Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/111804
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dc.contributor.authorOud, M.en
dc.contributor.authorRamos, L.en
dc.contributor.authorO'Bryan, M.en
dc.contributor.authorMcLachlan, R.en
dc.contributor.authorOkutman, Ö.en
dc.contributor.authorViville, S.en
dc.contributor.authorde Vries, P.en
dc.contributor.authorSmeets, D.en
dc.contributor.authorLugtenberg, D.en
dc.contributor.authorHehir-Kwa, J.en
dc.contributor.authorGilissen, C.en
dc.contributor.authorvan de Vorst, M.en
dc.contributor.authorVissers, L.en
dc.contributor.authorHoischen, A.en
dc.contributor.authorMeijerink, A.en
dc.contributor.authorFleischer, K.en
dc.contributor.authorVeltman, J.en
dc.contributor.authorNoordam, M.en
dc.date.issued2017en
dc.identifier.citationHuman Mutation, 2017; 38(11):1592-1605en
dc.identifier.issn1059-7794en
dc.identifier.issn1098-1004en
dc.identifier.urihttp://hdl.handle.net/2440/111804-
dc.description.abstractMicrodeletions of the Y chromosome (YCMs), Klinefelter syndrome (47,XXY), and CFTR mutations are known genetic causes of severe male infertility, but the majority of cases remain idiopathic. Here, we describe a novel method using single molecule Molecular Inversion Probes (smMIPs), to screen infertile men for mutations and copy number variations affecting known disease genes. We designed a set of 4,525 smMIPs targeting the coding regions of causal (n = 6) and candidate (n = 101) male infertility genes. After extensive validation, we screened 1,112 idiopathic infertile men with non-obstructive azoospermia or severe oligozoospermia. In addition to five chromosome YCMs and six other sex chromosomal anomalies, we identified five patients with rare recessive mutations in CFTR as well as a patient with a rare heterozygous frameshift mutation in SYCP3 that may be of clinical relevance. This results in a genetic diagnosis in 11-17 patients (1%-1.5%), a yield that may increase significantly when more genes are confidently linked to male infertility. In conclusion, we developed a flexible and scalable method to reliably detect genetic causes of male infertility. The assay consolidates the detection of different types of genetic variation while increasing the diagnostic yield and detection precision at the same or lower price compared with currently used methods.en
dc.description.statementofresponsibilityManon S. Oud, Liliana Ramos, Moira K. O'Bryan, Robert I. McLachlan, Özlem Okutman, Stephane Viville, Petra F. de Vries, Dominique F.C.M. Smeets, Dorien Lugtenberg, Jayne Y. Hehir-Kwa, Christian Gilissen, Maartje van de Vorst, Lisenka E.L.M. Vissers, Alexander Hoischen, Aukje M. Meijerink, Kathrin Fleischer, Joris A. Veltman, Michiel J. Noordamen
dc.language.isoenen
dc.publisherWileyen
dc.rights© 2017 Wiley Periodicals, Inc.en
dc.subjectAzoospermia; CBAVD; CFTR; diagnostics; male infertility; oligozoospermia; reproduction; smMIPs; targeted sequencingen
dc.titleValidation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermiaen
dc.typeJournal articleen
dc.identifier.rmid0030082193en
dc.identifier.doi10.1002/humu.23312en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1022327en
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1058356en
dc.identifier.pubid366934-
pubs.library.collectionMedicine publicationsen
pubs.library.teamDS14en
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidO'Bryan, M. [0000-0001-7298-4940]en
Appears in Collections:Medicine publications

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