ScholarIQanswers from OpenAlex & ORCID
Dagmar Wieczorek
ResearcherPublications, citations & collaboration network
Dagmar Wieczorek is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Dagmar Wieczorek have?
ScholarIQindexed works
Dagmar Wieczorek has 334 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Dagmar Wieczorek have?
ScholarIQcitation count
Dagmar Wieczorek has 23,807 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Dagmar Wieczorek?
ScholarIQh-index
Dagmar Wieczorek has an h-index of 82 in OpenAlex.
What is the i10-index of Dagmar Wieczorek?
ScholarIQi10-index
Dagmar Wieczorek has an i10-index of 232 in OpenAlex.
What is the ORCID of Dagmar Wieczorek?
ScholarIQorcid
The ORCID for Dagmar Wieczorek is on the source record.
What is the OpenAlex record for Dagmar Wieczorek?
ScholarIQopenalex
The OpenAlex for Dagmar Wieczorek is on the source record.
What are the most-cited papers on Dagmar Wieczorek?
ScholarIQmost cited works
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato, Andreas Dufke, Kirsten Cremer, Maja Hempel, Denise Horn, Juliane Hoyer, Pascal Joset, Albrecht Röpke, Ute Moog, Angelika Rieß, Christian T. Thiel, Andreas Tzschach, Antje Wiesener, Eva Wohlleber, Christiane Zweier, Arif B. Ekici, Alexander M. Zink, Andreas Rump, Christa Meisinger, Harald Grallert, Heinrich Sticht, Annette Schenck, Hartmut Engels, Gudrun Rappold, Evelin Schröck, Peter Wieacker, Olaf Rieß, Thomas Meitinger, André Reis, Tim M. Strom
Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome
Johannes G. Dauwerse, Jill Dixon, Saskia Seland, Claudia Ruivenkamp, Arie van Haeringen, Lies H. Hoefsloot, Dorien J.M. Peters, Agnes Clement-de Boers, Cornelia Daumer‐Haas, Robert Maiwald, Christiane Zweier, Bronwyn Kerr, Ana María Cobo, Joaquín Fernández Toral, A. Jeannette M. Hoogeboom, Dietmar Lohmann, Ute Hehr, Michael J. Dixon, Martijn H. Breuning, Dagmar Wieczorek
CEP152 is a genome maintenance protein disrupted in Seckel syndrome
Ersan Kalay, Gökhan Yigit, Yakup Aslan, Karen Brown, Esther Pohl, Louise S. Bicknell, Hülya Kayserili, Yun Li, Beyhan Tüysüz, Gudrun Nürnberg, Wieland Kieß, Manfred Koegl, Ingelore Baessmann, Celal Kurtuluş Buruk, Bayram Toraman, Saadettin Kayıpmaz, Sibel Kul, Mevlit Íkbal, Daniel J. Turner, Martin S. Taylor, Jan Aerts, Carol Scott, Karen Milstein, Hélène Dollfus, Dagmar Wieczorek, Han G. Brunner, Matthew E. Hurles, Andrew P. Jackson, Anita Rauch, Peter Nürnberg, Ahmet Karagüzel, Bernd Wollnik
ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6
Maimoona A. Zariwala, Heon Yung Gee, Małgorzata Kurkowiak, Dalal A. Al-Mutairi, Margaret W. Leigh, Toby W. Hurd, Rim Hjeij, Sharon Dell, Moumita Chaki, Gerard W. Dougherty, Mohamed Adan, Philip C. Spear, Julián Esteve-Rudd, Niki T. Loges, Margaret Rosenfeld, Katrina A. Diaz, Heike Olbrich, Whitney Wolf, Eamonn Sheridan, Trevor F.C. Batten, Jan Halbritter, Jonathan D. Porath, Stefan Kohl, Svjetlana Lovric, Daw‐Yang Hwang, Jessica E. Pittman, Kimberlie A. Burns, Thomas W. Ferkol, Scott D. Sagel, Kenneth N. Olivier, Lucy Morgan, Claudius Werner, Johanna Raidt, Petra Pennekamp, Zhaoxia Sun, Weibin Zhou, Rannar Airik, S. Natarajan, Susan J. Allen, Israel Amirav, Dagmar Wieczorek, Kerstin Landwehr, Kim G. Nielsen, Nicolaus Schwerk, Jadranka Sertić, Gabriele Köhler, Joseph Washburn, Shawn Levy, Shuling Fan, Cordula Koerner‐Rettberg, Serge Amselem, David S. Williams, Brian J. Mitchell, Iain A. Drummond, Edgar A. Otto, Heymut Omran, Michael R. Knowles, Friedhelm Hildebrandt