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2024	detectCilia: An R Package for Automated Detection and Length Measurement of Primary Cilia Bioinformatics and Biology Insights Kai Budde-Sagert, Simone Krueger, Clemens Sehlke, Heiko Lemcke, Anika Jonitz-Heincke, Robert David, Rainer Bader, Adelinde M Uhrmacher
2024	Bone Cell Biomechanics, Mechanobiology and Bone Diseases Hua Liu, Zihan Tian, Shuyu Liu, Wenhui Yang, Airong Qian, Lifang Hu, Zixiang Wu
2024	Early insights into the role of Exoc6B associated with spondyloepimetaphyseal dysplasia with joint laxity type 3 in primary ciliogenesis and chondrogenic differentiation in vitro Molecular Biology Reports Vishal Singh Guleria, Neha Quadri, Keshava Prasad, Ranajit Das, Priyanka Upadhyai
2023	Primary cilia in skeletal development and disease Experimental Cell Research Neha Quadri, Priyanka Upadhyai
2023	Emerging principles of primary cilia dynamics in controlling tissue organization and function The EMBO Journal Jay Gopalakrishnan, Kerstin Feistel, Benjamin M Friedrich, Anne Grapin‐Botton, Nathalie Jurisch‐Yaksi, Elvira Mass, David U Mick, Roman‐Ulrich Müller, Helen May‐Simera, Bernhard Schermer, Miriam Schmidts, Peter Walentek, Dagmar Wachten
2023	Airway ciliated cells in adult lung homeostasis and COPD European Respiratory Review Laure M.G. Petit, Randa Belgacemi, Julien Ancel, Lynda Saber Cherif, Myriam Polette, Jeanne-Marie Perotin, Nathalie Spassky, Charles Pilette, Denise Al Alam, Gaëtan Deslée, Valérian Dormoy
2022	The intraflagellar transport protein IFT52 associated with short-rib thoracic dysplasia is essential for ciliary function in osteogenic differentiation in vitro and for sensory perception in Drosophila Experimental Cell Research Vishal Singh Guleria, Rahul Parit, Neha Quadri, Ranajit Das, Priyanka Upadhyai
2022	Primary Cilia: A Cellular Regulator of Articular Cartilage Degeneration Stem Cells International Haiqi Zhou, Sha Wu, Huixian Ling, Changjie Zhang, Ying Kong
2022	Biallelic loss‐of‐function variants in EXOC6B are associated with impaired primary ciliogenesis and cause spondylo‐epi‐metaphyseal dysplasia with joint laxity type 3 Human Mutation Pelin Ozlem Simsek‐Kiper, Prince Jacob, Priyanka Upadhyai, Zihni Ekim Taşkıran, Vishal S. Guleria, Beren Karaosmanoglu, Gozde Imren, Rahsan Gocmen, Gandham S. Bhavani, Neethukrishna Kausthubham, Hitesh Shah, Gulen Eda Utine, Koray Boduroglu, Katta M. Girisha