An imprinted IMAGe: insights into growth regulation through genomic analysis of a rare disease

di Dias, Renuka P, Maher, Eamonn R
Pubblicazione 2012

Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects

di Ibrahim, Abdulla, Kirby, Gail, Hardy, Carol, Dias, Renuka P, Tee, Louise, Lim, Derek, Berg, Jonathan, MacDonald, Fiona, Nightingale, Peter, Maher, Eamonn R
Pubblicazione 2014

Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology

di Tee, Louise, Lim, Derek HK, Dias, Renuka P, Baudement, Marie-Odile, Slater, Amy A, Kirby, Gail, Hancocks, Tom, Stewart, Helen, Hardy, Carol, Macdonald, Fiona, Maher, Eamonn R
Pubblicazione 2013

Frequent Monitoring of C-Peptide Levels in Newly Diagnosed Type 1 Subjects Using Dried Blood Spots Collected at Home

di Willemsen, Ruben H, Burling, Keith, Barker, Peter, Ackland, Fran, Dias, Renuka P, Edge, Julie, Smith, Anne, Todd, John, Lopez, Boryana, Mander, Adrian P, Guy, Catherine, Dunger, David B
Pubblicato in J Clin Endocrinol Metab (2018)

Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty

di Idkowiak, Jan, Taylor, Angela E., Subtil, Sandra, O'Neil, Donna M., Vijzelaar, Raymon, Dias, Renuka P., Amin, Rakesh, Barrett, Timothy G., Shackleton, Cedric H. L., Kirk, Jeremy M. W., Moss, Celia, Arlt, Wiebke
Pubblicato in J Clin Endocrinol Metab (2016)

Causes, patterns and severity of androgen excess in 487 consecutively recruited pre- and post-pubertal children

di Idkowiak, Jan, Elhassan, Yasir S, Mannion, Pascoe, Smith, Karen, Webster, Rachel, Saraff, Vrinda, Barrett, Timothy G, Shaw, Nicholas J, Krone, Nils, Dias, Renuka P, Kershaw, Melanie, Kirk, Jeremy M, Högler, Wolfgang, Krone, Ruth E, O’Reilly, Michael W, Arlt, Wiebke
Pubblicato in Eur J Endocrinol (2018)