Candidate gene studies of bipolar disorder
Open accessAbstract
Genetic factors undoubtedly play an important role in determining vulnerability to bipolar disorder but the task of finding susceptibility genes is not trivial. Candidate gene studies, usually employing the association approach, offer the potential to discover the genes of relatively modest effect size that are expected for a complex genetic disorder. Candidate gene approaches depend crucially on our current understanding of disease pathophysiology, and attention has consequently been focussed on a limited range of neurotransmitter systems implicated by the action of drug treatments. Despite no unequivocal, consistently replicated findings, a number of intriguing results have emerged in the literature, both for bipolar disorder in general and for subtypes such as bipolar affective puerperal psychosis and rapid cycling bipolar illness. Genes of particular current interest include those encoding the serotonin transporter, monoamine oxidase A (MAOA) and catechol-O-methyl transferase (COMT). As susceptibility genes are found and knowledge of aetiology advanced it is likely that many more candidate genes in novel biological systems will attract attention.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Direct implications were demonstrated for the monoamine oxidase A, 5-hydroxytryptamine transporter, and catechol-O-methyltransferase genes in BD.
“In this way, direct implications were demonstrated for the monoamine oxidase A, 5-hydroxytryptamine transporter, and catechol-O-methyltransferase genes [217–220].”
From Oxidative Stress Implications in the Affective Disorders: Main Biomarkers, Animal Models Relevance, Genetic Perspectives, and Antioxidant Approaches (2016) · cites this paper as [219]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216 · see citing works
Introduction to Quantitative Genetics.
Edwards, A. W. F., & Falconer, D. S. (1982) · Biometrics · doi:10.2307/2529912 · Cited by 21,447 · see citing works
The Future of Genetic Studies of Complex Human Diseases
Risch, N., & Merikangas, K. (1996) · Science · doi:10.1126/science.273.5281.1516 · Cited by 5,355 · see citing works
Strittmatter, W. J., Saunders, A. M., Schmechel, D., Pericak-Vance, M., Enghild, J., Salvesen, G. S., & Roses, A. D. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.5.1977 · Cited by 4,268 · see citing works
Introduction to Quantitative Genetics
J.-M., G., & Falconer, D. S. (1962) · Population · doi:10.2307/1525780 · Cited by 3,773 · see citing works
Spielman, R. S., McGinnis, R. E., & Ewens, W. J. (1993) · PubMed · Cited by 3,679 · see citing works
Genetic Dissection of Complex Traits
Lander, E. S., & Schork, N. J. (1994) · Science · doi:10.1126/science.8091226 · Cited by 3,425 · see citing works
Genomic Control for Association Studies
Devlin, B., & Roeder, K. (1999) · Biometrics · doi:10.1111/j.0006-341x.1999.00997.x · Cited by 3,162 · see citing works
Sokoloff, P., Bruno Giros, A., Martres, M., Bouthenet, M.-L., & Schwartz, J. (1990) · Nature · doi:10.1038/347146a0 · Cited by 2,608 · see citing works
Association mapping in structured populations.
Pritchard, J. K., Stephens, M., Rosenberg, N., & Donnelly, P. (2000) · American Journal of Human Genetics · doi:10.1086/302959 · Cited by 2,066 · see citing works
Searching for genetic determinants in the new millennium
Risch, N. J. (2000) · Nature · doi:10.1038/35015718 · Cited by 1,839 · see citing works
Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A
Brunner, H. G., Nelen, M., Breakefield, X. O., Ropers, H. H., & van Oost, B. A. (1993) · Science · doi:10.1126/science.8211186 · Cited by 1,644 · see citing works
Use of Unlinked Genetic Markers to Detect Population Stratification in Association Studies
Pritchard, J. K., & Rosenberg, N. A. (1999) · The American Journal of Human Genetics · doi:10.1086/302449 · Cited by 1,198 · see citing works
The TDT and other family-based tests for linkage disequilibrium and association.
(1996) · PubMed Central · Cited by 901 · see citing works
Bipolar affective disorders linked to DNA markers on chromosome 11
Egeland, J. A., Gerhard, D. S., Pauls, D. L., Sussex, J. N., Kídd, K. K., Alien, C. R., Hostetter, A. M., & Housman, D. E. (1987) · Nature · doi:10.1038/325783a0 · Cited by 815 · see citing works
Bell, G. I., Horita, S., & Karam, J. H. (1984) · Diabetes · doi:10.2337/diab.33.2.176 · Cited by 744 · see citing works
A Sibship Test for Linkage in the Presence of Association: The Sib Transmission/Disequilibrium Test
Spielman, R. S., & Ewens, W. J. (1998) · The American Journal of Human Genetics · doi:10.1086/301714 · Cited by 666 · see citing works
Collier, D. A., Stöber, G., Li, T., Heils, A., Catalano, M., Bella, D. D., Arranz, M. J., Murray, R. M., Vallada, H., Bengel, D., et al. (1996) · PubMed · Cited by 665 · see citing works
Falk, C. T., & Rubinstein, P. G. (1987) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1987.tb00875.x · Cited by 618 · see citing works
Polymorphism in serotonin transporter gene associated with susceptibility to major depression
Ogilvie, A. D., Battersby, S., Fink, G., Harmar, A. J., Goodwin, G. M., Bubb, V. J., & Smith, C. A. (1996) · The Lancet · doi:10.1016/s0140-6736(96)90079-3 · Cited by 530 · see citing works
Craddock, N. J., & Jones, I. R. (1999) · Journal of Medical Genetics · doi:10.1136/jmg.36.8.585 · Cited by 523 · see citing works
Self-citationWacholder, S. (2000) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/92.14.1151 · Cited by 442 · see citing works
Long, A. D., & Langley, C. (1999) · Genome Research · doi:10.1101/gr.9.8.720 · Cited by 437 · see citing works
Khoury, M. J., & Flanders, W. D. (1996) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a008915 · Cited by 420 · see citing works
MacKenzie, A., & Quinn, J. P. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.26.15251 · Cited by 374 · see citing works
Risch, N., & Teng, J. (1998) · Genome Research · doi:10.1101/gr.8.12.1273 · Cited by 366 · see citing works
Bacanu, S.-A., Devlin, B., & Roeder, K. (2000) · The American Journal of Human Genetics · doi:10.1086/302929 · Cited by 340 · see citing works
Kunugi, H., Hattori, M., Kato, T., Tatsumi, M., Sakai, T., Sasaki, T., Hirose, T., & Nanko, S. (1997) · Molecular Psychiatry · doi:10.1038/sj.mp.4000334 · Cited by 305 · see citing works
Association between schizophrenia and homozygosity at the dopamine D3 receptor gene.
Crocq, M. A., Mant, R., Asherson, P. J., Williams, J. H., Hodé, Y., Mayerová, A., Collier, D. A., Lannfelt, L., Sokoloff, P., & Schwartz, J. (1992) · Journal of Medical Genetics · doi:10.1136/jmg.29.12.858 · Cited by 276 · see citing works
Population studies of polymorphisms of the serotonin transporter protein gene.
Gelernter, J. E., Cubells, J. F., Kidd, J. R., PAKSTIS, A. J., & Kídd, K. K. (1999) · PubMed · Cited by 256 · see citing works
Williams, J. H., Spurlock, G., McGuffin, P., Owen, M., Mallet, J. J., Nöthen, M. M., Gill, M., Aschauer, H. N., Nylander, P.-O., & Macciardi, F. M. (1996) · The Lancet · doi:10.1016/s0140-6736(96)90939-3 · Cited by 245 · see citing works
Du, L., Bakish, D., Lapierre, Y. D., Ravindran, A. V., & Hrdina, P. D. (2000) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(20000207)96:1 · Cited by 229 · see citing works
22q11 deletion syndrome in adults with schizophrenia
Bassett, A. S., Hodgkinson, K. A., Chow, E. W. C., Correia, S., Scutt, L. E., & Weksberg, R. (1998) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19980710)81:4 · Cited by 228 · see citing works
Comparison of statistics for candidate-gene association studies using cases and parents.
Schaid, D. J., & Sommer, S. S. (1994) · PubMed · Cited by 203 · see citing works
Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia
Williams, J. H., McGuffin, P., Nöthen, M. M., & Michael J Owen, A. T. E. C. G. (1997) · The Lancet · doi:10.1016/s0140-6736(05)62413-0 · Cited by 203 · see citing works
Use of siblings as controls in case‐control association studies
Curtis, D. (1997) · Annals of Human Genetics · doi:10.1046/j.1469-1809.1998.6210089.x · Cited by 189 · see citing works
The serotonin transporter is a potential susceptibility factor for bipolar affective disorder
Collier, D. A., Arranz, M. J., Sham, P. C., Battersby, S., Vallada, H., Gill, P., Aitchison, K. J., Sodhi, M., Li, T., Roberts, G. W., et al. (1996) · Neuroreport · doi:10.1097/00001756-199607080-00030 · Cited by 187 · see citing works
A note on the application of the transmission disequilibrium test when a parent is missing.
Curtis, D., & Sham, P. C. (1995) · PubMed · Cited by 182 · see citing works
Kirov, G., Murphy, K. C., Arranz, M. J., Jones, I. R., McCandles, F., Kunugi, H., Murray, R. M., McGuffin, P., Collier, D. A., Owen, M. J., et al. (1998) · Molecular Psychiatry · doi:10.1038/sj.mp.4000385 · Cited by 167 · see citing works
Self-citationPapolos, D. F., Veit, S., Faedda, G. L., Saito, T., & Lachman, H. M. (1998) · Molecular Psychiatry · doi:10.1038/sj.mp.4000410 · Cited by 166 · see citing works
Williams, J. H., Spurlock, G., Holmans, P., Mant, R., Murphy, K. C., Jones, L. A., Cardno, A. G., Asherson, P. J., Blackwood, D., Muir, W. J., et al. (1998) · Molecular Psychiatry · doi:10.1038/sj.mp.4000376 · Cited by 161 · see citing works
Hamer, D. H., & Sirota, L. A. (2000) · Molecular Psychiatry · doi:10.1038/sj.mp.4000662 · Cited by 158 · see citing works
Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT)
Rees, M. I., Norton, N., Jones, I. R., McCandless, F., Scourfield, J., Holmans, P., Moorhead, S., Feldman, E., Sadler, S., Cole, T. J., et al. (1997) · Molecular Psychiatry · doi:10.1038/sj.mp.4000256 · Cited by 146 · see citing works
Self-citationLow activity allele of catechol-o-methyltransferase gene and Japanese unipolar depression
Ohara, K., Nagai, M., Suzuki, Y., & Ohara, K. (1998) · Neuroreport · doi:10.1097/00001756-199805110-00009 · Cited by 145 · see citing works
Preisig, M., Bellivier, F., Fenton, B. T., Baud, P., Berney, A., Courtet, P., Hardy, P., Golaz, J., Leboyer, M., Mallet, J., et al. (2000) · American Journal of Psychiatry · doi:10.1176/appi.ajp.157.6.948 · Cited by 137 · see citing works
Serotonin transporter gene polymorphisms in patients with unipolar or bipolar depression
Bellivier, F., Henry, C., Szöke, A., Schürhoff, F., Nosten‐Bertrand, M., Feingold, J., Launay, J., Leboyer, M., & Laplanche, J. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00677-6 · Cited by 131 · see citing works
Battersby, S., Ogilvie, A. D., Smith, C., Blackwood, D., Muir, W. J., Quinn, J. P., Fink, G., Goodwin, G. M., & Harmar, A. J. (1996) · Psychiatric Genetics · doi:10.1097/00041444-199624000-00001 · Cited by 128 · see citing works
Farrer, L. A. (1997) · JAMA · doi:10.1001/jama.1997.03550160069041 · Cited by 124 · see citing works
Tyrosine hydroxylase polymorphisms associated with manic-depressive illness
Leboyer, M., Malafosse, A., Boularand, S., Campion, D., Gheysen, F., Samolyk, D., Henriksson, B., Denise, E., Lauriers, A. D., Lépine, J., et al. (1990) · The Lancet · doi:10.1016/0140-6736(90)92738-4 · Cited by 124 · see citing works
Seidman, L. J., Faraone, S. V., Goldstein, J. M., Goodman, J. M., Kremen, W. S., Matsuda, G., Hoge, E. A., Kennedy, D. N., Makris, N., Caviness, V. S., et al. (1997) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19970919)74:5 · Cited by 122 · see citing works
Mathematical limits of multilocus models: the genetic transmission of bipolar disorder.
Craddock, N. J., Khodel, V., Eerdewegh, P. V., & Reich, T. (1995) · PubMed Central · Cited by 118 · see citing works
Self-citationAssociation studies of bipolar disorder
Craddock, N. J., Dave, S., & Greening, J. (2001) · Bipolar Disorders · doi:10.1034/j.1399-5618.2001.30604.x · Cited by 118 · see citing works
Self-citationA functional polymorphism in the promoter region of monoamine oxidase-A gene and mood disorders
Kunugi, H., Ishida, S., Kato, T., Tatsumi, M., Sakai, T., Hattori, M., Hirose, T., & Nanko, S. (1999) · Molecular Psychiatry · doi:10.1038/sj.mp.4000558 · Cited by 115 · see citing works
Kunugi, H., Vallada, H., Hoda, F., Kirov, G., Gill, M., Aitchison, K. J., Ball, D., Arranz, M. J., Murray, R. M., & Collier, D. A. (1997) · Biological Psychiatry · doi:10.1016/s0006-3223(96)00366-6 · Cited by 106 · see citing works
Association studies in psychiatric genetics
Owen, M. J., Holmans, P., & McGuffin, P. (1997) · Molecular Psychiatry · doi:10.1038/sj.mp.4000292 · Cited by 102 · see citing works
Furlong, R. A., Ho, L. W., Rubinsztein, J. S., Walsh, C., Paykel, E. S., & Rubinsztein, D. C. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19990820)88:4 · Cited by 100 · see citing works
Use of siblings as controls in case-control association studies
Curtis, D. (1997) · Annals of Human Genetics · doi:10.1017/s000348009700626x · Cited by 100 · see citing works
Serotonin transporter gene polymorphism and affective disorder.
Kunugi, H., Tatsumi, M., Sakai, T., Hattori, M., & Nanko, S. (1996) · PubMed · Cited by 96 · see citing works
Sobell, J. L., Heston, L. L., & Sommer, S. S. (1992) · Genomics · doi:10.1016/0888-7543(92)90398-c · Cited by 95 · see citing works
DNA polymorphism and the study of disease associations
Cooper, D. N., & Clayton, J. F. (1988) · Human Genetics · doi:10.1007/bf00291724 · Cited by 94 · see citing works
Li, T., Vallada, H., Curtis, D., Arranz, M. J., Xu, K., Cai, G., Deng, H., Liu, J., Murray, R. M., Liu, X., et al. (1997) · Pharmacogenetics · doi:10.1097/00008571-199710000-00002 · Cited by 91 · see citing works
Schizophrenia and smoking: Evidence for a common neurobiological basis?
Stassen, H. H., Bridler, R., H�gele, S., Hergersberg, M., Mehmann, B., Schinzel, A., Weisbrod, M., & Scharfetter, C. (2000) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(20000403)96:2 · Cited by 89 · see citing works
Coyle, N. E., Jones, I. R., Robertson, E., Lendon, C. L., & Craddock, N. J. (2000) · The Lancet · doi:10.1016/s0140-6736(00)02877-4 · Cited by 88 · see citing works
Self-citationLim, L. C.-C., Powell, J. F., Sham, P. C., Castle, D. J., Hunt, N., Murray, R. M., & Gill, M. (1995) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320600413 · Cited by 88 · see citing works
Gutiérrez, B., Arranz, M. J., Collier, D. A., Vallès, V., Guillamat, R., Bertranpetit, J., Murray, R. M., & Fañanás, L. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(97)00540-4 · Cited by 85 · see citing works
Genetic Association Analysis of Serotonin System Genes in Bipolar Affective Disorder
Vincent, J. B., Masellis, M., Lawrence, J., Choi, V., Gurling, H., Parikh, S. V., & Kennedy, J. L. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.1.136 · Cited by 83 · see citing works
Mynett‐Johnson, L., Murphy, V., Claffey, E., Shields, D. C., & McKeon, P. (1998) · Psychiatric Genetics · doi:10.1097/00041444-199808040-00004 · Cited by 78 · see citing works
Association of manic-depressive illness with tyrosine hydroxylase microsatellite marker
Meloni, R., Leboyer, M., Bellivier, F., Barbe, B., Samolyk, D., Allilaire, J., & Mallet, J. J. (1995) · The Lancet · doi:10.1016/s0140-6736(95)90053-5 · Cited by 76 · see citing works
Rubinsztein, D. C. (1996) · Human Molecular Genetics · doi:10.1093/hmg/5.6.779 · Cited by 73 · see citing works
Relationship of sleep abnormalities to patient genotypes in Prader-Willi syndrome
Vgontzas, A. N., Kales, A., Seip, J. R., Mascari, M. J., Bixler, E. O., Myers, D. C., Vela‐Bueno, A., & Rogan, P. K. (1996) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19960920)67:5 · Cited by 73 · see citing works
Association analysis of the catechol O-methyltransferase gene and bipolar affective disorder
Gutiérrez, B., Bertranpetit, J., Guillamat, R., Vallès, V., Arranz, M. J., Kerwin, R., & Fañanás, L. (1997) · American Journal of Psychiatry · doi:10.1176/ajp.154.1.113 · Cited by 73 · see citing works
Craddock, N. J., Daniels, J., Roberts, E., Rees, M. I., McGuffin, P., & Owen, M. J. (1995) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320600412 · Cited by 68 · see citing works
Self-citation5 The genetic susceptibility to type I (insulin-dependent) diabetes mellitus
Cudworth, A. G., & Wolf, E. (1982) · Clinics in Endocrinology and Metabolism · doi:10.1016/s0300-595x(82)80021-2 · Cited by 66 · see citing works
The role of genetic factors in the etiology of seasonal affective disorder and seasonality
Sher, L., Goldman, D. A., Ozaki, N., & Rosenthal, N. E. (1999) · Journal of Affective Disorders · doi:10.1016/s0165-0327(98)00194-3 · Cited by 64 · see citing works
Liu, W., Gu, N., Feng, G., Li, S., Bai, S., Zhang, J., Shen, T., Xue, H., Breen, G. D., Clair, D. S., et al. (1999) · PubMed · Cited by 55 · see citing works
Chromosome workshop: Chromosomes 11, 14, and 15
Craddock, N. J., Lendon, C. L., Cichon, S., Culverhouse, R., Detera‐Wadleigh, S. D., Devon, R. S., Faraone, S. V., Foroud, T., Gejman, P. V., Leonard, S. S., et al. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19990618)88:3 · Cited by 51 · see citing works
Self-citationWhat Is Significant in Whole-Genome Linkage Disequilibrium Studies?
Kruglyak, L. (1997) · The American Journal of Human Genetics · doi:10.1086/514893 · Cited by 51 · see citing works
Turecki, G., Grof, P., Cavazzoni, P. A., Duffy, A. C., Grof, E., Ahrens, B., Berghöfer, A., Müller-Oerlinghausen, B., Dvorakova, M. C., Libigerová, E., et al. (1999) · Psychiatric Genetics · doi:10.1097/00041444-199903000-00003 · Cited by 49 · see citing works
Modern molecular genetic approaches to psychiatric disease
Craddock, N. J., & Owen, M. J. (1996) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a011558 · Cited by 49 · see citing works
Self-citationLachman, H. M., Kelsoe, J. R., Moreno, L., Katz, S., & Papolos, D. F. (1997) · Psychiatric Genetics · doi:10.1097/00041444-199700710-00002 · Cited by 48 · see citing works
Page, G. P., & Amos, C. I. (1999) · The American Journal of Human Genetics · doi:10.1086/302331 · Cited by 48 · see citing works
Bipolar disorder and the serotonin transporter gene: a family-based association study
Kirov, G., Rees, M. I., Jones, I. R., MacCandless, F., Owen, M. J., & Craddock, N. J. (1999) · Psychological Medicine · doi:10.1017/s003329179900882x · Cited by 44 · see citing works
Self-citationNo association between bipolar disorder and alleles at a functional polymorphism in the COMT gene
Craddock, N. J., Spurlock, G., McGuffin, P., Owen, M. J., Nosten‐Bertrand, M., Bellivier, F., Meloni, R., Leboyer, M., Mallet, J. J., Mynett‐Johnson, L., et al. (1997) · The British Journal of Psychiatry · doi:10.1192/bjp.170.6.526 · Cited by 39 · see citing works
Self-citationThe monoamine oxidase-a gene and major psychosis in japanese subjects
Sasaki, T., Hattori, M., Sakai, T., Kato, T., Kunugi, H., Hirose, T., & Nanko, S. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(97)00522-2 · Cited by 34 · see citing works
Editorial: Can we find genes for schizophrenia?
Kidd, K. (1997) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19970221)74:1 · Cited by 31 · see citing works
Elvidge, G. P., Jones, I. R., McCandless, F., Asherson, P. J., Owen, M. J., & Craddock, N. J. (2001) · American Journal of Medical Genetics · doi:10.1002/ajmg.1353 · Cited by 29 · see citing works
Self-citationZubenko, G. S., Stiffler, J. S., Hughes, H. B., Hurtt, M. R., & Kaplan, B. B. (1998) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19980207)81:1 · Cited by 29 · see citing works
Braun, T. G., & Ewald, H. (1999) · Molecular Psychiatry · doi:10.1038/sj.mp.4000600 · Cited by 23 · see citing works
Brockington, I. (1996) · doi:10.1093/oso/9780192621269.003.0004 · Cited by 15 · see citing works
Jorm, A. F., & Easteal, S. (2000) · Social Psychiatry and Psychiatric Epidemiology · doi:10.1007/s001270050001 · Cited by 13 · see citing works
Kallmann syndrome gene (KAL-X) is not mutated in schizophrenia
O’Neill, M. J., Brewer, W. J., Thornley, C., Copolov, D., Warne, G. L., Sinclair, A. H., Forrest, S., & Williamson, R. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19990205)88:1 · Cited by 7 · see citing works
Neale (2000) · doi:10.1002/(sici)1098-2272(200004)18:4
Jonnal (2000) · doi:10.1002/1096-8628(20001204)96:6
Flagged first, then by citations
3 of the 97 references couldn’t be matched to a known paper.
Research works printed but not linked: 12
- Natl Ac-ud Sci U S A 1993; 90: 1977-81. 1982; 11: 389-96. Candidate gene studies depend on good candidates. It is likely that as our knowledge of the patho- physiology of bipolar disorder increases, this will lead to an interest in previously uninvestigated genes. In particular, when susceptibility genes for bipolar dis- order are found this will suggest a number of other candidate genes in the relevant biological pathway. The completion of the human genome project (93) (http://www.nature.com/genomics) and ongoing devel- opments in laboratory and statistical methodology will provide exciting new opportunities to unravel the complex genetic basis of non-mendelian disorders (reviewed in (94)). Our hope and belief is that identifying genes for bipolar disorder will be the first step on a path leading to a better understanding of disease pathophysiology and to improved treatment options for our patients. It is by the latter criteria that the success of candidate gene studies of bipolar disorder must ultimately be judged.
- epidemiological studies. Soc Psychiatry Psychiatr Epidemiol 2000; 35: 1-4.
- van den Oord EJCG. Framework for identifying quantitative trait loci in association studies using structural equation modelling. Genet Epidemiol 2000; 18: 341-59.
- Mynett-Johnson L, Kealey C, Claffey E, Curtis D, Bouchier- Hayes L, Powell C, et al. Multimarker haplotypes within the serotonin transporter gene suggest evidence of an association with bipolar disorder. A m J Med Genet 2000; 96: 845-9. 92: 1151-8. 453-60. 29: 1249-54. 44. 45. 46. 47. 48. 49. 50. 51. 52. 53. 54. 55. 56. 57. 58. 59. 60. 61.
- Craddock N, Dave S , Greening J. Association studies of hipolar disorder. Bipolar Disord (in press).
- Hoehe MR, Wendel B, Grunewald I, Chiaroni P, Levy N, Morris-Rosendahl D, et al. Serotonin transporter (5-HTT) gene polymorphisms are not associated with susceptibility to mood disorders. A m ] Med Genet 1998; 81: 1-3.
- Furlong RA, Ho L, Walsh C, Rubinsztein JS, Jain S, Paykel ES, et al. Analysis and meta-analysis of two serotonin transporter gene polymorphisms in bipolar and unipolar affective disorders. A m J Med Genet 1998; 81: 58-63.
- Saleem Q , Ganesh S, Vijaykumar M, Reddy YCJ, Brahmachari SK, Jain S. Association analysis of SHT transporter gene in bipolar disorder in the Indian population. A m ] Med Genet 2000; 96: 170-2.
- Lin S, Jiang S, Wu X, Qian Y, Wang D, Tang G, et al. Association analysis between mood disorder and monoamine oxidase gene. A m J Med Genet 2000; 96: 12-4.
- Parsian A, Todd RD. Genetic association between mono- amine oxidase and manic-depressive illness: comparison of relative risk and haplotype relative risk data. A m J Med Genet 1997; 74: 475-9.
- Sasaki T, Hattori M, Sakai T, Kato T, Kunugi H, Hirose T, et al. The moiioamine oxidase-A gene and major psychosis in Japanesc subiects. B i d Psychiatry 1998; 44: 922-4.
- Turecki G , Grof P, Cavazzoni P, Duffy A, Grof E, Ahrens B, et al. MAOA: association and linkage studies with lithium responsive bipolar disorder. Psychiatr Genet 1999; 9: 13-6.
Cited by
Sorted by citations
The genetics of schizophrenia and bipolar disorder: dissecting psychosis
Craddock, N., O’Donovan, M. C., & Owen, M. J. (2005) · Journal of Medical Genetics · doi:10.1136/jmg.2005.030718 · Cited by 574 · see citing works
Self-citationJesulola, E., Micalos, P., & Baguley, I. J. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2017.12.025 · Cited by 379 · see citing works
Cytokine, sickness behavior, and depression
Dantzer, R. (2006) · Neurologic Clinics · doi:10.1016/j.ncl.2006.03.003 · Cited by 340 · see citing works
Pathophysiology of depression and mechanisms of treatment
Brigitta, B. (2002) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2002.4.1/bbondy · Cited by 286 · see citing works
Gene–environment interaction and the genetics of depression
Lesch, K. (2004) · Journal of Psychiatry and Neuroscience · doi:10.1139/jpn.0420 · Cited by 284 · see citing works
Genetics of affective (mood) disorders
Craddock, N. J., & Forty, L. (2006) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201549 · Cited by 233 · see citing works
Self-citationCo‐occurrence of bipolar and attention‐deficit hyperactivity disorders in children
Singh, M. K., DelBello, M. P., Kowatch, R. A., & Strakowski, S. M. (2006) · Bipolar Disorders · doi:10.1111/j.1399-5618.2006.00391.x · Cited by 160 · see citing works
Askland, K. D., Read, C., & Moore, J. H. (2008) · Human Genetics · doi:10.1007/s00439-008-0600-y · Cited by 144 · see citing works
Genetics of stress response and stress-related disorders
Ising, M., & Holsboer, F. (2006) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2006.8.4/mising · Cited by 118 · see citing works
Is there a relationship between attention deficit hyperactivity disorder and bipolar disorder?
Kent, L. (2003) · Journal of Affective Disorders · doi:10.1016/s0165-0327(02)00092-7 · Cited by 112 · see citing works
Balmus, I. M., Ciobica, A., Antioch, I., Dobrin, R., & Timofte, D. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/3975101 · Cited by 103 · see citing works
“In this way, direct implications were demonstrated for themonoamine oxidaseA, 5-hydroxytryptamine transporter, and catechol-O-methyltransferase genes [217–220].”
BackgroundJuengst, S. B., Kumar, R. G., Failla, M. D., Goyal, A., & Wagner, A. K. (2014) · Journal of Head Trauma Rehabilitation · doi:10.1097/htr.0000000000000031 · Cited by 96 · see citing works
Jones, I. R., MRCPsych, PhD, Craddock, N. J., MRCPsych, & PhD (2025) · Psychopharmacology Bulletin · doi:10.64719/pb.4125 · Cited by 54 · see citing works
Self-citationGreen, E., & Craddock, N. J. (2003) · Current Psychiatry Reports · doi:10.1007/s11920-003-0086-1 · Cited by 44 · see citing works
Self-citationAtypical antipsychotics in bipolar depression: Neurobiological basis and clinical implications
Brugue, E., & Vieta, E. (2007) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2006.06.014 · Cited by 54 · see citing works
Genetic linkage and association studies in bipolar affective disorder: A time for optimism
Schulze, T. G., & McMahon, F. J. (2003) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.20012 · Cited by 31 · see citing works
Rapid-cycling bipolar disorder
Elhaj, O., & Calabrese, J. R. (2005) · Cambridge University Press eBooks · doi:10.1017/cbo9780511544019.004 · Cited by 31 · see citing works
Chapter 23 Molecular genetic approaches to puerperal psychosis
Jones, I. R., Lendon, C. L., Coyle, N. E., Robertson, E., Brockington, I., & Craddock, N. J. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)33024-8 · Cited by 30 · see citing works
Self-citationGenetic and neurocognitive foundations of emotion abnormalities in bipolar disorder
Rheenen, T. E. V., & Rossell, S. L. (2012) · Cognitive Neuropsychiatry · doi:10.1080/13546805.2012.690938 · Cited by 24 · see citing works
Trouble hyperactif avec déficit de l'attention et trouble bipolaire sont-ils liés ?
Charfi, F., & Cohen, D. (2005) · Neuropsychiatrie de l Enfance et de l Adolescence · doi:10.1016/j.neurenf.2004.11.002 · Cited by 17 · see citing works
No association between two polymorphisms at the5HT2Agene and bipolar affective puerperal psychosis
Robertson, E., Jones, I. R., Middle, F., Moray, J., & Craddock, N. J. (2003) · Acta Psychiatrica Scandinavica · doi:10.1034/j.1600-0447.2003.00167.x · Cited by 17 · see citing works
Self-citationHara, T., Owada, Y., & Takata, A. (2022) · Journal of Human Genetics · doi:10.1038/s10038-022-01046-9 · Cited by 14 · see citing works
Inflammation, sickness behaviour and depression
Dantzer, R., Castanon, N., Lestage, J., Moreau, M. M., & Capuron, L. (2006) · Cambridge University Press eBooks · doi:10.1017/cbo9780511544293.013 · Cited by 12 · see citing works
Update on psychiatric genetics
Zuchner, S. L., Roberts, S. T., Speer, M. C., & Beckham, J. C. (2007) · Genetics in Medicine · doi:10.1097/gim.0b013e318065a9fa · Cited by 12 · see citing works
Translating knowledge of genetics and pharmacology into improving everyday practice
Yatham, L. N. (2005) · Bipolar Disorders · doi:10.1111/j.1399-5618.2005.00211.x · Cited by 12 · see citing works
The severity of mental disorders is linked to interaction among candidate genes
Tiwary, B. K. (2012) · Integrative Biology · doi:10.1039/c2ib20066j · Cited by 11 · see citing works
Xu, X., Breen, G. D., Luo, L., Sun, B., Chen, C., Paredes, U. M., Huang, Y., Wu, Y.-Y., & Asherson, P. J. (2013) · BMC Research Notes · doi:10.1186/1756-0500-6-29 · Cited by 8 · see citing works
No evidence of an association between tyrosine hydroxylase gene polymorphisms and suicide victims.
Hattori, H., Shirakawa, O., Nishiguchi, N., Nushida, H., Ueno, Y., & Maeda, K. (2006) · PubMed · doi:10.24546/81000095 · Cited by 8 · see citing works
Triplet repeats and bipolar disorder
Jones, I. R., Gordon‐Smith, K., & Craddock, N. J. (2002) · Current Psychiatry Reports · doi:10.1007/s11920-002-0047-0 · Cited by 4 · see citing works
Self-citationNeurotransmitter Systems in Bipolar Disorder
Nakic, M., Krystal, J. H., & Bhagwagar, Z. (2010) · Wiley eBooks · doi:10.1002/9780470661277.ch16 · Cited by 4 · see citing works
Genetik psychiatrischer Störugen
Maier, W., Schwab, S. G., & Rietschel, M. (2003) · Springer eBooks · doi:10.1007/3-540-27386-7_4 · Cited by 3 · see citing works
Lesch, K. (2005) · doi:10.1002/9783527619672.ch29 · Cited by 3 · see citing works
Green, E., & Craddock, N. J. (2004) · Current Psychosis & Therapeutics Reports · doi:10.1007/bf02629417 · Cited by 2 · see citing works
Self-citationNöthen, M. M., Cichon, S., Schmäl, C., & Rietschel, M. (2006) · Springer eBooks · doi:10.1007/3-540-29623-9_1280 · Cited by 1 · see citing works
Die Genetik der bipolaren Störung
Cichon, S., & Rietschel, M. (2007) · Medizinische Genetik · doi:10.1007/s11825-007-0044-0 · Cited by 1 · see citing works
Craddock, N. J. (2007) · Medical psychiatry · doi:10.3109/9781420021158.013 · Cited by 1 · see citing works
Self-citationGene expression and genetic association in bipolar disorder
Sears, C. (2012) · Otago University Research Archive (University of Otago) · Cited by 1 · see citing works
PERCEPTIONS OF GENETIC COUNSELING FROM ADULTS WITH BIPOLAR DISORDER
Perschke, S. M. (2010) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 1 · see citing works
Geneties of Schizophrenia and Bipolar Affective Disorder
Nöthen, M. M., Cichon, S., Schmael, C., & Rietschel, M. (2009) · Springer eBooks · doi:10.1007/978-3-540-37654-5_32
Neurobiologic Foundations of Mood Disorders
Polan, H. J., Duman, R. S., & Schatzberg, A. F. (2015) · Wiley eBooks · doi:10.1002/9781118753378.ch21
Phenotypic dissection of mood disorder
Forty, L. (2009) · ORCA Online Research @Cardiff (Cardiff University)
Bipolar affective disorder: advances in genetics and mood-stabilising medication
White, D. C., & Kelly, B. D. (2006) · Irish Journal of Psychological Medicine · doi:10.1017/s0790966700009423
Investigating susceptibility to bipolar disorder, migraine and epilepsy
Knott, S. (2016) · ORCA Online Research @Cardiff (Cardiff University)
(2013) · CRC Press eBooks · doi:10.1201/b15462-35
- Authors
- Jones, I., & Craddock, N.
- Affiliations
- University of Birmingham (GB)
- Corresponding author
- Craddock, Nick
- Venue
- Annals of Medicine
- Publisher
- Informa UK Limited
- Published
- 2001-01
- Volume
- 33
- Issue
- 4
- Pages
- 248-256
- ISSN
- 0785-3890 (ISSN-L)
- 1365-2060
- OpenAlex
- W2129061795
- Cited by
- 44
- References
- 97
- Citations by year
- 2025: 1 · 2022: 1 · 2017: 1 · 2016: 2 · 2015: 1 · 2014: 1 · 2013: 2 · 2012: 3
- FWCI
- 0.60
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Annals of Medicine (publishedVersion)
- PubMed (publishedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- bipolar disorder, candidate gene association, genetic susceptibility, rapid cycling bipolar disorder, serotonin transporter, monoamine oxidase A, catechol-O-methyltransferase, neurotransmitter systems, complex genetic disorders
- MeSH terms
- Bipolar Disorder, Carrier Proteins, Catechol O-Methyltransferase, Genetic Techniques, Genetics, Population, Humans, Membrane Glycoproteins, Monoamine Oxidase, Nerve Tissue Proteins, Receptors, Serotonin, Tyrosine 3-Monooxygenase, Case-Control Studies, Receptors, Dopamine D2, Genetic Predisposition to Disease, Membrane Transport Proteins, Serotonin Plasma Membrane Transport Proteins, Receptors, Dopamine D3
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review