The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Risk factors for congenital anomaly in a multiethnic birth cohort: an analysis of the Born in Bradford study
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“One study reported associations between education level and congenital anomalies106 with significantly increased odds of congenital anomalies for educational attainment levels below a diploma, degree or higher degree qualification (online supplemental appendix S11, table z).”
From Socioeconomic inequalities and adverse pregnancy outcomes in the UK and Republic of Ireland: a systematic review and meta-analysis (2021) · cites this paper as [106]
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Cites
Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report
Hamamy, H., Antonarakis, S. E., Cavalli-Sforza, L. L., Temtamy, S., Romeo, G., Ten Kate, L. P., Bennett, R. L., Shaw, A., Megarbane, A., van Duijn, C., et al. (2011) · Genetics in Medicine · doi:10.1097/gim.0b013e318217477f · Cited by 345
Quantification of homozygosity in consanguineous individuals with autosomal recessive disease
Woods, C. G., Cox, J., Springell, K., Hampshire, D. J., Mohamed, M. D., McKibbin, M., Stern, R., Raymond, F. L., Sandford, R., Malik Sharif, S., et al. (2006) · The American Journal of Human Genetics · doi:10.1086/503875 · Cited by 262
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Cited by
Prevalence and architecture of de novo mutations in developmental disorders
Study, D. D. D. (2017) · Nature · doi:10.1038/nature21062 · Cited by 1,480
Health and population effects of rare gene knockouts in adult humans with related parents
Narasimhan, V. M., Hunt, K. A., Mason, D., Baker, C. L., Karczewski, K. J., Barnes, M. R., Barnett, A. H., Bates, C., Bellary, S., Bockett, N. A., et al. (2016) · Science · doi:10.1126/science.aac8624 · Cited by 286
Self-citationQuantifying the contribution of recessive coding variation to developmental disorders
Martin, H. C., Jones, W. D., McIntyre, R., Sanchez-Andrade, G., Sanderson, M., Stephenson, J. D., Jones, C. P., Handsaker, J., Gallone, G., Bruntraeger, M., et al. (2018) · Science · doi:10.1126/science.aar6731 · Cited by 201
Thomson, K., Moffat, M., Arisa, O., Jesurasa, A., Richmond, C., Odeniyi, A., Bambra, C., Rankin, J., Brown, H., Bishop, J., et al. (2021) · BMJ Open · doi:10.1136/bmjopen-2020-042753 · Cited by 154
McRae, J. F., Clayton, S., Fitzgerald, T. W., Kaplanis, J., Prigmore, E., Rajan, D., Sifrim, A., Aitken, S., Akawi, N., Alvi, M., et al. (2016) · doi:10.1101/049056 · Cited by 30
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Metadata
- Authors
- Sheridan, E., Wright, J., Small, N., Corry, P. C., Oddie, S., Whibley, C., Petherick, E. S., Malik, T., Pawson, N., McKinney, P. A., & Parslow, R. C.
- Venue
- The Lancet
- Publisher
- Elsevier BV
- Published
- 2013-10
- Volume
- 382
- Issue
- 9901
- Pages
- 1350-1359
- ISSN
- 0140-6736
- Cited by
- 215
- References
- 2
- Language
- en
- Funders
- National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care (CLAHRC) programme (KRD/012/001/006)
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.