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CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.
Friedman JI, Vrijenhoek T, Markx S, Janssen IM, van der Vliet WA, Faas BH, Knoers NV, Cahn W, Kahn RS, Edelmann L, Davis KL, Silverman JM, Brunner HG, van Kessel AG, Wijmenga C, Ophoff RA, Veltman JA. Friedman JI, et al. Among authors: markx s. Mol Psychiatry. 2008 Mar;13(3):261-6. doi: 10.1038/sj.mp.4002049. Epub 2007 Jul 24. Mol Psychiatry. 2008. PMID: 17646849
Development of animal models for schizophrenia.
Arguello PA, Markx S, Gogos JA, Karayiorgou M. Arguello PA, et al. Among authors: markx s. Dis Model Mech. 2010 Jan-Feb;3(1-2):22-6. doi: 10.1242/dmm.003996. Dis Model Mech. 2010. PMID: 20075378 Free PMC article.
Copy Number Variation in Syndromic Forms of Psychiatric Illness: The Emerging Value of Clinical Genetic Testing in Psychiatry.
Bouwkamp CG, Kievit AJA, Markx S, Friedman JI, van Zutven L, van Minkelen R, Vrijenhoek T, Xu B, Sterrenburg-van de Nieuwegiessen I, Veltman JA, Bonifati V, Kushner SA. Bouwkamp CG, et al. Among authors: markx s. Am J Psychiatry. 2017 Nov 1;174(11):1036-1050. doi: 10.1176/appi.ajp.2017.16080946. Am J Psychiatry. 2017. PMID: 29088930 No abstract available.
Cortical overgrowth in a preclinical forebrain organoid model of CNTNAP2-associated autism spectrum disorder.
de Jong JO, Llapashtica C, Genestine M, Strauss K, Provenzano F, Sun Y, Zhu H, Cortese GP, Brundu F, Brigatti KW, Corneo B, Migliori B, Tomer R, Kushner SA, Kellendonk C, Javitch JA, Xu B, Markx S. de Jong JO, et al. Among authors: markx s. Nat Commun. 2021 Sep 1;12(1):4087. doi: 10.1038/s41467-021-24358-4. Nat Commun. 2021. PMID: 34471112 Free PMC article.
Neuroanatomical phenotypes in a mouse model of the 22q11.2 microdeletion.
Ellegood J, Markx S, Lerch JP, Steadman PE, Genç C, Provenzano F, Kushner SA, Henkelman RM, Karayiorgou M, Gogos JA. Ellegood J, et al. Among authors: markx s. Mol Psychiatry. 2014 Jan;19(1):99-107. doi: 10.1038/mp.2013.112. Epub 2013 Sep 3. Mol Psychiatry. 2014. PMID: 23999526 Free PMC article.
Signaling pathways in schizophrenia: emerging targets and therapeutic strategies.
Karam CS, Ballon JS, Bivens NM, Freyberg Z, Girgis RR, Lizardi-Ortiz JE, Markx S, Lieberman JA, Javitch JA. Karam CS, et al. Among authors: markx s. Trends Pharmacol Sci. 2010 Aug;31(8):381-90. doi: 10.1016/j.tips.2010.05.004. Epub 2010 Jun 25. Trends Pharmacol Sci. 2010. PMID: 20579747 Free PMC article. Review.
High-impact rare genetic variants in severe schizophrenia.
Zoghbi AW, Dhindsa RS, Goldberg TE, Mehralizade A, Motelow JE, Wang X, Alkelai A, Harms MB, Lieberman JA, Markx S, Goldstein DB. Zoghbi AW, et al. Among authors: markx s. Proc Natl Acad Sci U S A. 2021 Dec 21;118(51):e2112560118. doi: 10.1073/pnas.2112560118. Proc Natl Acad Sci U S A. 2021. PMID: 34903660 Free PMC article.
A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder.
Strauss KA, Markx S, Georgi B, Paul SM, Jinks RN, Hoshi T, McDonald A, First MB, Liu W, Benkert AR, Heaps AD, Tian Y, Chakravarti A, Bucan M, Puffenberger EG. Strauss KA, et al. Among authors: markx s. Hum Mol Genet. 2014 Dec 1;23(23):6395-406. doi: 10.1093/hmg/ddu335. Epub 2014 Jun 30. Hum Mol Genet. 2014. PMID: 24986916 Free PMC article.
21 results