Risk in Relatives, Heritability, SNP-Based Heritability, and Genetic Correlations in Psychiatric Disorders: A Review

GCTA: a tool for genome-wide complex trait analysis

Yang, J., Lee, S. H., Goddard, M. E., & Visscher, P. M. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2010.11.011 · Cited by 8,279 · see citing works

Biological insights from 108 schizophrenia-associated genetic loci

Schizophrenia Working Group of the Psychiatric Genomics Consortium (2014) · Nature · doi:10.1038/nature13595 · Cited by 7,577 · see citing works

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

Schizophrenia Working Group of the Psychiatric Genomics Consortium, Bulik-Sullivan, B. K., Loh, P.-R., Finucane, H. K., Ripke, S., Yang, J., Patterson, N., Daly, M. J., Price, A. L., & Neale, B. M. (2015) · Nature Genetics · doi:10.1038/ng.3211 · Cited by 5,559 · see citing works

Common SNPs explain a large proportion of the heritability for human height

Yang, J., Benyamin, B., McEvoy, B. P., Gordon, S., Henders, A. K., Nyholt, D. R., Madden, P. A., Heath, A. C., Martin, N. G., Montgomery, G. W., et al. (2010) · Nature Genetics · doi:10.1038/ng.608 · Cited by 4,446 · see citing works

An atlas of genetic correlations across human diseases and traits

ReproGen Consortium, Bulik-Sullivan, B., Psychiatric Genomics Consortium, Genetic Consortium for Anorexia Nervosa of the Wellcome Trust Case Control Consortium 3, Finucane, H. K., Anttila, V., Gusev, A., Day, F. R., Loh, P.-R., Duncan, L., et al. (2015) · Nature Genetics · doi:10.1038/ng.3406 · Cited by 4,255 · see citing works

Causal Relationship Between Stressful Life Events and the Onset of Major Depression

Kendler, K. S., Karkowski, L. M., & Prescott, C. A. (1999) · American Journal of Psychiatry · doi:10.1176/ajp.156.6.837 · Cited by 2,486 · see citing works

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Cross-Disorder Group of the Psychiatric Genomics Consortium (2013) · Nature Genetics · doi:10.1038/ng.2711 · Cited by 2,263 · see citing works

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

Lichtenstein, P., Yip, B. H., Björk, C., Pawitan, Y., Cannon, T. D., Sullivan, P. F., & Hultman, C. M. (2009) · The Lancet · doi:10.1016/s0140-6736(09)60072-6 · Cited by 2,125 · see citing works

Analysis of shared heritability in common disorders of the brain

The Brainstorm Consortium, Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., Duncan, L., Escott-Price, V., Falcone, G. J., Gormley, P., et al. (2018) · Science · doi:10.1126/science.aap8757 · Cited by 1,924 · see citing works

The inheritance of liability to certain diseases, estimated from the incidence among relatives

Falconer, D. (1965) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1965.tb00500.x · Cited by 1,662 · see citing works

The Danish Civil Registration System. A cohort of eight million persons.

Pedersen, C. B., Gøtzsche, H., Møller, J. O., & Mortensen, P. B. (2006) · PubMed · Cited by 1,617 · see citing works

Genome-wide association study identifies 30 loci associated with bipolar disorder

eQTLGen Consortium, Stahl, E. A., BIOS Consortium, the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Breen, G., Forstner, A. J., McQuillin, A., Ripke, S., Trubetskoy, V., Mattheisen, M., et al. (2019) · Nature Genetics · doi:10.1038/s41588-019-0397-8 · Cited by 1,519 · see citing works

Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

Lee, P. H., Anttila, V., Won, H., Feng, Y.-C. A., Rosenthal, J., Zhu, Z., Tucker-Drob, E. M., Nivard, M. G., Grotzinger, A. D., Posthuma, D., et al. (2019) · Cell · doi:10.1016/j.cell.2019.11.020 · Cited by 1,381 · see citing works

Estimating Missing Heritability for Disease from Genome-wide Association Studies

Lee, S. H., Wray, N. R., Goddard, M. E., & Visscher, P. M. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2011.02.002 · Cited by 1,064 · see citing works

Genome partitioning of genetic variation for complex traits using common SNPs

Yang, J., Manolio, T. A., Pasquale, L. R., Boerwinkle, E., Caporaso, N., Cunningham, J. M., de Andrade, M., Feenstra, B., Feingold, E., Hayes, M. G., et al. (2011) · Nature Genetics · doi:10.1038/ng.823 · Cited by 890 · see citing works

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

Zheng, J., Erzurumluoglu, A. M., Elsworth, B. L., Kemp, J. P., Howe, L., Haycock, P. C., Hemani, G., Tansey, K., Laurin, C., Early Genetics and Lifecourse Epidemiology (EAGLE) Eczema Consortium, et al. (2017) · Bioinformatics · doi:10.1093/bioinformatics/btw613 · Cited by 869 · see citing works

Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

Study, T. L. C., Yang, J., Bakshi, A., Zhu, Z., Hemani, G., Vinkhuyzen, A. A. E., Lee, S. H., Robinson, M. R., Perry, J. R. B., Nolte, I. M., et al. (2015) · Nature Genetics · doi:10.1038/ng.3390 · Cited by 745 · see citing works

The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood

Lichtenstein, P., Carlström, E., Råstam, M., Gillberg, C., & Anckarsäter, H. (2010) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2010.10020223 · Cited by 738 · see citing works

Improved Heritability Estimation from Genome-wide SNPs

Speed, D., Hemani, G., Johnson, M. R., & Balding, D. J. (2012) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2012.10.010 · Cited by 700 · see citing works

Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease

Lee, J.-M., Wheeler, V. C., Chao, M. J., Vonsattel, J. P. G., Pinto, R. M., Lucente, D., Abu-Elneel, K., Ramos, E. M., Mysore, J. S., Gillis, T., et al. (2015) · Cell · doi:10.1016/j.cell.2015.07.003 · Cited by 655 · cited 1× · see citing works

Comparative genetic architectures of schizophrenia in East Asian and European populations

Schizophrenia Working Group of the Psychiatric Genomics Consortium, Lam, M., Indonesia Schizophrenia Consortium, Genetic REsearch on schizophreniA neTwork-China and the Netherlands (GREAT-CN), Chen, C.-Y., Li, Z., Martin, A. R., Bryois, J., Ma, X., Gaspar, H., et al. (2019) · Nature Genetics · doi:10.1038/s41588-019-0512-x · Cited by 655 · see citing works

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

Lee, S. H., Yang, J., Goddard, M. E., Visscher, P. M., & Wray, N. R. (2012) · Bioinformatics · doi:10.1093/bioinformatics/bts474 · Cited by 635 · see citing works

Heritability of schizophrenia and schizophrenia spectrum based on the nationwide danish twin register

Hilker, R., Helenius, D., Fagerlund, B., Skytthe, A., Christensen, K., Werge, T. M., Nordentoft, M., & Glenthøj, B. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.08.017 · Cited by 615 · see citing works

Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings

Visscher, P. M., Medland, S. E., Ferreira, M. A. R., Morley, K. I., Zhu, G., Cornes, B. K., Montgomery, G. W., & Martin, N. G. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020041 · Cited by 613 · see citing works

The incidence and prevalence of Huntington's disease: A systematic review and meta‐analysis

Pringsheim, T. M., Wiltshire, K. M., Day, L., Dykeman, J., Steeves, T. D. L., & Jetté, N. (2012) · Movement Disorders · doi:10.1002/mds.25075 · Cited by 586 · see citing works

The Swedish Multi-Generation Register

Ekbom, A. (2011) · Methods in molecular biology · doi:10.1007/978-1-59745-423-0_10 · Cited by 553 · see citing works

Improved polygenic prediction by Bayesian multiple regression on summary statistics

Lloyd-Jones, L. R., Zeng, J., Sidorenko, J., Yengo, L., Moser, G., Kemper, K. E., Wang, H., Zheng, Z., Magi, R., Esko, T., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12653-0 · Cited by 528 · see citing works

Recovery of trait heritability from whole genome sequence data

Wainschtein, P., Jain, D., Zheng, Z., TOPMed Anthropometry Working Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Cupples, L. A., Shadyab, A. H., McKnight, B., Shoemaker, B. M., Mitchell, B. D., et al. (2019) · doi:10.1101/588020 · Cited by 515 · cited 1× · see citing works

Reevaluation of SNP heritability in complex human traits

Speed, D., Cai, N., Johnson, M. R., Nejentsev, S., & Balding, D. J. (2017) · Nature Genetics · doi:10.1038/ng.3865 · Cited by 436 · see citing works

Concepts, estimation and interpretation of SNP-based heritability

Yang, J., Zeng, J., Goddard, M. E., Wray, N. R., & Visscher, P. M. (2017) · Nature Genetics · doi:10.1038/ng.3941 · Cited by 435 · see citing works

Childhood maltreatment and unfavourable clinical outcomes in bipolar disorder: a systematic review and meta-analysis

Agnew‐Blais, J. C., & Danese, A. (2016) · The Lancet Psychiatry · doi:10.1016/s2215-0366(15)00544-1 · Cited by 421 · see citing works

The use of multiple thresholds in determining the mode of transmission of semi‐continuous traits*

Reich, T., James, J. W., & Morris, C. A. (1972) · Annals of Human Genetics · doi:10.1111/j.1469-1809.1972.tb00767.x · Cited by 420 · see citing works

Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration

Revez, J. A., Lin, T., Qiao, Z., Xue, A., Holtz, Y., Zhu, Z., Zeng, J., Wang, H., Sidorenko, J., Kemper, K. E., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-15421-7 · Cited by 408 · see citing works

Psychiatric genetics and the structure of psychopathology

Smoller, J. W., Andreassen, O. A., Edenberg, H. J., Faraone, S. V., Glatt, S. J., & Kendler, K. S. (2019) · Molecular Psychiatry · doi:10.1038/s41380-017-0010-4 · Cited by 398 · see citing works

Signatures of negative selection in the genetic architecture of human complex traits

Zeng, J., de Vlaming, R., Wu, Y., Robinson, M. R., Lloyd-Jones, L. R., Yengo, L., Yap, C. X., Xue, A., Sidorenko, J., McRae, A. F., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0101-4 · Cited by 391 · see citing works

Genetic correlations of polygenic disease traits: from theory to practice

van Rheenen, W., Peyrot, W. J., Schork, A. J., Lee, S., & Wray, N. R. (2019) · Nature Reviews Genetics · doi:10.1038/s41576-019-0137-z · Cited by 385 · see citing works

Using Extended Genealogy to Estimate Components of Heritability for 23 Quantitative and Dichotomous Traits

Paşaniuc, B., & Zaitlen, N. (2013) · eScholarship (California Digital Library) · Cited by 362 · see citing works

Neonatal Vitamin D Status and Risk of Schizophrenia

McGrath, J. J., Eyles, D. W., Pedersen, C. B., Anderson, C., Ko, P., Burne, T. H. J., Nørgaard‐Pedersen, B., HOUGAARD, D. M., & Mortensen, P. B. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.110 · Cited by 360 · see citing works

Minimal phenotyping yields genome-wide association signals of low specificity for major depression

MDD Working Group of the Psychiatric Genomics Consortium, Cai, N., Revez, J. A., Adams, M. J., Andlauer, T. F. M., Breen, G., Byrne, E. M., Clarke, T.-K., Forstner, A. J., Grabe, H. J., et al. (2020) · Nature Genetics · doi:10.1038/s41588-020-0594-5 · Cited by 344 · see citing works

Transethnic Genetic-Correlation Estimates from Summary Statistics

Brown, B. C., Ye, C. J., Price, A. L., & Zaitlen, N. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2016.05.001 · Cited by 340 · see citing works

Non-Genetic Factors in Schizophrenia

Stilo, S. A., & Murray, R. M. (2019) · Current Psychiatry Reports · doi:10.1007/s11920-019-1091-3 · Cited by 322 · see citing works

Vitamin D supplementation during the first year of life and risk of schizophrenia: a Finnish birth cohort study

McGrath, J., Saari, K., Hakko, H., Jokelainen, J., Jones, P., Järvelin, M.-R., Chant, D., & Isohanni, M. (2004) · Schizophrenia Research · doi:10.1016/j.schres.2003.08.005 · Cited by 288 · see citing works

Family History of Schizophrenia and Bipolar Disorder as Risk Factors for Autism

Sullivan, P. F., Magnusson, C., Reichenberg, A., Boman, M., Dalman, C., Davidson, M., Fruchter, E., Hultman, C. M., Lundberg, M., Långström, N., et al. (2012) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2012.730 · Cited by 256 · see citing works

Severe Mental Disorders in Offspring With 2 Psychiatrically Ill Parents

Gottesman, I. I., Laursen, T. M., Bertelsen, A., & Mortensen, P. B. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.1 · Cited by 246 · see citing works

Stress and neurodevelopmental processes in the emergence of psychosis

Holtzman, C. W., Trotman, H. D., Goulding, S. M., Ryan, A. T., MacDonald, A. N., Shapiro, D. I., Brasfield, J. L., & Walker, E. F. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.12.017 · Cited by 242 · see citing works

Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits

Haplotype Reference Consortium, Evans, L. M., Tahmasbi, R., Vrieze, S. I., Abecasis, G. R., Das, S., Gazal, S., Bjelland, D. W., de Candia, T. R., Goddard, M. E., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0108-x · Cited by 239 · see citing works

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Maier, R., Moser, G., Chen, G., Ripke, S., Absher, D., Agartz, I., Akil, H., D, F. A. M., Andreassen, O. A., Anjorin, A., et al. (2015) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.12.006 · Cited by 227 · see citing works

Genome-wide characteristics of de novo mutations in autism

Yuen, R. K., Merico, D., Cao, H., Pellecchia, G., Alipanahi, B., Thiruvahindrapuram, B., Tong, X., Sun, Y., Cao, D., Zhang, T., et al. (2016) · npj Genomic Medicine · doi:10.1038/npjgenmed.2016.27 · Cited by 216 · see citing works

Patterns of nonrandom mating within and across 11 major psychiatric disorders

Nordsletten, A. E., Larsson, H., Crowley, J. J., Almqvist, C., Lichtenstein, P., & Mataix-Cols, D. (2016) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.3192 · Cited by 210 · see citing works

Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database

Li, J., Cai, T., Jiang, Y. W., Chen, H., He, X., Chen, C., Li, X., Shao, Q., Xia, R., Li, Z., et al. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.40 · Cited by 208 · see citing works

Using summary data from the Danish National Registers to estimate heritabilities for schizophrenia, bipolar disorder, and major depressive disorder

Wray, N. R. (2012) · Frontiers in Genetics · doi:10.3389/fgene.2012.00118 · Cited by 203 · see citing works

Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank

Coleman, J. R. I., Peyrot, W. J., Purves, K. L., Davis, K. A. S., Rayner, C., Choi, S. W., Hübel, C., Gaspar, H. A., Kan, C., der Auwera, S. V., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-019-0546-6 · Cited by 195 · see citing works

Psychiatric family history and schizophrenia risk in Denmark: which mental disorders are relevant?

Mortensen, P. B., Pedersen, M. G., & Pedersen, C. B. (2009) · Psychological Medicine · doi:10.1017/s0033291709990419 · Cited by 165 · see citing works

Meta-analytic Evidence for Familial Coaggregation of Schizophrenia and Bipolar Disorder

Snellenberg, J. X. V., & de Candia, T. R. (2009) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.64 · Cited by 159 · see citing works

Etiological overlap between obsessive‐compulsive disorder and anorexia nervosa: a longitudinal cohort, multigenerational family and twin study

Cederlöf, M., Thornton, L. M., Baker, J. H., Lichtenstein, P., Larsson, H., Rück, C., Bulik, C. M., & Mataix‐Cols, D. (2015) · World Psychiatry · doi:10.1002/wps.20251 · Cited by 148 · see citing works

De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia

GROUP Investigators, Rees, E., Han, J., Morgan, J., Carrera, N., Escott-Price, V., Pocklington, A. J., Duffield, M., Hall, L. S., Legge, S. E., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-019-0565-2 · Cited by 129 · see citing works

Power of the classical twin design revisited.

Visscher, P. (2004) · Twin research : the official journal of the International Society for Twin Studies · doi:10.1375/1369052042335250 · Cited by 111 · see citing works

The associations of earlier trauma exposures and history of mental disorders with PTSD after subsequent traumas

Collaborators, O. B. O. T. W. W. M. H. S., Kessler, R. C., Aguilar‐Gaxiola, S., Alonso, J., Bromet, E. J., Gureje, O., Karam, E. G., Koenen, K. C., Lee, S., Liu, H., et al. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.194 · Cited by 85 · see citing works

Power of the Classical Twin Design Revisited: II Detection of Common Environmental Variance

Visscher, P., Gordon, S., & Neale, M. (2008) · Twin Research and Human Genetics · doi:10.1375/twin.11.1.48 · Cited by 80 · see citing works

Impact of diagnostic misclassification on estimation of genetic correlations using genome-wide genotypes

Wray, N. R., Lee, S., & Kendler, K. S. (2012) · European Journal of Human Genetics · doi:10.1038/ejhg.2011.257 · Cited by 79 · see citing works

HERITABILITY OF POLYCHOTOMOUS CHARACTERS

Gianola, D. (1979) · Genetics · doi:10.1093/genetics/93.4.1051 · Cited by 73 · see citing works

Genetic Basis of Complex Genetic Disease: The Contribution of Disease Heterogeneity to Missing Heritability

Wray, N. R., & Maier, R. (2014) · Current Epidemiology Reports · doi:10.1007/s40471-014-0023-3 · Cited by 67 · see citing works

Genetics of Anorexia Nervosa

Baker, J. H., Schaumberg, K., & Munn‐Chernoff, M. A. (2017) · Current Psychiatry Reports · doi:10.1007/s11920-017-0842-2 · Cited by 63 · see citing works

Age at onset and life table risks in genetic counselling for Huntington's disease.

Harper, P. S., & Newcombe, R. G. (1992) · Journal of Medical Genetics · doi:10.1136/jmg.29.4.239 · Cited by 44 · see citing works

Disease and Polygenic Architecture: Avoid Trio Design and Appropriately Account for Unscreened Control Subjects for Common Disease

Peyrot, W. J., Boomsma, D. I., Penninx, B. W. J. H., & Wray, N. R. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2015.12.017 · Cited by 42 · see citing works

Misestimation of heritability and prediction accuracy of male-pattern baldness

Yap, C. X., Sidorenko, J., Marioni, R. E., Yengo, L., Wray, N. R., & Visscher, P. M. (2018) · Nature Communications · doi:10.1038/s41467-018-04807-3 · Cited by 21 · see citing works

Eugen Bleuler’s Views on the Genetics of Schizophrenia in 1917

Kendler, K. S. (2019) · Schizophrenia Bulletin · doi:10.1093/schbul/sbz131 · Cited by 15 · see citing works

Assumptions and Properties of Limiting Pathway Models for Analysis of Epistasis in Complex Traits

Stringer, S., Derks, E. M., Kahn, R. S., Hill, W. G., & Wray, N. R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068913 · Cited by 13 · see citing works

Evaluating the Impact of Nonrandom Mating: Psychiatric Outcomes Among the Offspring of Pairs Diagnosed With Schizophrenia and Bipolar Disorder

Nordsletten, A. E., Brander, G., Larsson, H., Lichtenstein, P., Crowley, J. J., Sullivan, P. F., Wray, N. R., & Mataix‐Cols, D. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.06.025 · Cited by 12 · see citing works

Bayesian analysis of GWAS summary data reveals differential signatures of natural selection across human complex traits and functional genomic categoriesPreprint

Zeng, J., Xue, A., Jiang, L., Lloyd‐Jones, L. R., Wu, Y., Wang, H., Zheng, Z., Yengo, L., Kemper, K. E., Goddard, M. E., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/752527 · Cited by 7 · see citing works

Major depression, minor depression, and double depression: are they distinct clinical entities?

Remick, R. A., Sadovnick, A. D., Lam, R. W., Zis, A. P., & Yee, I. M. L. (1996) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19960726)67:4

From Basic Science to Clinical Application of Polygenic Risk Scores: A Primer

Wray, N. R., Lin, T., Austin, J., McGrath, J. J., Hickie, I. B., Murray, G. K., & Visscher, P. M. (2021) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2020.3049 · Cited by 367 · see citing works

Epigenetic regulation in major depression and other stress-related disorders: molecular mechanisms, clinical relevance and therapeutic potential

Yuan, M., Yang, B., Rothschild, G., Mann, J. J., Sanford, L. D., Tang, X., Huang, C., Wang, C., & Zhang, W. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01519-z · Cited by 246 · see citing works

Genetic heterogeneity and subtypes of major depression

Nguyen, T.-D., Harder, A., Xiong, Y., Kowalec, K., Hägg, S., Cai, N., Kuja-Halkola, R., Dalman, C., Sullivan, P. F., & Lu, Y. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01413-6 · Cited by 129 · see citing works

Genetic influences on neurodevelopmental disorders and their overlap with co-occurring conditions in childhood and adolescence: A meta-analysis

Gidziela, A., Ahmadzadeh, Y. I., Michelini, G., Allegrini, A. G., Agnew-Blais, J., Lau, L. Y., Duret, M., Procopio, F., Daly, E., Ronald, A., et al. (2022) · doi:10.1101/2022.02.17.22271089 · Cited by 2 · see citing works

Genetic architecture of Environmental Sensitivity reflects multiple heritable components: a twin study with adolescents

Assary, E., Zavos, H. M. S., Krapohl, E. M. L., Keers, R., & Pluess, M. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0783-8 · Cited by 141 · see citing works

Psychiatric Genetics: Methods, Findings and Ethical IssuesPreprint

Kendler, K. S. (2008) · Nature Precedings · doi:10.1038/npre.2008.2623.1 · Cited by 1 · see citing works

Psychiatric Genetics: Methods, Findings and Ethical IssuesPreprint

Kendler, K. S., & Kendler, K. S. (2008) · Nature Precedings · doi:10.1038/npre.2008.2623

Twin studies: A unique epidemiological tool

Sahu, M., & Prasuna, J. G. (2016) · Indian Journal of Community Medicine · doi:10.4103/0970-0218.183593 · Cited by 95 · see citing works

Theoretical underpinning for the use of twin studies in life course epidemiology

Loos, R. J. F., Ridgway, C. L., & Ong, K. K. (2009) · Family matters · doi:10.1093/acprof:oso/9780199231034.003.0004 · Cited by 5 · see citing works