X-linked Alport SyndromeJean Philippe Jaïs, Marie-Claire Gübler, Bertrand Knebelmann et al.|Journal of the American Society of Nephrology|2000Cited by 592
X-Linked Alport SyndromeJean Philippe Jaïs, Marie-Claire Gübler, Bertrand Knebelmann et al.|Journal of the American Society of Nephrology|2003Cited by 479
Transcriptional regulator PRDM12 is essential for human pain perceptionYa-Chun Chen, Jonathan Baets, Maria Schabhüttl et al.|Nature Genetics|2015Cited by 172
X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype CorrelationsMato Nagel, Helen Storey, Hae Il Cheong et al.|PLoS ONE|2016Cited by 102
FC044: Heterozygous Variants in Kinase Domain of NEK8 cause an Autosomal-Dominant CiliopathyLaura R. Claus, Richard Steet, Jennifer L. Stallworth et al.|Nephrology Dialysis Transplantation|2022Cited by 2