ScholarIQanswers from OpenAlex & ORCID
Patrick Nitschké
ResearcherPublications, citations & collaboration network
Patrick Nitschké is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Patrick Nitschké have?
ScholarIQindexed works
Patrick Nitschké has 209 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Patrick Nitschké have?
ScholarIQcitation count
Patrick Nitschké has 17,580 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Patrick Nitschké?
ScholarIQh-index
Patrick Nitschké has an h-index of 61 in OpenAlex.
What is the i10-index of Patrick Nitschké?
ScholarIQi10-index
Patrick Nitschké has an i10-index of 127 in OpenAlex.
What is the ORCID of Patrick Nitschké?
ScholarIQorcid
The ORCID for Patrick Nitschké is on the source record.
What is the OpenAlex record for Patrick Nitschké?
ScholarIQopenalex
The OpenAlex for Patrick Nitschké is on the source record.
What are the most-cited papers on Patrick Nitschké?
ScholarIQmost cited works
Gain-of-function human <i>STAT1</i> mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis
Luyan Liu, Satoshi Okada, Xiao‐Fei Kong, Alexandra Y. Kreins, Sophie Cypowyj, Avinash Abhyankar, Julie Toubiana, Yuval Itan, Magali Audry, Patrick Nitschké, Cécile Masson, Beáta Tóth, Jérome Flatot, Mélanie Migaud, Maya Chrabieh, Tatiana Kochetkov, Alexandre Bolze, A. Borghesi, A. Toulon, Julia Hiller, Stefanie Eyerich, Kilian Eyerich, Vera Gulácsy, Л.И. Чернышова, Chernyshov Vp, Анастасія Бондаренко, Rosa María Cortés Grimaldo, Lizbeth Blancas‐Galicia, Ileana María Madrigal Beas, Joachim Roesler, K. Magdorf, Dan Engelhard, C. Thumerelle, Pierre‐Régis Burgel, Miriam Hoernes, Barbara Drexel, Reinhard Seger, Theresia Kusuma, Annette Jansson, Julie Sawalle‐Belohradsky, Bernd H. Belohradsky, Emmanuelle Jouanguy, Jacinta Bustamante, Mélanie Bué, Nathan Karin, Gizi Wildbaum, Christine Bodemer, Olivier Lortholary, Alain Fischer, Stéphane Blanche, Saleh Al‐Muhsen, Janine Reichenbach, Masao Kobayashi, Francisco Espinosa‐Rosales, Carlos Torres Lozano, Sara Şebnem Kılıç, Matías Oleastro, Amos Etzioni, Claudia Traidl‐Hoffmann, Ellen D. Renner, Laurent Abel, Capucine Pïcard, László Maródi, Stéphanie Boisson‐Dupuis, Anne Puel, Jean‐Laurent Casanova
De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy
Giulia Barcia, Matthew R. Fleming, Aline Deligniere, Valeswara‐Rao Gazula, Maile R. Brown, Maéva Langouët, Haijun Chen, Jack Kronengold, Avinash Abhyankar, Roberta Cilio, Patrick Nitschké, Anna Kamińska, Nathalie Boddaert, Jean‐Laurent Casanova, Isabelle Desguerre, Arnold Münnich, Olivier Dulac, Leonard K. Kaczmarek, Laurence Colleaux, Rima Nabbout
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
Karine Poirier, Nicolas Lebrun, Loïc Broix, Guoling Tian, Yoann Saillour, Cécile Boscheron, Elena Parrini, Stéphanie Valence, Benjamin Saint Pierre, Madison Oger, Didier Lacombe, David Geneviève, Elena Fontana, Francesca Darra, Claude Cancès, Magalie Barth, Dominique Bonneau, Bernardo Dalla Bernadina, Sylvie Nguyen, Cyril Gitiaux, Philippe Parent, Vincent des Portes, Jean Michel Pedespan, Victoire Legrez, Laetitia Castelnau-Ptakine, Patrick Nitschké, Thierry Hieu, Cécile Masson, Diana Zélénika, Annie Andrieux, Fiona Francis, Renzo Guerrini, Nicholas J. Cowan, Nadia Bahi‐Buisson, Jamel Chelly
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
Shazia Ashraf, Heon Yung Gee, Stéphanie Woerner, Letian Xie, Virginia Vega-Warner, Svjetlana Lovric, Humphrey Fang, Xuewen Song, Daniel C. Cattran, Carmen Ávila-Casado, Andrew D. Paterson, Patrick Nitschké, Christine Bôle‐Feysot, Pierre Cochat, Julián Esteve-Rudd, Birgit Haberberger, Susan J. Allen, Weibin Zhou, Rannar Airik, Edgar A. Otto, Moumita Barua, Mohamed H. Al‐Hamed, Jameela A. Kari, Jonathan Evans, Agnieszka Bierżyńska, Moin A. Saleem, Detlef Böckenhauer, Robert Kleta, Sherif El Desoky, Duygu Övünç Hacıhamdioğlu, Faysal Gök, Joseph Washburn, Roger C. Wiggins, Murim Choi, Richard P. Lifton, Shawn Levy, Zhe Han, Leonardo Salviati, Holger Prokisch, David S. Williams, Martin R. Pollak, Catherine F. Clarke, York Pei, Corinne Antignac, Friedhelm Hildebrandt
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