Items where authors include "Rankin, J"

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Number of items: 12.

Article

Aggarwal, D, Warne, B, Jahun, AS et al. (725 more authors) (2022) Genomic epidemiology of SARS-CoV-2 in a UK university identifies dynamics of transmission. Nature Communications, 13 (1). 751. ISSN 2041-1723

Aitken, S, Firth, HV, McRae, J et al. (280 more authors) (2019) Finding diagnostically useful patterns in quantitative phenotypic data. The American Journal of Human Genetics, 105 (5). pp. 933-946. ISSN 0002-9297

Blok, LS, Rousseau, J, Twist, J et al. (77 more authors) (2019) Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications, 10. 2079. ISSN 2041-1723

Snijders Blok, L, Rousseau, J, Twist, J et al. (76 more authors) (2018) CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications, 9 (1). 4619. ISSN 2041-1723

Snijders Blok, L, Rousseau, J, Twist, J et al. (76 more authors) (2018) CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Nature Communications, 9 (1). 4619. ISSN 2041-1723

Whitworth, J, Smith, PS, Martin, J-E et al. (330 more authors) (2018) Comprehensive cancer-predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes. The American Journal of Human Genetics, 103 (1). pp. 3-18. ISSN 0002-9297

Best, KE, Tennant, PWG orcid.org/0000-0003-1555-069X and Rankin, J (2017) Survival, by birth weight and gestational age, in individuals with congenital heart disease: a population-based study. Journal of the American Heart Association, 6 (e005213). ISSN 2047-9980

Glinianaia, SV, Tennant, PWG orcid.org/0000-0003-1555-069X and Rankin, J (2017) Risk estimates of recurrent congenital anomalies in the UK: a population-based register study. BMC Medicine, 15 (20). ISSN 1741-7015

McRae, JF, Clayton, S, Fitzgerald, TW et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542. pp. 433-438. ISSN 0028-0836

McRae, JF, Clayton, S, Fitzgerald, TW et al. (298 more authors) (2016) Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study. bioRxiv. (Submitted)

Tennant, PWG, Glinianaia, SV, Bilous, RW et al. (2 more authors) (2014) Pre-existing diabetes, maternal glycated haemoglobin, and the risks of fetal and infant death: A population-based study. Diabetologia, 57 (2). pp. 285-294. ISSN 0012-186X

McParlin, C, Robson, SC, Tennant, PWG orcid.org/0000-0003-1555-069X et al. (5 more authors) (2010) Objectively measured physical activity during pregnancy: a study in obese and overweight women. BMC Pregnancy and Childbirth, 10 (1). 76.

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