The Genetics of Major Depression
Open accessAbstract
(Neuron 81, 484–503; February 5, 2014) The original publication contained errors in gene nomenclature in Table 2. The table has now been corrected in the article online. The Genetics of Major DepressionFlint et al.NeuronFebruary 05, 2014In BriefGenetic analysis of major depression lags behind that of other disease. Genome-wide association and linkage results provide constraints on major depression’s genetic architecture, indicating that candidate gene studies are underpowered. The disorder is heterogeneous; subtypes likely exist that represent more homogenous conditions suitable for genetic dissection. Full-Text PDF Open Access
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Psychiatric disorders run in families, indicating substantial heredity.
“It has long been known that psychiatric disorders run in families, indicating substantial heredity”
From Neandertal introgression partitions the genetic landscape of neuropsychiatric disorders and associated behavioral phenotypes (2022) · cites this paper as [1]
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“…14,903 0.007 1.09 1.02–1.16 44 bp ins/del 0.43 65.8% 9,575 Anguelova et al., 2003 11 941 2,110 0.198 1.08 0.96–1.22 44 bp ins/del 0.43 12.3% 11,958 Anguelova et al., 2003 10 592 2,094 >0.5 NA NA intron 2 VNTR 0.35 NA NA Furlong et al., 1998 4 275 739 0.049 1.2 1.00–1.45 44 bp ins/del 0.43…”
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“Is it possible that the endogenous form of MD is more genetically determined than others? The short answer to that question is no; in fact, contrary to the hypothesis that subjects whose MD appears to be devoid of precipitating events should have increased genetic predisposition (indexed by greater family history), th…”
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“Do the same genetic loci that increase susceptibility to MD also increase susceptibility to other disorders? Two quantitative Reviews (meta-analyses) agree that there is a high genetic correlation between anxiety and MD (Cerdá et al., 2010; Middeldorp et al., 2005).”
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“Distinguishing features are relatively nonspecific: those with a family history of MD have more clinically severe illness, tend to present at an earlier age, and suffer higher rates of recurrence (Kendler et al., 1994, 1999; Lieb et al., 2002; Weissman et al., 2006).”
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Seventy-five genetic loci influencing the human red blood cell
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Neurogenesis and affective disorders
Samuels, B. A., & Hen, R. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07614.x · Cited by 286 · cited 2× · see citing works
“, 1997]) and impaired corticosteroid receptor signaling (Holsboer, 2000), more recent hypotheses include the involvement of neurotrophins (Samuels and Hen, 2011), fibroblast growth factors (both ligands and receptors) (Turner et al.”
Genetic moderation of environmental risk for depression and anxiety in adolescent girls
Silberg, J., Rutter, M., Neale, M., & Eaves, L. (2001) · British Journal of Psychiatry · doi:10.1192/bjp.179.2.116 · Cited by 285 · cited 1× · see citing works
“Evidence from twin studies (Kendler et al., 1995a, 2004; Silberg et al., 2001) indicate that genetic risk factors for MD not only alter average risk but also impact on sensitivity to the depressogenic effects of environmental adversities, particularly various forms of childhood maltreatment and recent stressful life e…”
Replication of Linkage Studies of Complex Traits: An Examination of Variation in Location Estimates
Roberts, S. B., MacLean, C. J., Neale, M. C., Eaves, L. J., & Kendler, K. S. (1999) · The American Journal of Human Genetics · doi:10.1086/302528 · Cited by 274 · see citing works
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“Two meta-analyses found no evidence for an interaction (Munafò et al., 2009; Risch et al., 2009), while one meta-analysis concluded that there was an effect (Karg et al.”
Cannabis Use, Abuse, and Dependence in a Population-Based Sample of Female Twins
Kendler, K. S., & Prescott, C. A. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.8.1016 · Cited by 265 · see citing works
Self-citationHeterogeneity of DSM-IV Major Depressive Disorder as a Consequence of Subthreshold Bipolarity
Zimmermann, P., Brückl, T. M., Nocon, A., Pfister, H., Lieb, R., Wïttchen, H., Holsboer, F., & Angst, J. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.158 · Cited by 264 · cited 2× · see citing works
“When symptoms of subthreshold mania are sought (elevated mood, irritable mood, or increased activity), a large proportion of unipolar cases are found to qualify: up to half of all cases with unipolar illness (Angst et al., 2010, 2011; Zimmermann et al., 2009).”
The Genetics of Mood Disorders.
Taylor, M. (1991) · American Journal of Psychiatry · doi:10.1176/ajp.148.11.1594 · Cited by 253 · cited 1×
“The risk for bipolar disorder in relatives of MD probands is only modestly increased, approximately 2-fold across studies (on a relative risk scale) (Tsuang and Faraone, 1990).”
Genome-Wide Association Study of Major Recurrent Depression in the U.K. Population
Lewis, C. M., Ng, M., Butler, A. W., Cohen‐Woods, S., Uher, R., Pirlo, K. J., Weale, M. E., Schosser, A., Paredes, U. M., Rivera, M., et al. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.09091380 · Cited by 237 · see citing works
The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression
Kohli, M. A., Lucae, S., Saemann, P. G., Schmidt, M. V., Demirkan, A., Hek, K., Czamara, D., Alexander, M., Salyakina, D., Ripke, S., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.04.005 · Cited by 228 · cited 4× · see citing works
“However, one paper claims a genome-wide significant association: a marker within a gene desert on chromosome 12 (Kohli et al., 2011).”
InfluentialPrevalence of anxiety disorders comorbidity in bipolar depression, unipolar depression and dysthymia
Pini, S., Cassano, G. B., Simonini, E., Savino, M., Russo, A. G., & Montgomery, S. (1997) · Journal of Affective Disorders · doi:10.1016/s0165-0327(96)01405-x · Cited by 226 · see citing works
The inheritance of affective disorders: A review of data and of hypotheses
Gershon, E. S., Bunney, W. E., Leckman, J. F., Eerdewegh, M. M. V., & DeBauche, B. A. (1976) · Behavior Genetics · doi:10.1007/bf01065722 · Cited by 222 · see citing works
Cuijpers, P., van Straten, A., van Oppen, P., & Andersson, G. (2008) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v69n1102 · Cited by 219 · cited 1× · see citing works
“There is even dispute about the value of medication (Khin et al., 2011; Kirsch et al., 2008; Turner et al., 2008; Vöhringer and Ghaemi, 2011) and psychological therapies (Cuijpers et al., 2008, 2010, 2011).”
The Classification of Depressive Illnesses
Kendell, R. (1970) · British Journal of Psychiatry · doi:10.1192/s0007125000193468 · Cited by 216
Khin, N. A., Chen, Y., Yang, Y., Yang, P., & LAUGHREN, T. P. (2011) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.10m06191 · Cited by 211 · cited 2× · see citing works
“There is even dispute about the value of medication (Khin et al., 2011; Kirsch et al., 2008; Turner et al., 2008; Vöhringer and Ghaemi, 2011) and psychological therapies (Cuijpers et al.”
Methodological challenges of genome-wide association analysis in Africa
Teo, Y., Small, K. S., & Kwiatkowski, D. P. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2731 · Cited by 195 · cited 1× · see citing works
“Standard GWAS approaches do not work so well in African populations (Teo et al., 2010).”
Zubenko, G. S., Maher, B. S., Hughes, H. B., Zubenko, W. N., Stiffler, J. S., Kaplan, B. B., & Marazita, M. L. (2003) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.20073 · Cited by 191 · see citing works
Rietschel, M., Mattheisen, M., Frank, J., Treutlein, J., Degenhardt, F., Breuer, R., Steffens, M., Mier, D. U., Esslinger, C., Walter, H., et al. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.05.038 · Cited by 183 · cited 1× · see citing works
“…Discovery 353 366 365,676 MD/RMD rs1545843 2.84 5.53 3 10 8 chr12:84563818 Europe/U.S. Replication 3,738 10,635 – – rs1545843 1.315 1.40 3 10 9 chr12:84563818 Rietschel et al., 2010 German Discovery 604 1,364 491,238 MD rs2765493 1.45 2.26 3 10 7 chr1:157797750 German Meta 1,013 1,905 –…”
InfluentialAssociation of the5-HTTLPRgenotype and unipolar depression: a meta-analysis
Clarke, H. F., Flint, J., Attwood, A. S., & Munafo, M. R. (2010) · Psychological Medicine · doi:10.1017/s0033291710000516 · Cited by 177 · cited 1× · see citing works
“…2013 11 1,491 2,937 0.12 NA NA rs6311 0.44 NA NA 5HT-6R Fukuo et al., 2010 4 701 2,422 0.406 0.94 0.80–1.08 rs1805054 0.17 8.4% 19,021 5HTTP/SLC6A4 Clarke et al., 2010 39 6,836 14,903 0.007 1.09 1.02–1.16 44 bp ins/del 0.43 65.8% 9,575 Anguelova et al., 2003 11 941 2,110 0.198 1.08 0.96–1.22 44…”
InfluentialSelf-citationHeilig, M., Zachrisson, O., Thorsell, A., Ehnvall, A., Mottagui-Tabar, S., Sjögren, M., Åsberg, M., Ekman, R., Wahlestedt, C., & Ågren, H. (2004) · Journal of Psychiatric Research · doi:10.1016/s0022-3956(03)00101-8 · Cited by 177 · cited 1× · see citing works
“Two SNPs (in C5orf20 [Willis-Owen et al., 2006] and in NPY [Heilig et al., 2004]) scored p values less than 0.05, where four would have been expected by chance.”
InfluentialDeGiorgio, M., Jakobsson, M., & Rosenberg, N. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903341106 · Cited by 175 · see citing works
Genetic risk profiles for depression and anxiety in adult and elderly cohorts
Demirkan, A., Penninx, B. W. J. H., Hek, K., Wray, N. R., Amin, N., Aulchenko, Y. S., van Dyck, R., de Geus, E. J. C., Hofman, A., Uitterlinden, A. G., et al. (2010) · Molecular Psychiatry · doi:10.1038/mp.2010.65 · Cited by 175 · cited 1× · see citing works
“While lifetime prevalence estimates vary, from 3% in Japan to 16.9% in the U.S., in all countries the disorder is common, with a frequency typically varying from 8% to 12% (Demyttenaere et al., 2004; Kessler et al., 2003).”
InfluentialA Genome-Wide Association Study of Depressive Symptoms
Hek, K., Demirkan, A., Lahti, J., Terracciano, A., Teumer, A., Cornelis, M. C., Amin, N., Bakshis, E., Baumert, J., Ding, J., et al. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.033 · Cited by 172 · cited 1× · see citing works
“While Table 1 only includes GWASs of MD, there are also a number of studies of phenotypes that are genetically related to MD, such as the personality trait of neuroticism (Kendler et al., 1993; Shifman et al., 2008) or depressive symptoms (Foley et al., 2001; Hek et al., 2013).”
Understanding the Clinical Heterogeneity of Major Depression Using Family Data
Weissman, M. M. (1986) · Archives of General Psychiatry · doi:10.1001/archpsyc.1986.01800050028003 · Cited by 162 · see citing works
The Fibroblast Growth Factor Family: Neuromodulation of Affective Behavior
Turner, C. A., Watson, S. J., & Akil, H. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.037 · Cited by 160 · cited 1× · see citing works
“, 1997]) and impaired corticosteroid receptor signaling (Holsboer, 2000), more recent hypotheses include the involvement of neurotrophins (Samuels and Hen, 2011), fibroblast growth factors (both ligands and receptors) (Turner et al., 2012), GABAergic deficits (Luscher et al.”
Whole genome linkage scan of recurrent depressive disorder from the depression network study
McGuffin, P., Knight, J., Breen, G., Brewster, S., Boyd, P. R., Craddock, N., Gill, M., Korszun, A., Maier, W., Middleton, L., et al. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi363 · Cited by 159 · see citing works
A whole genome association study of neuroticism using DNA pooling
Shifman, S., Bhomra, A., Smiley, S., Wray, N. R., James, M. R., Martin, N. G., Hettema, J. M., An, S., Neale, M. C., van den Oord, E. J. C. G., et al. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4002048 · Cited by 156 · see citing works
Self-citationThe dopamine D4 receptor gene 48-base-pair-repeat polymorphism and mood disorders: A meta-analysis
López‐León, S., Croes, E. A., Sayed‐Tabatabaei, F. A., Claes, S. J., Broeckhoven, C. V., & van Duijn, C. M. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.01.030 · Cited by 156 · see citing works
Lewis, S. J., Lawlor, D. A., Smith, G. D., Araya, R., Timpson, N. J., Day, I. N. M., & Ebrahim, S. B. J. (2006) · Molecular Psychiatry · doi:10.1038/sj.mp.4001790 · Cited by 151 · cited 1× · see citing works
“Peerbooms et al., 2011 17 3,341 13,840 0.579 1.016 0.96–1.07 rs1801133 0.32 6.2% 250,625 Lewis et al., 2006 9 1,241 1,1021 0.003 1.36 1.11–1.67 rs1801133 0.32 99.1% 518 Gilbody et al., 2007 10 1,280 10,429 <0.05 1.14 11.04–1.26 rs1801133 0.32 43.4% 3,121 Zintzaras, 2006 5 291 897 >0.1 1.15…”
InfluentialEvidence for Multiple Genetic Factors Underlying DSM-IV Criteria for Major Depression
Kendler, K. S., Aggen, S. H., & Neale, M. C. (2013) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2013.751 · Cited by 146 · see citing works
Self-citationEstimating the genetic variance of Major Depressive Disorder (MDD) due to all SNPs
Lubke, G., Hottenga, J., Walters, R., Laurin, C., de Geus, E. D., Willemsen, G., Smit, J., Middeldorp, C., Penninx, B., Vink, J., et al. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.03.011 · Cited by 145 · cited 1× · see citing works
“Two papers report SNP heritabilities for MD ranging from 21% (Lee et al., 2013) to 30% (Lubke et al., 2012).”
Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4
Polymeropoulos, M., Swift, R., & Swift, M. (1994) · Nature Genetics · doi:10.1038/ng0994-95 · Cited by 145 · cited 1× · see citing works
“Table 4 contains one example of a Mendelian mutation that underlies pure MD: Wolfram syndrome, a rare autosomal recessive disorder due to a mutation on the short arm of chromosome 4 (Polymeropoulos et al., 1994).”
Clinical Characteristics of Major Depression That Predict Risk of Depression in Relatives
Kendler, K. S., Gardner, C. O., & Prescott, C. A. (1999) · Archives of General Psychiatry · doi:10.1001/archpsyc.56.4.322 · Cited by 142 · cited 1× · see citing works
“The two major studies that have addressed this question found reassuringly similar answers (Kendler et al., 2001, 2006).”
Self-citationStevens, V., Redwood, S. K., Bost, R. H., et al. (2007) · doi:10.1016/b978-0-323-04571-1.50021-4 · Cited by 139 · cited 2×
“…that the number of loci detected increases linearly with increasing sample size (data are from Frayling et al., 2007; Lango Allen et al., 2010; Loos et al., 2008; Park et al., 2010; Scuteri et al., 2007; Speliotes et al., 2010; Thorleifsson et al., 2009; Wen et al., 2012; Willer et al., 2009).”
Kendler, K. S., Pedersen, N. L., Neale, M. C., & Mathé, A. A. (1995) · Behavior Genetics · doi:10.1007/bf02197180 · Cited by 134 · cited 1× · see citing works
“A larger study of 486 twin pairs with affective illness provided some support for the threshold model, but the number of bipolar probands was small, so power to discriminate models was low (Kendler et al., 1995b).”
Self-citationGenetic and environmental influences on psychiatric comorbidity: a systematic review.
Cerdá, M., Sagdeo, A., Johnson, J., & Galea, S. (2010) · Journal of Affective Disorders · doi:10.1016/j.jad.2009.11.006 · Cited by 131 · see citing works
Genomewide Significant Linkage to Recurrent, Early-Onset Major Depressive Disorder on Chromosome 15q
Holmans, P., Zubenko, G. S., Crowe, R., DePaulo, J. R., Scheftner, W. A., Weissman, M. M., Zubenko, W. N., Boutelle, S., Murphy-Eberenz, K. P., MacKinnon, D. F., et al. (2004) · The American Journal of Human Genetics · doi:10.1086/421333 · Cited by 130 · see citing works
Life stress, 5-HTTLPR and mental disorder: findings from a 30-year longitudinal study
Fergusson, D. M., Horwood, L. J., Miller, A. L., & Kennedy, M. A. (2011) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.110.085993 · Cited by 124 · cited 1× · see citing works
“While Table 1 only includes GWASs of MD, there are also a number of studies of phenotypes that are genetically related to MD, such as the personality trait of neuroticism (Kendler et al., 1993; Shifman et al., 2008) or depressive symptoms (Foley et al., 2001; Hek et al., 2013).”
Stressful Life Events, Genetic Liability, and Onset of an Episode of Major Depression in Women
Kendler, K. S., Kessler, R. C., Walters, E. E., MacLean, C., Neale, M. C., Heath, A. C., & Eaves, L. J. (2010) · FOCUS The Journal of Lifelong Learning in Psychiatry · doi:10.1176/foc.8.3.foc459 · Cited by 114 · see citing works
Self-citationJun, T., Pae, C., Hoon-Han, Chae, J., Bahk, W., Kim, K., & Serretti, A. (2003) · Psychiatric Genetics · doi:10.1097/00041444-200309000-00008 · Cited by 113 · see citing works
Use of cognitive therapy for relapse prevention in chronic depression
Scott, J. L., Palmer, S., Paykel, E. S., Teasdale, J., & Hayhurst, H. (2003) · The British Journal of Psychiatry · doi:10.1192/bjp.182.3.221 · Cited by 109 · see citing works
Narrowing the Boundaries of the Genetic Architecture of Schizophrenia
Wray, N. R., & Visscher, P. M. (2009) · Schizophrenia Bulletin · doi:10.1093/schbul/sbp137 · Cited by 105 · cited 1× · see citing works
“Wray and Visscher asked this question about the genetic architecture of schizophrenia (Wray and Visscher, 2010).”
Kishi, T., Yoshimura, R., Fukuo, Y., Okochi, T., Matsunaga, S., Umene‐Nakano, W., Nakamura, J., Serretti, A., Correll, C. U., Kane, J. M., et al. (2012) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-012-0337-4 · Cited by 101 · cited 1× · see citing works
“Kishi et al., 2009 7 1,658 2,046 0.0327 0.821 0.695–0.984 rs6295 0.48 65.9% 2,315 López-León et al., 2008 4 NA NA NS 1.16 0.98–1.38 rs6295 0.48 NA NA Kishi et al., 2013 13 3,199 4,380 0.006 0.87 0.78–0.96 rs6295 0.48 61.9% 4,901”
InfluentialZintzaras, E. (2006) · Psychiatric Genetics · doi:10.1097/01.ypg.0000199444.77291.e2 · Cited by 101 · cited 1× · see citing works
“…2006 9 1,241 1,1021 0.003 1.36 1.11–1.67 rs1801133 0.32 99.1% 518 Gilbody et al., 2007 10 1,280 10,429 <0.05 1.14 11.04–1.26 rs1801133 0.32 43.4% 3,121 Zintzaras, 2006 5 291 897 >0.1 1.15 0.97–1.36 rs1801133 0.32 13.4% 3,223 López-León et al., 2008 6 875 3,859 0.05 1.2 1.07–1.34 rs1801133 0.32…”
InfluentialInference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs
Hemani, G., Yang, J., Vinkhuyzen, A. A. E., Powell, J. E., Willemsen, G. A. H. M., Hottenga, J., Abdellaoui, A., Mangino, M., Valdes, A. M., Medland, S. E., et al. (2013) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2013.10.005 · Cited by 101 · cited 2× · see citing works
“…et al., 2013; 490 Neuron 81, February 5, 2014 ª2014 Elsevier Inc. Speliotes et al., 2010) and it has a heritability similar to MD (a recent estimate based on 20,000 sibling pairs gave 40% [Hemani et al., 2013], though this is lower than a large meta-analysis of twin data [Nan et al., 2012]).”
Yang, J., Wray, N. R., & Visscher, P. M. (2009) · Genetic Epidemiology · doi:10.1002/gepi.20456 · Cited by 99 · see citing works
Genetic association study of BDNF in depression: Finding from two cohort studies and a meta‐analysis
Chen, L., Lawlor, D. A., Lewis, S. J., Yuan, W., Abdollahi, M. R., Timpson, N. J., Day, I. N. M., Ebrahim, S. B. J., Smith, G. D., & Shugart, Y. Y. (2008) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30686 · Cited by 90 · see citing works
Heritability of body mass index in pre-adolescence, young adulthood and late adulthood
Nan, C., Guo, B., Warner, C., Fowler, T., Barrett, T. G., Boomsma, D. I., Nelson, T., Whitfield, K. E., Beunen, G. P., Thomis, M. A., et al. (2012) · European Journal of Epidemiology · doi:10.1007/s10654-012-9678-6 · Cited by 90 · see citing works
Karg, K., Burmeister, M., Shedden, K., & Sen, S. (2011) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.189 · Cited by 87 · cited 2× · see citing works
“, 2009), while one meta-analysis concluded that there was an effect (Karg et al., 2011).”
The current state of play on the molecular genetics of depression
Cohen-Woods, S., Craig, I. W., & McGuffin, P. (2013) · Psychological Medicine · doi:10.1017/s0033291712001286 · Cited by 82 · cited 1× · see citing works
“A simple summary of Table 1 is that nothing significant has been found and indeed many of the papers and reviews of this field make that point (e.g., Cohen-Woods et al., 2013).”
Solving the Antidepressant Efficacy Question: Effect Sizes in Major Depressive Disorder
Vöhringer, P. A., & Ghaemi, S. N. (2011) · Clinical Therapeutics · doi:10.1016/j.clinthera.2011.11.019 · Cited by 81 · cited 2× · see citing works
“There is even dispute about the value of medication (Khin et al., 2011; Kirsch et al., 2008; Turner et al., 2008; Vöhringer and Ghaemi, 2011) and psychological therapies (Cuijpers et al.”
No association of genetic variants in BDNF with major depression: A meta‐ and gene‐based analysis
Gyekis, J. P., Yu, W., Dong, S., Wang, H., Qian, J., Kota, P., & Yang, J. (2012) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32122 · Cited by 81 · cited 1× · see citing works
“Two SNPs (in C5orf20 [Willis-Owen et al., 2006] and in NPY [Heilig et al., 2004]) scored p values less than 0.05, where four would have been expected by chance.”
InfluentialSo, H., Li, M., & Sham, P. C. (2011) · Genetic Epidemiology · doi:10.1002/gepi.20593 · Cited by 70 · cited 1× · see citing works
“There are currently two implementations of this idea (So et al., 2011; Yang et al., 2011).”
Hunt, C., Slade, T., & Andrews, G. (2004) · Depression and Anxiety · doi:10.1002/da.20019 · Cited by 70 · cited 1× · see citing works
“At the gene level (testing for enrichment of significant SNPs), two genes passed the 5% threshold, TNF (Jun et al., 2003) and the norepinephrine transport (NET) (Inoue et al., 2004), again compatible with chance expectations.”
Zimmerman, M. A., McGlinchey, J. B., Chelminski, I., & Young, D. (2007) · Psychological Medicine · doi:10.1017/s0033291707001717 · Cited by 66 · see citing works
Gaysina, D., Cohen‐Woods, S., Craddock, N. J., FARMER, A. E., Hoda, F., Korszun, A., Owen, M. J., Craig, I., & McGuffin, P. (2007) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30665 · Cited by 64 · cited 1× · see citing works
“…1,280 10,429 <0.05 1.14 11.04–1.26 rs1801133 0.32 43.4% 3,121 Zintzaras, 2006 5 291 897 >0.1 1.15 0.97–1.36 rs1801133 0.32 13.4% 3,223 López-León et al., 2008 6 875 3,859 0.05 1.2 1.07–1.34 rs1801133 0.32 51.5% 1,719 Gaysina et al., 2008 4 1,222 835 0.39 0.96 0.84–1.09 rs1801133 0.32 6.4% 80,906”
InfluentialWolframin mutations and hospitalization for psychiatric illness
Swift, M., & Swift, R. G. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001681 · Cited by 61 · see citing works
Levinson, D. F., Evgrafov, O. V., Knowles, J. A., Potash, J. B., Weissman, M. M., Scheftner, W. A., DePaulo, J. R., Crowe, R., Murphy-Eberenz, K. P., Marta, D. H., et al. (2007) · American Journal of Psychiatry · doi:10.1176/ajp.2007.164.2.259 · Cited by 60 · cited 1× · see citing works
“, 2005), chromosome 15, 87–92 Mb (Breen et al., 2011; Holmans et al., 2004, 2007; Levinson et al., 2007), chromosome 3, 4–9 Mb (Breen et al.”
The Clinical Characteristics of Major Depression as Indices of the Familial Risk to Illness
Kendler, K. S., Neale, M. C., Kessler, R. C., Heath, A. C., & Eaves, L. J. (1994) · The British Journal of Psychiatry · doi:10.1192/bjp.165.1.66 · Cited by 58 · see citing works
Self-citationInoue, K., Itoh, K., Yoshida, K., et al. (2004) · Neuropsychobiology · doi:10.1159/000080957 · Cited by 58 · cited 2× · see citing works
“, 2003) and the norepinephrine transport (NET) (Inoue et al., 2004), again compatible with chance expectations.”
The Mood Spectrum in Unipolar and Bipolar Disorder: Arguments for a Unitary Approach
Cassano, G. B., Rucci, P., Frank, E., Fagiolini, A. M., Dell’Osso, L., Shear, M. K., & Kupfer, D. J. (2005) · FOCUS The Journal of Lifelong Learning in Psychiatry · doi:10.1176/foc.3.1.61 · Cited by 51 · see citing works
McGuffin, P., Alsabban, S., & Uher, R. (2011) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.110.085225 · Cited by 47 · cited 1× · see citing works
“The original studywas carried out on a longitudinal cohort in New Zealand, and empirical literature dealing with whether that finding is robust, and replicable, is unclear and considerably polarized (Caspi et al., 2010; Kaufman et al., 2010; McGuffin et al., 2011).”
Linkage on chromosome 14 in a genome-wide linkage study of a broad anxiety phenotype
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Multiple threshold models for the affective disorders: The Yale-NIMH collaborative family study
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InfluentialLinkage analysis of depression spectrum disease.
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- Authors
- Flint, J., & Kendler, K. S.
- ORCID
- Kendler, Kenneth S.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2014-03
- Volume
- 81
- Issue
- 5
- Pages
- 1214
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
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- en
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- Licence
- Locations
- Neuron (publishedVersion, cc-by)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- major depressive disorder, genetic architecture, genome-wide association study, genetic linkage, candidate gene association, disease heterogeneity, depression subtypes, gene nomenclature
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 ›
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