ScholarIQanswers from OpenAlex & ORCID
Julia Hoefele
ResearcherPublications, citations & collaboration network
Julia Hoefele is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Julia Hoefele have?
ScholarIQindexed works
Julia Hoefele has 145 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Julia Hoefele have?
ScholarIQcitation count
Julia Hoefele has 5,102 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Julia Hoefele?
ScholarIQh-index
Julia Hoefele has an h-index of 34 in OpenAlex.
What is the i10-index of Julia Hoefele?
ScholarIQi10-index
Julia Hoefele has an i10-index of 71 in OpenAlex.
What is the ORCID of Julia Hoefele?
ScholarIQorcid
The ORCID for Julia Hoefele is on the source record.
What is the OpenAlex record for Julia Hoefele?
ScholarIQopenalex
The OpenAlex for Julia Hoefele is on the source record.
What are the most-cited papers on Julia Hoefele?
ScholarIQmost cited works
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
Edgar A. Otto, Bernhard Schermer, Tomoko Obara, John F. O’Toole, Karl S. Hiller, Adelheid M. Mueller, Rainer Ruf, Julia Hoefele, Frank Beekmann, Daniel Landau, John W. Foreman, Judith A. Goodship, Tom Strachan, Andreas Kispert, Matthias T. F. Wolf, M. F. Gagnadoux, Hubert Nivet, Corinne Antignac, Gerd Walz, Iain A. Drummond, Thomas Benzing, Friedhelm Hildebrandt
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis
Heike Olbrich, Manfred Fliegauf, Julia Hoefele, Andreas Kispert, Edgar A. Otto, Andreas Volz, Matthias T. F. Wolf, Gürsel Sasmaz, Ute Trauer, Richard Reinhardt, Ralf Sudbrak, Corinne Antignac, Norbert Gretz, Gerd Walz, Bernhard Schermer, Thomas Benzing, Friedhelm Hildebrandt, Heymut Omran
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling
Heon Yung Gee, Pawaree Saisawat, Shazia Ashraf, Toby W. Hurd, Virginia Vega-Warner, Humphrey Fang, Bodo B. Beck, Olivier Gribouval, Weibin Zhou, Katrina A. Diaz, S. Natarajan, Roger C. Wiggins, Svjetlana Lovric, Gil Chernin, Dominik S. Schoeb, Buğsu Övünç, Yaacov Frishberg, Neveen A. Soliman, Hanan Fathy, Heike Goebel, Julia Hoefele, Lutz T. Weber, Jeffrey W. Innis, Christian Faul, Zhe Han, Joseph Washburn, Corinne Antignac, Shawn Levy, Edgar A. Otto, Friedhelm Hildebrandt
Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease
Carsten Bergmann, Jennifer von Bothmer, Nadina Ortiz Brüchle, Andreas Venghaus, Valeska Frank, Henry Fehrenbach, Tobias Hampel, Lars Pape, Annegret Buske, Jón J. Jónsson, Nanette Sarioglu, Antónia Santos, José Carlos Ferreira, Jan U. Becker, Reinhold Cremer, Julia Hoefele, Marcus R. Benz, Lutz T. Weber, Reinhard Buettner, Klaus Zerres
A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution
Edgar A. Otto, Julia Hoefele, Rainer Ruf, Adelheid M. Mueller, Karl S. Hiller, Matthias T. F. Wolf, Maria J. Schuermann, Achim Becker, Ralf Birkenhäger, Ralf Sudbrak, Hans Christian Hennies, Peter Nürnberg, Friedhelm Hildebrandt