-
2
-
-
40149094771
-
Gene and expression analyses reveal enhanced expression of pericentrin 2 (PCNT2) in bipolar disorder
-
Anitha A., Nakamura K., Yamada K., Iwayama Y., Toyota T., Takei N., Iwata Y., Suzuki K., Sekine Y., Matsuzaki H., Kawai M., Miyoshi K., Katayama T., Matsuzaki S., Baba K., Honda A., Hattori T., Shimizu S., Kumamoto N., Tohyama M., Yoshikawa T., Mori N. Gene and expression analyses reveal enhanced expression of pericentrin 2 (PCNT2) in bipolar disorder. Biol. Psychiatry 2008, 63:678-685.
-
(2008)
Biol. Psychiatry
, vol.63
, pp. 678-685
-
-
Anitha, A.1
Nakamura, K.2
Yamada, K.3
Iwayama, Y.4
Toyota, T.5
Takei, N.6
Iwata, Y.7
Suzuki, K.8
Sekine, Y.9
Matsuzaki, H.10
Kawai, M.11
Miyoshi, K.12
Katayama, T.13
Matsuzaki, S.14
Baba, K.15
Honda, A.16
Hattori, T.17
Shimizu, S.18
Kumamoto, N.19
Tohyama, M.20
Yoshikawa, T.21
Mori, N.22
more..
-
3
-
-
38749096303
-
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
-
Arking D.E., Cutler D.J., Brune C.W., Teslovich T.M., West K., Ikeda M., Rea A., Guy M., Lin S., Cook E.H., Chakravarti A. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am. J. Hum. Genet. 2008, 82:160-164.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 160-164
-
-
Arking, D.E.1
Cutler, D.J.2
Brune, C.W.3
Teslovich, T.M.4
West, K.5
Ikeda, M.6
Rea, A.7
Guy, M.8
Lin, S.9
Cook, E.H.10
Chakravarti, A.11
-
4
-
-
33745818375
-
Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP)
-
Baird G., Simonoff E., Pickles A., Chandler S., Loucas T., Meldrum D., Charman T. Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP). Lancet 2006, 368:210-215.
-
(2006)
Lancet
, vol.368
, pp. 210-215
-
-
Baird, G.1
Simonoff, E.2
Pickles, A.3
Chandler, S.4
Loucas, T.5
Meldrum, D.6
Charman, T.7
-
5
-
-
33744810884
-
The Autism-Spectrum Quotient (AQ)-adolescent version
-
Baron-Cohen S., Hoekstra R.A., Knickmeyer R., Wheelwright S. The Autism-Spectrum Quotient (AQ)-adolescent version. J. Autism Dev. Disord. 2006, 36:343-350.
-
(2006)
J. Autism Dev. Disord.
, vol.36
, pp. 343-350
-
-
Baron-Cohen, S.1
Hoekstra, R.A.2
Knickmeyer, R.3
Wheelwright, S.4
-
6
-
-
37349008925
-
Attachment, aggression and affiliation: the role of oxytocin in female social behavior
-
Campbell A. Attachment, aggression and affiliation: the role of oxytocin in female social behavior. Biol. Psychol. 2008, 77:1-10.
-
(2008)
Biol. Psychol.
, vol.77
, pp. 1-10
-
-
Campbell, A.1
-
7
-
-
42749090959
-
CD38 at the junction between prognostic marker and therapeutic target
-
Deaglio S., Aydin S., Vaisitti T., Bergui L., Malavasi F. CD38 at the junction between prognostic marker and therapeutic target. Trends Mol. Med. 2008, 14:210-218.
-
(2008)
Trends Mol. Med.
, vol.14
, pp. 210-218
-
-
Deaglio, S.1
Aydin, S.2
Vaisitti, T.3
Bergui, L.4
Malavasi, F.5
-
8
-
-
63449098569
-
Intranasal oxytocin increases positive communication and reduces cortisol levels during couple conflict
-
Ditzen B., Schaer M., Gabriel B., Bodenmann G., Ehlert U., Heinrichs M. Intranasal oxytocin increases positive communication and reduces cortisol levels during couple conflict. Biol. Psychiatry 2009, 65:728-731.
-
(2009)
Biol. Psychiatry
, vol.65
, pp. 728-731
-
-
Ditzen, B.1
Schaer, M.2
Gabriel, B.3
Bodenmann, G.4
Ehlert, U.5
Heinrichs, M.6
-
9
-
-
33847273564
-
Oxytocin improves " mind-reading" in humans
-
Domes G., Heinrichs M., Michel A., Berger C., Herpertz S.C. Oxytocin improves " mind-reading" in humans. Biol. Psychiatry 2007, 61:731-733.
-
(2007)
Biol. Psychiatry
, vol.61
, pp. 731-733
-
-
Domes, G.1
Heinrichs, M.2
Michel, A.3
Berger, C.4
Herpertz, S.C.5
-
10
-
-
55849119537
-
Oxytocin, vasopressin, and the neurogenetics of sociality
-
Donaldson Z.R., Young L.J. Oxytocin, vasopressin, and the neurogenetics of sociality. Science 2008, 322:900-904.
-
(2008)
Science
, vol.322
, pp. 900-904
-
-
Donaldson, Z.R.1
Young, L.J.2
-
11
-
-
67649635335
-
Arginine vasopressin and oxytocin modulate human social behavior
-
Ebstein R.P., Israel S., Lerer E., Uzefovsky F., Shalev I., Gritsenko I., Riebold M., Salomon S., Yirmiya N. Arginine vasopressin and oxytocin modulate human social behavior. Ann. NY Acad. Sci. 2009, 1167:87-102.
-
(2009)
Ann. NY Acad. Sci.
, vol.1167
, pp. 87-102
-
-
Ebstein, R.P.1
Israel, S.2
Lerer, E.3
Uzefovsky, F.4
Shalev, I.5
Gritsenko, I.6
Riebold, M.7
Salomon, S.8
Yirmiya, N.9
-
12
-
-
0033943538
-
Social amnesia in mice lacking the oxytocin gene
-
Ferguson J.N., Young L.J., Hearn E.F., Matzuk M.M., Insel T.R., Winslow J.T. Social amnesia in mice lacking the oxytocin gene. Nat. Genet. 2000, 25:284-288.
-
(2000)
Nat. Genet.
, vol.25
, pp. 284-288
-
-
Ferguson, J.N.1
Young, L.J.2
Hearn, E.F.3
Matzuk, M.M.4
Insel, T.R.5
Winslow, J.T.6
-
13
-
-
0034916325
-
The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions
-
AGRE Steering Committee
-
Geschwind D.H., Sowinski J., Lord C., Iversen P., Shestack J., Jones P., Ducat L., Spence S.J. The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions. Am. J. Hum. Genet. 2001, 69:463-466. AGRE Steering Committee.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 463-466
-
-
Geschwind, D.H.1
Sowinski, J.2
Lord, C.3
Iversen, P.4
Shestack, J.5
Jones, P.6
Ducat, L.7
Spence, S.J.8
-
14
-
-
0035057149
-
The Asperger Syndrome (and high-functioning autism) Diagnostic Interview (ASDI): a preliminary study of a new structured clinical interview
-
Gillberg C., Gillberg C., Rastam M., Wentz E. The Asperger Syndrome (and high-functioning autism) Diagnostic Interview (ASDI): a preliminary study of a new structured clinical interview. Autism 2001, 5:57-66.
-
(2001)
Autism
, vol.5
, pp. 57-66
-
-
Gillberg, C.1
Gillberg, C.2
Rastam, M.3
Wentz, E.4
-
15
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
Glessner J.T., Wang K., Cai G., Korvatska O., Kim C.E., Wood S., Zhang H., Estes A., Brune C.W., Bradfield J.P., Imielinski M., Frackelton E.C., Reichert J., Crawford E.L., Munson J., Sleiman P.M., Chiavacci R., Annaiah K., Thomas K., Hou C., Glaberson W., Flory J., Otieno F., Garris M., Soorya L., Klei L., Piven J., Meyer K.J., Anagnostou E., Sakurai T., Game R.M., Rudd D.S., Zurawiecki D., McDougle C.J., Davis L.K., Miller J., Posey D.J., Michaels S., Kolevzon A., Silverman J.M., Bernier R., Levy S.E., Schultz R.T., Dawson G., Owley T., McMahon W.M., Wassink T.H., Sweeney J.A., Nurnberger J.I., Coon H., Sutcliffe J.S., Minshew N.J., Grant S.F., Bucan M., Cook E.H., Buxbaum J.D., Devlin B., Schellenberg G.D., Hakonarson H. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009, 459:569-573.
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
Korvatska, O.4
Kim, C.E.5
Wood, S.6
Zhang, H.7
Estes, A.8
Brune, C.W.9
Bradfield, J.P.10
Imielinski, M.11
Frackelton, E.C.12
Reichert, J.13
Crawford, E.L.14
Munson, J.15
Sleiman, P.M.16
Chiavacci, R.17
Annaiah, K.18
Thomas, K.19
Hou, C.20
Glaberson, W.21
Flory, J.22
Otieno, F.23
Garris, M.24
Soorya, L.25
Klei, L.26
Piven, J.27
Meyer, K.J.28
Anagnostou, E.29
Sakurai, T.30
Game, R.M.31
Rudd, D.S.32
Zurawiecki, D.33
McDougle, C.J.34
Davis, L.K.35
Miller, J.36
Posey, D.J.37
Michaels, S.38
Kolevzon, A.39
Silverman, J.M.40
Bernier, R.41
Levy, S.E.42
Schultz, R.T.43
Dawson, G.44
Owley, T.45
McMahon, W.M.46
Wassink, T.H.47
Sweeney, J.A.48
Nurnberger, J.I.49
Coon, H.50
Sutcliffe, J.S.51
Minshew, N.J.52
Grant, S.F.53
Bucan, M.54
Cook, E.H.55
Buxbaum, J.D.56
Devlin, B.57
Schellenberg, G.D.58
Hakonarson, H.59
more..
-
16
-
-
71149104488
-
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
-
Gregory S.G., Connelly J.J., Towers A.J., Johnson J., Biscocho D., Markunas C.A., Lintas C., Abramson R.K., Wright H.H., Ellis P., Langford C.F., Worley G., Delong G.R., Murphy S.K., Cuccaro M.L., Persico A., Pericak-Vance M.A. Genomic and epigenetic evidence for oxytocin receptor deficiency in autism. BMC Med. 2009, 7:62.
-
(2009)
BMC Med.
, vol.7
, pp. 62
-
-
Gregory, S.G.1
Connelly, J.J.2
Towers, A.J.3
Johnson, J.4
Biscocho, D.5
Markunas, C.A.6
Lintas, C.7
Abramson, R.K.8
Wright, H.H.9
Ellis, P.10
Langford, C.F.11
Worley, G.12
Delong, G.R.13
Murphy, S.K.14
Cuccaro, M.L.15
Persico, A.16
Pericak-Vance, M.A.17
-
18
-
-
46249099558
-
Oxytocin enhances the encoding of positive social memories in humans
-
Guastella A.J., Mitchell P.B., Mathews F. Oxytocin enhances the encoding of positive social memories in humans. Biol. Psychiatry 2008, 64:256-258.
-
(2008)
Biol. Psychiatry
, vol.64
, pp. 256-258
-
-
Guastella, A.J.1
Mitchell, P.B.2
Mathews, F.3
-
19
-
-
77949486670
-
Intranasal oxytocin improves emotion recognition for youth with autism spectrum disorders
-
Guastella A.J., Einfeld S.L., Gray K.M., Rinehart N.J., Tonge B.J., Lambert T.J., Hickie I.B. Intranasal oxytocin improves emotion recognition for youth with autism spectrum disorders. Biol. Psychiatry 2010, 67:692-694.
-
(2010)
Biol. Psychiatry
, vol.67
, pp. 692-694
-
-
Guastella, A.J.1
Einfeld, S.L.2
Gray, K.M.3
Rinehart, N.J.4
Tonge, B.J.5
Lambert, T.J.6
Hickie, I.B.7
-
20
-
-
25444440088
-
Second messenger function and the structure-activity relationship of cyclic adenosine diphosphoribose (cADPR)
-
Guse A.H. Second messenger function and the structure-activity relationship of cyclic adenosine diphosphoribose (cADPR). FEBS J. 2005, 272:4590-4597.
-
(2005)
FEBS J.
, vol.272
, pp. 4590-4597
-
-
Guse, A.H.1
-
21
-
-
0036888353
-
Improvements in the analysis of domain motions in proteins from conformational change: DynDom version 1.50
-
Hayward S., Lee R.A. Improvements in the analysis of domain motions in proteins from conformational change: DynDom version 1.50. J. Mol. Graph. Model. 2002, 21:181-183.
-
(2002)
J. Mol. Graph. Model.
, vol.21
, pp. 181-183
-
-
Hayward, S.1
Lee, R.A.2
-
22
-
-
34547459564
-
Cyclic ADP-ribose as a universal calcium signal molecule in the nervous system
-
Higashida H., Salmina A.B., Olovyannikova R.Y., Hashii M., Yokoyama S., Koizumi K., Jin D., Liu H.X., Lopatina O., Amina S., Islam M.S., Huang J.J., Noda M. Cyclic ADP-ribose as a universal calcium signal molecule in the nervous system. Neurochem. Int. 2007, 51:192-199.
-
(2007)
Neurochem. Int.
, vol.51
, pp. 192-199
-
-
Higashida, H.1
Salmina, A.B.2
Olovyannikova, R.Y.3
Hashii, M.4
Yokoyama, S.5
Koizumi, K.6
Jin, D.7
Liu, H.X.8
Lopatina, O.9
Amina, S.10
Islam, M.S.11
Huang, J.J.12
Noda, M.13
-
23
-
-
33846624633
-
O xytocin increases retention of social cognition in autism
-
Hollander E., Bartz J., Chaplin W., Phillips A., Sumner J., Soorya L., Anagnostou E., Wasserman S. O xytocin increases retention of social cognition in autism. Biol. Psychiatry 2007, 61:498-503.
-
(2007)
Biol. Psychiatry
, vol.61
, pp. 498-503
-
-
Hollander, E.1
Bartz, J.2
Chaplin, W.3
Phillips, A.4
Sumner, J.5
Soorya, L.6
Anagnostou, E.7
Wasserman, S.8
-
24
-
-
12744278201
-
Cumulative incidence of childhood autism: a total population study of better accuracy and precision
-
Honda H., Shimizu Y., Imai M., Nitto Y. Cumulative incidence of childhood autism: a total population study of better accuracy and precision. Dev. Med. Child Neurol. 2005, 47:10-18.
-
(2005)
Dev. Med. Child Neurol.
, vol.47
, pp. 10-18
-
-
Honda, H.1
Shimizu, Y.2
Imai, M.3
Nitto, Y.4
-
25
-
-
3943064343
-
How the brain processes social information: searching for the social brain
-
Insel T.R., Fernald R.D. How the brain processes social information: searching for the social brain. Annu. Rev. Neurosci. 2004, 27:697-722.
-
(2004)
Annu. Rev. Neurosci.
, vol.27
, pp. 697-722
-
-
Insel, T.R.1
Fernald, R.D.2
-
26
-
-
34047153763
-
Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism
-
Jacob S., Brune C.W., Carter C.S., Leventhal B.L., Lord C., Cook E.H. Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism. Neurosci Lett. 2007, 417:6-9.
-
(2007)
Neurosci Lett.
, vol.417
, pp. 6-9
-
-
Jacob, S.1
Brune, C.W.2
Carter, C.S.3
Leventhal, B.L.4
Lord, C.5
Cook, E.H.6
-
27
-
-
64549101682
-
CD38 gene polymorphisms contribute to genetic susceptibility to B-cell chronic lymphocytic leukemia: evidence from two case-control studies in Polish Caucasians
-
Jamroziak K., Szemraj Z., Grzybowska-Izydorczyk O., Szemraj J., Bieniasz M., Cebula B., Giannopoulos K., Balcerczak E., Jesionek-Kupnicka D., Kowal M., Kostyra A., Calbecka M., Wawrzyniak E., Mirowski M., Kordek R., Robak T. CD38 gene polymorphisms contribute to genetic susceptibility to B-cell chronic lymphocytic leukemia: evidence from two case-control studies in Polish Caucasians. Cancer Epidemiol. Biomarkers Prev. 2009, 18:945-953.
-
(2009)
Cancer Epidemiol. Biomarkers Prev.
, vol.18
, pp. 945-953
-
-
Jamroziak, K.1
Szemraj, Z.2
Grzybowska-Izydorczyk, O.3
Szemraj, J.4
Bieniasz, M.5
Cebula, B.6
Giannopoulos, K.7
Balcerczak, E.8
Jesionek-Kupnicka, D.9
Kowal, M.10
Kostyra, A.11
Calbecka, M.12
Wawrzyniak, E.13
Mirowski, M.14
Kordek, R.15
Robak, T.16
-
28
-
-
33847398002
-
CD38 is critical for social behaviour by regulating oxytocin secretion
-
Jin D., Liu H.X., Hirai H., Torashima T., Nagai T., Lopatina O., Shnayder N.A., Yamada K., Noda M., Seike T., Fujita K., Takasawa S., Yokoyama S., Koizumi K., Shiraishi Y., Tanaka S., Hashii M., Yoshihara T., Higashida K., Islam M.S., Yamada N., Hayashi K., Noguchi N., Kato I., Okamoto H., Matsushima A., Salmina A., Munesue T., Shimizu N., Mochida S., Asano M., Higashida H. CD38 is critical for social behaviour by regulating oxytocin secretion. Nature 2007, 446:41-45.
-
(2007)
Nature
, vol.446
, pp. 41-45
-
-
Jin, D.1
Liu, H.X.2
Hirai, H.3
Torashima, T.4
Nagai, T.5
Lopatina, O.6
Shnayder, N.A.7
Yamada, K.8
Noda, M.9
Seike, T.10
Fujita, K.11
Takasawa, S.12
Yokoyama, S.13
Koizumi, K.14
Shiraishi, Y.15
Tanaka, S.16
Hashii, M.17
Yoshihara, T.18
Higashida, K.19
Islam, M.S.20
Yamada, N.21
Hayashi, K.22
Noguchi, N.23
Kato, I.24
Okamoto, H.25
Matsushima, A.26
Salmina, A.27
Munesue, T.28
Shimizu, N.29
Mochida, S.30
Asano, M.31
Higashida, H.32
more..
-
29
-
-
20444497343
-
Oxytocin increases trust in humans
-
Kosfeld M., Heinrichs M., Zak P.J., Fischbacher U., Fehr E. Oxytocin increases trust in humans. Nature 2005, 435:673-676.
-
(2005)
Nature
, vol.435
, pp. 673-676
-
-
Kosfeld, M.1
Heinrichs, M.2
Zak, P.J.3
Fischbacher, U.4
Fehr, E.5
-
30
-
-
0035033022
-
Physiological functions of cyclic ADP-ribose and NAADP as calcium messengers
-
Lee H.C. Physiological functions of cyclic ADP-ribose and NAADP as calcium messengers. Annu. Rev. Pharmacol. Toxicol. 2001, 41:317-345.
-
(2001)
Annu. Rev. Pharmacol. Toxicol.
, vol.41
, pp. 317-345
-
-
Lee, H.C.1
-
31
-
-
55549122291
-
Locomotor activity, ultrasonic vocalization and oxytocin levels in infant CD38 knockout mice
-
Liu H.X., Lopatina O., Higashida C., Tsuji T., Kato I., Takasawa S., Okamoto H., Yokoyama S., Higashida H. Locomotor activity, ultrasonic vocalization and oxytocin levels in infant CD38 knockout mice. Neurosci. Lett. 2008, 448:67-70.
-
(2008)
Neurosci. Lett.
, vol.448
, pp. 67-70
-
-
Liu, H.X.1
Lopatina, O.2
Higashida, C.3
Tsuji, T.4
Kato, I.5
Takasawa, S.6
Okamoto, H.7
Yokoyama, S.8
Higashida, H.9
-
32
-
-
31444453954
-
Dendritic peptide release and peptide-dependent behaviours
-
Ludwig M., Leng G. Dendritic peptide release and peptide-dependent behaviours. Nat. Rev. Neurosci. 2006, 7:126-136.
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 126-136
-
-
Ludwig, M.1
Leng, G.2
-
33
-
-
65249140471
-
The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders
-
Levitt P., Campbell D.B. The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders. J. Clin. Invest. 2009, 119:747-754.
-
(2009)
J. Clin. Invest.
, vol.119
, pp. 747-754
-
-
Levitt, P.1
Campbell, D.B.2
-
34
-
-
0027997172
-
Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
Lord C., Rutter M., Le Couteur A. Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J. Autism Dev. Disord. 1994, 24:659-685.
-
(1994)
J. Autism Dev. Disord.
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
35
-
-
0035085646
-
Autoantibody response to CD38 in Caucasian patients with type 1 and type 2 diabetes: immunological and genetic characterization
-
Mallone R., Ortolan E., Baj G., Funaro A., Giunti S., Lillaz E., Saccucci F., Cassader M., Cavallo-Perin P., Malavasi F. Autoantibody response to CD38 in Caucasian patients with type 1 and type 2 diabetes: immunological and genetic characterization. Diabetes 2001, 50:752-762.
-
(2001)
Diabetes
, vol.50
, pp. 752-762
-
-
Mallone, R.1
Ortolan, E.2
Baj, G.3
Funaro, A.4
Giunti, S.5
Lillaz, E.6
Saccucci, F.7
Cassader, M.8
Cavallo-Perin, P.9
Malavasi, F.10
-
36
-
-
50349083286
-
Evolution and function of the ADP ribosyl cyclase/CD38 gene family in physiology and pathology
-
Malavasi F., Deaglio S., Funaro A., Ferrero E., Horenstein A.L., Ortolan E., Vaisitti T., Aydin S. Evolution and function of the ADP ribosyl cyclase/CD38 gene family in physiology and pathology. Physiol. Rev. 2008, 88:841-886.
-
(2008)
Physiol. Rev.
, vol.88
, pp. 841-886
-
-
Malavasi, F.1
Deaglio, S.2
Funaro, A.3
Ferrero, E.4
Horenstein, A.L.5
Ortolan, E.6
Vaisitti, T.7
Aydin, S.8
-
37
-
-
52949098630
-
High prevalence of bipolar disorder comorbidity in adolescents and young adults with high-functioning autism spectrum disorder: a preliminary study of 44 outpatients
-
Munesue T., Ono Y., Mutoh K., Shimoda K., Nakatani H., Kikuchi M. High prevalence of bipolar disorder comorbidity in adolescents and young adults with high-functioning autism spectrum disorder: a preliminary study of 44 outpatients. J. Affect. Disord. 2008, 111:170-175.
-
(2008)
J. Affect. Disord.
, vol.111
, pp. 170-175
-
-
Munesue, T.1
Ono, Y.2
Mutoh, K.3
Shimoda, K.4
Nakatani, H.5
Kikuchi, M.6
-
38
-
-
0028817072
-
Assignment of CD38, the gene encoding human leukocyte antigen CD38 (ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase), to chromosome 4p15
-
Nakagawara K., Mori M., Takasawa S., Nata K., Takamura T., Berlova A., Tohgo A., Karasawa T., Yonekura H., Takeuchi T., Okamoto H. Assignment of CD38, the gene encoding human leukocyte antigen CD38 (ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase), to chromosome 4p15. Cytogenet. Cell Genet. 1995, 69:38-39.
-
(1995)
Cytogenet. Cell Genet.
, vol.69
, pp. 38-39
-
-
Nakagawara, K.1
Mori, M.2
Takasawa, S.3
Nata, K.4
Takamura, T.5
Berlova, A.6
Tohgo, A.7
Karasawa, T.8
Yonekura, H.9
Takeuchi, T.10
Okamoto, H.11
-
39
-
-
18844471424
-
Human gene encoding CD38 (ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase): organization, nucleotide sequence and alternative splicing
-
Nata K., Takamura T., Karasawa T., Kumagai T., Hashioka W., Tohgo A., Yonekura H., Takasawa S., Nakamura S., Okamoto H. Human gene encoding CD38 (ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase): organization, nucleotide sequence and alternative splicing. Gene 1997, 186:285-292.
-
(1997)
Gene
, vol.186
, pp. 285-292
-
-
Nata, K.1
Takamura, T.2
Karasawa, T.3
Kumagai, T.4
Hashioka, W.5
Tohgo, A.6
Yonekura, H.7
Takasawa, S.8
Nakamura, S.9
Okamoto, H.10
-
40
-
-
45549103898
-
Brain oxytocin: a key regulator of emotional and social behaviours in both females and males
-
Neumann I.D. Brain oxytocin: a key regulator of emotional and social behaviours in both females and males. J. Neuroendocrinol. 2008, 20:858-865.
-
(2008)
J. Neuroendocrinol.
, vol.20
, pp. 858-865
-
-
Neumann, I.D.1
-
41
-
-
0034917719
-
High-throughput genotyping with single nucleotide polymorphisms
-
Ranade K. High-throughput genotyping with single nucleotide polymorphisms. Genome Res. 2001, 11:1262-1268.
-
(2001)
Genome Res.
, vol.11
, pp. 1262-1268
-
-
Ranade, K.1
-
42
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J., Lakshmi B., Malhotra D., Troge J., Lese-Martin C., Walsh T., Yamrom B., Yoon S., Krasnitz A., Kendall J., Leotta A., Pai D., Zhang R., Lee Y.H., Hicks J., Spence S.J., Lee A.T., Puura K., Lehtimäki T., Ledbetter D., Gregersen P.K., Bregman J., Sutcliffe J.S., Jobanputra V., Chung W., Warburton D., King M.C., Skuse D., Geschwind D.H., Gilliam T.C., Ye K., Wigler M. Strong association of de novo copy number mutations with autism. Science 2007, 316:445-449.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
Yamrom, B.7
Yoon, S.8
Krasnitz, A.9
Kendall, J.10
Leotta, A.11
Pai, D.12
Zhang, R.13
Lee, Y.H.14
Hicks, J.15
Spence, S.J.16
Lee, A.T.17
Puura, K.18
Lehtimäki, T.19
Ledbetter, D.20
Gregersen, P.K.21
Bregman, J.22
Sutcliffe, J.S.23
Jobanputra, V.24
Chung, W.25
Warburton, D.26
King, M.C.27
Skuse, D.28
Geschwind, D.H.29
Gilliam, T.C.30
Ye, K.31
Wigler, M.32
more..
-
43
-
-
33745460591
-
Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan
-
Sumi S., Taniai H., Miyachi T., Tanemura M. Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan. J. Hum. Genet. 2006, 51:518-522.
-
(2006)
J. Hum. Genet.
, vol.51
, pp. 518-522
-
-
Sumi, S.1
Taniai, H.2
Miyachi, T.3
Tanemura, M.4
-
44
-
-
67650175927
-
Heterogeneity and the design of genetic studies in autism
-
Sutcliffe J.S. Heterogeneity and the design of genetic studies in autism. Autism Res. 2008, 1:205-206.
-
(2008)
Autism Res.
, vol.1
, pp. 205-206
-
-
Sutcliffe, J.S.1
-
45
-
-
27644476955
-
Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice
-
Takayanagi Y., Yoshida M., Bielsky I.F., Ross H.E., Kawamata M., Onaka T., Yanagisawa T., Kimura T., Matzuk M.M., Young L.J., Nishimori K. Pervasive social deficits, but normal parturition, in oxytocin receptor-deficient mice. Proc. Natl. Acad. Sci. U.S.A. 2005, 102:16096-16101.
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 16096-16101
-
-
Takayanagi, Y.1
Yoshida, M.2
Bielsky, I.F.3
Ross, H.E.4
Kawamata, M.5
Onaka, T.6
Yanagisawa, T.7
Kimura, T.8
Matzuk, M.M.9
Young, L.J.10
Nishimori, K.11
-
46
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
Wang K., Zhang H., Ma D., Bucan M., Glessner J.T., Abrahams B.S., Salyakina D., Imielinski M., Bradfield J.P., Sleiman P.M., Kim C.E., Hou C., Frackelton E., Chiavacci R., Takahashi N., Sakurai T., Rappaport E., Lajonchere C.M., Munson J., Estes A., Korvatska O., Piven J., Sonnenblick L.I., Alvarez Retuerto A.I., Herman E.I., Dong H., Hutman T., Sigman M., Ozonoff S., Klin A., Owley T., Sweeney J.A., Brune C.W., Cantor R.M., Bernier R., Gilbert J.R., Cuccaro M.L., McMahon W.M., Miller J., State M.W., Wassink T.H., Coon H., Levy S.E., Schultz R.T., Nurnberger J.I., Haines J.L., Sutcliffe J.S., Cook E.H., Minshew N.J., Buxbaum J.D., Dawson G., Grant S.F., Geschwind D.H., Pericak-Vance M.A., Schellenberg G.D., Hakonarson H. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature 2009, 459:528-533.
-
(2009)
Nature
, vol.459
, pp. 528-533
-
-
Wang, K.1
Zhang, H.2
Ma, D.3
Bucan, M.4
Glessner, J.T.5
Abrahams, B.S.6
Salyakina, D.7
Imielinski, M.8
Bradfield, J.P.9
Sleiman, P.M.10
Kim, C.E.11
Hou, C.12
Frackelton, E.13
Chiavacci, R.14
Takahashi, N.15
Sakurai, T.16
Rappaport, E.17
Lajonchere, C.M.18
Munson, J.19
Estes, A.20
Korvatska, O.21
Piven, J.22
Sonnenblick, L.I.23
Alvarez Retuerto, A.I.24
Herman, E.I.25
Dong, H.26
Hutman, T.27
Sigman, M.28
Ozonoff, S.29
Klin, A.30
Owley, T.31
Sweeney, J.A.32
Brune, C.W.33
Cantor, R.M.34
Bernier, R.35
Gilbert, J.R.36
Cuccaro, M.L.37
McMahon, W.M.38
Miller, J.39
State, M.W.40
Wassink, T.H.41
Coon, H.42
Levy, S.E.43
Schultz, R.T.44
Nurnberger, J.I.45
Haines, J.L.46
Sutcliffe, J.S.47
Cook, E.H.48
Minshew, N.J.49
Buxbaum, J.D.50
Dawson, G.51
Grant, S.F.52
Geschwind, D.H.53
Pericak-Vance, M.A.54
Schellenberg, G.D.55
Hakonarson, H.56
more..
-
47
-
-
70349956425
-
-
Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly, M.J., Chakravarti, A., 2009. A genome-wide linkage and association scan reveals novel loci for autism. Nature 461, 802-808.
-
Weiss, L.A., Arking, D.E., Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly, M.J., Chakravarti, A., 2009. A genome-wide linkage and association scan reveals novel loci for autism. Nature 461, 802-808.
-
-
-
Weiss, L.A.1
Arking, D.E.2
-
48
-
-
77349094557
-
Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level
-
Wermter A.K., Kamp-Becker I., Hesse P., Schulte-Körne G., Strauch K., Remschmidt H. Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level. Am. J. Med. Genet. B: Neuropsychiatr. Genet. 2010, 153B:629-639.
-
(2010)
Am. J. Med. Genet. B: Neuropsychiatr. Genet.
, vol.153 B
, pp. 629-639
-
-
Wermter, A.K.1
Kamp-Becker, I.2
Hesse, P.3
Schulte-Körne, G.4
Strauch, K.5
Remschmidt, H.6
-
49
-
-
30344439519
-
Systematic review of prevalence studies of autism spectrum disorders
-
Williams J.G., Higgins J.P., Brayne C.E. Systematic review of prevalence studies of autism spectrum disorders. Arch. Dis. Child. 2006, 91:8-15.
-
(2006)
Arch. Dis. Child.
, vol.91
, pp. 8-15
-
-
Williams, J.G.1
Higgins, J.P.2
Brayne, C.E.3
-
50
-
-
0042199134
-
The Diagnostic Interview for Social and Communication Disorders: background, inter-rater reliability and clinical use
-
Wing L., Leekam S.R., Libby S.J., Gould J., Larcombe M. The Diagnostic Interview for Social and Communication Disorders: background, inter-rater reliability and clinical use. J. Child Psychol. Psychiat. 2002, 43:307-325.
-
(2002)
J. Child Psychol. Psychiat.
, vol.43
, pp. 307-325
-
-
Wing, L.1
Leekam, S.R.2
Libby, S.J.3
Gould, J.4
Larcombe, M.5
-
51
-
-
21344444796
-
Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population
-
Wu S., Jia M., Ruan Y., Liu J., Guo Y., Shuang M., Gong X., Zhang Y., Yang X., Zhang D. Positive association of the oxytocin receptor gene (OXTR) with autism in the Chinese Han population. Biol. Psychiatry 2005, 58:74-77.
-
(2005)
Biol. Psychiatry
, vol.58
, pp. 74-77
-
-
Wu, S.1
Jia, M.2
Ruan, Y.3
Liu, J.4
Guo, Y.5
Shuang, M.6
Gong, X.7
Zhang, Y.8
Yang, X.9
Zhang, D.10
-
52
-
-
15144357923
-
A missense mutation in the CD38 gene, a novel factor for insulin secretion: association with Type II diabetes mellitus in Japanese subjects and evidence of abnormal function when expressed in vitro
-
Yagui K., Shimada F., Mimura M., Hashimoto N., Suzuki Y., Tokuyama Y., Nata K., Tohgo A., Ikehata F., Takasawa S., Okamoto H., Makino H., Saito Y., Kanatsuka A. A missense mutation in the CD38 gene, a novel factor for insulin secretion: association with Type II diabetes mellitus in Japanese subjects and evidence of abnormal function when expressed in vitro. Diabetologia 1998, 41:1024-1028.
-
(1998)
Diabetologia
, vol.41
, pp. 1024-1028
-
-
Yagui, K.1
Shimada, F.2
Mimura, M.3
Hashimoto, N.4
Suzuki, Y.5
Tokuyama, Y.6
Nata, K.7
Tohgo, A.8
Ikehata, F.9
Takasawa, S.10
Okamoto, H.11
Makino, H.12
Saito, Y.13
Kanatsuka, A.14
-
53
-
-
0036828144
-
Identification of cell-specific messenger ribonucleic acids in oxytocinergic and vasopressinergic magnocellular neurons in rat supraoptic nucleus by single-cell differential hybridization
-
Yamashita M., Glasgow E., Zhang B.J., Kusano K., Gainer H. Identification of cell-specific messenger ribonucleic acids in oxytocinergic and vasopressinergic magnocellular neurons in rat supraoptic nucleus by single-cell differential hybridization. Endocrinology 2002, 143:4464-4476.
-
(2002)
Endocrinology
, vol.143
, pp. 4464-4476
-
-
Yamashita, M.1
Glasgow, E.2
Zhang, B.J.3
Kusano, K.4
Gainer, H.5
-
54
-
-
62949122605
-
Oxytocin, sexually dimorphic features of the social brain, and autism
-
Yamasue H., Kuwabara H., Kawakubo Y., Kasai K. Oxytocin, sexually dimorphic features of the social brain, and autism. Psychiatry Clin. Neurosci. 2009, 63:129-140.
-
(2009)
Psychiatry Clin. Neurosci.
, vol.63
, pp. 129-140
-
-
Yamasue, H.1
Kuwabara, H.2
Kawakubo, Y.3
Kasai, K.4
-
55
-
-
34249714340
-
The neurobiology of love
-
Zeki S. The neurobiology of love. FEBS Lett. 2007, 581:2575-2579.
-
(2007)
FEBS Lett.
, vol.581
, pp. 2575-2579
-
-
Zeki, S.1
-
56
-
-
33845889727
-
Essential function of HIPK2 in TGFbeta-dependent survival of midbrain dopamine neurons
-
Zhang J., Pho V., Bonasera S.J., Holtzman J., Tang A.T., Hellmuth J., Tang S., Janak P.H., Tecott L.H., Huang E.J. Essential function of HIPK2 in TGFbeta-dependent survival of midbrain dopamine neurons. Nat. Neurosci. 2007, 10:77-86.
-
(2007)
Nat. Neurosci.
, vol.10
, pp. 77-86
-
-
Zhang, J.1
Pho, V.2
Bonasera, S.J.3
Holtzman, J.4
Tang, A.T.5
Hellmuth, J.6
Tang, S.7
Janak, P.H.8
Tecott, L.H.9
Huang, E.J.10
-
57
-
-
34547886497
-
A unified genetic theory for sporadic and inherited autism
-
Zhao X., Leotta A., Kustanovich V., Lajonchere C., Geschwind D.H., Law K., Law P., Qiu S., Lord C., Sebat J., Ye K., Wigler M. A unified genetic theory for sporadic and inherited autism. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:12831-12836.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 12831-12836
-
-
Zhao, X.1
Leotta, A.2
Kustanovich, V.3
Lajonchere, C.4
Geschwind, D.H.5
Law, K.6
Law, P.7
Qiu, S.8
Lord, C.9
Sebat, J.10
Ye, K.11
Wigler, M.12
|