Literature DB >> 30311372

The progression of the ClinGen gene clinical validity classification over time.

Jennifer L McGlaughon1, Jennifer L Goldstein1, Courtney Thaxton1, Sarah E Hemphill2, Jonathan S Berg1.   

Abstract

In order for ClinGen to maintain up-to-date gene-disease clinical validity classifications for use by clinicians and clinical laboratories, an appropriate timeline for reevaluating curated gene-disease associations will need to be determined. To provide guidance on how often a gene-disease association should be recurated, a retrospective analysis of 30 gene curations was performed. Curations were simulated at one-year intervals starting with the year of the first publication to assert disease-causing variants in the gene to observe trends in the classification over time, as well as factors that influenced changes in classification. On average, gene-disease associations spent the least amount of time in the "Moderate" classification before progressing to "Strong" or "Definitive." In contrast, gene-disease associations that spent five or more years in the "Limited" classification were most likely to remain "Limited" or become "Disputed/Refuted." Large population datasets contributed to the reclassification of several gene-disease associations from "Limited" to "Disputed/Refuted." Finally, recent advancements in sequencing technology correlated with an increase in the quantity of case-level evidence that was curated per paper. This study provided a number of key points to consider when determining how often to recurate a gene-disease association.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  ClinGen; Clinical Genome Resource; clinical validity; curation; gene-disease association; reevaluation

Mesh:

Year:  2018        PMID: 30311372      PMCID: PMC6190678          DOI: 10.1002/humu.23604

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  40 in total

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2.  Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.

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Journal:  Am J Hum Genet       Date:  2006-11-02       Impact factor: 11.025

3.  Pelger-huet anomaly and a mild skeletal phenotype secondary to mutations in LBR.

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4.  De novo mutations in the genome organizer CTCF cause intellectual disability.

Authors:  Anne Gregor; Martin Oti; Evelyn N Kouwenhoven; Juliane Hoyer; Heinrich Sticht; Arif B Ekici; Susanne Kjaergaard; Anita Rauch; Hendrik G Stunnenberg; Steffen Uebe; Georgia Vasileiou; André Reis; Huiqing Zhou; Christiane Zweier
Journal:  Am J Hum Genet       Date:  2013-06-06       Impact factor: 11.025

5.  Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy.

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6.  Mutation of an A-kinase-anchoring protein causes long-QT syndrome.

Authors:  Lei Chen; Michelle L Marquardt; David J Tester; Kevin J Sampson; Michael J Ackerman; Robert S Kass
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7.  Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita.

Authors:  Tom Vulliamy; Richard Beswick; Michael Kirwan; Anna Marrone; Martin Digweed; Amanda Walne; Inderjeet Dokal
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8.  SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling.

Authors:  Kishan Kumar Chudasama; Jonathon Winnay; Stefan Johansson; Tor Claudi; Rainer König; Ingfrid Haldorsen; Bente Johansson; Ju Rang Woo; Dagfinn Aarskog; Jørn V Sagen; C Ronald Kahn; Anders Molven; Pål Rasmus Njølstad
Journal:  Am J Hum Genet       Date:  2013-06-27       Impact factor: 11.025

9.  Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosa.

Authors:  Alice E Davidson; Nele Schwarz; Lina Zelinger; Gabriele Stern-Schneider; Amelia Shoemark; Benjamin Spitzbarth; Menachem Gross; Uri Laxer; Jacob Sosna; Panagiotis I Sergouniotis; Naushin H Waseem; Robert Wilson; Richard A Kahn; Vincent Plagnol; Uwe Wolfrum; Eyal Banin; Alison J Hardcastle; Michael E Cheetham; Dror Sharon; Andrew R Webster
Journal:  Am J Hum Genet       Date:  2013-07-11       Impact factor: 11.025

10.  Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment.

Authors:  Eberhard Schneider; Tina Märker; Angelika Daser; Gabriele Frey-Mahn; Vera Beyer; Ruxandra Farcas; Brigitte Schneider-Rätzke; Nicolai Kohlschmidt; Bärbel Grossmann; Katharina Bauss; Ulrike Napiontek; Annerose Keilmann; Oliver Bartsch; Ulrich Zechner; Uwe Wolfrum; Thomas Haaf
Journal:  Hum Mol Genet       Date:  2008-11-20       Impact factor: 6.150

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Journal:  Hum Mutat       Date:  2021-11-15       Impact factor: 4.700

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Journal:  Hum Mutat       Date:  2020-05-21       Impact factor: 4.878

3.  ClinGen expert clinical validity curation of 164 hearing loss gene-disease pairs.

Authors:  Marina T DiStefano; Sarah E Hemphill; Andrea M Oza; Rebecca K Siegert; Andrew R Grant; Madeline Y Hughes; Brandon J Cushman; Hela Azaiez; Kevin T Booth; Alex Chapin; Hatice Duzkale; Tatsuo Matsunaga; Jun Shen; Wenying Zhang; Margaret Kenna; Lisa A Schimmenti; Mustafa Tekin; Heidi L Rehm; Ahmad N Abou Tayoun; Sami S Amr
Journal:  Genet Med       Date:  2019-03-21       Impact factor: 8.822

4.  Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.

Authors:  Elizabeth Jordan; Laiken Peterson; Tomohiko Ai; Babken Asatryan; Lucas Bronicki; Emily Brown; Rudy Celeghin; Matthew Edwards; Judy Fan; Jodie Ingles; Cynthia A James; Olga Jarinova; Renee Johnson; Daniel P Judge; Najim Lahrouchi; Ronald H Lekanne Deprez; R Thomas Lumbers; Francesco Mazzarotto; Argelia Medeiros Domingo; Rebecca L Miller; Ana Morales; Brittney Murray; Stacey Peters; Kalliopi Pilichou; Alexandros Protonotarios; Christopher Semsarian; Palak Shah; Petros Syrris; Courtney Thaxton; J Peter van Tintelen; Roddy Walsh; Jessica Wang; James Ware; Ray E Hershberger
Journal:  Circulation       Date:  2021-05-05       Impact factor: 29.690

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