA Pediatrics · 2017 · 431 citations · Full text

, , +14

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants

Stephen F. Kingsmore, Julie A. Cakici, Michelle M. Clark et al. · The American Journal of Human Genetics · 2019 · 358 citations · Full text

, , +17

Mutations in EZH2 Cause Weaver Syndrome

William T. Gibson, Rebecca L. Hood, Shing H. Zhan et al. · The American Journal of Human Genetics · 2011 · 328 citations · Full text

, , +17

Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing

Claire Redin, Bénédicte Gérard, Julia Lauer et al. · Journal of Medical Genetics · 2014 · 273 citations · Full text

, , +17

1–5 of 199

Authors

2.6K

  1. CT
    Christel Thauvin‐Robinet

    Inserm, France

    7 publications · 552 citations

    7

    h-index

  2. LF
    Laurence Faivre

    Inserm, France

    6 publications · 279 citations

    6

    h-index

  3. AV
    Antonio Vitobello

    Inserm, France

    5 publications · 105 citations

    5

    h-index

  4. CG
    Christian Gilissen

    Radboud University Nijmegen, Netherlands

    5 publications · 415 citations

    5

    h-index

  5. WG
    Weiyue Gu

    BeiGene (China), China

    5 publications · 162 citations

    5

    h-index

1–5 of 2.6K

Institutions

852

  1. Inserm

    Paris, France

    13 h-index

    174 publications

    11.2K citations

  2. Baylor College of Medicine

    Houston, United States

    11 h-index

    85 publications

    22.5K citations

  3. The University of Melbourne

    Melbourne, Australia

    10 h-index

    59 publications

    2.2K citations

  4. Murdoch Children's Research Institute

    Melbourne, Australia

    9 h-index

    57 publications

    2.1K citations

  5. Guangzhou Medical University

    Guangzhou, China

    9 h-index

    53 publications

    2.8K citations

  6. University of Cambridge

    Cambridge, United Kingdom

    8 h-index

    40 publications

    3.8K citations

  7. Royal Children's Hospital

    Melbourne, Australia

    8 h-index

    25 publications

    698 citations

  8. Radboud University Nijmegen

    Nijmegen, The Netherlands

    8 h-index

    63 publications

    4.9K citations

1–8 of 852

Venues

  1. Journal of Medical Genetics

    JMG · 12 publications · 810 citations

    11

    h-index

  2. Frontiers in Genetics

    12 publications · 385 citations

    11

    h-index

  3. Scientific Reports

    9 publications · 459 citations

    9

    h-index

  4. Clinical Genetics

    8 publications · 347 citations

    8

    h-index

  5. Molecular Genetics & Genomic Medicine

    7 publications · 217 citations

    7

    h-index

1–5