ScholarIQanswers from OpenAlex & ORCID
Bernd Wissinger
ResearcherPublications, citations & collaboration network
Bernd Wissinger is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Bernd Wissinger have?
ScholarIQindexed works
Bernd Wissinger has 420 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Bernd Wissinger have?
ScholarIQcitation count
Bernd Wissinger has 17,802 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Bernd Wissinger?
ScholarIQh-index
Bernd Wissinger has an h-index of 70 in OpenAlex.
What is the i10-index of Bernd Wissinger?
ScholarIQi10-index
Bernd Wissinger has an i10-index of 228 in OpenAlex.
What is the ORCID of Bernd Wissinger?
ScholarIQorcid
The ORCID for Bernd Wissinger is on the source record.
What is the OpenAlex record for Bernd Wissinger?
ScholarIQopenalex
The OpenAlex for Bernd Wissinger is on the source record.
What are the most-cited papers on Bernd Wissinger?
ScholarIQmost cited works
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
Patrizia Amati‐Bonneau, Maria Lucia Valentino, Pascal Reynier, M. Esther Gallardo, Belén Bornstein, Anne Boissière, Yolanda Campos, Horacio Rivera, J. G. de la Aleja, Rosanna Carroccia, Luisa Iommarini, Pierre Labauge, D. Figarella-Branger, P. Marcorelles, A. Furby, Katell Beauvais, Franck Letournel, Rocco Liguori, Chiara La Morgia, P. Montagna, Maria Liguori, Claudia Zanna, Michela Rugolo, Andrea Cossarizza, Bernd Wissinger, Christophe Verny, Robert Schwarzenbacher, Miguel Á. Martín, Joaquı́n Arenas, Carmen Ayuso, Rafael Garesse, Guy Lenaers, Dominique Bonneau, Valério Carelli
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
Jessica N. Cooke Bailey, Stephanie Loomis, Jae H. Kang, R. Rand Allingham, Puya Gharahkhani, Chiea Chuen Khor, Kathryn P. Burdon, Hugues Aschard, Daniel I. Chasman, Robert P. Igo, Pirro G. Hysi, Craig A. Glastonbury, Allison E. Ashley‐Koch, Murray H. Brilliant, Andrew Brown, Donald L. Budenz, Alfonso Buil, Ching‐Yu Cheng, Hyon K. Choi, William G. Christen, Gary C. Curhan, Immaculata De Vivo, John H. Fingert, Paul J. Foster, Charles S. Fuchs, Douglas Gaasterland, Terry Gaasterland, Alex W. Hewitt, Frank B. Hu, David J. Hunter, Anthony P. Khawaja, Richard K. Lee, Zheng Li, Paul R. Lichter, David A. Mackey, Peter McGuffin, Paul Mitchell, Sayoko E. Moroi, Shamira Perera, Keating W. Pepper, Qibin Qi, Tony Realini, Julia E. Richards, Paul M. Ridker, Eric B. Rimm, Robert Ritch, Marylyn D. Ritchie, Joel S. Schuman, William K. Scott, Kuldev Singh, Arthur J. Sit, Yeunjoo E. Song, Rulla M. Tamimi, Fotis Topouzis, Ananth C. Viswanathan, Shefali S. Verma, Douglas Vollrath, Jie Jin Wang, Nicole Weisschuh, Bernd Wissinger, Gadi Wollstein, Tien Yin Wong, Brian L. Yaspan, Donald J. Zack, Kang Zhang, EPIC-Norfolk Eye Study, Robert N. Weinreb, Margaret A. Pericak‐Vance, Kerrin S. Small, Christopher J. Hammond, Tin Aung, Yutao Liu, Eranga N. Vithana, Stuart MacGregor, Jamie E. Craig, Peter Kraft, Gareth R. Howell, Michael A. Hauser, Louis R. Pasquale, Jonathan L. Haines, Janey L. Wiggs
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
Isabelle Audo, Kinga M. Bujakowska, Elise Orhan, Charlotte M. Poloschek, Sabine Defoort‐Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien Dao Luu, Odile Lecompte, Eberhart Zrenner, Marie‐Elise Lancelot, Aline Antonio, Aurore Germain, Christelle Michiels, Claire Audier, Mélanie Letexier, Jean‐Paul Saraiva, Bart P. Leroy, Francis L. Munier, Saddek Mohand‐Saïd, Birgit Lorenz, Christoph Friedburg, Markus N. Preising, Ulrich Kellner, Agnes B. Renner, Veselina Moskova‐Doumanova, Wolfgang Berger, Bernd Wissinger, Christian Hamel, Daniel F. Schorderet, Elfride De Baere, Dror Sharon, Eyal Banin, Samuel G. Jacobson, Dominique Bonneau, Xavier Zanlonghi, Guylène Le Meur, Ingele Casteels, Robert K. Koenekoop, Vernon Long, Françoise Meire, Katrina Prescott, Thomy de Ravel, Ian Simmons, Hoan Nguyen, Hélène Dollfus, Olivier Poch, Thierry Léveillard, Kim T. Nguyen-Ba-Charvet, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz
Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein
Hans K. Biesalski, Jürgen Frank, Susanne Beck, Felix Heinrich, Beate Illek, Ram Reifen, Harald Gollnick, Mathias W. Seeliger, Bernd Wissinger, Eberhart Zrenner