Tuula Rinne, Phd
Radboud University Medical Centre, Department of Human Genetics, Nijmegen, The Netherlands
Clinical laboratory geneticist
Tuula Rinne obtained a PhD in medical sciences where she studied p63-associated diseases, their molecular disease mechanisms and the role of p63 and its downstream signaling in these diseases (ectodermal dysplasia, orofacial clefting and limb defects). In 2012, she finished her training as a clinical laboratory geneticist in Nijmegen. Since then, she has specialized in the fields of Kallmann syndrome and hypogonadotrophic hypogonadism, disorders of sex development and Noonan syndrome. She is also involved in the diagnostics of intellectual disability and multiple congenital anomaly syndromes. Currently she works on the interpretation and reporting of sequencing, MLPA and exome data.
Click HERE to see her publications in Researchgate.net