ScholarIQanswers from OpenAlex & ORCID
Jan Halbritter
ResearcherPublications, citations & collaboration network
Jan Halbritter is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Jan Halbritter have?
ScholarIQindexed works
Jan Halbritter has 168 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Jan Halbritter have?
ScholarIQcitation count
Jan Halbritter has 5,860 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Jan Halbritter?
ScholarIQh-index
Jan Halbritter has an h-index of 39 in OpenAlex.
What is the i10-index of Jan Halbritter?
ScholarIQi10-index
Jan Halbritter has an i10-index of 71 in OpenAlex.
What is the ORCID of Jan Halbritter?
ScholarIQorcid
The ORCID for Jan Halbritter is on the source record.
What is the OpenAlex record for Jan Halbritter?
ScholarIQopenalex
The OpenAlex for Jan Halbritter is on the source record.
What are the most-cited papers on Jan Halbritter?
ScholarIQmost cited works
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
Fourteen Monogenic Genes Account for 15% of Nephrolithiasis/Nephrocalcinosis
Jan Halbritter, Michelle A. Baum, Ann Marie Hynes, Sarah J. Rice, David T. Thwaites, Zoran Gucev, Brittany Fisher, Leslie Spaneas, Jonathan D. Porath, Daniela A. Braun, Ari J. Wassner, Caleb P. Nelson, Velibor Tasić, John A. Sayer, Friedhelm Hildebrandt
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy
The GPN Study Group, Jan Halbritter, Jonathan D. Porath, Katrina A. Diaz, Daniela A. Braun, Stefan Kohl, Moumita Chaki, Susan J. Allen, Neveen A. Soliman, Friedhelm Hildebrandt, Edgar A. Otto
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans
Jan Halbritter, Albane A. Bizet, Miriam Schmidts, Jonathan D. Porath, Daniela A. Braun, Heon Yung Gee, Aideen McInerney‐Leo, Pauline Krug, Emilie Filhol, Erica E. Davis, Rannar Airik, Peter G. Czarnecki, Anna Lehman, Peter Trnka, Patrick Nitschké, Christine Bôle‐Feysot, Markus Schueler, Bertrand Knebelmann, Stéphane Burtey, Attila J. Szabó, Kálmán Tory, Paul Leo, Brooke Gardiner, Fiona A. McKenzie, Andreas Zankl, Matthew A. Brown, Jane Hartley, Eamonn R. Maher, Chunmei Li, Michel R. Leroux, Peter Scambler, Shing H. Zhan, Steven J.M. Jones, Hülya Kayserili, Beyhan Tüysüz, Khemchand N Moorani, Alexandru R. Constantinescu, Ian D. Krantz, Bernard S. Kaplan, Jagesh V. Shah, Toby W. Hurd, Dan Doherty, Nicholas Katsanis, Emma L. Duncan, Edgar A. Otto, Philip L. Beales, Hannah M. Mitchison, Sophie Saunier, Friedhelm Hildebrandt
Mutations in <i>RSPH1</i> Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype
Michael R. Knowles, Lawrence E. Ostrowski, Margaret W. Leigh, Patrick R. Sears, Stephanie D. Davis, Whitney Wolf, Milan J. Hazucha, Johnny L. Carson, Kenneth N. Olivier, Scott D. Sagel, Margaret Rosenfeld, Thomas W. Ferkol, Sharon Dell, Carlos Milla, Scott H. Randell, Weining Yin, Aruna Sannuti, Hilda Metjian, Peadar G. Noone, Peter J. Noone, Christina A. Olson, Michael V. Patrone, Hong Dang, Hye Seung Lee, Toby W. Hurd, Heon Yung Gee, Edgar A. Otto, Jan Halbritter, Stefan Kohl, Martin Kircher, Jeffrey P. Krischer, Michael J. Bamshad, Deborah A. Nickerson, Friedhelm Hildebrandt, Jay Shendure, Maimoona A. Zariwala