-
1
-
-
0038003196
-
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia
-
Lewis C.M., Levinson D.F., Wise L.H., DeLisi L.E., Straub R.E., Hovatta I., et al. Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia. Am J Hum Genet 73 (2003) 34-48
-
(2003)
Am J Hum Genet
, vol.73
, pp. 34-48
-
-
Lewis, C.M.1
Levinson, D.F.2
Wise, L.H.3
DeLisi, L.E.4
Straub, R.E.5
Hovatta, I.6
-
2
-
-
3142767559
-
Genetic abnormalities of chromosome 22 and the development of psychosis
-
Williams N.M., and Owen M.J. Genetic abnormalities of chromosome 22 and the development of psychosis. Curr Psychiatry Rep 6 (2004) 176-182
-
(2004)
Curr Psychiatry Rep
, vol.6
, pp. 176-182
-
-
Williams, N.M.1
Owen, M.J.2
-
3
-
-
1442357651
-
A nonsense mutation in the synaptogyrin 1 gene in a family with schizophrenia
-
Verma R., Chauhan C., Saleem Q., Gandhi C., Jain S., and Brahmachari S.K. A nonsense mutation in the synaptogyrin 1 gene in a family with schizophrenia. Biol Psychiatry 55 (2004) 196-199
-
(2004)
Biol Psychiatry
, vol.55
, pp. 196-199
-
-
Verma, R.1
Chauhan, C.2
Saleem, Q.3
Gandhi, C.4
Jain, S.5
Brahmachari, S.K.6
-
4
-
-
10744226205
-
Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia
-
Takahashi S., Ohtsuki T., Yu S.Y., Tanabe E., Yara K., Kamioka M., et al. Significant linkage to chromosome 22q for exploratory eye movement dysfunction in schizophrenia. Am J Med Genet B Neuropsychiatr Genet 123 (2003) 27-32
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.123
, pp. 27-32
-
-
Takahashi, S.1
Ohtsuki, T.2
Yu, S.Y.3
Tanabe, E.4
Yara, K.5
Kamioka, M.6
-
5
-
-
10744228601
-
Family-based association study of markers on chromosome 22 in schizophrenia using African-American, European-American, and Chinese families
-
Takahashi S., Cui Y.H., Kojima T., Han Y.H., Zhou R.L., Kamioka M., et al. Family-based association study of markers on chromosome 22 in schizophrenia using African-American, European-American, and Chinese families. Am J Med Genet B Neuropsychiatr Genet 120 (2003) 11-17
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.120
, pp. 11-17
-
-
Takahashi, S.1
Cui, Y.H.2
Kojima, T.3
Han, Y.H.4
Zhou, R.L.5
Kamioka, M.6
-
6
-
-
0036258079
-
Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia
-
Badner J.A., and Gershon E.S. Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia. Mol Psychiatry 7 (2002) 405-411
-
(2002)
Mol Psychiatry
, vol.7
, pp. 405-411
-
-
Badner, J.A.1
Gershon, E.S.2
-
7
-
-
0029874880
-
A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22)
-
Gill M., Vallada H., Collier D., Sham P., Holmans P., Murray R., et al. A combined analysis of D22S278 marker alleles in affected sib-pairs: Support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). Am J Med Genet 67 (1996) 40-45
-
(1996)
Am J Med Genet
, vol.67
, pp. 40-45
-
-
Gill, M.1
Vallada, H.2
Collier, D.3
Sham, P.4
Holmans, P.5
Murray, R.6
-
8
-
-
0028786445
-
Potential linkage disequilibrium between schizophrenia and locus D22S278 on the long arm of chromosome 22
-
Moises H.W., Yang L., Li T., Havsteen B., Fimmers R., Baur M.P., et al. Potential linkage disequilibrium between schizophrenia and locus D22S278 on the long arm of chromosome 22. Am J Med Genet 60 (1995) 465-467
-
(1995)
Am J Med Genet
, vol.60
, pp. 465-467
-
-
Moises, H.W.1
Yang, L.2
Li, T.3
Havsteen, B.4
Fimmers, R.5
Baur, M.P.6
-
9
-
-
0032572612
-
A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: Further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Collaborative Linkage Group for Chromosome 22
-
Group S.C.L. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: Further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Collaborative Linkage Group for Chromosome 22. Schizophr Res 32 (1998) 115-121
-
(1998)
Schizophr Res
, vol.32
, pp. 115-121
-
-
Group, S.C.L.1
-
10
-
-
0028937526
-
Linkage studies on chromosome 22 in familial schizophrenia
-
Vallada H.P., Gill M., Sham P., Lim L.C., Nanko S., Asherson P., et al. Linkage studies on chromosome 22 in familial schizophrenia. Am J Med Genet 60 (1995) 139-146
-
(1995)
Am J Med Genet
, vol.60
, pp. 139-146
-
-
Vallada, H.P.1
Gill, M.2
Sham, P.3
Lim, L.C.4
Nanko, S.5
Asherson, P.6
-
11
-
-
0029561772
-
Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia
-
Vallada H., Curtis D., Sham P.C., Murray R.M., McGuffin P., Nanko S., et al. Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia. Psychiatr Genet 5 (1995) 127-130
-
(1995)
Psychiatr Genet
, vol.5
, pp. 127-130
-
-
Vallada, H.1
Curtis, D.2
Sham, P.C.3
Murray, R.M.4
McGuffin, P.5
Nanko, S.6
-
12
-
-
18244398975
-
Search for common haplotypes on chromosome 22q in patients with schizophrenia or bipolar disorder from the Faroe Islands
-
Jorgensen T.H., Borglum A.D., Mors O., Wang A.G., Pinaud M., Flint T.J., et al. Search for common haplotypes on chromosome 22q in patients with schizophrenia or bipolar disorder from the Faroe Islands. Am J Med Genet 114 (2002) 245-252
-
(2002)
Am J Med Genet
, vol.114
, pp. 245-252
-
-
Jorgensen, T.H.1
Borglum, A.D.2
Mors, O.3
Wang, A.G.4
Pinaud, M.5
Flint, T.J.6
-
13
-
-
0038823525
-
The endophenotype concept in psychiatry: Etymology and strategic intentions
-
Gottesman I.I., and Gould T.D. The endophenotype concept in psychiatry: Etymology and strategic intentions. Am J Psychiatry 160 (2003) 636-645
-
(2003)
Am J Psychiatry
, vol.160
, pp. 636-645
-
-
Gottesman, I.I.1
Gould, T.D.2
-
14
-
-
33751310482
-
A continuous performance test of brain damage
-
Rosvold H.E., Mirsky A.F., Sarason I., Bransome Jr. E.D., and Beck L.H. A continuous performance test of brain damage. J Consult Psychol 20 (1956) 343-350
-
(1956)
J Consult Psychol
, vol.20
, pp. 343-350
-
-
Rosvold, H.E.1
Mirsky, A.F.2
Sarason, I.3
Bransome Jr., E.D.4
Beck, L.H.5
-
15
-
-
0034059094
-
Sustained attention deficits as markers of genetic susceptibility to schizophrenia
-
Chen W.J., and Faraone S.V. Sustained attention deficits as markers of genetic susceptibility to schizophrenia. Am J Med Genet 97 (2000) 52-57
-
(2000)
Am J Med Genet
, vol.97
, pp. 52-57
-
-
Chen, W.J.1
Faraone, S.V.2
-
16
-
-
0028261613
-
Impaired attention, genetics, and the pathophysiology of schizophrenia
-
Cornblatt B.A., and Keilp J.G. Impaired attention, genetics, and the pathophysiology of schizophrenia. Schizophr Bull 20 (1994) 31-46
-
(1994)
Schizophr Bull
, vol.20
, pp. 31-46
-
-
Cornblatt, B.A.1
Keilp, J.G.2
-
17
-
-
0031708881
-
Sustained attention deficit and schizotypal personality features in nonpsychotic relatives of schizophrenic patients
-
Chen W.J., Liu S.K., Chang C.J., Lien Y.J., Chang Y.H., and Hwu H.G. Sustained attention deficit and schizotypal personality features in nonpsychotic relatives of schizophrenic patients. Am J Psychiatry 155 (1998) 1214-1220
-
(1998)
Am J Psychiatry
, vol.155
, pp. 1214-1220
-
-
Chen, W.J.1
Liu, S.K.2
Chang, C.J.3
Lien, Y.J.4
Chang, Y.H.5
Hwu, H.G.6
-
18
-
-
2342590773
-
Sustained attention deficits in nonpsychotic relatives of schizophrenic patients: A recurrence risk ratio analysis
-
Collaborators from the Multidimensional Psychopathology Group Research Project
-
Chen W.J., Chang C.-H., Liu S.K., Hwang T.J., Hwu H.-G., and Collaborators from the Multidimensional Psychopathology Group Research Project. Sustained attention deficits in nonpsychotic relatives of schizophrenic patients: A recurrence risk ratio analysis. Biol Psychiatry 55 (2004) 995-1000
-
(2004)
Biol Psychiatry
, vol.55
, pp. 995-1000
-
-
Chen, W.J.1
Chang, C.-H.2
Liu, S.K.3
Hwang, T.J.4
Hwu, H.-G.5
-
19
-
-
0019131721
-
The utility of the Wisconsin Card Sorting Test in detecting and localizing frontal lobe lesions
-
Robinson A.L., Heaton R.K., Lehman R.A., and Stilson D.W. The utility of the Wisconsin Card Sorting Test in detecting and localizing frontal lobe lesions. J Consult Clin Psychol 48 (1980) 605-614
-
(1980)
J Consult Clin Psychol
, vol.48
, pp. 605-614
-
-
Robinson, A.L.1
Heaton, R.K.2
Lehman, R.A.3
Stilson, D.W.4
-
20
-
-
0023507317
-
Further evidence for dementia of the prefrontal type in schizophrenia?. A controlled study of teaching the Wisconsin Card Sorting Test
-
Goldberg T.E., Weinberger D.R., Berman K.F., Pliskin N.H., and Podd M.H. Further evidence for dementia of the prefrontal type in schizophrenia?. A controlled study of teaching the Wisconsin Card Sorting Test. Arch Gen Psychiatry 44 (1987) 1008-1014
-
(1987)
Arch Gen Psychiatry
, vol.44
, pp. 1008-1014
-
-
Goldberg, T.E.1
Weinberger, D.R.2
Berman, K.F.3
Pliskin, N.H.4
Podd, M.H.5
-
21
-
-
7144252536
-
Factor structure of the Wisconsin Card Sorting Test: Dimensions of deficit in schizophrenia
-
Koren D., Seidman L.J., Harrison R.H., Lyons M.J., Kremen W.S., Caplan B., et al. Factor structure of the Wisconsin Card Sorting Test: Dimensions of deficit in schizophrenia. Neuropsychology 12 (1998) 289-302
-
(1998)
Neuropsychology
, vol.12
, pp. 289-302
-
-
Koren, D.1
Seidman, L.J.2
Harrison, R.H.3
Lyons, M.J.4
Kremen, W.S.5
Caplan, B.6
-
22
-
-
0036773647
-
Wisconsin Card Sorting deficits in the offspring of schizophrenics in the New York High-Risk Project
-
Wolf L.E., Cornblatt B.A., Roberts S.A., Shapiro B.M., and Erlenmeyer-Kimling L. Wisconsin Card Sorting deficits in the offspring of schizophrenics in the New York High-Risk Project. Schizophr Res 57 (2002) 173
-
(2002)
Schizophr Res
, vol.57
, pp. 173
-
-
Wolf, L.E.1
Cornblatt, B.A.2
Roberts, S.A.3
Shapiro, B.M.4
Erlenmeyer-Kimling, L.5
-
23
-
-
0036641258
-
Symptom patterns and subgrouping of schizophrenic patients: Significance of negative symptoms assessed on admission
-
Hwu H.G., Chen C.H., Hwang T.J., Liu C.M., Cheng J.J., Lin S.K., et al. Symptom patterns and subgrouping of schizophrenic patients: Significance of negative symptoms assessed on admission. Schizophr Res 56 (2002) 105-119
-
(2002)
Schizophr Res
, vol.56
, pp. 105-119
-
-
Hwu, H.G.1
Chen, C.H.2
Hwang, T.J.3
Liu, C.M.4
Cheng, J.J.5
Lin, S.K.6
-
24
-
-
20144381752
-
Taiwan schizophrenia linkage study: The field study
-
Hwu H.G., Faraone S.V., Liu C.M., Chen W.J., Liu S.K., Shieh M.H., et al. Taiwan schizophrenia linkage study: The field study. Am J Med Genet B Neuropsychiatr Genet 134 (2005) 30-36
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.134
, pp. 30-36
-
-
Hwu, H.G.1
Faraone, S.V.2
Liu, C.M.3
Chen, W.J.4
Liu, S.K.5
Shieh, M.H.6
-
25
-
-
33745083236
-
-
Publication Committee, College of Medicine, National Taiwan University, Taipei, Taiwan
-
Hwu H.G. Psychiatric Diagnostic Assessment. 2nd ed. (1999), Publication Committee, College of Medicine, National Taiwan University, Taipei, Taiwan
-
(1999)
Psychiatric Diagnostic Assessment. 2nd ed.
-
-
Hwu, H.G.1
-
26
-
-
33745078458
-
-
Institute of Epidemiology, College of Public Health, National Taiwan University, Taipei, Taiwan
-
Chen W.J. Diagnostic Interview for Genetic Studies (DIGS) Mandarin Version 2.0 (1999), Institute of Epidemiology, College of Public Health, National Taiwan University, Taipei, Taiwan
-
(1999)
Diagnostic Interview for Genetic Studies (DIGS) Mandarin Version 2.0
-
-
Chen, W.J.1
-
27
-
-
0033909546
-
A general test of association for quantitative traits in nuclear families
-
Abecasis G.R., Cardon L.R., and Cookson W.O. A general test of association for quantitative traits in nuclear families. Am J Hum Genet 66 (2000) 279-292
-
(2000)
Am J Hum Genet
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.3
-
28
-
-
0031907796
-
Performance of the continuous performance test among community samples
-
Chen W.J., Hsiao C.K., Hsiao L.-L., and Hwu H.-G. Performance of the continuous performance test among community samples. Schizophr Bull 24 (1998) 163-174
-
(1998)
Schizophr Bull
, vol.24
, pp. 163-174
-
-
Chen, W.J.1
Hsiao, C.K.2
Hsiao, L.-L.3
Hwu, H.-G.4
-
29
-
-
0001516060
-
Vigilance in schizophrenia and related disorders
-
Steinhauer S.R., Gruzelier J.H., and Zubin J. (Eds), Elsevier, Amsterdam
-
Nuechterlein K.H. Vigilance in schizophrenia and related disorders. In: Steinhauer S.R., Gruzelier J.H., and Zubin J. (Eds). Handbook of Schizophrenia, Vol. 5: Neuropsychology, Psychophysiology and Information Processing (1991), Elsevier, Amsterdam 397-433
-
(1991)
Handbook of Schizophrenia, Vol. 5: Neuropsychology, Psychophysiology and Information Processing
, pp. 397-433
-
-
Nuechterlein, K.H.1
-
30
-
-
0030209761
-
Computerized Wisconsin Card Sorting Test: comparison with manual administration
-
Tien A.Y., Spevack T.V., Jones D.W., Pearlson G.D., Schlaepfer T.E., and Strauss M.E. Computerized Wisconsin Card Sorting Test: comparison with manual administration. Kaohsiung J Med Sci 12 (1996) 479-485
-
(1996)
Kaohsiung J Med Sci
, vol.12
, pp. 479-485
-
-
Tien, A.Y.1
Spevack, T.V.2
Jones, D.W.3
Pearlson, G.D.4
Schlaepfer, T.E.5
Strauss, M.E.6
-
31
-
-
0034089322
-
Performance on the Wisconsin Card Sorting Test among adolescents in Taiwan: Norms, factorial structure, and relation to schizotypy
-
Lin C.C.H., Chen W.J., Yang H.-J., Hsiao C.K., and Tien A.Y. Performance on the Wisconsin Card Sorting Test among adolescents in Taiwan: Norms, factorial structure, and relation to schizotypy. J Clin Exp Neuropsychol 22 (2000) 69-79
-
(2000)
J Clin Exp Neuropsychol
, vol.22
, pp. 69-79
-
-
Lin, C.C.H.1
Chen, W.J.2
Yang, H.-J.3
Hsiao, C.K.4
Tien, A.Y.5
-
32
-
-
0003968285
-
-
Psychological Assessment Resources, Odessa, Florida
-
Heaton R.K., Chelune G.I., Talley J.L., Kay G.G., and Curtiss G. Wisconsin Card Sorting Test Manual: Revised and Expanded (1993), Psychological Assessment Resources, Odessa, Florida
-
(1993)
Wisconsin Card Sorting Test Manual: Revised and Expanded
-
-
Heaton, R.K.1
Chelune, G.I.2
Talley, J.L.3
Kay, G.G.4
Curtiss, G.5
-
33
-
-
0036594904
-
A strategy for the rapid discovery of disease markers using the MassARRAY system
-
68-69
-
Rodi C.P., Darnhofer-Patel B., Stanssens P., Zabeau M., and van den Boom D. A strategy for the rapid discovery of disease markers using the MassARRAY system. Biotechniques Suppl (2002) 62-66 68-69
-
(2002)
Biotechniques
, Issue.SUPPL
, pp. 62-66
-
-
Rodi, C.P.1
Darnhofer-Patel, B.2
Stanssens, P.3
Zabeau, M.4
van den Boom, D.5
-
34
-
-
14844303718
-
Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications
-
Tost J., and Gut I.G. Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications. Clin Biochem 38 (2005) 335-350
-
(2005)
Clin Biochem
, vol.38
, pp. 335-350
-
-
Tost, J.1
Gut, I.G.2
-
35
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell J.R., and Weeks D.E. PedCheck: A program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 63 (1998) 259-266
-
(1998)
Am J Hum Genet
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
37
-
-
0345821169
-
-
SAS, SAS Institute, Cary, North Carolina
-
SAS. SAS/Genetics User's Guide (2002), SAS Institute, Cary, North Carolina
-
(2002)
SAS/Genetics User's Guide
-
-
-
38
-
-
0023430504
-
Gametic disequilibrium measures: Proceed with caution
-
Hedrick P.W. Gametic disequilibrium measures: Proceed with caution. Genetics 117 (1987) 331-341
-
(1987)
Genetics
, vol.117
, pp. 331-341
-
-
Hedrick, P.W.1
-
39
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett J.C., Fry B., Maller J., and Daly M.J. Haploview: Analysis and visualization of LD and haplotype maps. Bioinformatics 21 (2005) 263-265
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
40
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E., and Lange K. Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 58 (1996) 1323-1337
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
41
-
-
0035741831
-
Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees
-
Sobel E., Sengul H., and Weeks D.E. Multipoint estimation of identity-by-descent probabilities at arbitrary positions among marker loci on general pedigrees. Hum Hered 52 (2001) 121-131
-
(2001)
Hum Hered
, vol.52
, pp. 121-131
-
-
Sobel, E.1
Sengul, H.2
Weeks, D.E.3
-
42
-
-
0036157589
-
Detection and integration of genotyping errors in statistical genetics
-
Sobel E., Papp J.C., and Lange K. Detection and integration of genotyping errors in statistical genetics. Am J Hum Genet 70 (2002) 496-508
-
(2002)
Am J Hum Genet
, vol.70
, pp. 496-508
-
-
Sobel, E.1
Papp, J.C.2
Lange, K.3
-
43
-
-
0035055544
-
The family based association test method: Strategies for studying general genotype-phenotype associations
-
Horvath S., Xu X., and Laird N.M. The family based association test method: Strategies for studying general genotype-phenotype associations. Eur J Hum Genet 9 (2001) 301-306
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 301-306
-
-
Horvath, S.1
Xu, X.2
Laird, N.M.3
-
44
-
-
0033814928
-
Implementing a unified approach to family-based tests of association
-
Laird N.M., Horvath S., and Xu X. Implementing a unified approach to family-based tests of association. Genet Epidemiol 19 (2000) S36-S42
-
(2000)
Genet Epidemiol
, vol.19
-
-
Laird, N.M.1
Horvath, S.2
Xu, X.3
-
45
-
-
0347992868
-
Family-based tests for associating haplotypes with general phenotype data: Application to asthma genetics
-
Horvath S., Xu X., Lake S.L., Silverman E.K., Weiss S.T., and Laird N.M. Family-based tests for associating haplotypes with general phenotype data: Application to asthma genetics. Genet Epidemiol 26 (2004) 61-69
-
(2004)
Genet Epidemiol
, vol.26
, pp. 61-69
-
-
Horvath, S.1
Xu, X.2
Lake, S.L.3
Silverman, E.K.4
Weiss, S.T.5
Laird, N.M.6
-
46
-
-
0033237335
-
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission
-
Clayton D. A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. Am J Hum Genet 65 (1999) 1170-1177
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1170-1177
-
-
Clayton, D.1
-
47
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis G.R., Cherny S.S., Cookson W.O., and Cardon L.R. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30 (2002) 97-101
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
48
-
-
33646749338
-
A comparison of major histocompatibility complex SNPs in Han Chinese residing in Taiwan and Caucasians
-
Yang H.C., Lin C.H., Hsu C.L., Hung S.I., Wu J.Y., Pan W.H., et al. A comparison of major histocompatibility complex SNPs in Han Chinese residing in Taiwan and Caucasians. J Biomed Sci 13 (2006) 489-498
-
(2006)
J Biomed Sci
, vol.13
, pp. 489-498
-
-
Yang, H.C.1
Lin, C.H.2
Hsu, C.L.3
Hung, S.I.4
Wu, J.Y.5
Pan, W.H.6
-
49
-
-
33748741474
-
A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention
-
Liu Y.L., Fann C.S., Liu C.M., Chen W.J., Wu J.Y., Hung S.I., et al. A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention. Biol Psychiatry 60 (2006) 554-562
-
(2006)
Biol Psychiatry
, vol.60
, pp. 554-562
-
-
Liu, Y.L.1
Fann, C.S.2
Liu, C.M.3
Chen, W.J.4
Wu, J.Y.5
Hung, S.I.6
-
50
-
-
0042827374
-
Polymorphism screening of PIK4CA: Possible candidate gene for chromosome 22q11-linked psychiatric disorders
-
Saito T., Stopkova P., Diaz L., Papolos D.F., Boussemart L., and Lachman H.M. Polymorphism screening of PIK4CA: Possible candidate gene for chromosome 22q11-linked psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet 116 (2003) 77-83
-
(2003)
Am J Med Genet B Neuropsychiatr Genet
, vol.116
, pp. 77-83
-
-
Saito, T.1
Stopkova, P.2
Diaz, L.3
Papolos, D.F.4
Boussemart, L.5
Lachman, H.M.6
-
51
-
-
0035116270
-
Polymorphism in SNAP29 gene promoter region associated with schizophrenia
-
Saito T., Guan F., Papolos D.F., Rajouria N., Fann C.S., and Lachman H.M. Polymorphism in SNAP29 gene promoter region associated with schizophrenia. Mol Psychiatry 6 (2001) 193-201
-
(2001)
Mol Psychiatry
, vol.6
, pp. 193-201
-
-
Saito, T.1
Guan, F.2
Papolos, D.F.3
Rajouria, N.4
Fann, C.S.5
Lachman, H.M.6
-
52
-
-
1842326196
-
Mapping of the human adenosine A2a receptor gene: Relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region
-
Deckert J., Nothen M.M., Bryant S.P., Schuffenhauer S., Schofield P.R., Spurr N.K., et al. Mapping of the human adenosine A2a receptor gene: Relationship to potential schizophrenia loci on chromosome 22q and exclusion from the CATCH 22 region. Hum Genet 99 (1997) 326-328
-
(1997)
Hum Genet
, vol.99
, pp. 326-328
-
-
Deckert, J.1
Nothen, M.M.2
Bryant, S.P.3
Schuffenhauer, S.4
Schofield, P.R.5
Spurr, N.K.6
-
53
-
-
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 Psychiatry 9 (2004) 962-967
-
(2004)
Mol Psychiatry
, vol.9
, pp. 962-967
-
-
Chen, X.1
Wang, X.2
O'Neill, A.F.3
Walsh, D.4
Kendler, K.S.5
-
54
-
-
0033766762
-
A myosin family tree
-
Hodge T., and Cope M.J. A myosin family tree. J Cell Sci 113 Pt 19 (2000) 3353-3354
-
(2000)
J Cell Sci
, vol.113
, Issue.PART 19
, pp. 3353-3354
-
-
Hodge, T.1
Cope, M.J.2
-
55
-
-
0034677906
-
Myosins: A diverse superfamily
-
Sellers J.R. Myosins: A diverse superfamily. Biochim Biophys Acta 1496 (2000) 3-22
-
(2000)
Biochim Biophys Acta
, vol.1496
, pp. 3-22
-
-
Sellers, J.R.1
-
56
-
-
0033822065
-
Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly
-
Kelley M.J., Jawien W., Ortel T.L., and Korczak J.F. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. Nat Genet 26 (2000) 106-108
-
(2000)
Nat Genet
, vol.26
, pp. 106-108
-
-
Kelley, M.J.1
Jawien, W.2
Ortel, T.L.3
Korczak, J.F.4
-
57
-
-
0037910378
-
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness
-
Seri M., Pecci A., Di Bari F., Cusano R., Savino M., Panza E., et al. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) 82 (2003) 203-215
-
(2003)
Medicine (Baltimore)
, vol.82
, pp. 203-215
-
-
Seri, M.1
Pecci, A.2
Di Bari, F.3
Cusano, R.4
Savino, M.5
Panza, E.6
-
58
-
-
8844261172
-
Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: Hematological, nephrological, and otological studies of heterozygous KO mice
-
Matsushita T., Hayashi H., Kunishima S., Hayashi M., Ikejiri M., Takeshita K., et al. Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: Hematological, nephrological, and otological studies of heterozygous KO mice. Biochem Biophys Res Commun 325 (2004) 1163-1171
-
(2004)
Biochem Biophys Res Commun
, vol.325
, pp. 1163-1171
-
-
Matsushita, T.1
Hayashi, H.2
Kunishima, S.3
Hayashi, M.4
Ikejiri, M.5
Takeshita, K.6
-
60
-
-
0031824669
-
Stargazing nets new calcium channel subunit
-
Puranam R.S., and McNamara J.O. Stargazing nets new calcium channel subunit. Nat Genet 19 (1998) 313-314
-
(1998)
Nat Genet
, vol.19
, pp. 313-314
-
-
Puranam, R.S.1
McNamara, J.O.2
-
62
-
-
0037109042
-
Direct interactions between PSD-95 and stargazin control synaptic AMPA receptor number
-
Schnell E., Sizemore M., Karimzadegan S., Chen L., Bredt D.S., and Nicoll R.A. Direct interactions between PSD-95 and stargazin control synaptic AMPA receptor number. Proc Natl Acad Sci U S A 99 (2002) 13902-13907
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 13902-13907
-
-
Schnell, E.1
Sizemore, M.2
Karimzadegan, S.3
Chen, L.4
Bredt, D.S.5
Nicoll, R.A.6
-
64
-
-
0032884754
-
Single gene defects in mice: The role of voltage-dependent calcium channels in absence models
-
Burgess D.L., and Noebels J.L. Single gene defects in mice: The role of voltage-dependent calcium channels in absence models. Epilepsy Res 36 (1999) 111-122
-
(1999)
Epilepsy Res
, vol.36
, pp. 111-122
-
-
Burgess, D.L.1
Noebels, J.L.2
-
65
-
-
33144482985
-
DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling
-
Wilson G.M., Flibotte S., Chopra V., Melnyk B.L., Honer W.G., and Holt R.A. DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling. Hum Mol Genet 15 (2006) 743-749
-
(2006)
Hum Mol Genet
, vol.15
, pp. 743-749
-
-
Wilson, G.M.1
Flibotte, S.2
Chopra, V.3
Melnyk, B.L.4
Honer, W.G.5
Holt, R.A.6
|