Sarah Hewitt - Concepedia

Author

Sarah Hewitt

Also Known As

Alex Henderson, Alison Kraus, Angus Dobbie, Georgina Hollingsworth, Hewitt, Sarah, Lucy Hildyard, S. Hewitt, Sarah Edkins, Sarah Hewitt, Sarah K. Hewitt

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

University of Manchester St James's University Hospital University of Leeds University of Liverpool Wessex Regional Genetics Laboratory

About

Sarah Hewitt is an author at University of Manchester specializing in genetics, medicine, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	276
2	Engineering	1	1	33
3	Natural Sciences	1	1	44
4	Public Health	1	1	36
5	Social Sciences	1	1	97

Sarah Hewitt

Publications

456

Citations

H-Index

Page 1

	Year	Citations
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy Anne O’Donnell‐Luria, Lynn Pais, Víctor Faúndes, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental BiologyHeterozygous VariantsKmt2e CauseGenetics	2019	97
Sequencing and Characterisation of Rearrangements in Three S. pastorianus Strains Reveals the Presence of Chimeric Genes and Gives Evidence of Breakpoint Reuse Sarah Hewitt, Ian J. Donaldson, Simon C. Lovell, PLoS ONE	2014	71
Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation Josie Hayes, Antigoni Tzika, Helene Thygesen, Genomics Dna SequencingPopulation GeneticsMolecular EcologyMedicineGenetics	2013	66
Phenotypic heterogeneity in fungi: Importance and methodology Sarah Hewitt, David S. Foster, Paul S. Dyer, Fungal Biology Reviews	2016	61
Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplications Christopher M. Watson, Laura A. Crinnion, Sarah Hewitt, Laboratory Investigation Dna SequencingSingle-molecule SequencingSequencingFunctional GenomicsGenomic Duplications	2019	44
Prevalence, phenotype and architecture of developmental disorders caused by <i>de novo</i> mutation: The Deciphering Developmental Disorders Study Jeremy F. McRae, Stephen Clayton, Tomas Fitzgerald, Exome SequencingGeneticsGenetic EpidemiologyDisease Gene IdentificationGenomics	2016	36
Diagnostic whole genome sequencing and split‐read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome Christopher M. Watson, Laura A. Crinnion, Antigoni Tzika, American Journal of Medical Genetics Part A Cntnap2 Deficiency SyndromeEngineeringWhole Genome SequencingSplit‐read MappingGenetic Disorder	2014	33
Plasticity of Mitochondrial DNA Inheritance and Its Impact on Nuclear Gene Transcription in Yeast Hybrids Sarah Hewitt, Kobchai Duangrattanalert, Tim Burgis, Microorganisms	2020	30
New colours for old in the blue-cheese fungus Penicillium roqueforti Matthew M. Cleere, Michaela Novodvorska, Elena Geib, npj Science of Food	2024	18

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