Literature DB >> 35899841

A retrospective cohort analysis of the Yale pediatric genomics discovery program.

Samir Al-Ali1, Lauren Jeffries1, E Vincent S Faustino1, Weizhen Ji1, Emily Mis1, Monica Konstantino1, Cynthia Zerillo1, Yong-Hui Jiang1,2, Michele Spencer-Manzon1,2, Allen Bale2, Hui Zhang2, Julie McGlynn1,2, James M McGrath2, Thierry Tremblay3, Nina N Brodsky1, Carrie L Lucas4, Richard Pierce1, Engin Deniz1, Mustafa K Khokha1,2, Saquib A Lakhani1.   

Abstract

The Pediatric Genomics Discovery Program (PGDP) at Yale uses next-generation sequencing (NGS) and translational research to evaluate complex patients with a wide range of phenotypes suspected to have rare genetic diseases. We conducted a retrospective cohort analysis of 356 PGDP probands evaluated between June 2015 and July 2020, querying our database for participant demographics, clinical characteristics, NGS results, and diagnostic and research findings. The three most common phenotypes among the entire studied cohort (n = 356) were immune system abnormalities (n = 105, 29%), syndromic or multisystem disease (n = 103, 29%), and cardiovascular system abnormalities (n = 62, 17%). Of 216 patients with final classifications, 77 (36%) received new diagnoses and 139 (64%) were undiagnosed; the remaining 140 patients were still actively being investigated. Monogenetic diagnoses were found in 67 (89%); the largest group had variants in known disease genes but with new contributions such as novel variants (n = 31, 40%) or expanded phenotypes (n = 14, 18%). Finally, five PGDP diagnoses (8%) were suggestive of novel gene-to-phenotype relationships. A broad range of patients can benefit from single subject studies combining NGS and functional molecular analyses. All pediatric providers should consider further genetics evaluations for patients lacking precise molecular diagnoses.
© 2022 Wiley Periodicals LLC.

Entities:  

Keywords:  functional characterization; gene discovery; genetic reanalysis; next generation sequencing (NGS); single subject studies; undiagnosed disease

Mesh:

Year:  2022        PMID: 35899841      PMCID: PMC9474639          DOI: 10.1002/ajmg.a.62918

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.578


  46 in total

1.  Functional testing for variant prioritization in a family with long QT syndrome.

Authors:  Maliheh Najari Beidokhti; Alexander C Bertalovitz; Weizhen Ji; Jorge McCormack; Lauren Jeffries; Emily Sempou; Mustafa K Khokha; Thomas V McDonald; Saquib A Lakhani
Journal:  Mol Genet Genomics       Date:  2021-04-19       Impact factor: 3.291

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

Authors:  Stephen F Kingsmore; Julie A Cakici; Michelle M Clark; Mary Gaughran; Michele Feddock; Sergey Batalov; Matthew N Bainbridge; Jeanne Carroll; Sara A Caylor; Christina Clarke; Yan Ding; Katarzyna Ellsworth; Lauge Farnaes; Amber Hildreth; Charlotte Hobbs; Kiely James; Cyrielle I Kint; Jerica Lenberg; Shareef Nahas; Lance Prince; Iris Reyes; Lisa Salz; Erica Sanford; Peter Schols; Nathaly Sweeney; Mari Tokita; Narayanan Veeraraghavan; Kelly Watkins; Kristen Wigby; Terence Wong; Shimul Chowdhury; Meredith S Wright; David Dimmock
Journal:  Am J Hum Genet       Date:  2019-09-26       Impact factor: 11.025

3.  The latest FADS: Functional analysis of GLDN patient variants and classification of GLDN-associated AMC as a type of viable fetal akinesia deformation sequence.

Authors:  Emily K Mis; Samir Al-Ali; Weizhen Ji; Michele Spencer-Manzon; Monica Konstantino; Mustafa K Khokha; Lauren Jeffries; Saquib A Lakhani
Journal:  Am J Med Genet A       Date:  2020-08-19       Impact factor: 2.802

4.  WDR5 Stabilizes Actin Architecture to Promote Multiciliated Cell Formation.

Authors:  Saurabh S Kulkarni; John N Griffin; Priya P Date; Karel F Liem; Mustafa K Khokha
Journal:  Dev Cell       Date:  2018-09-10       Impact factor: 12.270

5.  Siblings with lethal primary pulmonary hypoplasia and compound heterozygous variants in the AARS2 gene: further delineation of the phenotypic spectrum.

Authors:  Catherine Kiraly-Borri; Gareth Jevon; Weizhen Ji; Lauren Jeffries; Jamie-Lee Ricciardi; Monica Konstantino; Kate G Ackerman; Saquib A Lakhani
Journal:  Cold Spring Harb Mol Case Stud       Date:  2019-06-03

6.  The Human Phenotype Ontology in 2021.

Authors:  Sebastian Köhler; Michael Gargano; Nicolas Matentzoglu; Leigh C Carmody; David Lewis-Smith; Nicole A Vasilevsky; Daniel Danis; Ganna Balagura; Gareth Baynam; Amy M Brower; Tiffany J Callahan; Christopher G Chute; Johanna L Est; Peter D Galer; Shiva Ganesan; Matthias Griese; Matthias Haimel; Julia Pazmandi; Marc Hanauer; Nomi L Harris; Michael J Hartnett; Maximilian Hastreiter; Fabian Hauck; Yongqun He; Tim Jeske; Hugh Kearney; Gerhard Kindle; Christoph Klein; Katrin Knoflach; Roland Krause; David Lagorce; Julie A McMurry; Jillian A Miller; Monica C Munoz-Torres; Rebecca L Peters; Christina K Rapp; Ana M Rath; Shahmir A Rind; Avi Z Rosenberg; Michael M Segal; Markus G Seidel; Damian Smedley; Tomer Talmy; Yarlalu Thomas; Samuel A Wiafe; Julie Xian; Zafer Yüksel; Ingo Helbig; Christopher J Mungall; Melissa A Haendel; Peter N Robinson
Journal:  Nucleic Acids Res       Date:  2021-01-08       Impact factor: 16.971

7.  Systematic assessment of outcomes following a genetic diagnosis identified through a large-scale research study into developmental disorders.

Authors:  H Copeland; E Kivuva; H V Firth; C F Wright
Journal:  Genet Med       Date:  2021-02-18       Impact factor: 8.822

8.  Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.

Authors:  Michelle M Clark; Zornitza Stark; Lauge Farnaes; Tiong Y Tan; Susan M White; David Dimmock; Stephen F Kingsmore
Journal:  NPJ Genom Med       Date:  2018-07-09       Impact factor: 8.617

9.  Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome.

Authors:  Reham Alharatani; Athina Ververi; Ana Beleza-Meireles; Weizhen Ji; Emily Mis; Quinten T Patterson; John N Griffin; Nabina Bhujel; Caitlin A Chang; Abhijit Dixit; Monica Konstantino; Christopher Healy; Sumayyah Hannan; Natsuko Neo; Alex Cash; Dong Li; Elizabeth Bhoj; Elaine H Zackai; Ruth Cleaver; Diana Baralle; Meriel McEntagart; Ruth Newbury-Ecob; Richard Scott; Jane A Hurst; Ping Yee Billie Au; Marie Therese Hosey; Mustafa Khokha; Denise K Marciano; Saquib A Lakhani; Karen J Liu
Journal:  Hum Mol Genet       Date:  2020-07-21       Impact factor: 6.150

10.  Rapid exome sequencing in PICU patients with new-onset metabolic or neurological disorders.

Authors:  Abigail S Carey; John P Schacht; Christine Umandap; David Fasel; Chunhua Weng; Joshua Cappell; Wendy K Chung; Steven G Kernie
Journal:  Pediatr Res       Date:  2020-03-27       Impact factor: 3.756

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