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Nerses Bebek

ResearcherPublications, citations & collaboration network

Nerses Bebek is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 230 works, 3,495 citations, an h-index of 29 and an i10-index of 80.

230
Works
3,495
Citations
29
h-index
80
i10-index

How has Nerses Bebek's publication output changed over time?

ScholarIQpublication output · 2001–2024

Output grew0% over the shown period — from 1 works in 2001 to 1 in 2024.

1
1
2
1
1
1
1
1
1
1
2001200820122014201720182019202020232024

What are the most-cited papers on Nerses Bebek?

ScholarIQmost cited works
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
S134425043. 2019309 CitationsOPEN ACCESS
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Remi Stevelink, Ciarán Campbell, Siwei Chen, Bassel Abou‐Khalil, Oluyomi M. Adesoji, Zaid Afawi, Elisabetta Amadori, Alison Anderson, Joseph Anderson, Danielle M. Andrade, Grazia Annesi, Pauls Auce, Andreja Avberšek, Melanie Bahlo, Mark D. Baker, Ganna Balagura, Simona Balestrini, Carmen Barba, Karen Barboza, Fabrice Bartoloméi, Thomas Bast, Larry Baum, Tobias Baumgartner, Betül Baykan, Nerses Bebek, Albert J. Becker, Felicitas Becker, Caitlin A. Bennett, Bianca Berghuis, Samuel F. Berkovic, Ahmad Beydoun, Claudia Bianchini, Francesca Bisulli, Ilan Blatt, Dheeraj Reddy Bobbili, Ingo Borggraefe, Christian M. Boßelmann, Vera Braatz, Jonathan P. Bradfield, Knut Brockmann, Lawrence C. Brody, Russell J. Buono, Robyn M. Busch, Hande Çağlayan, Ellen Campbell, Laura Canafoglia, Christina Canavati, Gregory D. Cascino, Barbara Castellotti, Claudia B. Catarino, Gianpiero L. Cavalleri, Felecia Cerrato, Francine Chassoux, Stacey S. Cherny, Ching‐Lung Cheung, Krishna Chinthapalli, I‐Jun Chou, Seo‐Kyung Chung, Claire Churchhouse, Peggy O. Clark, Andrew J. Cole, Alastair Compston, Antonietta Coppola, Mahgenn Cosico, Patrick Cossette, John Craig, Caroline Cusick, Mark J. Daly, Lea K. Davis, Gerrit‐Jan de Haan, Norman Delanty, Chantal Depondt, Philippe Derambure, Orrin Devinsky, Lidia Di Vito, Dennis Dlugos, Viola Doccini, Colin P. Doherty, Hany El-Naggar, Christian E. Elger, Colin A. Ellis, Johan G. Eriksson, Annika Faucon, Yen‐Chen Anne Feng, Lisa Ferguson, Thomas N. Ferraro, Lorenzo Ferri, Martha Feucht, Mark P. Fitzgerald, Beata Fonferko‐Shadrach, Francesco Fortunato, Silvana Franceschetti, Andre Franke, Jacqueline A. French, Elena Freri, Monica Gagliardi, Antonio Gambardella, Eric B. Geller, Tania Giangregorio, Leif Gjerstad
S137905309. 2023217 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
S166515463. 2012152 CitationsOPEN ACCESS
Myoclonic seizures subside in the fourth decade in juvenile myoclonic epilepsy
Betül Baykan, Ebru Altındağ, Nerses Bebek, Ayhan Öztürk, Begüm Aslantaş, C. Gurses, Isin Baral-Kulaksizoglu, Ayşen Gökyiğit
Neurology. 2008132 Citations
PRRT2 Mutations are the major cause of benign familial infantile seizures
Julian Schubert, Roberta Paravidino, Felicitas Becker, Andrea Berger, Nerses Bebek, Amedeo Bianchi, Knut Brockmann, Giuseppe Capovilla, Bernardo Dalla Bernardina, Yukio Fukuyama, Georg F. Hoffmann, Karin Jurkat‐Rott, Anna-Kaisa Anttonen, Gerhard Kurlemann, Anna-Elina Lehesjoki, Frank Lehmann‐Horn, Massimo Mastrangelo, Ulrike Mause, Stephan A. Müller, Bernd A. Neubauer, B Püst, D. Rating, Angela Robbiano, Susanne Ruf, Christopher Schroeder, Andreas Seidel, Nicola Specchio, Ulrich Stephani, Pasquale Striano, Jens Teichler, Dilşad Türkdoğan, Federico Vigevano, Maurizio Viri, Peter Bauer, Federico Zara, Holger Lerche, Yvonne Weber
S98809561. 2012107 Citations

Related on ScholarIQ

Istanbul University
Institution
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
Paper
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Paper
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32
Paper
Myoclonic seizures subside in the fourth decade in juvenile myoclonic epilepsy
Paper
PRRT2 Mutations are the major cause of benign familial infantile seizures
Paper
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