-
1
-
-
60749134716
-
Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4
-
Backx L, Ceulemans B, Vermeesch JR, Devriendt K, Van Esch H. 2009. Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4. Eur J Hum Genet 17:378-382.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 378-382
-
-
Backx, L.1
Ceulemans, B.2
Vermeesch, J.R.3
Devriendt, K.4
Van Esch, H.5
-
3
-
-
0028785406
-
Aberrant neural and cardiac development in mice lacking the erbB4 neuregulin receptor
-
Gassman M, Casagranda F, Orioll D, Simon H, Lai C, Klein R, Lemke G. 1995. Aberrant neural and cardiac development in mice lacking the erbB4 neuregulin receptor. Nature 378:390-394.
-
(1995)
Nature
, vol.378
, pp. 390-394
-
-
Gassman, M.1
Casagranda, F.2
Orioll, D.3
Simon, H.4
Lai, C.5
Klein, R.6
Lemke, G.7
-
4
-
-
0034112445
-
Heregulin, but not ErbB2 or ErbB3, heterozygous mutant mice exhibit hyperactivity in multiple behavioral tasks
-
Gerlai R, Pisacane P, Erickson S. 2000. Heregulin, but not ErbB2 or ErbB3, heterozygous mutant mice exhibit hyperactivity in multiple behavioral tasks. Behav Brain Res 109:219-227.
-
(2000)
Behav Brain Res
, vol.109
, pp. 219-227
-
-
Gerlai, R.1
Pisacane, P.2
Erickson, S.3
-
5
-
-
3042640878
-
Behavioral characteristics of a nervous system-specific erbB4 knock-out mouse
-
Golub MS, Germann SL, Lloyd KC. 2004. Behavioral characteristics of a nervous system-specific erbB4 knock-out mouse. Behav Brain Res 153:159-170.
-
(2004)
Behav Brain Res
, vol.153
, pp. 159-170
-
-
Golub, M.S.1
Germann, S.L.2
Lloyd, K.C.3
-
6
-
-
33846589304
-
Disease-associated intronic variants in the ErbB4 gene are related to altered ErbB4 splice-variant expression in the brain in schizophrenia
-
Law AJ, Kleinman JE, Weinberger DR, Weickert CS. 2007. Disease-associated intronic variants in the ErbB4 gene are related to altered ErbB4 splice-variant expression in the brain in schizophrenia. Hum Mol Genet 16:129-141.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 129-141
-
-
Law, A.J.1
Kleinman, J.E.2
Weinberger, D.R.3
Weickert, C.S.4
-
7
-
-
80053106248
-
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders
-
Mikhail FM, Lose EJ, Robin NH, Descartes MD, Rutledge KD, Rutledge SL, Korf BR, Carroll AJ. 2011. Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders. Am J Med Genet A 155A:2386-2396.
-
(2011)
Am J Med Genet A
, vol.155 A
, pp. 2386-2396
-
-
Mikhail, F.M.1
Lose, E.J.2
Robin, N.H.3
Descartes, M.D.4
Rutledge, K.D.5
Rutledge, S.L.6
Korf, B.R.7
Carroll, A.J.8
-
8
-
-
77953053247
-
Selective populations of hippocampal interneurons express ErbB4 and their number and distribution is altered in ErbB4 knockout mice
-
Neddens J, Buonanno A. 2010. Selective populations of hippocampal interneurons express ErbB4 and their number and distribution is altered in ErbB4 knockout mice. Hippocampus 20:724-744.
-
(2010)
Hippocampus
, vol.20
, pp. 724-744
-
-
Neddens, J.1
Buonanno, A.2
-
9
-
-
80052863881
-
ErbB4 is not detected in pyramidal cells but is confined to interneurons in the frontal cortex of humans, monkeys and rodents: Implications for schizophrenia
-
Neddens J, Fish KN, Tricoire L, Vullhorst D, Shamir A, Chung W, Lewis DA, McBain CJ, Buonanno A. 2011. ErbB4 is not detected in pyramidal cells but is confined to interneurons in the frontal cortex of humans, monkeys and rodents: Implications for schizophrenia. Biol Psychiatry 70:636-645.
-
(2011)
Biol Psychiatry
, vol.70
, pp. 636-645
-
-
Neddens, J.1
Fish, K.N.2
Tricoire, L.3
Vullhorst, D.4
Shamir, A.5
Chung, W.6
Lewis, D.A.7
McBain, C.J.8
Buonanno, A.9
-
10
-
-
77957719415
-
Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls
-
Nicodemus KK, Law AJ, Radulescu E, Luna A, Kolachana B, Vakkalanka R, Rujescu D, Giegling I, Straub RE, McGee K, Gold B, Dean M, Muglia P, Callicott JH, Tan HY, Weinberger DR. 2010. Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls. Arch Gen Psychiatry 67:991-1001.
-
(2010)
Arch Gen Psychiatry
, vol.67
, pp. 991-1001
-
-
Nicodemus, K.K.1
Law, A.J.2
Radulescu, E.3
Luna, A.4
Kolachana, B.5
Vakkalanka, R.6
Rujescu, D.7
Giegling, I.8
Straub, R.E.9
McGee, K.10
Gold, B.11
Dean, M.12
Muglia, P.13
Callicott, J.H.14
Tan, H.Y.15
Weinberger, D.R.16
-
11
-
-
84878255390
-
Schizophrenia Candidate Gene ERB B4: Covert routes of vulnerability to psychosis detected at the population level
-
Epub ahead of print
-
Stefanis NC, Hatzimanolis A, Smyrnis N, Avramopoulos D, Evdokimidis I, van Os J, Stefanis CN, Straub RE, Weinberger DR. 2011. Schizophrenia Candidate Gene ERB B4: Covert routes of vulnerability to psychosis detected at the population level. Schizophr Bull [Epub ahead of print].
-
(2011)
Schizophr Bull
-
-
Stefanis, N.C.1
Hatzimanolis, A.2
Smyrnis, N.3
Avramopoulos, D.4
Evdokimidis, I.5
van Os, J.6
Stefanis, C.N.7
Straub, R.E.8
Weinberger, D.R.9
-
12
-
-
0013375948
-
Neuregulin 1 and susceptibility to schizophrenia
-
Stefansson H, Sigurdsson E, Steinthorsdottir V, Bjornsdottir S, Sigmundsson T, Ghosh S, Brynjolfsson J, Gunnarsdottir S, Ivarsson O, Chou TT, Hjaltason O, Birgisdottir B, Jonsson H, Gudnadottir VG, Gudmundsdottir E, Bjornsson A, Ingvarsson B, Ingason A, Sigfusson S, Hardardottir H, Harvey RP, Lai D, Zhou M, Brunner D, Mutel V, Gonzalo A, Lemke G, Sainz J, Johannesson G, Andresson T, Gudbjartsson D, Manolescu A, Frigge ML, Gurney ME, Kong A, Gulcher JR, Petursson H, Stefansson K. 2002. Neuregulin 1 and susceptibility to schizophrenia. Am J Hum Genet 71:877-892.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 877-892
-
-
Stefansson, H.1
Sigurdsson, E.2
Steinthorsdottir, V.3
Bjornsdottir, S.4
Sigmundsson, T.5
Ghosh, S.6
Brynjolfsson, J.7
Gunnarsdottir, S.8
Ivarsson, O.9
Chou, T.T.10
Hjaltason, O.11
Birgisdottir, B.12
Jonsson, H.13
Gudnadottir, V.G.14
Gudmundsdottir, E.15
Bjornsson, A.16
Ingvarsson, B.17
Ingason, A.18
Sigfusson, S.19
Hardardottir, H.20
Harvey, R.P.21
Lai, D.22
Zhou, M.23
Brunner, D.24
Mutel, V.25
Gonzalo, A.26
Lemke, G.27
Sainz, J.28
Johannesson, G.29
Andresson, T.30
Gudbjartsson, D.31
Manolescu, A.32
Frigge, M.L.33
Gurney, M.E.34
Kong, A.35
Gulcher, J.R.36
Petursson, H.37
Stefansson, K.38
more..
-
13
-
-
84856245459
-
Neuregulin 1 represses limbic epileptogenesis through ErbB4 in parvalbumin-expressing interneurons
-
DOI: 10.1038/nn.3005
-
Tan GH, Liu YY, Hu XL, Yin DM, Mei L, Xiong ZQ. 2011. Neuregulin 1 represses limbic epileptogenesis through ErbB4 in parvalbumin-expressing interneurons. Nat Neurosci 15:258-266 DOI: 10.1038/nn.3005.
-
(2011)
Nat Neurosci
, vol.15
, pp. 258-266
-
-
Tan, G.H.1
Liu, Y.Y.2
Hu, X.L.3
Yin, D.M.4
Mei, L.5
Xiong, Z.Q.6
-
14
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, Stray SM, Rippey CF, Roccanova P, Makarov V, Lakshmi B, Findling RL, Sikich L, Stromberg T, Merriman B, Gogtay N, Butler P, Eckstrand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Meltzer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J. 2008. Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320:539-543.
-
(2008)
Science
, vol.320
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
Addington, A.M.4
Pierce, S.B.5
Cooper, G.M.6
Nord, A.S.7
Kusenda, M.8
Malhotra, D.9
Bhandari, A.10
Stray, S.M.11
Rippey, C.F.12
Roccanova, P.13
Makarov, V.14
Lakshmi, B.15
Findling, R.L.16
Sikich, L.17
Stromberg, T.18
Merriman, B.19
Gogtay, N.20
Butler, P.21
Eckstrand, K.22
Noory, L.23
Gochman, P.24
Long, R.25
Chen, Z.26
Davis, S.27
Baker, C.28
Eichler, E.E.29
Meltzer, P.S.30
Nelson, S.F.31
Singleton, A.B.32
Lee, M.K.33
Rapoport, J.L.34
King, M.C.35
Sebat, J.36
more..
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