Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Topics Community

Article

Long-term economic impacts of exome sequencing for suspected monogenic disorders: diagnosis, management, and reproductive outcomes

20 May 2019

Abstract excerpt

No abstract is available from the source.

Source

Identifiers

PMID: 31110331
DOI: 10.1038/s41436-019-0534-x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Long-term economic impacts of exome sequencing for suspected monogenic disorders: diagnosis, management, and reproductive outcomesPMID 31110331Read ↗

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disordersSemantic proximity Read ↗

Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseasesSemantic proximity Read ↗

The long tail and rare disease research: the impact of next-generation sequencing for rare Mendelian disorders.Semantic proximity Read ↗

Insights from exome sequencing for endocrine disordersSemantic proximity Read ↗

Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysisSemantic proximity Read ↗

Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort studySemantic proximity Read ↗

Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center studySemantic proximity Read ↗

Exome and genome sequencing in reproductive medicine.Semantic proximity Read ↗

Exome sequencing and the genetic basis of complex traits.Semantic proximity Read ↗

The usefulness of whole-exome sequencing in routine clinical practice.Semantic proximity Read ↗

Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders.Semantic proximity Read ↗

Rare-disease genetics in the era of next-generation sequencing: discovery to translation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.