PubMed (GeneRIF) for id: 93664

Year	Number of Results
2003	1
2007	1
2008	2
2009	2
2010	2
2011	2
2012	1
2014	1
2017	2
2019	1
2021	1
2024	0

1

Down-regulation of habenular calcium-dependent secretion activator 2 induces despair-like behavior.

Yoo H, Yang SH, Kim JY, Yang E, Park HS, Lee SJ, Rhyu IJ, Turecki G, Lee HW, Kim H. Yoo H, et al. Sci Rep. 2021 Feb 12;11(1):3700. doi: 10.1038/s41598-021-83310-0. Sci Rep. 2021. PMID: 33580180 Free PMC article.

2

Genetic analysis for cognitive flexibility in the trail-making test in attention deficit hyperactivity disorder patients from single nucleotide polymorphism, gene to pathway level.

Zhang K, Fan Z, Wang Y, Faraone SV, Yang L, Chang S. Zhang K, et al. World J Biol Psychiatry. 2019 Jul;20(6):476-485. doi: 10.1080/15622975.2017.1386324. Epub 2017 Oct 25. World J Biol Psychiatry. 2019. PMID: 28971736 Free PMC article.

3

CADPS2 gene expression is oppositely regulated by LRRK2 and alpha-synuclein.

Obergasteiger J, Überbacher C, Pramstaller PP, Hicks AA, Corti C, Volta M. Obergasteiger J, et al. Biochem Biophys Res Commun. 2017 Aug 26;490(3):876-881. doi: 10.1016/j.bbrc.2017.06.134. Epub 2017 Jun 21. Biochem Biophys Res Commun. 2017. PMID: 28647363

4

Maternally inherited genetic variants of CADPS2 are present in autism spectrum disorders and intellectual disability patients.

Bonora E, Graziano C, Minopoli F, Bacchelli E, Magini P, Diquigiovanni C, Lomartire S, Bianco F, Vargiolu M, Parchi P, Marasco E, Mantovani V, Rampoldi L, Trudu M, Parmeggiani A, Battaglia A, Mazzone L, Tortora G; IMGSAC; Maestrini E, Seri M, Romeo G. Bonora E, et al. EMBO Mol Med. 2014 Jun;6(6):795-809. doi: 10.1002/emmm.201303235. Epub 2014 Apr 6. EMBO Mol Med. 2014. PMID: 24737869 Free PMC article.

5

Blood CADPS2ΔExon3 expression is associated with intelligence and memory in healthy adults.

Hattori K, Tanaka H, Yamamoto N, Teraishi T, Hori H, Kinoshita Y, Matsuo J, Kawamoto Y, Kunugi H. Hattori K, et al. Biol Psychol. 2012 Jan;89(1):117-22. doi: 10.1016/j.biopsycho.2011.09.017. Epub 2011 Oct 12. Biol Psychol. 2012. PMID: 22001167

6

Submicroscopic deletion in 7q31 encompassing CADPS2 and TSPAN12 in a child with autism spectrum disorder and PHPV.

Okamoto N, Hatsukawa Y, Shimojima K, Yamamoto T. Okamoto N, et al. Am J Med Genet A. 2011 Jul;155A(7):1568-73. doi: 10.1002/ajmg.a.34028. Epub 2011 May 27. Am J Med Genet A. 2011. PMID: 21626674

7

Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.

Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR. Rose JE, et al. Mol Med. 2010 Jul-Aug;16(7-8):247-53. doi: 10.2119/molmed.2009.00159. Epub 2010 Mar 17. Mol Med. 2010. PMID: 20379614 Free PMC article. Clinical Trial.

8

Voxelwise genome-wide association study (vGWAS).

Stein JL, Hua X, Lee S, Ho AJ, Leow AD, Toga AW, Saykin AJ, Shen L, Foroud T, Pankratz N, Huentelman MJ, Craig DW, Gerber JD, Allen AN, Corneveaux JJ, Dechairo BM, Potkin SG, Weiner MW, Thompson P; Alzheimer's Disease Neuroimaging Initiative. Stein JL, et al. Neuroimage. 2010 Nov 15;53(3):1160-74. doi: 10.1016/j.neuroimage.2010.02.032. Epub 2010 Feb 17. Neuroimage. 2010. PMID: 20171287 Free PMC article.

9

A common variant in DRD3 receptor is associated with autism spectrum disorder.

de Krom M, Staal WG, Ophoff RA, Hendriks J, Buitelaar J, Franke B, de Jonge MV, Bolton P, Collier D, Curran S, van Engeland H, van Ree JM. de Krom M, et al. Biol Psychiatry. 2009 Apr 1;65(7):625-30. doi: 10.1016/j.biopsych.2008.09.035. Epub 2008 Dec 5. Biol Psychiatry. 2009. PMID: 19058789

10

Ca2+-dependent activator proteins of secretion promote vesicular monoamine uptake.

Brunk I, Blex C, Speidel D, Brose N, Ahnert-Hilger G. Brunk I, et al. J Biol Chem. 2009 Jan 9;284(2):1050-6. doi: 10.1074/jbc.M805328200. Epub 2008 Nov 13. J Biol Chem. 2009. PMID: 19008227 Free article.

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