about
DoCM: a database of curated mutations in cancer.Prioritization of retinal disease genes: an integrative approachOptic nerve crush induces spatial and temporal gene expression patterns in retina and optic nerve of BALB/cJ mice.Transcriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-SeqDGIdb 2.0: mining clinically relevant drug-gene interactions.Exon-level expression profiling of ocular tissues.GenVisR: Genomic Visualizations in RNon-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease.Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standardsGenVisR: Genomic Visualizations in RA deep learning approach to automate refinement of somatic variant calling from cancer sequencing dataRecurrent WNT pathway alterations are frequent in relapsed small cell lung cancerFHIR Genomics: enabling standardization for precision medicine use casesA harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer
P50
Q27942768-43448274-22D3-4E4E-A255-2D02092A43E4Q31113482-9130F6E5-DC9C-4362-9051-69017B360D95Q33960323-C0E4EEBA-E0A6-4E1E-BF42-620499D40B0AQ34657009-EFEAB74C-62C4-4804-9E61-0F2092563FD0Q36434749-363232BE-E6FF-43F6-862D-43E6D5707140Q36875675-76DBDD8D-0006-4E3B-A3AC-47657FB4B7D5Q37291788-5D7AA91C-285B-4E77-8588-0A1529E12819Q37346967-0635AA63-C76D-4A80-8C8D-ECDECDFE28C1Q57455605-40C2C870-2E19-4642-8D57-019F56834100Q57903508-301865F8-0BBE-4975-9903-45E5CD59D5B8Q58611495-A4B6513B-055B-40EA-8509-B9B5B981452AQ58734416-EB8BDF1E-372C-4CC1-B3DA-0B9771BDC633Q90482590-1996E7A3-FAD7-43CF-B761-5DC3918717BCQ91556269-D36D2AE0-84C4-4DAD-9997-0CD7DCA19DCF
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-2502-8961
@en
name
Alex H Wagner
@ast
Alex H Wagner
@en
Alex H Wagner
@nl
type
label
Alex H Wagner
@ast
Alex H Wagner
@en
Alex H Wagner
@nl
prefLabel
Alex H Wagner
@ast
Alex H Wagner
@en
Alex H Wagner
@nl
P106
P31
P496
0000-0002-2502-8961