ScholarIQanswers from OpenAlex & ORCID
Ulrich Stephani
ResearcherPublications, citations & collaboration network
Ulrich Stephani is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Ulrich Stephani have?
ScholarIQindexed works
Ulrich Stephani has 887 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Ulrich Stephani have?
ScholarIQcitation count
Ulrich Stephani has 16,213 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Ulrich Stephani?
ScholarIQh-index
Ulrich Stephani has an h-index of 69 in OpenAlex.
What is the i10-index of Ulrich Stephani?
ScholarIQi10-index
Ulrich Stephani has an i10-index of 229 in OpenAlex.
What is the ORCID of Ulrich Stephani?
ScholarIQorcid
The ORCID for Ulrich Stephani is on the source record.
What is the OpenAlex record for Ulrich Stephani?
ScholarIQopenalex
The OpenAlex for Ulrich Stephani is on the source record.
What are the most-cited papers on Ulrich Stephani?
ScholarIQmost cited works
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Johannes R. Lemke, Dennis Lal, Eva M. Reinthaler, Isabelle Steiner, Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin Finsterwalder, André Franke, Markus B. Schilhabel, Johanna Jähn, Hiltrud Muhle, Rainer Boor, Wim Van Paesschen, Roberto Caraballo, Natalio Fejerman, Sarah Weckhuysen, Peter De Jonghe, Jan Larsen, Rikke S. Møller, Helle Hjalgrim, Laura Addis, Shan Tang, Elaine Hughes, Deb K. Pal, Kadi Veri, Ulvi Vaher, Tiina Talvik, Petia Dimova, Rosa Guerrero, José M. Serratosa, Tarja Linnankivi, Anna‐Elina Lehesjoki, Susanne Ruf, Markus Wolff, Sarah E. Buerki, Gabriele Wohlrab, Judith Kroell, Alexandre Datta, Barbara Fiedler, Gerhard Kurlemann, Gerhard Kluger, Andreas Hahn, D Edda Haberlandt, Christina Kutzer, Jürgen Sperner, Felicitas Becker, Yvonne Weber, Martha Feucht, Hannelore Steinböck, Birgit Neophythou, Gabriel M. Ronen, U Gruber‐Sedlmayr, Julia Geldner, Robert J Harvey, Per Hoffmann, Stefan Herms, Janine Altmüller, Mohammad R. Toliat, Hölger Thiele, Peter Nürnberg, Christian Wilhelm, Ulrich Stephani, Ingo Helbig, Holger Lerche, Fritz Zimprich, Bernd A. Neubauer, Saskia Biskup, Sarah von Spiczak
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott, Katherine Tashman, Felecia Cerrato, Tarjinder Singh, Henrike Heyne, Andrea Byrnes, Claire Churchhouse, Nick Watts, Matthew Solomonson, Dennis Lal, Erin L. Heinzen, Ryan S. Dhindsa, Kate E. Stanley, Gianpiero L. Cavalleri, Håkon Håkonarson, Ingo Helbig, Roland Krause, Patrick May, Sarah Weckhuysen, Slavé Petrovski, Sitharthan Kamalakaran, Sanjay M. Sisodiya, Patrick Cossette, Chris Cotsapas, Peter De Jonghe, Tracy Dixon‐Salazar, Renzo Guerrini, Patrick Kwan, Anthony G Marson, Randy Stewart, Chantal Depondt, Dennis Dlugos, Ingrid E. Scheffer, Pasquale Striano, Catharine Freyer, Kevin E. McKenna, Brigid M. Regan, Susannah T. Bellows, Costin Leu, Caitlin A. Bennett, Esther M.C. Johns, Alexandra MacDonald, Hannah Shilling, Rosemary Burgess, Dorien Weckhuysen, Melanie Bahlo, Terence J. O’Brien, Marian Todaro, Hannah Stamberger, Danielle M. Andrade, Tara Sadoway, Kelly Mo, Heinz Krestel, Sabina Gallati, Savvas Papacostas, Ioanna Kousiappa, George A. Tanteles, Katalin Štěrbová, Markéta Vlčková, Lucie Sedláčková, Petra Laššuthová, Karl Martin Klein, Felix Rosenow, Philipp S. Reif, Susanne Knake, Wolfram S. Kunz, Gábor Zsurka, Christian E. Elger, Jürgen Bauer, Michael Rademacher, Manuela Pendziwiat, Hiltrud Muhle, Annika Rademacher, Andreas van Baalen, Sarah von Spiczak, Ulrich Stephani, Zaid Afawi, Amos D. Korczyn, Moien Kanaan, Christina Canavati, Gerhard Kurlemann, Karen Müller‐Schlüter, Gerhard Kluger, Martin Häusler, Ilan Blatt, Johannes R. Lemke, Ilona Krey, Yvonne Weber, Stefan Wolking, Felicitas Becker, Christian Hengsbach, Sarah Rau, Ana F. Maisch, Bernhard J. Steinhoff, Andreas Schulze‐Bonhage, Susanne Schubert‐Bast, Herbert Schreiber, Ingo Borggräfe
Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens
Rima Nabbout, Arun Mistry, Sameer M. Zuberi, Nathalie Villeneuve, António Gil‐Nagel, Rocı́o Sánchez-Carpintero, Ulrich Stephani, Linda Laux, Elaine Wirrell, Kelly G. Knupp, Catherine Chiron, Gail Farfel, Bradley S. Galer, Glenn Morrison, Michael Lock, Anupam Agarwal, Stéphane Auvin, for the FAiRE, DS Study Group
Long‐term seizure outcome in 211 patients with focal cortical dysplasia
Susanne Fauser, Charles Essang, Dirk‐Matthias Altenmüller, Anke M. Staack, Bernhard J. Steinhoff, Karl Strobl, Thomas Bast, Susanne Schubert‐Bast, Ulrich Stephani, Gert Wiegand, Marco Prinz, Armin Brandt, Josef Zentner, Andreas Schulze‐Bonhage
Consensus on diagnosis and management of JME: From founder's observations to current trends
Dorothée G.A. Kasteleijn- Nolst Trenité, Bettina Schmitz, Diéter Janz, Antonio V. Delgado‐Escueta, Pierre Thomas, Édouard Hirsch, Holger Lerche, Carol Camfield, Betül Baykan, Martha Feucht, Iris E. Martínez‐Juárez, Reyna M. Durón, Marco T. Medina, Guido Rubboli, Judith Jerney, Bruce P. Hermann, Elza Márcia Targas Yacubian, Michael Koutroumanidis, Ulrich Stephani, Javier Salas‐Puig, Ronald C. Reed, Friedrich G. Woermann, Britta Wandschneider, Michelle Bureau, Antonio Gambardella, Matthias J. Koepp, Philippe Gélisse, C. Gurses, Arielle Crespel, Vi Huong Nguyen-Michel, Edoardo Ferlazzo, Thierry Grisar, Ingo Helbig, Bobby P.C. Koeleman, Pasquale Striano, Michael Trimble, Russel Buono, Patrick Cossette, Alfonso Represa, Charlotte Dravet, Anna Serafini, Ivanka Savic- Berglund, Sanjay M. Sisodiya, Kazuhiro Yamakawa, Pierre Genton