Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndromeKinga M. Bujakowska, Eric A. Pierce, Qi Zhang et al.|Human Molecular Genetics|2014Cited by 160
<scp> <i>WDR34</i> </scp> , a candidate gene for non‐syndromic rod‐cone dystrophyMaria Solaguren‐Beascoa, Christina Zeitz, Kinga M. Bujakowska et al.|Clinical Genetics|2020Cited by 12
Gene‐ and pathway‐level analyses of <scp>iCOGS</scp> variants highlight novel signaling pathways underlying familial breast cancer susceptibilityChristine Lonjou, Fabienne Lesueur, Noura Mebirouk et al.|International Journal of Cancer|2020Cited by 6
Atlas of Cancer Signaling Network: A Resource of Multi-Scale Biological Maps to Study Disease MechanismsLuis Cristóbal Monraz Gómez, Inna Kuperstein, Maria Kondratova et al.|Systems Medicine|2020Cited by 1
Models including pathological and radiomic features vs clinical models in predicting outcome of patients with metastatic non-small cell lung cancer treated with immunotherapy.Nicolas Captier, Emmanuel Barillot, Marvin Lerousseau et al.|Journal of Clinical Oncology|2023Cited by 1