Education:
06/1996 Graduation from High School
10/1997 - 05/2005 Medical Studies, University of Halle-Wittenberg, Halle, Germany
10/2002 – 01/2007 Doctoral Research Fellow at the Institute of Anatomy and Cell Biology, University of Halle-Wittenberg
Employment:
11/2005 – 11/2006 House Officer, Children’s Hospital, University of Dresden, Germany
12/2006 – 11/2008 Senior House Officer, Children’s Hospital, University of Dresden, Germany
12/2008 – 11/2009 SpR Endocrinology and Diabetes, Children’s Hospital, University of Dresden, Germany
since 01/2009 Research Fellow at the Centre for Endocrinology, Diabetes and Metabolism, University of Birmingham, UK
since 01/2009 Honorary SpR, Paediatric Endocrinology and Diabetes, Birmingham Children’s Hospital, Birmingham, UK
Idkowiak J, Randell T, Dhir V, Patel P, Shackleton CHL, Taylor NF, Krone N, Arlt W. A missense mutation in the human cytochrome b5 gene causes 46,XY disorder of sex development due to true isolated 17,20 lyase deficiency. (submitted to J Clin Endocrinol Metab August 2011)
Krone N, Reisch N, Idkowiak J, Dhir V, Ivison HE, Hughes BA, Rose IT, O’Neil DM, Vijzelaar R, Smith MH, MacDonald F, Cole TR, Barton J, Blair, EM, Braddock SR, Collins F, Cragun DL, Dattani MT, Day R, Dougan S, Gottschalk ME, Graul-Neumann LM, Gregory JW, Haim M, Haskins Olney A, Hauffa BP, Hindmarsh PC, Hopkin RJ, Jira PE, Kempers M, Kerstens MN, Khalifa M, Köhler B, Maiter D, Nielsen S, O’Riordan SM, Roth CL, Shane KP, Silink M, Stikkelbroek NMML, Sweeney E, Szarras-Czapnik, Waterson JR, Williamson L, Zipf WB, Hartmann M, Taylor NF, Wudy SA, Malunowicz EM, Shackleton CHL, Arlt W. Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency. (revised version submitted to J Clin Endocrinol Metab August 2011)
Idkowiak J, Lavery GG, Dhir V, Barrett T, Stewart PM, Krone N, Arlt W. Premature adrenarche – novel lessons from early onset androgen excess. Eur J Endocrinol 2011 Aug; 165(2):189-207.
Idkowiak J, O’Riordan S, Reisch N, Malunowicz EM, Collins F, Kerstens MN, Köhler B, Graul-Neumann LM, Szarras-Czapnik M, Silink M, Dattani MT, Shackleton CHL, Maiter D, Krone N, Arlt W. Pubertal presentation in in seven patients with congenital adrenal hyperplasia due to P450 oxidoreductase deficiency. J Clin Endocrinol Metab 2011, 96(3):E453-62.
Idkowiak J, Malunowicz EM, Dhir V, Reisch N, Szarras-Czapnik M, Holmes DM, Shackleton, CHL, Davies JD, Hughes IA, Krone N, Arlt W. Concomitant mutations in the P450 oxidoreductase and androgen receptor genes presenting with 46,XY disordered sex development and androgenization at adrenarche. J Clin Endocrinol Metab 2010, 95(7): 3418-3427.
Idkowiak J, Weisheit G, Viebahn C. (2004) Polarity in the rabbit embryo. (Review) Sem Cell Dev Biol 15: 607-617
Idkowiak J, Weisheit G, PlitznerJ, und Viebahn C (2004) Hypoblast controls mesoderm generation and axial patterning in the gastrulating rabbit embryo. Dev Gen Evol. 214: 591-605
Idkowiak J „Natural scientific glossary“ in Damschen, G., Schönecker, D. (eds) (2002) The ethical state of human embryos (de Gruyter study book) ISBN 3-11-017365-4