James Cleak

Mary Lyon Centre at MRC Harwell — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

14h-index4.8kcitations25works6.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Mitochondrial Function and Pathology(4), CRISPR and Genetic Engineering(4), Genetic Mapping and Diversity in Plants and Animals(4), Microtubule and mitosis dynamics(3), RNA and protein synthesis mechanisms(3)

Publications24 total

Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines
Scientific Reports·2024· 6 citedOpen Access
Cleft palate and minor metabolic disturbances in a mouse global <i>Arl15</i> gene knockout
The FASEB Journal·2023Open Access
Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice
Orphanet Journal of Rare Diseases·2022· 5 citedOpen Access
Mendelian gene identification through mouse embryo viability screening
Genome Medicine·2022· 14 citedOpen Access
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
Nature Cardiovascular Research·2022· 4 citedOpen Access
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
Nature Cardiovascular Research·2022· 66 citedOpen Access
Mendelian gene identification through mouse embryo viability screening
2022· 2 citedOpen Access
A novel knockout mouse for the small EDRK-rich factor 2 (Serf2) showing developmental and other deficits
Mammalian Genome·2021· 12 citedOpen Access
Collaborative Cross mice and their power to map host susceptibility to Aspergillus fumigatus infection
UNC Libraries·2020· 7 citedOpen Access
Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations
Scientific Reports·2020· 17 citedOpen Access
Diverse Species-Specific Phenotypic Consequences of Loss of Function <i>Sorting Nexin 14</i> Mutations
2019Open Access
Identification of genetic elements in metabolism by high-throughput mouse phenotyping
Nature Communications·2018· 71 citedOpen Access
Erratum: Corrigendum: High-throughput discovery of novel developmental phenotypes
Nature·2017· 14 citedOpen Access
Prevalence of sexual dimorphism in mammalian phenotypic traits
Nature Communications·2017· 267 citedOpen Access
High-throughput discovery of novel developmental phenotypes
Nature·2016· 1.3k citedOpen Access
The Architecture of Parent-of-Origin Effects in Mice
Cell·2014· 89 citedOpen Access
Sequence-based characterization of structural variation in the mouse genome
Nature·2011· 324 cited
Mouse genomic variation and its effect on phenotypes and gene regulation
Nature·2011· 1.7k citedOpen Access
Cytoarchitectural disruption of the superior colliculus and an enlarged acoustic startle response in the Tuba1a mutant mouse
Neuroscience·2011· 7 citedOpen Access
Collaborative Cross mice and their power to map host susceptibility to<i>Aspergillus fumigatus</i>infection
Genome Research·2011· 154 citedOpen Access
page 1 of 2Next →

Frequent Co-authors

Lydia Teboul(12), Jonathan Flint(8), Jeremy Mason(8), Richard Mott(7), David J. Adams(7), Sara Johnson(7), Henrik Westerberg(6), Chih‐Wei Hsu(6), Kevin A. Peterson(6), Zsombor Szoke-Kovacs(6), Helen Parkinson(6), Ann‐Marie Mallon(6), K. C. Kent Lloyd(6), Colin McKerlie(6), Michelle Stewart(6), Binnaz Yalcin(5), Ann M. Flenniken(5), Jacqueline K. White(5), Lynette Bower(5), Sowmya Kalaga(5)