Annick Raas-Rothschild

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4

Alfonso Baldi, Val C. Sheffield, Edwin M. Stone, 2001, Nature Genetics.

[RARE DISEASES DTC: DIAGNOSIS, TREATMENT AND CARE].

Hagith Yonath, Hila Barash, Annick Raas-Rothschild, 2016, Harefuah.

P35S mutation in the NOG gene associated with Teunissen-Cremers syndrome and features of multiple NOG joint-fusion syndromes.

Jacob Sosna, J. Sosna, E. Banin, 2008, European journal of medical genetics.

The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.

Francesca Forzano, Hui Zou, Susan Chang, 2008, Human molecular genetics.