| 37186866 | The SHDRA syndrome-associated gene <i>TMEM260</i> encodes a protein-specific O-mannosyltransferase. | Proc Natl Acad Sci U S A | 2023 |
| 34716235 | Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100,000 Genomes Project. | J Med Genet | 2022 |
| 35217805 | Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease. | Eur J Hum Genet | 2022 |
| 35181706 | RNA-Seq analysis of a Pax3-expressing myoblast clone in-vitro and effect of culture surface stiffness on differentiation. | Sci Rep | 2022 |
| 35297555 | Activation of autophagy reverses progressive and deleterious protein aggregation in PRPF31 patient-induced pluripotent stem cell-derived retinal pigment epithelium cells. | Clin Transl Med | 2022 |
| 35170427 | Regulation of canonical Wnt signalling by the ciliopathy protein MKS1 and the E2 ubiquitin-conjugating enzyme UBE2E1. | Elife | 2022 |
| 34964473 | Interpreting ciliopathy-associated missense variants of uncertain significance (VUS) in Caenorhabditis elegans. | Hum Mol Genet | 2022 |
| 32571899 | Novel loss-of-function mutation in <i>HERC2</i> is associated with severe developmental delay and paediatric lethality. | J Med Genet | 2021 |
| 33220177 | Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly. | Neuron | 2021 |
| 32203228 | Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome. | Genet Med | 2020 |
| 31949313 | A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome. | Genet Med | 2020 |
| 33392209 | Primary Cilia, Ciliogenesis and the Actin Cytoskeleton: A Little Less Resorption, A Little More Actin Please. | Front Cell Dev Biol | 2020 |
| 30931988 | The ciliary Frizzled-like receptor Tmem67 regulates canonical Wnt/β-catenin signalling in the developing cerebellum via Hoxb5. | Sci Rep | 2019 |
| 31014478 | The Nuclear Arsenal of Cilia. | Dev Cell | 2019 |
| 31095607 | CiliaCarta: An integrated and validated compendium of ciliary genes. | PLoS One | 2019 |
| 29228333 | DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport. | Hum Mol Genet | 2018 |
| 30002499 | Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants. | Eur J Hum Genet | 2018 |
| 30095490 | Characterization of Primary Cilia in Normal Fallopian Tube Epithelium and Serous Tubal Intraepithelial Carcinoma. | Int J Gynecol Cancer | 2018 |
| 30315276 | Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa. | Nat Commun | 2018 |
| 27634431 | The Cilium: Cellular Antenna and Central Processing Unit. | Trends Cell Biol | 2017 |
| 28289185 | Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes. | J Med Genet | 2017 |
| 29209597 | Meckel-Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances. | Front Pediatr | 2017 |
| 29100095 | Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia. | Am J Hum Genet | 2017 |
| 27021811 | Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport. | Nat Commun | 2016 |
| 26490104 | MKS1 regulates ciliary INPP5E levels in Joubert syndrome. | J Med Genet | 2016 |
| 26595381 | TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome. | Nat Cell Biol | 2016 |
| 26560041 | A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency. | J Allergy Clin Immunol | 2016 |
| 27693231 | Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta. | Am J Hum Genet | 2016 |
| 27894351 | Characterizing the morbid genome of ciliopathies. | Genome Biol | 2016 |
| 27523597 | Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2. | Am J Hum Genet | 2016 |
| 27335639 | Ciliogenesis and the DNA damage response: a stressful relationship. | Cilia | 2016 |
| 26996948 | Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia. | Am J Hum Genet | 2016 |
| 25564561 | The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes. | J Med Genet | 2015 |
| 26546361 | Screen-based identification and validation of four new ion channels as regulators of renal ciliogenesis. | J Cell Sci | 2015 |
| 26626625 | Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain. | Am J Hum Genet | 2015 |
| 26044572 | TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport. | Nat Commun | 2015 |
| 26035863 | The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway. | Dis Model Mech | 2015 |
| 26167768 | An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes. | Nat Cell Biol | 2015 |
| 25928877 | Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations. | BMC Med Genet | 2015 |
| 25983245 | Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with early macular involvement. | Am J Hum Genet | 2015 |
| 26026149 | Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome. | Elife | 2015 |
| 25794656 | A new case of Fas-associated death domain protein deficiency and update on treatment outcomes. | J Allergy Clin Immunol | 2015 |
| 24162842 | The role of primary cilia in the development and disease of the retina. | Organogenesis | 2014 |
| 25729630 | Unraveling the genetics of Joubert and Meckel-Gruber syndromes. | J Pediatr Genet | 2014 |
| 25446516 | IFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment. | Dev Cell | 2014 |
| 25294941 | ATMIN is a transcriptional regulator of both lung morphogenesis and ciliogenesis. | Development | 2014 |
| 25133751 | Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing. | PLoS One | 2014 |
| 24614073 | Mutations in TJP2 cause progressive cholestatic liver disease. | Nat Genet | 2014 |
| 24705253 | De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. | Nat Genet | 2014 |
| 24336167 | Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. | Nat Genet | 2014 |