Shifeng Xue
Singapore, Singapore
Last Updated: 09/26/2026
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Found 19 publications
Cranial placode differentiation defect in individuals born without a nose.
Journal: Stem cell reports
Published: June 05, 2025
Genotypic and phenotypic spectrum of anophthalmia/microphthalmia in families from Khyber Pakhtunkhwa, Pakistan.
Journal: Journal of human genetics
Published: May 07, 2025
Epigenetic regulation of DUX4: From embryogenesis to muscular degeneration.
Journal: Current opinion in cell biology
Published: February 06, 2025
Deep transcriptome profiling reveals limited conservation of A-to-I RNA editing in Xenopus.
Journal: BMC biology
Published: July 25, 2023
DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 07, 2023
In skeletal muscle and neural crest cells, SMCHD1 regulates biological pathways relevant for Bosma syndrome and facioscapulohumeral dystrophy phenotype.
Journal: Nucleic acids research
Published: March 24, 2023
A novel variant in AFF3 underlying isolated syndactyly.
Journal: Clinical genetics
Published: August 09, 2022
Direct identification of A-to-I editing sites with nanopore native RNA sequencing.
Journal: Nature methods
Published: August 02, 2021
HOX epimutations driven by maternal SMCHD1/LRIF1 haploinsufficiency trigger homeotic transformations in genetically wildtype offspring.
Journal: Nature communications
Published: July 15, 2021
Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy.
Journal: American journal of human genetics
Published: July 02, 2021
Novel variants in the LRP4 underlying Cenani-Lenz Syndactyly syndrome.
Journal: Journal of human genetics
Published: May 19, 2021
Last Updated: 09/26/2026