R01 MH107431/MH/NIMH NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2017	4
2018	2
2019	3
2020	4
2021	5
2022	3
2023	2
2024	0

1

Genetic Testing in Neurodevelopmental Disorders.

Savatt JM, Myers SM. Savatt JM, et al. Front Pediatr. 2021 Feb 19;9:526779. doi: 10.3389/fped.2021.526779. eCollection 2021. Front Pediatr. 2021. PMID: 33681094 Free PMC article. Review.

2

Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy.

Moreno-De-Luca A, Millan F, Pesacreta DR, Elloumi HZ, Oetjens MT, Teigen C, Wain KE, Scuffins J, Myers SM, Torene RI, Gainullin VG, Arvai K, Kirchner HL, Ledbetter DH, Retterer K, Martin CL. Moreno-De-Luca A, et al. JAMA. 2021 Feb 2;325(5):467-475. doi: 10.1001/jama.2020.26148. JAMA. 2021. PMID: 33528536 Free PMC article.

3

Insufficient Evidence for "Autism-Specific" Genes.

Myers SM, Challman TD, Bernier R, Bourgeron T, Chung WK, Constantino JN, Eichler EE, Jacquemont S, Miller DT, Mitchell KJ, Zoghbi HY, Martin CL, Ledbetter DH. Myers SM, et al. Am J Hum Genet. 2020 May 7;106(5):587-595. doi: 10.1016/j.ajhg.2020.04.004. Epub 2020 Apr 30. Am J Hum Genet. 2020. PMID: 32359473 Free PMC article. Review.

4

Long overdue: including adults with brain disorders in precision health initiatives.

Finucane BM, Myers SM, Martin CL, Ledbetter DH. Finucane BM, et al. Curr Opin Genet Dev. 2020 Dec;65:47-52. doi: 10.1016/j.gde.2020.05.001. Epub 2020 Jun 13. Curr Opin Genet Dev. 2020. PMID: 32544666 Free PMC article. Review.

5

Editorial: Taking the Next Step Towards Validating Social Processes From the Research Domain Criteria.

Wallace GL, Yerys BE. Wallace GL, et al. J Am Acad Child Adolesc Psychiatry. 2020 Nov;59(11):1212-1214. doi: 10.1016/j.jaac.2019.11.027. Epub 2020 Jun 15. J Am Acad Child Adolesc Psychiatry. 2020. PMID: 32553786

6

All for one and one for all: heterogeneity of genetic etiologies in neurodevelopmental psychiatric disorders.

Moreno-De-Luca D, Martin CL. Moreno-De-Luca D, et al. Curr Opin Genet Dev. 2021 Jun;68:71-78. doi: 10.1016/j.gde.2021.02.015. Epub 2021 Mar 25. Curr Opin Genet Dev. 2021. PMID: 33773394 Free PMC article. Review.

7

Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome.

Taylor CM, Finucane BM, Moreno-De-Luca A, Walsh LK, Martin CL, Ledbetter DH. Taylor CM, et al. Genet Med. 2023 Jan;25(1):151-154. doi: 10.1016/j.gim.2022.09.011. Epub 2022 Nov 6. Genet Med. 2023. PMID: 36609147 Free PMC article.

8

Missing heritability and where to find it.

Girirajan S. Girirajan S. Genome Biol. 2017 May 11;18(1):89. doi: 10.1186/s13059-017-1227-x. Genome Biol. 2017. PMID: 28494787 Free PMC article.

9

Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.

Martin CL, Wain KE, Oetjens MT, Tolwinski K, Palen E, Hare-Harris A, Habegger L, Maxwell EK, Reid JG, Walsh LK, Myers SM, Ledbetter DH. Martin CL, et al. JAMA Psychiatry. 2020 Dec 1;77(12):1276-1285. doi: 10.1001/jamapsychiatry.2020.2159. JAMA Psychiatry. 2020. PMID: 32697297 Free PMC article.

10

Birt-Hogg-Dubé symptoms in Smith-Magenis syndrome include pediatric-onset pneumothorax.

Finucane B, Savatt JM, Shimelis H, Girirajan S, Myers SM. Finucane B, et al. Am J Med Genet A. 2021 Jun;185(6):1922-1924. doi: 10.1002/ajmg.a.62159. Epub 2021 Mar 5. Am J Med Genet A. 2021. PMID: 33666332 Free PMC article. No abstract available.

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