Andrea H. Sorenson - Concepedia

Concepedia

Author

Andrea H. Sorenson

Indiana University – Purdue University Indianapolis

Also Known As

A H Sorenson, Andrea H. Sorenson

9

Publications

1.2K

Citations

9

H-Index

15

Concepts

All Affiliations

Indiana University – Purdue University Indianapolis Indiana University School of Medicine

AH

About

Andrea H. Sorenson is an author at Indiana University – Purdue University Indianapolis specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	582
2	Natural Sciences	2	2	517
3	Biochemistry	2	2	517
4	Metabolism	2	2	517
5	Molecular Biology	1	1	65

Andrea H. Sorenson

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9

Publications

1.2K

Citations

9

H-Index

	Year	Citations
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis Shoji Ichikawa, Erik A. Imel, Mary L. Kreiter, Journal of Clinical Investigation GeneticsPathologyTumor BiologyVitamin D HomeostasisParathyroid Hormone	2007	471
Ablation of the Galnt3 Gene Leads to Low-Circulating Intact Fibroblast Growth Factor 23 (Fgf23) Concentrations and Hyperphosphatemia Despite Increased Fgf23 Expression Shoji Ichikawa, Andrea H. Sorenson, Anthony M. Austin, Endocrinology	2009	146
Intronic Deletions in the<i>SLC34A3</i>Gene Cause Hereditary Hypophosphatemic Rickets with Hypercalciuria Shoji Ichikawa, Andrea H. Sorenson, Erik A. Imel, The Journal of Clinical Endocrinology & Metabolism	2006	135
Clinical variability of familial tumoral calcinosis caused by novel <i>GALNT3</i> mutations Shoji Ichikawa, Geneviève Baujat, Aksel Seyahi, American Journal of Medical Genetics Part A	2010	122
Novel GALNT3 Mutations Causing Hyperostosis-Hyperphosphatemia Syndrome Result in Low Intact Fibroblast Growth Factor 23 Concentrations Shoji Ichikawa, Vincent Guigonis, Erik A. Imel, The Journal of Clinical Endocrinology & Metabolism	2007	90
Tumoral Calcinosis Presenting with Eyelid Calcifications due to Novel Missense Mutations in the Glycosyl Transferase Domain of the<i>GALNT3</i>Gene Shoji Ichikawa, Erik A. Imel, Andrea H. Sorenson, The Journal of Clinical Endocrinology & Metabolism	2006	85
Mutational survey of the PHEX gene in patients with X-linked hypophosphatemic rickets Shoji Ichikawa, Elizabeth A. Traxler, Selina A. Estwick, Bone Molecular PhysiologyMutational SurveyGenetic DisorderGeneticsInherited Metabolic Disease	2008	65
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis. Shoji Ichikawa, Erik A. Imel, Mary L. Kreiter, PubMed GeneticsPathologyTumor BiologyVitamin D HomeostasisParathyroid Hormone	2008	46
Discordance for X-Linked Hypophosphataemic Rickets in Identical Twin Girls Catherine Owen, Abdul Habeb, Simon H. S. Pearce, Hormone Research in Paediatrics	2009	11

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