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Genotype-phenotype correlations with autism spectrum disorder-related traits in noonan syndrome and noonan syndrome with multiple lentigines: a cross-sectional study.

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Title: Genotype-phenotype correlations with autism spectrum disorder-related traits in noonan syndrome and noonan syndrome with multiple lentigines: a cross-sectional study.
Authors: McGhee CA; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA. camcghee@stanford.edu., Plank JR; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA., Pannone L; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Department of Oncology and Molecular Medicine, Istituto Superiore Di Sanità, Rome, Italy., Russo O; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA., Fuhrmann N; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA., Ruggeri A; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Radio FC; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Martinelli S; Department of Oncology and Molecular Medicine, Istituto Superiore Di Sanità, Rome, Italy., Tartaglia M; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Green T; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA.
Source: Molecular autism [Mol Autism] 2025 Oct 11; Vol. 16 (1), pp. 51. Date of Electronic Publication: 2025 Oct 11.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101534222 Publication Model: Electronic Cited Medium: Internet ISSN: 2040-2392 (Electronic) NLM ISO Abbreviation: Mol Autism Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Genotype-phenotype correlations with autism spectrum disorder-related traits in noonan syndrome and noonan syndrome with multiple lentigines: a cross-sectional study.
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  Data: <searchLink fieldCode="AU" term="%22McGhee+CA%22">McGhee CA</searchLink>; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA. camcghee@stanford.edu.<br /><searchLink fieldCode="AU" term="%22Plank+JR%22">Plank JR</searchLink>; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA.<br /><searchLink fieldCode="AU" term="%22Pannone+L%22">Pannone L</searchLink>; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.; Department of Oncology and Molecular Medicine, Istituto Superiore Di Sanità, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Russo+O%22">Russo O</searchLink>; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA.<br /><searchLink fieldCode="AU" term="%22Fuhrmann+N%22">Fuhrmann N</searchLink>; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA.<br /><searchLink fieldCode="AU" term="%22Ruggeri+A%22">Ruggeri A</searchLink>; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Radio+FC%22">Radio FC</searchLink>; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Martinelli+S%22">Martinelli S</searchLink>; Department of Oncology and Molecular Medicine, Istituto Superiore Di Sanità, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Tartaglia+M%22">Tartaglia M</searchLink>; Molecular Genetics and Functional Genomics Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Green+T%22">Green T</searchLink>; Department of Psychiatry & Behavioral Sciences, Stanford University, Stanford, USA.
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  Data: <searchLink fieldCode="JN" term="%22101534222%22">Molecular autism</searchLink> [Mol Autism] 2025 Oct 11; Vol. 16 (1), pp. 51. <i>Date of Electronic Publication: </i>2025 Oct 11.
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  Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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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>101534222 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2040-2392 (Electronic) <i>NLM ISO Abbreviation: </i>Mol Autism <i>Subsets: </i>MEDLINE
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              Text: 2025 Oct 11
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