You are here

Identifying the genes causing Turner syndrome (45,XO) and Klinefelter syndrome (47,XXY)

Description 
Differences of sex development include sex chromosome aneuploidies such as Turner syndrom (TS) and Klinefelter syndrome (KS). Women with TS lack one X chromosome leading to various health issues, including growth impairment and infertility. The X chromosome carries about 900 genes and while most of these genes on the second X chromosome is inactivated, about 15% remain active and are therefore candidate genes causing TS. Men with KS carry an additional X chromosome often leading to neurocognitive challenges and infertility. We have developed rat models for TS and KS and using transcriptomic approaches we will identify when expression of X and Y genes and downstream targets are first affected in various organs and tissues. We will intergrate our data with patients data obtained from international collaborators.
Essential criteria: 
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords 
X chromosome, Y chromosome, infertility, cognition, intersex, genomics, human genetics
School 
School of Clinical Sciences at Monash Health / Hudson Institute of Medical Research » Molecular and Translational Sciences
Available options 
PhD/Doctorate
Masters by research
Honours
BMedSc(Hons)
Graduate Diploma
Time commitment 
Full-time
Top-up scholarship funding available 
No
Physical location 
Monash Health Translation Precinct (Monash Medical Centre)
Co-supervisors 
Dr 
Shanie Landen

Want to apply for this project? Submit an Expression of Interest by clicking on Contact the researcher.