Associated Papers
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Supplement: 13073_2024_1370_MOESM3_ESM.xlsx › SNV
Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia.
Chen L et al.
Translational Psychiatry, 2024
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Supplement: 41398_2024_2984_MOESM1_ESM.pdf
Identification of NCAN as a candidate gene for developmental dyslexia.
Einarsdottir E et al.
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Supplement: 41598_2017_10175_MOESM4_ESM.xls › 3821-rare_exonic_variants
Exome sequencing reveals comprehensive genomic alterations across eight cancer cell lines.
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Plos One, 2011
21701589 (PubMed )
Supplement: pone.0021097.s002.xls › a549_f40r3
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