Howard TD - Search Results

1

Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.

Shashi V, Keshavan MS, Howard TD, Berry MN, Basehore MJ, Lewandowski E, Kwapil TR. Shashi V, et al. Among authors: howard td. Clin Genet. 2006 Mar;69(3):234-8. doi: 10.1111/j.1399-0004.2006.00569.x. Clin Genet. 2006. PMID: 16542388

2

Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.

Shashi V, Kwapil TR, Kaczorowski J, Berry MN, Santos CS, Howard TD, Goradia D, Prasad K, Vaibhav D, Rajarethinam R, Spence E, Keshavan MS. Shashi V, et al. Among authors: howard td. Psychiatry Res. 2010 Jan 30;181(1):1-8. doi: 10.1016/j.pscychresns.2009.07.003. Psychiatry Res. 2010. PMID: 19962860 Free PMC article.

3

COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.

Shashi V, Howard TD, Keshavan MS, Kaczorowski J, Berry MN, Schoch K, Spence EJ, Kwapil TR. Shashi V, et al. Among authors: howard td. Psychiatry Res. 2010 Jul 30;178(2):433-6. doi: 10.1016/j.psychres.2010.04.048. Epub 2010 May 20. Psychiatry Res. 2010. PMID: 20488547 Free PMC article.

4

Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.

Shashi V, Francis A, Hooper SR, Kranz PG, Zapadka M, Schoch K, Ip E, Tandon N, Howard TD, Keshavan MS. Shashi V, et al. Among authors: howard td. Eur J Hum Genet. 2012 Oct;20(10):1051-7. doi: 10.1038/ejhg.2012.138. Epub 2012 Jun 27. Eur J Hum Genet. 2012. PMID: 22763378 Free PMC article.

5

Dysregulation of DGCR6 and DGCR6L: psychopathological outcomes in chromosome 22q11.2 deletion syndrome.

Das Chakraborty R, Bernal AJ, Schoch K, Howard TD, Ip EH, Hooper SR, Keshavan MS, Jirtle RL, Shashi V. Das Chakraborty R, et al. Among authors: howard td. Transl Psychiatry. 2012 Apr 24;2(4):e105. doi: 10.1038/tp.2012.31. Transl Psychiatry. 2012. PMID: 22832905 Free PMC article.

6

The RBMX gene as a candidate for the Shashi X-linked intellectual disability syndrome.

Shashi V, Xie P, Schoch K, Goldstein DB, Howard TD, Berry MN, Schwartz CE, Cronin K, Sliwa S, Allen A, Need AC. Shashi V, et al. Among authors: howard td. Clin Genet. 2015 Oct;88(4):386-90. doi: 10.1111/cge.12511. Epub 2014 Dec 5. Clin Genet. 2015. PMID: 25256757 Free article.

7

Effects of early- and mid-life stress on DNA methylation of genes associated with subclinical cardiovascular disease and cognitive impairment: a systematic review.

Vidrascu EM, Bashore AC, Howard TD, Moore JB. Vidrascu EM, et al. Among authors: howard td. BMC Med Genet. 2019 Mar 12;20(1):39. doi: 10.1186/s12881-019-0764-4. BMC Med Genet. 2019. PMID: 30866842 Free PMC article.

8

Germline BAP1 Mutational Landscape of Asbestos-Exposed Malignant Mesothelioma Patients with Family History of Cancer.

Ohar JA, Cheung M, Talarchek J, Howard SE, Howard TD, Hesdorffer M, Peng H, Rauscher FJ, Testa JR. Ohar JA, et al. Among authors: howard se, howard td. Cancer Res. 2016 Jan 15;76(2):206-15. doi: 10.1158/0008-5472.CAN-15-0295. Epub 2015 Dec 30. Cancer Res. 2016. PMID: 26719535 Free PMC article.

9

Validation of Epigenetic Markers for the Prediction of Response to Topical Corticosteroid Treatment in Eosinophilic Esophagitis.

Jensen ET, Langefeld CD, Howard TD, Dellon ES. Jensen ET, et al. Among authors: howard td. Clin Transl Gastroenterol. 2023 Sep 1;14(9):e00622. doi: 10.14309/ctg.0000000000000622. Clin Transl Gastroenterol. 2023. PMID: 37439560 Free PMC article.

10

The modifying influence of HLA class II DQB1∗06:02 on the Streptococcus and clinical phenotype correlation among anti-Ro+ mothers of children with neonatal lupus.

Clancy RM, Guthridge CJ, Marion MC, Guthridge J, Howard TD, Izmirly PM, Masson M, Buyon JP, James JA, Langefeld CD. Clancy RM, et al. Among authors: howard td. Genes Dis. 2022 Dec 13;10(4):1169-1171. doi: 10.1016/j.gendis.2022.11.006. eCollection 2023 Jul. Genes Dis. 2022. PMID: 37397545 Free PMC article. No abstract available.

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