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Jürg Ott

Active 1976–2023

Also published as
Jurg Ott
141
Papers
30,962
Citations
93
h-index
133
i10-index

Citations

Citations per year for Jürg Ott1971: 1 citations1977: 1 citations1978: 1 citations1980: 1 citations1982: 1 citations1983: 5 citations1985: 4 citations1986: 8 citations1987: 13 citations1988: 28 citations1989: 14 citations1990: 50 citations1991: 49 citations1992: 70 citations1993: 74 citations1994: 127 citations1995: 150 citations1996: 142 citations1997: 159 citations1998: 237 citations1999: 224 citations2000: 243 citations2001: 252 citations2002: 266 citations2003: 303 citations2004: 311 citations2005: 331 citations2006: 434 citations2007: 392 citations2008: 391 citations2009: 322 citations2010: 412 citations2011: 352 citations2012: 312 citations2013: 248 citations2014: 202 citations2015: 184 citations2016: 172 citations2017: 171 citations2018: 135 citations2019: 347 citations2020: 319 citations2021: 353 citations2022: 187 citations2023: 155 citations2024: 226 citations2025: 100 citations2026: 6 citations1972–1976: no citations, so these years are not shown1979: no citations, so this year is not shown1981: no citations, so this year is not shown1984: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,961 citing papers, 34.7% of this breakdownUnited Kingdom: 1,116 citing papers, 9.8% of this breakdownGermany: 685 citing papers, 6% of this breakdownChina: 549 citing papers, 4.8% of this breakdownFrance: 418 citing papers, 3.7% of this breakdownCanada: 406 citing papers, 3.5% of this breakdownAustralia: 359 citing papers, 3.1% of this breakdownItaly: 344 citing papers, 3% of this breakdownNetherlands: 342 citing papers, 3% of this breakdownJapan: 319 citing papers, 2.8% of this breakdownSwitzerland: 242 citing papers, 2.1% of this breakdownSweden: 187 citing papers, 1.6% of this breakdown
0%34.7%Other 21.9%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology42.1%
  • Medicine34.2%
  • Neuroscience10.3%
  • Immunology and Microbiology3.5%
  • Psychology3.5%
  • Nursing1.7%
  • Other4.7%

Topics

  • 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%
  • Other83.2%

Coauthors

All papers

Open in search
  1. Complement Factor H Polymorphism in Age-Related Macular Degeneration

    Authors: 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 cited by 4,530

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

    Authors: 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 and 61 more - Nature Genetics 2023 cited by 73

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

    Authors: Jürg Ott, Jing Wang, Suzanne M. Leal - Nature Reviews Genetics 2015 cited by 285

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

    Authors: 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 cited by 238

  5. PDE3A mutations cause autosomal dominant hypertension with brachydactyly

    Authors: 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 cited by 171

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

    Authors: 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 cited by 623

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

    Authors: 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 cited by 368

  8. Dysfunctional nitric oxide signalling increases risk of myocardial infarction

    Authors: 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 cited by 283

  9. Machine learning approaches to explore digenic inheritance

    Authors: Atsuko Okazaki, Jürg Ott - Trends in Genetics 2022 cited by 55

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

    Authors: 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 cited by 369

  11. Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion

    Authors: 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 cited by 325

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

    Authors: 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 cited by 113

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

    Authors: 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 cited by 106

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

    Authors: 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 cited by 1,654

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

    Authors: Jürg Ott, Yoichiro Kamatani, Mark Lathrop - Nature Reviews Genetics 2011 cited by 281

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

    Authors: 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 cited by 110

  17. Population genetics: past, present, and future

    Authors: Atsuko Okazaki, Satoru Yamazaki, Ituro Inoue, Jürg Ott - Human Genetics 2020 cited by 22

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

    Authors: 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 cited by 333

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

    Authors: Jacek Majewski, Jürg Ott - Genome Research 2002 cited by 310

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

    Authors: 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 cited by 208

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

    Authors: 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 cited by 158

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

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

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

    Authors: 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 cited by 509

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

    Authors: 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 cited by 303