Sian Ellard - Concepedia

Author

Sian Ellard

Also Known As

; Consiglione, A. Hadonou, Andrew T. Hattersley, Bingham, C, Christopher Hyde, Corin A. Yeats, David G. Partridge, E. Renström, Ellard S, Ellard S.

918

Publications

54.5K

Citations

118

H-Index

243

Concepts

All Affiliations

University of Exeter Royal Devon & Exeter NHS Foundation Trust Peninsula College of Medicine and Dentistry University College London University of Oxford

About

Sian Ellard is an author at University of Exeter specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	57	138	15.8K
2	Health Sciences	15	17	1.8K
3	Public Health	12	15	3K
4	Natural Sciences	9	9	410
5	Engineering	2	2	290

Sian Ellard

433

Publications

44K

Citations

106

H-Index

Page 1

	Year	Citations
A Common Variant in the <i>FTO</i> Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity Timothy M. Frayling, Nicholas J. Timpson, Michael N. Weedon, Science	2007	4.4K
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes Eleftheria Zeggini, Michael N. Weedon, Cecilia M. Lindgren, Science GeneticsGenetic EpidemiologyGenomicsGenome-wide Association SignalsInsulin Signaling	2007	2.2K
Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes Anna L. Gloyn, Ewan R. Pearson, Jennifer F. Antcliff, New England Journal of Medicine	2004	1.1K
Switching from Insulin to Oral Sulfonylureas in Patients with Diabetes Due to Kir6.2 Mutations Ewan R. Pearson, Isabelle Flechtner, Pål R. Njølstad, New England Journal of Medicine	2006	979
Maturity-onset diabetes of the young (MODY): how many cases are we missing? Beverley M. Shields, Sarah Hicks, Maggie Shepherd, Diabetologia Metabolic SyndromeMany CasesDiabetes ManagementLongevityInsulin Management	2010	699
Mutations in the glucokinase gene of the fetus result in reduced birth weight Andrew T. Hattersley, Frances Beards, Elizabeth Ballantyne, Nature Genetics Glucokinase GeneDevelopmental BiologyGeneticsInherited Metabolic DiseaseFetal Medicine	1998	601
Insulin gene mutations as a cause of permanent neonatal diabetes Julie Støy, Emma L. Edghill, Sarah E. Flanagan, Proceedings of the National Academy of Sciences GeneticsInsulin SignalingMetabolic SyndromeProtein FoldingNeonatal Diabetes	2007	552
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57 Deborah Mackay, Jonathan L A Callaway, Sophie M Marks, Nature Genetics Developmental BiologyGenetic DisorderMultiple Imprinted LociGeneticsDiabetes	2008	524
Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease Sarah E. Flanagan, Emma Haapaniemi, Mark A. Russell, Nature Genetics ImmunogeneticsAutoimmune DiseaseAutoantibody ProductionImmune Cell DevelopmentImmunodeficiencies	2014	484
Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria Vikas Pejaver, Alicia B. Byrne, Bing Feng, The American Journal of Human Genetics	2022	471

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