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American Journal of Human Genetics|December 9, 2022
Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genesLisa A Lansdon, Amanda Dickinson, Sydney Arlis, et al.Elife|January 13, 2021
MITF reprograms the extracellular matrix and focal adhesion in melanomaRamile Dilshat, Valerie Fock, Colin Kenny, et al.Cancer Research|June 10, 2026
GNAQ Induces Melanomagenesis in Mitfa-Independent Melanocyte Progenitors in a Zebrafish Model of Uveal MelanomaJulius I Yevdash, Delaney Robinson, Rachel Moore, et al.American Journal of Human Genetics|December 24, 2013
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm developmentMyriam Peyrard-Janvid, Elizabeth J Leslie, Youssef A Kousa, et al.Nature Communications|June 18, 2021
BRN2 is a non-canonical melanoma tumor-suppressorMichael Hamm, Pierre Sohier, Valérie Petit, et al.Nature Communications|November 5, 2024
High incidence and geographic distribution of cleft palate in Finland are associated with the IRF6 geneFedik Rahimov, Pekka Nieminen, Priyanka Kumari, et al.Medrxiv : the Preprint Server for Health Sciences|July 23, 2024
High incidence and geographic distribution of cleft palate cases in Finland are associated with a regulatory variant in IRF6Fedik Rahimov, Pekka Nieminen, Priyanka Kumari, et al.Developmental Cell|September 16, 2021
Cooperation between melanoma cell states promotes metastasis through heterotypic cluster formationNathaniel R Campbell, Anjali Rao, Miranda V Hunter, et al.Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.American Journal of Human Genetics|September 3, 2025
Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathyKelsey Robinson, Sunil K Singh, Rachel B Walkup, et al.Pageof 7