Concepedia

Author

Stephanie Halford

University of OxfordORCID

Also Known As

Angela Howard, H. J. Kim, Michael E. Cheetham, S HALFORD, S Halford, S. Halford, Stephanie Halford, Susan Downes

114

Publications

4.7K

Citations

37

H-Index

89

Concepts

All Affiliations

University of OxfordUniversity College LondonCentre for Human GeneticsNewcastle UniversitySt. Mary's Hospital
SH

About

Stephanie Halford is an author at University of Oxford specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

19

21

1.4K

2

Natural Sciences

7

7

520

3

Public Health

3

3

171

4

Health Sciences

1

1

120

5

Social Sciences

1

1

167

Stephanie Halford

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47

Publications

3.6K

Citations

31

H-Index

YearCitations

Large-Scale Association Studies of Variants in Genes Encoding the Pancreatic β-Cell KATP Channel Subunits Kir6.2 (<i>KCNJ11</i>) and SUR1 (<i>ABCC8</i>) Confirm That the <i>KCNJ11</i> E23K Variant Is Associated With Type 2 Diabetes

Anna L. Gloyn, Michael N. Weedon, Katharine R. Owen,

Diabetes

2003

753

VA Opsin-Based Photoreceptors in the Hypothalamus of Birds

Stephanie Halford, Susana S. Pires, Michael Turton,

Current Biology

2009

167

Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome.

A H Carey, David A. Kelly, Stephanie Halford,

PubMed

1992

158

Targeted Mutagenesis of the <i>Hira</i> Gene Results in Gastrulation Defects and Patterning Abnormalities of Mesoendodermal Derivatives Prior to Early Embryonic Lethality

Catherine Roberts, Helen Sutherland, Hannah Farmer,

Molecular and Cellular Biology

2002

153

Functional diversity of melanopsins and their global expression in the teleost retina

Wayne I. L. Davies, Lei Zheng, Steven Hughes,

Cellular and Molecular Life Sciences

2011

120

Identification of a New Human Catenin Gene Family Member (ARVCF) from the Region Deleted in Velo–Cardio–Facial Syndrome

Howard I. Sirotkin, Hilary O‘Donnell, Ruchira DasGupta,

Genomics

1997

107

Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)☆

Samantha Johnson, Stephanie Halford, Alex Morris,

Genomics

2003

105

Characterization of a Novel Human Opsin Gene with Wide Tissue Expression and Identification of Embedded and Flanking Genes on Chromosome 1q43

Stephanie Halford, Melanie S. Freedman, James Bellingham,

Genomics

2001

102

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.

Helen Sutherland, R Wadey, Judith M. McKie,

PubMed

1996

101

Detailed Phenotypic and Genotypic Characterization of Bietti Crystalline Dystrophy

Stephanie Halford, Gerald Liew, Donna S. Mackay,

Ophthalmology

2014

100

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