Evidence map›Paper›PMID 39663844›Full record

ArticleClinical genetics2025

Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study.

Luise Kessler, Jeremias Krause, Florian Kraft, Asmaa K Amin, Gyorgy Fekete, Anna Lengyel, Eva Pinti, Arpad Kovacs, Annette Lischka, Katja Eggermann and 5 more

Abstract read
In one paragraph

Article in Clinical genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Genes · 2026
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Luise KesslerInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0009-0000-4542-8471
Jeremias KrauseInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0001-9915-7400
Florian KraftInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-5324-9155
Asmaa K AminDepartment of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, Egypt.ORCID 0000-0003-1691-5101
Gyorgy Fekete2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.ORCID 0009-0005-7666-342X
Anna Lengyel2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-3477-7411
Eva Pinti2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-5724-6859
Arpad Kovacs2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-7742-160X
Annette LischkaInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0001-8042-4361
Katja EggermannInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-8706-137X
Ingo KurthInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-5642-8378
Cordula KnoppInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-6126-6078
Miriam ElbrachtInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-4659-8437
Matthias BegemannInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0001-5088-1369
Thomas EggermannInstitute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-8419-0264

Funding

Deutsche Forschungsgemeinschaft EG 115/13-1Illumina
6 · The paper itself

Abstract

To assess the suitability of genome sequencing (GS) as the second step in the diagnostics of patients with the features of 11p15.5-associated imprinting disorders (ImpDis: Silver-Russell syndrome [SRS], Beckwith-Wiedemann syndrome [BWS]), we performed short-read GS in patients negatively tested for imprinting disturbances. Obtaining a genetic diagnosis for patients with the features of these syndromes is challenging due to the clinical and molecular heterogeneity and overlap, and many patients remain undiagnosed after the currently suggested stepwise diagnostic workup. GS was conducted in 48 patients (SRS features: n = 37 and BWS features: n = 11). The detection rate differed markedly between the ImpDis: although a genetic cause could be identified in 51% of patients referred with SRS features, no pathogenic variants were detected in patients with BWS features. Thus, GS substantially improves the diagnostic yield and broadens the spectrum of overlapping disorders with SRS features. Obtaining a precise molecular diagnosis provides the basis for a personalized clinical management. Our findings support the use of GS as a second-tier diagnostic tool for patients with growth disturbances, as it addresses all currently known variant types and shortens the diagnostic odyssey.

Indexed as

Beckwith-Wiedemann SyndromeChromosomes, Human, Pair 11Genomic ImprintingSilver-Russell SyndromeAdolescentChildChild, PreschoolFemaleHumansImprinting DisordersInfantMalePilot ProjectsWhole Genome SequencingBeckwith–Wiedemann syndromediagnostic yieldgenome sequencingSilver–Russell syndrome

Identifiers

PMID39663844
PMCPMC11790513

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.