Shira G. Ziegler - Concepedia

Author

Shira G. Ziegler

National Human Genome Research Institute ORCID

Also Known As

S Ziegler, S. Ziegler, S.G. Ziegler, Shira G. Ziegler, Shira Ziegler

Publications

3.7K

Citations

H-Index

Concepts

All Affiliations

National Human Genome Research Institute National Institutes of Health Johns Hopkins Medicine Johns Hopkins University National Heart Lung and Blood Institute

About

Shira G. Ziegler is an author at National Human Genome Research Institute specializing in medicine, pathology, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	613
2	Social Sciences	3	3	115
3	Health Sciences	2	2	42
4	Education	1	1	82
5	Natural Sciences	1	1	12

Shira G. Ziegler

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease E. Sidransky, Mike A. Nalls, Jan Aasly, New England Journal of Medicine	2009	2.1K
<i>NT5E</i> Mutations and Arterial Calcifications Cynthia St. Hilaire, Shira G. Ziegler, Thomas C. Markello, New England Journal of Medicine	2011	444
Vascular pathology of medial arterial calcifications in NT5E deficiency: Implications for the role of adenosine in pseudoxanthoma elasticum Thomas C. Markello, Laura K. Pak, Cynthia St. Hilaire, Molecular Genetics and Metabolism MechanobiologyNt5e DeficiencyVascular DiseaseVascular AdaptationPhysiology	2011	115
Lineage-specific events underlie aortic root aneurysm pathogenesis in Loeys-Dietz syndrome Elena Gallo MacFarlane, Sarah J. Parker, Joseph Shin, Journal of Clinical Investigation	2019	115
Ectopic calcification in pseudoxanthoma elasticum responds to inhibition of tissue-nonspecific alkaline phosphatase Shira G. Ziegler, Carlos R. Ferreira, Elena Gallo MacFarlane, Science Translational Medicine	2017	108
Glucocerebrosidase mutations in Chinese subjects from Taiwan with sporadic Parkinson disease Shira G. Ziegler, Michael J. Eblan, Usha Gutti, Molecular Genetics and Metabolism Chinese SubjectsMendelian DisorderGeneticsParkinson DiseasePathology	2007	107
PKHD1 sequence variations in 78 children and adults with autosomal recessive polycystic kidney disease and congenital hepatic fibrosis Meral Gunay‐Aygun, M. Tuchman, Esperanza Font–Montgomery, Molecular Genetics and Metabolism Pkhd1 Sequence VariationsHepatologyMendelian DisorderGenetic DisorderMedicine	2009	98
Prospective phenotyping of long-term survivors of generalized arterial calcification of infancy (GACI) Carlos R. Ferreira, Mary E. Hackbarth, Shira G. Ziegler, Genetics in Medicine NeonatologyCardiovascular DiseasePediatric Heart DiseaseMedicineArterial Reconstructions	2020	82
The phenotype of the musculocontractural type of Ehlers‐Danlos syndrome due to <i>CHST14</i> mutations Andreas Janecke, Ben Li, Manfred Boehm, American Journal of Medical Genetics Part A	2015	62
Hypercementosis Associated with <i>ENPP1</i> Mutations and GACI Vivek Thumbigere‐Math, Areej Alqadi, Natalia I. Chalmers, Journal of Dental Research	2017	61

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