Zohn IE - Search Results

1

Identification and functional analysis of rare HECTD1 missense variants in human neural tube defects.

Oxman E, Li H, Wang HY, Zohn IE. Oxman E, et al. Among authors: zohn ie. Hum Genet. 2024 Mar;143(3):263-277. doi: 10.1007/s00439-024-02647-4. Epub 2024 Mar 7. Hum Genet. 2024. PMID: 38451291 Free PMC article.

2

Parental obesity-induced changes in developmental programming.

Cechinel LR, Batabyal RA, Freishtat RJ, Zohn IE. Cechinel LR, et al. Among authors: zohn ie. Front Cell Dev Biol. 2022 Oct 7;10:918080. doi: 10.3389/fcell.2022.918080. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36274855 Free PMC article. Review.

3

ALDH1A2-related disorder: A new genetic syndrome due to alteration of the retinoic acid pathway.

Leon E, Nde C, Ray RS, Preciado D, Zohn IE. Leon E, et al. Among authors: zohn ie. Am J Med Genet A. 2023 Jan;191(1):90-99. doi: 10.1002/ajmg.a.62991. Epub 2022 Oct 19. Am J Med Genet A. 2023. PMID: 36263470 Free PMC article.

4

Model organisms and mechanisms of gene-environment interactions in structural birth defects.

Zohn IE. Zohn IE. Genesis. 2021 Nov;59(11):e23461. doi: 10.1002/dvg.23461. Epub 2021 Nov 5. Genesis. 2021. PMID: 34739742 No abstract available.

5

Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome.

Yitsege G, Stokes BA, Sabatino JA, Sugrue KF, Banyai G, Paronett EM, Karpinski BA, Maynard TM, LaMantia AS, Zohn IE. Yitsege G, et al. Among authors: zohn ie. Birth Defects Res. 2020 Oct;112(16):1194-1208. doi: 10.1002/bdr2.1709. Epub 2020 May 20. Birth Defects Res. 2020. PMID: 32431076 Free PMC article.

6

Mouse Models of Neural Tube Defects.

Zohn IE. Zohn IE. Adv Exp Med Biol. 2020;1236:39-64. doi: 10.1007/978-981-15-2389-2_2. Adv Exp Med Biol. 2020. PMID: 32304068 Review.

7

Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology.

Maynard TM, Zohn IE, Moody SA, LaMantia AS. Maynard TM, et al. Among authors: zohn ie. Annu Rev Neurosci. 2020 Jul 8;43:315-336. doi: 10.1146/annurev-neuro-100419-100636. Epub 2020 Feb 26. Annu Rev Neurosci. 2020. PMID: 32101484 Free PMC article. Review.

8

Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome.

Welby L, Caudill H, Yitsege G, Hamad A, Bunyak F, Zohn IE, Maynard T, LaMantia AS, Mendelowitz D, Lever TE. Welby L, et al. Among authors: zohn ie. Front Neurol. 2020 Jan 31;11:4. doi: 10.3389/fneur.2020.00004. eCollection 2020. Front Neurol. 2020. PMID: 32082240 Free PMC article.

9

Hsp90 and complex birth defects: A plausible mechanism for the interaction of genes and environment.

Zohn IE. Zohn IE. Neurosci Lett. 2020 Jan 18;716:134680. doi: 10.1016/j.neulet.2019.134680. Epub 2019 Dec 9. Neurosci Lett. 2020. PMID: 31821846 Free PMC article. Review.

10

Reduced maternal vitamin A status increases the incidence of normal aortic arch variants.

Sugrue KF, Zohn IE. Sugrue KF, et al. Among authors: zohn ie. Genesis. 2019 Nov;57(11-12):e23343. doi: 10.1002/dvg.23343. Epub 2019 Nov 4. Genesis. 2019. PMID: 31682315 No abstract available.

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