Items where authors include "Lees, M"

Article

Al-Jawahiri, R orcid.org/0000-0002-5689-3368, Foroutan, A, Kerkhof, J et al. (111 more authors) (2022) SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile. Genetics in Medicine, 24 (6). pp. 1261-1273. ISSN 1098-3600

Rossi, C, Lees, M, Mehta, V et al. (9 more authors) (2020) Comparison of Efficiency and Function of Vascular Endothelial Growth Factor Adenovirus Vectors in Endothelial Cells for Gene Therapy of Placental Insufficiency. Human Gene Therapy, 31 (21-22). pp. 1190-1202. ISSN 1043-0342

Rossi, C, Lees, M, Mehta, V et al. (9 more authors) (2020) Comparison of Efficiency and Function of Vascular Endothelial Growth Factor Adenovirus Vectors in Endothelial Cells for Gene Therapy of Placental Insufficiency. Human Gene Therapy, 31 (21-22). pp. 1190-1202. ISSN 1043-0342

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

Spencer, R, Rossi, C, Lees, M et al. (9 more authors) (2019) Achieving orphan designation for placental insufficiency: annual incidence estimations in Europe. BJOG: An International Journal of Obstetrics & Gynaecology, 126 (9). pp. 1157-1167. ISSN 1470-0328

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

Bengani, H, Handley, M orcid.org/0000-0001-7200-747X, Alvi, M et al. (31 more authors) (2017) Clinical and molecular consequences of disease-associated de novo mutations in SATB2. Genetics in Medicine, 19 (8). pp. 900-908. ISSN 1098-3600

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)

Kang, Y-J, Lees, M, Matthews, LC et al. (3 more authors) (2015) miR-145 suppresses embryo–epithelial juxtacrine communication at implantation by modulating maternal IGF1R. Journal of Cell Science, 128 (4). pp. 804-814. ISSN 0021-9533

Forbes, K, Lees, M, Kang, Y-J et al. (2 more authors) (2014) O-079 Regulation of Implantation by Interaction between the Type-1 IGF Receptor (IGF1R) and MiR-145. Reproductive Sciences, 21 (3). 102A-102A. ISSN 1933-7191