-
1
-
-
0017187975
-
Catatonia. A prospective clinical study
-
Abrams R., and Taylor M.A. Catatonia. A prospective clinical study. Arch. Gen. Psychiat. 33 (1976) 579-581
-
(1976)
Arch. Gen. Psychiat.
, vol.33
, pp. 579-581
-
-
Abrams, R.1
Taylor, M.A.2
-
2
-
-
0036138102
-
Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
-
Alarcon M., Cantor R.M., Liu J., Gilliam T.C., and Geschwind D.H. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am. J. Hum. Genet. 70 (2002) 60-71
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 60-71
-
-
Alarcon, M.1
Cantor, R.M.2
Liu, J.3
Gilliam, T.C.4
Geschwind, D.H.5
-
3
-
-
0036780698
-
A genomewide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27
-
Auranen M., Vanhala R., Varilo T., Ayers K., Kempas E., Ylisaukko-Oja T., Sinsheimer J.S., Peltonen L., and Jarvela I. A genomewide screen for autism-spectrum disorders: Evidence for a major susceptibility locus on chromosome 3q25-27. Am. J. Hum. Genet. 71 (2002) 777-790
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 777-790
-
-
Auranen, M.1
Vanhala, R.2
Varilo, T.3
Ayers, K.4
Kempas, E.5
Ylisaukko-Oja, T.6
Sinsheimer, J.S.7
Peltonen, L.8
Jarvela, I.9
-
4
-
-
0036360702
-
Higher scores of self reported schizotypy in healthy young males carrying the COMT high activity allele
-
Avramopoulos D., Stefanis N.C., Hantoumi I., Smyrnis N., Evdokimidis I., and Stefanis C.N. Higher scores of self reported schizotypy in healthy young males carrying the COMT high activity allele. Mol. Psychiatr. 7 (2002) 706-711
-
(2002)
Mol. Psychiatr.
, vol.7
, pp. 706-711
-
-
Avramopoulos, D.1
Stefanis, N.C.2
Hantoumi, I.3
Smyrnis, N.4
Evdokimidis, I.5
Stefanis, C.N.6
-
5
-
-
0034088447
-
Genetic studies in autistic disorder and chromosome 15
-
Bass M.P., Menold M.M., Wolpert C.M., Donnelly S.L., Ravan S.A., Hauser E.R., Maddox L.O., Vance J.M., Abramson R.K., Wright H.H., Gilbert J.R., Cuccaro M.L., et al. Genetic studies in autistic disorder and chromosome 15. Neurogenetics 2 (2000) 219-226
-
(2000)
Neurogenetics
, vol.2
, pp. 219-226
-
-
Bass, M.P.1
Menold, M.M.2
Wolpert, C.M.3
Donnelly, S.L.4
Ravan, S.A.5
Hauser, E.R.6
Maddox, L.O.7
Vance, J.M.8
Abramson, R.K.9
Wright, H.H.10
Gilbert, J.R.11
Cuccaro, M.L.12
-
6
-
-
4444362182
-
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome
-
Bearden C.E., Jawad A.F., Lynch D.R., Sokol S., Kanes S.J., McDonald-McGinn D.M., Saitta S.C., Harris S.E., Moss E., Wang P.P., Zackai E., Emanuel B.S., et al. Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome. Am. J. Psychiatr. 161 (2004) 1700-1702
-
(2004)
Am. J. Psychiatr.
, vol.161
, pp. 1700-1702
-
-
Bearden, C.E.1
Jawad, A.F.2
Lynch, D.R.3
Sokol, S.4
Kanes, S.J.5
McDonald-McGinn, D.M.6
Saitta, S.C.7
Harris, S.E.8
Moss, E.9
Wang, P.P.10
Zackai, E.11
Emanuel, B.S.12
-
7
-
-
14044270114
-
Trisomy 15q25.2-qter in an autistic child: Genotype-phenotype correlations
-
Bonati M.T., Finelli P., Giardino D., Gottardi G., Roberts W., and Larizza L. Trisomy 15q25.2-qter in an autistic child: Genotype-phenotype correlations. Am. J. Med. Genet. A 133 (2005) 184-188
-
(2005)
Am. J. Med. Genet. A
, vol.133
, pp. 184-188
-
-
Bonati, M.T.1
Finelli, P.2
Giardino, D.3
Gottardi, G.4
Roberts, W.5
Larizza, L.6
-
8
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
Broman K.W., Murray J.C., Sheffield V.C., White R.L., and Weber J.L. Comprehensive human genetic maps: Individual and sex-specific variation in recombination. Am. J. Hum. Genet. 63 (1998) 861-869
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
9
-
-
0034982149
-
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity
-
Buxbaum J.D., Silverman J.M., Smith C.J., Kilifarski M., Reichert J., Hollander E., Lawlor B.A., Fitzgerald M., Greenberg D.A., and Davis K.L. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am. J. Hum. Genet. 68 (2001) 1514-1520
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1514-1520
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Kilifarski, M.4
Reichert, J.5
Hollander, E.6
Lawlor, B.A.7
Fitzgerald, M.8
Greenberg, D.A.9
Davis, K.L.10
-
10
-
-
85047700330
-
Association between a GABRB3 polymorphism and autism
-
Buxbaum J.D., Silverman J.M., Smith C.J., Greenberg D.A., Kilifarski M., Reichert J., Cook Jr. E.H., Fang Y., Song C.Y., and Vitale R. Association between a GABRB3 polymorphism and autism. Mol. Psychiatr. 7 (2002) 311-316
-
(2002)
Mol. Psychiatr.
, vol.7
, pp. 311-316
-
-
Buxbaum, J.D.1
Silverman, J.M.2
Smith, C.J.3
Greenberg, D.A.4
Kilifarski, M.5
Reichert, J.6
Cook Jr., E.H.7
Fang, Y.8
Song, C.Y.9
Vitale, R.10
-
11
-
-
18944365556
-
Replication of autism linkage: Fine-mapping peak at 17q21
-
Cantor R.M., Kono N., Duvall J.A., Alvarez-Retuerto A., Stone J.L., Alarcon M., Nelson S.F., and Geschwind D.H. Replication of autism linkage: Fine-mapping peak at 17q21. Am. J. Hum. Genet. 76 (2005) 1050-1056
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 1050-1056
-
-
Cantor, R.M.1
Kono, N.2
Duvall, J.A.3
Alvarez-Retuerto, A.4
Stone, J.L.5
Alarcon, M.6
Nelson, S.F.7
Geschwind, D.H.8
-
12
-
-
6044246071
-
Variants in the catechol-O-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families
-
Chen X., Wang X., O'Neill A.F., Walsh D., and Kendler K.S. Variants in the catechol-O-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families. Mol. Psychiatr. 9 (2004) 962-967
-
(2004)
Mol. Psychiatr.
, vol.9
, pp. 962-967
-
-
Chen, X.1
Wang, X.2
O'Neill, A.F.3
Walsh, D.4
Kendler, K.S.5
-
13
-
-
0029988255
-
A metric map of humans: 23,500 loci in 850 bands
-
Collins A., Frezal J., Teague J., and Morton N.E. A metric map of humans: 23,500 loci in 850 bands. Proc. Natl. Acad. Sci. USA 93 (1996) 14,771-14,775
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
-
-
Collins, A.1
Frezal, J.2
Teague, J.3
Morton, N.E.4
-
14
-
-
17344364660
-
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
-
Cook Jr. E.H., Courchesne R.Y., Cox N.J., Lord C., Gonen D., Guter S.J., Lincoln A., Nix K., Haas R., Leventhal B.L., and Courchesne E. Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. Am. J. Hum. Genet. 62 (1998) 1077-1083
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 1077-1083
-
-
Cook Jr., E.H.1
Courchesne, R.Y.2
Cox, N.J.3
Lord, C.4
Gonen, D.5
Guter, S.J.6
Lincoln, A.7
Nix, K.8
Haas, R.9
Leventhal, B.L.10
Courchesne, E.11
-
15
-
-
0035056929
-
The genomic organisation of the metabotropic glutamate receptor subtype 5 gene, and its association with schizophrenia
-
Devon R.S., Anderson S., Teague P.W., Muir W.J., Murray V., Pelosi A.J., Blackwood D.H., and Porteous D.J. The genomic organisation of the metabotropic glutamate receptor subtype 5 gene, and its association with schizophrenia. Mol. Psychiatr. 6 (2001) 311-314
-
(2001)
Mol. Psychiatr.
, vol.6
, pp. 311-314
-
-
Devon, R.S.1
Anderson, S.2
Teague, P.W.3
Muir, W.J.4
Murray, V.5
Pelosi, A.J.6
Blackwood, D.H.7
Porteous, D.J.8
-
16
-
-
0031852985
-
Brief report: Catatonia in autistic disorders
-
Dhossche D. Brief report: Catatonia in autistic disorders. J. Autism Dev. Disord. 28 (1998) 329-331
-
(1998)
J. Autism Dev. Disord.
, vol.28
, pp. 329-331
-
-
Dhossche, D.1
-
17
-
-
0035810850
-
Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia
-
Egan M.F., Goldberg T.E., Kolachana B.S., Callicott J.H., Mazzanti C.M., Straub R.E., Goldman D., and Weinberger D.R. Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia. Proc. Natl. Acad. Sci. USA 98 (2001) 6917-6922
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 6917-6922
-
-
Egan, M.F.1
Goldberg, T.E.2
Kolachana, B.S.3
Callicott, J.H.4
Mazzanti, C.M.5
Straub, R.E.6
Goldman, D.7
Weinberger, D.R.8
-
18
-
-
0037335094
-
Genetic origins of anxiety in women: A role for a functional catechol-O-methyltransferase polymorphism
-
Enoch M.A., Xu K., Ferro E., Harris C.R., and Goldman D. Genetic origins of anxiety in women: A role for a functional catechol-O-methyltransferase polymorphism. Psychiatr. Genet. 13 (2003) 33-41
-
(2003)
Psychiatr. Genet.
, vol.13
, pp. 33-41
-
-
Enoch, M.A.1
Xu, K.2
Ferro, E.3
Harris, C.R.4
Goldman, D.5
-
19
-
-
12644303225
-
Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus
-
Freedman R., Coon H., Myles-Worsley M., Orr-Urtreger A., Olincy A., Davis A., Polymeropoulos M., Holik J., Hopkins J., Hoff M., Rosenthal J., Waldo M.C., et al. Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus. Proc. Natl. Acad. Sci. USA 94 (1997) 587-592
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 587-592
-
-
Freedman, R.1
Coon, H.2
Myles-Worsley, M.3
Orr-Urtreger, A.4
Olincy, A.5
Davis, A.6
Polymeropoulos, M.7
Holik, J.8
Hopkins, J.9
Hoff, M.10
Rosenthal, J.11
Waldo, M.C.12
-
20
-
-
0035829977
-
Evidence for the multigenic inheritance of schizophrenia
-
Freedman R., Leonard S., Olincy A., Kaufmann C.A., Malaspina D., Cloninger C.R., Svrakic D., Faraone S.V., and Tsuang M.T. Evidence for the multigenic inheritance of schizophrenia. Am. J. Med. Genet. 105 (2001) 794-800
-
(2001)
Am. J. Med. Genet.
, vol.105
, pp. 794-800
-
-
Freedman, R.1
Leonard, S.2
Olincy, A.3
Kaufmann, C.A.4
Malaspina, D.5
Cloninger, C.R.6
Svrakic, D.7
Faraone, S.V.8
Tsuang, M.T.9
-
21
-
-
6344237686
-
Association of the DTNBP1 locus with schizophrenia in a U.S. population
-
Funke B., Finn C.T., Plocik A.M., Lake S., DeRosse P., Kane J.M., Kucherlapati R., and Malhotra A.K. Association of the DTNBP1 locus with schizophrenia in a U.S. population. Am. J. Hum. Genet. 75 (2004) 891-898
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 891-898
-
-
Funke, B.1
Finn, C.T.2
Plocik, A.M.3
Lake, S.4
DeRosse, P.5
Kane, J.M.6
Kucherlapati, R.7
Malhotra, A.K.8
-
22
-
-
0346101809
-
Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa
-
Gabrovsek M., Brecelj-Anderluh M., Bellodi L., Cellini E., Di Bella D., Estivill X., Fernandez-Aranda F., Freeman B., Geller F., Gratacos M., Haigh R., Hebebrand J., et al. Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 124 (2004) 68-72
-
(2004)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.124
, pp. 68-72
-
-
Gabrovsek, M.1
Brecelj-Anderluh, M.2
Bellodi, L.3
Cellini, E.4
Di Bella, D.5
Estivill, X.6
Fernandez-Aranda, F.7
Freeman, B.8
Geller, F.9
Gratacos, M.10
Haigh, R.11
Hebebrand, J.12
-
23
-
-
0037365978
-
Association between a functional catechol-O-methyltransferase gene polymorphism and schizophrenia: Meta-analysis of case-control and family-based studies
-
Glatt S.J., Faraone S.V., and Tsuang M.T. Association between a functional catechol-O-methyltransferase gene polymorphism and schizophrenia: Meta-analysis of case-control and family-based studies. Am. J. Psychiatry 160 (2003) 469-476
-
(2003)
Am. J. Psychiatry
, vol.160
, pp. 469-476
-
-
Glatt, S.J.1
Faraone, S.V.2
Tsuang, M.T.3
-
24
-
-
0041819686
-
CAG-repeat length in exon 1 of KCNN3 does not influence risk for schizophrenia or bipolar disorder: A meta-analysis of association studies
-
Glatt S.J., Faraone S.V., and Tsuang M.T. CAG-repeat length in exon 1 of KCNN3 does not influence risk for schizophrenia or bipolar disorder: A meta-analysis of association studies. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 121 (2003) 14-20
-
(2003)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.121
, pp. 14-20
-
-
Glatt, S.J.1
Faraone, S.V.2
Tsuang, M.T.3
-
25
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
IMGSAC
-
IMGSAC. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum. Mol. Genet. 7 (1998) 571-578
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 571-578
-
-
-
26
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
IMGSAC
-
IMGSAC. A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am. J. Hum. Genet. 69 (2001) 570-581
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 570-581
-
-
-
27
-
-
0035830310
-
An autosomal genomic screen for autism
-
IMGSAC
-
IMGSAC. An autosomal genomic screen for autism. Am. J. Med. Genet. 105 (2001) 609-615
-
(2001)
Am. J. Med. Genet.
, vol.105
, pp. 609-615
-
-
-
28
-
-
3042722158
-
Linkage disequilibrium in the DTNBP1 (dysbindin) gene region and on chromosome 1p36 among psychotic patients from a genetic isolate in Israel: Findings from identity by descent haplotype sharing analysis
-
Kohn Y., Danilovich E., Filon D., Oppenheim A., Karni O., Kanyas K., Turetsky N., Korner M., and Lerer B. Linkage disequilibrium in the DTNBP1 (dysbindin) gene region and on chromosome 1p36 among psychotic patients from a genetic isolate in Israel: Findings from identity by descent haplotype sharing analysis. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 128 (2004) 65-70
-
(2004)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.128
, pp. 65-70
-
-
Kohn, Y.1
Danilovich, E.2
Filon, D.3
Oppenheim, A.4
Karni, O.5
Kanyas, K.6
Turetsky, N.7
Korner, M.8
Lerer, B.9
-
29
-
-
0344196966
-
Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15
-
Kury S., Rubie C., Moisan J.P., and Stober G. Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15. J. Neural. Transm. 110 (2003) 1329-1332
-
(2003)
J. Neural. Transm.
, vol.110
, pp. 1329-1332
-
-
Kury, S.1
Rubie, C.2
Moisan, J.P.3
Stober, G.4
-
30
-
-
13444269226
-
Analysis of IMGSAC autism susceptibility loci: Evidence for sex limited and parent of origin specific effects
-
Lamb J.A., Barnby G., Bonora E., Sykes N., Bacchelli E., Blasi F., Maestrini E., Broxholme J., Tzenova J., Weeks D., Bailey A.J., and Monaco A.P. Analysis of IMGSAC autism susceptibility loci: Evidence for sex limited and parent of origin specific effects. J. Med. Genet. 42 (2005) 132-137
-
(2005)
J. Med. Genet.
, vol.42
, pp. 132-137
-
-
Lamb, J.A.1
Barnby, G.2
Bonora, E.3
Sykes, N.4
Bacchelli, E.5
Blasi, F.6
Maestrini, E.7
Broxholme, J.8
Tzenova, J.9
Weeks, D.10
Bailey, A.J.11
Monaco, A.P.12
-
31
-
-
18544369453
-
Risk factors for autism: Perinatal factors, parental psychiatric history, and socioeconomic status
-
Larsson H.J., Eaton W.W., Madsen K.M., Vestergaard M., Olesen A.V., Agerbo E., Schendel D., Thorsen P., and Mortensen P.B. Risk factors for autism: Perinatal factors, parental psychiatric history, and socioeconomic status. Am. J. Epidemiol. 161 (2005) 916-925
-
(2005)
Am. J. Epidemiol.
, vol.161
, pp. 916-925
-
-
Larsson, H.J.1
Eaton, W.W.2
Madsen, K.M.3
Vestergaard, M.4
Olesen, A.V.5
Agerbo, E.6
Schendel, D.7
Thorsen, P.8
Mortensen, P.B.9
-
32
-
-
0033569931
-
Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSAC families. The International Molecular Genetic Study of Autism Consortium
-
Maestrini E., Lai C., Marlow A., Matthews N., Wallace S., Bailey A., Cook E.H., Weeks D.E., and Monaco A.P. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSAC families. The International Molecular Genetic Study of Autism Consortium. Am. J. Med. Genet. 88 (1999) 492-496
-
(1999)
Am. J. Med. Genet.
, vol.88
, pp. 492-496
-
-
Maestrini, E.1
Lai, C.2
Marlow, A.3
Matthews, N.4
Wallace, S.5
Bailey, A.6
Cook, E.H.7
Weeks, D.E.8
Monaco, A.P.9
-
33
-
-
20844457467
-
Shared and specific susceptibility loci for schizophrenia and bipolar disorder: A dense genome scan in Eastern Quebec families
-
Maziade M., Roy M., Chagnon Y., Cliche D., Fournier J., Montgrain N., Dion C., Lavallee J., Garneau Y., Gingras N., Nicole L., Pires L., et al. Shared and specific susceptibility loci for schizophrenia and bipolar disorder: A dense genome scan in Eastern Quebec families. Mol. Psychiatry 10 (2005) 486-499
-
(2005)
Mol. Psychiatry
, vol.10
, pp. 486-499
-
-
Maziade, M.1
Roy, M.2
Chagnon, Y.3
Cliche, D.4
Fournier, J.5
Montgrain, N.6
Dion, C.7
Lavallee, J.8
Garneau, Y.9
Gingras, N.10
Nicole, L.11
Pires, L.12
-
34
-
-
7644221741
-
A linkage disequilibrium map of the 1 Mb 15q12 GABA(A) receptor subunit cluster and association to autism
-
McCauley J.L., Olson L.M., Delahanty R., Amin T., Nurmi E.L., Organ E.L., Jacobs M.M., Folstein S.E., Haines J.L., and Sutcliffe J.S. A linkage disequilibrium map of the 1 Mb 15q12 GABA(A) receptor subunit cluster and association to autism. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 131 (2004) 51-59
-
(2004)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.131
, pp. 51-59
-
-
McCauley, J.L.1
Olson, L.M.2
Delahanty, R.3
Amin, T.4
Nurmi, E.L.5
Organ, E.L.6
Jacobs, M.M.7
Folstein, S.E.8
Haines, J.L.9
Sutcliffe, J.S.10
-
35
-
-
4444269807
-
Association between catechol-O-methyltransferase and phobic anxiety
-
McGrath M., Kawachi I., Ascherio A., Colditz G.A., Hunter D.J., and De Vivo I. Association between catechol-O-methyltransferase and phobic anxiety. Am. J. Psychiatr. 161 (2004) 1703-1705
-
(2004)
Am. J. Psychiatr.
, vol.161
, pp. 1703-1705
-
-
McGrath, M.1
Kawachi, I.2
Ascherio, A.3
Colditz, G.A.4
Hunter, D.J.5
De Vivo, I.6
-
36
-
-
16844373134
-
No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families
-
McKeane D.P., Meyer J., Dobrin S.E., Melmed K.M., Ekawardhani S., Tracy N.A., Lesch K.P., and Stephan D.A. No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families. Schizophr. Res. 75 (2005) 1-3
-
(2005)
Schizophr. Res.
, vol.75
, pp. 1-3
-
-
McKeane, D.P.1
Meyer, J.2
Dobrin, S.E.3
Melmed, K.M.4
Ekawardhani, S.5
Tracy, N.A.6
Lesch, K.P.7
Stephan, D.A.8
-
37
-
-
18344386200
-
Association analysis of chromosome 15 GABAA receptor subunit genes in autistic disorder
-
Menold M.M., Shao Y., Wolpert C.M., Donnelly S.L., Raiford K.L., Martin E.R., Ravan S.A., Abramson R.K., Wright H.H., Delong G.R., Cuccaro M.L., Pericak-Vance M.A., et al. Association analysis of chromosome 15 GABAA receptor subunit genes in autistic disorder. J. Neurogenet. 15 (2001) 245-259
-
(2001)
J. Neurogenet.
, vol.15
, pp. 245-259
-
-
Menold, M.M.1
Shao, Y.2
Wolpert, C.M.3
Donnelly, S.L.4
Raiford, K.L.5
Martin, E.R.6
Ravan, S.A.7
Abramson, R.K.8
Wright, H.H.9
Delong, G.R.10
Cuccaro, M.L.11
Pericak-Vance, M.A.12
-
38
-
-
85047697752
-
Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus
-
Meyer J., Ortega G., Schraut K., Nurnberg G., Ruschendorf F., Saar K., Mossner R., Wienker T.F., Reis A., Stober G., and Lesch K.P. Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus. Mol. Psychiatr. 7 (2002) 220-223
-
(2002)
Mol. Psychiatr.
, vol.7
, pp. 220-223
-
-
Meyer, J.1
Ortega, G.2
Schraut, K.3
Nurnberg, G.4
Ruschendorf, F.5
Saar, K.6
Mossner, R.7
Wienker, T.F.8
Reis, A.9
Stober, G.10
Lesch, K.P.11
-
39
-
-
0033637841
-
Molecular characterization of schizophrenia viewed by microarray analysis of gene expression in prefrontal cortex
-
Mirnics K., Middleton F.A., Marquez A., Lewis D.A., and Levitt P. Molecular characterization of schizophrenia viewed by microarray analysis of gene expression in prefrontal cortex. Neuron 28 (2000) 53-67
-
(2000)
Neuron
, vol.28
, pp. 53-67
-
-
Mirnics, K.1
Middleton, F.A.2
Marquez, A.3
Lewis, D.A.4
Levitt, P.5
-
40
-
-
0042611650
-
Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3
-
Mizuno Y., Puca A.A., O'Brien K.F., Beggs A.H., and Kunkel L.M. Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3. BMC Genet. 2 (2001) 8
-
(2001)
BMC Genet.
, vol.2
, pp. 8
-
-
Mizuno, Y.1
Puca, A.A.2
O'Brien, K.F.3
Beggs, A.H.4
Kunkel, L.M.5
-
41
-
-
0035933037
-
Desmuslin, an intermediate filament protein that interacts with alpha-dystrobrevin and desmin
-
Mizuno Y., Thompson T.G., Guyon J.R., Lidov H.G., Brosius M., Imamura M., Ozawa E., Watkins S.C., and Kunkel L.M. Desmuslin, an intermediate filament protein that interacts with alpha-dystrobrevin and desmin. Proc. Natl. Acad. Sci. USA 98 (2001) 6156-6161
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 6156-6161
-
-
Mizuno, Y.1
Thompson, T.G.2
Guyon, J.R.3
Lidov, H.G.4
Brosius, M.5
Imamura, M.6
Ozawa, E.7
Watkins, S.C.8
Kunkel, L.M.9
-
42
-
-
0035417396
-
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families
-
Nurmi E.L., Bradford Y., Chen Y., Hall J., Arnone B., Gardiner M.B., Hutcheson H.B., Gilbert J.R., Pericak-Vance M.A., Copeland-Yates S.A., Michaelis R.C., Wassink T.H., et al. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics 77 (2001) 105-113
-
(2001)
Genomics
, vol.77
, pp. 105-113
-
-
Nurmi, E.L.1
Bradford, Y.2
Chen, Y.3
Hall, J.4
Arnone, B.5
Gardiner, M.B.6
Hutcheson, H.B.7
Gilbert, J.R.8
Pericak-Vance, M.A.9
Copeland-Yates, S.A.10
Michaelis, R.C.11
Wassink, T.H.12
-
43
-
-
10744229245
-
Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism
-
570.
-
Nurmi E.L., Amin T., Olson L.M., Jacobs M.M., McCauley J.L., Lam A.Y., Organ E.L., Folstein S.E., Haines J.L., and Sutcliffe J.S. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism. Mol. Psychiatr. 8 (2003) 624570-634570 570.
-
(2003)
Mol. Psychiatr.
, vol.8
, pp. 624570-634570
-
-
Nurmi, E.L.1
Amin, T.2
Olson, L.M.3
Jacobs, M.M.4
McCauley, J.L.5
Lam, A.Y.6
Organ, E.L.7
Folstein, S.E.8
Haines, J.L.9
Sutcliffe, J.S.10
-
44
-
-
21044435639
-
The GABA type A receptor alpha5 subunit gene is associated with bipolar I disorder
-
Otani K., Ujike H., Tanaka Y., Morita Y., Katsu T., Nomura A., Uchida N., Hamamura T., Fujiwara Y., and Kuroda S. The GABA type A receptor alpha5 subunit gene is associated with bipolar I disorder. Neurosci. Lett. 381 (2005) 108-113
-
(2005)
Neurosci. Lett.
, vol.381
, pp. 108-113
-
-
Otani, K.1
Ujike, H.2
Tanaka, Y.3
Morita, Y.4
Katsu, T.5
Nomura, A.6
Uchida, N.7
Hamamura, T.8
Fujiwara, Y.9
Kuroda, S.10
-
45
-
-
0035070109
-
Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onset
-
Papadimitriou G., Dikeos D., Daskalopoulou E., Karadima G., Avramopoulos D., Contis C., and Stefanis C. Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onset. Neuropsychobiology 43 (2001) 141-144
-
(2001)
Neuropsychobiology
, vol.43
, pp. 141-144
-
-
Papadimitriou, G.1
Dikeos, D.2
Daskalopoulou, E.3
Karadima, G.4
Avramopoulos, D.5
Contis, C.6
Stefanis, C.7
-
46
-
-
0032492215
-
Association between the GABA(A) receptor alpha5 subunit gene locus (GABRA5) and bipolar affective disorder
-
Papadimitriou G.N., Dikeos D.G., Karadima G., Avramopoulos D., Daskalopoulou E.G., Vassilopoulos D., and Stefanis C.N. Association between the GABA(A) receptor alpha5 subunit gene locus (GABRA5) and bipolar affective disorder. Am. J. Med. Genet. 81 (1998) 73-80
-
(1998)
Am. J. Med. Genet.
, vol.81
, pp. 73-80
-
-
Papadimitriou, G.N.1
Dikeos, D.G.2
Karadima, G.3
Avramopoulos, D.4
Daskalopoulou, E.G.5
Vassilopoulos, D.6
Stefanis, C.N.7
-
47
-
-
0035826542
-
GABA-A receptor beta3 and alpha5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: A genetic association study
-
Papadimitriou G.N., Dikeos D.G., Karadima G., Avramopoulos D., Daskalopoulou E.G., and Stefanis C.N. GABA-A receptor beta3 and alpha5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: A genetic association study. Am. J. Med. Genet. 105 (2001) 317-320
-
(2001)
Am. J. Med. Genet.
, vol.105
, pp. 317-320
-
-
Papadimitriou, G.N.1
Dikeos, D.G.2
Karadima, G.3
Avramopoulos, D.4
Daskalopoulou, E.G.5
Stefanis, C.N.6
-
48
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
-
Philippe A., Martinez M., Guilloud-Bataille M., Gillberg C., Rastam M., Sponheim E., Coleman M., Zappella M., Aschauer H., Van Maldergem L., Penet C., Feingold J., et al. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum. Mol. Genet. 8 (1999) 805-812
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
Coleman, M.7
Zappella, M.8
Aschauer, H.9
Van Maldergem, L.10
Penet, C.11
Feingold, J.12
-
49
-
-
0035856428
-
Postmortem brain abnormalities of the glutamate neurotransmitter system in autism
-
Purcell A.E., Jeon O.H., Zimmerman A.W., Blue M.E., and Pevsner J. Postmortem brain abnormalities of the glutamate neurotransmitter system in autism. Neurology 57 (2001) 1618-1628
-
(2001)
Neurology
, vol.57
, pp. 1618-1628
-
-
Purcell, A.E.1
Jeon, O.H.2
Zimmerman, A.W.3
Blue, M.E.4
Pevsner, J.5
-
50
-
-
20144387173
-
Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1)
-
Raybould R., Green E.K., MacGregor S., Gordon-Smith K., Heron J., Hyde S., Caesar S., Nikolov I., Williams N., Jones L., O'Donovan M.C., Owen M.J., et al. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biol. Psychiatr. 57 (2005) 696-701
-
(2005)
Biol. Psychiatr.
, vol.57
, pp. 696-701
-
-
Raybould, R.1
Green, E.K.2
MacGregor, S.3
Gordon-Smith, K.4
Heron, J.5
Hyde, S.6
Caesar, S.7
Nikolov, I.8
Williams, N.9
Jones, L.10
O'Donovan, M.C.11
Owen, M.J.12
-
51
-
-
0026348447
-
Catatonia in autistic disorder: A sign of comorbidity or variable expression?
-
Realmuto G.M., and August G.J. Catatonia in autistic disorder: A sign of comorbidity or variable expression?. J. Autism Dev. Disord. 21 (1991) 517-528
-
(1991)
J. Autism Dev. Disord.
, vol.21
, pp. 517-528
-
-
Realmuto, G.M.1
August, G.J.2
-
52
-
-
0033362024
-
A genomic screen of autism: Evidence for a multilocus etiology
-
Risch N., Spiker D., Lotspeich L., Nouri N., Hinds D., Hallmayer J., Kalaydjieva L., McCague P., Dimiceli S., Pitts T., Nguyen L., Yang J., et al. A genomic screen of autism: Evidence for a multilocus etiology. Am. J. Hum. Genet. 65 (1999) 493-507
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
Nouri, N.4
Hinds, D.5
Hallmayer, J.6
Kalaydjieva, L.7
McCague, P.8
Dimiceli, S.9
Pitts, T.10
Nguyen, L.11
Yang, J.12
-
53
-
-
8844248677
-
Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: Association is more significant in women
-
Sazci A., Ergul E., Kucukali I., Kilic G., Kaya G., and Kara I. Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: Association is more significant in women. Brain. Res. Mol. Brain. Res. 132 (2004) 51-56
-
(2004)
Brain. Res. Mol. Brain. Res.
, vol.132
, pp. 51-56
-
-
Sazci, A.1
Ergul, E.2
Kucukali, I.3
Kilic, G.4
Kaya, G.5
Kara, I.6
-
54
-
-
0037222276
-
Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families
-
Schwab S.G., Knapp M., Mondabon S., Hallmayer J., Borrmann-Hassenbach M., Albus M., Lerer B., Rietschel M., Trixler M., Maier W., and Wildenauer D.B. Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families. Am. J. Hum. Genet. 72 (2003) 185-190
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 185-190
-
-
Schwab, S.G.1
Knapp, M.2
Mondabon, S.3
Hallmayer, J.4
Borrmann-Hassenbach, M.5
Albus, M.6
Lerer, B.7
Rietschel, M.8
Trixler, M.9
Maier, W.10
Wildenauer, D.B.11
-
55
-
-
0037371673
-
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes
-
Shao Y., Cuccaro M.L., Hauser E.R., Raiford K.L., Menold M.M., Wolpert C.M., Ravan S.A., Elston L., Decena K., Donnelly S.L., Abramson R.K., Wright H.H., et al. Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. Am. J. Hum. Genet. 72 (2003) 539-548
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 539-548
-
-
Shao, Y.1
Cuccaro, M.L.2
Hauser, E.R.3
Raiford, K.L.4
Menold, M.M.5
Wolpert, C.M.6
Ravan, S.A.7
Elston, L.8
Decena, K.9
Donnelly, S.L.10
Abramson, R.K.11
Wright, H.H.12
-
56
-
-
3042806953
-
COMT: A common susceptibility gene in bipolar disorder and schizophrenia
-
Shifman S., Bronstein M., Sternfeld M., Pisante A., Weizman A., Reznik I., Spivak B., Grisaru N., Karp L., Schiffer R., Kotler M., Strous R.D., et al. COMT: A common susceptibility gene in bipolar disorder and schizophrenia. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 128 (2004) 61-64
-
(2004)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.128
, pp. 61-64
-
-
Shifman, S.1
Bronstein, M.2
Sternfeld, M.3
Pisante, A.4
Weizman, A.5
Reznik, I.6
Spivak, B.7
Grisaru, N.8
Karp, L.9
Schiffer, R.10
Kotler, M.11
Strous, R.D.12
-
57
-
-
0034606205
-
Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13
-
Smith M., Filipek P.A., Wu C., Bocian M., Hakim S., Modahl C., and Spence M.A. Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13. Am. J. Med. Genet. 96 (2000) 765-770
-
(2000)
Am. J. Med. Genet.
, vol.96
, pp. 765-770
-
-
Smith, M.1
Filipek, P.A.2
Wu, C.3
Bocian, M.4
Hakim, S.5
Modahl, C.6
Spence, M.A.7
-
60
-
-
0033847848
-
hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia
-
Stöber G., Meyer J., Nanda I., Wienker T.F., Saar K., Jatzke S., Schmid M., Lesch K.P., and Beckmann H. hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia. Eur. Arch. Psychiatry Clin. Neurosci. 250 (2000) 163-168
-
(2000)
Eur. Arch. Psychiatry Clin. Neurosci.
, vol.250
, pp. 163-168
-
-
Stöber, G.1
Meyer, J.2
Nanda, I.3
Wienker, T.F.4
Saar, K.5
Jatzke, S.6
Schmid, M.7
Lesch, K.P.8
Beckmann, H.9
-
61
-
-
0033754079
-
Splitting schizophrenia: Periodic catatonia-susceptibility locus on chromosome 15q15
-
Stöber G., Saar K., Ruschendorf F., Meyer J., Nurnberg G., Jatzke S., Franzek E., Reis A., Lesch K.P., Wienker T.F., and Beckmann H. Splitting schizophrenia: Periodic catatonia-susceptibility locus on chromosome 15q15. Am. J. Hum. Genet. 67 (2000) 1201-1207
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 1201-1207
-
-
Stöber, G.1
Saar, K.2
Ruschendorf, F.3
Meyer, J.4
Nurnberg, G.5
Jatzke, S.6
Franzek, E.7
Reis, A.8
Lesch, K.P.9
Wienker, T.F.10
Beckmann, H.11
-
62
-
-
0036780845
-
Periodic catatonia: Confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity
-
Stöber G., Seelow D., Ruschendorf F., Ekici A., Beckmann H., and Reis A. Periodic catatonia: Confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity. Hum. Genet. 111 (2002) 323-330
-
(2002)
Hum. Genet.
, vol.111
, pp. 323-330
-
-
Stöber, G.1
Seelow, D.2
Ruschendorf, F.3
Ekici, A.4
Beckmann, H.5
Reis, A.6
-
63
-
-
2142653598
-
Evidence for linkage between regulatory enzymes in glycolysis and schizophrenia in a multiplex sample
-
Stone W.S., Faraone S.V., Su J., Tarbox S.I., Van Eerdewegh P., and Tsuang M.T. Evidence for linkage between regulatory enzymes in glycolysis and schizophrenia in a multiplex sample. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 127 (2004) 5-10
-
(2004)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.127
, pp. 5-10
-
-
Stone, W.S.1
Faraone, S.V.2
Su, J.3
Tarbox, S.I.4
Van Eerdewegh, P.5
Tsuang, M.T.6
-
64
-
-
18444364206
-
Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog on the mouse dysbindin gene, is associated with schizophrenia
-
Straub R.E., Jiang Y., MacLean C.J., Ma Y., Webb B.T., Myakishev M.V., Harris-Kerr C., Wormley B., Sadek H., Kadambi B., Cesare A.J., Gibberman A., et al. Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog on the mouse dysbindin gene, is associated with schizophrenia. Am. J. Hum. Genet. 71 (2002) 337-348
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 337-348
-
-
Straub, R.E.1
Jiang, Y.2
MacLean, C.J.3
Ma, Y.4
Webb, B.T.5
Myakishev, M.V.6
Harris-Kerr, C.7
Wormley, B.8
Sadek, H.9
Kadambi, B.10
Cesare, A.J.11
Gibberman, A.12
-
65
-
-
0035957960
-
N-methyl-D-aspartate receptors regulate a group of transiently expressed genes in the developing brain
-
Sugiura N., Patel R.G., and Corriveau R.A. N-methyl-D-aspartate receptors regulate a group of transiently expressed genes in the developing brain. J. Biol. Chem. 276 (2001) 14,257-14,263
-
(2001)
J. Biol. Chem.
, vol.276
-
-
Sugiura, N.1
Patel, R.G.2
Corriveau, R.A.3
-
66
-
-
9144267763
-
The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease
-
Van Den Bogaert A., Schumacher J., Schulze T.G., Otte A.C., Ohlraun S., Kovalenko S., Becker T., Freudenberg J., Jonsson E.G., Mattila-Evenden M., Sedvall G.C., Czerski P.M., et al. The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease. Am. J. Hum. Genet. 73 (2003) 1438-1443
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 1438-1443
-
-
Van Den Bogaert, A.1
Schumacher, J.2
Schulze, T.G.3
Otte, A.C.4
Ohlraun, S.5
Kovalenko, S.6
Becker, T.7
Freudenberg, J.8
Jonsson, E.G.9
Mattila-Evenden, M.10
Sedvall, G.C.11
Czerski, P.M.12
-
67
-
-
0038235907
-
Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families
-
van den Oord E.J., Sullivan P.F., Jiang Y., Walsh D., O'Neill F.A., Kendler K.S., and Riley B.P. Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families. Mol. Psychiatr. 8 (2003) 499-510
-
(2003)
Mol. Psychiatr.
, vol.8
, pp. 499-510
-
-
van den Oord, E.J.1
Sullivan, P.F.2
Jiang, Y.3
Walsh, D.4
O'Neill, F.A.5
Kendler, K.S.6
Riley, B.P.7
-
69
-
-
0033625728
-
Catatonia in autistic spectrum disorders
-
Wing L., and Shah A. Catatonia in autistic spectrum disorders. Br. J. Psychiatry 176 (2000) 357-362
-
(2000)
Br. J. Psychiatry
, vol.176
, pp. 357-362
-
-
Wing, L.1
Shah, A.2
-
70
-
-
0041413380
-
Association between Val108/158 Met polymorphism of the COMT gene and schizophrenia
-
Wonodi I., Stine O.C., Mitchell B.D., Buchanan R.W., and Thaker G.K. Association between Val108/158 Met polymorphism of the COMT gene and schizophrenia. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 120 (2003) 47-50
-
(2003)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.120
, pp. 47-50
-
-
Wonodi, I.1
Stine, O.C.2
Mitchell, B.D.3
Buchanan, R.W.4
Thaker, G.K.5
-
71
-
-
0035826536
-
Evidence for an association with the serotonin transporter promoter region polymorphism and autism
-
Yirmiya N., Pilowsky T., Nemanov L., Arbelle S., Feinsilver T., Fried I., and Ebstein R.P. Evidence for an association with the serotonin transporter promoter region polymorphism and autism. Am. J. Med. Genet. 105 (2001) 381-386
-
(2001)
Am. J. Med. Genet.
, vol.105
, pp. 381-386
-
-
Yirmiya, N.1
Pilowsky, T.2
Nemanov, L.3
Arbelle, S.4
Feinsilver, T.5
Fried, I.6
Ebstein, R.P.7
-
72
-
-
1542284670
-
Genome-wide scan for loci of Asperger syndrome
-
Ylisaukko-Oja T., Nieminen-von Wendt T., Kempas E., Sarenius S., Varilo T., von Wendt L., Peltonen L., and Jarvela I. Genome-wide scan for loci of Asperger syndrome. Mol. Psychiatr. 9 (2004) 161-168
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(2004)
Mol. Psychiatr.
, vol.9
, pp. 161-168
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Ylisaukko-Oja, T.1
Nieminen-von Wendt, T.2
Kempas, E.3
Sarenius, S.4
Varilo, T.5
von Wendt, L.6
Peltonen, L.7
Jarvela, I.8
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