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An ontogenetic switch drives the positive and negative selection of B cells.

Journal article

Xu X. et al, (2020), Proc Natl Acad Sci U S A, 117, 3718 - 3727

Co-transcriptional Loading of RNA Export Factors Shapes the Human Transcriptome.

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Viphakone N. et al, (2019), Mol Cell, 75, 310 - 323.e8

CGAT-core: a python framework for building scalable, reproducible computational biology workflows

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Cribbs AP. et al, (2019), F1000Research, 8, 377 - 377

An essential role for the Zn2+ transporter ZIP7 in B cell development.

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Anzilotti C. et al, (2019), Nat Immunol, 20, 350 - 361

Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.

Journal article

Morgan MD. et al, (2018), Nat Commun, 9

The epigenetic regulation of mouse cerebellar development

Conference paper

Riegman KLH. et al, (2018), GENETICS RESEARCH, 100

Genomic Response to Vitamin D Supplementation in the Setting of a Randomized, Placebo-Controlled Trial.

Journal article

Berlanga-Taylor AJ. et al, (2018), EBioMedicine, 31, 133 - 142

Stem cell modeling of mitochondrial parkinsonism reveals key functions of OPA1.

Journal article

Jonikas M. et al, (2018), Ann Neurol, 83, 915 - 925

De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.

Journal article

Fry AE. et al, (2018), Brain, 141, 698 - 712

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44.

Journal article

Watson LM. et al, (2017), Am J Hum Genet, 101

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44.

Journal article

Watson LM. et al, (2017), Am J Hum Genet, 101

Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44.

Journal article

Watson LM. et al, (2017), Am J Hum Genet, 101, 451 - 458

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