Author

Danielle Whittaker

Guy's HospitalORCID 0000-0003-0240-8141Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 2 Assay:ATAC-seq· 1 Assay:ChIP-seq· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:Hi-C· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Kimberley L. H. Riegman· 2 shared M. Albert BassoniD· 2 shared Alyssa Julia Jennifer PaganoniiD· 1 shared Anna Maria CariboniiD· 1 shared Antonella LettieriiD· 1 shared Brian J.P. HuntlyiD· 1 shared Cameron S. OsborneiD· 1 shared Charlotte GeorgeiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersNeuroscience

Kimberley L. H. Riegman

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintAug 22, 2024

The long-range gene regulatory landscape of cerebellar granule neuron progenitors

Kimberley L. H. Riegman, Charlotte George, Danielle Whittaker…·M. Albert Basson

The paper identifies long-range gene regulatory interactions in cerebellar granule neuron progenitors using pcHi-C, ATAC-seq, and ChIP-seq, revealing co-regulation by Atoh1 and CHD7.

DOI 10.1101/2024.08.22.609103

mouseHi-C

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Genetic & Genomic MedicineJournal of Clinical InvestigationPeer-reviewedNov 3, 2021

A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia

Danielle Whittaker, Roberto Oleari, Louise Cheryl Gregory…·Mehul Dattani

This study identifies a recessive PRDM13 mutation causing congenital hypogonadotropic hypogonadism and cerebellar hypoplasia through mouse models and human expression analysis.

31 citationstop 4%

humanmouse

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