Upload Records Snowball Search Search OpenAlex
About the database ScholarIQanswers from OpenAlex & ORCID
Detlef Böckenhauer
ResearcherPublications, citations & collaboration network
Detlef Böckenhauer is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 487 works, 18,626 citations, an h-index of 72 and an i10-index of 192.
487
Works
18,626
Citations
72
h-index
192
i10-index
How has Detlef Böckenhauer's publication output changed over time?
ScholarIQpublication output · 2001–2021
Output grew0% over the shown period — from 1 works in 2001 to 1 in 2021.
1
2
1
1
1
1
1
1
2
1
2001200920112012201320142016201920202021
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
Kidney International. 2020723 CitationsOPEN ACCESS
Potassium leak channels and the KCNK family of two-p-domain subunits
Steven A. Goldstein, Detlef Böckenhauer, Anne M. Kelly, Noam Zilberberg
S26843219. 2001719 CitationsOPEN ACCESS
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
Journal of the American Society of Nephrology. 2014663 CitationsOPEN ACCESS
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
Nature. 2012638 Citations
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
Nature. 2020586 CitationsOPEN ACCESS
Related on ScholarIQ
Great Ormond Street Hospital
Institution
Nomenclature for kidney function and disease: report of a Kidney Disease: Improving Global Outcomes (KDIGO) Consensus Conference
Paper
Potassium leak channels and the KCNK family of two-p-domain subunits
Paper
A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome
Paper
Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities
Paper
Whole-genome sequencing of patients with rare diseases in a national health system
Paper