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Thaddeus P. Dryja

Active 1982–2022

Also published as
Thaddeus P Dryja
98
Papers
28,292
Citations
84
h-index
97
i10-index

Citations

Citations per year for Thaddeus P. Dryja1980: 2 citations1983: 1 citations1984: 20 citations1985: 27 citations1986: 52 citations1987: 90 citations1988: 102 citations1989: 178 citations1990: 210 citations1991: 215 citations1992: 234 citations1993: 246 citations1994: 199 citations1995: 149 citations1996: 189 citations1997: 206 citations1998: 219 citations1999: 252 citations2000: 207 citations2001: 207 citations2002: 175 citations2003: 167 citations2004: 205 citations2005: 180 citations2006: 198 citations2007: 148 citations2008: 136 citations2009: 155 citations2010: 194 citations2011: 195 citations2012: 220 citations2013: 194 citations2014: 183 citations2015: 203 citations2016: 139 citations2017: 178 citations2018: 90 citations2019: 431 citations2020: 417 citations2021: 359 citations2022: 275 citations2023: 192 citations2024: 272 citations2025: 100 citations2026: 4 citations1981–1982: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,029 citing papers, 39.7% of this breakdownUnited Kingdom: 660 citing papers, 8.7% of this breakdownGermany: 414 citing papers, 5.4% of this breakdownChina: 349 citing papers, 4.6% of this breakdownJapan: 311 citing papers, 4.1% of this breakdownFrance: 302 citing papers, 4% of this breakdownCanada: 290 citing papers, 3.8% of this breakdownNetherlands: 222 citing papers, 2.9% of this breakdownItaly: 212 citing papers, 2.8% of this breakdownSwitzerland: 198 citing papers, 2.6% of this breakdownSpain: 183 citing papers, 2.4% of this breakdownAustralia: 136 citing papers, 1.8% of this breakdown
0%39.7%Other 17.2%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology58.1%
  • Medicine29.8%
  • Neuroscience6%
  • Immunology and Microbiology4.4%
  • Agricultural and Biological Sciences0.4%
  • Nursing0.2%
  • Other1.1%

Topics

  • Retinal Development and Disorders12.7%
  • Retinal Diseases and Treatments5.2%
  • Cancer-related Molecular Pathways4.1%
  • Photoreceptor and optogenetics research3.9%
  • Ocular Oncology and Treatments2.9%
  • Epigenetics and DNA Methylation2%
  • Other69.2%

Coauthors

All papers

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  1. Retinitis pigmentosa

    Authors: Dyonne T. Hartong, Eliot L. Berson, Thaddeus P. Dryja - The Lancet 2006 cited by 2,881

  2. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

    Authors: Thaddeus P. Dryja, Terri L. McGee, Elias Reichel, Lauri B. Hahn, Glenn S. Cowley, David W. Yandell, Michael A. Sandberg, Eliot L. Berson - Nature 1990 cited by 1,085

  3. Effects of AIN457, a Fully Human Antibody to Interleukin-17A, on Psoriasis, Rheumatoid Arthritis, and Uveitis

    Authors: Wolfgang Hueber, Dhavalkumar D. Patel, Thaddeus P. Dryja, A. Wright, И. А. Королева, Gerard Bruin, Christian Antoni, Zoe Draelos, Michael H. Gold, the Psoriasis Study Group, Patrick Durez, Paul P. Tak, Juan J. Gómez‐Reino, the Rheumatoid Arthritis Study Group, C. Stephen Foster, Rosa Y. Kim, C. Michael Samson, Naomi S. Falk, David Chu, David Callanan, Quan Dong Nguyen, the Uveitis Study Group, Kristine Rose, Asifa Haider, Franco Di Padova - Science Translational Medicine 2010 cited by 861

  4. A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

    Authors: Stephen Friend, René Bernards, Snezna Rogelj, Robert A. Weinberg, Joyce M. Rapaport, Daniel M. Albert, Thaddeus P. Dryja - Nature 1986 cited by 2,984

  5. Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

    Authors: Webster K. Cavenee, Thaddeus P. Dryja, Robert A. Phillips, W. F. Benedict, Roseline Godbout, Brenda L. Gallie, A. Linn Murphree, Louise C. Strong, R. White - Nature 1983 cited by 1,948

  6. Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa

    Authors: Thaddeus P. Dryja, Terri L. McGee, Lauri B. Hahn, Glenn S. Cowley, J E Olsson, Elias Reichel, Michael A. Sandberg, Eliot L. Berson - New England Journal of Medicine 1990 cited by 503

  7. Digenic Retinitis Pigmentosa Due to Mutations at the Unlinked Peripherin/ RDS and ROM1 Loci

    Authors: Kazuto Kajiwara, Eliot L. Berson, Thaddeus P. Dryja - Science 1994 cited by 786

  8. The RB1 Story: Characterization and Cloning of the First Tumor Suppressor Gene

    Authors: Jesse L. Berry, Ashley Polski, Webster K. Cavenee, Thaddeus P. Dryja, A. Linn Murphree, Brenda L. Gallie - Genes 2019 cited by 73

  9. Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis

    Authors: Hiroyuki Morimura, Gerald A. Fishman, Sandeep Grover, Anne B. Fulton, Eliot L. Berson, Thaddeus P. Dryja - National Academy of Sciences, Proceedings of the National Academy of Sciences 1998 cited by 489

  10. Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6

    Authors: Thaddeus P. Dryja, Terri L. McGee, Eliot L. Berson, Gerald A. Fishman, Michael A. Sandberg, Kenneth R. Alexander, Deborah J. Derlacki, Aruna S. Rajagopalan - National Academy of Sciences, Proceedings of the National Academy of Sciences 2005 cited by 250

  11. Disease Course of Patients with X-linked Retinitis Pigmentosa due toRPGRGene Mutations

    Authors: Michael A. Sandberg, Bernard Rosner, Carol Weigel-DiFranco, Thaddeus P. Dryja, Eliot L. Berson - Investigative Ophthalmology & Visual Science 2007 cited by 159

  12. Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa

    Authors: Hiroyuki Morimura, Florence Saindelle-Ribeaudeau, Eliot L. Berson, Thaddeus P. Dryja - Nature Genetics 1999 cited by 145

  13. A Review of Next-Generation Sequencing (NGS): Applications to the Diagnosis of Ocular Infectious Diseases

    Authors: Lina Ma, Frederick A. Jakobiec, Thaddeus P. Dryja - Seminars in Ophthalmology 2019 cited by 63

  14. Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa

    Authors: Margaret E. McLaughlin, Michael A. Sandberg, Eliot L. Berson, Thaddeus P. Dryja - Nature Genetics 1993 cited by 606

  15. Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus

    Authors: Hiroyuki Yamamoto, András Simon, Ulf Eriksson, Eddie Harris, Eliot L. Berson, Thaddeus P. Dryja - Nature Genetics 1999 cited by 294

  16. Transgenic mice carrying the dominant rhodopsin mutation P347S: Evidence for defective vectorial transport of rhodopsin to the outer segments

    Authors: Tiansen Li, Wendy K. Snyder, J E Olsson, Thaddeus P. Dryja - National Academy of Sciences, Proceedings of the National Academy of Sciences 1996 cited by 244

  17. RP2 and RPGR Mutations and Clinical Correlations in Patients with X-Linked Retinitis Pigmentosa

    Authors: Dror Sharon, Michael A. Sandberg, Vivian W. Rabe, Melissa A. Stillberger, Thaddeus P. Dryja, Eliot L. Berson - The American Journal of Human Genetics 2003 cited by 228

  18. A Homozygous Missense Mutation in theIRBPGene (RBP3) Associated with Autosomal Recessive Retinitis Pigmentosa

    Authors: Anneke I. den Hollander, Terri L. McGee, Carmela Ziviello, Sandro Banfi, Thaddeus P. Dryja, Federico Gonzalez-Fernandez, Debashis Ghosh, Eliot L. Berson - Investigative Ophthalmology & Visual Science 2009 cited by 109

  19. Systemic Medication Associations with Presumed Advanced or Uncontrolled Primary Open-Angle Glaucoma

    Authors: Wei Zheng, Thaddeus P. Dryja, Zhongyuan Wei, Dongying Song, Haijun Tian, Kristijan H. Kahler, Anthony P. Khawaja - Ophthalmology 2018 cited by 85

  20. Allele-specific hypermethylation of the retinoblastoma tumor-suppressor gene.

    Authors: Toshiyuki Sakai, Junya Toguchida, Naoko Ohtani, David W. Yandell, Joyce M. Rapaport, Thaddeus P. Dryja - 1991 cited by 475

  21. Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa

    Authors: J E Olsson, Jon W. Gordon, Basil S. Pawlyk, Dorothy Roof, Annmarie Hayes, Robert S. Molday, Shizuo Mukai, Glenn S. Cowley, Eliot L. Berson, Thaddeus P. Dryja - Neuron 1992 cited by 458

  22. Missense Mutation in the USH2A Gene: Association with Recessive Retinitis Pigmentosa without Hearing Loss

    Authors: Carlo Rivolta, Elizabeth A. Sweklo, Eliot L. Berson, Thaddeus P. Dryja - The American Journal of Human Genetics 2000 cited by 259

  23. Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle

    Authors: Dyonne T. Hartong, Mayura Dange, Terri L. McGee, Eliot L. Berson, Thaddeus P. Dryja, Roberta F. Colman - Nature Genetics 2008 cited by 174

  24. Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa

    Authors: Terri L. McGee, B. Jian Seyedahmadi, Meredith O. Sweeney, Thaddeus P Dryja, Eliot L. Berson - Journal of Medical Genetics 2010 cited by 170