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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 1
2012 1
2014 1
2015 1
2016 3
2019 3
2020 4
2021 6
2022 5
2023 0
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Page 1
Imputing cognitive impairment in SPARK, a large autism cohort.
Shu C, Green Snyder L, Shen Y, Chung WK; SPARK Consortium. Shu C, et al. Among authors: green snyder l. Autism Res. 2022 Jan;15(1):156-170. doi: 10.1002/aur.2622. Epub 2021 Oct 11. Autism Res. 2022. PMID: 34636158
Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication.
Linden SC, Watson CJ, Smith J, Chawner SJRA, Lancaster TM, Evans F, Williams N, Skuse D, Raymond FL, Hall J, Owen MJ, Linden DEJ, Green-Snyder L, Chung WK, Maillard AM, Jacquemont S, van den Bree MBM. Linden SC, et al. Among authors: green snyder l. Transl Psychiatry. 2021 Jun 18;11(1):372. doi: 10.1038/s41398-021-01296-9. Transl Psychiatry. 2021. PMID: 34226486 Free PMC article. No abstract available.
Psychotic symptoms in 16p11.2 copy-number variant carriers.
Jutla A, Turner JB, Green Snyder L, Chung WK, Veenstra-VanderWeele J. Jutla A, et al. Among authors: green snyder l. Autism Res. 2020 Feb;13(2):187-198. doi: 10.1002/aur.2232. Epub 2019 Nov 14. Autism Res. 2020. PMID: 31724820
The psychiatric phenotypes of 1q21 distal deletion and duplication.
Linden SC, Watson CJ, Smith J, Chawner SJRA, Lancaster TM, Evans F, Williams N, Skuse D, Raymond FL, Hall J, Owen MJ, Linden DEJ, Green-Snyder L, Chung WK, Maillard AM, Jacquemont S, van den Bree MBM. Linden SC, et al. Among authors: green snyder l. Transl Psychiatry. 2021 Feb 4;11(1):105. doi: 10.1038/s41398-021-01226-9. Transl Psychiatry. 2021. PMID: 33542195 Free PMC article.
Language characterization in 16p11.2 deletion and duplication syndromes.
Kim SH, Green-Snyder L, Lord C, Bishop S, Steinman KJ, Bernier R, Hanson E, Goin-Kochel RP, Chung WK. Kim SH, et al. Among authors: green snyder l. Am J Med Genet B Neuropsychiatr Genet. 2020 Sep;183(6):380-391. doi: 10.1002/ajmg.b.32809. Epub 2020 Jul 11. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 32652891 Free PMC article.
Clinical Characteristics of Seizures and Epilepsy in Individuals With Recurrent Deletions and Duplications in the 16p11.2 Region.
Moufawad El Achkar C, Rosen A, Kessler SK, Steinman KJ, Spence SJ, Ramocki M, Marco EJ, Green Snyder L, Spiro JE, Chung WK, Annapurna P, Sherr EH. Moufawad El Achkar C, et al. Among authors: green snyder l. Neurol Genet. 2022 Aug 5;8(5):e200018. doi: 10.1212/NXG.0000000000200018. eCollection 2022 Oct. Neurol Genet. 2022. PMID: 36531974 Free PMC article.
20 results