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Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes.
Genet Med. 2022 Jun;24(6):1336-1348. doi: 10.1016/j.gim.2022.02.007. Epub 2022 Mar 16.
Genet Med. 2022.
PMID: 35305867
Free article.
Single-cell analysis of human adipose tissue identifies depot and disease specific cell types.
Vijay J, Gauthier MF, Biswell RL, Louiselle DA, Johnston JJ, Cheung WA, Belden B, Pramatarova A, Biertho L, Gibson M, Simon MM, Djambazian H, Staffa A, Bourque G, Laitinen A, Nystedt J, Vohl MC, Fraser JD, Pastinen T, Tchernof A, Grundberg E.
Vijay J, et al. Among authors: biswell rl.
Nat Metab. 2020 Jan;2(1):97-109. doi: 10.1038/s42255-019-0152-6. Epub 2019 Dec 23.
Nat Metab. 2020.
PMID: 32066997
Free PMC article.
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ASCL2 reciprocally controls key trophoblast lineage decisions during hemochorial placenta development.
Varberg KM, Iqbal K, Muto M, Simon ME, Scott RL, Kozai K, Choudhury RH, Aplin JD, Biswell R, Gibson M, Okae H, Arima T, Vivian JL, Grundberg E, Soares MJ.
Varberg KM, et al. Among authors: biswell r.
Proc Natl Acad Sci U S A. 2021 Mar 9;118(10):e2016517118. doi: 10.1073/pnas.2016517118.
Proc Natl Acad Sci U S A. 2021.
PMID: 33649217
Free PMC article.
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Antibody Responses after a Single Dose of SARS-CoV-2 mRNA Vaccine.
Bradley T, Grundberg E, Selvarangan R, LeMaster C, Fraley E, Banerjee D, Belden B, Louiselle D, Nolte N, Biswell R, Pastinen T, Myers A, Schuster J.
Bradley T, et al.
N Engl J Med. 2021 May 20;384(20):1959-1961. doi: 10.1056/NEJMc2102051. Epub 2021 Mar 23.
N Engl J Med. 2021.
PMID: 33755375
Free PMC article.
No abstract available.
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Insurance denials and diagnostic rates in a pediatric genomic research cohort.
Zion TN, Berrios CD, Cohen ASA, Bartik L, Cross LA, Engleman KL, Fleming EA, Gadea RN, Hughes SS, Jenkins JL, Kussmann J, Lawson C, Schwager C, Strenk ME, Welsh H, Rush ET, Amudhavalli SM, Sullivan BR, Zhou D, Gannon JL, Heese BA, Moore R, Boillat E, Biswell RL, Louiselle DA, Puckett LMB, Beyer S, Neal SH, Sierant V, McBeth M, Belden B, Walter AM, Gibson M, Cheung WA, Johnston JJ, Thiffault I, Farrow EG, Grundberg E, Pastinen T.
Zion TN, et al. Among authors: biswell rl.
Genet Med. 2023 May;25(5):100020. doi: 10.1016/j.gim.2023.100020. Epub 2023 Jan 28.
Genet Med. 2023.
PMID: 36718845
Free PMC article.
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Case of CLPB deficiency solved by HiFi long read genome sequencing and RNAseq.
Farrow E, Jay A, Means J, Younger S, Biswell R, Koseva B, Thiffault I, Pastinen T, Pappas K, Toriello H.
Farrow E, et al.
Am J Med Genet A. 2023 Dec;191(12):2908-2912. doi: 10.1002/ajmg.a.63365. Epub 2023 Aug 7.
Am J Med Genet A. 2023.
PMID: 37548286
No abstract available.
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