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

Por Dias, Renuka P, Maher, Eamonn R
Publicado em 2012

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

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

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

Por 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
Publicado em 2013

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

Por 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
Publicado no J Clin Endocrinol Metab (2018)

Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty

Por 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
Publicado no J Clin Endocrinol Metab (2016)

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

Por 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
Publicado no Eur J Endocrinol (2018)