S

Stephanie M. Ware

Indiana University School of Medicine

ORCID: 0000-0003-4714-0142

251 papers and 8.6k citations.

PubIndex Score65Top 35% · seniorHow it's scored

251Publications

8.6kTotal Citations

First publication: 2002First senior author: 2006

Top publicationsby citations

High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders

J. Pablo Abonia, Marc E. Rothenberg, James P. Franciosi et al.|Journal of Allergy and Clinical Immunology|2013

Cited by 192

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations

Bhagyalaxmi Mohapatra, Stephanie M. Ware|Human Molecular Genetics|2008

Cited by 173

Spectrum of Clinical Diseases Caused By Disorders of Primary Cilia

Stephanie M. Ware, Friedhelm Hildebrandt, Mahmure Aygün|Proceedings of the American Thoracic Society|2011

Cited by 106

Single cell RNA analysis of the left–right organizer transcriptome reveals potential novel heterotaxy genes

Helen M. Bellchambers, Stephanie M. Ware, Amruta R. Phatak et al.|Scientific Reports|2023

Cited by 4

Non-coding cause of congenital heart defects: Abnormal RNA splicing with multiple isoforms as a mechanism for heterotaxy

John R Wells, Stephanie M. Ware|Human Genetics and Genomics Advances|2024

Cited by 2

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