Dr Jillian Bryce
- Project Manager (Medicine)
telephone:
01414515843
email:
Jillian.Bryce@glasgow.ac.uk
School of Medicine, Child Health, Level 0, Zone 1, Office Block (Paediatrics), Queen Elizabeth University Hospital Campus, Govan Rd, Glasgow, G51 4TF
https://orcid.org/0000-0002-4316-9477Publications
2023
Scougall, K. et al. (2023) Predictors of surgical complications in boys with hypospadias: data from an international registry. World Journal of Pediatric Surgery, 6, e000599. (doi: 10.1136/wjps-2023-000599) (PMID:37860275) (PMCID:PMC10582860)
Tseretopoulou, X., Bryce, J. , Chen, M., McMillan, M., Lucas-Herald, A. K. , Ali, S. R. and Ahmed, S.F. (2023) The I‐CAH registry: a platform for international collaboration for improving knowledge and clinical care in congenital adrenal hyperplasia. Clinical Endocrinology, (doi: 10.1111/cen.14961) (PMID:37602832) (Early Online Publication)
Righi, B. et al. (2023) Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia. Endocrine, 80(3), pp. 630-638. (doi: 10.1007/s12020-023-03330-w) (PMID:36857009) (PMCID:PMC10199864)
Nowotny, H. F. et al. (2023) Outcome of COVID-19 infections in patients with adrenal insufficiency and excess. Endocrine Connections, 12(4), e220416. (doi: 10.1530/EC-22-0416) (PMID:36715679) (PMCID:PMC10083676)
2022
Lawrence, N. et al. (2022) Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry. Clinical Endocrinology, 97(5), pp. 551-561. (doi: 10.1111/cen.14796) (PMID:35781728)
Neumann, U. et al. (2022) Treatment of congenital adrenal hyperplasia in children aged 0–3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure. European Journal of Endocrinology, 186(5), pp. 587-596. (doi: 10.1530/eje-21-1085) (PMID:35290211) (PMCID:PMC9066592)
2021
Ali, S. R., Bryce, J. , Kodra, Y., Taruscio, D., Persani, L. and Ahmed, S. F. (2021) The quality evaluation of rare disease registries—an assessment of the essential features of a disease registry. International Journal of Environmental Research and Public Health, 18(22), 11968. (doi: 10.3390/ijerph182211968) (PMID:34831724) (PMCID:PMC8620980)
Lucas-Herald, A. K. et al. (2021) Gonadectomy in conditions affecting sex development – a registry-based cohort study. European Journal of Endocrinology, 184(6), pp. 791-801. (doi: 10.1530/EJE-20-1058) (PMID:33780351)
Ali, S.R., Bryce, J. , Smythe, C., Hytiris, M., Priego, A.L., Appelman-Dijkstra, N.M. and Ahmed, S.F. (2021) Supporting international networks through platforms for standardised data collection—the European Registries for Rare Endocrine Conditions (EuRRECa) model. Endocrine, 71(3), pp. 555-560. (doi: 10.1007/s12020-021-02617-0) (PMID:33512655) (PMCID:PMC7844549)
Ali, S. R. et al. (2021) Real world estimates of adrenal insufficiency related adverse events in children with congenital adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 106(1), e192-e203. (doi: 10.1210/clinem/dgaa694) (PMID:32995889) (PMCID:PMC7990061)
2020
Ali, S. R. et al. (2020) The EuRRECa project as a model for data access and governance policies for rare disease registries that collect clinical outcomes. International Journal of Environmental Research and Public Health, 17(23), 8743. (doi: 10.3390/ijerph17238743) (PMID:33255540) (PMCID:PMC7727867)
2019
Ali, S. R., Lucas-Herald, A. , Bryce, J. and Ahmed, S. F. (2019) The role of international databases in understanding the aetiology and consequences of differences/disorders of sex development. International Journal of Molecular Sciences, 20, 4405. (doi: 10.3390/ijms20184405)
Ali, S. R. et al. (2019) The current landscape of European registries for rare endocrine conditions. European Journal of Endocrinology, 180(1), pp. 89-98. (doi: 10.1530/EJE-18-0861) (PMID:30407922) (PMCID:PMC6347278)
2018
Sanders, C. et al. (2018) Involving individuals with disorders of sex development and their parents in exploring new models of shared learning: Proceedings from a DSDnet COST Action workshop. Sexual Development, 12(5), pp. 225-231. (doi: 10.1159/000490081) (PMID:29936513)
2017
Dessens, A. et al. (2017) Understanding the needs of professionals who provide psychosocial care for children and adults with disorders of sex development. BMJ Paediatrics Open, 1(1), e000132. (doi: 10.1136/bmjpo-2017-000132) (PMID:29637150) (PMCID:PMC5843008)
Kourime, M., Bryce, J. , Jiang, J., Nixon, R., Rodie, M. and Ahmed, S.F. (2017) An assessment of the quality of the I-DSD and the I-CAH registries - international registries for rare conditions affecting sex development. Orphanet Journal of Rare Diseases, 12(1), 56. (doi: 10.1186/s13023-017-0603-7) (PMID:28320446) (PMCID:PMC5360059)
Poyrazoglu, S. et al. (2017) Birth weight in different etiologies of disorders of sex development. Journal of Clinical Endocrinology and Metabolism, 102(3), pp. 1044-1050. (doi: 10.1210/jc.2016-3460) (PMID:28359094)
2016
Kyriakou, A. et al. (2016) Current models of care for disorders of sex development – results from an International survey of specialist centres. Orphanet Journal of Rare Diseases, 11, 155. (doi: 10.1186/s13023-016-0534-8) (PMID:27871307) (PMCID:PMC5117601)
Lucas-Herald, A. et al. (2016) The Long term outcome of boys with partial androgen insensitivity syndrome and androgen receptor gene mutations. Journal of Clinical Endocrinology and Metabolism, 101(11), pp. 3959-3967. (doi: 10.1210/jc.2016-1372) (PMID:27403927) (PMCID:PMC5095251)
2014
Kolesinska, Z. et al. (2014) Changes over time in sex assignment for disorders of sex development. Pediatrics, 134(3), e710-e715. (doi: 10.1542/peds.2014-1088)
Cox, K. et al. (2014) Novel associations in disorders of sex development: findings from the I-DSD registry. Journal of Clinical Endocrinology and Metabolism, 99(2), E348-E355. (doi: 10.1210/jc.2013-2918) (PMID:24302751) (PMCID:PMC3955252)
Articles
Scougall, K. et al. (2023) Predictors of surgical complications in boys with hypospadias: data from an international registry. World Journal of Pediatric Surgery, 6, e000599. (doi: 10.1136/wjps-2023-000599) (PMID:37860275) (PMCID:PMC10582860)
Tseretopoulou, X., Bryce, J. , Chen, M., McMillan, M., Lucas-Herald, A. K. , Ali, S. R. and Ahmed, S.F. (2023) The I‐CAH registry: a platform for international collaboration for improving knowledge and clinical care in congenital adrenal hyperplasia. Clinical Endocrinology, (doi: 10.1111/cen.14961) (PMID:37602832) (Early Online Publication)
Righi, B. et al. (2023) Long-term cardiometabolic morbidity in young adults with classic 21-hydroxylase deficiency congenital adrenal hyperplasia. Endocrine, 80(3), pp. 630-638. (doi: 10.1007/s12020-023-03330-w) (PMID:36857009) (PMCID:PMC10199864)
Nowotny, H. F. et al. (2023) Outcome of COVID-19 infections in patients with adrenal insufficiency and excess. Endocrine Connections, 12(4), e220416. (doi: 10.1530/EC-22-0416) (PMID:36715679) (PMCID:PMC10083676)
Lawrence, N. et al. (2022) Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry. Clinical Endocrinology, 97(5), pp. 551-561. (doi: 10.1111/cen.14796) (PMID:35781728)
Neumann, U. et al. (2022) Treatment of congenital adrenal hyperplasia in children aged 0–3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure. European Journal of Endocrinology, 186(5), pp. 587-596. (doi: 10.1530/eje-21-1085) (PMID:35290211) (PMCID:PMC9066592)
Ali, S. R., Bryce, J. , Kodra, Y., Taruscio, D., Persani, L. and Ahmed, S. F. (2021) The quality evaluation of rare disease registries—an assessment of the essential features of a disease registry. International Journal of Environmental Research and Public Health, 18(22), 11968. (doi: 10.3390/ijerph182211968) (PMID:34831724) (PMCID:PMC8620980)
Lucas-Herald, A. K. et al. (2021) Gonadectomy in conditions affecting sex development – a registry-based cohort study. European Journal of Endocrinology, 184(6), pp. 791-801. (doi: 10.1530/EJE-20-1058) (PMID:33780351)
Ali, S.R., Bryce, J. , Smythe, C., Hytiris, M., Priego, A.L., Appelman-Dijkstra, N.M. and Ahmed, S.F. (2021) Supporting international networks through platforms for standardised data collection—the European Registries for Rare Endocrine Conditions (EuRRECa) model. Endocrine, 71(3), pp. 555-560. (doi: 10.1007/s12020-021-02617-0) (PMID:33512655) (PMCID:PMC7844549)
Ali, S. R. et al. (2021) Real world estimates of adrenal insufficiency related adverse events in children with congenital adrenal hyperplasia. Journal of Clinical Endocrinology and Metabolism, 106(1), e192-e203. (doi: 10.1210/clinem/dgaa694) (PMID:32995889) (PMCID:PMC7990061)
Ali, S. R. et al. (2020) The EuRRECa project as a model for data access and governance policies for rare disease registries that collect clinical outcomes. International Journal of Environmental Research and Public Health, 17(23), 8743. (doi: 10.3390/ijerph17238743) (PMID:33255540) (PMCID:PMC7727867)
Ali, S. R., Lucas-Herald, A. , Bryce, J. and Ahmed, S. F. (2019) The role of international databases in understanding the aetiology and consequences of differences/disorders of sex development. International Journal of Molecular Sciences, 20, 4405. (doi: 10.3390/ijms20184405)
Ali, S. R. et al. (2019) The current landscape of European registries for rare endocrine conditions. European Journal of Endocrinology, 180(1), pp. 89-98. (doi: 10.1530/EJE-18-0861) (PMID:30407922) (PMCID:PMC6347278)
Sanders, C. et al. (2018) Involving individuals with disorders of sex development and their parents in exploring new models of shared learning: Proceedings from a DSDnet COST Action workshop. Sexual Development, 12(5), pp. 225-231. (doi: 10.1159/000490081) (PMID:29936513)
Dessens, A. et al. (2017) Understanding the needs of professionals who provide psychosocial care for children and adults with disorders of sex development. BMJ Paediatrics Open, 1(1), e000132. (doi: 10.1136/bmjpo-2017-000132) (PMID:29637150) (PMCID:PMC5843008)
Kourime, M., Bryce, J. , Jiang, J., Nixon, R., Rodie, M. and Ahmed, S.F. (2017) An assessment of the quality of the I-DSD and the I-CAH registries - international registries for rare conditions affecting sex development. Orphanet Journal of Rare Diseases, 12(1), 56. (doi: 10.1186/s13023-017-0603-7) (PMID:28320446) (PMCID:PMC5360059)
Poyrazoglu, S. et al. (2017) Birth weight in different etiologies of disorders of sex development. Journal of Clinical Endocrinology and Metabolism, 102(3), pp. 1044-1050. (doi: 10.1210/jc.2016-3460) (PMID:28359094)
Kyriakou, A. et al. (2016) Current models of care for disorders of sex development – results from an International survey of specialist centres. Orphanet Journal of Rare Diseases, 11, 155. (doi: 10.1186/s13023-016-0534-8) (PMID:27871307) (PMCID:PMC5117601)
Lucas-Herald, A. et al. (2016) The Long term outcome of boys with partial androgen insensitivity syndrome and androgen receptor gene mutations. Journal of Clinical Endocrinology and Metabolism, 101(11), pp. 3959-3967. (doi: 10.1210/jc.2016-1372) (PMID:27403927) (PMCID:PMC5095251)
Kolesinska, Z. et al. (2014) Changes over time in sex assignment for disorders of sex development. Pediatrics, 134(3), e710-e715. (doi: 10.1542/peds.2014-1088)
Cox, K. et al. (2014) Novel associations in disorders of sex development: findings from the I-DSD registry. Journal of Clinical Endocrinology and Metabolism, 99(2), E348-E355. (doi: 10.1210/jc.2013-2918) (PMID:24302751) (PMCID:PMC3955252)
Research datasets
2020
Ali, S., Bryce, J. , Haghpanahan, H., Lewsey, J. D., Tan, L. E., Atapattu, N., Birkebaek, N. H., Blankenstein, O., Neumann, U., Balsamo, A., Ortolano, R., Bonfig, W., Claahsen-van der Grinten, H. L., Cools, M., Correa Costa, E., Darendeliler, F., Poyrazoglu, S., Elsedfy, H., Finken, M. J.J., Fluck, C. E., Gevers, E., Korbonits, M., Guaragna-Filho, G., Guran, T., Guven, A., Hannema, S. E., Higham, C., Hughes, I. A., Tadokoro-Cuccaro, R., Thankamony, A., Iotova, V., Krone, N. P., Krone, R., Lichiardopol, C., Luczay, A., Mendonca, B. B., Bachega, T. A.S.S., Miranda, M. C., Milenkovic, T., Mohnike, K., Nordenstrom, A., Einaudi, S., van der Kamp, H., Vieites, A., de Vries, L., Ross, R. J. M. and Ahmed, S. F. (2020) Real World Estimates Of Adrenal Insufficiency Related Adverse Events In Children With Congenital Adrenal Hyperplasia. [Data Collection]