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Year | Number of Results |
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2023 | 1 |
2024 | 2 |
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Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape.
Nat Commun. 2023 Aug 10;14(1):4826. doi: 10.1038/s41467-023-40424-5.
Nat Commun. 2023.
PMID: 37563143
Free PMC article.
Complex trait associations in rare diseases and impacts on Mendelian variant interpretation.
Smail C, Ge B, Keever-Keigher MR, Schwendinger-Schreck C, Cheung W, Johnston JJ, Barrett C; Genomic Answers for Kids Consortium; Feldman K, Cohen ASA, Farrow EG, Thiffault I, Grundberg E, Pastinen T.
Smail C, et al.
medRxiv [Preprint]. 2024 Jan 11:2024.01.10.24301111. doi: 10.1101/2024.01.10.24301111.
medRxiv. 2024.
PMID: 38260377
Free PMC article.
Preprint.
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Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scores.
LeMaster C, Schwendinger-Schreck C, Ge B, Cheung WA, McLennan R, Johnston JJ, Pastinen T, Smail C.
LeMaster C, et al.
medRxiv [Preprint]. 2024 May 16:2024.03.15.24304216. doi: 10.1101/2024.03.15.24304216.
medRxiv. 2024.
PMID: 38562793
Free PMC article.
Preprint.
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