The DOI matches its Crossref record; 91 of the 91 references it cites were found in a registry or an index.
The heritability of human disease: estimation, uses and abuses.
Abstract
Relatives provide the basic material for the study of inheritance of human disease. However, the methodologies for the estimation of heritability and the interpretation of the results have been controversial. The debate arises from the plethora of methods used, the validity of the methodological assumptions and the inconsistent and sometimes erroneous genetic interpretations made. We will discuss how to estimate disease heritability, how to interpret it, how biases in heritability estimates arise and how heritability relates to other measures of familial disease aggregation.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“In addition to providing exceptional statistical power, the study directly addresses the concern of lack of replication in research findings 31,32 replicating results across 5 countries and health systems.”
From Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort (2019) · cites this paper as [32]
Citations
Cites
A new look at the statistical model identification
Akaike, H. (1974) · IEEE Transactions on Automatic Control · doi:10.1109/tac.1974.1100705 · Cited by 51,879
Introduction to Quantitative Genetics.
Edwards, A. W. F., & Falconer, D. S. (1982) · Biometrics · doi:10.2307/2529912 · Cited by 21,447
Finding the missing heritability of complex diseases
Manolio, T. A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., Hunter, D. J., McCarthy, M. I., Ramos, E. M., Cardon, L. R., Chakravarti, A., et al. (2009) · Nature · doi:10.1038/nature08494 · Cited by 8,336
Nelder, J. A., & Wedderburn, R. W. M. (1972) · Journal of the Royal Statistical Society Series A (General) · doi:10.2307/2344614 · Cited by 7,703
Genetics and Analysis of Quantitative Traits
(2002) · Journal of Animal Breeding and Genetics · doi:10.1046/j.1439-0388.2002.00356.x · Cited by 6,176
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
The International Schizophrenia Consortium (2009) · Nature · doi:10.1038/nature08185 · Cited by 4,821
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
Lichtenstein, P., Holm, N. V., Verkasalo, P. K., Iliadou, A., Kaprio, J., Koskenvuo, M., Pukkala, E., Skytthe, A., & Hemminki, K. (2000) · New England Journal of Medicine · doi:10.1056/nejm200007133430201 · Cited by 4,114
Recovery of Inter-Block Information when Block Sizes are Unequal
Patterson, H. D., & Thompson, R. (1971) · Biometrika · doi:10.1093/biomet/58.3.545 · Cited by 4,073
Methodology for Genetic Studies of Twins and Families
Neale, M. C., & Cardon, L. R. (1992) · doi:10.1007/978-94-015-8018-2 · Cited by 4,005
Research works printed but not linked: 1
- Trimble, B. K. An Empirical Simulation of Quasi-Continuous Inheritance Using Human Birthweight Data. Thesis, McGill Univ. (1971).
Cited by
Sorted by citations
Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort
Bai, D., Yip, B. H. K., Windham, G. C., Sourander, A., Francis, R., Yoffe, R., Glasson, E., Mahjani, B., Suominen, A., Leonard, H., et al. (2019) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2019.1411 · Cited by 683
Pitfalls of predicting complex traits from SNPs
Wray, N. R., Yang, J., Hayes, B. J., Price, A. L., Goddard, M. E., & Visscher, P. M. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3457 · Cited by 690
Research Review: Polygenic methods and their application to psychiatric traits
Wray, N. R., Lee, S., Mehta, D., Vinkhuyzen, A. A. E., Dudbridge, F., & Middeldorp, C. M. (2014) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12295 · Cited by 683
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
Genetic architecture: the shape of the genetic contribution to human traits and disease
Timpson, N. J., Greenwood, C. M. T., Soranzo, N., Lawson, D. J., & Richards, J. B. (2018) · Nature Reviews Genetics · doi:10.1038/nrg.2017.101 · Cited by 434
Using genetic data to strengthen causal inference in observational research
Pingault, J.-B., O’Reilly, P. F., Schoeler, T., Ploubidis, G. B., Rijsdijk, F., & Dudbridge, F. (2018) · Nature Reviews Genetics · doi:10.1038/s41576-018-0020-3 · Cited by 444
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 402
Melzer, D. R., Pilling, L. C., & Ferrucci, L. (2019) · Nature Reviews Genetics · doi:10.1038/s41576-019-0183-6 · Cited by 387
Kuo, C., Grainge, M. J., Valdes, A. M., See, L., Luo, S., Yu, K., Zhang, W., & Doherty, M. (2015) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2015.3528 · Cited by 314
Dixon, L. E., Greenwood, J. R., Bencivenga, S., Zhang, P., Cockram, J., Mellers, G., Ramm, K., Cavanagh, C. R., Swain, S. M., & Boden, S. A. (2018) · The Plant Cell · doi:10.1105/tpc.17.00961 · Cited by 254
Quantitative analysis of population-scale family trees with millions of relatives
Kaplanis, J., Gordon, A., Shor, T., Weissbrod, O., Geiger, D., Wahl, M., Gershovits, M., Markus, B., Sheikh, M., Gymrek, M., et al. (2018) · Science · doi:10.1126/science.aam9309 · Cited by 245
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
The road to precision psychiatry: translating genetics into disease mechanisms
Gandal, M. J., Leppa, V., Won, H., Parikshak, N. N., & Geschwind, D. H. (2016) · Nature Neuroscience · doi:10.1038/nn.4409 · Cited by 223
Missing heritability of complex diseases: case solved?
Génin, E. (2019) · Human Genetics · doi:10.1007/s00439-019-02034-4 · Cited by 219
Delay discounting of different outcomes: Review and theory
Odum, A. L., Becker, R. J., Haynes, J. M., Galizio, A., Frye, C. C. J., Downey, H., Friedel, J. E., & Pérez, D. M. (2020) · Journal of the Experimental Analysis of Behavior · doi:10.1002/jeab.589 · Cited by 207
Sauce, B., & Matzel, L. D. (2017) · Psychological Bulletin · doi:10.1037/bul0000131 · Cited by 185
Estimation and Partition of Heritability in Human Populations Using Whole-Genome Analysis Methods
Vinkhuyzen, A. A. E., Wray, N. R., Yang, J., Goddard, M. E., & Visscher, P. M. (2013) · Annual Review of Genetics · doi:10.1146/annurev-genet-111212-133258 · Cited by 173
The contribution of genetic variants to disease depends on the ruler
Witte, J. S., Visscher, P. M., & Wray, N. R. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3786 · Cited by 163
Assessing the Heritability of Complex Traits in Humans: Methodological Challenges and Opportunities
Mayhew, A., & Meyre, D. (2017) · Current Genomics · doi:10.2174/1389202918666170307161450 · Cited by 169
Bennett, B. J., Davis, R. C., Civelek, M., Orozco, L. D., Wu, J., Qi, H., Pan, C., Packard, R. R. S., Eskin, E., Yan, M., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005711 · Cited by 138
Spritz, R. A., & Santorico, S. A. (2020) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2020.06.004 · Cited by 135
Fernandez-Pujals, A. M., Adams, M. J., Thomson, P. A., McKechanie, A. G., Blackwood, D., Smith, B. H., Dominiczak, A. F., Morris, A. D., Matthews, K., Campbell, A., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0142197 · Cited by 132
Marenholz, I., Grosche, S., Kalb, B., Rüschendorf, F., Blümchen, K., Schlags, R., Harandi, N., Price, M., Hansen, G., Seidenberg, J., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01220-0 · Cited by 121
Disease Heritability Inferred from Familial Relationships Reported in Medical Records
Polubriaginof, F. C. G., Vanguri, R., Quinnies, K. M., Belbin, G. M., Yahi, A., Salmasian, H., Lorberbaum, T., Nwankwo, V., Li, L., Shervey, M. M., et al. (2018) · Cell · doi:10.1016/j.cell.2018.04.032 · Cited by 106
Muñoz, M., Pong‐Wong, R., Canela‐Xandri, O., Rawlik, K., Haley, C., & Tenesa, A. (2016) · Nature Genetics · doi:10.1038/ng.3618 · Cited by 106
Genetic and molecular architecture of complex traits
Lappalainen, T., Li, Y., Ramachandran, S., & Gusev, A. (2024) · Cell · doi:10.1016/j.cell.2024.01.023 · Cited by 125
What Is the Heritability of Periodontitis? A Systematic Review
Nibali, L., Bayliss-Chapman, J., Almofareh, S. A., Zhou, Y., Divaris, K., & Vieira, A. R. (2019) · Journal of Dental Research · doi:10.1177/0022034519842510 · Cited by 103
Low-copper diet as a preventive strategy for Alzheimer's disease
Squitti, R., Siotto, M., & Polimanti, R. A. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.02.031 · Cited by 101
Inference 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 100
Polygenic Risk for Externalizing Disorders
Salvatore, J. E., Alıev, F., Bucholz, K. K., Arpana Agrawal, A., HESSELBROCK, V. M., Hesselbrock, M. N., Bauer, L. O., Kuperman, S., Schuckit, M. A., Kramer, J., et al. (2014) · Clinical Psychological Science · doi:10.1177/2167702614534211 · Cited by 104
Statistical methods for SNP heritability estimation and partition: A review
Zhu, H., & Zhou, X. (2020) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2020.06.011 · Cited by 103
Cultural evolution of genetic heritability
Uchiyama, R., Spicer, R., & Muthukrishna, M. (2021) · Behavioral and Brain Sciences · doi:10.1017/s0140525x21000893 · Cited by 103
Familial aggregation and heritability of sarcoidosis: a Swedish nested case−control study
Rossides, M., Grünewald, J., Eklúnd, A., Kullberg, S., Giuseppe, D. D., Askling, J., & Arkema, E. V. (2018) · European Respiratory Journal · doi:10.1183/13993003.00385-2018 · Cited by 90
Periodontal health and disease: The contribution of genetics
Shaddox, L. M., Morford, L. A., & Nibali, L. (2020) · Periodontology 2000 · doi:10.1111/prd.12357 · Cited by 85
Computational approaches for prioritizing candidate disease genes based on PPI networks
Lan, W., Wang, J., Li, M., Peng, W., & Wu, F. (2015) · Tsinghua Science & Technology · doi:10.1109/tst.2015.7297749 · Cited by 84
Variations of cingulate sulcal organization and link with cognitive performance
Amiez, C., Wilson, C. R. E., & Procyk, E. (2018) · Scientific Reports · doi:10.1038/s41598-018-32088-9 · Cited by 87
Sexual dimorphisms in genetic loci linked to body fat distribution
Pulit, S. L., Karaderi, T., & Lindgren, C. M. (2017) · Bioscience Reports · doi:10.1042/bsr20160184 · Cited by 82
A Swedish Nationwide Adoption Study of the Heritability of Heart Failure
Lindgren, M. P., Pirouzifard, M., Smith, J. G., Sundquist, J., Sundquist, K., & Zöller, B. (2018) · JAMA Cardiology · doi:10.1001/jamacardio.2018.1919 · Cited by 69
The genetic architecture of vitiligo
Roberts, G. H. L., Santorico, S. A., & Spritz, R. A. (2019) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12848 · Cited by 76
Bossini‐Castillo, L., López‐Isac, E., & Martin, J. J. (2015) · Journal of Autoimmunity · doi:10.1016/j.jaut.2015.07.005 · Cited by 74
On the power of epigenome-wide association studies using a disease-discordant twin design
Li, W., Christiansen, L., Hjelmborg, J., Baumbach, J., & Tan, Q. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty532 · Cited by 74
Xia, C., Amador, C., Huffman, J. E., Trochet, H., Campbell, A., Porteous, D. J., Scotland, G., Hastie, N. D., Hayward, C., Vitart, V., et al. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1005804 · Cited by 69
Multidimensional heritability analysis of neuroanatomical shape
Ge, T., Reuter, M., Winkler, A. M., Holmes, A. J., Lee, P. H., Tirrell, L. S., Roffman, J. L., Buckner, R. L., Smoller, J. W., & Sabuncu, M. R. (2016) · Nature Communications · doi:10.1038/ncomms13291 · Cited by 76
The familial risk of autism spectrum disorder with and without intellectual disability
Xie, S., Karlsson, H., Dalman, C., Widman, L., Rai, D., Gardner, R. M., Magnusson, C., Sandin, S., Tabb, L. P., Newschaffer, C. J., et al. (2020) · Autism Research · doi:10.1002/aur.2417 · Cited by 64
Wray, N. R., & Maier, R. (2014) · Current Epidemiology Reports · doi:10.1007/s40471-014-0023-3 · Cited by 67
Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study
Chen, F., Childs, E. J., Mocci, E., Bracci, P. M., Gallinger, S., Li, D., Neale, R. Ε., Olson, S. H., Scélo, G., Bamlet, W. R., et al. (2019) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-18-1235 · Cited by 70
Debes, P. V., Gross, R., & Vasemägi, A. (2017) · The American Naturalist · doi:10.1086/692536 · Cited by 59
Heritability of glaucoma and glaucoma-related endophenotypes: Systematic review and meta-analysis
Asefa, N. G., Neustaeter, A., Jansonius, N. M., & Snieder, H. (2019) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2019.06.002 · Cited by 57
Direct-to-Consumer Nutrigenetics Testing: An Overview
Floris, M., Cano, A., Porru, L., Addis, R., Cambedda, A., Idda, M. L., Steri, M., Ventura, C., & Maioli, M. (2020) · Nutrients · doi:10.3390/nu12020566 · Cited by 62
Chen, X., Kuja‐Halkola, R., Rahman, I., Arpegård, J., Viktorin, A., Karlsson, R., Hägg, S., Svensson, P., Pedersen, N. L., & Magnusson, P. K. E. (2015) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2015.10.004 · Cited by 57
Schizophrenia as a pseudogenetic disease: A call for more gene-environmental studies
Torrey, E. F., & Yolken, R. H. (2019) · Psychiatry Research · doi:10.1016/j.psychres.2019.06.006 · Cited by 56
Assumption-free estimation of the genetic contribution to refractive error across childhood.
Guggenheim, J. A., Pourcain, B. S., McMahon, G., Timpson, N. J., Evans, D. M., & Williams, C. (2015) · PubMed Central · Cited by 52
Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics
Holland, D., Wang, Y., Thompson, W. K., Schork, A. J., Chen, C., Lo, M., Witoelar, A., Werge, T. M., O’Donovan, M. C., Andreassen, O. A., et al. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00015 · Cited by 49
Glaucoma Heritability: Molecular Mechanisms of Disease
Zukerman, R. J., Harris, A., Oddone, F., Siesky, B. A., Vercellin, A. C. V., & Ciulla, T. A. (2021) · Genes · doi:10.3390/genes12081135 · Cited by 50
Wu, W., Witherspoon, D. J., Fraser, A., Clark, E., Rogers, A. R., Stoddard, G. J., Manuck, T. A., Chen, K., Esplin, M. S., Smith, K. R., et al. (2015) · Human Genetics · doi:10.1007/s00439-015-1558-1 · Cited by 50
What does heritability of Alzheimer’s disease represent?
Baker, E. A., Leonenko, G., Schmidt, K. M., Hill, M., Myers, A., Shoai, M., de Rojas, I., Tesi, N., Holstege, H. H., van der Flier, W. M., et al. (2023) · PLoS ONE · doi:10.1371/journal.pone.0281440 · Cited by 55
Howe, L. J., Tudball, M., Davey Smith, G., & Davies, N. M. (2022) · International Journal of Epidemiology · doi:10.1093/ije/dyab208 · Cited by 48
An Evolutionary Genetic Perspective of Eating Disorders
Mayhew, A., Pigeyre, M., Couturier, J. L., & Meyre, D. (2017) · Neuroendocrinology · doi:10.1159/000484525 · Cited by 53
Genome-Wide Polygenic Score and the Risk of Ischemic Stroke in a Prospective Cohort
Hachiya, T., Hata, J., Hirakawa, Y., Yoshida, D., Furuta, Y., Kitazono, T., Shimizu, A., & Ninomiya, T. (2020) · Stroke · doi:10.1161/strokeaha.119.027520 · Cited by 44
Genetically transitional disease: a new concept in genomic medicine
Yao, Q., Gorevic, P. D., Shen, B., & Gibson, G. C. (2022) · Trends in Genetics · doi:10.1016/j.tig.2022.11.002 · Cited by 44
Endocrinology Meets Metabolomics: Achievements, Pitfalls, and Challenges
Tokarz, J., Haid, M., Cecil, A., Prehn, C. P., Artati, A., Möller, G., & Adamski, J. (2017) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2017.07.001 · Cited by 44
A review of SNP heritability estimation methods
Tang, M., Wang, T., & Zhang, X. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbac067 · Cited by 46
Tang, N. L. S., Dobbs, M. B., Gurnett, C. A., Qiu, Y., Lam, T. P., Cheng, J. C. Y., & Hadley-Miller, N. A. (2021) · Genes · doi:10.3390/genes12071033 · Cited by 41
Estimation of kinship coefficient in structured and admixed populations using sparse sequencing data
Dou, J., Sun, B., Sim, X., Hughes, J. D., Reilly, D. F., Tai, E. S., Liu, J., & Wang, C. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1007021 · Cited by 39
Sauce, B., Bendrath, S. C., Herzfeld, M., Siegel, D., Style, C., Rab, S., Korabelnikov, J., & Matzel, L. D. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2017.0289 · Cited by 43
Zeng, Y., Navarro, P., Xia, C., Amador, C., Fernandez-Pujals, A. M., Thomson, P. A., Campbell, A., Nagy, R., Clarke, T., Hafferty, J. D., et al. (2016) · EBioMedicine · doi:10.1016/j.ebiom.2016.11.003 · Cited by 35
Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder
Mahjani, B., Klei, L., Hultman, C. M., Larsson, H., Devlin, B., Buxbaum, J. D., Sandin, S., & Grice, D. E. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.01.006 · Cited by 36
Heritability of Sleep EEG Topography in Adolescence: Results from a Longitudinal Twin Study
Markovic, A., Achermann, P., Rusterholz, T., & Tarokh, L. (2018) · Scientific Reports · doi:10.1038/s41598-018-25590-7 · Cited by 37
Family-Based Association Analysis of Alcohol Dependence Criteria and Severity
Wetherill, L. F., Kapoor, M., Arpana Agrawal, A., Bucholz, K. K., Koller, D. L., Bertelsen, S. E., Le, N., Wang, J., Almasy, L. A., HESSELBROCK, V. M., et al. (2013) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.12251 · Cited by 33
A Twin Study Examining Rumination as a Transdiagnostic Correlate of Psychopathology
Johnson, D. P., Rhee, S. H., Friedman, N. P., Corley, R. P., Munn‐Chernoff, M. A., Hewitt, J. K., & Whisman, M. A. (2016) · Clinical Psychological Science · doi:10.1177/2167702616638825 · Cited by 43
Individual differences: Case studies of rodent and primate intelligence.
Matzel, L. D., & Sauce, B. (2017) · Journal of Experimental Psychology Animal Learning and Cognition · doi:10.1037/xan0000152 · Cited by 37
Familial risk and heritability of intellectual disability: a population‐based cohort study in Sweden
Lichtenstein, P., Tideman, M., Sullivan, P. F., Serlachius, E., Larsson, H., Kuja‐Halkola, R., & Butwicka, A. (2021) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.13560 · Cited by 37
Genetic and environmental influences on rumination and its covariation with depression
Johnson, D. P., Whisman, M. A., Corley, R. P., Hewitt, J. K., & Friedman, N. P. (2014) · Cognition & Emotion · doi:10.1080/02699931.2014.881325 · Cited by 32
Heritability Estimation Approaches Utilizing Genome‐Wide Data
Srivastava, A. K., Williams, S. M., & Zhang, G. (2023) · Current Protocols · doi:10.1002/cpz1.734 · Cited by 37
Haljas, K., Amare, A. T., Alizadeh, B. Z., Hsu, Y., Mosley, T. H., Newman, A. B., Murabito, J. M., Tiemeier, H. W., Tanaka, T., van Duijn, C. M., et al. (2017) · Psychosomatic Medicine · doi:10.1097/psy.0000000000000555 · Cited by 30
GenoMatrix: A Software Package for Pedigree-Based and Genomic Prediction Analyses on Complex Traits
Nazarian, A., & Gezan, S. A. (2016) · Journal of Heredity · doi:10.1093/jhered/esw020 · Cited by 33
Heritability of Choroidal Thickness in the Amish
Sardell, R. J., Nittala, M. G., Adams, L. D., Laux, R. A., Bailey, J. N. C., Fuzzell, D., Fuzzell, S. L., Reinhart‐Mercer, L., Caywood, L. J., Horst, V., et al. (2016) · Ophthalmology · doi:10.1016/j.ophtha.2016.09.001 · Cited by 30
Familiality and SNP heritability of age at onset and episodicity in major depressive disorder
Ferentinos, P. P., Koukounari, A., Power, R. A., Rivera, M., Uher, R., Craddock, N. J., Owen, M. J., Korszun, A., Jones, L. A., Jones, I. R., et al. (2015) · Psychological Medicine · doi:10.1017/s0033291715000215 · Cited by 29
Deep genotype imputation captures virtually all heritability of autoimmune vitiligo
Roberts, G. H. L., Santorico, S. A., & Spritz, R. A. (2020) · Human Molecular Genetics · doi:10.1093/hmg/ddaa005 · Cited by 32
Genetic and environmental contributions to psychological resilience and coping
Navrady, L. B., Zeng, Y., Clarke, T., Adams, M. J., Howard, D. M., Deary, I. J., & McIntosh, A. M. (2018) · Wellcome Open Research · doi:10.12688/wellcomeopenres.13854.1 · Cited by 28
Testing the validity of value‐added measures of educational progress with genetic data
Morris, T., Davies, N. M., Dorling, D., Richmond, R. C., & Smith, G. D. (2018) · British Educational Research Journal · doi:10.1002/berj.3466 · Cited by 29
Narrow-sense heritability estimation of complex traits using identity-by-descent information
Evans, L. M., Tahmasbi, R., Jones, M., Vrieze, S. I., Abecasis, G. R., Das, S., Bjelland, D. W., de Candia, T. R., Abecasis, G., Altshuler, D., et al. (2018) · Heredity · doi:10.1038/s41437-018-0067-0 · Cited by 29
Did the human genome project affect research on Schizophrenia?
Torrey, Ε. F. (2023) · Psychiatry Research · doi:10.1016/j.psychres.2023.115691 · Cited by 32
Heritability of periodontal bone loss in mice
Hiyari, S., Atti, E., Camargo, P. M., Eskin, E., Lusis, A. J., Tetradis, S., & Pirih, F. Q. M. (2015) · Journal of Periodontal Research · doi:10.1111/jre.12258 · Cited by 28
Familiality of Psychotic Disorders: A Polynosologic Study in Multiplex Families
Peralta, V., Goldberg, X., Ribeiro, M., Sánchez-Torres, A. M., Fañanás, L., & Cuesta, M. J. (2015) · Schizophrenia Bulletin · doi:10.1093/schbul/sbv192 · Cited by 28
A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR
Safarova, M. S., Satterfield, B. A., Fan, X., Austin, E. E., Ye, Z., Bastarache, L. A., Zheng, N. S., Ritchie, M. D., Borthwick, K. M., Williams, M. S., et al. (2019) · npj Genomic Medicine · doi:10.1038/s41525-019-0078-7 · Cited by 29
The Role and Sources of Individual Differences in Critical-Analytic Thinking: a Capsule Overview
Bolger, D. J., Mackey, A. P., Wang, M., & Grigorenko, E. L. (2014) · Educational Psychology Review · doi:10.1007/s10648-014-9279-x · Cited by 30
Hiyari, S., Green, E. B., Pan, C., Lari, S., Davar, M., Davis, R. C., Camargo, P. M., Tetradis, S., Lusis, A. J., & Pirih, F. Q. M. (2018) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3440 · Cited by 28
State, M. W., & Thapar, A. (2015) · Wiley eBooks · doi:10.1002/9781118381953.ch24 · Cited by 27
Peripheral Blood-Based Gene Expression Studies in Schizophrenia: A Systematic Review
Wagh, V. V., Vyas, P., Agrawal, S., Pachpor, T. A., Paralikar, V. P., & Khare, S. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.736483 · Cited by 25
A systematic heritability analysis of the human whole blood transcriptome
Huan, T., Liu, C., Joehanes, R., Zhang, X., Chen, B. H., Johnson, A. D., Yao, C., Courchesne, P. L., O’Donnell, C. J., Munson, P. J., et al. (2015) · Human Genetics · doi:10.1007/s00439-014-1524-3 · Cited by 26
Inequality in genetic cancer risk suggests bad genes rather than bad luck
Stensrud, M. J., & Valberg, M. (2017) · Nature Communications · doi:10.1038/s41467-017-01284-y · Cited by 23
The goldmine of GWAS summary statistics: a systematic review of methods and tools
Kontou, P. I., & Bagos, P. G. (2024) · BioData Mining · doi:10.1186/s13040-024-00385-x · Cited by 23
Gorlov, I. P., Gorlova, O. Y., & Amos, C. I. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005371 · Cited by 21
Fundamentals of Complex Trait Genetics and Association Studies
Alghamdi, J., & Padmanabhan, S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-386882-4.00012-8 · Cited by 24
Population phenomena inflate genetic associations of complex social traits
Morris, T. T., Davies, N. M., Hemani, G., & Smith, G. D. (2020) · Science Advances · doi:10.1126/sciadv.aay0328 · Cited by 20
Peralta, V., Fañanás, L., Reyes, M. M., & Cuesta, M. J. (2017) · Schizophrenia Research · doi:10.1016/j.schres.2017.09.013 · Cited by 20
Xhaard, C., Dandine‐Roulland, C., de Villemereuil, P., Floch, É. L., Bacq‐Daian, D., Machu, J., Ferreira, J. P., Deleuze, J., Zannad, F. M., Rossignol, P., et al. (2019) · European Journal of Preventive Cardiology · doi:10.1177/2047487319890763 · Cited by 20
Revisiting heritability accounting for shared environmental effects and maternal inheritance
Liu, C., Dupuis, J., Larson, M. G., Cupples, L. A., Ordovás, J. M., Vasan, R. S., Meigs, J. B., Jacques, P. F., & Levy, D. A. (2014) · Human Genetics · doi:10.1007/s00439-014-1505-6 · Cited by 21
Genetic Influence on Accessory Navicular Bone in the Foot: A Korean Twin and Family Study
Cheong, I. Y., Kang, H. J., Ko, H., Sung, J., Song, Y., & Hwang, J. H. (2017) · Twin Research and Human Genetics · doi:10.1017/thg.2017.21 · Cited by 19
Metadata
- Authors
- Tenesa, A., & Haley, C. S.
- Affiliations
- Roslin Institute (GB)
- Corresponding author
- Tenesa, Albert
- Venue
- Nature Reviews Genetics
- Published
- 2013-01-18
- Volume
- 14
- Issue
- 2
- Pages
- 139-149
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W2040924786
- Cited by
- 283
- References
- 90
- Citations by year
- 2026: 10 · 2025: 13 · 2024: 13 · 2023: 15 · 2022: 20 · 2021: 24 · 2020: 22 · 2019: 30 · 2018: 35 · 2017: 20 · 2016: 23 · 2015: 27 · 2014: 22 · 2013: 9
- FWCI
- 3.27
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Cancer Research UK (C12229/A13154, 13154)
- Medical Research Council
- Biotechnology and Biological Sciences Research Council (BBS/E/D/20211553, BB/K000195/1)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and phenotypic traits in livestock
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- heritability, human disease, heritability estimation, genetic and environmental contributions, phenotypic variance, familial aggregation, relatives
- MeSH terms
- Disease, Environment, Female, Humans, Male, Models, Genetic, Pedigree, Models, Statistical, Bias, Linear Models, Twin Studies as Topic, Genetic Predisposition to Disease, Genetic Association Studies
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