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Andreas Janecke

ResearcherPublications, citations & collaboration network

Andreas Janecke is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Andreas Janecke have?

ScholarIQindexed works

Andreas Janecke has 10,029 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Andreas Janecke have?

ScholarIQcitation count

Andreas Janecke has 17,866 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Andreas Janecke?

ScholarIQh-index

Andreas Janecke has an h-index of 62 in OpenAlex.

What is the i10-index of Andreas Janecke?

ScholarIQi10-index

Andreas Janecke has an i10-index of 335 in OpenAlex.

What is the ORCID of Andreas Janecke?

ScholarIQorcid

The ORCID for Andreas Janecke is on the source record.

What is the OpenAlex record for Andreas Janecke?

ScholarIQopenalex

The OpenAlex for Andreas Janecke is on the source record.

What are the most-cited papers on Andreas Janecke?

ScholarIQmost cited works
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema
Aileen Sandilands, Ana Terron-Kwiatkowski, Peter Hull, Gráinne M. O’Regan, Timothy Clayton, Rosemarie M. Watson, Thomas Carrick, Alan Evans, Haihui Liao, Yiwei Zhao, Linda Campbell, Matthias Schmuth, Robert Gruber, Andreas Janecke, Peter M. Elias, Maurice A. M. Van Steensel, Ivo F. Nagtzaam, Michel van Geel, Peter M. Steijlen, Colin S. Munro, Daniel G. Bradley, Colin N A Palmer, Frances J.D. Smith, W.H. Irwin McLean, Alan D. Irvine
Nature Genetics. 2007665 Citations
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study
Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, Sandrine Marlin, Françoise Denoyelle, J Waligora, Małgorzata Mueller‐Malesińska, Agneszka Pollak, Rafał Płoski, Alessandra Murgia, Eva Orzan, Pierangela Castorina, Umberto Ambrosetti, Ewa Nowakowska-Szyrwińska, Jerzy Bal, Wojciech Wiszniewski, Andreas Janecke, Doris Nekahm-Heis, Pavel Seeman, O. Bendová, Margaret A. Kenna, Anna Frangulov, Heidi L. Rehm, Mustafa Tekin, Armağan İncesulu, Hans‐Henrik M. Dahl, Desirée du Sart, Lucy Jenkins, Deirdre Lucas, Maria Bitner‐Glindzicz, Karen B. Avraham, Zippora Brownstein, Ignacio del Castillo, Felipe Moreno, Nikolaus Blin, Markus Pfister, István Sziklai, Tímea Tóth, Philip M. Kelley, Edward Cohn, Lionel Van Maldergem, Pascale Hilbert, Anne‐Françoise Roux, M. Mondain, Lies H. Hoefsloot, Cor W. R. J. Cremers, Tuija Löppönen, Heikki Löppönen, Agnete Parving, Karen Grønskov, Iris Schrijver, Joseph Roberson, Francesca Gualandi, Alessandro Martini, Geneviève Lina‐Granade, Nathalie Pallarès-Ruiz, Céu Correia, Graça Fialho, Kim Cryns, Nele Hilgert, Paul Van de Heyning, Carla Nishimura, Richard J. Smith, Guy Van Camp
The American Journal of Human Genetics. 2005561 CitationsOPEN ACCESS
Variants in CPA1 are strongly associated with early onset chronic pancreatitis
Heiko Witt, Sebastian Beer, Jonas Rosendahl, Jian‐Min Chen, Giriraj R. Chandak, Atsushi Masamune, Melinda Bence, Richárd Szmola, Grzegorz Oracz, Milan Maçek, Eesh Bhatia, Sandra Steigenberger, Denise Lasher, Florence Bühler, Catherine Delaporte, Johanna Tebbing, Maren Ludwig, Claudia Pilsak, Karolin Saum, Peter Bugert, Emmanuelle Masson, Sumit Paliwal, Seema Bhaskar, Agnieszka Sobczyńska‐Tomaszewska, Daniel Bąk, Ivan Balaščák, Gourdas Choudhuri, D. Nageshwar Reddy, G.V. Rao, Varghese Thomas, Kiyoshi Kume, Eriko Nakano, Yoichi Kakuta, Tooru Shimosegawa, Łukasz Durko, András Szabó, Andrea Schnúr, Péter Hegyi, Zoltán Rakonczay, Roland H. Pfützer, Alexander Schneider, David A. Groneberg, Markus Braun, Hartmut Schmidt, Ulrike Witt, Helmut Frieß, Hana Algül, Olfert Landt, Markus Schuelke, Renate Krüger, Bertram Wiedenmann, Frank Schmidt, Klaus‐Peter Zimmer, Péter Kovács, Michael Stümvoll, Matthias Blüher, Thomas Müller, Andreas Janecke, Niels Teich, Robert Grützmann, Hans-Ulrich Schulz, Joachim Mössner, Volker Keim, Matthias Löhr, Claude Férec, Miklós Sahin‐Tóth
Nature Genetics. 2013304 CitationsOPEN ACCESS
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics
Claudia Dafinger, Max C. Liebau, Solaf M. Elsayed, Yorck Hellenbroich, Eugen Boltshauser, Georg Christoph Korenke, Francesca Fabretti, Andreas Janecke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg, Hanswalter Zentgraf, Friederike Koerber, Klaus Addicks, Ezzat Elsobky, Thomas Benzing, Bernhard Schermer, Hanno J. Bolz
Journal of Clinical Investigation. 2011214 CitationsOPEN ACCESS

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