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A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discovery.
HGG Adv. 2024 Oct 10;6(1):100371. doi: 10.1016/j.xhgg.2024.100371. Online ahead of print.
HGG Adv. 2024.
PMID: 39394689
Free PMC article.
How Interoperability Can Enable Artificial Intelligence in Clinical Applications.
Rehburg F, Graefe A, Hübner M, Thun S.
Rehburg F, et al.
Stud Health Technol Inform. 2024 Aug 22;316:596-600. doi: 10.3233/SHTI240485.
Stud Health Technol Inform. 2024.
PMID: 39176813
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Review of Key Elements in Developing a Common Data Model for Rare Diseases: Identifying Common Success Factors.
Graefe ASL, Rehburg F, Hübner M, Thun S, Beyan O.
Graefe ASL, et al. Among authors: rehburg f.
Stud Health Technol Inform. 2024 Aug 22;316:1396-1400. doi: 10.3233/SHTI240672.
Stud Health Technol Inform. 2024.
PMID: 39176641
Review.
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A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery.
Danis D, Bamshad MJ, Bridges Y, Cacheiro P, Carmody LC, Chong JX, Coleman B, Dalgleish R, Freeman PJ, Graefe ASL, Groza T, Jacobsen JOB, Klocperk A, Kusters M, Ladewig MS, Marcello AJ, Mattina T, Mungall CJ, Munoz-Torres MC, Reese JT, Rehburg F, Reis BCS, Schuetz C, Smedley D, Strauss T, Sundaramurthi JC, Thun S, Wissink K, Wagstaff JF, Zocche D, Haendel MA, Robinson PN.
Danis D, et al. Among authors: rehburg f.
medRxiv [Preprint]. 2024 May 29:2024.05.29.24308104. doi: 10.1101/2024.05.29.24308104.
medRxiv. 2024.
Update in:
HGG Adv. 2024 Oct 10;6(1):100371. doi: 10.1016/j.xhgg.2024.100371
PMID: 38854034
Free PMC article.
Updated.
Preprint.
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