Associated Papers
Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma.
Villa M et al.
British Journal of Cancer, 2024
39478125 (PubMed )
Supplement: 41416_2024_2881_MOESM1_ESM.pdf
Association between idiopathic hypersomnia and a genetic variant in the PER3 gene.
Cherasse Y et al.
Journal of Sleep Research, 2024
Identification and functional assays of single-nucleotide variants of opsins genes in melanocytic tumors.
Zhang W et al.
Pigment Cell & Melanoma Research, 2022
Whole genome, exon mutation and transcriptomic profiling of acute myeloid leukemia: A case report.
Lai SH et al.
Oncology Letters, 2021
Functional characterisation of naturally occurring mutations in human melanopsin.
Rodgers J et al.
Cellular and Molecular Life Sciences : Cmls, 2018
Defining the impact of melanopsin missense polymorphisms using in vivo functional rescue.
Rodgers J et al.
Human Molecular Genetics, 2018
Melanopsin gene variations interact with season to predict sleep onset and chronotype.
Roecklein KA et al.
Chronobiology International, 2012
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