Lee BB, Cripps RA, Fitzharris M, Wing PC (2014) The global map for traumatic spinal cord injury
epidemiology: update 2011, global incidence rate. Spinal Cord 52:110–116
Li J, Luo M, Xu X, Sheng W (2012) Association between 1425G/A SNP in PRKCH and ischemic
stroke among Chinese and Japanese populations: a meta-analysis including 3686 cases and
4589 controls. Neurosci Lett 506:55–58
Malik R, Bevan S, Nalls MA, Holliday EG, Devan WJ, Cheng YC, Ibrahim-Verbaas CA,
Verhaaren BF, Bis JC, Joon AY, de Stefano AL, Fornage M, Psaty BM, Ikram MA, Launer
LJ, van Duijn CM, Sharma P, Mitchell BD, Rosand J, Meschia JF, Levi C, Rothwell PM,
Sudlow C, Markus HS, Seshadri S, Dichgans M; WellcomeTrust Case Control Consortium
2 (2014) Multilocus genetic risk score associates with ischemic stroke in case-control and
prospective cohort studies. Stroke 45:394–402
Markus HS (2012) Stroke genetics: prospects for personalized medicine. BMC Med 10:113
Miura Y, Tam T, Ido A, Morinaga T, Miki T, Hashimoto T, Tamaoki T (1995) Cloning and
characterization of an ATBF1 isoform that expresses in a neuronal differentiation-dependent
manner. J Biol Chem 270:26840–26848
Mladinic M, Muller KJ, Nicholls JG (2009) Central nervous system regeneration: from leech to
opossum. J Physiol 587(Pt 12):2775–2782
Mladinic M, Bianchetti E, Dekanic A, Mazzone GL, Nistri A (2014) ATF3 is a novel nuclear
marker for migrating ependymal stem cells in the rat spinal cord. Stem Cell Res. doi:10.1016/j.
scr.2014.03.006
Muramatsu R, Ueno M, Yamashita T (2009) Intrinsic regenerative mechanisms of central nervous
system neurons. Biosci Trends 3:179–183
New PW, Cripps RA, Bonne Lee B (2014) Global maps of non-traumatic spinal cord injury
epidemiology: towards a living data repository. Spinal Cord 52:97–109
Nori S, Okada Y, Yasuda A, Tsuji O, Takahashi Y, Kobayashi Y, Fujiyoshi K, Koike M,
Uchiyama Y, Ikeda E, Toyama Y, Yamanaka S, Nakamura M, Okano H (2011) Grafted
human-induced pluripotent stem-cell-derived neurospheres promote motor functional recovery
after spinal cord injury in mice. Proc Natl Acad Sci U S A 108:16825–16830
Ozomaro U, Wahlestedt C, Nemeroff CB (2013) Personalized medicine in psychiatry: problems
and promises. BMC Med 11:132
Rosenthal D (ed) (1963) The genain quadruplets: a case study and theoretical analysis of heredity
and environment in Schizophrenia. Basic Books, New York
Roussos P, Haroutunian V (2014) Schizophrenia: susceptibility genes and oligodendroglial and
myelin related abnormalities. Front Cell Neurosci 8:5, eCollection 2014
Sacco RL, Ellenberg JH, Mohr JP, Tatemichi TK, Hier DB, Price TR, Wolf PA (1989) Infarcts of
undetermined cause: the NINCDS Stroke Data Bank. Ann Neurol 25:382–390
Schierding W, Cutfield WS, O’Sullivan JM (2014) The missing story behind Genome Wide
Association Studies: single nucleotide polymorphisms in gene deserts have a story to tell.
Front Genet 5:39, eCollection 2014
Segal NL (2001) Genain quadruplets: variations on the schizophrenic syndrome. Twin Res 4
(57-9):61
Shi J, Levinson DF, Duan J, Sanders AR, Zheng Y, Pe’er I, Dudbridge F, Holmans PA,
Whittemore AS, Mowry BJ, Olincy A, Amin F, Cloninger CR, Silverman JM, Buccola NG,
Byerley WF, Black DW, Crowe RR, Oksenberg JR, Mirel DB, Kendler KS, Freedman R,
Gejman PV (2009) Common variants on chromosome 6p22.1 are associated with schizophre-
nia. Nature 460:753–757
Silva H (2013) Ethnopsychopharmacology and pharmacogenomics. Adv Psychosom Med
33:88–96
Smith K (2011) Mental disorders affect more than a third of Europeans. Nature. doi:10.1038/news.
2011.514, Accessed 5 Sept 2011
Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D, Werge T,
Pietila ̈inen OP, Mors O, Mortensen PB, Sigurdsson E, Gustafsson O, Nyegaard M, Tuulio-
Henriksson A, Ingason A, Hansen T, Suvisaari J, Lonnqvist J, Paunio T, Børglum AD,
254 M.M. Pejatovic ́and S. Anzic ́