CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

13 citing papers in PubMed.

1. The prevalence of pathogenic variants in medically actionable genes among individuals with idiopathic hypogonadotropic hypogonadism/Kallmann syndrome.Journal of assisted reproduction and genetics · 2026
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2. Analytical Validation of a Genomic Newborn Screening Workflow.International journal of neonatal screening · 2025
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3. Navigating the Intersection between Genomic Research and Clinical Practice.Cancer prevention research (Philadelphia, Pa.) · 2020
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4. Genome analysis and knowledge-driven variant interpretation with TGex.BMC medical genomics · 2019
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5. Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy-associated genes among children undergoing exome sequencing reflect healthy population variation.Molecular genetics & genomic medicine · 2019
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6. Precision Medicine in Internal Medicine.Annals of internal medicine · 2019
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7. Genetic alterations of triple negative breast cancer (TNBC) in women from Northeastern Mexico.Oncology letters · 2019
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8. KRAS mutations in the parental tumour accelerate in vitro growth of tumoroids established from colorectal adenocarcinoma.International journal of experimental pathology · 2019
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9. Physicians' perspectives on receiving unsolicited genomic results.Genetics in medicine : official journal of the American College of Medical Genetics · 2019
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10. GENETICS IN ENDOCRINOLOGY: Approaches to molecular genetic diagnosis in the management of differences/disorders of sex development (DSD): position paper of EU COST Action BM 1303 ‘DSDnet’European journal of endocrinology · 2018
    Review
11. Targeted high-throughput sequencing technique for the molecular diagnosis of primary immunodeficiency disorders.Medicine · 2018
    Observational
12. Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.Journal of the American Society of Nephrology : JASN · 2018
    Article
13. Incidentalome in Neurogenetics: Pathogenic Variant ofFrontiers in genetics · 2018
    Article

Corrections and comments

• Erratum for
  ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.2013

Authors and funding

14 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.