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Edgar A. Otto

ResearcherPublications, citations & collaboration network

Edgar A. Otto is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Edgar A. Otto have?

ScholarIQindexed works

Edgar A. Otto has 248 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Edgar A. Otto have?

ScholarIQcitation count

Edgar A. Otto has 21,373 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Edgar A. Otto?

ScholarIQh-index

Edgar A. Otto has an h-index of 80 in OpenAlex.

What is the i10-index of Edgar A. Otto?

ScholarIQi10-index

Edgar A. Otto has an i10-index of 151 in OpenAlex.

What is the ORCID of Edgar A. Otto?

ScholarIQorcid

The ORCID for Edgar A. Otto is on the source record.

What is the OpenAlex record for Edgar A. Otto?

ScholarIQopenalex

The OpenAlex for Edgar A. Otto is on the source record.

What are the most-cited papers on Edgar A. Otto?

ScholarIQmost cited works
An atlas of healthy and injured cell states and niches in the human kidney
Blue B. Lake, Rajasree Menon, Seth Winfree, Qiwen Hu, Ricardo Melo Ferreira, Kian Kalhor, Daria Barwinska, Edgar A. Otto, Michael J. Ferkowicz, Dinh Diep, Nongluk Plongthongkum, Amanda Knoten, Sarah Urata, Laura H. Mariani, Abhijit S. Naik, Sean Eddy, Bo Zhang, Yan Wu, Diane Salamon, James C. Williams, Xin Wang, Karol S. Balderrama, Paul Hoover, Evan Murray, Jamie L. Marshall, Teia Noel, Anitha Vijayan, Austin Hartman, Fei Chen, Sushrut S. Waikar, Sylvia E. Rosas, F. Perry Wilson, Paul M. Palevsky, Krzysztof Kiryluk, John R. Sedor, Robert D. Toto, Chirag R. Parikh, Eric H. Kim, Rahul Satija, Anna Greka, Evan Z. Macosko, Peter V. Kharchenko, Joseph P. Gaut, Jeffrey B. Hodgin, Richard A. Knight, Stewart H. Lecker, Isaac E. Stillman, Afolarin Amodu, Titlayo Ilori, Shana Maikhor, Insa M. Schmidt, Gearoid M. McMahon, Astrid Weins, Nir Hacohen, Lakeshia Bush, Agustin Gonzalez‐Vicente, Jonathan J. Taliercio, John O’Toole, Emilio D. Poggio, Leslie Cooperman, Stacey E. Jolly, Leal Herlitz, Jane Nguyen, Ellen L. Palmer, Dianna Sendrey, Kassandra Spates-Harden, Paul S. Appelbaum, Jonathan Barasch, Andrew S. Bomback, Vivette D. D’Agati, Karla Mehl, Pietro A. Canetta, Ning Shang, Olivia Balderes, Satoru Kudose, Laura Barisoni, Theodore Alexandrov, Ying‐Hua Cheng, Kenneth W. Dunn, Katherine J. Kelly, Timothy A. Sutton, Yumeng Wen, Celia P. Corona-Villalobos, Steven Menez, Avi Z. Rosenberg, Mohammed Atta, Camille Johansen, Jennifer K. Sun, Neil Roy, Mark Williams, Evren U. Azeloglu, Cijang He, Ravi Iyengar, Jens Hansen, Yuguang Xiong, Brad H. Rovin, Samir V. Parikh, Sethu M. Madhavan, Christopher Anderton, Ljiljana Paša‐Tolić
Nature. 2023678 CitationsOPEN ACCESS
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
Nature Genetics. 2003651 CitationsOPEN ACCESS
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
John A. Sayer, Edgar A. Otto, John F. O’Toole, Gudrun Nürnberg, Michael A. Kennedy, Christian Becker, Hans Christian Hennies, Juliana Helou, Massimo Attanasio, Blake V. Fausett, Boris Utsch, Hemant Khanna, Yan Liu, Iain A. Drummond, I. Kawakami, Takehiro Kusakabe, Motoyuki Tsuda, Li Ma, Hwankyu Lee, Ronald G. Larson, Susan J. Allen, Christopher J. Wilkinson, Erich A. Nigg, Chengchao Shou, Concepción Lillo, David S. Williams, Bernd Höppe, Markus J. Kemper, Thomas J. Neuhaus, Melissa A. Parisi, Ian A. Glass, Marianne Petry, Andreas Kispert, Joachim Gloy, Athina Ganner, Gerd Walz, Xueliang Zhu, Daniel Goldman, Peter Nürnberg, Anand Swaroop, Michel R. Leroux, Friedhelm Hildebrandt
Nature Genetics. 2006578 Citations
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
Bernward Hinkes, Roger C. Wiggins, Rasheed Gbadegesin, Christopher N. Vlangos, Dominik Seelow, Gudrun Nürnberg, Puneet Garg, Rakesh Verma, Hassan Chaı̈b, Bethan E. Hoskins, Shazia Ashraf, Christian Becker, Hans Christian Hennies, Meera Goyal, Bryan L. Wharram, Asher D. Schachter, Sudha Mudumana, Iain A. Drummond, Dontscho Kerjaschki, Rüdiger Waldherr, Alexander Dietrich, Fatih Özaltın, Ayşı̇n Bakkaloğlu, Roxana Cleper, Lina Basel‐Vanagaite, Martin Pöhl, Martin Griebel, А.Н. Цыгин, Alper Soylu, Dominik Müller, Caroline S Sorli, Tom D. Bunney, Matilda Katan, Jinhong Liu, Massimo Attanasio, John F. O’Toole, K Hasselbacher, Bettina E. Mucha, Edgar A. Otto, Rannar Airik, Andreas Kispert, Grant G. Kelley, Alan V. Smrcka, Thomas Gudermann, Lawrence B. Holzman, Peter Nürnberg, Friedhelm Hildebrandt
Nature Genetics. 2006567 Citations
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
Ralf Birkenhäger, Edgar A. Otto, Maria J. Schürmann, Martin Vollmer, Eva-Maria Ruf, Irina Maier-Lutz, Frank Beekmann, Andrea Fekete, Heymut Omran, Delphine Feldmann, David V. Milford, Nicola Jeck, Martin Konrad, Daniel Landau, Nine V.A.M. Knoers, Corinne Antignac, Ralf Sudbrak, Andreas Kispert, Friedhelm Hildebrandt
Nature Genetics. 2001538 Citations

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