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Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.

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Title: Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
Authors: Curtis SW; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA., Carlson JC; Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, 15621, USA.; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA., Beaty TH; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 21205, USA., Murray JC; Department of Pediatrics, University of Iowa, Iowa City, IA, 52242, USA., Weinberg SM; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA, 15261, USA., Marazita ML; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA, 15261, USA., Cotney JL; Department of Genetics and Genome Sciences, University of Connecticut, Farmington, CT, 06030, USA., Cutler DJ; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA., Epstein MP; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA., Leslie EJ; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA. ejlesli@emory.edu.
Source: Human genetics [Hum Genet] 2023 Oct; Vol. 142 (10), pp. 1531-1541. Date of Electronic Publication: 2023 Sep 07.
Publication Type: Journal Article
Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
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  Data: <searchLink fieldCode="AU" term="%22Curtis+SW%22">Curtis SW</searchLink>; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.<br /><searchLink fieldCode="AU" term="%22Carlson+JC%22">Carlson JC</searchLink>; Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA, 15621, USA.; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.<br /><searchLink fieldCode="AU" term="%22Beaty+TH%22">Beaty TH</searchLink>; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 21205, USA.<br /><searchLink fieldCode="AU" term="%22Murray+JC%22">Murray JC</searchLink>; Department of Pediatrics, University of Iowa, Iowa City, IA, 52242, USA.<br /><searchLink fieldCode="AU" term="%22Weinberg+SM%22">Weinberg SM</searchLink>; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA, 15261, USA.<br /><searchLink fieldCode="AU" term="%22Marazita+ML%22">Marazita ML</searchLink>; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, 15261, USA.; Center for Craniofacial and Dental Genetics, Department of Oral and Craniofacial Sciences, University of Pittsburgh, Pittsburgh, PA, 15261, USA.<br /><searchLink fieldCode="AU" term="%22Cotney+JL%22">Cotney JL</searchLink>; Department of Genetics and Genome Sciences, University of Connecticut, Farmington, CT, 06030, USA.<br /><searchLink fieldCode="AU" term="%22Cutler+DJ%22">Cutler DJ</searchLink>; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.<br /><searchLink fieldCode="AU" term="%22Epstein+MP%22">Epstein MP</searchLink>; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA.<br /><searchLink fieldCode="AU" term="%22Leslie+EJ%22">Leslie EJ</searchLink>; Department of Human Genetics, Emory University, Atlanta, GA, 30322, USA. ejlesli@emory.edu.
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  Data: <searchLink fieldCode="JN" term="%227613873%22">Human genetics</searchLink> [Hum Genet] 2023 Oct; Vol. 142 (10), pp. 1531-1541. <i>Date of Electronic Publication: </i>2023 Sep 07.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer+Verlag%22">Springer Verlag </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>7613873 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1432-1203 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2203406717%22">03406717 </searchLink><i>NLM ISO Abbreviation: </i>Hum Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1007/s00439-023-02596-4
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              Text: 2023 Oct
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