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Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders.

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Title: Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders.
Authors: Wootton O; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Campbell P; Department of Medical and Molecular Genetics, King's College London, London, UK., Richardson S; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK., Lindsay SJ; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Huang QQ; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Delage E; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Amanat S; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Wong HS; Cambridge University Hospitals Foundation Trust, Addenbrooke's Hospital, Cambridge, UK., Firth HV; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.; Cambridge University Hospitals Foundation Trust, Addenbrooke's Hospital, Cambridge, UK., Hurles ME; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK., Simpson MA; Department of Medical and Molecular Genetics, King's College London, London, UK., Radford EJ; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.; Department of Paediatrics, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK., Martin HC; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK. hcm@sanger.ac.uk.
Source: Genome medicine [Genome Med] 2025 Oct 30; Vol. 17 (1), pp. 134. Date of Electronic Publication: 2025 Oct 30.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X (Electronic) Linking ISSN: 1756994X NLM ISO Abbreviation: Genome Med Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Investigating the interplay between prematurity and genetic variation in the context of rare developmental disorders.
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  Data: <searchLink fieldCode="AU" term="%22Wootton+O%22">Wootton O</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.<br /><searchLink fieldCode="AU" term="%22Campbell+P%22">Campbell P</searchLink>; Department of Medical and Molecular Genetics, King's College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Richardson+S%22">Richardson S</searchLink>; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Lindsay+SJ%22">Lindsay SJ</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.<br /><searchLink fieldCode="AU" term="%22Huang+QQ%22">Huang QQ</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.<br /><searchLink fieldCode="AU" term="%22Delage+E%22">Delage E</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.<br /><searchLink fieldCode="AU" term="%22Amanat+S%22">Amanat S</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.<br /><searchLink fieldCode="AU" term="%22Wong+HS%22">Wong HS</searchLink>; Cambridge University Hospitals Foundation Trust, Addenbrooke's Hospital, Cambridge, UK.<br /><searchLink fieldCode="AU" term="%22Firth+HV%22">Firth HV</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.; Cambridge University Hospitals Foundation Trust, Addenbrooke's Hospital, Cambridge, UK.<br /><searchLink fieldCode="AU" term="%22Hurles+ME%22">Hurles ME</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.<br /><searchLink fieldCode="AU" term="%22Simpson+MA%22">Simpson MA</searchLink>; Department of Medical and Molecular Genetics, King's College London, London, UK.<br /><searchLink fieldCode="AU" term="%22Radford+EJ%22">Radford EJ</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK.; Department of Paediatrics, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.<br /><searchLink fieldCode="AU" term="%22Martin+HC%22">Martin HC</searchLink>; Human Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 1SA, UK. hcm@sanger.ac.uk.
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  Data: <searchLink fieldCode="JN" term="%22101475844%22">Genome medicine</searchLink> [Genome Med] 2025 Oct 30; Vol. 17 (1), pp. 134. <i>Date of Electronic Publication: </i>2025 Oct 30.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101475844 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1756-994X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%221756994X%22">1756994X </searchLink><i>NLM ISO Abbreviation: </i>Genome Med <i>Subsets: </i>MEDLINE
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