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D. Porteous, P. Thomson, Nicholas Brandon, J. Millar (2006)
The Genetics and Biology of Disc1—An Emerging Role in Psychosis and CognitionBiological Psychiatry, 60
C. Bourgain, E. Génin (2005)
Complex trait mapping in isolated populations: Are specific statistical methods required?European Journal of Human Genetics, 13
M. McQueen, B. Devlin, S. Faraone, V. Nimgaonkar, P. Sklar, P. Sklar, J. Smoller, R. Jamra, M. Albus, S. Bacanu, M. Baron, T. Barrett, W. Berrettini, D. Blacker, W. Byerley, S. Cichon, W. Coryell, N. Craddock, M. Daly, J. DePaulo, H. Edenberg, T. Foroud, M. Gill, T. Gilliam, M. Hamshere, I. Jones, Lisa Jones, S. Juo, J. Kelsoe, David Lambert, C. Lange, B. Lerer, Jianjun Liu, W. Maier, J. Mackinnon, M. McInnis, F. McMahon, D. Murphy, M. Nöthen, J. Nurnberger, C. Pato, M. Pato, J. Potash, P. Propping, A. Pulver, J. Rice, M. Rietschel, W. Scheftner, J. Schumacher, R. Segurado, K. Steen, Weiting Xie, P. Zandi, N. Laird (2005)
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.American journal of human genetics, 77 4
Frank Middleton, M. Pato, M. Pato, K. Gentile, C. Morley, X. Zhao, A. Eisener, A. Brown, T. Petryshen, A. Kirby, A. Kirby, H. Medeiros, H. Medeiros, C. Carvalho, A. Macedo, A. Dourado, I. Coelho, J. Valente, M. Soares, C. Ferreira, M. Lei, M. Azevedo, James Kennedy, Mark Daly, Pamela Sklar, Pamela Sklar, C. Pato (2004)
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.American journal of human genetics, 74 5
W. Hennah, A. Tuulio-Henriksson, T. Paunio, J. Ekelund, T. Varilo, T. Partonen, Tyrone Cannon, J. Lönnqvist, L. Peltonen (2005)
A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophreniaMolecular Psychiatry, 10
Xiaodong Zhang, R. Gainetdinov, J. Beaulieu, T. Sotnikova, L. Burch, Redford Williams, D. Schwartz, K. Krishnan, M. Caron (2005)
Loss-of-Function Mutation in Tryptophan Hydroxylase-2 Identified in Unipolar Major DepressionNeuron, 45
M. Harvey, E. Shink, M. Tremblay, B. Gagné, C. Raymond, M. Labbé, D. Walther, Michael Bader, Nicholas Barden (2004)
Support for the involvement of TPH2 gene in affective disordersMolecular Psychiatry, 9
Agnar Helgason, George Nicholson, Kári Stefánsson, P. Donnelly (2003)
A Reassessment of Genetic Diversity in Icelanders: Strong Evidence from Multiple Loci for Relative Homogeneity Caused by Genetic DriftAnnals of Human Genetics, 67
S. Service, R. Ophoff, N. Freimer (2001)
The genome-wide distribution of background linkage disequilibrium in a population isolate.Human molecular genetics, 10 5
K. Hong, L. McInnes, S. Service, Terry Song, J. Lucas, Sandra Silva, E. Fournier, P. León, J. Molina, V. Reus, L. Sandkuijl, N. Freimer (2004)
Genetic mapping using haplotype and model‐free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31‐33American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 125B
U. Bailer, F. Leisch, K. Meszaros, E. Lenzinger, U. Willinger, R. Strobl, A. Heiden, C. Gebhardt, Elisabeth Döge, K. Fuchs, W. Sieghart, S. Kasper, K. Hornik, H. Aschauer (2002)
Genome scan for susceptibility loci for schizophrenia and bipolar disorderBiological Psychiatry, 52
Yu-Li Liu, C. Fann, Chih-Min Liu, Chien-Ching Chang, Jer-Yuarn Wu, S. Hung, Shih‐Kai Liu, M. Hsieh, T. Hwang, H. Chan, Jiahn‐Jyh Chen, S. Faraone, M. Tsuang, Wei Chen, H. Hwu (2006)
No association of G72 and d-amino acid oxidase genes with schizophreniaSchizophrenia Research, 87
M. Olivier (2003)
A haplotype map of the human genome.Nature, 437 7063
D. Curtis, G. Kalsi, J. Brynjólfsson, M. McInnis, J. O'Neill, C. Smyth, E. Moloney, P. Murphy, A. McQuillin, H. Pétursson, H. Gurling (2003)
Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23‐q24, and suggests the presence of additional loci on 1p and 1qPsychiatric Genetics, 13
H. Ibrahim, A. Hogg, D. Healy, V. Haroutunian, K. Davis, J. Meador-Woodruff (2000)
Ionotropic glutamate receptor binding and subunit mRNA expression in thalamic nuclei in schizophrenia.The American journal of psychiatry, 157 11
M. Escamilla, A. Ontiveros, Humberto Nicolini, H. Raventós, Ricardo Mendoza, R. Medina, Rodrigo Muñoz, D. Levinson, Juan Peralta, Juan Peralta, A. Dassori, L. Almasy (2007)
A genome‐wide scan for schizophrenia and psychosis susceptibility loci in families of Mexican and Central American ancestryAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 144B
A. Bogaert, K. Sleegers, S. Zutter, L. Heyrman, K. Norrback, R. Adolfsson, C. Broeckhoven, J. Del-Favero (2006)
Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population.Archives of general psychiatry, 63 10
G. MacQueen, T. Hajek, M. Alda (2005)
The phenotypes of bipolar disorder: relevance for genetic investigationsMolecular Psychiatry, 10
J. Smoller, Christine Finn (2003)
Family, twin, and adoption studies of bipolar disorderAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, 123C
J. Ekholm, T. Kieseppä, T. Hiekkalinna, T. Partonen, T. Paunio, M. Perola, J. Ekelund, J. Lönnqvist, Petra Pekkarinen-Ijäs, L. Peltonen (2003)
Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder.Human molecular genetics, 12 15
B. Degn, M. Lundorf, A. Wang, M. Vang, O. Mors, T. Kruse, H. Ewald (2001)
Further evidence for a bipolar risk gene on chromosome 12q24 suggested by investigation of haplotype sharing and allelic association in patients from the Faroe IslandsMolecular Psychiatry, 6
A. Cardno, F. Rijsdijk, P. Sham, R. Murray, P. McGuffin (2002)
A twin study of genetic relationships between psychotic symptoms.The American journal of psychiatry, 159 4
R. Segurado, S. Detera-Wadleigh, D. Levinson, C. Lewis, M. Gill, J. Nurnberger, N. Craddock, J. DePaulo, M. Baron, E. Gershon, J. Ekholm, S. Cichon, G. Turecki, S. Claes, J. Kelsoe, P. Schofield, R. Badenhop, J. Morissette, H. Coon, D. Blackwood, L. McInnes, T. Foroud, H. Edenberg, T. Reich, J. Rice, A. Goate, M. McInnis, F. McMahon, J. Badner, L. Goldin, P. Bennett, V. Willour, P. Zandi, Jianjun Liu, C. Gilliam, S. Juo, W. Berrettini, T. Yoshikawa, L. Peltonen, J. Lönnqvist, M. Nöthen, J. Schumacher, C. Windemuth, M. Rietschel, P. Propping, W. Maier, M. Alda, P. Grof, G. Rouleau, J. Del-Favero, C. Broeckhoven, J. Mendlewicz, R. Adolfsson, M. Spence, H. Luebbert, L. Adams, J. Donald, P. Mitchell, N. Barden, E. Shink, W. Byerley, W. Muir, P. Visscher, S. Macgregor, H. Gurling, G. Kalsi, A. McQuillin, M. Escamilla, V. Reus, P. León, N. Freimer, H. Ewald, T. Kruse, O. Mors, U. Radhakrishna, J. Blouin, S. Antonarakis, N. Akarsu (2003)
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.American journal of human genetics, 73 1
L. Brzustowicz, K. Hodgkinson, E. Chow, W. Honer, A. Bassett (2000)
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22.Science, 288 5466
D. Fallin, V. Lasseter, P. Wolyniec, J. McGrath, G. Nestadt, D. Valle, K. Liang, A. Pulver (2003)
Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.American journal of human genetics, 73 3
J. Kelsoe, M. Spence, E. Loetscher, M. Foguet, A. Sadovnick, R. Remick, P. Flodman, J. Khristich, Z. Mroczkowski-Parker, John Brown, Diane Masser, Sharon Ungerleider, M. Rapaport, W. Wishart, H. Luebbert (2001)
A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22.Proceedings of the National Academy of Sciences of the United States of America, 98 2
S. Detera-Wadleigh, J. Badner, J. Badner, W. Berrettini, T. Yoshikawa, L. Goldin, G. Turner, D. Rollins, T. Moses, A. Sanders, A. Sanders, J. Karkera, L. Esterling, Jin Zeng, T. Ferraro, J. Guroff, Diane Kazuba, M. Maxwell, J. Nurnberger, E. Gershon, E. Gershon (1999)
A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.Proceedings of the National Academy of Sciences of the United States of America, 96 10
I. Herzberg, A. Jasinska, Jenny García, D. Jawaheer, S. Service, B. Kremeyer, C. Duque, M. Parra, J. Vega, D. Ortiz, Luis Carvajal, Guadalupe Polanco, G. Restrepo, C. López, C. Palacio, M. Levinson, I. Aldana, C. Mathews, P. Davanzo, J. Molina, E. Fournier, J. Bejarano, M. Ramírez, C. Ortiz, X. Araya, C. Sabatti, V. Reus, G. Macaya, G. Bedoya, J. Ospina, N. Freimer, A. Ruiz-Linares (2006)
Convergent linkage evidence from two Latin-American population isolates supports the presence of a susceptibility locus for bipolar disorder in 5q31-34.Human molecular genetics, 15 21
T. Venken, S. Claes, S. Sluijs, A. Paterson, C. Duijn, R. Adolfsson, J. Del-Favero, C. Broeckhoven (2005)
Genomewide scan for affective disorder susceptibility Loci in families of a northern Swedish isolated population.American journal of human genetics, 76 2
堀川 幸男 (2003)
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
Bin Xu, Naomi Wratten, Erik Charych, Steven Buyske, Bonnie Firestein, L. Brzustowicz (2005)
Increased Expression in Dorsolateral Prefrontal Cortex of CAPON in Schizophrenia and Bipolar DisorderPLoS Medicine, 2
S. Schwab, G. Eckstein, Joachim Hallmayer, B. Lerer, Margot Albus, M. Borrmann, D. Lichtermann, M. Ertl, Wolfgang Maier, D. Wildenauer (1997)
Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysisMolecular Psychiatry, 2
Edward Smith, Xujing Wang, Jack Littrell, J. Eckert, R. Cole, A. Kissebah, Michael Olivier (2006)
Comparison of linkage disequilibrium patterns between the HapMap CEPH samples and a family-based cohort of Northern European descent.Genomics, 88 4
I. Gottesman, T. Gould (2003)
The endophenotype concept in psychiatry: etymology and strategic intentions.The American journal of psychiatry, 160 4
L. McInnes, T. Lauriat (2006)
RNA metabolism and dysmyelination in schizophreniaNeuroscience & Biobehavioral Reviews, 30
M. Dean (2003)
Approaches to identify genes for complex human diseases: Lessons from Mendelian disordersHuman Mutation, 22
S. Grant, G. Thorleifsson, I. Reynisdottir, R. Benediktsson, A. Manolescu, J. Sainz, Agnar Helgason, H. Stefánsson, V. Emilsson, A. Helgadóttir, U. Styrkársdóttir, K. Magnússon, G. Walters, E. Pálsdóttir, T. Jonsdottir, T. Gudmundsdóttir, Arnaldur Gylfason, Jona Saemundsdottir, R. Wilensky, M. Reilly, D. Rader, Y. Bagger, C. Christiansen, V. Gudnason, Gunnar Sigurdsson, U. Thorsteinsdóttir, J. Gulcher, A. Kong, K. Stefánsson (2006)
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetesNature Genetics, 38
S. Faraone, H. Hwu, Chih-Min Liu, Wei Chen, M. Tsuang, Shih‐Kai Liu, Ming-Hsien Shieh, T. Hwang, W-C Ou-Yang, Chun‐Ying Chen, Chwen-Cheng Chen, Jin‐Jia Lin, F. Chou, C. Chueh, Wei-ming Liu, M. Hall, Jessica Su, P. Eerdewegh, M. Tsuang (2006)
Genome scan of Han Chinese schizophrenia families from Taiwan: confirmation of linkage to 10q22.3.The American journal of psychiatry, 163 10
Yonglan Zheng, Hua-fang Li, W. Qin, Wu-yan Chen, Yun Duan, Yue Xiao, Chao Li, Jing Zhang, Xing-wang Li, G. Feng, Lin He (2005)
Association of the carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase gene with schizophrenia in the Chinese Han population.Biochemical and biophysical research communications, 328 4
P. Nylander, L. Beckman (1991)
Population studies in northern Sweden. XVII. Estimates of Finnish and Saamish influence.Human heredity, 41 3
S. Detera-Wadleigh, F. McMahon (2006)
G72/G30 in Schizophrenia and Bipolar Disorder: Review and Meta-analysisBiological Psychiatry, 60
L. Walter, Thien Dinh, N. Stella (2004)
ATP Induces a Rapid and Pronounced Increase in 2-Arachidonoylglycerol Production by Astrocytes, a Response Limited by Monoacylglycerol LipaseThe Journal of Neuroscience, 24
D. Wildenauer, S. Schwab (1999)
Chromosomes 8 and 10 workshop.American journal of medical genetics, 88 3
J. Stankovich, Charles Cox, Rachel Tan, D. Montgomery, S. Huxtable, J. Rubio, M. Ehm, L. Johnson, H. Butzkueven, T. Kilpatrick, T. Speed, A. Roses, M. Bahlo, S. Foote (2006)
On the utility of data from the International HapMap Project for Australian association studiesHuman Genetics, 119
A. Ingason, K. Søeby, S. Timm, August Wang, K. Jakobsen, A. Fink-Jensen, R. Hemmingsen, H. Rasmussen, T. Werge (2006)
No significant association of the 5′ end of neuregulin 1 and schizophrenia in a large Danish sampleSchizophrenia Research, 83
M. Escamilla, L. McInnes, M. Spesny, V. Reus, N. Shimayoshi, David Tyler, Sandra Silva, J. Molina, A. Gallegos, L. Meza, M. Cruz, S. Batki, S. Vinogradov, T. Neylan, Jasmine Nguyen, E. Fournier, Carmen Araya, S. Barondes, P. León, L. Sandkuijl, L. Sandkuijl, L. Sandkuijl, N. Freimer (1999)
Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: an initial screen for bipolar disorder loci on chromosome 18.American journal of human genetics, 64 6
Jong Kim, Yu‐Sang Lee, E. Cho, Y. Jang, D. Park, Kyeong-Sook Choi, H. Jeun, Seunghee Cho, S. Jang, K. Hong (2006)
Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean populationAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141B
T. Gasperoni, J. Ekelund, M. Huttunen, C. Palmer, A. Tuulio-Henriksson, J. Lönnqvist, J. Kaprio, L. Peltonen, Tyrone Cannon (2003)
Genetic linkage and association between chromosome 1q and working memory function in schizophreniaAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 116B
J. Potash, P. Zandi, V. Willour, T. Lan, Y. Huo, D. Avramopoulos, Y. Shugart, D. MacKinnon, S. Simpson, F. McMahon, J. DePaulo, M. McInnis (2003)
Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder.The American journal of psychiatry, 160 4
Victor Lopez, S. Detera-Wadleigh, I. Cardona, L. Kassem, F. McMahon (2007)
Nested Association Between Genetic Variation in Tryptophan Hydroxylase II, Bipolar Affective Disorder, and Suicide AttemptsBiological Psychiatry, 61
C. Garner, L. McInnes, S. Service, M. Spesny, E. Fournier, P. León, N. Freimer (2001)
Linkage analysis of a complex pedigree with severe bipolar disorder, using a Markov chain Monte Carlo method.American journal of human genetics, 68 4
H. Gurling, G. Kalsi, Jon Brynjolfson, T. Sigmundsson, R. Sherrington, B. Mankoo, T. Read, P. Murphy, E. Blaveri, A. McQuillin, H. Pétursson, D. Curtis (2001)
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.American journal of human genetics, 68 3
C. Fan, C. Sikström (1988)
Population Studies in Northern SwedenHuman Heredity, 44
C. Glatt, E. Carlson, Travis Taylor, N. Risch, V. Reus, C. Schaefer (2005)
Response to Zhang et al. (2005) Loss-of-Function Mutation in Tryptophan Hydroxylase-2 Identified in Unipolar Major Depression. Neuron 45, 11–16Neuron, 48
N. Freimer, V. Reus, M. Escamilla, L. Mclnnes, M. Spesny, P. León, S. Service, Lauren Smith, Sandra Silva, E. Rojas, A. Gallegos, L. Meza, E. Fournier, S. Baharloo, Kathleen Blankenship, David Tyler, S. Batki, S. Vinogradov, J. Weissenbach, S. Barondes, L. Sandkuijl (1996)
Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23Nature Genetics, 12
(2003)
Psychiatry 2:148–155
P. Zill, T. Baghai, P. Zwanzger, C. Schüle, D. Eser, R. Rupprecht, H. Möller, B. Bondy, M. Ackenheil (2004)
SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depressionMolecular Psychiatry, 9
A. Addington, M. Gornick, P. Shaw, J. Seal, N. Gogtay, Dede Greenstein, L. Clasen, M. Coffey, P. Gochman, R. Long, J. Rapoport (2007)
Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectoriesMolecular Psychiatry, 12
C. Willer, L. Scott, L. Bonnycastle, A. Jackson, P. Chines, R. Pruim, Craig Bark, Ya‐Yu Tsai, E. Pugh, K. Doheny, L. Kinnunen, K. Mohlke, T. Valle, R. Bergman, J. Tuomilehto, F. Collins, M. Boehnke (2006)
Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap databaseGenetic Epidemiology, 30
K. Åberg, P. Saetre, E. Lindholm, B. Ekholm, U. Pettersson, R. Adolfsson, E. Jazin (2006)
Human QKI, a new candidate gene for schizophrenia involved in myelinationAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141B
Pamela Sklar, Pamela Sklar, M. Pato, M. Pato, A. Kirby, T. Petryshen, T. Petryshen, H. Medeiros, C. Carvalho, A. Macedo, A. Dourado, I. Coelho, J. Valente, M. Soares, C. Ferreira, M. Lei, A. Verner, Thomas Hudson, C. Morley, James Kennedy, M. Azevedo, Eric Lander, Mark Daly, Carlos Pato, Carlos Pato (2004)
Genome-wide scan in Portuguese Island families identifies 5q31–5q35 as a susceptibility locus for schizophrenia and psychosisMolecular Psychiatry, 9
B. Étain, Flavie Mathieu, M. Rietschel, Wolfgang Maier, M. Albus, P. Mckeon, S. Roche, C. Kealey, D. Blackwood, W. Muir, F. Bellivier, C. Henry, C. Dina, Sophie Gallina, H. Gurling, A. Malafosse, M. Preisig, F. Ferrero, S. Cichon, J. Schumacher, S. Ohlraun, M. Borrmann-Hassenbach, P. Propping, R. Jamra, T. Schulze, A. Marušič, Z. Dernovsek, B. Giros, T. Bourgeron, A. Lemainque, D. Bacq, C. Bétard, C. Charon, M. Nöthen, M. Lathrop, M. Leboyer (2006)
Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14Molecular Psychiatry, 11
M. Hamshere, P. Bennett, N. Williams, R. Segurado, A. Cardno, N. Norton, David Lambert, H. Williams, G. Kirov, A. Corvin, P. Holmans, L. Jones, I. Jones, M. Gill, M. O’Donovan, M. Owen, N. Craddock (2005)
Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13.Archives of general psychiatry, 62 10
H. Garriock, J. Allen, P. Delgado, Z. Nahaz, M Kling, L. Carpenter, M. Burke, W. Burke, T. Schwartz, L. Marangell, M. Husain, R Erickson, F Moreno (2005)
Lack of association of TPH2 exon XI polymorphisms with major depression and treatment resistanceMolecular Psychiatry, 10
N. Craddock, M. O’Donovan, M. Owen (2005)
The genetics of schizophrenia and bipolar disorder: dissecting psychosisJournal of Medical Genetics, 42
L. Brzustowicz, L. Brzustowicz, William Honer, E. Chow, Dawn Little, Jackie Hogan, Kathy Hodgkinson, A. Bassett (1999)
Linkage of familial schizophrenia to chromosome 13q32.American journal of human genetics, 65 4
N. Barden, M. Harvey, B. Gagné, E. Shink, M. Tremblay, C. Raymond, M. Labbé, A. Villeneuve, Denis Rochette, Lise Bordeleau, H. Stadler, F. Holsboer, B. Müller-Myhsok (2006)
Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorderAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141B
K. Åberg, P. Saetre, N. Jareborg, E. Jazin (2006)
Human QKI, a potential regulator of mRNA expression of human oligodendrocyte-related genes involved in schizophrenia.Proceedings of the National Academy of Sciences of the United States of America, 103 19
C. Walss-Bass, H. Raventós, A. Montero, R. Armas, A. Dassori, S. Contreras, W. Liu, R. Medina, D. Levinson, Mariana Pereira, R. Leach, L. Almasy, M. Escamilla (2006)
Association analyses of the neuregulin 1 gene with schizophrenia and manic psychosis in a Hispanic populationActa Psychiatrica Scandinavica, 113
(2007)
Association of Neuregulin 1 Human Mutation
L. McInnes, S. Service, V. Reus, G. Barnes, O. Charlat, S. Jawahar, S. Lewitzky, Qing Yang, Quyen Duong, M. Spesny, Carmen Araya, X. Araya, A. Gallegos, L. Meza, J. Molina, Rolando Ramirez, Roxana Mendez, Sandra Silva, E. Fournier, S. Batki, C. Mathews, T. Neylan, C. Glatt, M. Escamilla, David Luo, P. Gajiwala, Terry Song, Stephen Crook, Jasmine Nguyen, E. Roche, Joanne Meyer, P. León, L. Sandkuijl, N. Freimer, Hong Chen (2001)
Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican populationProceedings of the National Academy of Sciences of the United States of America, 98
V. Abkevich, N. Camp, C. Hensel, C. Neff, Deanna Russell, Dana Hughes, Agnes Plenk, M. Lowry, R. Richards, C. Carter, G. Frech, S. Stone, K. Rowe, C. Chau, Kathleen Cortado, Angelene Hunt, Karanina Luce, G. O'Neil, J. Poarch, J. Potter, Gregg Poulsen, H. Saxton, Michelle Bernat-Sestak, Victor Thompson, A. Gutin, M. Skolnick, D. Shattuck, L. Cannon-Albright (2003)
Predisposition locus for major depression at chromosome 12q22-12q23.2.American journal of human genetics, 73 6
M. Munafo, D. Thiselton, T. Clark, J. Flint (2006)
Association of the NRG1 gene and schizophrenia: a meta-analysisMolecular Psychiatry, 11
L. Wood, Eve Pickering, B. DeChairo (2007)
Significant Support for DAO as a Schizophrenia Susceptibility Locus: Examination of Five Genes Putatively Associated with SchizophreniaBiological Psychiatry, 61
B. Devlin, S. Bacanu, K. Roeder, F. Reimherr, P. Wender, B. Galke, D. Novasad, A. Chu, K. Tcuenco, S. Tiobek, C. Otto, W. Byerley (2002)
Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of PalauMolecular Psychiatry, 7
D. Fallin, V. Lasseter, P. Wolyniec, J. McGrath, G. Nestadt, D. Valle, K. Liang, A. Pulver (2004)
Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish families.American journal of human genetics, 75 2
D. Dick, T. Foroud, L. Flury, Elizabeth Bowman, Marvin Miller, N. Rau, P. Moe, Nalini Samavedy, R. El-Mallakh, H. Manji, D. Glitz, Eric Meyer, Carrie Smiley, Rhoda Hahn, C. Widmark, R. Mckinney, Laura Sutton, C. Ballas, D. Grice, W. Berrettini, W. Byerley, W. Coryell, R. Depaulo, D. MacKinnon, E. Gershon, J. Kelsoe, F. McMahon, M. McInnis, D. Murphy, T. Reich, W. Scheftner, J. Nurnberger (2003)
Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.American journal of human genetics, 73 1
H. Ostrer (2001)
A genetic profile of contemporary Jewish populationsNature Reviews Genetics, 2
Dawei Li, D. Collier, Lin He (2006)
Meta-analysis shows strong positive association of the neuregulin 1 (NRG1) gene with schizophrenia.Human molecular genetics, 15 12
L. Carvajal-Carmona, R. Ophoff, S. Service, J. Hartiala, J. Molina, P. León, J. Ospina, G. Bedoya, N. Freimer, A. Ruiz-Linares (2003)
Genetic demography of Antioquia (Colombia) and the Central Valley of Costa RicaHuman Genetics, 112
J. Millar, Julie Wilson-Annan, S. Anderson, S. Christie, Martin Taylor, C. Semple, R. Devon, D. Clair, W. Muir, Douglas Blackwood, D. Porteous (2000)
Disruption of two novel genes by a translocation co-segregating with schizophrenia.Human molecular genetics, 9 9
R. Cheng, S. Juo, S. Juo, J. Loth, J. Nee, I. Iossifov, R. Blumenthal, L. Sharpe, K. Kanyas, B. Lerer, B. Lilliston, M. Smith, K. Trautman, T. Gilliam, T. Gilliam, J. Endicott, M. Baron (2006)
Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorderMolecular Psychiatry, 11
H. Stefánsson, E. Sigurdsson, V. Steinthorsdottir, S. Bjornsdottir, T. Sigmundsson, Shyamali Ghosh, J. Brynjólfsson, Steinunn Gunnarsdottir, Ó. Ívarsson, T. Chou, Ómar Hjaltason, B. Birgisdottir, H. Jonsson, Vala Gudnadottir, E. Gudmundsdottir, A. Bjornsson, Brynjólfur Ingvarsson, A. Ingason, S. Sigfússon, H. Hardardottir, R. Harvey, D. Lai, M. Zhou, D. Brunner, V. Mutel, A. Gonzalo, G. Lemke, J. Sainz, G. Jóhannesson, T. Andresson, D. Gudbjartsson, A. Manolescu, M. Frigge, M. Gurney, A. Kong, J. Gulcher, H. Pétursson, K. Stefánsson (2002)
Neuregulin 1 and susceptibility to schizophrenia.American journal of human genetics, 71 4
A. Pulver, V. Lasseter, L. Kasch, P. Wolyniec, G. Nestadt, J. Blouin, J. Blouin, M. Kimberland, R. Babb, Sophia Vourlis, Sophia Vourlis, Haiming Chen, Haiming Chen, M. Lalioti, M. Lalioti, M. Morris, M. Morris, M. Karayiorgou, J. Ott, D. Meyers, S. Antonarakis, D. Housman, H. Kazazian (1995)
Schizophrenia: a genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes.American journal of medical genetics, 60 3
David Lambert, F. Middle, M. Hamshere, R. Segurado, R. Raybould, A. Corvin, E. Green, E. O’Mahony, I. Nikolov, T. Mulcahy, S. Haque, S. Bort, P. Bennett, N. Norton, M. Owen, G. Kirov, C. Lendon, L. Jones, I. Jones, P. Holmans, M. Gill, N. Craddock (2006)
Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22Molecular Psychiatry, 11
D. Blackwood, D. Blackwood, A. Fordyce, M. Walker, D. Clair, D. Porteous, W. Muir, W. Muir (2001)
Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.American journal of human genetics, 69 2
J. Ekelund, D. Lichtermann, I. Hovatta, P. Ellonen, J. Suvisaari, J. Terwilliger, H. Juvonen, T. Varilo, R. Arajärvi, Marja-Liisa Kokko-Sahin, J. Lönnqvist, L. Peltonen (2000)
Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22.Human molecular genetics, 9 7
P. Lin, M. McInnis, J. Potash, V. Willour, D. MacKinnon, Kuangyi Miao, J. DePaulo, P. Zandi (2005)
Assessment of the effect of age at onset on linkage to bipolar disorder: evidence on chromosomes 18p and 21q.American journal of human genetics, 77 4
Xinmin Liu, G. He, Xiaoyan Wang, Qi Chen, X. Qian, Wei Lin, Dawei Li, N. Gu, G. Feng, Lin He (2004)
Association of DAAO with schizophrenia in the Chinese populationNeuroscience Letters, 369
D. Clair, D. Blackwood, W. Muir, M. Walker, A. Carothers, G. Spowart, C. Gosden, H. Evans (1990)
Association within a family of a balanced autosomal translocation with major mental illnessThe Lancet, 336
P. Zill, A. Büttner, W. Eisenmenger, H. Möller, B. Bondy, M. Ackenheil (2004)
Single nucleotide polymorphism and haplotype analysis of a novel tryptophan hydroxylase Isoform (TPH2) gene in suicide victimsBiological Psychiatry, 56
B. Lerer, R. Segman, A. Hamdan, K. Kanyas, O. Karni, Y. Kohn, M. Korner, M. Lanktree, M. Kaadan, N. Turetsky, A. Yakir, B. Kerem, F. Macciardi, F. Macciardi (2003)
Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24Molecular Psychiatry, 8
J. Ekelund, W. Hennah, T. Hiekkalinna, A. Parker, J. Meyer, J. Lönnqvist, L. Peltonen, L. Peltonen (2004)
Replication of 1q42 linkage in Finnish schizophrenia pedigreesMolecular Psychiatry, 9
Zhifeng Zhou, A. Roy, Robert Lipsky, Kavi Kuchipudi, Guanshan Zhu, J. Taubman, M. Enoch, M. Virkkunen, D. Goldman (2005)
Haplotype-based linkage of tryptophan hydroxylase 2 to suicide attempt, major depression, and cerebrospinal fluid 5-hydroxyindoleacetic acid in 4 populations.Archives of general psychiatry, 62 10
S. Gretarsdottir, G. Thorleifsson, S. Reynisdottir, A. Manolescu, S. Jónsdóttir, T. Jonsdottir, T. Gudmundsdóttir, S. Bjarnadottir, O. Einarsson, H. Gudjonsdottir, M. Hawkins, G. Gudmundsson, H. Gudmundsdóttir, H. Andrason, A. Gudmundsdottir, M. Sigurdardottir, T. Chou, J. Nahmias, S. Goss, S. Sveinbjörnsdóttir, E. Valdimarsson, F. Jakobsson, U. Agnarsson, V. Gudnason, G. Thorgeirsson, J. Fingerle, M. Gurney, D. Gudbjartsson, M. Frigge, A. Kong, K. Stefánsson, J. Gulcher (2003)
The gene encoding phosphodiesterase 4D confers risk of ischemic strokeNature Genetics, 35
C. Pato, M. Azevedo, M. Pato, J. Kennedy, I. Coelho, A. Dourado, A. Macedo, J. Valente, C. Ferreira, José Madeira, J. Camara, M. Moniz, C. Correia (1997)
Selection of homogeneous populations for genetic study: the Portugal genetics of psychosis project.American journal of medical genetics, 74 3
Tyrone Cannon, W. Hennah, T. Erp, P. Thompson, J. Lonnqvist, M. Huttunen, T. Gasperoni, A. Tuulio-Henriksson, T. Pirkola, A. Toga, J. Kaprio, J. Mazziotta, L. Peltonen (2005)
Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory.Archives of general psychiatry, 62 11
N. Williams, E. Green, S. Macgregor, S. Dwyer, N. Norton, H. Williams, R. Raybould, D. Grozeva, M. Hamshere, S. Zammit, L. Jones, A. Cardno, G. Kirov, I. Jones, M. O’Donovan, M. Owen, N. Craddock (2006)
Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder.Archives of general psychiatry, 63 4
T. Ketter, Po Wang, Olga Becker, C. Nowakowska, Yen-shou Yang (2004)
Psychotic bipolar disorders: dimensionally similar to or categorically different from schizophrenia?Journal of psychiatric research, 38 1
T. Paunio, A. Tuulio-Henriksson, T. Hiekkalinna, M. Perola, T. Varilo, T. Partonen, Tyrone Cannon, J. Lönnqvist, L. Peltonen (2004)
Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.Human molecular genetics, 13 16
J. Duan, Maria Martinez, A. Sanders, C. Hou, Aaron Krasner, Daniel Schwartz, P. Gejman (2005)
Neuregulin 1 (NRG1) and schizophrenia: analysis of a US family sample and the evidence in the balancePsychological Medicine, 35
M. Maziade, M. Roy, Y. Chagnon, D. Cliche, Fournier Jp, N. Montgrain, C. Dion, J. Lavallee, Y. Garneau, N. Gingras, L. Nicole, A. Pirès, A.-M. Ponton, A. Potvin, H. Wallot, C. Mérette (2005)
Shared and specific susceptibility loci for schizophrenia and bipolar disorder: a dense genome scan in Eastern Quebec familiesMolecular Psychiatry, 10
The International HapMap Consortium (2005)
10.1038/nature04226Nature, 437
J. Blouin, B. Dombroski, S. Nath, V. Lasseter, P. Wolyniec, G. Nestadt, M. Thornquist, Gail Ullrich, J. Mcgrath, L. Kasch, M. Lamacz, M. Thomas, C. Gehrig, U. Radhakrishna, S. Snyder, Katherine Balk, K. Neufeld, K. Swartz, N. deMarchi, G. Papadimitriou, D. Dikeos, C. Stefanis, A. Chakravarti, B. Childs, D. Housman, H. Kazazian, S. Antonarakis, A. Pulver (1998)
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21Nature Genetics, 20
I. Chumakov, M. Blumenfeld, O. Guerassimenko, L. Cavarec, M. Palicio, H. Abderrahim, L. Bougueleret, Caroline Barry, Hiroaki Tanaka, P. Rosa, A. Puech, N. Tahri, A. Cohen-Akenine, Sylvain Delabrosse, S. Lissarrague, Françoise-Pascaline Picard, Karelle Maurice, L. Essioux, P. Millasseau, Pascale Grel, V. Debailleul, A. Simon, D. Caterina, I. Dufaure, K. Malekzadeh, M. Belova, J. Luan, M. Bouillot, J. Sambucy, Gwenael Primas, M. Saumier, Nadia Boubkiri, Sandrine Martin-Saumier, M. Nasroune, H. Peixoto, A. Delaye, Virginie Pinchot, Mariam Bastucci, S. Guillou, M. Chevillon, R. Sainz-Fuertes, S. Meguenni, J. Aurich-Costa, D. Chérif, Anne Gimalac, C. Duijn, D. Gauvreau, G. Ouellette, I. Fortier, J. Raelson, T. Sherbatich, N. Riazanskaia, E. Rogaev, P. Raeymaekers, J. Aerssens, F. Konings, W. Luyten, F. Macciardi, P. Sham, R. Straub, D. Weinberger, Nadine Cohen, D. Cohen (2002)
Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.Nature Reviews Genetics, 3
P. Thomson, A. Christoforou, S. Morris, E. Adie, B. Pickard, D. Porteous, W. Muir, D. Blackwood, K. Evans (2007)
Association of Neuregulin 1 with schizophrenia and bipolar disorder in a second cohort from the Scottish populationMolecular Psychiatry, 12
J. Morissette, A. Villeneuve, Lise Bordeleau, Denis Rochette, C. Laberge, B. Gagné, C. Laprise, G. Bouchard, M. Plante, L. Gobeil, E. Shink, J. Weissenbach, N. Barden (1999)
Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in quebec points to a locus of major effect on chromosome 12q23-q24.American journal of medical genetics, 88 5
Muller-Oerlinghausen (2002)
10.1016/S0140-6736(02)07450-0Lancet, 359
N. Fukui, T. Muratake, N. Kaneko, Hideki Amagane, T. Someya (2006)
Supportive evidence for neuregulin 1 as a susceptibility gene for schizophrenia in a Japanese populationNeuroscience Letters, 396
Ian Jones, N. Jacobsen, E. Green, G. Elvidge, M. Owen, N. Craddock (2002)
Evidence for familial cosegregation of major affective disorder and genetic markers flanking the gene for Darier's diseaseMolecular Psychiatry, 7
R. Houwen, S. Baharloo, Kathleen Blankenship, P. Raeymaekers, J. Juyn, L. Sandkuijl, N. Freimer (1994)
Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasisNature Genetics, 8
B. Marcheco-Teruel, T. Flint, F. Wikman, M. Torralbas, L. González, L. Blanco, Q. Tan, H. Ewald, T. Orntoft, T. Kruse, A. Borglum, O. Mors (2006)
A genome‐wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of CubaAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141B
N. Sachs, A. Sawa, S. Holmes, C. Ross, L. DeLisi, R. Margolis (2005)
A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorderMolecular Psychiatry, 10
D. Amann-Zalcenstein, N. Avidan, K. Kanyas, R. Ebstein, Y. Kohn, A. Hamdan, E. Ben‐Asher, O. Karni, M. Mujaheed, R. Segman, W. Maier, F. Macciardi, J. Beckmann, D. Lancet, B. Lerer (2006)
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophreniaEuropean Journal of Human Genetics, 14
Chumakov (2002)
10.1073/pnas.182412499Proc Natl Acad Sci USA, 99
N. Craddock, P. McGuffin, M. Owen (1994)
Darier's disease cosegregating with affective disorderBritish Journal of Psychiatry, 165
D. Levinson, P. Holmans, C. Laurent, B. Riley, A. Pulver, P. Gejman, S. Schwab, N. Williams, M. Owen, D. Wildenauer, A. Sanders, G. Nestadt, B. Mowry, B. Wormley, S. Bauché, S. Soubigou, R. Ribble, D. Nertney, K. Liang, L. Martinolich, W. Maier, N. Norton, H. Williams, M. Albus, Eric Carpenter, N. deMarchi, K. Ewen-White, D. Walsh, M. Jay, J. Deleuze, F. O’Neill, G. Papadimitriou, Ann Weilbaecher, B. Lerer, M. O’Donovan, D. Dikeos, J. Silverman, K. Kendler, J. Mallet, R. Crowe, M. Walters (2002)
No Major Schizophrenia Locus Detected on Chromosome 1q in a Large Multicenter SampleScience, 296
S. Shaw, Mary Kelly, Angela Smith, G. Shields, Penelope Hopkins, Josephine Loftus, Steven Laval, Antonio Vita, Marc Hert, L. Cardon, Timothy Crow, R. Sherrington, Lynn DeLisi (1998)
A genome-wide search for schizophrenia susceptibility genes.American journal of medical genetics, 81 5
M. Fallin, V. Lasseter, D. Avramopoulos, K. Nicodemus, P. Wolyniec, J. McGrath, G. Steel, G. Nestadt, K. Liang, R. Huganir, D. Valle, A. Pulver (2005)
Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios.American journal of human genetics, 77 6
T. Schulze, S. Ohlraun, P. Czerski, J. Schumacher, L. Kassem, Monika Deschner, M. Gross, Monja Tullius, V. Heidmann, S. Kovalenko, R. Jamra, T. Becker, A. Leszczynska-rodziewicz, J. Hauser, T. Illig, N. Klopp, S. Wellek, S. Cichon, F. Henn, F. McMahon, W. Maier, P. Propping, M. Nöthen, M. Rietschel (2005)
Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes.The American journal of psychiatry, 162 11
R. Shih, P. Belmonte, P. Zandi (2004)
A review of the evidence from family, twin and adoption studies for a genetic contribution to adult psychiatric disordersInternational Review of Psychiatry, 16
Paul Harrison, A. Law (2006)
Neuregulin 1 and Schizophrenia: Genetics, Gene Expression, and NeurobiologyBiological Psychiatry, 60
L. Brzustowicz, J. Simone, P. Mohseni, Jared Hayter, K. Hodgkinson, E. Chow, A. Bassett (2004)
Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22.American journal of human genetics, 74 5
N. Williams, N. Norton, H. Williams, B. Ekholm, M. Hamshere, Y. Lindblom, K. Chowdari, A. Cardno, S. Zammit, Lisa Jones, K. Murphy, R. Sanders, G. McCarthy, M. Gray, G. Jones, P. Holmans, V. Nimgaonkar, R. Adolfson, U. Ösby, L. Terenius, G. Sedvall, M. O’Donovan, M. Owen (2003)
A systematic genomewide linkage study in 353 sib pairs with schizophrenia.American journal of human genetics, 73 6
V. Puri, A. McQuillin, K. Choudhury, S. Datta, J. Pimm, S. Thirumalai, R. Krasucki, J. Lawrence, D. Quested, N. Bass, H. Moorey, J. Morgan, B. Punukollu, Gomathinayagam Kandasami, D. Curtis, H. Gurling (2007)
Fine Mapping by Genetic Association Implicates the Chromosome 1q23.3 Gene UHMK1, Encoding a Serine/Threonine Protein Kinase, as a Novel Schizophrenia Susceptibility GeneBiological Psychiatry, 61
Richard Straub, C. Maclean, F. O’Neill, D. Walsh, K. Kendler (1997)
Support for a possible schizophrenia vulnerability locus in region 5q22–31 in Irish familiesMolecular Psychiatry, 2
E. Lindholm, B. Ekholm, S. Shaw, P. Jalonen, G. Johansson, U. Pettersson, R. Sherrington, R. Adolfsson, E. Jazin (2001)
A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.American journal of human genetics, 69 1
L. Ke, Zhang Qi, Y. Ping, Cheng Ren (2006)
Effect of SNP at position 40237 in exon 7 of the TPH2 gene on susceptibility to suicideBrain Research, 1122
T. Paunio, J. Ekelund, T. Varilo, A. Parker, I. Hovatta, J. Turunen, Kate Rinard, Alessandro Foti, J. Terwilliger, H. Juvonen, J. Suvisaari, R. Arajärvi, J. Suokas, T. Partonen, J. Lönnqvist, Joanne Meyer, L. Peltonen (2001)
Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q.Human molecular genetics, 10 26
L. McInnes, M. Escamilla, V. Reus, P. León, Sandra Silva, E. Rojas, M. Spesny, S. Baharloo, Kathleen Blankenship, A. Peterson, David Tyler, N. Shimayoshi, Christa Tobey, S. Batki, S. Vinogradov, L. Meza, A. Gallegos, E. Fournier, Lauren Smith, S. Barondes, L. Sandkuijl, L. Sandkuijl, L. Sandkuijl, N. Freimer (1996)
A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees.Proceedings of the National Academy of Sciences of the United States of America, 93 23
Agnar Helgason, Bryndís Yngvadóttir, B. Hrafnkelsson, J. Gulcher, K. Stefánsson (2005)
An Icelandic example of the impact of population structure on association studiesNature Genetics, 37
Lambert (2005)
10.1038/sj.mp.4001684Mol Psychiatry, 10
R. Delorme, C. Durand, C. Betancur, M. Wagner, S. Ruhrmann, H. Grabe, G. Nygren, C. Gillberg, M. Leboyer, T. Bourgeron, P. Courtet, F. Jollant, C. Buresi, J. Aubry, P. Baud, G. Bondolfi, G. Bertschy, N. Perroud, A. Malafosse (2006)
No Human Tryptophan Hydroxylase-2 Gene R441H Mutation in a Large Cohort of Psychiatric Patients and Control SubjectsBiological Psychiatry, 60
H. Lôo (2008)
[On bipolar disorder].L'Encephale, 34 Suppl 4
C. Lewis, D. Levinson, L. Wise, L. DeLisi, R. Straub, I. Hovatta, N. Williams, S. Schwab, A. Pulver, S. Faraone, L. Brzustowicz, C. Kaufmann, D. Garver, H. Gurling, E. Lindholm, H. Coon, H. Moises, W. Byerley, S. Shaw, Andrea Mesén, R. Sherrington, F. O’Neill, D. Walsh, K. Kendler, J. Ekelund, T. Paunio, J. Lönnqvist, L. Peltonen, M. O’Donovan, M. Owen, D. Wildenauer, W. Maier, G. Nestadt, J. Blouin, S. Antonarakis, B. Mowry, J. Silverman, R. Crowe, C. Cloninger, M. Tsuang, D. Malaspina, J. Harkavy-Friedman, D. Svrakic, A. Bassett, J. Holcomb, G. Kalsi, A. McQuillin, Jon Brynjolfson, T. Sigmundsson, H. Pétursson, E. Jazin, T. Zoëga, T. Helgason (2003)
Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.American journal of human genetics, 73 1
E. Green, R. Raybould, S. Macgregor, K. Gordon-Smith, J. Heron, Sally Hyde, D. Grozeva, M. Hamshere, N. Williams, M. Owen, M. O’Donovan, L. Jones, I. Jones, G. Kirov, N. Craddock (2005)
Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder.Archives of general psychiatry, 62 6
G. Ribas, A. González-Neira, A. Salas, R. Milne, A. Vega, B. Carracedo, Emilio González, E. Barroso, Lara Fernández, P. Yankilevich, M. Robledo, Á. Carracedo, J. Benítez (2006)
Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genesHuman Genetics, 118
E. Shink, J. Morissette, Nicholas Barden (2003)
Genetic heterogeneity in a very large bipolar affective disorder pedigree from QuebecAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 119B
L. Peltonen, A. Palotie, K. Lange (2000)
Use of population isolates for mapping complex traitsNature Reviews Genetics, 1
J. Schumacher, R. Jamra, J. Freudenberg, T. Becker, S. Ohlraun, Andreas Otte, Monja Tullius, S. Kovalenko, A. Bogaert, Wolfgang Maier, M. Rietschel, P. Propping, M. Nöthen, S. Cichon (2004)
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorderMolecular Psychiatry, 9
H. Ewald, T. Flint, T. Jorgensen, August Wang, P. Jensen, M. Vang, O. Mors, T. Kruse (2002)
Search for a shared segment on chromosome 10q26 in patients with bipolar affective disorder or schizophrenia from the Faroe Islands.American journal of medical genetics, 114 2
C. Hong, Sheue-Jane Hou, Feng-Chang Yen, Y. Liou, S. Tsai (2006)
Family-based association study between G72/G30 genetic polymorphism and schizophreniaNeuroReport, 17
J. Deyoung, M. Karayiorgou, J. Roos, Herman Pretorious, G. Bedoya, J. Ospina, A. Ruiz-Linares, A. Ruiz-Linares, A. Macedo, J. Palha, P. Heutink, Y. Aulchenko, B. Oostra, C. Duijn, M. Järvelin, M. Järvelin, T. Varilo, L. Peddle, P. Rahman, G. Piras, M. Monne, S. Murray, L. Galver, L. Peltonen, C. Sabatti, A. Collins, N. Freimer, N. Freimer (2006)
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studiesNature Genetics, 38
S. Cichon, Gabriele Schmidt-Wolf, J. Schumacher, Daniel Müller, Martina Hürter, T. Schulze, M. Albus, M. Borrmann-Hassenbach, Ernst Franzek, M. Lanczik, Jürgen Fritze, R. Kreiner, B. Weigelt, J. Minges, D. Lichtermann, B. Lerer, K. Kanyas, Nicolas Produit, C. Windemuth, Max Baur, T. Wienker, Wolfgang Maier, M. Rietschel, P. Propping, M. Nöthen, M. Nöthen (2001)
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25–q26Molecular Psychiatry, 6
M. Korostishevsky, M. Kaganovich, Alina Cholostoy, M. Ashkenazi, Y. Ratner, Dvir Dahary, Jeanne Bernstein, Ullrike Bening-Abu-Shach, E. Ben‐Asher, D. Lancet, M. Ritsner, R. Navon (2004)
Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysisBiological Psychiatry, 56
J. Badner, E. Gershon (2002)
Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophreniaMolecular Psychiatry, 7
B. Riley, K. Kendler (2006)
Molecular genetic studies of schizophreniaEuropean Journal of Human Genetics, 14
A. Levi, Y. Kohn, K. Kanyas, D. Amann, C. Pae, A. Hamdan, R. Segman, N. Avidan, O. Karni, M. Korner, T. Jun, J. Beckmann, F. Macciardi, B. Lerer (2005)
Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage intervalEuropean Journal of Human Genetics, 13
Michael Escamilla, L. McInnes, M. Spesny, V. Reus, J. Molina, A. Gallegos, E. Fournier, S. Batki, T. Neylan, Carol Matthews, S. Vinogradov, E. Roche, David Tyler, N. Shimayoshi, Roxana Mendez, Rolando Ramirez, M. Ramírez, Carmen Araya, X. Araya, P. León, L. Sandkuijl, L. Sandkuijl, L. Sandkuijl, N. Freimer (2001)
Genome screening for linkage disequilibrium in a Costa Rican sample of patients with bipolar-I disorder: a follow-up study on chromosome 18.American journal of medical genetics, 105 2
E. Shink, J. Morissette, R. Sherrington, N. Barden (2005)
A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12Molecular Psychiatry, 10
C. Pato, M. Pato, A. Kirby, T. Petryshen, T. Petryshen, H. Medeiros, C. Carvalho, A. Macedo, A. Dourado, I. Coelho, J. Valente, M. Soares, C. Ferreira, M. Lei, A. Verner, T. Hudson, C. Morley, J. Kennedy, M. Azevedo, M. Daly, P. Sklar, P. Sklar (2004)
Genome‐wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: Fine mapping adds support on chromosomes 6 and 11American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 127B
H. Ewald, T. Flint, T. Kruse, O. Mors (2002)
A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22–21, 4p16, 6q14–22, 10q26 and 16p13.3Molecular Psychiatry, 7
J. Millar, R. James, S. Christie, D. Porteous (2005)
Disrupted In Schizophrenia 1 (DISC1): Subcellular targeting and induction of ring mitochondriaMolecular and Cellular Neuroscience, 30
Michael Korostishevsky, Ilana Kremer, M. Kaganovich, Alina Cholostoy, I. Murad, M. Muhaheed, I. Bannoura, M. Rietschel, M. Dobrusin, U. Bening-Abu-Shach, R. Belmaker, Wolfgang Maier, R. Ebstein, R. Ebstein, R. Navon (2006)
Transmission disequilibrium and haplotype analyses of the G72/G30 locus: Suggestive linkage to schizophrenia in Palestinian Arabs living in the North of IsraelAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141B
Toshihiro Tanaka (2003)
The International HapMap ProjectNature, 426
E. Lindholm, K. Åberg, B. Ekholm, U. Pettersson, R. Adolfsson, E. Jazin (2004)
Reconstruction of ancestral haplotypes in a 12-generation schizophrenia pedigreePsychiatric Genetics, 14
D. Parton, R. Snow, W. Seibert (1964)
Review of the Evidence.Science, 146 3651
E. Shink, M. Harvey, M. Tremblay, B. Gagné, P. Belleau, C. Raymond, M. Labbé, M. Dubé, R. Lafreniére, N. Barden (2005)
Analysis of microsatellite markers and single nucleotide polymorphisms in candidate genes for susceptibility to bipolar affective disorder in the chromosome 12Q24.31 regionAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 135B
W. Hennah, T. Varilo, M. Kestilä, T. Paunio, R. Arajärvi, J. Haukka, A. Parker, Rory Martin, Steve Levitzky, T. Partonen, Joanne Meyer, J. Lönnqvist, L. Peltonen, J. Ekelund (2003)
Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects.Human molecular genetics, 12 23
M. McInnis, M. McInnis, T. Lan, T. Lan, V. Willour, F. McMahon, F. McMahon, S. Simpson, A. Addington, D. MacKinnon, J. Potash, A. Mahoney, J. Chellis, Y. Huo, T. Swift-Scanlan, H. Chen, R. Koskela, O. Stine, O. Stine, K. Jamison, P. Holmans, S. Folstein, K. Ranade, C. Friddle, D. Botstein, T. Marr, T. Beaty, Peter Zandi, J. DePaulo (2003)
Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12Molecular Psychiatry, 8
Jieqiong Ma, Jieqiong Ma, W. Qin, W. Qin, X. Wang, Tingwei Guo, L. Bian, Shiwei Duan, Xiaoyan Li, F. Zou, Y. Fang, J. Fang, G. Feng, N. Gu, D. Clair, Lin He, Lin He (2006)
Further evidence for the association between G72/G30 genes and schizophrenia in two ethnically distinct populationsMolecular Psychiatry, 11
L. DeLisi, Andrea Mesén, C. Rodriguez, A. Bertheau, B. Laprade, M. Llach, S. Riondet, K. Razi, M. Relja, W. Byerley, R. Sherrington (2002)
Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica.American journal of medical genetics, 114 5
Y. Horikawa, N. Oda, N. Cox, Xiangquan Li, M. Orho-Melander, M. Hara, Y. Hinokio, T. Lindner, H. Mashima, P. Schwarz, L. Bosque-Plata, Y. Horikawa, Y. Oda, I. Yoshiuchi, S. Colilla, K. Polonsky, Shan Wei, P. Concannon, N. Iwasaki, Jan Schulze, L. Baier, C. Bogardus, L. Groop, E. Boerwinkle, C. Hanis, G. Bell (2000)
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitusNature Genetics, 26
I. Hovatta, T. Varilo, J. Suvisaari, J. Terwilliger, V. Ollikainen, R. Arajärvi, H. Juvonen, Marja-Liisa Kokko-Sahin, L. Väisänen, H. Mannila, J. Lönnqvist, L. Peltonen (1999)
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci.American journal of human genetics, 65 4
T. Venken, M. Alaerts, D. Souery, D. Goossens, S. Sluijs, R. Navon, C. Broeckhoven, J. Mendlewicz, J. Del-Favero, S. Claes (2008)
Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish familiesMolecular Psychiatry, 13
N. Craddock, L. Forty (2006)
Genetics of affective (mood) disordersEuropean Journal of Human Genetics, 14
J. Ekelund, I. Hovatta, A. Parker, T. Paunio, T. Varilo, Rory Martin, J. Suhonen, P. Ellonen, G. Chan, J. Sinsheimer, E. Sobel, H. Juvonen, R. Arajärvi, T. Partonen, J. Suvisaari, J. Lönnqvist, Joanne Meyer, L. Peltonen (2001)
Chromosome 1 loci in Finnish schizophrenia families.Human molecular genetics, 10 15
Major affective disorders and schizophrenia are among the most common brain diseases worldwide and their predisposition is influenced by a complex interaction of genetic and environmental factors. So far, traditional linkage mapping studies for these complex disorders have not achieved the same success as the positional cloning of genes for Mendelian diseases. The struggle to identify susceptibility genes for complex disorders has stimulated the development of alternative approaches, including studies in genetically isolated populations. Since isolated populations are likely to have both a reduced number of genetic vulnerability factors and environmental background and are therefore considered to be more homogeneous compared to outbred populations, the use of isolated populations in genetic studies is expected to improve the chance of finding susceptibility loci and genes. Here we review the role of isolated populations, based on linkage and association studies, in the identification of susceptibility genes for bipolar disorder and schizophrenia. Hum Mutat 28(12), 1156–1170, 2007. © 2007 Wiley‐Liss, Inc.
Human Mutation – Wiley
Published: Dec 1, 2007
Keywords: complex genetics; isolated population; association studies; linkage analysis; bipolar disorder; schizophrenia
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