ScholarIQanswers from OpenAlex & ORCID
Detlef Böckenhauer
ResearcherPublications, citations & collaboration network
Detlef Böckenhauer is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Detlef Böckenhauer have?
ScholarIQindexed works
Detlef Böckenhauer has 487 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Detlef Böckenhauer have?
ScholarIQcitation count
Detlef Böckenhauer has 18,626 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Detlef Böckenhauer?
ScholarIQh-index
Detlef Böckenhauer has an h-index of 72 in OpenAlex.
What is the i10-index of Detlef Böckenhauer?
ScholarIQi10-index
Detlef Böckenhauer has an i10-index of 192 in OpenAlex.
What is the ORCID of Detlef Böckenhauer?
ScholarIQorcid
The ORCID for Detlef Böckenhauer is on the source record.
What is the OpenAlex record for Detlef Böckenhauer?
ScholarIQopenalex
The OpenAlex for Detlef Böckenhauer is on the source record.
What are the most-cited papers on Detlef Böckenhauer?
ScholarIQmost cited works
Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference
Andrew S. Levey, Kai‐Uwe Eckardt, Nijsje Dorman, Stacy Christiansen, Ewout J. Hoorn, Julie R. Ingelfinger, Lesley A. Inker, Adeera Levin, Rajnish Mehrotra, Paul M. Palevsky, Mark A. Perazella, Allison Tong, Susan J. Allison, Detlef Böckenhauer, Josephine P. Briggs, Jonathan S. Bromberg, Andrew Davenport, Harold I. Feldman, Denis Fouque, Ron T. Gansevoort, John S. Gill, Eddie L. Greene, Brenda R. Hemmelgarn, Matthias Kretzler, Mark Lambie, Pascale H. Lane, Joseph Laycock, Shari E. Leventhal, Michael Mittelman, Patricia Morrissey, Marlies Ostermann, Lesley Rees, Pierre Ronco, Franz Schaefer, Jennifer St. Clair Russell, Caroline Vinck, Stephen B. Walsh, Daniel E. Weiner, Michael Cheung, Michel Jadoul, Wolfgang C. Winkelmayer
Potassium leak channels and the KCNK family of two-p-domain subunits
Steven A. Goldstein, Detlef Böckenhauer, Anne M. Kelly, Noam Zilberberg
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 kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Lynn M. Boyden, Murim Choi, Keith A. Choate, Carol Nelson‐Williams, Anita Farhi, Hakan R. Toka, Irina R. Tikhonova, Robert Bjornson, Shrikant Mane, Giacomo Colussi, Marcel Lebel, Richard D. Gordon, Ben A. Semmekrot, A. Poujol, Matti Välimäki, Maria Elisabetta De Ferrari, Sami A. Sanjad, Michael Gutkin, Fiona E. Karet, Joseph Tucci, Jim Stockigt, Kim M. Keppler‐Noreuil, Craig Porter, Sudhir Anand, Margo L. Whiteford, Ira D. Davis, Stephanie Dewar, Alberto Bettinelli, Jeffrey J. Fadrowski, Craig W. Belsha, Tracy E. Hunley, Raoul D. Nelson, Howard Trachtman, Trevor Cole, Maury Pinsk, Detlef Böckenhauer, Mohan Shenoy, Priya Vaidyanathan, John W. Foreman, Majid Rasoulpour, Farook Thameem, Hania Z. Al-Shahrouri, Jai Radhakrishnan, Ali G. Gharavi, Béatrice Goilav, Richard P. Lifton
Whole-genome sequencing of patients with rare diseases in a national health system
Ernest Turro, William J. Astle, Karyn Mégy, Stefan Gräf, Daniel Greene, Olga Shamardina, Hana Lango Allen, Alba Sanchis‐Juan, Mattia Frontini, Chantal Thys, Jonathan Stephens, Rutendo Mapeta, Oliver S. Burren, Kate Downes, Matthias Haimel, Salih Tuna, Sri V. V. Deevi, Timothy J. Aitman, David Bennett, Paul Calleja, Keren Carss, Mark J. Caulfield, Patrick F. Chinnery, Peter Dixon, Daniel P. Gale, Roger James, Ania Koziell, Michael A. Laffan, Adam P. Levine, Eamonn R. Maher, Hugh S. Markus, Joannella Morales, Nicholas W. Morrell, Andrew Mumford, Elizabeth Ormondroyd, Stuart Rankin, Augusto Rendon, Sylvia Richardson, Irene Roberts, Noémi Roy, Moin A. Saleem, Kenneth G. C. Smith, Hannah Stark, Rhea Tan, Andreas C. Themistocleous, Adrian J. Thrasher, Hugh Watkins, Andrew R. Webster, Martin R. Wilkins, Catherine Williamson, James Whitworth, Sean Humphray, David R. Bentley, NIHR BioResource for the 100,000 Genomes Project, Stephen Abbs, Lara Abulhoul, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, J. P. Almeida, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Paul Aurora, Christian Babbs, Chiara Bacchelli, Tamam Bakchoul, Siddharth Banka, Tadbir K. Bariana, Julian Barwell, Joana Batista, Helen Baxendale, Phil Beales, David Bennett, David R. Bentley, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Graeme C. Black, Marta Bleda, Iulia Blesneac, Detlef Böckenhauer, Harm Jan Bogaard, Christian Bourne, Sara Boyce, John R. Bradley, Eugene Bragin, Gerome Breen, Paul Brennan, Carole Brewer, Matthew A. Brown, Andrew C. Browning, Michael J. Browning, Rachel Buchan