Kaczorowski J - Search Results

1

Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.

Shashi V, Keshavan M, Kaczorowski J, Schoch K, Lewandowski KE, McConkie-Rosell A, Hooper SR, Kwapil TR. Shashi V, et al. Among authors: kaczorowski j. J Genet Couns. 2010 Oct;19(5):535-44. doi: 10.1007/s10897-010-9309-x. Epub 2010 Aug 3. J Genet Couns. 2010. PMID: 20680421 Free PMC article.

2

Neurological soft signs in psychometrically identified schizotypy.

Kaczorowski JA, Barrantes-Vidal N, Kwapil TR. Kaczorowski JA, et al. Schizophr Res. 2009 Dec;115(2-3):293-302. doi: 10.1016/j.schres.2009.06.018. Epub 2009 Aug 3. Schizophr Res. 2009. PMID: 19651490

3

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: kaczorowski j. 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.

4

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: kaczorowski j. 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.

5

Association of Multidimensional Schizotypy with PID-5 Domains and Facets.

Kemp KC, Kaczorowski JA, Burgin CJ, Raulin ML, Lynam DR, Sleep C, Miller JD, Barrantes-Vidal N, Kwapil TR. Kemp KC, et al. Among authors: kaczorowski ja. J Pers Disord. 2022 Dec;36(6):680-700. doi: 10.1521/pedi.2022.36.6.680. J Pers Disord. 2022. PMID: 36454161

6

Neuropsychological Profile of an Adolescent Female With Ectodermal Dysplasia With Hypohidrosis.

Kaczorowski JA, Doty N, Shrewsbury A, Doyle AE, Tan QK, Braaten E. Kaczorowski JA, et al. Cogn Behav Neurol. 2021 Sep 2;34(3):212-219. doi: 10.1097/WNN.0000000000000281. Cogn Behav Neurol. 2021. PMID: 34473673

7

Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders.

Kaczorowski JA, Smith TF, Shrewsbury AM, Thomas LR, Knopik VS, Acosta MT. Kaczorowski JA, et al. Behav Genet. 2020 Jul;50(4):191-202. doi: 10.1007/s10519-020-09991-x. Epub 2020 Feb 5. Behav Genet. 2020. PMID: 32026187 Review.

8

An executive functioning perspective in neurofibromatosis type 1: from ADHD and autism spectrum disorder to research domains.

Smith TF, Kaczorowski JA, Acosta MT. Smith TF, et al. Childs Nerv Syst. 2020 Oct;36(10):2321-2332. doi: 10.1007/s00381-020-04745-w. Epub 2020 Jul 3. Childs Nerv Syst. 2020. PMID: 32617712 Review.

9

Pre- and Perinatal Ischemia-Hypoxia, the Ischemia-Hypoxia Response Pathway, and ADHD Risk.

Smith TF, Schmidt-Kastner R, McGeary JE, Kaczorowski JA, Knopik VS. Smith TF, et al. Behav Genet. 2016 May;46(3):467-77. doi: 10.1007/s10519-016-9784-4. Epub 2016 Feb 26. Behav Genet. 2016. PMID: 26920003 Review.

10

A comparison of self-reported chronic disease, health awareness and behaviours in social housing residents: cross-sectional study of communities in Ontario and Quebec.

Agarwal G, Pirrie M, Koester C, Pete D, Antolovich J, Angeles R, Marzanek F, Girard M, Kaczorowski J. Agarwal G, et al. Among authors: kaczorowski j. BMC Res Notes. 2024 Jul 30;17(1):211. doi: 10.1186/s13104-024-06849-x. BMC Res Notes. 2024. PMID: 39080733 Free PMC article.

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