Associated Papers
Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes.
Marianski K et al.
Human Genetics, 2025
41442065 (PubMed )
Supplement: 439_2025_2796_MOESM4_ESM.xlsx › ST2
Whole exome sequencing identifies novel predisposing genes in neural tube defects.
Lemay P et al.
Molecular Genetics & Genomic Medicine, 2019
Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing.
Husson T et al.
Translational Psychiatry, 2018
30518751 (PubMed )
Supplement: 41398_2018_291_MOESM1_ESM.pdf
Molecular Guided Therapy Provides Sustained Clinical Response in Refractory Choroid Plexus Carcinoma.
Cornelius A et al.
Frontiers in Pharmacology, 2017
28993730 (PubMed )
Supplement: Table3.xlsx › Germline
Integrated analysis of germline and somatic variants in ovarian cancer.
Kanchi KL et al.
Nature Communications, 2014
24448499 (PubMed )
Supplement: NIHMS551112-supplement-9.xlsx › S_Data_8
Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome.
McCarthy HJ et al.
Clinical Journal of the American Society of Nephrology : Cjasn, 2013
MYO1E mutations and childhood familial focal segmental glomerulosclerosis.
Mele C et al.
The New England Journal of Medicine, 2011
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