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Wolfgang Berger

1968–2026 年に発表

91
論文数
20,782
被引用数
63
h 指数
85
i10 指数

被引用数

Wolfgang Berger の年別被引用数1970 年: 被引用 3 件1971 年: 被引用 9 件1972 年: 被引用 3 件1973 年: 被引用 2 件1975 年: 被引用 1 件1976 年: 被引用 10 件1977 年: 被引用 5 件1978 年: 被引用 5 件1979 年: 被引用 1 件1980 年: 被引用 3 件1981 年: 被引用 7 件1982 年: 被引用 7 件1983 年: 被引用 5 件1984 年: 被引用 6 件1985 年: 被引用 4 件1986 年: 被引用 5 件1987 年: 被引用 8 件1988 年: 被引用 7 件1989 年: 被引用 16 件1990 年: 被引用 10 件1991 年: 被引用 8 件1992 年: 被引用 15 件1993 年: 被引用 27 件1994 年: 被引用 13 件1995 年: 被引用 18 件1996 年: 被引用 24 件1997 年: 被引用 14 件1998 年: 被引用 28 件1999 年: 被引用 51 件2000 年: 被引用 55 件2001 年: 被引用 48 件2002 年: 被引用 85 件2003 年: 被引用 82 件2004 年: 被引用 84 件2005 年: 被引用 127 件2006 年: 被引用 131 件2007 年: 被引用 110 件2008 年: 被引用 131 件2009 年: 被引用 140 件2010 年: 被引用 175 件2011 年: 被引用 135 件2012 年: 被引用 152 件2013 年: 被引用 128 件2014 年: 被引用 114 件2015 年: 被引用 96 件2016 年: 被引用 98 件2017 年: 被引用 94 件2018 年: 被引用 81 件2019 年: 被引用 228 件2020 年: 被引用 228 件2021 年: 被引用 234 件2022 年: 被引用 170 件2023 年: 被引用 126 件2024 年: 被引用 225 件2025 年: 被引用 70 件2026 年: 被引用 3 件1974 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 1,433 件、この内訳の 26.8%イギリス: 引用元論文 521 件、この内訳の 9.7%ドイツ: 引用元論文 376 件、この内訳の 7%カナダ: 引用元論文 265 件、この内訳の 5%中国: 引用元論文 251 件、この内訳の 4.7%フランス: 引用元論文 241 件、この内訳の 4.5%オーストラリア: 引用元論文 226 件、この内訳の 4.2%オランダ: 引用元論文 202 件、この内訳の 3.8%スイス: 引用元論文 188 件、この内訳の 3.5%イタリア: 引用元論文 167 件、この内訳の 3.1%スペイン: 引用元論文 134 件、この内訳の 2.5%日本: 引用元論文 120 件、この内訳の 2.2%
0%26.8%その他 23%

機関

分野

  • Biochemistry, Genetics and Molecular Biology33.9%
  • Environmental Science18.4%
  • Medicine13.3%
  • Earth and Planetary Sciences11.4%
  • Neuroscience8.3%
  • Computer Science4.8%
  • その他9.9%

トピック

  • Retinal Development and Disorders5.4%
  • Coral and Marine Ecosystems Studies3.2%
  • Marine and fisheries research3%
  • Geology and Paleoclimatology Research2.6%
  • Retinal Diseases and Treatments2.1%
  • Marine Bivalve and Aquaculture Studies1.6%
  • その他82.1%

共著者

全論文

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  1. The molecular basis of human retinal and vitreoretinal diseases

    著者: Wolfgang Berger, Barbara Kloeckener‐Gruissem, John Neidhardt - Progress in Retinal and Eye Research 2010 被引用: 611

  2. Historical Overfishing and the Recent Collapse of Coastal Ecosystems

    著者: Jeremy B. C. Jackson, Michael X. Kirby, Wolfgang Berger, Karen A. Bjorndal, Louis W. Botsford, Bruce J. Bourque, Roger Bradbury, Richard G. Cooke, Jon M. Erlandson, James A. Estes, Terry P. Hughes, Susan M. Kidwell, Carina B. Lange, Hunter S. Lenihan, John M. Pandolfi, Charles H. Peterson, Robert S. Steneck, Mia J. Tegner, Robert R. Warner - Science 2001 被引用: 6,633

  3. Diversity of Planktonic Foraminifera in Deep-Sea Sediments

    著者: Wolfgang Berger, Frances L. Parker - Science 1970 被引用: 1,044

  4. Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease−associated genes

    著者: Suzanne E. de Bruijn, Kim Rodenburg, Jordi Corominas, Tamar Ben‐Yosef, Janine Reurink, Hannie Kremer, Laura Whelan, Astrid S. Plomp, Wolfgang Berger, G. Jane Farrar, Árpád Ferenc Kovács, Isabelle Fajardy, Rebekkah J. Hitti‐Malin, Nicole Weisschuh, Marianna E. Weener, Dror Sharon, Ronald J. E. Pennings, Lonneke Haer‐Wigman, Carel B. Hoyng, Marcel Nelen, Lisenka E.L.M. Vissers, L. Ingeborgh van den Born, Christian Gilissen, Frans P.M. Cremers, Alexander Hoischen, Kornelia Neveling, Susanne Roosing - Genetics in Medicine 2022 被引用: 41

  5. ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature

    著者: Rob W.J. Collin, Konstantinos Nikopoulos, Margo Dona, Christian Gilissen, Alexander Hoischen, F. Nienke Boonstra, James A. Poulter, Hiroyuki Kondo, Wolfgang Berger, Carmel Toomes, Tomoko Tahira, Lucas Mohn, Ellen A.W. Blokland, Lisette Hetterschijt, Manir Ali, Johanne M. Groothuismink, Lonneke Duijkers, Chris F. Inglehearn, Lea Sollfrank, Tim M. Strom, Eiichi Uchio, C. E. van Nouhuys, Hannie Kremer, Joris A. Veltman, Erwin van Wijk, Frans P.M. Cremers - National Academy of Sciences, Proceedings of the National Academy of Sciences 2013 被引用: 188

  6. Haplotype of the astrocytic water channel AQP4 is associated with slow wave energy regulation in human NREM sleep

    著者: Sara Marie Ulv Larsen, Hans‐Peter Landolt, Wolfgang Berger, Maiken Nedergaard, Gitte M. Knudsen, Sebastian C. Holst - PLoS Biology 2020 被引用: 60

  7. A Genetic Variation in the Adenosine A2A Receptor Gene (ADORA2A) Contributes to Individual Sensitivity to Caffeine Effects on Sleep

    著者: Julia Rétey, Martin Adam, Ramin Khatami, Ulrich F. O. Luhmann, Hae Hyuk Jung, Wolfgang Berger, H-P Landolt - Clinical Pharmacology & Therapeutics 2007 被引用: 280

  8. TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

    著者: Isabelle Audo, Susanne Kohl, Bart P. Leroy, Francis L. Munier, Xavier Guillonneau, Saddek Mohand‐Saïd, Kinga M. Bujakowska, Emeline F. Nandrot, Birgit Lorenz, Markus N. Preising, Ulrich Kellner, Agnes B. Renner, Antje Bernd, Aline Antonio, Veselina Moskova‐Doumanova, Marie‐Elise Lancelot, Charlotte M. Poloschek, Isabelle Drumare, Sabine Defoort‐Dhellemmes, Bernd Wissinger, Thierry Léveillard, Christian Hamel, Daniel F. Schorderet, Elfride De Baere, Wolfgang Berger, Samuel G. Jacobson, Eberhart Zrenner, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz - The American Journal of Human Genetics 2009 被引用: 262

  9. Mutations in CABP4, the Gene Encoding the Ca2+-Binding Protein 4, Cause Autosomal Recessive Night Blindness

    著者: Christina Zeitz, Barbara Kloeckener‐Gruissem, U. Förster, Susanne Kohl, I Magyar, Bernd Wissinger, Gábor Mátyás, François‐Xavier Borruat, Daniel F. Schorderet, Eberhart Zrenner, Francis L. Munier, Wolfgang Berger - The American Journal of Human Genetics 2006 被引用: 181

  10. Role of the Norrie Disease Pseudoglioma Gene in Sprouting Angiogenesis during Development of the Retinal Vasculature

    著者: Ulrich F. O. Luhmann, Jihong Lin, Niyazi Acar, Stefanie Lammel, Silke Feil, Christian Grimm, Mathias W. Seeliger, Hans‐Peter Hammes, Wolfgang Berger - Investigative Ophthalmology & Visual Science 2005 被引用: 155

  11. Integrin-linked kinase controls retinal angiogenesis and is linked to Wnt signaling and exudative vitreoretinopathy

    著者: Hongryeol Park, Hiroyuki Yamamoto, Lucas Mohn, Lea Maria Margareta Ambühl, Kenichi Kanai, Inga Schmidt, Kee-Pyo Kim, Alessia Fraccaroli, Silke Feil, Harald J. Junge, Eloi Montañez, Wolfgang Berger, Ralf H. Adams - Nature Communications 2019 被引用: 84

  12. A Multi-Threading Architecture to Support Interactive Visual Exploration

    著者: Harald Piringer, Christian Tominski, Philipp Muigg, Wolfgang Berger - IEEE Transactions on Visualization and Computer Graphics, IEEE Trans. Vis. Comput. Graph. 2009 被引用: 69

  13. Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction

    著者: Janine Reurink, Nicole Weisschuh, Alejandro Garanto, Adrian Dockery, L. Ingeborgh van den Born, Isabelle Fajardy, Lonneke Haer‐Wigman, Susanne Kohl, Bernd Wissinger, G. Jane Farrar, Tamar Ben‐Yosef, Fatma Kivrak Pfiffner, Wolfgang Berger, Marianna E. Weener, Ľubica Ďuďáková, Petra Lišková, Dror Sharon, Manar Salameh, Ashley Offenheim, Elise Héon, Giorgia Girotto, Paolo Gasparini, Anna Morgan, Arthur A. Bergen, Jacoline B. ten Brink, Caroline C. W. Klaver, Lisbeth Tranebjærg, Nanna Dahl Rendtorff, Sascha Vermeer, Jeroen J. Smits, Ronald J. E. Pennings, Marco Aben, Jaap Oostrik, Galuh Astuti, Jordi Corominas Galbany, Hester Y. Kroes, Milan Phan, Wendy A.G. van Zelst–Stams, Alberta A. H. J. Thiadens, Joke B.G.M. Verheij, Mary J. van Schooneveld, Suzanne E. de Bruijn, Catherina H. Z. Li, Carel B. Hoyng, Christian Gilissen, Lisenka E.L.M. Vissers, Frans P.M. Cremers, Hannie Kremer, Erwin van Wijk, Susanne Roosing - Human Genetics and Genomics Advances 2023 被引用: 28

  14. Long-Range PCR-Based NGS Applications to Diagnose Mendelian Retinal Diseases

    著者: Jordi Maggi, Samuel Koller, Luzy Bähr, Silke Feil, Fatma Kivrak Pfiffner, James V. M. Hanson, Alessandro Maspoli, Christina Gerth‐Kahlert, Wolfgang Berger - International Journal of Molecular Sciences 2021 被引用: 25

  15. Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies

    著者: Nicola Glöckle, Susanne Kohl, Julia Mohr, Tim Scheurenbrand, Andrea Sprecher, Nicole Weisschuh, Antje Bernd, Günther Rudolph, Max Schubach, Charlotte M. Poloschek, Eberhart Zrenner, Saskia Biskup, Wolfgang Berger, Bernd Wissinger, John Neidhardt - European Journal of Human Genetics 2013 被引用: 246

  16. Whole Exome Sequencing in Coloboma/Microphthalmia: Identification of Novel and Recurrent Variants in Seven Genes

    著者: Patricia Haug, Samuel Koller, Jordi Maggi, Elena Lang, Silke Feil, Agnès Wlodarczyk, Luzy Bähr, Katharina Steindl, Marianne Rohrbach, Christina Gerth‐Kahlert, Wolfgang Berger - Genes 2021 被引用: 32

  17. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

    著者: Nandita Quaderi, Susann Schweiger, Karin Gaudenz, Brunella Franco, Elena I. Rugarli, Wolfgang Berger, George Feldman, Manuela Volta, Grazia Andolfi, S Gilgenkrantz, Robert W. Marion, Raoul C. M. Hennekam, John M. Opitz, Maximilian Muenke, Hilger H. Ropers, Andrea Ballabio - Nature Genetics 1997 被引用: 370

  18. Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease

    著者: Heidi L. Rehm, Duan-Sun Zhang, M. Christian Brown, Barbara J. Burgess, Chris Halpin, Wolfgang Berger, Cynthia C. Morton, David P. Corey, Zheng‐Yi Chen - Journal of Neuroscience 2002 被引用: 156

  19. Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

    著者: 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 - The American Journal of Human Genetics 2012 被引用: 134

  20. Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestalt

    著者: Nataliya Di Donato, Teresa Neuhann, Anne-Karin Kahlert, Barbara Klink, Karl Hackmann, Irmingard M. Neuhann, Barbora Novotná, Jens Schallner, Claudia Krause, Ian A. Glass, Shawn E. Parnell, Anna Benet‐Pagès, Anke M. Nissen, Wolfgang Berger, Janine Altmüller, Hölger Thiele, Bernhard H. F. Weber, Evelin Schröck, William B. Dobyns, Andrea Bier, Andreas Rump - Journal of Medical Genetics 2016 被引用: 97

  21. Genetic Analysis in a Swiss Cohort of Bilateral Congenital Cataract

    著者: Delia Rechsteiner, Lydia S. Issler, Samuel Koller, Elena Lang, Luzy Bähr, Silke Feil, Christoph M. Rüegger, Raimund Kottke, Sandra P. Toelle, Noëmi Zweifel, Katharina Steindl, Pascal Joset, Markus Zweier, Aude‐Annick Suter, Laura Gogoll, Cordula Haas, Wolfgang Berger, Christina Gerth‐Kahlert - JAMA Ophthalmology 2021 被引用: 50

  22. Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans

    著者: Emilia Boiadjieva Knöpfel, Clara Vilches, Simone M. R. Camargo, Ekaitz Errasti‐Murugarren, Andrina Stäubli, Clara Mayayo‐Vallverdú, Francis L. Munier, Nataliya Miroshnikova, Nadège Poncet, Alexandra Junza, Shomi S. Bhattacharya, Esther Prat, Vanita Berry, Wolfgang Berger, Elise Héon, Anthony T. Moore, Óscar Yanes, Virginia Nunes, Manuel Palacı́n, François Verrey, Barbara Kloeckener‐Gruissem - Frontiers in Physiology 2019 被引用: 48

  23. Impact of Genetic Variant Reassessment on the Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy Based on the 2010 Task Force Criteria

    著者: Sarah Costa, Argelia Medeiros‐Domingo, Alessio Gasperetti, Deniz Akdiş, Wolfgang Berger, Cynthia A. James, Frank Ruschitzka, Corinna Brunckhorst, Fırat Duru, Ardan M. Saguner - Circulation Genomic and Precision Medicine 2020 被引用: 26

  24. Isolation of a candidate gene for Norrie disease by positional cloning

    著者: Wolfgang Berger, A Meindl, T.J.R. van de Pol, Frans P.M. Cremers, H.-H. Ropers, C. Döerner, Anthony P. Monaco, Arthur A. Bergen, R V Lebo, Mette Warburg, L Zergollern, Bettina Lorenz, Andreas Gal, E. M. Bleeker‐Wagemakers, Thomas Meitinger - Nature Genetics 1992 被引用: 253