ScholarIQanswers from OpenAlex & ORCID
Friedhelm Hildebrandt
ResearcherPublications, citations & collaboration network
Friedhelm Hildebrandt is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Friedhelm Hildebrandt have?
ScholarIQindexed works
Friedhelm Hildebrandt has 588 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Friedhelm Hildebrandt have?
ScholarIQcitation count
Friedhelm Hildebrandt has 38,478 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Friedhelm Hildebrandt?
ScholarIQh-index
Friedhelm Hildebrandt has an h-index of 108 in OpenAlex.
What is the i10-index of Friedhelm Hildebrandt?
ScholarIQi10-index
Friedhelm Hildebrandt has an i10-index of 315 in OpenAlex.
What is the ORCID of Friedhelm Hildebrandt?
ScholarIQorcid
The ORCID for Friedhelm Hildebrandt is on the source record.
What is the OpenAlex record for Friedhelm Hildebrandt?
ScholarIQopenalex
The OpenAlex for Friedhelm Hildebrandt is on the source record.
What are the most-cited papers on Friedhelm Hildebrandt?
ScholarIQmost cited works
Ciliopathies
Friedhelm Hildebrandt, Thomas Benzing, Nicholas Katsanis
A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome
Carolin E. Sadowski, Svjetlana Lovric, Shazia Ashraf, Werner L. Pabst, Heon Yung Gee, Stefan Kohl, Susanne Engelmann, Virginia Vega-Warner, Humphrey Fang, Jan Halbritter, Michael J.G. Somers, Weizhen Tan, Shirlee Shril, Inès Fessi, Richard P. Lifton, Detlef Böckenhauer, Sherif M. El-Desoky, Jameela A. Kari, Martin Zenker, Markus J. Kemper, Dominik Mueller, Hanan Fathy, Neveen A. Soliman, Friedhelm Hildebrandt
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
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
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