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Samuel G. Jacobson

1971–2023 年に発表

191
論文数
31,134
被引用数
110
h 指数
191
i10 指数

被引用数

Samuel G. Jacobson の年別被引用数1973 年: 被引用 1 件1974 年: 被引用 1 件1976 年: 被引用 1 件1977 年: 被引用 3 件1978 年: 被引用 5 件1979 年: 被引用 3 件1980 年: 被引用 1 件1981 年: 被引用 1 件1982 年: 被引用 3 件1983 年: 被引用 1 件1985 年: 被引用 3 件1986 年: 被引用 1 件1987 年: 被引用 1 件1989 年: 被引用 3 件1990 年: 被引用 4 件1991 年: 被引用 15 件1992 年: 被引用 29 件1993 年: 被引用 41 件1994 年: 被引用 24 件1995 年: 被引用 43 件1996 年: 被引用 43 件1997 年: 被引用 53 件1998 年: 被引用 104 件1999 年: 被引用 112 件2000 年: 被引用 138 件2001 年: 被引用 209 件2002 年: 被引用 177 件2003 年: 被引用 237 件2004 年: 被引用 292 件2005 年: 被引用 269 件2006 年: 被引用 334 件2007 年: 被引用 263 件2008 年: 被引用 283 件2009 年: 被引用 364 件2010 年: 被引用 431 件2011 年: 被引用 381 件2012 年: 被引用 384 件2013 年: 被引用 358 件2014 年: 被引用 302 件2015 年: 被引用 331 件2016 年: 被引用 263 件2017 年: 被引用 279 件2018 年: 被引用 206 件2019 年: 被引用 814 件2020 年: 被引用 887 件2021 年: 被引用 797 件2022 年: 被引用 583 件2023 年: 被引用 375 件2024 年: 被引用 579 件2025 年: 被引用 195 件2026 年: 被引用 2 件1975 年は被引用が無いため表示していません1984 年は被引用が無いため表示していません1988 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 2,843 件、この内訳の 37.3%イギリス: 引用元論文 777 件、この内訳の 10.2%ドイツ: 引用元論文 466 件、この内訳の 6.1%フランス: 引用元論文 350 件、この内訳の 4.6%中国: 引用元論文 302 件、この内訳の 3.9%オランダ: 引用元論文 278 件、この内訳の 3.6%カナダ: 引用元論文 268 件、この内訳の 3.5%イタリア: 引用元論文 249 件、この内訳の 3.3%日本: 引用元論文 214 件、この内訳の 2.8%オーストラリア: 引用元論文 192 件、この内訳の 2.5%スイス: 引用元論文 180 件、この内訳の 2.4%スペイン: 引用元論文 158 件、この内訳の 2.1%
0%37.3%その他 17.7%

機関

分野

  • Biochemistry, Genetics and Molecular Biology70.1%
  • Medicine17.9%
  • Neuroscience7.6%
  • Immunology and Microbiology1.7%
  • Engineering0.6%
  • Computer Science0.5%
  • その他1.6%

トピック

  • Retinal Development and Disorders19.5%
  • Retinal Diseases and Treatments9.7%
  • Photoreceptor and optogenetics research4.5%
  • CRISPR and Genetic Engineering3.1%
  • Virus-based gene therapy research3.1%
  • Genetic and Kidney Cyst Diseases2.4%
  • その他57.7%

共著者

全論文

検索で開く
  1. Intravitreal antisense oligonucleotide sepofarsen in Leber congenital amaurosis type 10: a phase 1b/2 trial

    著者: Stephen R. Russell, Arlene V. Drack, Artur V. Cideciyan, Samuel G. Jacobson, Bart P. Leroy, Caroline Van Cauwenbergh, Allen C. Ho, Alina V. Dumitrescu, Ian C. Han, M. Carmen Marcos Martin, Wanda Pfeifer, Elliott H. Sohn, Jean Walshire, Alexandra V. Garafalo, Arun K. Krishnan, Christian A. Powers, Alexander Sumaroka, Alejandro J. Román, Eva Vanhonsebrouck, Eltanara A. Jones, Fanny Nerinckx, Julie De Zaeytijd, Rob W.J. Collin, Carel B. Hoyng, Peter Adamson, Michael E. Cheetham, Michael R. Schwartz, Wilhelmina den Hollander, Friedrich Asmus, Gerard Platenburg, David M. Rodman, Aniz Girach - Nature Medicine 2022 被引用: 130

  2. Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations

    著者: Sanae Sakami, Tadao Maeda, Grzegorz Bereta, Kiichiro Okano, Marcin Golczak, Alexander Sumaroka, Alejandro J. Román, Artur V. Cideciyan, Samuel G. Jacobson, Krzysztof Palczewski - Journal of Biological Chemistry 2011 被引用: 304

  3. Treatment of Leber Congenital Amaurosis Due to RPE65 Mutations by Ocular Subretinal Injection of Adeno-Associated Virus Gene Vector: Short-Term Results of a Phase I Trial

    著者: William W. Hauswirth, Tomás S. Alemán, Shalesh Kaushal, Artur V. Cideciyan, Sharon Schwartz, Lili Wang, Thomas J. Conlon, Sanford L. Boye, Terence R. Flotte, Barry J. Byrne, Samuel G. Jacobson - Human Gene Therapy 2008 被引用: 947

  4. Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 Mutations

    著者: Samuel G. Jacobson - Archives of Ophthalmology 2011 被引用: 636

  5. Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

    著者: Andreas Gal, Yun Li, Debra A. Thompson, Jessica Weir, Ulrike Orth, Samuel G. Jacobson, Eckart Apfelstedt-Sylla, Douglas Vollrath - Nature Genetics 2000 被引用: 665

  6. Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement

    著者: Artur V. Cideciyan, Samuel G. Jacobson, William A. Beltran, Alexander Sumaroka, Małgorzata Świder, Simone Iwabe, Alejandro J. Román, Melani B. Olivares, Sharon Schwartz, András M. Komáromy, William W. Hauswirth, Gustavo D. Aguirre - National Academy of Sciences, Proceedings of the National Academy of Sciences 2013 被引用: 440

  7. Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

    著者: Artur V. Cideciyan, Samuel G. Jacobson, Arlene V. Drack, Allen C. Ho, Jason Charng, Alexandra V. Garafalo, Alejandro J. Román, Alexander Sumaroka, Ian C. Han, Maria D. Hochstedler, Wanda Pfeifer, Elliott H. Sohn, Magali Taiel, Michael R. Schwartz, Patricia Biasutto, Wilma de Wit, Michael E. Cheetham, Peter Adamson, David M. Rodman, Gerard Platenburg, Maria D. Tome, Irina Balikova, Fanny Nerinckx, Julie De Zaeytijd, Caroline Van Cauwenbergh, Bart P. Leroy, Stephen R. Russell - Nature Medicine 2018 被引用: 216

  8. Improvement and Decline in Vision with Gene Therapy in Childhood Blindness

    著者: Samuel G. Jacobson, Artur V. Cideciyan, Alejandro J. Román, Alexander Sumaroka, Sharon Schwartz, Elise Héon, William W. Hauswirth - New England Journal of Medicine 2015 被引用: 377

  9. Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives

    著者: Alexandra V. Garafalo, Artur V. Cideciyan, Elise Héon, Rebecca Sheplock, Alexander Pearson, Caberry W. Yu, Alexander Sumaroka, Geoffrey K. Aguirre, Samuel G. Jacobson - Progress in Retinal and Eye Research 2019 被引用: 178

  10. In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations

    著者: Hiroko Shimada, Quanlong Lü, Christine Insinna-Kettenhofen, Kunio Nagashima, Milton A. English, Elizabeth M. Semler, Jacklyn Mahgerefteh, Artur V. Cideciyan, Tiansen Li, Brian P. Brooks, Meral Gunay‐Aygun, Samuel G. Jacobson, Tiziana Cogliati, Christopher J. Westlake, Anand Swaroop - Cell Reports 2017 被引用: 149

  11. Gene therapy restores vision in a canine model of childhood blindness

    著者: Gregory M. Acland, Geoffrey K. Aguirre, Jharna Ray, Qí Zhāng, Tomás S. Alemán, Artur V. Cideciyan, Susan E. Pearce-Kelling, Vibha Anand, Yong Zeng, Albert M. Maguire, Samuel G. Jacobson, William W. Hauswirth, Jean Bennett - Nature Genetics 2001 被引用: 1,195

  12. Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics

    著者: Artur V. Cideciyan, Tomás S. Alemán, Sanford L. Boye, Sharon Schwartz, Shalesh Kaushal, Alejandro J. Román, Jijing Pang, Alexander Sumaroka, Elizabeth A. M. Windsor, James M. Wilson, Terence R. Flotte, Gerald A. Fishman, Elise Héon, Edwin M. Stone, Barry J. Byrne, Samuel G. Jacobson, William W. Hauswirth - National Academy of Sciences, Proceedings of the National Academy of Sciences 2008 被引用: 664

  13. Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate

    著者: Neena B. Haider, Samuel G. Jacobson, Artur V. Cideciyan, Ruth E. Swiderski, Luan M. Streb, Charles Searby, Gretel Beck, Robin R. Hockey, David B. Hanna, Susan W. Gorman, David M. Duhl, Rivka Carmi, Jean Bennett, Richard G. Weleber, Gerald A. Fishman, Alan F. Wright, Edwin M. Stone, Val C. Sheffield - Nature Genetics 2000 被引用: 508

  14. Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence

    著者: Artur V. Cideciyan, Tomás S. Alemán, Małgorzata Świder, Sharon Schwartz, Janet D. Steinberg, Alexander J. Brucker, Albert M. Maguire, Jean Bennett, Edwin M. Stone, Samuel G. Jacobson - Human Molecular Genetics 2004 被引用: 268

  15. Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector

    著者: Artur V. Cideciyan, Raghavi Sudharsan, Valérie Dufour, Michael T. Massengill, Simone Iwabe, Małgorzata Świder, B Lisi, Alexander Sumaroka, Luis Felipe Marinho, Tatyana Appelbaum, Brian Rossmiller, William W. Hauswirth, Samuel G. Jacobson, Alfred S. Lewin, Gustavo D. Aguirre, William A. Beltran - National Academy of Sciences, Proceedings of the National Academy of Sciences 2018 被引用: 147

  16. Full-field stimulus testing: Role in the clinic and as an outcome measure in clinical trials of severe childhood retinal disease

    著者: Alejandro J. Román, Artur V. Cideciyan, Vivian Wu, Alexandra V. Garafalo, Samuel G. Jacobson - Progress in Retinal and Eye Research 2021 被引用: 60

  17. Night vision restored in days after decades of congenital blindness

    著者: Samuel G. Jacobson, Artur V. Cideciyan, Allen C. Ho, Alejandro J. Román, Vivian Wu, Alexandra V. Garafalo, Alexander Sumaroka, Arun K. Krishnan, Małgorzata Świder, Abraham A. Mascio, Christine N. Kay, Dan Yoon, Kenji P. Fujita, Sanford L. Boye, Igor V. Peshenko, Alexander M. Dizhoor, Sanford L. Boye - iScience 2022 被引用: 36

  18. Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease

    著者: Terry A. Braun, Robert F. Mullins, Alex H. Wagner, Jeaneen L. Andorf, Rebecca M. Johnston, Benjamin Bakall, Adam P. DeLuca, Gerald A. Fishman, Byron L. Lam, Richard G. Weleber, Artur V. Cideciyan, Samuel G. Jacobson, Val C. Sheffield, Budd A. Tucker, Edwin M. Stone - Human Molecular Genetics 2013 被引用: 182

  19. Full-field stimulus testing (FST) to quantify visual perception in severely blind candidates for treatment trials

    著者: Alejandro J. Román, Artur V. Cideciyan, Tomás S. Alemán, Samuel G. Jacobson - Physiological Measurement 2007 被引用: 116

  20. Durable vision improvement after a single intravitreal treatment with antisense oligonucleotide in CEP290-LCA: Replication in two eyes

    著者: Artur V. Cideciyan, Samuel G. Jacobson, Allen C. Ho, Małgorzata Świder, Alexander Sumaroka, Alejandro J. Román, Vivian Wu, Robert C. Russell, Iryna Viarbitskaya, Alexandra V. Garafalo, Michael R. Schwartz, Aniz Girach - American Journal of Ophthalmology Case Reports 2023 被引用: 15

  21. Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene () Essential for Maintenance of the Photoreceptor

    著者: Carol L. Freund, Cheryl Y. Gregory‐Evans, Takahisa Furukawa, Myrto Papaioannou, Jens Looser, Lynda Ploder, James Bellingham, David Ng, Jo-Anne Herbrick, Alessandra M.V. Duncan, Stephen W. Scherer, Lap-Chee Tsui, Aphrodite Loutradis-Anagnostou, Samuel G. Jacobson, Constance L. Cepko, Shomi S. Bhattacharya, Roderick R. McInnes - Cell 1997 被引用: 565

  22. Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man

    著者: Artur V. Cideciyan, Donald C. Hood, Yijun Huang, Eyal Banin, Zongyi Li, Edwin M. Stone, Ann H. Milam, Samuel G. Jacobson - National Academy of Sciences, Proceedings of the National Academy of Sciences 1998 被引用: 283

  23. Quantifying rod photoreceptor-mediated vision in retinal degenerations: dark-adapted thresholds as outcome measures

    著者: Alejandro J. Román, Sharon Schwartz, Tomás S. Alemán, Artur V. Cideciyan, John D. Chico, Elizabeth A. M. Windsor, Leigh M. Gardner, Gui‐Shuang Ying, E.E. Smilko, Maureen G. Maguire, Samuel G. Jacobson - Experimental Eye Research 2004 被引用: 162

  24. Human cone photoreceptor dependence on RPE65 isomerase

    著者: Samuel G. Jacobson, Tomás S. Alemán, Artur V. Cideciyan, Elise Héon, Marcin Golczak, William A. Beltran, Alexander Sumaroka, Sharon Schwartz, Alejandro J. Román, Elizabeth A. M. Windsor, James M. Wilson, Geoffrey K. Aguirre, Edwin M. Stone, Krzysztof Palczewski - National Academy of Sciences, Proceedings of the National Academy of Sciences 2007 被引用: 157