Telomere length (TL) has been associated with aging and mortality, but individual differences are also influenced by genetic factors, with previous studies reporting heritability estimates ranging from 34 to 82%. Here we investigate the heritability, mode of inheritance and the influence of parental age at birth on TL in six large, independent cohort studies with a total of 19 713 participants. The meta-analysis estimate of TL heritability was 0.70 (95% CI 0.64–0.76) and is based on a pattern of results that is highly similar for twins and other family members. We observed a stronger mother–offspring (r=0.42; P-value=3.60 × 10−61) than father–offspring correlation (r=0.33; P-value=7.01 × 10−5), and a significant positive association with paternal age at offspring birth (β=0.005; P-value=7.01 × 10−5). Interestingly, a significant and quite substantial correlation in TL between spouses (r=0.25; P-value=2.82 × 10−30) was seen, which appeared stronger in older spouse pairs (mean age ≥55 years; r=0.31; P-value=4.27 × 10−23) than in younger pairs (mean age<55 years; r=0.20; P-value=3.24 × 10−10). In summary, we find a high and very consistent heritability estimate for TL, evidence for a maternal inheritance component and a positive association with paternal age.


Telomeres are specialized DNA structures located at the terminal ends of chromosomes.1 Their primary function is to maintain genomic stability. Because of the inability of DNA polymerase to fully replicate the 3′ end of the DNA strand, that is, the ‘end-replication problem’, telomeres naturally shorten with each cell division and, therefore, with age.2, 3, 4 In epidemiological studies, both of cross-sectional and prospective design, decreased telomere length (TL) in leukocytes was associated with increased mortality,5, 6, 7, 8 although this finding was not consistent.9, 10 Increased TL in leukocytes has been associated with longevity in a comparison of long-lived Ashkenazi Jews and their offspring with younger controls.11 Genetic association studies have revealed associations between single-nucleotide polymorphisms (SNPs) in the TERC and TERT genes and TL.11, 12, 13, 14, 15, 16, 17 Other studies reported associations between SNPs in TERC and POT1 with human longevity,11, 17, 18 suggesting that genes regulating TL may influence human longevity.

That genetic variants would be found associated with TL was expected from earlier twin and family studies indicating genetic influence on TL. An early study in twins of different ages showed a heritability of 78% for TL in 4-, 17- and 44-year-old individuals,4 with no evidence for genotype × age interaction in this age range. In older twins (N=287 pairs aged 73 to 95 years) estimates for heritability were 34% in women, whereas for the smaller male sample the heritability was lower.19 In a sample of 55 female monozygotic (MZ) and 1025 dizygotic (DZ) middle-aged twin pairs, Andrew et al20 reported a heritability estimate of 36% and an unexpectedly large shared familial effect of 49%. Another study comprising 258 sib-pairs returned a heritability estimate of 82%.21 There is a need to reconcile these divergent estimates, which might in part be caused by differences in sample composition or TL assessments.22 A remaining question that also needs to be addressed is the extent to which estimates of heritability based on twin data are comparable to those based on other relatives such as parents and offspring from multigenerational studies or non-twin sibling pairs.

Several studies have been conducted to assess the potential mechanisms for telomere inheritance. An early study suggested that TL was maternally inherited via an X-linked mechanism.23 However, an increasing number of larger studies have reported stronger father–offspring than mother–offspring correlations for TL, suggesting that inheritance of this trait is mainly paternally determined.8, 24, 25, 26 In addition to a paternal pattern of inheritance, a positive correlation between offspring TL and paternal age at birth has been observed.24, 27, 28 Unlike somatic cells, sperm cell TL has been shown to increase with the age of the donor24, 29 because of the presence of active telomerase, suggesting that offspring of older fathers would inherit longer telomeres.

In the current study, we investigated the heritability, mode of inheritance and influence of parental age at birth on TL in six large, independent cohort studies with a total of 19 713 participants.

Materials and methods


The Erasmus Rucphen Family (ERF) study is a cross-sectional cohort including more than 3000 living descendants of 22 couples who had at least 6 children baptized in the community church between 1850 and 1900. The participants were not selected on the basis of any disease or other outcome. Details about the genealogy of the population have been previously described.30, 31 The study protocol was approved by the medical ethics board of the Erasmus MC Rotterdam, the Netherlands.

The GRAPHIC study comprises individuals from 520 white Caucasian nuclear families recruited from the general population in Leicestershire, UK, between 2003 and 2005, for the purpose of investigating the genetic determinants of blood pressure and related cardiovascular traits. Inclusion criteria were that both parents (aged 40–60 years) and two offspring ≥18 years were willing to participate. Further details are provided elsewhere.32

For the Leiden Longevity Study (LLS), long-lived siblings of Dutch descent were recruited together with their offspring and the partners of the offspring. Families were included if at least two long-lived siblings were alive and fulfilled the age criterion of ≥89 years for males and ≥91 years for females, representing <0.5% of the Dutch population in 2001.33 In total, 944 long-lived proband siblings were included with a mean age of 94 years (range, 89–104), 1671 offspring (61 years, 39–81) and 744 partners (60 years, 36–79). For this study only the offspring and their partners were included.

The Netherlands Twin Register (NTR: http://www.tweelingenregister.org/) recruits twins and their family members to study the causes of individual differences in health, behavior and lifestyle. Participants are followed longitudinally; details about the cohort have been published previously.34 A subsample of unselected twins and their family members has taken part in the NTR-Biobank,35 in which biological samples, including DNA and RNA, were collected in a standardized manner after overnight fasting. Study protocols were approved by the medical ethics board of the VUMC Amsterdam, the Netherlands.

The Queensland Institute of Medical Research (QIMR) adolescent study comprised twins and their non-twin siblings living in south-east Queensland, Australia.36 Most (98% by self-report) are of mixed European ancestry, mainly from the British Isles. The participants are not selected on the basis of any disease or other outcome. Blood samples were collected at the end of testing sessions from participants and, if possible, from their parents. Pedigree relationships and zygosity were confirmed by genotype data. Further details are provided elsewhere.37

The TwinsUK cohort (www.twinsuk.ac.uk) is an adult twin British registry shown to be representative of singleton populations and the UK population.38 A total of 6038 twins with TL measurement were included in the analysis. The age range of the TwinsUK cohort was 16–99 years. Ethical approval was obtained from the Guy’s and St Thomas’ Hospital Ethics Committee. Written informed consent was obtained from every participant in the study.

TL assessment

All samples from all studies were measured in the same laboratory under standard conditions. Mean leukocyte TL was measured by quantitative PCR-based technique as previously described.12, 39 This method expresses TL as a ratio (T/S) of telomere repeat length (T) to copy number of a single copy gene, 36B4(S), within each sample. Samples were quantified relative to a calibrator sample used on each run (DNA from the K562 cell line).12 Mean interrun coefficient of variations (CVs) were calculated for all study cohorts and these ranged from 3.30 to 3.72%.


To summarize resemblance between family members, correlations of TL between monozygotic (MZ) and dizygotic (DZ) twins, non-twin siblings, parents and offspring and between spouses, adjusting for age, gender and potential batch effects were calculated in R, version If data on more than two siblings were available, the data from the oldest two non-twin siblings were analyzed.

Maximum likelihood analyses as implemented in POLY41 were used to evaluate different models of familial resemblance and these analyses were based on all data (ie, allowing for more than 2 siblings per family). In these analyses, TL was adjusted for age, gender and batch by specifying these as fixed effects on TL. Data from the six cohorts were first analyzed individually followed by meta-analysis, whereby each cohort took into account the unique structure in the data, such as the highly complex pedigree structure in the ERF cohort. In those studies where the pedigree structure allowed for evaluating sub models that included an additive genetic variance component, a nonadditive genetic variance component (dominance) or a sibling-shared environment variance component, respectively, were compared. A model in which variance was partitioned into an additive genetic variance component and a random environmental variance component gave the best description of all data and heritability was estimated based on this model.

In order to investigate differences between maternal or paternal inheritance for TL, family trios or duos were selected. When data on two or more children were available, data from the oldest child were selected for this analysis. We assessed the age-, gender- and batch-adjusted correlations between fathers and their offspring and mothers and their offspring.

Paternal and maternal ages at the birth of their children were obtained based on the date of birth of the parents and offspring if available, or by subtracting the child’s age from the parental age. The associations of paternal and maternal age with TL were compared by regressing TL on parental age in addition to own age and gender (eg, TL−age+gender+parental age). In order to correct significance testing for familial dependencies, these analyses were also done in POLY. Meta-analyses were performed using the R package rmeta.42


General characteristics of each cohort are described in Table 1. The mean age ranged from 27.9 (QIMR) to 59.2 (LLS). Overall, approximately half of the participants are female in each population. Three cohorts (NTR, QIMR and TwinsUK) had twin data, with NTR and TwinsUK having more MZ twins and QIMR having more DZ twins. As expected, TL showed a significant negative association with age and was significantly longer in women in each population (Supplementary Table 1).

Table 1: General characteristics of the study populations

MZ twins were significantly more alike than DZ twins (P-value=1.85 × 10−24, Table 2) and siblings were significantly correlated within each cohort and this correlation was very similar to that of DZ twins (Table 2). Spouses had significantly correlated TLs (r=0.25; P-value=2.82 × 10−30) and this effect was more pronounced in older spouses (mean age ≥55 years) compared with younger spouses (mean age<55 years; P-value=0.010; Table 2) suggesting that there is a significant influence of environmental factors.

Table 2: Sibling, twin and spousal correlations, adjusted for age, gender and batch effects

Despite the evidence for the influence of environmental factors, neither the dominant variance component nor the sibling-shared variance component influenced the estimates of familial resemblance in those studies where the analysis could be performed (Supplementary Table 2) suggesting that any residual shared-environment or nonadditive genetic effects are small. In the heritability analyses, three cohorts (ERF, NTR and QIMR) had nearly identical heritability estimates of 0.62 (Table 3). The highest heritability estimate was found in LLS (h2=0.86). In the meta-analysis of all six cohorts, the heritability was estimated to be 0.70 (95% confidence interval (CI) 0.64–0.76; P-value=2.31 × 10−111).

Table 3: Heritability of telomere length

The correlations between parental and offspring TL as a function of gender showed an effect of parental gender, but not of offspring gender. Both father–offspring (r=0.33; P-value=5.66 × 10−4) and mother–offspring (r=0.42; P-value=5.01 × 10−5) TLs were significantly correlated (Table 4). The mother–offspring correlation was significantly larger than the father–offspring correlation (P-value=0.007). There was no difference in correlation structure between male and female offspring and their parents.

Table 4: Inheritance patterns: father–offspring and mother–offspring correlations in telomere length

Finally, we investigated whether parental age plays a role in TL (Table 5). In each cohort the association between paternal age and TL went in the positive direction. After meta-analysis, we found a significant association between paternal age and TL (n=5127; β=0.005; P-value=7.01 × 10−5). Maternal age was found to be significantly associated with TL after meta-analysis (n=5500; β=0.003; P-value=0.012). This association was no longer significant when additionally adjusting for paternal age (β=−0.003; P-value=0.357). The paternal age association remained significant when additionally adjusting for maternal age (β=0.007; P-value=0.011).

Table 5: Association of paternal and maternal age at birth with telomere length


In six independent family-based cohorts from Europe and Australia, we investigated three aspects of familial relationships in TL, namely the heritability, mode of inheritance and parental age at birth of their children. We found a high heritability, a significant stronger maternal than paternal inheritance and a positive association with paternal age.

The meta-analysis estimate for heritability of TL in the six populations was 0.70. Heritability estimates from the separate studies were remarkably similar across populations, with three of them showing near identical estimates. The highest estimate was observed in the oldest participants (LLS; h2: 0.86), which may reflect a selection effect.33 Although only the offspring with their spouses of long-living participants were selected from the LLS study, the selection of the parents for old age might have influenced the total TL distribution in their relatives.

Spousal correlations for TL have not been reported before.25 Interestingly, we observed a significant correlation in TL between spouses. This was more pronounced in older spouses (mean age ≥55; r=0.31) compared with younger spouses (mean age <55; r=0.20), suggesting a possible influence on TL because of living together for an extended amount of time. The hypothesis that resemblance in adults is induced by living together for extended periods of time does not need to be conflicting with the finding that modeling of the twin-family data did not detect shared-environmental influences. In a twin design shared environment is reflected in the portion of the phenotypic correlation in MZ and DZ twins that exceeds above the pattern expected if the similarity of twins was only a function of their genetic resemblance. By assuming that the common environment applies to those factors that are always shared 100% between twins, or siblings, the scope of this component for quantifying shared family environment tends to be limited to influences of the early environment, and ignores factors that are shared by individuals who share a household later in life. Another explanation could be an ascertainment effect. In older spouse pairs, both individuals have survived for extended periods of time, and are therefore likely to have above average TL for their age. The age correction performed might not completely control for this.

Mother–offspring correlations were significantly higher than the father–offspring correlations (P-value=0.007), although both were statistically significant on their own. This did not change when additionally adjusting the father–offspring correlation for paternal age (data not shown). In 2004, Nawrot et al23 also showed a significant correlation between mother–offspring (n=71) and father–daughter (n=47), but not between father–son (n=34). Recently, a paternal inheritance model has been gaining favor.8, 24, 25, 26 The most recent study suggesting paternal inheritance from Nordfjall et al26 contained a total of 217 parent–offspring pairs. In our study we included a total of 1244 father–offspring pairs and 1388 mother–offspring pairs and found both significant mother–offspring and father–offspring correlations for TL. Our findings are in contrast with those from other studies, as we found a significantly stronger mother–offspring than father–offspring correlation, which previously was attributed to an X-linked mechanism in TL determination.23 A prime candidate gene for this X-linked mechanism is DKC1 encoding dyskerin, which is important for the function of telomerase and has been found to cause congenital dyskeratosis that is characterized by short telomeres.43 However, if an X-linked mechanism is in effect, a stronger father–daughter correlation would be expected, compared with the father–son correlation, which we did not observe. Other potential explanations for the larger mother–offspring correlation include mitochondrial DNA or other parent-specific ‘imprinting’. Nonpaternities were excluded as an explanation, based on genotype data.

Finally, we found significant evidence for a positive association of paternal age with TL, supporting earlier reports.24, 27, 28 At first glance, any positive association of TL with age seems counterintuitive. However, TL is known to be maintained, and even lengthened, in sperm, despite both mitotic and meiotic divisions during the proliferation and differentiation of the cells.44 In humans, this leads to a gain of 71 base pairs of TL per year.29 Recently, it was shown that the paternal age effect may be cumulative over generations.45 Our findings are opposite of the recent publication that paternal age is the major determinant of novel mutations leading to autism.46 Thus, high paternal age may have both positive and negative effects on the health of the offspring, assuming that long telomeres in children are healthy.

In summary, we find a high and very consistent heritability estimate for TL. In addition, we find evidence for a maternal inheritance component and a positive association with paternal age.


  1. 1.

    , : A tandemly repeated sequence at the termini of the extrachromosomal ribosomal RNA genes in Tetrahymena. J Mol Biol 1978; 120: 33–53.

  2. 2.

    : Switching and signaling at the telomere. Cell 2001; 106: 661–673.

  3. 3.

    , , , , : In vivo loss of telomeric repeats with age in humans. Mutat Res 1991; 256: 45–48.

  4. 4.

    , , : Genetic determination of telomere size in humans: a twin study of three age groups. Am J Hum Genet 1994; 55: 876–882.

  5. 5.

    , , et al: Telomere length predicts survival independent of genetic influences. Aging Cell 2007; 6: 769–774.

  6. 6.

    , , , , : Association between telomere length in blood and mortality in people aged 60 years or older. Lancet 2003; 361: 393–395.

  7. 7.

    , , et al: Telomere length and mortality: a study of leukocytes in elderly Danish twins. Am J Epidemiol 2008; 167: 799–806.

  8. 8.

    , , et al: Telomere length is paternally inherited and is associated with parental lifespan. Proc Natl Acad Sci USA 2007; 104: 12135–12139.

  9. 9.

    , , et al: No association between telomere length and survival among the elderly and oldest old. Epidemiology 2006; 17: 190–194.

  10. 10.

    , , , , : Telomere length in white blood cells is not associated with morbidity or mortality in the oldest old: a population-based study. Aging Cell 2005; 4: 287–290.

  11. 11.

    , , et al: Evolution in health and medicine Sackler colloquium: genetic variation in human telomerase is associated with telomere length in Ashkenazi centenarians. Proc Natl Acad Sci USA 2010; 107 (Suppl 1): 1710–1717.

  12. 12.

    , , et al: Common variants near TERC are associated with mean telomere length. Nat Genet 2010; 42: 197–199.

  13. 13.

    , , et al: Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. Proc Natl Acad Sci USA 2010; 107: 9293–9298.

  14. 14.

    , , et al: The association of telomere length and genetic variation in telomere biology genes. Hum Mutat 2010; 31: 1050–1058.

  15. 15.

    , , et al: Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Nat Genet 2009; 41: 221–227.

  16. 16.

    , , et al: Common variants near TERC are associated with leukocyte telomere length in the Chinese Han population. Eur J Hum Genet 2011; 19: 721–723.

  17. 17.

    , , et al: Genetic variation in TERT and TERC and human leukocyte telomere length and longevity: a cross-sectional and longitudinal analysis. Aging Cell 2012; 11: 223–227.

  18. 18.

    , , et al: Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways. Age (Dordr) 2011, doi:10.1007/s11357-011-9340-3.

  19. 19.

    , , et al: The heritability of telomere length among the elderly and oldest-old. Twin Res Hum Genet 2005; 8: 433–439.

  20. 20.

    , , et al: Mapping genetic loci that determine leukocyte telomere length in a large sample of unselected female sibling pairs. Am J Hum Genet 2006; 78: 480–486.

  21. 21.

    , , et al: Mapping of a major locus that determines telomere length in humans. Am J Hum Genet 2005; 76: 147–151.

  22. 22.

    , , : The use of telomere length in ecology and evolutionary biology. Heredity (Edinb) 2010; 105: 497–506.

  23. 23.

    , , , : Telomere length and possible link to X chromosome. Lancet 2004; 363: 507–510.

  24. 24.

    , , et al: Offspring’s leukocyte telomere length, paternal age, and telomere elongation in sperm. PLoS Genet 2008; 4: e37.

  25. 25.

    , , , , : Telomere length and heredity: indications of paternal inheritance. Proc Natl Acad Sci USA 2005; 102: 16374–16378.

  26. 26.

    , , , , : Large-scale parent-child comparison confirms a strong paternal influence on telomere length. Eur J Hum Genet 2010; 18: 385–389.

  27. 27.

    , , et al: Paternal age at birth is an important determinant of offspring telomere length. Hum Mol Genet 2007; 16: 3097–3102.

  28. 28.

    , , : Paternal age is positively linked to telomere length of children. Aging Cell 2005; 4: 97–101.

  29. 29.

    , , et al: Telomere length predicts replicative capacity of human fibroblasts. Proc Natl Acad Sci USA 1992; 89: 10114–10118.

  30. 30.

    , , et al: Linkage disequilibrium in young genetically isolated Dutch population. Eur J Hum Genet 2004; 12: 527–534.

  31. 31.

    , , , , : The effect of genetic drift in a young genetically isolated population. Ann Hum Genet 2005; 69: 288–295.

  32. 32.

    , , et al: Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension 2008; 51: 1658–1664.

  33. 33.

    , , et al: Evidence of genetic enrichment for exceptional survival using a family approach: the Leiden Longevity Study. Eur J Hum Genet 2006; 14: 79–84.

  34. 34.

    , , et al: Netherlands Twin Register: from twins to twin families. Twin Res Hum Genet 2006; 9: 849–857.

  35. 35.

    , , et al: The Netherlands Twin Register biobank: a resource for genetic epidemiological studies. Twin Res Hum Genet 2010; 13: 231–245.

  36. 36.

    , : Brisbane adolescent twin study: outline of study methods and research projects. Aust J Psychol 2004; 56: 65–78.

  37. 37.

    , , et al: Common variants in the trichohyalin gene are associated with straight hair in Europeans. Am J Hum Genet 2009; 85: 750–755.

  38. 38.

    , , , : Cohort Profile: TwinsUK and Healthy Ageing Twin Study. Int J Epidemiol 2012, doi:10.1093/ije/dyr207.

  39. 39.

    : Telomere measurement by quantitative PCR. Nucleic Acids Res 2002; 30: e47.

  40. 40.

    R Development Core Team: R: A Language and Environment for Statistical Computing. Vienna, Austria: R foundation for Statistical Computing, 2010, 2.12.1 edn.

  41. 41.

    , , et al: Heritability of cardiovascular and personality traits in 6148 Sardinians. PLoS Genet 2006; 2: e132.

  42. 42.

    : rmeta: Meta-analysis 2009, R package version 2.16 edn.

  43. 43.

    , , : A telomerase component is defective in the human disease dyskeratosis congenita. Nature 1999; 402: 551–555.

  44. 44.

    , , : Telomere length in male germ cells is inversely correlated with telomerase activity. Biol Reprod 2000; 63: 591–598.

  45. 45.

    , , : Delayed paternal age of reproduction in humans is associated with longer telomeres across two generations of descendants. Proc Natl Acad Sci USA 2012; 109: 10251–10256.

  46. 46.

    , , et al: Rate of de novo mutations and the importance of father’s age to disease risk. Nature 2012; 488: 471–475.

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ERF: The study was supported by grants from The Netherlands Organisation for Scientific Research (NWO), Erasmus MC and the Centre for Medical Systems Biology (CMSB). Telomere length assessment was supported through funds from the European Community’s Seventh Framework Programme (FP7/2007-2013), ENGAGE Consortium, grant agreement HEALTH-F4-2007-201413. We are grateful to all general practitioners for their contributions, to Petra Veraart for her help in genealogy, Jeannette Vergeer for the supervision of the laboratory work and Peter Snijders for his help in data collection. GRAPHIC: The GRAPHIC study was funded by the BHF. VC and NJS are supported by the BHF and VC, CN and NJS are supported by the Leicester National Institute of Health Research (NIHR) Biomedical Research Unit in Cardiovascular Disease. Additionally, this research was supported through funds from The European Community’s Seventh Framework Programme (FP7/2007-2013), ENGAGE Consortium, grant agreement HEALTH-F4-2007- 201413. LLS: We thank all participants of the Leiden Longevity Study. The research leading to these results has received funding from the European Union’s Seventh Framework Programme (FP7/2007-2011) under grant agreement number 259679. This study was supported by a grant from the Innovation-Oriented Research Program on Genomics (SenterNovem IGE05007), the Centre for Medical Systems Biology and the Netherlands Consortium for Healthy Ageing (grant 050-060-810), all in the framework of the Netherlands Genomics Initiative, Netherlands Organization for Scientific Research (NWO), and by Unilever Colworth. NTR: We thank all participants in the Netherlands Twin Register. Research was funded by the Netherlands Organization for Scientific Research (NWO: MagW/ZonMW grants 904-61-090, 985-10-002,904-61-193,480-04-004, 400-05-717, Addiction-31160008 Middelgroot-911-09-032, Spinozapremie 56-464-14192), Center for Medical Systems Biology (CSMB, NWO Genomics), NBIC/BioAssist/RK(2008.024), Biobanking and Biomolecular Resources Research Infrastructure (BBMRI –NL, 184.021.007), the VU University’s Institute for Health and Care Research (EMGO+), the European Community’s Seventh Framework Program (FP7/2007-2013), ENGAGE (HEALTH-F4-2007-201413) and the European Science Council (ERC–230374 and ERC-284167). QIMR: We thank Marlene Grace and Ann Eldridge for twin recruitment and data collection, Lisa Bardsley for preparation of DNA samples, David Smyth for IT/database support and the twins and their families for their participation. Data collection was supported by grants to NGM and MJW from the Australian Research Council and Australian National Health and Medical Research Council (NHMRC). Telomere length assessment was co-funded by the European Community’s Seventh Framework Programme (FP7/2007-2013), ENGAGE project, grant agreement HEALTH-F4-2007-201413 and NHMRC-European Union Collaborative Research Grant 496739. GWM and DRN were supported by the NHMRC Fellowship (619667) and ARC Future Fellowship (FT0991022) schemes, respectively. TwinsUK: The study was funded by the Wellcome Trust; European Community’s Seventh Framework Programme (FP7/2007-2013), ENGAGE project grant agreement (HEALTH-F4-2007-201413). The study also receives support from the Dept of Health via the National Institute for Health Research (NIHR) comprehensive Biomedical Research Centre award to Guy’s & St Thomas’ NHS Foundation Trust in partnership with King’s College London. TDS is an NIHR senior Investigator and is holder of an ERC Advanced Principal Investigator award. Genotyping was performed by The Wellcome Trust Sanger Institute, support of the National Eye Institute via an NIH/CIDR genotyping project.

Author information

Author notes

    • Linda Broer

    Shared first.

    • Cornelia M van Duijn
    •  & Dorret I Boomsma

    Shared last.


  1. Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands

    • Linda Broer
    • , Veryan Codd
    • , Najaf Amin
    • , Aaron Isaacs
    • , Ben A Oostra
    •  & Cornelia M van Duijn
  2. Netherlands Consortium for Healthy Aging, Leiden University Medical Center, Leiden, The Netherlands

    • Linda Broer
    • , Joris Deelen
    • , Marian Beekman
    • , P Eline Slagboom
    •  & Cornelia M van Duijn
  3. Department of Cardiovascular Sciences, University of Leicester, Leicester, UK

    • Veryan Codd
    • , Christopher P Nelson
    • , Mary Matthews
    •  & Nilesh J Samani
  4. Queensland Institute of Medical Research, Herston, Queensland, Australia

    • Dale R Nyholt
    • , Anjali Henders
    • , Margie J Wright
    • , Grant W Montgomery
    •  & Nicholas G Martin
  5. Section of Molecular Epidemiology, Leiden University Medical Center, Leiden, The Netherlands

    • Joris Deelen
    • , Marian Beekman
    •  & P Eline Slagboom
  6. Department of Twin Research and Genetic Epidemiology, King’s College London, London, UK

    • Massimo Mangino
    • , Claire J Steves
    • , Alireza Moayyeri
    •  & Tim D Spector
  7. Netherlands Twin Register, Department of Biological Psychology, VU Univ Amsterdam, Amsterdam, The Netherlands

    • Gonneke Willemsen
    • , Eco J C de Geus
    • , Jacqueline M Vink
    •  & Dorret I Boomsma
  8. Institute of Genetic Epidemiology, Helmholtz Zentrum München German Research Center for Environmental Health, Neuherberg, Germany

    • Eva Albrecht
  9. Deparment of Gerontology and Geriatrics, Leiden University Medical Center, Leiden, The Netherlands

    • Anton J M de Craen
  10. Centre for Medical Systems Biology, Leiden, The Netherlands

    • Aaron Isaacs


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Competing interests

The authors declare no conflict of interest.

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Correspondence to Cornelia M van Duijn or Dorret I Boomsma.

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Supplementary Information accompanies this paper on European Journal of Human Genetics website (http://www.nature.com/ejhg)

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