| Recurrent de novo mutations affecting residue Arg138 of pyrroline-5-carboxylate synthase cause a progeroid form of autosomal-dominant cutis laxa B Fischer-Zirnsak, N Escande-Beillard, J Ganesh, YX Tan, M Al Bughaili, ... The American Journal of Human Genetics 97 (3), 483-492, 2015 | 81 | 2015 |
| Discriminative features in three autosomal recessive cutis laxa syndromes: cutis laxa IIA, cutis laxa IIB, and geroderma osteoplastica A Kariminejad, F Afroozan, B Bozorgmehr, A Ghanadan, S Akbaroghli, ... International journal of molecular sciences 18 (3), 635, 2017 | 33 | 2017 |
| Pioneer factor ASCL1 cooperates with the mSWI/SNF complex at distal regulatory elements to regulate human neural differentiation O Păun, YX Tan, H Patel, S Strohbuecker, A Ghanate, C Cobolli-Gigli, ... Genes & Development 37 (5-6), 218-242, 2023 | 15 | 2023 |
| RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis S Wong, YX Tan, AYT Loh, KY Tan, H Lee, Z Aziz, SF Nelson, E Özkan, ... EMBO Molecular Medicine 15 (5), e17078, 2023 | 4 | 2023 |
