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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1992 1
1994 2
1995 1
1997 2
1998 2
1999 6
2000 3
2001 4
2002 2
2003 5
2004 3
2005 1
2006 4
2007 4
2008 4
2009 6
2010 4
2011 3
2012 7
2013 8
2014 6
2015 2
2016 4
2017 3
2018 9
2019 3
2020 3
2021 9
2022 3
2023 6
2024 1

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110 results

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Page 1
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome.
Jain P, Miller-Fleming T, Topaloudi A, Yu D, Drineas P, Georgitsi M, Yang Z, Rizzo R, Müller-Vahl KR, Tumer Z, Mol Debes N, Hartmann A, Depienne C, Worbe Y, Mir P, Cath DC, Boomsma DI, Roessner V, Wolanczyk T, Janik P, Szejko N, Zekanowski C, Barta C, Nemoda Z, Tarnok Z, Buxbaum JD, Grice D, Glennon J, Stefansson H, Hengerer B, Benaroya-Milshtein N, Cardona F, Hedderly T, Heyman I, Huyser C, Morer A, Mueller N, Munchau A, Plessen KJ, Porcelli C, Walitza S, Schrag A, Martino D; Psychiatric Genomics Consortium Tourette Syndrome Working Group (PGC-TS); EMTICS collaborative group; Dietrich A; TS-EUROTRAIN Network; Mathews CA, Scharf JM, Hoekstra PJ, Davis LK, Paschou P. Jain P, et al. Among authors: zekanowski c. Transl Psychiatry. 2023 Feb 23;13(1):69. doi: 10.1038/s41398-023-02341-5. Transl Psychiatry. 2023. PMID: 36823209 Free PMC article.
Genome-wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome.
Tsetsos F, Topaloudi A, Jain P, Yang Z, Yu D, Kolovos P, Tumer Z, Rizzo R, Hartmann A, Depienne C, Worbe Y, Müller-Vahl KR, Cath DC, Boomsma DI, Wolanczyk T, Zekanowski C, Barta C, Nemoda Z, Tarnok Z, Padmanabhuni SS, Buxbaum JD, Grice D, Glennon J, Stefansson H, Hengerer B, Yannaki E, Stamatoyannopoulos JA, Benaroya-Milshtein N, Cardona F, Hedderly T, Heyman I, Huyser C, Mir P, Morer A, Mueller N, Munchau A, Plessen KJ, Porcelli C, Roessner V, Walitza S, Schrag A, Martino D; PGC TS Working Group; TSAICG; TSGeneSEE Initiative; EMTICS Collaborative Group; TS-EUROTRAIN Network; TIC Genetics Collaborative Group; Tischfield JA, Heiman GA, Willsey AJ, Dietrich A, Davis LK, Crowley JJ, Mathews CA, Scharf JM, Georgitsi M, Hoekstra PJ, Paschou P. Tsetsos F, et al. Among authors: zekanowski c. Biol Psychiatry. 2023 Feb 2:S0006-3223(23)00051-3. doi: 10.1016/j.biopsych.2023.01.023. Online ahead of print. Biol Psychiatry. 2023. PMID: 36738982
Myofibrillar myopathy in the genomic context.
Fichna JP, Maruszak A, Żekanowski C. Fichna JP, et al. Among authors: zekanowski c. J Appl Genet. 2018 Nov;59(4):431-439. doi: 10.1007/s13353-018-0463-4. Epub 2018 Sep 10. J Appl Genet. 2018. PMID: 30203143 Review.
Mitochondrial dysfunction and Alzheimer's disease.
Maruszak A, Żekanowski C. Maruszak A, et al. Among authors: zekanowski c. Prog Neuropsychopharmacol Biol Psychiatry. 2011 Mar 30;35(2):320-30. doi: 10.1016/j.pnpbp.2010.07.004. Epub 2010 Jul 16. Prog Neuropsychopharmacol Biol Psychiatry. 2011. PMID: 20624441 Review.
Role of BRCA1 in Neuronal Death in Alzheimer's Disease.
Wezyk M, Zekanowski C. Wezyk M, et al. Among authors: zekanowski c. ACS Chem Neurosci. 2018 May 16;9(5):870-872. doi: 10.1021/acschemneuro.8b00149. Epub 2018 Apr 10. ACS Chem Neurosci. 2018. PMID: 29634233 Review.
Genetic aspects of Alzheimer's disease.
Zekanowski C, Religa D, Graff C, Filipek S, Kuźnicki J. Zekanowski C, et al. Acta Neurobiol Exp (Wars). 2004;64(1):19-31. doi: 10.55782/ane-2004-1488. Acta Neurobiol Exp (Wars). 2004. PMID: 15190677 Free article. Review.
TREM2 Gene Compound Heterozygosity in Neurodegenerative Disorders.
Berdyński M, Ludwiczak J, Barczak A, Barcikowska-Kotowicz M, Kuźma-Kozakiewicz M, Dunin-Horkawicz S, Żekanowski C, Borzemska B. Berdyński M, et al. Among authors: zekanowski c. J Alzheimers Dis. 2022;89(4):1211-1219. doi: 10.3233/JAD-220210. J Alzheimers Dis. 2022. PMID: 36031890
110 results