Crossmark

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

Crossref DOI link: https://doi.org/10.1186/s13229-025-00681-1

Published Online: 2025-10-11

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

McGhee, Chloe Alexa https://orcid.org/0000-0002-6357-9721
Plank, Julia R. https://orcid.org/0009-0008-5929-0651
Pannone, Luca https://orcid.org/0000-0001-7027-8196
Russo, Odeya

Fuhrmann, Naomi

Ruggeri, Aurora

Radio, Francesca Clementina https://orcid.org/0000-0003-1993-8018
Martinelli, Simone https://orcid.org/0000-0002-5843-419X
Tartaglia, Marco https://orcid.org/0000-0001-7736-9672
Green, Tamar https://orcid.org/0000-0001-5661-8297
Funding

Funding for this research was provided by:

Associazione Italiana per la Ricerca sul Cancro (IG 28768)

National Institute of Child Health and Human Development (123752K23)

Neurofibromatosis Therapeutic Acceleration Program

Stanford Maternal and Child Health Research Institute
License Information

Text and Data Mining valid from 2025-10-11

Version of Record valid from 2025-10-11
More Information

Article History

Received: 26 April 2025

Accepted: 22 August 2025

First Online: 11 October 2025

Declarations

:

: This study was approved by the Stanford University School of Medicine's Institutional Review Board. All procedures involving human participants follow the institutional/national committees and the Helsinki Declaration of 1975, as revised in 2008. Informed consent was obtained from all participants included in this study. Consent for publication Written informed consent for publication was obtained from all participants (or their legal guardians).

: The authors declare no competing interests.

Document is current

Any future updates will be listed below