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Year Number of Results
2020 39
2021 156
2022 139
2023 146
2024 85

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PubMed for id: 410155

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Page 1
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure.
Summers J, Baribeau D, Perlman P, Hoang N, Cui S, Krakowski A, Ambrozewicz P, Ho A, Selvanayagam T, Sándor-Bajusz KA, Palad K, Patel N, McGaughey S, Gallagher L, Scherer SW, Szatmari P, Vorstman J. Summers J, et al. J Neurodev Disord. 2024 Jul 5;16(1):37. doi: 10.1186/s11689-024-09552-x. J Neurodev Disord. 2024. PMID: 38970057 Free PMC article.
Evolutionary and biomedical implications of sex differences in the primate brain transcriptome.
DeCasien AR, Chiou KL, Testard C, Mercer A, Negrón-Del Valle JE, Bauman Surratt SE, González O, Stock MK, Ruiz-Lambides AV, Martínez MI; Cayo Biobank Research Unit; Antón SC, Walker CS, Sallet J, Wilson MA, Brent LJN, Montague MJ, Sherwood CC, Platt ML, Higham JP, Snyder-Mackler N. DeCasien AR, et al. Cell Genom. 2024 Jul 10;4(7):100589. doi: 10.1016/j.xgen.2024.100589. Epub 2024 Jun 27. Cell Genom. 2024. PMID: 38942023 Free article.
Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes.
Heimdörfer D, Vorleuter A, Eschlböck A, Spathopoulou A, Suarez-Cubero M, Farhan H, Reiterer V, Spanjaard M, Schaaf CP, Huber LA, Kremser L, Sarg B, Edenhofer F, Geley S, de Araujo MEG, Huettenhofer A. Heimdörfer D, et al. Am J Hum Genet. 2024 Jul 11;111(7):1383-1404. doi: 10.1016/j.ajhg.2024.05.023. Epub 2024 Jun 21. Am J Hum Genet. 2024. PMID: 38908375 Free article.
500 results