guest ::
| Home > Publications Database > Unraveling undiagnosed rare disease cases by HiFi long-read genome sequencing. > print |
| Home > Publications Database > Unraveling undiagnosed rare disease cases by HiFi long-read genome sequencing. > print |
| 001 | 277999 | ||
| 005 | 20260105131056.0 | ||
| 024 | 7 | _ | |a pmc:PMC12047270 |2 pmc |
| 024 | 7 | _ | |a 10.1101/gr.279414.124 |2 doi |
| 024 | 7 | _ | |a pmid:40138663 |2 pmid |
| 024 | 7 | _ | |a 1054-9803 |2 ISSN |
| 024 | 7 | _ | |a 1088-9051 |2 ISSN |
| 024 | 7 | _ | |a 1549-5469 |2 ISSN |
| 024 | 7 | _ | |a altmetric:175800512 |2 altmetric |
| 037 | _ | _ | |a DZNE-2025-00526 |
| 041 | _ | _ | |a English |
| 082 | _ | _ | |a 540 |
| 100 | 1 | _ | |a Steyaert, Wouter |0 0000-0001-8393-0788 |b 0 |
| 245 | _ | _ | |a Unraveling undiagnosed rare disease cases by HiFi long-read genome sequencing. |
| 260 | _ | _ | |a Stanford, Calif. |c 2025 |b HighWire Press |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1745920641_31475 |2 PUB:(DE-HGF) |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
| 336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 520 | _ | _ | |a Solve-RD is a pan-European rare disease (RD) research program that aims to identify disease-causing genetic variants in previously undiagnosed RD families. We utilized 10-fold coverage HiFi long-read sequencing (LRS) for detecting causative structural variants (SVs), single-nucleotide variants (SNVs), insertion-deletions (indels), and short tandem repeat (STR) expansions in previously studied RD families without a clear molecular diagnosis. Our cohort includes 293 individuals from 114 genetically undiagnosed RD families selected by European Reference Network (ERN) experts. Of these, 21 families were affected by so-called 'unsolvable' syndromes for which genetic causes remain unknown and for which prior testing was not a prerequisite. The remaining 93 families had at least one individual affected by a rare neurological, neuromuscular, or epilepsy disorder without a genetic diagnosis despite extensive prior testing. Clinical interpretation and orthogonal validation of variants in known disease genes yielded 12 novel genetic diagnoses due to de novo and rare inherited SNVs, indels, SVs, and STR expansions. In an additional five families, we identified a candidate disease-causing variant, including an MCF2/FGF13 fusion and a PSMA3 deletion. However, no common genetic cause was identified in any of the 'unsolvable' syndromes. Taken together, we found (likely) disease-causing genetic variants in 11.8% of previously unsolved families and additional candidate disease-causing SVs in another 5.4% of these families. In conclusion, our results demonstrate the potential added value of HiFi long-read genome sequencing in undiagnosed rare diseases. |
| 536 | _ | _ | |a 353 - Clinical and Health Care Research (POF4-353) |0 G:(DE-HGF)POF4-353 |c POF4-353 |f POF IV |x 0 |
| 588 | _ | _ | |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de |
| 650 | _ | 2 | |a Humans |2 MeSH |
| 650 | _ | 2 | |a Rare Diseases: genetics |2 MeSH |
| 650 | _ | 2 | |a Rare Diseases: diagnosis |2 MeSH |
| 650 | _ | 2 | |a Male |2 MeSH |
| 650 | _ | 2 | |a Female |2 MeSH |
| 650 | _ | 2 | |a Whole Genome Sequencing: methods |2 MeSH |
| 650 | _ | 2 | |a Polymorphism, Single Nucleotide |2 MeSH |
| 650 | _ | 2 | |a Genome, Human |2 MeSH |
| 650 | _ | 2 | |a Pedigree |2 MeSH |
| 650 | _ | 2 | |a Undiagnosed Diseases: genetics |2 MeSH |
| 650 | _ | 2 | |a INDEL Mutation |2 MeSH |
| 700 | 1 | _ | |a Sagath, Lydia |0 0000-0002-6754-3830 |b 1 |
| 700 | 1 | _ | |a Demidov, German |b 2 |
| 700 | 1 | _ | |a Yépez, Vicente A |b 3 |
| 700 | 1 | _ | |a Esteve-Codina, Anna |b 4 |
| 700 | 1 | _ | |a Gagneur, Julien |0 0000-0002-8924-8365 |b 5 |
| 700 | 1 | _ | |a Ellwanger, Kornelia |b 6 |
| 700 | 1 | _ | |a Derks, Ronny |b 7 |
| 700 | 1 | _ | |a Weiss, Marjan |b 8 |
| 700 | 1 | _ | |a den Ouden, Amber |b 9 |
| 700 | 1 | _ | |a van den Heuvel, Simone |b 10 |
| 700 | 1 | _ | |a Swinkels, Hilde |b 11 |
| 700 | 1 | _ | |a Zomer, Nick |b 12 |
| 700 | 1 | _ | |a Steehouwer, Marloes |b 13 |
| 700 | 1 | _ | |a O'Gorman, Luke |b 14 |
| 700 | 1 | _ | |a Astuti, Galuh |b 15 |
| 700 | 1 | _ | |a Neveling, Kornelia |b 16 |
| 700 | 1 | _ | |a Schüle-Freyer, Rebecca |0 P:(DE-2719)2812018 |b 17 |u dzne |
| 700 | 1 | _ | |a Xu, Jishu |b 18 |
| 700 | 1 | _ | |a Synofzik, Matthis |0 P:(DE-2719)2811275 |b 19 |
| 700 | 1 | _ | |a Beijer, Danique |0 P:(DE-2719)9002605 |b 20 |u dzne |
| 700 | 1 | _ | |a Hengel, Holger |b 21 |
| 700 | 1 | _ | |a Schöls, Ludger |0 P:(DE-2719)2810795 |b 22 |u dzne |
| 700 | 1 | _ | |a Claeys, Kristl G |b 23 |
| 700 | 1 | _ | |a Baets, Jonathan |b 24 |
| 700 | 1 | _ | |a Van de Vondel, Liedewei |b 25 |
| 700 | 1 | _ | |a Ferlini, Alessandra |b 26 |
| 700 | 1 | _ | |a Selvatici, Rita |b 27 |
| 700 | 1 | _ | |a Morsy, Heba |b 28 |
| 700 | 1 | _ | |a Saeed Abd Elmaksoud, Marwa |b 29 |
| 700 | 1 | _ | |a Straub, Volker |0 0000-0001-9046-3540 |b 30 |
| 700 | 1 | _ | |a Müller, Juliane |b 31 |
| 700 | 1 | _ | |a Pini, Veronica |b 32 |
| 700 | 1 | _ | |a Perry, Luke |b 33 |
| 700 | 1 | _ | |a Sarkozy, Anna |b 34 |
| 700 | 1 | _ | |a Zaharieva, Irina |b 35 |
| 700 | 1 | _ | |a Muntoni, Francesco |0 0000-0002-9102-5232 |b 36 |
| 700 | 1 | _ | |a Bugiardini, Enrico |0 0000-0002-9709-6699 |b 37 |
| 700 | 1 | _ | |a Polavarapu, Kiran |b 38 |
| 700 | 1 | _ | |a Horvath, Rita |b 39 |
| 700 | 1 | _ | |a Reid, Evan |b 40 |
| 700 | 1 | _ | |a Lochmüller, Hanns |b 41 |
| 700 | 1 | _ | |a Spinazzi, Marco |0 0000-0003-0048-9558 |b 42 |
| 700 | 1 | _ | |a Savarese, Marco |0 0000-0002-2591-244X |b 43 |
| 700 | 1 | _ | |a Solve-RD DITF-ITHACA, Solve-RD DITF-Euro-NMD, Solve-RD DITF-RND, Solve-RD DITF-EpiCARE |b 44 |e Collaboration Author |
| 700 | 1 | _ | |a Matalonga, Leslie |b 45 |
| 700 | 1 | _ | |a Laurie, Steven |b 46 |
| 700 | 1 | _ | |a Brunner, Han G |b 47 |
| 700 | 1 | _ | |a Graessner, Holm |b 48 |
| 700 | 1 | _ | |a Beltran, Sergi |b 49 |
| 700 | 1 | _ | |a Ossowski, Stephan |0 0000-0002-7416-9568 |b 50 |
| 700 | 1 | _ | |a Vissers, Lisenka E L M |0 0000-0001-6470-5497 |b 51 |
| 700 | 1 | _ | |a Gilissen, Christian |0 0000-0003-1693-9699 |b 52 |
| 700 | 1 | _ | |a Hoischen, Alexander |b 53 |
| 700 | 1 | _ | |a consortium, Solve-RD |b 54 |e Collaboration Author |
| 773 | _ | _ | |a 10.1101/gr.279414.124 |g Vol. 35, no. 4, p. 755 - 768 |0 PERI:(DE-600)1483456-X |n 4 |p 755 - 768 |t Genome research |v 35 |y 2025 |x 1054-9803 |
| 856 | 4 | _ | |u https://pub.dzne.de/record/277999/files/DZNE-2025-00526%20SUP.zip |
| 856 | 4 | _ | |y OpenAccess |u https://pub.dzne.de/record/277999/files/DZNE-2025-00526.pdf |
| 856 | 4 | _ | |y OpenAccess |x pdfa |u https://pub.dzne.de/record/277999/files/DZNE-2025-00526.pdf?subformat=pdfa |
| 909 | C | O | |o oai:pub.dzne.de:277999 |p openaire |p open_access |p VDB |p driver |p dnbdelivery |
| 910 | 1 | _ | |a External Institute |0 I:(DE-HGF)0 |k Extern |b 17 |6 P:(DE-2719)2812018 |
| 910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 19 |6 P:(DE-2719)2811275 |
| 910 | 1 | _ | |a External Institute |0 I:(DE-HGF)0 |k Extern |b 20 |6 P:(DE-2719)9002605 |
| 910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 22 |6 P:(DE-2719)2810795 |
| 913 | 1 | _ | |a DE-HGF |b Gesundheit |l Neurodegenerative Diseases |1 G:(DE-HGF)POF4-350 |0 G:(DE-HGF)POF4-353 |3 G:(DE-HGF)POF4 |2 G:(DE-HGF)POF4-300 |4 G:(DE-HGF)POF |v Clinical and Health Care Research |x 0 |
| 914 | 1 | _ | |y 2025 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0200 |2 StatID |b SCOPUS |d 2025-01-07 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0160 |2 StatID |b Essential Science Indicators |d 2025-01-07 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1050 |2 StatID |b BIOSIS Previews |d 2025-01-07 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1190 |2 StatID |b Biological Abstracts |d 2025-01-07 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0600 |2 StatID |b Ebsco Academic Search |d 2025-01-07 |
| 915 | _ | _ | |a JCR |0 StatID:(DE-HGF)0100 |2 StatID |b GENOME RES : 2022 |d 2025-01-07 |
| 915 | _ | _ | |a Creative Commons Attribution-NonCommercial CC BY-NC 4.0 |0 LIC:(DE-HGF)CCBYNC4 |2 HGFVOC |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1030 |2 StatID |b Current Contents - Life Sciences |d 2025-01-07 |
| 915 | _ | _ | |a WoS |0 StatID:(DE-HGF)0113 |2 StatID |b Science Citation Index Expanded |d 2025-01-07 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0150 |2 StatID |b Web of Science Core Collection |d 2025-01-07 |
| 915 | _ | _ | |a OpenAccess |0 StatID:(DE-HGF)0510 |2 StatID |
| 915 | _ | _ | |a Peer Review |0 StatID:(DE-HGF)0030 |2 StatID |b ASC |d 2025-01-07 |
| 915 | _ | _ | |a IF >= 5 |0 StatID:(DE-HGF)9905 |2 StatID |b GENOME RES : 2022 |d 2025-01-07 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0300 |2 StatID |b Medline |d 2025-01-07 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0199 |2 StatID |b Clarivate Analytics Master Journal List |d 2025-01-07 |
| 920 | 1 | _ | |0 I:(DE-2719)1210000 |k AG Gasser |l Parkinson Genetics |x 0 |
| 920 | 1 | _ | |0 I:(DE-2719)5000005 |k AG Schöls |l Clinical Neurogenetics |x 1 |
| 980 | _ | _ | |a journal |
| 980 | _ | _ | |a VDB |
| 980 | _ | _ | |a UNRESTRICTED |
| 980 | _ | _ | |a I:(DE-2719)1210000 |
| 980 | _ | _ | |a I:(DE-2719)5000005 |
| 980 | 1 | _ | |a FullTexts |
| Library | Collection | CLSMajor | CLSMinor | Language | Author |
|---|