ScholarIQanswers from OpenAlex & ORCID
Marie C. Hogan
ResearcherPublications, citations & collaboration network
Marie C. Hogan is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Marie C. Hogan have?
ScholarIQindexed works
Marie C. Hogan has 207 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Marie C. Hogan have?
ScholarIQcitation count
Marie C. Hogan has 10,869 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Marie C. Hogan?
ScholarIQh-index
Marie C. Hogan has an h-index of 54 in OpenAlex.
What is the i10-index of Marie C. Hogan?
ScholarIQi10-index
Marie C. Hogan has an i10-index of 112 in OpenAlex.
What is the ORCID of Marie C. Hogan?
ScholarIQorcid
The ORCID for Marie C. Hogan is on the source record.
What is the OpenAlex record for Marie C. Hogan?
ScholarIQopenalex
The OpenAlex for Marie C. Hogan is on the source record.
What are the most-cited papers on Marie C. Hogan?
ScholarIQmost cited works
The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein
Christopher J. Ward, Marie C. Hogan, Sandro Rossetti, Denise L. Walker, Tam P. Sneddon, Xiaofang Wang, Vicky Kubly, Julie M. Cunningham, Robert L. Bacallao, Masahiko Ishibashi, Dawn S. Milliner, Vicente E. Torres, Peter C. Harris
Imaging Classification of Autosomal Dominant Polycystic Kidney Disease
María V. Irazabal, Laureano J. Rangel, Eric J. Bergstralh, Sara L. Osborn, Amber J. Harmon, Jamie L. Sundsbak, Kyongtae T. Bae, Arlene B. Chapman, Jared J. Grantham, Michal Mrug, Marie C. Hogan, Ziad Zoghby, Peter C. Harris, Bradley J. Erickson, Bernard F. King, Vicente E. Torres
Blood Pressure in Early Autosomal Dominant Polycystic Kidney Disease
Robert W. Schrier, Kaleab Z. Abebe, Ronald D. Perrone, Vicente E. Torres, William E. Braun, Theodore I. Steinman, Franz T. Winklhofer, Godela Brosnahan, Peter G. Czarnecki, Marie C. Hogan, Dana C. Miskulin, Frederic F. Rahbari-Oskoui, Jared J. Grantham, Peter C. Harris, Michael F. Flessner, Kyongtae T. Bae, Charity G. Moore, Arlene B. Chapman
Mutations in GANAB , Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease
Binu Porath, Vladimir G. Gainullin, Émilie Cornec-Le Gall, Elizabeth K. Dillinger, Christina M. Heyer, Katharina Hopp, Marie E. Edwards, Charles D. Madsen, Sarah R. Mauritz, Carly J. Banks, Saurabh Baheti, Bharathi Reddy, J.I. Herrero, Jesús M. Bañales, Marie C. Hogan, Velibor Tasić, Terry Watnick, Arlene B. Chapman, Cécile Vigneau, Frédéric Lavainne, M.‐P. Audrézet, Claude Férec, Yannick Le Meur, Vicente E. Torres, Peter C. Harris
Response of Wegener's granulomatosis to anti-CD20 chimeric monoclonal antibody therapy
Ulrich Specks, Fernando C. Fervenza, Thomas J. McDonald, Marie C. Hogan