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A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders.

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Title: A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders.
Authors: Ben-Mahmoud A; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar., Jun KR; Department of Laboratory Medicine, Inje University Haeundae Paik Hospital, Busan, South Korea., Gupta V; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar., Shastri P; Department of Cardiovascular Medicine, Cape Fear Valley Medical Center, Fayetteville, NC, United States., de la Fuente A; Diabetes Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar., Park Y; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar., Shin KC; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar., Kim CA; Faculdade de Medicina, Unidade de Genética do Instituto da Criança - Hospital das Clínicas HCFMUSP, Universidade de São Paulo, São Paulo, Brazil., da Cruz AD; School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.; Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil., Pinto IP; School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.; Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil., Minasi LB; School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.; Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil., Silva da Cruz A; School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.; Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil., Faivre L; Inserm UMR 1231 GAD, Genetics of Developmental Disorders, Université de Bourgogne-Franche Comté, Dijon, France.; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, Dijon, France., Callier P; UMR 1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France., Racine C; UMR 1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France., Layman LC; Section of Reproductive Endocrinology, Infertility and Genetics, Department of Obstetrics and Gynecology, Augusta University, Augusta, GA, United States.; Department of Neuroscience and Regenerative Medicine, Augusta University, Augusta, GA, United States., Kong IK; Department of Animal Science, Division of Applied Life Science (BK21 Four), Gyeongsang National University, Jinju, South Korea., Kim CH; Department of Biology, Chungnam National University, Daejeon, South Korea., Kim WY; Department of Biological Sciences, Kent State University, Kent, OH, United States., Kim HG; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
Source: Frontiers in molecular neuroscience [Front Mol Neurosci] 2022 Oct 06; Vol. 15, pp. 979061. Date of Electronic Publication: 2022 Oct 06 (Print Publication: 2022).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101477914 Publication Model: eCollection Cited Medium: Print ISSN: 1662-5099 (Print) Linking ISSN: 16625099 NLM ISO Abbreviation: Front Mol Neurosci Subsets: PubMed not MEDLINE
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  Data: A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders.
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  Data: <searchLink fieldCode="AU" term="%22Ben-Mahmoud+A%22">Ben-Mahmoud A</searchLink>; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.<br /><searchLink fieldCode="AU" term="%22Jun+KR%22">Jun KR</searchLink>; Department of Laboratory Medicine, Inje University Haeundae Paik Hospital, Busan, South Korea.<br /><searchLink fieldCode="AU" term="%22Gupta+V%22">Gupta V</searchLink>; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.<br /><searchLink fieldCode="AU" term="%22Shastri+P%22">Shastri P</searchLink>; Department of Cardiovascular Medicine, Cape Fear Valley Medical Center, Fayetteville, NC, United States.<br /><searchLink fieldCode="AU" term="%22de+la+Fuente+A%22">de la Fuente A</searchLink>; Diabetes Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.<br /><searchLink fieldCode="AU" term="%22Park+Y%22">Park Y</searchLink>; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.<br /><searchLink fieldCode="AU" term="%22Shin+KC%22">Shin KC</searchLink>; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.<br /><searchLink fieldCode="AU" term="%22Kim+CA%22">Kim CA</searchLink>; Faculdade de Medicina, Unidade de Genética do Instituto da Criança - Hospital das Clínicas HCFMUSP, Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22da+Cruz+AD%22">da Cruz AD</searchLink>; School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.; Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil.<br /><searchLink fieldCode="AU" term="%22Pinto+IP%22">Pinto IP</searchLink>; School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.; Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil.<br /><searchLink fieldCode="AU" term="%22Minasi+LB%22">Minasi LB</searchLink>; School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.; Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil.<br /><searchLink fieldCode="AU" term="%22Silva+da+Cruz+A%22">Silva da Cruz A</searchLink>; School of Medical and Life Sciences, Genetics Master Program, Replicon Research Group, Pontifical Catholic University of Goiás, Goiânia, Brazil.; Genetics Master Program, Replicon Research Nucleus, School of Agrarian and Biological Sciences, Pontifical Catholic University of Goias, Goiás, Brazil.<br /><searchLink fieldCode="AU" term="%22Faivre+L%22">Faivre L</searchLink>; Inserm UMR 1231 GAD, Genetics of Developmental Disorders, Université de Bourgogne-Franche Comté, Dijon, France.; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Hôpital d'Enfants, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Callier+P%22">Callier P</searchLink>; UMR 1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Racine+C%22">Racine C</searchLink>; UMR 1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Layman+LC%22">Layman LC</searchLink>; Section of Reproductive Endocrinology, Infertility and Genetics, Department of Obstetrics and Gynecology, Augusta University, Augusta, GA, United States.; Department of Neuroscience and Regenerative Medicine, Augusta University, Augusta, GA, United States.<br /><searchLink fieldCode="AU" term="%22Kong+IK%22">Kong IK</searchLink>; Department of Animal Science, Division of Applied Life Science (BK21 Four), Gyeongsang National University, Jinju, South Korea.<br /><searchLink fieldCode="AU" term="%22Kim+CH%22">Kim CH</searchLink>; Department of Biology, Chungnam National University, Daejeon, South Korea.<br /><searchLink fieldCode="AU" term="%22Kim+WY%22">Kim WY</searchLink>; Department of Biological Sciences, Kent State University, Kent, OH, United States.<br /><searchLink fieldCode="AU" term="%22Kim+HG%22">Kim HG</searchLink>; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
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  Data: <searchLink fieldCode="JN" term="%22101477914%22">Frontiers in molecular neuroscience</searchLink> [Front Mol Neurosci] 2022 Oct 06; Vol. 15, pp. 979061. <i>Date of Electronic Publication: </i>2022 Oct 06 (<i>Print Publication: </i>2022).
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