VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q79747949 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000340.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q79747949‏
024 ‎‡a 0000-0001-8470-9719‏ ‎‡2 orcid‏
024 ‎‡a 12809642500‏ ‎‡2 scopus‏
035 ‎‡a (OCoLC)Q79747949‏
100 0 ‎‡a María M Abad-Grau‏ ‎‡c researcher‏ ‎‡9 en‏
400 0 ‎‡a María M Abad-Grau‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's A comparison of genomic profiles of complex diseases under different models.‏
670 ‎‡a Author's A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis.‏
670 ‎‡a Author's Building chromosome-wide LD maps‏
670 ‎‡a Author's Evolution and challenges in the design of computational systems for triage assistance.‏
670 ‎‡a Author's GeneOnEarth: fitting genetic PC plots on the globe.‏
670 ‎‡a Author's Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis‏
670 ‎‡a Author's IL2RA/CD25 gene polymorphisms: uneven association with multiple sclerosis (MS) and type 1 diabetes (T1D).‏
670 ‎‡a Author's Increasing power by using haplotype similarity in a multimarker transmission/disequilibrium test.‏
670 ‎‡a Author's Members 6B and 14 of the TNF receptor superfamily in multiple sclerosis predisposition‏
670 ‎‡a Author's Sample reproducibility of genetic association using different multimarker TDTs in genome-wide association studies: characterization and a new approach.‏
909 ‎‡a (orcid) 0000000184709719‏ ‎‡9 1‏
909 ‎‡a (scopus) 12809642500‏ ‎‡9 1‏
919 ‎‡a comparisonofgenomicprofilesofcomplexdiseasesunderdifferentmodels‏ ‎‡A A comparison of genomic profiles of complex diseases under different models.‏ ‎‡9 1‏
919 ‎‡a functionalvariantthataffectsexonskippingandproteinexpressionofsp140asgeneticmechanismpredisposingtomultiplesclerosis‏ ‎‡A A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis.‏ ‎‡9 1‏
919 ‎‡a buildingchromosomewideldmaps‏ ‎‡A Building chromosome-wide LD maps‏ ‎‡9 1‏
919 ‎‡a evolutionandchallengesinthedesignofcomputationalsystemsfortriageassistance‏ ‎‡A Evolution and challenges in the design of computational systems for triage assistance.‏ ‎‡9 1‏
919 ‎‡a geneonearthfittinggeneticpcplotsontheglobe‏ ‎‡A GeneOnEarth: fitting genetic PC plots on the globe.‏ ‎‡9 1‏
919 ‎‡a identificationofafunctionalvariantinthekif5acyp27b1mettl1fam119blocusassociatedwithmultiplesclerosis‏ ‎‡A Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis‏ ‎‡9 1‏
919 ‎‡a il2racd25genepolymorphismsunevenassociationwithmultiplesclerosismsandtype1diabetest1d‏ ‎‡A IL2RA/CD25 gene polymorphisms: uneven association with multiple sclerosis (MS) and type 1 diabetes (T1D).‏ ‎‡9 1‏
919 ‎‡a increasingpowerbyusinghaplotypesimilarityinamultimarkertransmissiondisequilibriumtest‏ ‎‡A Increasing power by using haplotype similarity in a multimarker transmission/disequilibrium test.‏ ‎‡9 1‏
919 ‎‡a members6band14ofthetnfreceptorsuperfamilyinmultiplesclerosispredisposition‏ ‎‡A Members 6B and 14 of the TNF receptor superfamily in multiple sclerosis predisposition‏ ‎‡9 1‏
919 ‎‡a samplereproducibilityofgeneticassociationusingdifferentmultimarkertdtsingenomewideassociationstudiescharacterizationandanewapproach‏ ‎‡A Sample reproducibility of genetic association using different multimarker TDTs in genome-wide association studies: characterization and a new approach.‏ ‎‡9 1‏
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏