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Bernhard J. Steinhoff

ResearcherPublications, citations & collaboration network

Bernhard J. Steinhoff is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Bernhard J. Steinhoff have?

ScholarIQindexed works

Bernhard J. Steinhoff has 497 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Bernhard J. Steinhoff have?

ScholarIQcitation count

Bernhard J. Steinhoff has 17,393 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Bernhard J. Steinhoff?

ScholarIQh-index

Bernhard J. Steinhoff has an h-index of 64 in OpenAlex.

What is the i10-index of Bernhard J. Steinhoff?

ScholarIQi10-index

Bernhard J. Steinhoff has an i10-index of 195 in OpenAlex.

What is the ORCID of Bernhard J. Steinhoff?

ScholarIQorcid

The ORCID for Bernhard J. Steinhoff is on the source record.

What is the OpenAlex record for Bernhard J. Steinhoff?

ScholarIQopenalex

The OpenAlex for Bernhard J. Steinhoff is on the source record.

What are the most-cited papers on Bernhard J. Steinhoff?

ScholarIQmost cited works
Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
Ingmar Blümcke, Roberto Spreafico, Gerrit Haaker, Roland Coras, Katja Kobow, Christian G. Bien, Margarete Pfäfflin, Christian E. Elger, Guido Widman, Johannes Schramm, Albert J. Becker, Kees P. J. Braun, Frans S. S. Leijten, Johannes C. Baayen, Eleonora Aronica, Francine Chassoux, Hajo M. Hamer, Hermann Stefan, Karl Rössler, Maria Thom, Matthew C. Walker, Sanjay M. Sisodiya, John S. Duncan, Andrew W. McEvoy, Tom Pieper, Hans Holthausen, Manfred Kudernatsch, H. J. Meencke, Philippe Kahane, Andreas Schulze‐Bonhage, Josef Zentner, Dieter Henrik Heiland, Horst Urbach, Bernhard J. Steinhoff, Thomas Bast, Laura Tassi, Giorgio Lo Russo, Çiğdem Özkara, Büğe Öz, Pavel Kršek, Silke Vogelgesang, Uwe Runge, Holger Lerche, Yvonne Weber, Mrinalini Honavar, José Pimentel, Alexis Arzimanoglou, Adriana Ulate-Campos, Soheyl Noachtar, Elisabeth Härtl, Olaf Schijns, Renzo Guerrini, Carmen Barba, Thomas S. Jacques, J. Helen Cross, Martha Feucht, Angelika Mühlebner, Thomas Grünwald, Eugen Trinka, Peter Winkler, António Gil‐Nagel, Rafael Toledano, Thomas Mayer, Martin Lutz, Basilios Zountsas, Kyriakos Garganis, Felix Rosenow, Anke Hermsen, Tim J. von Oertzen, Thomas L. Diepgen, G. Avanzini
New England Journal of Medicine. 2017929 CitationsOPEN ACCESS
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
The American Journal of Human Genetics. 2019309 CitationsOPEN ACCESS
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
Epilepsia. 2014175 CitationsOPEN ACCESS
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
Michael Steffens, Costin Leu, Ann‐Kathrin Ruppert, Federico Zara, Pasquale Striano, Angela Robbiano, Giuseppe Capovilla, Paolo Tinuper, Antonio Gambardella, Amedeo Bianchi, Angela La Neve, Giovanni Crichiutti, Carolien G. F. de Kovel, Dorothée Kasteleijn‐Nolst Trenité, Gerrit‐Jan de Haan, Dick Lindhout, Verena Gaus, Bettina Schmitz, Diéter Janz, Yvonne Weber, Felicitas Becker, Holger Lerche, Bernhard J. Steinhoff, Ailing A. Kleefuß‐Lie, Wolfram S. Kunz, Rainer Surges, Christian E. Elger, Hiltrud Muhle, Sarah von Spiczak, P Ostertag, Ingo Helbig, Ulrich Stephani, Rikke S. Møller, Helle Hjalgrim, Leanne M. Dibbens, Susannah T. Bellows, Karen Oliver, Saul A. Mullen, Ingrid E. Scheffer, Samuel F. Berkovic, Kate V. Everett, M. R. Gardiner, Carla Marini, Renzo Guerrini, Anna‐Elina Lehesjoki, Auli Sirén, Michel Guipponi, Alain Malafosse, Pierre Thomas, Rima Nabbout, Stéphanie Baulac, Éric Leguern, Rosa Guerrero, José M. Serratosa, Philipp S. Reif, Felix Rosenow, Martina Mörzinger, Martha Feucht, Fritz Zimprich, Claudia Kapser, Christoph J. Schankin, Arvid Suls, Kaat Smets, Peter De Jonghe, Albena Jordanova, Hande Çağlayan, Zühal Yapıcı, Demet Yalcin, Betül Baykan, Nerses Bebek, Uğur Özbek, Christian Gieger, H.‐Erich Wichmann, Tobias Balschun, David Ellinghaus, André Franke, Christian Meesters, Tim Becker, T. F. Wienker, Anne Hempelmann, Herbert Schulz, Franz Rüschendorf, Markus Leber, S. M. Pauck, Holger Trucks, Mohammad-Reza Toliat, Peter Nürnberg, G. Avanzini, Bobby P.C. Koeleman, T. Sander
Human Molecular Genetics. 2012152 CitationsOPEN ACCESS

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