ScholarIQanswers from OpenAlex & ORCID
Lutz T. Weber
ResearcherPublications, citations & collaboration network
Lutz T. Weber is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Lutz T. Weber have?
ScholarIQindexed works
Lutz T. Weber has 362 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Lutz T. Weber have?
ScholarIQcitation count
Lutz T. Weber has 7,432 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Lutz T. Weber?
ScholarIQh-index
Lutz T. Weber has an h-index of 45 in OpenAlex.
What is the i10-index of Lutz T. Weber?
ScholarIQi10-index
Lutz T. Weber has an i10-index of 133 in OpenAlex.
What is the ORCID of Lutz T. Weber?
ScholarIQorcid
The ORCID for Lutz T. Weber is on the source record.
What is the OpenAlex record for Lutz T. Weber?
ScholarIQopenalex
The OpenAlex for Lutz T. Weber is on the source record.
What are the most-cited papers on Lutz T. Weber?
ScholarIQmost cited works
Opportunities to Optimize Tacrolimus Therapy in Solid Organ Transplantation: Report of the European Consensus Conference
Pierre Wallemacq, Victor W. Armstrong, Merçè Brunet, Vincent Haufroid, David W. Holt, A. E. Johnston, Dirk Kuypers, Yannick Le Meur, Pierre Marquet, Michael Oellerich, Éric Thervet, Burkhand Toenshoff, N. Undre, Lutz T. Weber, Ian S Westley, Michel Mourad
The Pharmacokinetic-Pharmacodynamic Relationship for Total and Free Mycophenolic Acid in Pediatric Renal Transplant Recipients
Lutz T. Weber, Maria Shipkova, Victor W. Armstrong, Natalie Wagner, Ekkehard Schütz, Otto Mehls, Lothar Bernd Zimmerhackl, Michael Oellerich, Burkhard Tönshoff
IPNA clinical practice recommendations for the diagnosis and management of children with steroid-sensitive nephrotic syndrome
Agnes Trautmann, Olivia Boyer, Elisabeth M Hodson, Arvind Bagga, Debbie S. Gipson, Susan Samuel, Jack F.M. Wetzels, Khalid Alhasan, Sushmita Banerjee, Rajendra Bhimma, Melvin Bonilla‐Félix, Francisco Cano, Martin Christian, Deirdré Hahn, Hee Gyung Kang, Koichi Nakanishi, Hesham Safouh, Howard Trachtman, Hong Xu, Wendy L. Cook, Marina Vivarelli, Dieter Haffner, Antonia H. Bouts, Claire Dossier, Francesco Emma, Markus J. Kemper, Rezan Topaloğlu, Aoife Waters, Lutz T. Weber, Alexandra Zurowska, Keisha L. Gibson, Larry A. Greenbaum, Susan F. Massengill, David T. Selewski, Tarak Srivastava, Chia-shi Wang, Scott E. Wenderfer, Lilian Johnstone, Nicholas Larkins, William Wong, Agnes A. Alba, T. S. Ha, Masoumeh Mokham, Xuhui Zhong, Riku Hamada, Kazumoto Iijima, Kenji Ishikura, Kandai Nozu, Nilzete Liberato Bresolin, Nilka De Jesus Gonzalez, Jaime Restrepo, Ifeoma Anochie, Mignon McCulloch
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