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Read about Simons Searchlight’s commitment to data privacy and security.

Publications

Date Revised: December 2025

Thank you to all the families for participating in Simons Searchlight. Through your involvement, we aim to assist researchers and geneticists worldwide in understanding genetic disorders affecting you or your family.

The research conducted using Simons Searchlight data has resulted in numerous published papers. These papers undergo a peer-review process, where other scientists assess and validate the research before publication in scientific journals. Additionally, some findings are shared via preprints, allowing rapid dissemination of information to the scientific community.

Many of the publications feature the name “Simons Variation in Individuals Project” (SimonsVIP), which was the original name of our research program, now known as Simons Searchlight.

The listed articles are organized from newest to oldest. You can explore publications by specific genetic conditions using the categories below.

As of December 2025, Simons Searchlight has contributed to 135 publications and preprints, and we will continue to summarize new publications.

For accessibility, the Simons Foundation encourages researchers to make their publications open access. If you cannot access a journal article, we recommend reaching out to the last author listed on the paper to request a copy.

Understanding Publication Reference Titles:

-The article title is followed by publication details, including where and when it was published.
– If there are more than three authors, we use “et al.” to represent additional contributors.
– Journals are referenced using shorthand names.

Disclaimer: Please be aware that papers posted on medRxiv (pronounced med-archive) or bioRxiv (pronounced bio-archive) are not peer-reviewed or edited before online publication. In contrast, all other articles listed here have undergone review by fellow researchers to ensure quality and accuracy. While posting on medRxiv or bioRxiv allows researchers to share findings quickly, the final published results may differ after undergoing formal peer review for journal publication.

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Genetic Condition
Year of Publication
134 Publications
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders
  • People registered in Simons VIP and from European research projects carrying the 16p11.2 deletion, were tested for their mental abilities, given behavioral questionnaires and had medical data collected. Show More
  • Researchers found that 16p11.2 deletion carriers are more likely to have a lower IQ, a higher incidence of psychiatric diagnoses and suffer from obesity, as compared to their family members without this deletion. Show Less
J Med Genet 49, 660-668 (2012)
Zufferey et al.

16p11.2 deletion
2012