Associated Papers
Quadruple primary tumors in a lynch syndrome patient surviving more than 26 years with genetic analysis: a case report and literature review.
Zhu B et al.
Frontiers in Oncology, 2024
38894864 (PubMed )
Supplement: Table_1.xlsx › Sheet1
Identifying therapeutic drug targets using bidirectional effect genes.
Estrada K et al.
Nature Communications, 2021
33850126 (PubMed )
Supplement: 41467_2021_21843_MOESM7_ESM.xlsx › Supplementary_Data_6
Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.
Ye X et al.
Plastic and Reconstructive Surgery, 2016
Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.
Heuzé Y et al.
Current Genetic Medicine Reports, 2014
Transcriptome correlation analysis identifies two unique craniosynostosis subtypes associated with IRS1 activation.
Stamper BD et al.
Physiological Genomics, 2012
Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications.
Lattanzi W et al.
Child's Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery, 2012
IGF1R variants associated with isolated single suture craniosynostosis.
Cunningham ML et al.
American Journal of Medical Genetics. Part A, 2011
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