R01 HD083181/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2016	1
2017	1
2020	2
2021	1
2022	2
2023	4
2024	1

1

Genetic rodent models of brain disorders: Perspectives on experimental approaches and therapeutic strategies.

McGraw CM, Ward CS, Samaco RC. McGraw CM, et al. Am J Med Genet C Semin Med Genet. 2017 Sep;175(3):368-379. doi: 10.1002/ajmg.c.31570. Am J Med Genet C Semin Med Genet. 2017. PMID: 28910526 Free PMC article. Review.

2

Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study.

Neul JL, Benke TA, Marsh ED, Suter B, Silveira L, Fu C, Peters SU, Percy AK; Rett syndrome Natural History Study Group. Neul JL, et al. J Neurodev Disord. 2023 Oct 13;15(1):33. doi: 10.1186/s11689-023-09502-z. J Neurodev Disord. 2023. PMID: 37833681 Free PMC article.

3

Top Caregiver Concerns in Rett syndrome and related disorders: data from the US Natural History Study.

Neul JL, Benke TA, Marsh ED, Suter B, Silveira L, Fu C, Peters SU, Percy AK; Rett syndrome Natural History Study Group. Neul JL, et al. Res Sq [Preprint]. 2023 Mar 20:rs.3.rs-2566253. doi: 10.21203/rs.3.rs-2566253/v1. Res Sq. 2023. PMID: 36993737 Free PMC article. Updated. Preprint.

4

Behavioral and brain anatomical analysis of Foxg1 heterozygous mice.

Erickson KR, Farmer R, Merritt JK, Miletic Lanaghan Z, Does MD, Ramadass K, Landman BA, Cutting LE, Neul JL. Erickson KR, et al. PLoS One. 2022 Oct 12;17(10):e0266861. doi: 10.1371/journal.pone.0266861. eCollection 2022. PLoS One. 2022. PMID: 36223387 Free PMC article.

5

Detection of neurophysiological features in female R255X MeCP2 mutation mice.

Dong HW, Erickson K, Lee JR, Merritt J, Fu C, Neul JL. Dong HW, et al. Neurobiol Dis. 2020 Nov;145:105083. doi: 10.1016/j.nbd.2020.105083. Epub 2020 Sep 12. Neurobiol Dis. 2020. PMID: 32927061 Free PMC article.

6

Magel2 truncation alters select behavioral and physiological outcomes in a rat model of Schaaf-Yang syndrome.

Reznik DL, Yang MV, Albelda de la Haza P, Jain A, Spanjaard M, Theiss S, Schaaf CP, Malovannaya A, Strong TV, Veeraragavan S, Samaco RC. Reznik DL, et al. Dis Model Mech. 2023 Feb 1;16(2):dmm049829. doi: 10.1242/dmm.049829. Epub 2023 Feb 3. Dis Model Mech. 2023. PMID: 36637363 Free PMC article.

7

Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndrome.

Collins BE, Merritt JK, Erickson KR, Neul JL. Collins BE, et al. Genes Brain Behav. 2022 Jan;21(1):e12739. doi: 10.1111/gbb.12739. Epub 2021 May 19. Genes Brain Behav. 2022. PMID: 33942492 Free PMC article.

8

Distribution of hand function by age in individuals with Rett syndrome.

Neul JL, Benke TA, Marsh ED, Lane JB, Lieberman DN, Skinner SA, Glaze DG, Suter B, Heydemann PT, Beisang AA, Standridge SM, Ryther RCC, Haas RH, Edwards LJ, Ananth A, Percy AK. Neul JL, et al. Ann Child Neurol Soc. 2023 Sep;1(3):228-238. doi: 10.1002/cns3.20038. Epub 2023 Sep 12. Ann Child Neurol Soc. 2023. PMID: 38496825

9

Rett syndrome diagnostic odyssey: Limitations of NextGen sequencing.

Abbott M, Angione K, Forbes E, Stoecker M, Saenz M, Neul JL, Marsh ED, Skinner SA, Percy AK, Benke TA. Abbott M, et al. Am J Med Genet A. 2024 May 22:e63725. doi: 10.1002/ajmg.a.63725. Online ahead of print. Am J Med Genet A. 2024. PMID: 38775384

10

Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndrome.

Merritt JK, Collins BE, Erickson KR, Dong H, Neul JL. Merritt JK, et al. Hum Mol Genet. 2020 Aug 29;29(15):2461-2470. doi: 10.1093/hmg/ddaa102. Hum Mol Genet. 2020. PMID: 32469049 Free PMC article.

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