Author

Christopher M. Richmond

Griffith UniversityORCID 0000-0002-9778-4344Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

Tahsin Stefan BarakatiD· 2 shared Ahmed Aly IbrahimiD· 1 shared Alain VerloèsiD· 1 shared Albena Todorova· 1 shared Alekh ParanjapyeiD· 1 shared Aleš MaveriD· 1 shared Alexander J.M. DingemansiD· 1 shared Allan Micheil InnesiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Tahsin Stefan BarakatORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 31, 2024

Loss of DOT1L disrupts neuronal transcription, behavior, and leads to a neurodevelopmental disorder

Marissa J. Maroni, Melissa Barton, Katherine Lynch…·Erica Korb

This study shows that partial loss of DOT1L causes transcriptional, morphological, and behavioral defects in neurons across multiple models.

3 citations

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedMar 25, 2022

Inherited variants in CHD3 demonstrate variable expressivity in Snijders Blok-Campeau syndrome

Jet van der Spek, Joery den Hoed, Lot Snijders Blok…·Tjitske Kleefstra

The paper shows inherited CHD3 variants cause Snijders Blok-Campeau syndrome with variable expressivity, overlapping with de novo variants' phenotypes, and suggests reduced penetrance is not due to expression compensation.

33 citationstop 5%

humanwhole-exome sequencing