Author

Dianne F. Newbury

Oxford Brookes UniversityORCID 0000-0002-9557-268XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:eQTL / molecular QTL mapping· 1

Frequent Co-Authors

A. Kuechler· 1 shared A. Petersen· 1 shared A. Vaknin-Dembinsky· 1 shared A. Waheeb· 1 shared Adam JacksoniD· 1 shared Alexander J.M. DingemansiD· 1 shared Alexander P.A. StegmanniD· 1 shared Alexandre ReymondiD· 1 shared

Activity by Year

2021-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

A. Kuechler

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJun 29, 2021

Analysis of expression Quantitative Trait Loci for NLGN4X in relation to language and neurodevelopmental function: an exploratory analysis using FUSION and GTEx workflows

Nuala H. Simpson, Dorothy Bishop, Dianne F. Newbury

The paper explores eQTLs for NLGN4X in relation to language and neurodevelopmental traits using FUSION and GTEx, finding no significant associations in twin samples.

DOI 10.1101/2021.06.29.450314

humanbulk RNA-seq

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GeneticsThe American Journal of Human GeneticsPeer-reviewedJan 28, 2021

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Joery den Hoed, Elke de Boer, Norine Voisin…·Lisenka E.L.M. Vissers

The paper identifies mutation-specific pathophysiological mechanisms in SATB1 variants causing distinct neurodevelopmental disorders.

52 citationstop 2%

humanstatistical model

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