Associated Papers
Whole exome sequencing reveals an FCGBP variant associated with spontaneous intraabdominal hemorrhage in severe acute pancreatitis.
Tang QY et al.
Imetaomics, 2025
41675706 (PubMed )
Supplement: IMO2-2-e52-s002.xlsx › 2D
De novo mutations identified by whole-genome sequencing implicate chromatin modifications in obsessive-compulsive disorder.
Lin GN et al.
Science Advances, 2022
35020433 (PubMed )
Supplement: sciadv.abi6180_tables_s2_to_s5.zip › sciadv.abi6180_table_s2.xlsx › Sheet1
BIRC2-BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia.
Roohollahi K et al.
Scientific Reports, 2022
34997070 (PubMed )
Supplement: 41598_2021_4042_MOESM2_ESM.xlsx › Supp.File.1
A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.
Zlotina A et al.
Bmc Medical Genomics, 2020
33218365 (PubMed )
Supplement: 12920_2020_821_MOESM1_ESM.xlsx › Sheet_1
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