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2022
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2026
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Risk Variants in the Exomes of Children With Critical Illness.
Not available
S-EPMC9617179
|
biostudies-literature
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Interstitial Cystitis: a phenotype and rare variant exome sequencing study: Interstitial Cystitis: a phenotype and exome sequencing study.
Not available
S-EPMC11875234
|
biostudies-literature
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Interstitial cystitis: a phenotype and rare variant exome sequencing study.
Not available
S-EPMC12933612
|
biostudies-literature
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Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS.
Not available
S-EPMC11218304
|
biostudies-literature
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Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study.
Not available
S-EPMC8891088
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biostudies-literature
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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
Not available
S-EPMC8206159
|
biostudies-literature
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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.
Not available
S-EPMC10359300
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biostudies-literature
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