R01 HD042974/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2004	1
2005	3
2006	2
2007	7
2008	7
2009	3
2010	6
2011	4
2012	6
2013	2
2014	8
2015	5
2017	2
2018	3
2019	2
2020	2
2021	3
2022	2
2023	1
2024	0

1

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.

Karayiorgou M, Simon TJ, Gogos JA. Karayiorgou M, et al. Nat Rev Neurosci. 2010 Jun;11(6):402-16. doi: 10.1038/nrn2841. Nat Rev Neurosci. 2010. PMID: 20485365 Free PMC article. Review.

2

Rewards and challenges of cognitive neuroscience studies of persons with intellectual and developmental disabilities.

Simon TJ. Simon TJ. Am J Intellect Dev Disabil. 2010 Mar;115(2):79-82. doi: 10.1352/1944-7558-115.2.79. Am J Intellect Dev Disabil. 2010. PMID: 20441387 No abstract available.

3

The Alzheimer's Disease Neuroimaging Initiative phase 2: Increasing the length, breadth, and depth of our understanding.

Beckett LA, Donohue MC, Wang C, Aisen P, Harvey DJ, Saito N; Alzheimer's Disease Neuroimaging Initiative. Beckett LA, et al. Alzheimers Dement. 2015 Jul;11(7):823-31. doi: 10.1016/j.jalz.2015.05.004. Alzheimers Dement. 2015. PMID: 26194315 Free PMC article. Review.

4

Cognitive characteristics of children with genetic syndromes.

Simon TJ. Simon TJ. Child Adolesc Psychiatr Clin N Am. 2007 Jul;16(3):599-616. doi: 10.1016/j.chc.2007.03.002. Child Adolesc Psychiatr Clin N Am. 2007. PMID: 17562581 Free PMC article. Review.

5

A Health-Literacy Intervention for Early Childhood Obesity Prevention: A Cluster-Randomized Controlled Trial.

Sanders LM, Perrin EM, Yin HS, Delamater AM, Flower KB, Bian A, Schildcrout JS, Rothman RL; Greenlight Study Team. Sanders LM, et al. Pediatrics. 2021 May;147(5):e2020049866. doi: 10.1542/peds.2020-049866. Pediatrics. 2021. PMID: 33911032 Free PMC article. Clinical Trial.

6

A new account of the neurocognitive foundations of impairments in space, time and number processing in children with chromosome 22q11.2 deletion syndrome.

Simon TJ. Simon TJ. Dev Disabil Res Rev. 2008;14(1):52-8. doi: 10.1002/ddrr.8. Dev Disabil Res Rev. 2008. PMID: 18612330 Free PMC article. Review.

7

Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome.

Deng Y, Goodrich-Hunsaker NJ, Cabaral M, Amaral DG, Buonocore MH, Harvey D, Kalish K, Carmichael OT, Schumann CM, Lee A, Dougherty RF, Perry LM, Wandell BA, Simon TJ. Deng Y, et al. Psychiatry Res. 2015 Apr 30;232(1):106-14. doi: 10.1016/j.pscychresns.2015.02.002. Epub 2015 Feb 11. Psychiatry Res. 2015. PMID: 25748884 Free PMC article.

8

Decreased DGCR8 expression and miRNA dysregulation in individuals with 22q11.2 deletion syndrome.

Sellier C, Hwang VJ, Dandekar R, Durbin-Johnson B, Charlet-Berguerand N, Ander BP, Sharp FR, Angkustsiri K, Simon TJ, Tassone F. Sellier C, et al. PLoS One. 2014 Aug 1;9(8):e103884. doi: 10.1371/journal.pone.0103884. eCollection 2014. PLoS One. 2014. PMID: 25084529 Free PMC article.

9

Registration based cortical thickness measurement.

Das SR, Avants BB, Grossman M, Gee JC. Das SR, et al. Neuroimage. 2009 Apr 15;45(3):867-79. doi: 10.1016/j.neuroimage.2008.12.016. Epub 2008 Dec 25. Neuroimage. 2009. PMID: 19150502 Free PMC article.

10

Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implications.

Howell S, Buchanan C, Davis SM, Miyazawa H, Furuta GT, Tartaglia NR, Nguyen N. Howell S, et al. Mol Genet Genomic Med. 2021 Dec;9(12):e1833. doi: 10.1002/mgg3.1833. Epub 2021 Nov 5. Mol Genet Genomic Med. 2021. PMID: 34738344 Free PMC article.

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