The DOI matches its Crossref record; 78 of the 78 references it cites were found in a registry or an index.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Open accessAbstract
Here 106 genomic loci associated with age at menarche, a marker of puberty timing in females, are identified; these loci show enrichment for genes involved in nuclear hormone receptor function, body mass index, and rare disorders of puberty, and for genes located in imprinted regions, with parent-of-origin specific effects at several loci. The age at which females first experience menstruation, called menarche, is a heritable trait associated with risks for obesity, type 2 diabetes, cardiovascular disease, breast cancer and general mortality. This large-scale genome-wide association study identifies 123 signals at 106 genomic loci associated with age at menarche. New findings include parent-of-origin-specific allelic associations (both maternally and paternally driven) at three imprinted loci and the implication of retinoic acid and GABAB receptor II signalling and lysine-specific histone demethylation. These data bring new insights into the genetic architecture of puberty timing and suggest a model involving thousands of genetic variants. Age at menarche is a marker of timing of puberty in females. It varies widely between individuals, is a heritable trait and is associated with risks for obesity, type 2 diabetes, cardiovascular disease, breast cancer and all-cause mortality1. Studies of rare human disorders of puberty and animal models point to a complex hypothalamic-pituitary-hormonal regulation2,3, but the mechanisms that determine pubertal timing and underlie its links to disease risk remain unclear. Here, using genome-wide and custom-genotyping arrays in up to 182,416 women of European descent from 57 studies, we found robust evidence (P < 5 × 10−8) for 123 signals at 106 genomic loci associated with age at menarche. Many loci were associated with other pubertal traits in both sexes, and there was substantial overlap with genes implicated in body mass index and various diseases, including rare disorders of puberty. Menarche signals were enriched in imprinted regions, with three loci (DLK1-WDR25, MKRN3-MAGEL2 and KCNK9) demonstrating parent-of-origin-specific associations concordant with known parental expression patterns. Pathway analyses implicated nuclear hormone receptors, particularly retinoic acid and γ-aminobutyric acid-B2 receptor signalling, among novel mechanisms that regulate pubertal timing in humans. Our findings suggest a genetic architecture involving at least hundreds of common variants in the coordinated timing of the pubertal transition.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In a recent meta-analysis of genome-wide association and custom-genotyping array studies of age at menarche in up to 182 416 women of European descent, a variant downstream of MKRN3 had the largest effect size for association with menarche when the variant was paternally inherited.80”
From Pubertal development and regulation (2016) · cites this paper as [80]
In the citing paper
“After identification of the association of MKRN3 with puberty regulation, single nucleotide polymorphisms in imprinted gene regions were linked to the age of menarche, supporting puberty timing as a selective trait.80”
From Pubertal development and regulation (2016) · cites this paper as [80]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
Genetics of Food Intake Self-Regulation in Childhood: Literature Review and Research Opportunities
Faith, M. S., Carnell, S., & Kral, T. V. E. (2013) · Human Heredity · doi:10.1159/000353879 · Cited by 7,633
METAL: fast and efficient meta-analysis of genomewide association scans
Willer, C. J., Li, Y., & Abecasis, G. R. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq340 · Cited by 5,205
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
MAGIC, Speliotes, E. K., on behalf of Procardis Consortium, Willer, C. J., Berndt, S. I., Monda, K. L., Thorleifsson, G., Jackson, A. U., Allen, H. L., Lindgren, C. M., et al. (2010) · Nature Genetics · doi:10.1038/ng.686 · Cited by 2,912
Self-citationHundreds of variants clustered in genomic loci and biological pathways affect human height
Lango Allen, H., Estrada, K., Lettre, G., Berndt, S. I., Weedon, M. N., Rivadeneira, F., Willer, C. J., Jackson, A. U., Vedantam, S., Raychaudhuri, S., et al. (2010) · Nature · doi:10.1038/nature09410 · Cited by 1,945
Self-citationThe Type 1 Diabetes Genetics Consortium, Barrett, J. C., Clayton, D. G., Concannon, P., Akolkar, B., Cooper, J. D., Erlich, H. A., Julier, C., Morahan, G., Nerup, J., et al. (2009) · Nature Genetics · doi:10.1038/ng.381 · Cited by 1,746
Genetic Investigation of ANthropometric Traits (GIANT) Consortium, Yang, J., DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium, Ferreira, T., Morris, A. P., Medland, S. E., Madden, P. A. F., Heath, A. C., Martin, N. G., Montgomery, G. W., et al. (2012) · Nature Genetics · doi:10.1038/ng.2213 · Cited by 1,712
Self-citationSystematic identification of trans eQTLs as putative drivers of known disease associations
Westra, H.-J., Peters, M. J., Esko, T., Yaghootkar, H., Schurmann, C., Kettunen, J., Christiansen, M. W., Fairfax, B. P., Schramm, K., Powell, J. E., et al. (2013) · Nature Genetics · doi:10.1038/ng.2756 · Cited by 1,658
Self-citationIntegrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer’s Disease
Zhang, B., Gaiteri, C., Bodea, L.-G., Wang, Z., McElwee, J., Podtelezhnikov, A. A., Zhang, C., Xie, T., Tran, L., Dobrin, R., et al. (2013) · Cell · doi:10.1016/j.cell.2013.03.030 · Cited by 1,657
Self-citationGenetics of gene expression and its effect on disease
Emilsson, V., Thorleifsson, G., Zhang, B., Leonardson, A. S., Zink, F., Zhu, J., Carlson, S., Helgason, A., Walters, G. B., Gunnarsdottir, S., et al. (2008) · Nature · doi:10.1038/nature06758 · Cited by 1,296
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Verbanck, M., Chen, C.-Y., Neale, B., & Do, R. (2018) · Nature Genetics · doi:10.1038/s41588-018-0099-7 · Cited by 8,591
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
Self-citationeQTLGen, Wray, N. R., 23andMe, the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Ripke, S., Mattheisen, M., Trzaskowski, M., Byrne, E. M., Abdellaoui, A., Adams, M. J., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0090-3 · Cited by 3,005
Self-citationVõsa, U., Claringbould, A., Westra, H.-J., Bonder, M. J., Deelen, P., Zeng, B., Kirsten, H., Saha, A., Kreuzhuber, R., Yazar, S., et al. (2021) · Nature Genetics · doi:10.1038/s41588-021-00913-z · Cited by 2,607
Self-citationPartitioning heritability by functional annotation using genome-wide association summary statistics
ReproGen Consortium, Finucane, H. K., Schizophrenia Working Group of the Psychiatric Genomics Consortium, The RACI Consortium, Bulik-Sullivan, B., Gusev, A., Trynka, G., Reshef, Y., Loh, P.-R., Anttila, V., et al. (2015) · Nature Genetics · doi:10.1038/ng.3404 · Cited by 2,604
Self-citationDetection and interpretation of shared genetic influences on 42 human traits
Pickrell, J. K., Berisa, T., Liu, J. Z., Ségurel, L., Tung, J. Y., & Hinds, D. A. (2016) · Nature Genetics · doi:10.1038/ng.3570 · Cited by 1,151
Boehm, U., Bouloux, P.-M., Dattani, M. T., de Roux, N., Dodé, C., Dunkel, L., Dwyer, A. A., Giacobini, P., Hardelin, J.-P., Juul, A., et al. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.112 · Cited by 874
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
Self-citationA molecular census of arcuate hypothalamus and median eminence cell types
Campbell, J. N., Macosko, E. Z., Fenselau, H., Pers, T. H., Lyubetskaya, A., Tenen, D., Goldman, M., Verstegen, A. M. J., Resch, J. M., McCarroll, S. A., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4495 · Cited by 817
Self-citationStudy, 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
Self-citationSex-dependent dominance at a single locus maintains variation in age at maturity in salmon
Barson, N. J., Aykanat, T., Hindar, K., Baranski, M., Bolstad, G. H., Fiske, P., Jacq, C., Jensen, A. J., Johnston, S. E., Karlsson, S., et al. (2015) · Nature · doi:10.1038/nature16062 · Cited by 663
Day, F., Karaderi, T., Jones, M. R., Meun, C., He, C., Drong, A., Kraft, P., Lin, N., Huang, H., Broer, L., et al. (2018) · PLOS Genetics · doi:10.1371/journal.pgen.1007813 · Cited by 619
“Publicly available genome-wide summary statistics for body mass index (BMI) [60], childhood obesity [61], fasting insulin levels (adjusted for BMI) [62], type 2 diabetes [63], high-density lipoprotein (HDL) levels [64], menarche timing [65], triglyceride levels [64], coronary artery disease [66], depression [36], meno…”
MethodSelf-citationPubertal development and regulation
Abreu, A. P., & Kaiser, U. B. (2016) · The Lancet Diabetes & Endocrinology · doi:10.1016/s2213-8587(15)00418-0 · Cited by 611
Study, T. L. C., Day, F. R., The InterAct Consortium, kConFab/AOCS Investigators, Endometrial Cancer Association Consortium, Ovarian Cancer Association Consortium, PRACTICAL consortium, Thompson, D. J., Helgason, H., Chasman, D. I., et al. (2017) · Nature Genetics · doi:10.1038/ng.3841 · Cited by 587
Self-citationUnraveling the polygenic architecture of complex traits using blood eQTL metaanalysis
Võsa, U., Claringbould, A., Westra, H.-J., Bonder, M. J., Deelen, P., Zeng, B., Kirsten, H., Saha, A., Kreuzhuber, R., Kasela, S., et al. (2018) · doi:10.1101/447367 · Cited by 2,607
Self-citationWidespread seasonal gene expression reveals annual differences in human immunity and physiology
Dopico, X. C., Evangelou, M., Ferreira, R. C., Guo, H., Pekalski, M. L., Smyth, D. J., Cooper, N., Burren, O. S., Fulford, A. J., Hennig, B. J., et al. (2015) · Nature Communications · doi:10.1038/ncomms8000 · Cited by 472
Gazal, S., Finucane, H. K., Furlotte, N. A., Loh, P.-R., Palamara, P. F., Liu, X., Schoech, A., Bulik-Sullivan, B., Neale, B. M., Gusev, A., et al. (2017) · Nature Genetics · doi:10.1038/ng.3954 · Cited by 525
Dissecting the genetics of complex traits using summary association statistics
Paşaniuc, B., & Price, A. L. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.142 · Cited by 461
The PRACTICAL Consortium, Day, F. R., kConFab Investigators, AOCS Investigators, Scotland, G., EPIC-InterAct Consortium, Study, L. C., Ruth, K. S., Thompson, D. J., Lunetta, K. L., et al. (2015) · Nature Genetics · doi:10.1038/ng.3412 · Cited by 402
Self-citationLarge-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior
Ganna, A., Verweij, K. J. H., Nivard, M. G., Maier, R., Wedow, R., Busch, A. S., Abdellaoui, A., Guo, S., Sathirapongsasuti, J. F., 23andMe Research Team, et al. (2019) · Science · doi:10.1126/science.aat7693 · Cited by 406
Self-citationContrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data
Shi, H., Kichaev, G., & Pasaniuc, B. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2016.05.013 · Cited by 387
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
Zhang, G., Feenstra, B., Bačelis, J., Liu, X., Muglia, L. M., Juodakis, J., Miller, D. E., Litterman, N. K., Jiang, P., Russell, L. E., et al. (2017) · New England Journal of Medicine · doi:10.1056/nejmoa1612665 · Cited by 385
Self-citationBryois, J., Skene, N., Hansen, T. F., Kogelman, L. J. A., Watson, H. J., Liu, Z., Adan, R. A. H., Alfredsson, L. S., Ando, T., Andreassen, O. A., et al. (2020) · Nature Genetics · doi:10.1038/s41588-020-0610-9 · Cited by 381
Self-citationA population genetic interpretation of GWAS findings for human quantitative traits
Simons, Y. B., Bullaughey, K., Hudson, R. R., & Sella, G. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2002985 · Cited by 367
Bayesian weighted Mendelian randomization for causal inference based on summary statistics
Zhao, J., Ming, J., Hu, X., Chen, G., Liu, J., & Yang, C. (2019) · Bioinformatics · doi:10.1093/bioinformatics/btz749 · Cited by 355
Local Genetic Correlation Gives Insights into the Shared Genetic Architecture of Complex Traits
Shi, H., Mancuso, N., Spendlove, S. J., & Paşaniuc, B. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.09.022 · Cited by 351
Can the impact of childhood adiposity on disease risk be reversed? A Mendelian randomization study.
Richardson, T. G., Sanderson, E., Elsworth, B., Tilling, K., & Davey Smith, G. (2019) · doi:10.1101/19008011 · Cited by 321
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Barban, N., Study, L. C., Jansen, R., de Vlaming, R., Vaez, A., Mandemakers, J. J., Tropf, F. C., Shen, X., Wilson, J. F., Chasman, D. I., et al. (2016) · Nature Genetics · doi:10.1038/ng.3698 · Cited by 324
Self-citationPaediatric and adult-onset male hypogonadism
Salonia, A., Rastrelli, G., Hackett, G., Seminara, S. B., Huhtaniemi, I. T., Rey, R. A., Hellstrom, W. J. G., Palmert, M. R., Corona, G., Dohle, G. R., et al. (2019) · Nature Reviews Disease Primers · doi:10.1038/s41572-019-0087-y · Cited by 286
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Lu, Y., Day, F. R., Gustafsson, S., Buchkovich, M. L., Na, J., Bataille, V. A., Cousminer, D. L., Dastani, Z., Drong, A., Esko, T., et al. (2016) · Nature Communications · doi:10.1038/ncomms10495 · Cited by 294
Self-citationMancuso, N., Shi, H., Goddard, P. C., Kichaev, G., Gusev, A., & Paşaniuc, B. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.01.031 · Cited by 266
Thinking About the Evolution of Complex Traits in the Era of Genome-Wide Association Studies
Sella, G., & Barton, N. (2019) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-083115-022316 · Cited by 290
Trajanoska, K., Morris, J. A., Oei, L., Zheng, H.-F., Evans, D. M., Kiel, D. P., Ohlsson, C., Richards, J. B., & Rivadeneira, F. (2018) · BMJ · doi:10.1136/bmj.k3225 · Cited by 270
Self-citationSumHer better estimates the SNP heritability of complex traits from summary statistics
Speed, D., & Balding, D. J. (2019) · Nature Genetics · doi:10.1038/s41588-018-0279-5 · Cited by 254
Schork, A. J., Won, H., Appadurai, V., Nudel, R., Gandal, M., Delaneau, O., Revsbech Christiansen, M., Hougaard, D. M., Bækved-Hansen, M., Bybjerg-Grauholm, J., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0320-0 · Cited by 223
Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
Dauber, A. N., Cunha-Silva, M., Macedo, D. B., Brito, V. N., Abreu, A. P., Roberts, S. A., Montenegro, L. R., Andrew, M., Kirby, A. W., Weirauch, M. T., et al. (2017) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2016-3677 · Cited by 219
Neuroendocrine control of the onset of puberty
Plant, T. M. (2015) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2015.04.002 · Cited by 223
Cohort Profile Update: The TRacking Adolescents' Individual Lives Survey (TRAILS)
Oldehinkel, A. J., Rosmalen, J. G. M., Buitelaar, J. K., Hoek, H. W., Ormel, J., Raven, D., Reijneveld, S. A., Veenstra, R., Verhulst, F. C., Vollebergh, W., et al. (2014) · International Journal of Epidemiology · doi:10.1093/ije/dyu225 · Cited by 216
Self-citationQi, G., & Chatterjee, N. (2019) · Nature Communications · doi:10.1038/s41467-019-09432-2 · Cited by 207
Copy Number Variations and Cognitive Phenotypes in Unselected Populations
Männik, K., Mägi, R., Macé, A., Cole, B., Guyatt, A. L., Shihab, H. A., Maillard, A. M., Alavere, H., Kolk, A., Reigo, A., et al. (2015) · JAMA · doi:10.1001/jama.2015.4845 · Cited by 205
Self-citationKim-Hellmuth, S., Bechheim, M., Pütz, B., Mohammadi, P., Nédélec, Y., Giangreco, N., Becker, J., Kaiser, V. B., Fricker, N., Beier, E., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00366-1 · Cited by 201
Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism
Stamou, M. I., & Georgopoulos, N. A. (2017) · Metabolism · doi:10.1016/j.metabol.2017.10.012 · Cited by 200
Taylor, A. E., Jones, H. J., Sallis, H., Euesden, J., Stergiakouli, E., Davies, N. M., Zammit, S., Lawlor, D. A., Munafò, M. R., Davey Smith, G., et al. (2018) · International Journal of Epidemiology · doi:10.1093/ije/dyy060 · Cited by 192
Self-citationNead, K. T., Sharp, S. J., Thompson, D. J., Painter, J. N., Savage, D. B., Semple, R. K., Barker, A., Perry, J. R. B., Attia, J., Dunning, A. M., et al. (2015) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djv178 · Cited by 189
Self-citationPhysical and neurobehavioral determinants of reproductive onset and success
Day, F. R., Helgason, H., Chasman, D. I., Rose, L. M., Loh, P., Scott, R. A., Helgason, A., Kong, A., Másson, G., Magnússon, Ó. Þ., et al. (2016) · Nature Genetics · doi:10.1038/ng.3551 · Cited by 174
Self-citationExome sequencing of Finnish isolates enhances rare-variant association power
Locke, A. E., Steinberg, K. M., Chiang, C. W. K., Service, S. K., Havulinna, A. S., Stell, L., Pirinen, M., Abel, H., Chiang, C., Fulton, R. S., et al. (2019) · Nature · doi:10.1038/s41586-019-1457-z · Cited by 173
Self-citationResource profile and user guide of the Polygenic Index Repository
Becker, J., Burik, C. A. P., Goldman, G., Wang, N., Jayashankar, H., Bennett, M., Belsky, D. W., Linnér, R. K., Ahlskog, R., Kleinman, A., et al. (2021) · Nature Human Behaviour · doi:10.1038/s41562-021-01119-3 · Cited by 179
Self-citationEvaluating and improving heritability models using summary statistics
Speed, D., Holmes, J., & Balding, D. J. (2020) · Nature Genetics · doi:10.1038/s41588-020-0600-y · Cited by 168
EMBRACE, Dunning, A. M., Collaborators, G. S., HEBON, kConFab Investigators, Michailidou, K., Kuchenbaecker, K. B., Thompson, D., French, J. D., Beesley, J., et al. (2016) · Nature Genetics · doi:10.1038/ng.3521 · Cited by 161
Self-citationSociology, Genetics, and the Coming of Age of Sociogenomics
Mills, M. C., & Tropf, F. C. (2020) · Annual Review of Sociology · doi:10.1146/annurev-soc-121919-054756 · Cited by 162
Rizzardi, L. F., Hickey, P. F., Rodriguez DiBlasi, V., Tryggvadóttir, R., Callahan, C. M., Idrizi, A., Hansen, K. D., & Feinberg, A. P. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0297-8 · Cited by 146
Childhood obesity and central precocious puberty
Shi, L., Jiang, Z., & Zhang, L. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1056871 · Cited by 146
Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patients
Kagami, M., Nagasaki, K., Kosaki, R., Horikawa, R., Naiki, Y., Saitoh, S., Tajima, T., Yorifuji, T., Numakura, C., Mizuno, S., et al. (2017) · Genetics in Medicine · doi:10.1038/gim.2017.53 · Cited by 144
Avendaño, M. S., Vazquez, M. J., & Tena‐Sempere, M. (2017) · Human Reproduction Update · doi:10.1093/humupd/dmx025 · Cited by 143
Genetic evidence for natural selection in humans in the contemporary United States
Beauchamp, J. P. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1600398113 · Cited by 138
PLAG1 and NCAPG‐LCORL in livestock
Takasuga, A. (2015) · Animal Science Journal · doi:10.1111/asj.12417 · Cited by 138
Adult Consequences of Self-Limited Delayed Puberty
Zhu, J., & Chan, Y.-M. (2017) · PEDIATRICS · doi:10.1542/peds.2016-3177 · Cited by 133
Wells, J. C. K., & Stock, J. T. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00325 · Cited by 139
Cassatella, D., Howard, S. R., Acierno, J. S., Xu, C., Papadakis, G. E., Santoni, F. A., Dwyer, A. A., Santini, S., Sykiotis, G. P., Chambion, C., et al. (2018) · European Journal of Endocrinology · doi:10.1530/eje-17-0568 · Cited by 131
Shared genetic aetiology of puberty timing between sexes and with health-related outcomes
Day, F. R., Bulik-Sullivan, B. K., Hinds, D. A., Finucane, H. K., Murabito, J. M., Tung, J. Y., Ong, K. K., & Perry, J. R. B. (2015) · Nature Communications · doi:10.1038/ncomms9842 · Cited by 131
Self-citationA new pathway in the control of the initiation of puberty: the MKRN3 gene
Abreu, A. P., Macedo, D. B., Brito, V. N., Kaiser, U. B., & Latronico, A. C. (2015) · Journal of Molecular Endocrinology · doi:10.1530/jme-14-0315 · Cited by 126
Disruption of Circadian Rhythms: A Crucial Factor in the Etiology of Infertility
Sciarra, F., Franceschini, E., Campolo, F., Gianfrilli, D., Pallotti, F., Paoli, D., Isidori, A. M., & Venneri, M. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21113943 · Cited by 132
Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
Yap, C. X., Sidorenko, J., Wu, Y., Kemper, K. E., Yang, J., Wray, N. R., Robinson, M. R., & Visscher, P. M. (2018) · Nature Communications · doi:10.1038/s41467-018-07862-y · Cited by 124
Yarmolinsky, J., Bull, C. J., Vincent, E. E., Robinson, J., Walther, A., Smith, G. D., Lewis, S. J., Relton, C. L., & Martin, R. M. (2020) · JAMA · doi:10.1001/jama.2020.0150 · Cited by 124
Insights into imprinting from parent-of-origin phased methylomes and transcriptomes
Zink, F., Magnúsdóttir, D. N., Magnússon, Ó. Þ., Walker, N. J., Morris, T. J., Sigurðsson, Á., Halldorsson, G. H., Gudjonsson, S. A., Melsted, P., Ingimundardóttir, H., et al. (2018) · Nature Genetics · doi:10.1038/s41588-018-0232-7 · Cited by 123
Self-citationFarello, G., Altieri, C., Cutini, M., Pozzobon, G. C., & Verrotti, A. (2019) · Frontiers in Pediatrics · doi:10.3389/fped.2019.00147 · Cited by 131
The Role of Growth Hormone on Ovarian Functioning and Ovarian Angiogenesis
Devesa, J., & Caicedo, D. (2019) · Frontiers in Endocrinology · doi:10.3389/fendo.2019.00450 · Cited by 120
DLK1 Is a Novel Link Between Reproduction and Metabolism
Gomes, L. G., Cunha-Silva, M., Crespo, R. P., Ramos, C. O., Montenegro, L. R., Canton, A. P. M., Lees, M. M., Spoudeas, H. A., Dauber, A. N., Macedo, D. B., et al. (2018) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2018-02010 · Cited by 119
Mbarek, H., Steinberg, S., Nyholt, D. R., Gordon, S. D., Miller, M., McRae, A. F., Hottenga, J., Day, F. R., Willemsen, G. A. H. M., de Geus, E. J. C., et al. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2016.03.008 · Cited by 120
Self-citationSinclair‐Waters, M., Ødegård, J., Korsvoll, S. A., Moen, T., Lien, S., Primmer, C. R., & Barson, N. J. (2020) · Genetics Selection Evolution · doi:10.1186/s12711-020-0529-8 · Cited by 124
Detecting Polygenic Adaptation in Admixture Graphs
Racimo, F., Berg, J. J., & Pickrell, J. K. (2018) · Genetics · doi:10.1534/genetics.117.300489 · Cited by 118
The Congenital and Acquired Mechanisms Implicated in the Etiology of Central Precocious Puberty
Brito, V. N., Canton, A. P. M., Seraphim, C. E., Abreu, A. P., Macedo, D. B., Mendonca, B. B., Kaiser, U. B., Argente, J., & Latronico, A. C. (2022) · Endocrine Reviews · doi:10.1210/endrev/bnac020 · Cited by 119
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
Duffy, D. L., Zhu, G., Li, X., Sanna, M., Iles, M. M., Jacobs, L. C., Evans, D. M., Yazar, S., Beesley, J., Law, M. H., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06649-5 · Cited by 115
Self-citationDelayed Puberty—Phenotypic Diversity, Molecular Genetic Mechanisms, and Recent Discoveries
Howard, S. R., & Dunkel, L. (2019) · Endocrine Reviews · doi:10.1210/er.2018-00248 · Cited by 116
Roberts, S. A., & Kaiser, U. B. (2020) · European Journal of Endocrinology · doi:10.1530/eje-20-0103 · Cited by 118
Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty
Simon, D., Ba, I., Mekhail, N., Écosse, E., Paulsen, A., Zénaty, D., Houang, M., Jésuran-Pérelroizen, M., FILIPPO, G. D., Salerno, M., et al. (2015) · European Journal of Endocrinology · doi:10.1530/eje-15-0488 · Cited by 115
Quach, B. C., Bray, M. A., Gaddis, N., Liu, M., Palviainen, T., Minică, C. C., Zellers, S. M., Sherva, R., Alıev, F., Nothnagel, M., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19265-z · Cited by 113
Self-citationSequeira, M., Lewis, S. J., Bonilla, C., Smith, G. D., & Joinson, C. J. (2016) · The British Journal of Psychiatry · doi:10.1192/bjp.bp.115.168617 · Cited by 118
A Shared Genetic Basis for Self-Limited Delayed Puberty and Idiopathic Hypogonadotropic Hypogonadism
Zhu, J., Choa, R., Guo, M. H., Plummer, L., Buck, C. L., Palmert, M. R., Hirschhorn, J. N., Seminara, S. B., & Chan, Y.-M. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2015-1080 · Cited by 112
Maione, L., Bouvattier, C. M., & Kaiser, U. B. (2021) · Clinical Endocrinology · doi:10.1111/cen.14475 · Cited by 113
MKRN3 Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis
Valadares, L. P., Meireles, C. G., de Toledo, I. P., Oliveira, R., Castro, L. C., Abreu, A. P., Carroll, R. S., Latronico, A. C., Kaiser, U. B., Guerra, E. N. S., et al. (2019) · Journal of the Endocrine Society · doi:10.1210/js.2019-00041 · Cited by 106
Endocrine-Disrupting Chemicals and Their Effects during Female Puberty: A Review of Current Evidence
Lucaccioni, L., Trevisani, V., Marrozzini, L., Bertoncelli, N. M., Predieri, B., Lugli, L., Berardi, A., & Iughetti, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21062078 · Cited by 106
Breast cancer risk factors and their effects on survival: a Mendelian randomisation study
Escala-Garcia, M., Morra, A., Canisius, S., Chang-Claude, J. C., Kar, S., Zheng, W., Bojesen, S. E., Easton, D. F., Pharoah, P. D. P., & Schmidt, M. K. (2020) · BMC Medicine · doi:10.1186/s12916-020-01797-2 · Cited by 109
Self-citationPhenotype-Specific Enrichment of Mendelian Disorder Genes near GWAS Regions across 62 Complex Traits
Freund, M. K., Burch, K. S., Shi, H., Mancuso, N., Kichaev, G., Garske, K. M., Pan, D. Z., Miao, Z., Mohlke, K. L., Laakso, M., et al. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2018.08.017 · Cited by 102
Epigenetic regulation of puberty via Zinc finger protein-mediated transcriptional repression
Lomniczi, A., Wright, H., Castellano, J. M., Matagne, V., Toro, C. A., Ramaswamy, S., Plant, T. M., & Ojeda, S. R. (2015) · Nature Communications · doi:10.1038/ncomms10195 · Cited by 103
Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants
Hauberg, M. E., Roussos, P., Grove, J., Børglum, A. D., & Mattheisen, M. (2016) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2015.3018 · Cited by 105
Age at menarche and adult body mass index: a Mendelian randomization study
Gill, D., Brewer, C. F., Fabiola Del Greco, M., Sivakumaran, P., Bowden, J., Sheehan, N. A., & Minelli, C. (2018) · International Journal of Obesity · doi:10.1038/s41366-018-0048-7 · Cited by 105
Perez, J. D., Rubinstein, N. D., & Dulac, C. G. (2016) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113708 · Cited by 106
Heilmann‐Heimbach, S., Herold, C., Hochfeld, L. M., Hillmer, A. M., Nyholt, D. R., Hecker, J., Javed, A., Chew, E. G. Y., Pechlivanis, S., Drichel, D., et al. (2017) · Nature Communications · doi:10.1038/ncomms14694 · Cited by 101
Self-citationEarly-life exposure to endocrine-disrupting chemicals and pubertal development in girls
Lee, J. E., Jung, H. W., Lee, Y. J., & Lee, Y. A. (2019) · Annals of Pediatric Endocrinology & Metabolism · doi:10.6065/apem.2019.24.2.78 · Cited by 99
Mobley, K. B., Aykanat, T., Czorlich, Y., House, A. H., Kurko, J., Miettinen, A., Moustakas-Verho, J. E., Salgado, A., Sinclair‐Waters, M., Verta, J., et al. (2021) · Reviews in Fish Biology and Fisheries · doi:10.1007/s11160-021-09656-w · Cited by 98
The epigenomic landscape of African rainforest hunter-gatherers and farmers
Fagny, M., Patin, É., MacIsaac, J. L., Rotival, M., Flutre, T., Jones, M. J., Siddle, K. J., Quach, H., Harmant, C., McEwen, L. M., et al. (2015) · Nature Communications · doi:10.1038/ncomms10047 · Cited by 97
Pubertal development in healthy children is mirrored by DNA methylation patterns in peripheral blood
Almstrup, K., Johansen, M. L., Busch, A. S., Hagen, C. P., Nielsen, J. E., Petersen, J. H., & Juul, A. (2016) · Scientific Reports · doi:10.1038/srep28657 · Cited by 94
Stamou, M. I., Cox, K. H., & Crowley, W. F. (2015) · Endocrine Reviews · doi:10.1210/er.2015-1045 · Cited by 91
RetractedPutative Effects of Obesity on Linear Growth and Puberty
Shalitin, S., & Kieß, W. (2017) · Hormone Research in Paediatrics · doi:10.1159/000455968 · Cited by 91
Ostrom, Q. T., Kinnersley, B., Wrensch, M., Eckel‐Passow, J. E., Armstrong, G., Rice, T., Chen, Y., Wiencke, J. K., Mccoy, L. S., Hansen, H. M., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-24580-z · Cited by 93
Self-citationVitamin D Receptor Signaling and Cancer
Campbell, M. J., & Trump, D. L. (2017) · Endocrinology and Metabolism Clinics of North America · doi:10.1016/j.ecl.2017.07.007 · Cited by 91
Genome sequencing in the clinic: the past, present, and future of genomic medicine
Prokop, J. W., May, T., Strong, K. A., Bilinovich, S. M., Bupp, C. P., Rajasekaran, S., Worthey, E. A., & Lazar, J. (2018) · Physiological Genomics · doi:10.1152/physiolgenomics.00046.2018 · Cited by 89
Sex-specific genetic effects across biomarkers
Flynn, E., Tanigawa, Y., Rodríguez, F., Altman, R. B., Sinnott-Armstrong, N., & Rivas, M. A. (2020) · European Journal of Human Genetics · doi:10.1038/s41431-020-00712-w · Cited by 89
Hagen, C. P., Sørensen, K., Mieritz, M. G., Johannsen, T. H., Almstrup, K., & Juul, A. (2015) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-4462 · Cited by 86
Metadata
- Authors
- Study, A. O. C., Perry, J. R. B., The GENICA Network, kConFab, Study, T. L. C., The InterAct Consortium, Early Growth Genetics (EGG) Consortium, Day, F., Elks, C. E., Sulem, P., Thompson, D. J., Ferreira, T., He, C., Chasman, D. I., Esko, T., Thorleifsson, G., Albrecht, E., Ang, W. Q., Corre, T., Cousminer, D. L., Feenstra, B., Franceschini, N., Ganna, A., Johnson, A. D., Kjellqvist, S., Lunetta, K. L., McMahon, G., Nolte, I. M., Paternoster, L., Porcu, E., Smith, A. V., Stolk, L., Teumer, A., Tšernikova, N., Tikkanen, E., Ulivi, S., Wagner, E. K., Amin, N., Bierut, L. J., Byrne, E. M., Hottenga, J.-J., Koller, D. L., Mangino, M., Pers, T. H., Yerges-Armstrong, L. M., Hua Zhao, J., Andrulis, I. L., Anton-Culver, H., Atsma, F., Bandinelli, S., Beckmann, M. W., Benitez, J., Blomqvist, C., Bojesen, S. E., Bolla, M. K., Bonanni, B., Brauch, H., Brenner, H., Buring, J. E., Chang-Claude, J., Chanock, S., Chen, J., Chenevix-Trench, G., Collée, J. M., Couch, F. J., Couper, D., Coviello, A. D., Cox, A., Czene, K., D’adamo, A. P., Davey Smith, G., De Vivo, I., Demerath, E. W., Dennis, J., Devilee, P., Dieffenbach, A. K., Dunning, A. M., Eiriksdottir, G., Eriksson, J. G., Fasching, P. A., Ferrucci, L., Flesch-Janys, D., Flyger, H., Foroud, T., Franke, L., Garcia, M. E., García-Closas, M., Geller, F., de Geus, E. E. J., Giles, G. G., Gudbjartsson, D. F., Gudnason, V., Guénel, P., Guo, S., Hall, P., Hamann, U., Haring, R., Hartman, C. A., Heath, A. C., Hofman, A., Hooning, M. J., Hopper, J. L., Hu, F. B., Hunter, D. J., Karasik, D., Kiel, D. P., Knight, J. A., Kosma, V.-M., Kutalik, Z., Lai, S., Lambrechts, D., Lindblom, A., Mägi, R., Magnusson, P. K., Mannermaa, A., Martin, N. G., Masson, G., McArdle, P. F., McArdle, W. L., Melbye, M., Michailidou, K., Mihailov, E., Milani, L., Milne, R. L., Nevanlinna, H., Neven, P., Nohr, E. A., Oldehinkel, A. J., Oostra, B. A., Palotie, A., Peacock, M., Pedersen, N. L., Peterlongo, P., Peto, J., Pharoah, P. D. P., Postma, D. S., Pouta, A., Pylkäs, K., Radice, P., Ring, S., Rivadeneira, F., Robino, A., Rose, L. M., Rudolph, A., Salomaa, V., Sanna, S., Schlessinger, D., Schmidt, M. K., Southey, M. C., Sovio, U., Stampfer, M. J., Stöckl, D., Storniolo, A. M., Timpson, N. J., Tyrer, J., Visser, J. A., Vollenweider, P., Völzke, H., Waeber, G., Waldenberger, M., Wallaschofski, H., Wang, Q., Willemsen, G., Winqvist, R., Wolffenbuttel, B. H. R., Wright, M. J., Boomsma, D. I., Econs, M. J., Khaw, K.-T., Loos, R. J. F., McCarthy, M. I., Montgomery, G. W., Rice, J. P., Streeten, E. A., Thorsteinsdottir, U., van Duijn, C. M., Alizadeh, B. Z., Bergmann, S., Boerwinkle, E., Boyd, H. A., Crisponi, L., Gasparini, P., Gieger, C., Harris, T. B., Ingelsson, E., Järvelin, M.-R., Kraft, P., Lawlor, D., Metspalu, A., Pennell, C. E., Ridker, P. M., Snieder, H., Sørensen, T. I. A., Spector, T. D., Strachan, D. P., Uitterlinden, A. G., Wareham, N. J., Widen, E., Zygmunt, M., Murray, A., Easton, D. F., Stefansson, K., Murabito, J. M., & Ong, K. K.
- Affiliations
- Centre for Human Genetics (GB)
- University of Bonn (DE)
- deCODE Genetics (Iceland) (IS)
- University of Cambridge (GB)
- Indiana University Health (US)
- Brigham and Women's Hospital (US)
- Broad Institute (US)
- Statens Serum Institut (DK)
- University of North Carolina at Chapel Hill (US)
- SIB Swiss Institute of Bioinformatics (CH)
- Boston University (US)
- Karolinska Institutet (SE)
- Science for Life Laboratory (SE)
- University of Bristol (GB)
- University Medical Center Groningen (NL)
- Universitätsmedizin Greifswald (DE)
- University of Sassari (IT)
- University of Helsinki (FI)
- IRCCS Materno Infantile Burlo Garofolo (IT)
- Erasmus MC (NL)
- The University of Queensland (AU)
- King's College London (GB)
- University of Maryland, Baltimore (US)
- Mount Sinai Hospital (CA)
- University of Copenhagen (DK)
- Friedrich-Alexander-Universität Erlangen-Nürnberg (DE)
- Spanish National Cancer Research Centre (ES)
- German Cancer Research Center (DE)
- Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology (DE)
- Mayo Clinic (US)
- University of Minnesota (US)
- Institute of Cancer Research (GB)
- National Institutes of Health (US)
- The University of Melbourne (AU)
- University of Iceland (IS)
- Université Paris-Sud (FR)
- Washington University in St. Louis (US)
- Harvard University (US)
- Beth Israel Deaconess Medical Center (US)
- University of Eastern Finland (FI)
- QIMR Berghofer Medical Research Institute (AU)
- University of Tartu (EE)
- University of Southern Denmark (DK)
- Finnish Institute for Health and Welfare (FI)
- Oulu University Hospital (FI)
- University of Trieste (IT)
- National Research Council (IT)
- The Netherlands Cancer Institute (NL)
- Centre Hospitalier Universitaire Vaudois (CH)
- Vrije Universiteit Amsterdam (NL)
- Icahn School of Medicine at Mount Sinai (US)
- Churchill Hospital (GB)
- Centre for Medical Systems Biology (NL)
- Helmholtz Munich (DE)
- Uppsala University (SE)
- The University of Western Australia (AU)
- St George's, University of London (GB)
- University of Exeter (GB)
- Corresponding author
- Perry, John R. B.
- Murabito, Joanne M.
- ORCID
- Perry, John R. B.
- Day, Felix
- Sulem, Patrick
- Thompson, Deborah J.
- Ferreira, Teresa
- He, Chunyan
- Chasman, Daniel I.
- Esko, Tõnu
- Corre, Tanguy
- Feenstra, Bjarke
- Franceschini, Nora
- Ganna, Andrea
- Johnson, Andrew D.
- Lunetta, Kathryn L.
- Nolte, Ilja M.
- Paternoster, Lavinia
- Porcu, Eleonora
- Smith, Albert V.
- Teumer, Alexander
- Tikkanen, Emmi
- Ulivi, Sheila
- Amin, Najaf
- Bierut, Laura J.
- Byrne, Enda M.
- Hottenga, Jouke-Jan
- Mangino, Massimo
- Pers, Tune H.
- Yerges-Armstrong, Laura M.
- Andrulis, Irene L.
- Atsma, Femke
- Bandinelli, Stefania
- Beckmann, Matthias W.
- Benitez, Javier
- Blomqvist, Carl
- Bojesen, Stig E.
- Bolla, Manjeet K.
- Bonanni, Bernardo
- Brauch, Hiltrud
- Brenner, Hermann
- Buring, Julie E.
- Chang-Claude, Jenny
- Chanock, Stephen
- Chen, Jinhui
- Couch, Fergus J.
- Couper, David
- Coviello, Andrea D.
- Cox, Angela
- Czene, Kamila
- Demerath, Ellen W.
- Dennis, Joe
- Devilee, Peter
- Dunning, Alison M.
- Eriksson, Johan G.
- Fasching, Peter A.
- Ferrucci, Luigi
- Foroud, Tatiana
- Franke, Lude
- Geller, Frank
- Giles, Graham G.
- Gudbjartsson, Daniel F.
- Gudnason, Vilmundur
- Guénel, Pascal
- Guo, Suiqun
- Hall, Per
- Hamann, Ute
- Haring, Robin
- Hartman, Catharina A.
- Heath, Andrew C.
- Hooning, Maartje J.
- Hopper, John L.
- Hu, Frank B.
- Karasik, David
- Kiel, Douglas P.
- Knight, Julia A.
- Lai, Sandra
- Lambrechts, Diether
- Lindblom, Annika
- Mägi, Reedik
- Magnusson, Patrik K.
- Martin, Nicholas G.
- McArdle, Patrick F.
- McArdle, Wendy L.
- Melbye, Mads
- Michailidou, Kyriaki
- Milani, Lili
- Milne, Roger L.
- Nevanlinna, Heli
- Neven, Patrick
- Nohr, Ellen A.
- Oldehinkel, Albertine J.
- Palotie, Aarno
- Peacock, Munro
- Pedersen, Nancy L.
- Peterlongo, Paolo
- Peto, Julian
- Pharoah, Paul D. P.
- Postma, Dirkje S.
- Pylkäs, Katri
- Radice, Paolo
- Ring, Susan
- Rivadeneira, Fernando
- Robino, Antonietta
- Rose, Lynda M.
- Rudolph, Anja
- Salomaa, Veikko
- Sanna, Serena
- Schmidt, Marjanka K.
- Sovio, Ulla
- Stampfer, Meir J.
- Storniolo, Anna M.
- Timpson, Nicholas J.
- Tyrer, Jonathan
- Völzke, Henry
- Wang, Qin
- Willemsen, Gonneke
- Winqvist, Robert
- Wolffenbuttel, Bruce H. R.
- Wright, Margaret J.
- Boomsma, Dorret I.
- Econs, Michael J.
- Khaw, Kay-Tee
- Loos, Ruth J. F.
- McCarthy, Mark I.
- Montgomery, Grant W.
- Rice, John P.
- Streeten, Elizabeth A.
- Alizadeh, Behrooz Z.
- Bergmann, Sven
- Boerwinkle, Eric
- Boyd, Heather A.
- Crisponi, Laura
- Gasparini, Paolo
- Gieger, Christian
- Harris, Tamara B.
- Ingelsson, Erik
- Järvelin, Marjo-Riitta
- Kraft, Peter
- Lawlor, Debbie
- Metspalu, Andres
- Pennell, Craig E.
- Ridker, Paul M.
- Snieder, Harold
- Sørensen, Thorkild I. A.
- Spector, Tim D.
- Strachan, David P.
- Uitterlinden, André G.
- Wareham, Nicholas J.
- Zygmunt, Marek
- Murray, Anna
- Easton, Douglas F.
- Murabito, Joanne M.
- Ong, Ken K.
- Venue
- Nature
- Published
- 2014-07-23
- Volume
- 514
- Issue
- 7520
- Pages
- 92-97
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4185210
- OpenAlex
- W2155441570
- Cited by
- 604
- References
- 78
- Citations by year
- 2026: 13 · 2025: 35 · 2024: 55 · 2023: 42 · 2022: 45 · 2021: 41 · 2020: 49 · 2019: 81 · 2018: 69 · 2017: 58 · 2016: 59 · 2015: 50 · 2014: 5
- FWCI
- 69.48
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- other-oa
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion, other-oa)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (publishedVersion, other-oa)
- VU Research Portal (publishedVersion, other-oa)
- University of Southern Denmark Research Portal (University of Southern Denmark) (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- St George's Online Research Archive (St George's University of London) (acceptedVersion)
- Open Research Exeter (University of Exeter) (acceptedVersion)
- LSHTM Research Online (London School of Hygiene and Tropical Medicine) (acceptedVersion)
- IRIS (submittedVersion)
- Lirias (KU Leuven) (submittedVersion, other-oa)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- UWA Profiles and Research Repository (UWA) (submittedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Leiden Repository (Leiden University) (submittedVersion)
- ArTS Archivio della ricerca di Trieste (University of Trieste https://www.units.it/) (submittedVersion)
- Minerva Access (University of Melbourne) (submittedVersion)
- Research Portal (King's College London) (submittedVersion)
- Site cant be reached (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion)
- Bristol Research (University of Bristol) (submittedVersion)
- IUScholarWorks (Indiana University) (submittedVersion)
- Purdue University Indianapolis (Indiana University) (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion, other-oa)
- Spiral (Imperial College London) (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Funders
- Brigham and Women's Hospital
- University of Minnesota
- School of Medicine, Boston University
- Helsingin Yliopisto
- Helsingin ja Uudenmaan Sairaanhoitopiiri
- Deutsches Krebsforschungszentrum
- Wellcome Trust (098381, 102215)
- QIMR Berghofer Medical Research Institute
- Cancer Research UK (10119, 16561, 16565, 10118, 16563, 11022, 10124)
- National Institute for Health and Care Research (NF-SI-0512-10114)
- Universiteit Leiden
- Rijksuniversiteit Groningen
- Eberhard Karls Universität Tübingen
- Gentofte Hospital
- Herlev Hospital
- Novo Nordisk
- Leids Universitair Medisch Centrum
- Oulun Yliopisto
- Uppsala Universitet
- Science for Life Laboratory
- Faculty of Health and Medical Sciences, University of Western Australia
- Novo Nordisk Foundation Center for Basic Metabolic Research
- Deutschen Konsortium für Translationale Krebsforschung
- Terveyden ja hyvinvoinnin laitos
- National Institutes of Health (UL1TR001108, 20892, MD 20892)
- University of North Carolina at Chapel Hill
- School of Medicine, Indiana University
- Geriatric Research Education and Clinical Center
- Medical Research Council (MR/J012165/1, MC_UU_12015/2, MC_PC_15018, MC_UU_12015/1)
- Det Sundhedsvidenskabelige Fakultet, Københavns Universitet
- Erasmus Universitair Medisch Centrum Rotterdam
- Biocenter, University of Oulu
- National Institute on Aging (U01AG049505, R01AG041517)
- National Cancer Institute (MD 20892, 20892, P50CA116201)
- National Institute of Neurological Disorders and Stroke (R01NS017950)
- NIH Clinical Center
- National Center for Advancing Translational Sciences
- Division of Cancer Epidemiology and Genetics, National Cancer Institute
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Syndromes and Imprinting
- Keywords
- age at menarche, puberty timing, parent-of-origin effects, genomic imprinting, nuclear receptors, retinoic acid signaling, body mass index, KCNK9, genetic architecture, European women
- MeSH terms
- Adolescent, Age Factors, Alleles, Breast Neoplasms, Calcium-Binding Proteins, Cardiovascular Diseases, Child, Diabetes Mellitus, Type 2, Europe, Female, Humans, Hypothalamo-Hypophyseal System, Male, Membrane Proteins, Menarche, Obesity, Ovary, Parents, Proteins, Ribonucleoproteins, Body Mass Index, Receptors, GABA-B, Receptors, Retinoic Acid, Genomic Imprinting, Polymorphism, Single Nucleotide, Potassium Channels, Tandem Pore Domain, Intercellular Signaling Peptides and Proteins, Quantitative Trait Loci, Ubiquitin-Protein Ligases, Intracellular Signaling Peptides and Proteins, Genome-Wide Association Study, Genetic Loci, Intrinsically Disordered Proteins
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