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Jürg Ott

1976–2023 年に発表

別表記
Jurg Ott
141
論文数
30,962
被引用数
93
h 指数
133
i10 指数

被引用数

Jürg Ott の年別被引用数1971 年: 被引用 1 件1977 年: 被引用 1 件1978 年: 被引用 1 件1980 年: 被引用 1 件1982 年: 被引用 1 件1983 年: 被引用 5 件1985 年: 被引用 4 件1986 年: 被引用 8 件1987 年: 被引用 13 件1988 年: 被引用 28 件1989 年: 被引用 14 件1990 年: 被引用 50 件1991 年: 被引用 49 件1992 年: 被引用 70 件1993 年: 被引用 74 件1994 年: 被引用 127 件1995 年: 被引用 150 件1996 年: 被引用 142 件1997 年: 被引用 159 件1998 年: 被引用 237 件1999 年: 被引用 224 件2000 年: 被引用 243 件2001 年: 被引用 252 件2002 年: 被引用 266 件2003 年: 被引用 303 件2004 年: 被引用 311 件2005 年: 被引用 331 件2006 年: 被引用 434 件2007 年: 被引用 392 件2008 年: 被引用 391 件2009 年: 被引用 322 件2010 年: 被引用 412 件2011 年: 被引用 352 件2012 年: 被引用 312 件2013 年: 被引用 248 件2014 年: 被引用 202 件2015 年: 被引用 184 件2016 年: 被引用 172 件2017 年: 被引用 171 件2018 年: 被引用 135 件2019 年: 被引用 347 件2020 年: 被引用 319 件2021 年: 被引用 353 件2022 年: 被引用 187 件2023 年: 被引用 155 件2024 年: 被引用 226 件2025 年: 被引用 100 件2026 年: 被引用 6 件1972〜1976 年は被引用が無いため表示していません1979 年は被引用が無いため表示していません1981 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

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 3,961 件、この内訳の 34.7%イギリス: 引用元論文 1,116 件、この内訳の 9.8%ドイツ: 引用元論文 685 件、この内訳の 6%中国: 引用元論文 549 件、この内訳の 4.8%フランス: 引用元論文 418 件、この内訳の 3.7%カナダ: 引用元論文 406 件、この内訳の 3.5%オーストラリア: 引用元論文 359 件、この内訳の 3.1%イタリア: 引用元論文 344 件、この内訳の 3%オランダ: 引用元論文 342 件、この内訳の 3%日本: 引用元論文 319 件、この内訳の 2.8%スイス: 引用元論文 242 件、この内訳の 2.1%スウェーデン: 引用元論文 187 件、この内訳の 1.6%
0%34.7%その他 21.9%

機関

分野

  • Biochemistry, Genetics and Molecular Biology42.1%
  • Medicine34.2%
  • Neuroscience10.3%
  • Immunology and Microbiology3.5%
  • Psychology3.5%
  • Nursing1.7%
  • その他4.7%

トピック

  • Genetic Associations and Epidemiology5.4%
  • Retinal Diseases and Treatments3.7%
  • Genetic Mapping and Diversity in Plants and Animals2.2%
  • Genetics and Neurodevelopmental Disorders2.1%
  • Retinal Development and Disorders1.7%
  • Genomic variations and chromosomal abnormalities1.7%
  • その他83.2%

共著者

全論文

検索で開く
  1. Complement Factor H Polymorphism in Age-Related Macular Degeneration

    著者: Robert J. Klein, Caroline J. Zeiss, Emily Y. Chew, Jen-Yue Tsai, Richard S. Sackler, Chad Haynes, Alice K. Henning, John Paul SanGiovanni, Shrikant Mane, Susan T. Mayne, Michael B. Bracken, Frederick L. Ferris, Jürg Ott, Colin J. Barnstable, Josephine Hoh - Science 2005 被引用: 4,530

  2. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

    著者: Dongjing Liu, Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica Johnson, You Jeong Park, Marysia-Kolbe Rieder, Steven Ascolillo, Agathe de Pins, Amanda Dobbyn, Dannielle Lebovitch, Emily Moya, Tan-Hoang Nguyen, Lillian Wilkins, Arsalan Hassan, Henry S. Aghanwa, Moin Ahmad Ansari, Aftab Asif, Rubina Aslam, José Luis Ayuso, Tim B. Bigdeli, Stefano Bignotti, Julio Bobes, Bekh Bradley, P.F. Buckley, Murray J. Cairns, Stanley V. Catts, Abdul Rashid Chaudhry, David Cohen, Brett Collins, Angèle Consoli, Javier Costas, Benedicto Crespo‐Facorro, Nikolaos P. Daskalakis, Michael Davidson, Kenneth L. Davis, Faith Dickerson, Imtiaz Ahmad Dogar, Elodie Drapeau, Lourdes Fañanás, Ayman H. Fanous, Warda Fatima, Mar Fatjó‐Vilas, Cheryl Filippich, Joseph I. Friedman, John F. Fullard, Penelope Georgakopoulos, Marianna Giannitelli, Ina Giegling, Melissa J. Green, Olivier Guillin, Blanca Gutiérrez, Herlina Y. Handoko, Stella Kim Hansen, Maryam Haroon, Vahram Haroutunian, Frans Henskens, Fahad Hussain, Assen Jablensky, Jamil Junejo, Brian Kelly, Shams-ud-Din Ahmad Khan, Muhammad Nasar Sayeed Khan, Anisuzzaman Khan, Hamid R. Khawaja, Bakht Khizar, Steven P. Kleopoulos, James A. Knowles, Bettina Konte, Agung Kusumawardhani, Naeemullah Leghari, Xudong Liu, Adriana Lori, Carmel M. Loughland, Khalid Mahmood, Saqib Mahmood, Dolores Malaspina, Danish J. Malik, Amy J. M. McNaughton, Patricia T. Michie, Vasiliki Michopolous, Esther Molina, María Dolores Moltó, Asim Munir, Gerard Muntané, Farooq Naeem, Derek J. Nancarrow, Amina Nasar, Tanvir Nasr, Jude U. Ohaeri, Jürg Ott, Christos Pantelis, Sathish Periyasamy, Ana González‐Pinto, Abigail Powers, Belén Ramos, Nusrat Habib Rana, Mark Hyman Rapaport, Abraham Reichenberg ほか 61 名 - Nature Genetics 2023 被引用: 73

  3. Genetic linkage analysis in the age of whole-genome sequencing

    著者: Jürg Ott, Jing Wang, Suzanne M. Leal - Nature Reviews Genetics 2015 被引用: 285

  4. A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23

    著者: Yongzhe Li, Kunlin Zhang, Hua Chen, Fei Sun, Juanjuan Xu, Ziyan Wu, Ping Li, Liuyan Zhang, Yang Du, Haixia Luan, Xi Li, Lijun Wu, Hongbin Li, Huaxiang Wu, Xiang-Pei Li, Xiaomei Li, Xiao Zhang, Lu Gong, Lie Dai, Lingyun Sun, Xiaoxia Zuo, Jianhua Xu, Huiping Gong, Zhijun Li, Shengquan Tong, Min Wu, Xiaofeng Li, Weiguo Xiao, Guochun Wang, Ping Zhu, Min Shen, Shengyun Liu, Dongbao Zhao, Wei Liu, Yi Wang, Cibo Huang, Quan Jiang, Guijian Liu, Bin Liu, Shaoxian Hu, Wen Zhang, Zhuoli Zhang, Xin You, Mengtao Li, Weixin Hao, Cheng Zhao, Xiaomei Leng, Liqi Bi, Yongfu Wang, Fengxiao Zhang, Qun Shi, Wencheng Qi, Xuewu Zhang, Yuan Jia, Jinmei Su, Qin Li, Yong Hou, Qingjun Wu, Dong Xu, Wenjie Zheng, Miaojia Zhang, Qian Wang, Yunyun Fei, Xuan Zhang, Jing Li, Ying Jiang, Xinping Tian, Lidan Zhao, Li Wang, Bin Zhou, Yang Li, Yan Zhao, Xiaofeng Zeng, Jürg Ott, Jing Wang, Fengchun Zhang, Fengchun Zhang, Fengchun Zhang - Nature Genetics 2013 被引用: 238

  5. PDE3A mutations cause autosomal dominant hypertension with brachydactyly

    著者: Philipp G. Maass, Atakan Aydın, Friedrich C. Luft, Carolin Schächterle, Anja Weise, Sigmar Stricker, Carsten Lindschau, Martin Vaegler, Fatimunnisa Qadri, Hakan R. Toka, Herbert Schulz, Peter Krawitz, Dmitri Parkhomchuk, Jochen Hecht, Irene Hollfinger, Yvette Wefeld‐Neuenfeld, Eireen Bartels‐Klein, Astrid Mühl, Martin Kann, Herbert Schuster, David Chitayat, Martin G. Bialer, Thomas F. Wienker, Jürg Ott, Katharina Rittscher, Thomas Liehr, Jens Jordan, Ghislaine Plessis, Jens Tank, Knut Mai, Ramin Naraghi, Russell Hodge, M Hopp, Lars‐Olof Hattenbach, Andreas Busjahn, Anita Rauch, Fabrice Vandeput, Maolian Gong, Franz Rüschendorf, Norbert Hübner, Hermann Haller, Stefan Mundlos, N Bilginturan, Matthew A. Movsesian, Enno Klußmann, Okan Toka, Sylvia Bähring - Nature Genetics 2015 被引用: 171

  6. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3

    著者: Linda M. Brzustowicz, Thomas Lehner, Lucio H. Castilla, Graciela K. Penchaszadeh, K. C. Wilhelmsen, R.J. Daniels, K.E. Davies, M. Leppert, F. A. Ziter, David Wood, Victor Dubowitz, Klaus Zerres, I Hausmanowa-Pétrusewicz, Jürg Ott, T. L. Munsat, T. Conrad Gilliam - Nature 1990 被引用: 623

  7. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

    著者: Orna Levran, Claire Attwooll, Rashida Henry, Kelly Milton, Kornelia Neveling, Paula Rı́o, Sat Dev Batish, Reinhard Kalb, Eunike Velleuer, Sandra Barral, Jürg Ott, John H.J. Petrini, Detlev Schindler, Helmut Hanenberg, Arleen D. Auerbach - Nature Genetics 2005 被引用: 368

  8. Dysfunctional nitric oxide signalling increases risk of myocardial infarction

    著者: CARDIoGRAM, Jeanette Erdmann, Klaus Stark, Ulrike Esslinger, P. Rumpf, Doris Koesling, Cor de Wit, Frank J. Kaiser, Diana Braunholz, Anja Medack, Marcus Fischer, Martina E. Zimmermann, Stephanie Tennstedt, Elisabeth Graf, Sebastian Eck, Zouhair Aherrahrou, Janja Nahrstaedt, Christina Willenborg, Petra Bruse, Ingrid Brænne, Markus M. Nöthen, P. Hofmann, Peter S. Braund, Evanthia Mergia, Wibke Reinhard, Christof Burgdorf, Stefan Schreiber, Anthony J. Balmforth, Alistair S. Hall, Lars Bertram, Elisabeth Steinhagen–Thiessen, Shu Li, Winfried März, Muredach P. Reilly, Sekar Kathiresan, Ruth McPherson, Ulrich Walter, Jürg Ott, Nilesh J. Samani, Tim M. Strom, Thomas Meitinger, Christian Hengstenberg, Heribert Schunkert - Nature 2013 被引用: 283

  9. Machine learning approaches to explore digenic inheritance

    著者: Atsuko Okazaki, Jürg Ott - Trends in Genetics 2022 被引用: 55

  10. Strong Association of the Y402H Variant in Complement Factor H at 1q32 with Susceptibility to Age-Related Macular Degeneration

    著者: Sepideh Zareparsi, Kari Branham, Mingyao Li, Sapna Shah, Robert J. Klein, Jürg Ott, Josephine Hoh, Gonçalo R. Abecasis, Anand Swaroop - The American Journal of Human Genetics 2005 被引用: 369

  11. Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion

    著者: Ana Kljuic, Hisham Bazzi, John P. Sundberg, Amalia Martı́nez-Mir, Ryan F.L. O’Shaughnessy, Mỹ G. Mahoney, Moise L. Levy, Xavier Montagutelli, Wasim Ahmad, Vincent M. Aita, Derek Gordon, Jouni Uitto, David Whiting, Jürg Ott, Stuart G. Fischer, T. Conrad Gilliam, Colin A.B. Jahoda, Rebecca J. Morris, Andrey A. Panteleyev, Vu Thuong Nguyen, Angela M. Christiano - Cell 2003 被引用: 325

  12. Rhesus monkeys and humans share common susceptibility genes for age-related macular disease

    著者: Paul Francis, Binoy Appukuttan, Emily Simmons, N. Landauer, Jennifer Stoddard, Sara Hamon, Jürg Ott, Betsy Ferguson, Michael L. Klein, J. Timothy Stout, Martha Neuringer - Human Molecular Genetics 2008 被引用: 113

  13. Joint Identification of Multiple Genetic Variants via Elastic‐Net Variable Selection in a Genome‐Wide Association Analysis

    著者: Seoae Cho, Kyunga Kim, Young Jin Kim, Jong‐Keuk Lee, Yoon Shin Cho, Jong‐Young Lee, Bok‐Ghee Han, Heebal Kim, Jürg Ott, Taesung Park - Annals of Human Genetics 2010 被引用: 106

  14. Interaction Between the Serotonin Transporter Gene (5-HTTLPR), Stressful Life Events, and Risk of Depression

    著者: Neil Risch, Richard Herrell, Thomas Lehner, Kung‐Yee Liang, Lindon J. Eaves, Josephine Hoh, Andrea Griem, Mária Kovács, Jürg Ott, Kathleen R. Merikangas - JAMA 2009 被引用: 1,654

  15. Family-based designs for genome-wide association studies

    著者: Jürg Ott, Yoichiro Kamatani, Mark Lathrop - Nature Reviews Genetics 2011 被引用: 281

  16. Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study

    著者: Patricia L. Kramer, Haiyan Xu, Randall L. Woltjer, Shawn K. Westaway, David Clark, Deniz Erten‐Lyons, Jeffrey Kaye, Kathleen A. Welsh‐Bohmer, Juan C. Troncoso, William R. Markesbery, Ronald C. Petersen, Raymond Scott Turner, Walter A. Kukull, David A. Bennett, Douglas Galasko, John C. Morris, Jürg Ott - Neurobiology of Aging 2010 被引用: 110

  17. Population genetics: past, present, and future

    著者: Atsuko Okazaki, Satoru Yamazaki, Ituro Inoue, Jürg Ott - Human Genetics 2020 被引用: 22

  18. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy

    著者: T. Conrad Gilliam, Linda M. Brzustowicz, Lucio H. Castilla, Thomas Lehner, Graciela K. Penchaszadeh, R.J. Daniels, Barbara C. Byth, James A. Knowles, Jenni Hislop, Yehudah Shapira, Victor Dubowitz, T. L. Munsat, Jürg Ott, Kay E. Davies - Nature 1990 被引用: 333

  19. Distribution and Characterization of Regulatory Elements in the Human Genome

    著者: Jacek Majewski, Jürg Ott - Genome Research 2002 被引用: 310

  20. Complement factor H polymorphism in age-related macular degeneration

    著者: Robert J. Klein, Caroline J. Zeiss, Emily Y. Chew, J.–Y. Tsai, Richard S. Sackler, Charles M. Haynes, Alice K. Henning, J.P. SanGiovanni, Sasikanth Manne, S. T. Mayne, Michael B. Bracken, F. L. Ferris, Jürg Ott, Colin J. Barnstable, J. Hoh - American Journal of Ophthalmology 2005 被引用: 208

  21. TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa

    著者: Poulabi Banerjee, Patrick W. Kleyn, James A. Knowles, Charles A. Lewis, Barbara M. Ross, Enrico Parano, Steve G. Kovats, John J. Lee, Graciela K. Penchaszadeh, Jürg Ott, Samuel G. Jacobson, T. Conrad Gilliam - Nature Genetics 1998 被引用: 158

  22. Progression of Geographic Atrophy and Genotype in Age-Related Macular Degeneration

    著者: Michael L. Klein, Frederick L. Ferris, Peter J. Francis, Anne S. Lindblad, Emily Y. Chew, Sara Hamon, Jürg Ott - Ophthalmology 2010 被引用: 83

  23. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene

    著者: Konstantin Petrukhin, S G Fischer, Mario Pirastu, Rudolph E. Tanzi, И. П. Чернов, Marcella Devoto, Linda M. Brzustowicz, Eftìhia Cayanis, Emilia Vitale, James J. Russo, D Matseoane, Boris Boukhgalter, Wilma Wasco, A Figus, Jorgos Loudianos, Aili Cao, Irmin Sternlieb, Oleg V. Evgrafov, Enrico Parano, Piero Pavone, Dorothy Warburton, Jürg Ott, Graciela K. Penchaszadeh, I. Herbert Scheinberg, T. Conrad Gilliam - Nature Genetics 1993 被引用: 509

  24. A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis

    著者: Cynthia Helms, Li Cao, James G. Krueger, Ellen M. Wijsman, Francesca Chamian, Derek Gordon, Michael Heffernan, Jil Daw, Jason Robarge, Jürg Ott, Pui–Yan Kwok, Alan Menter, A. Bowcock - Nature Genetics 2003 被引用: 303