Jacqueline K. White - Concepedia

Author

Jacqueline K. White

Also Known As

Cheryl L. Scudamore, Chris Lelliott, David J Adams, Day, Diane Gleeson, J K White, Jacqueline K White, Jacqueline K. White, Jacqueline Katie White, Jacqueline White

154

Publications

7.4K

Citations

H-Index

129

Concepts

All Affiliations

Wellcome Sanger Institute Jackson Laboratory University of Cambridge University of Oxford Toronto Centre for Phenogenomics

About

Jacqueline K. White is an author at Wellcome Sanger Institute specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	27	4.7K
2	Engineering	5	5	402
3	Health Sciences	5	5	240
4	Arts	1	1	67
5	Natural Sciences	1	1	92

Jacqueline K. White

Publications

Citations

H-Index

Page 1

	Year	Citations
High-throughput discovery of novel developmental phenotypes Mary E. Dickinson, Ann M. Flenniken, Xiao Ji, Nature Genetic AnalysisHigh-throughput DiscoveryFunctional GenomicsDevelopmental BiologyGenetics	2016	1.3K
Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion Jacqueline K. White, Wojtek Auerbach, Mabel P. Duyao, Nature Genetics Knockout MouseDisease Cag ExpansionDevelopmental BiologyGeneticsDegenerative Disease	1997	521
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains Michelle M. Simon, Simon Greenaway, Jacqueline K. White, Genome biology	2013	520
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis John P. Kemp, John Morris, Carolina Medina‐Gómez, Nature Genetics Bone DiseaseBone HealthFunctional InvolvementPathologyBone Metabolism	2017	503
Placentation defects are highly prevalent in embryonic lethal mouse mutants Vicente Pérez-García, Elena Fineberg, Robert Wilson, Nature Knockout MouseDevelopmental BiologyGeneticsMorphogenesisPlacentation Defects	2018	371
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium Terrence F. Meehan, Nathalie Conte, David B. West, Nature Genetics BioinformaticsDisease ModelsKnockout MouseGeneticsGenetic Epidemiology	2017	260
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement Yu Sun, Beata Bąk, Nadia Schoenmakers, Nature Genetics Developmental BiologyMendelian DisorderCentral HypothyroidismGenetic DisorderGenetics	2012	215
Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesis Leslie O. Goodwin, Erik Splinter, Tiffany L. Davis, Genome Research EngineeringLarge-scale DiscoveryTransgenic Mouse ModelsGeneticsGenomic Mechanism	2019	215
Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics Martin Hrabě de Angelis, George Nicholson, Mohammed Selloum, Nature Genetics Knockout MouseFunctional GenomicsTransgenic Mouse ModelsGeneticsMouse Clinics	2015	157
Genomic Organization and Sequence of the Human NRAMP Gene: Identification and Mapping of a Promoter Region Polymorphism Jenefer M. Blackwell, Chris Barton, Jacqueline K. White, Molecular Medicine Genetic AnalysisGenomic OrganizationPromoter Region PolymorphismGeneticsHuman Polymorphism	1995	144

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