PubMed for id: 769787

Year	Number of Results
2017	63
2018	83
2019	87
2020	97
2021	107
2022	85
2023	76

1

The impact of placental genomic risk for schizophrenia and birth asphyxia on brain development.

Wortinger LA, Shadrin AA, Szabo A, Nerland S, Smelror RE, Jørgensen KN, Barth C, Andreou D, Thoresen M, Andreassen OA, Djurovic S, Ursini G, Agartz I. Wortinger LA, et al. Transl Psychiatry. 2023 Nov 8;13(1):343. doi: 10.1038/s41398-023-02639-4. Transl Psychiatry. 2023. PMID: 37938559 Free PMC article.

2

Compound heterozygous mutations in the helicase RTEL1 causing Hoyeraal-Hreidarsson syndrome with Blake`s pouch cyst: a case report.

He M, Lian G, Hu H, He H, Wang M. He M, et al. Turk J Pediatr. 2023;65(5):845-852. doi: 10.24953/turkjped.2022.344. Turk J Pediatr. 2023. PMID: 37853975 Free article.

3

Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene.

Fernandez TV, Williams ZP, Kline T, Rajendran S, Augustine F, Wright N, Sullivan CAW, Olfson E, Abdallah SB, Liu W, Hoffman EJ, Gupta AR, Singer HS. Fernandez TV, et al. PLoS One. 2023 Oct 3;18(10):e0291978. doi: 10.1371/journal.pone.0291978. eCollection 2023. PLoS One. 2023. PMID: 37788244 Free PMC article.

4

Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex.

Salamon I, Park Y, Miškić T, Kopić J, Matteson P, Page NF, Roque A, McAuliffe GW, Favate J, Garcia-Forn M, Shah P, Judaš M, Millonig JH, Kostović I, De Rubeis S, Hart RP, Krsnik Ž, Rasin MR. Salamon I, et al. Nat Commun. 2023 Sep 27;14(1):6025. doi: 10.1038/s41467-023-41730-8. Nat Commun. 2023. PMID: 37758766 Free PMC article.

5

Abnormal fetal ultrasound leading to the diagnosis of ADNP syndrome.

Rosenblum J, Van der Veeken L, Aertsen M, Meuwissen M, Jansen AC. Rosenblum J, et al. Eur J Med Genet. 2023 Nov;66(11):104855. doi: 10.1016/j.ejmg.2023.104855. Epub 2023 Sep 25. Eur J Med Genet. 2023. PMID: 37758165

6

Prenatal Alcohol Exposure Impairs the Placenta-Cortex Transcriptomic Signature, Leading to Dysregulation of Angiogenic Pathways.

Sautreuil C, Lecointre M, Derambure C, Brasse-Lagnel C, Leroux P, Laquerrière A, Nicolas G, Gil S, Savage DD, Marret S, Marguet F, Falluel-Morel A, Gonzalez BJ. Sautreuil C, et al. Int J Mol Sci. 2023 Aug 30;24(17):13484. doi: 10.3390/ijms241713484. Int J Mol Sci. 2023. PMID: 37686296 Free PMC article.

7

Epigenetics of Trauma Transmission and Fetal Alcohol Spectrum Disorder: What Does the Evidence Support?

Orton SM, Millis K, Choate P. Orton SM, et al. Int J Environ Res Public Health. 2023 Sep 3;20(17):6706. doi: 10.3390/ijerph20176706. Int J Environ Res Public Health. 2023. PMID: 37681846 Free PMC article. Review.

8

Transcript levels of 4 genes in umbilical cord blood are predictive of later autism development: a longitudinal follow-up study.

Jia Q, Li H, Wang M, Wei C, Xu L, Ye L, Wang C, Ke S, Li L, Yao P. Jia Q, et al. J Psychiatry Neurosci. 2023 Sep 6;48(5):E334-E344. doi: 10.1503/jpn.230046. Print 2023 Sep-Oct. J Psychiatry Neurosci. 2023. PMID: 37673435 Free PMC article.

9

Are CUL3 variants an underreported cause of congenital heart disease?

Di Francesco D, Swenerton A, Li WL, Dunham C, Hendson G, Boerkoel CF. Di Francesco D, et al. Am J Med Genet A. 2023 Dec;191(12):2903-2907. doi: 10.1002/ajmg.a.63387. Epub 2023 Sep 4. Am J Med Genet A. 2023. PMID: 37665043

10

Prenatal diagnosis of lanosterol synthase deficiency: Fetal ultrasound findings as a window on family genetics.

Matza Porges S, Mor-Shaked H, Shaag A, Porat S, Daum H. Matza Porges S, et al. Eur J Med Genet. 2023 Oct;66(10):104825. doi: 10.1016/j.ejmg.2023.104825. Epub 2023 Sep 1. Eur J Med Genet. 2023. PMID: 37659595

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