litlas
Log inCreate account

Rando Allikmets

Active 1986–2024

80
Papers
22,574
Citations
67
h-index
79
i10-index

Citations

Citations per year for Rando Allikmets1980: 1 citations1987: 1 citations1988: 6 citations1989: 5 citations1990: 6 citations1991: 6 citations1992: 2 citations1994: 6 citations1995: 2 citations1996: 10 citations1997: 103 citations1998: 138 citations1999: 175 citations2000: 204 citations2001: 258 citations2002: 146 citations2003: 228 citations2004: 180 citations2005: 224 citations2006: 304 citations2007: 258 citations2008: 215 citations2009: 205 citations2010: 281 citations2011: 243 citations2012: 224 citations2013: 211 citations2014: 194 citations2015: 148 citations2016: 134 citations2017: 147 citations2018: 99 citations2019: 445 citations2020: 501 citations2021: 555 citations2022: 384 citations2023: 238 citations2024: 412 citations2025: 196 citations2026: 4 citations1981–1986: no citations, so these years are not shown1993: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,656 citing papers, 33.1% of this breakdownUnited Kingdom: 681 citing papers, 8.5% of this breakdownGermany: 555 citing papers, 6.9% of this breakdownChina: 397 citing papers, 4.9% of this breakdownNetherlands: 335 citing papers, 4.2% of this breakdownFrance: 317 citing papers, 4% of this breakdownCanada: 302 citing papers, 3.8% of this breakdownJapan: 256 citing papers, 3.2% of this breakdownAustralia: 236 citing papers, 2.9% of this breakdownItaly: 223 citing papers, 2.8% of this breakdownSwitzerland: 188 citing papers, 2.3% of this breakdownSpain: 167 citing papers, 2.1% of this breakdown
0%33.1%Other 21.3%

Institutions

Fields

  • Medicine46.3%
  • Biochemistry, Genetics and Molecular Biology34.6%
  • Immunology and Microbiology13.4%
  • Neuroscience2.2%
  • Agricultural and Biological Sciences0.9%
  • Nursing0.7%
  • Other1.9%

Topics

  • Retinal Diseases and Treatments9.5%
  • Retinal Development and Disorders7.8%
  • Drug Transport and Resistance Mechanisms5.7%
  • HIV Research and Treatment3.4%
  • Cholesterol and Lipid Metabolism3.1%
  • Retinal Imaging and Analysis2.6%
  • Other67.9%

Coauthors

All papers

Open in search
  1. Targeted long-read sequencing identifies missing disease-causing variation

    Authors: Danny E. Miller, Arvis Sulovari, Tianyun Wang, Hailey Loucks, Kendra Hoekzema, Katherine M. Munson, Alexandra P. Lewis, Edith P. Almanza Fuerte, Catherine R. Paschal, Tom Walsh, Jenny Thies, James T. Bennett, Ian A. Glass, Katrina M. Dipple, Karynne Patterson, Emily Bonkowski, Zoe Nelson, Audrey Squire, Megan Sikes, Erika Beckman, Robin L. Bennett, Dawn Earl, Winston Lee, Rando Allikmets, Seth J. Perlman, Penny Chow, Anne Hing, Tara Wenger, Margaret P Adam, Angela Sun, Christina Lam, Irene J. Chang, Xue Zou, Stephanie Austin, Erin Huggins, Alexias Safi, Apoorva K. Iyengar, Timothy E. Reddy, William H. Majoros, Andrew S. Allen, Gregory E. Crawford, Priya S. Kishnani, Mary‐Claire King, Tim Cherry, Jessica X. Chong, Michael J. Bamshad, Deborah A. Nickerson, Heather C. Mefford, Dan Doherty, Evan E. Eichler - The American Journal of Human Genetics 2021 cited by 239

  2. Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations

    Authors: Frans P.M. Cremers, Winston Lee, Rob W.J. Collin, Rando Allikmets - Progress in Retinal and Eye Research 2020 cited by 312

  3. A common haplotype in the complement regulatory gene factor H ( HF1/CFH ) predisposes individuals to age-related macular degeneration

    Authors: Gregory S. Hageman, Don H. Anderson, Lincoln V. Johnson, Lisa S. Hancox, Andrew J. Taiber, Lisa I. Hardisty, Jill L. Hageman, Heather Stockman, James D. Borchardt, Karen M. Gehrs, Richard J. Smith, Giuliana Silvestri, Stephen R. Russell, Caroline C. W. Klaver, Irene Barbazetto, Stanley Chang, Lawrence A. Yannuzzi, Gaetano R. Barile, John C. Merriam, R. Theodore Smith, Adam Olsh, Julie Bergeron, Jana Zernant, Joanna E. Merriam, Bert Gold, Michael Dean, Rando Allikmets - National Academy of Sciences, Proceedings of the National Academy of Sciences 2005 cited by 1,968

  4. The human ATP‐binding cassette (ABC) transporter superfamily

    Authors: Michael Dean, Karobi Moitra, Rando Allikmets - Human Mutation 2022 cited by 168

  5. The Human ATP-Binding Cassette (ABC) Transporter Superfamily

    Authors: Michael Dean, Andrey Rzhetsky, Rando Allikmets - Genome Research 2001 cited by 1,748

  6. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophy

    Authors: Rando Allikmets, Nanda Singh, Hui Sun, Noah F. Shroyer, Amy Hutchinson, Abirami Chidambaram, Bernard Gerrard, Lisa Baird, Dora Stauffer, Andy Peiffer, Amir Rattner, Philip M. Smallwood, Yixin Li, Kent L. Anderson, Richard A. Lewis, Jeremy Nathans, Mark Leppert, Michael Dean, James R. Lupski - Nature Genetics 1997 cited by 1,437

  7. Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

    Authors: Irene Perea‐Romero, Gema Gordo, Ionut-Florin Iancu, Marta Del Pozo‐Valero, Berta Almoguera, Fiona Blanco‐Kelly, Ester Carreño, Belén Jimenez‐Rolando, Rosario López‐Rodríguez, Isabel Lorda‐Sánchez, Inmaculada Martín-Mérida, Lucía Pérez de Ayala, Rosa Riveiro-Álvarez, Elvira Rodríguez‐Pinilla, Saoud Tahsin Swafiri, María José Trujillo-Tiebas, The ESRETNET Study Group, Ana Bustamante‐Aragonés, Rocio Cardero‐Merlo, Ruth Fernández‐Sánchez, J. Gallego‐Merlo, Ines Garcia-Vara, Ascensión Gimenez-Pardo, Laura Horcajada-Burgos, Fernando Infantes‐Barbero, Esther Lantero, Miguel Ángel López-Martínez, Andrea Martínez‐Ramas, Lorena Ondo, Marta Rodríguez de Alba, C. Sánchez-Jimeno, C. Vélez-Monsalve, Cristina Villaverde, Olga Zurita, Domingo Aguilera‐Garcia, Jana Aguirre-Lambán, Ana Arteche‐López, Diego Cantalapiedra, Patrícia José, Liliana Galbis-Martinez, Maria García‐Hoyos, Carlos Lombardia, María Isabel López-Molina, Raquel Pérez-Carro, Luciana Rodrigues Jacy da Silva, Carmen Ramos, Rocío Sánchez-Alcudia, Iker Sánchez‐Navarro, Sorina D. Tatu, Elena Vallespín, Elena Aller, Sara Bernal, Maria J. Gamundi, Gema García‐García, Inmaculada Hernan, Teresa Jaijo, Guillermo Antiñolo, Montserrat Baiget, Miguel Carballo, José M. Millán, Diana Valverde, The ERDC Study Group, Rando Allikmets, Sandro Banfi, Frans P.M. Cremers, Rob W.J. Collin, Elfride De Baere, Håkon Håkonarson, Susanne Kohl, Carlo Rivolta, Dror Sharon, María Concepción Alonso‐Cerezo, María Juliana Ballesta‐Martínez, Sergi Beltrán, Carmen Benito López, Jaume Catalá‐Mora, Claudio Catalli, Carmen Cotarelo-Pérez, Miguel Fernández‐Burriel, Ana Fontalba-Romero, Enrique Galán‐Gómez, María García‐Barcina, Loida M. Garcia-Cruz, Blanca Gener, Belén Gil-Fournier, Nancy Govea, Encarna Guillén‐Navarro, I. Hernando Acero, Cristina Irigoyen, Silvia Izquierdo Álvarez, Isabel Llano‐Rivas, Maria A. López-Ariztegui, Vanesa López‐González, Fermina Lopez-Grondona, Loreto Martorell, Pilar Mendez-Perez, María Moreno‐Igoa, Raluca Oancea-Ionescu, Francesc Palau, Guiomar Pérez de Nanclares and 16 more - Scientific Reports 2021 cited by 160

  8. Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene ( LIPC )

    Authors: Benjamin M. Neale, Jesen Fagerness, Robyn Reynolds, Lucia Sobrin, Margaret M. Parker, Soumya Raychaudhuri, Perciliz L. Tan, Edwin C. Oh, Joanna E. Merriam, Eric H. Souied, Paul S. Bernstein, Binxing Li, Jeanne M. Frederick, Kang Zhang, Milam A. Brantley, Aaron Lee, Donald J. Zack, Betsy Campochiaro, Peter A. Campochiaro, Stephan Ripke, R. Theodore Smith, Gaetano R. Barile, Nicholas Katsanis, Rando Allikmets, Mark J. Daly, Johanna M. Seddon - National Academy of Sciences, Proceedings of the National Academy of Sciences 2010 cited by 451

  9. Serine and Lipid Metabolism in Macular Disease and Peripheral Neuropathy

    Authors: Marin L. Gantner, Kevin Eade, Martina Wallace, Michal K. Handzlik, Regis Fallon, Jennifer Trombley, Roberto Bonelli, Sarah Giles, Sarah Harkins‐Perry, Tjebo Heeren, Lydia Sauer, Yoichiro Ideguchi, M Baldini, Lea Scheppke, Michael I. Dorrell, Maki Kitano, Barbara Hart, Carolyn Cai, Takayuki Nagasaki, Mehmet G. Badur, Mali Okada, Sasha M. Woods, Catherine Egan, Mark C. Gillies, Robyn H. Guymer, Florian Eichler, Melanie Bahlo, Marcus Fruttiger, Rando Allikmets, Paul S. Bernstein, Christian M. Metallo, Martin Friedlander - New England Journal of Medicine 2019 cited by 255

  10. Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration

    Authors: Bert Gold, Joanna E. Merriam, Jana Zernant, Lisa S. Hancox, Andrew J. Taiber, Karen M. Gehrs, Kevin Cramer, Julia Neel, Julie Bergeron, Gaetano R. Barile, R. Theodore Smith, Gregory S. Hageman, Michael Dean, Rando Allikmets - Nature Genetics 2006 cited by 1,077

  11. A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases

    Authors: Shinya Yamamoto, Manish Jaiswal, Wu‐Lin Charng, Tomasz Gambin, Ender Karaca, Ghayda Mirzaa, Wojciech Wiszniewski, Héctor Sandoval, Nele A Haelterman, Bo Xiong, Ke Zhang, Vafa Bayat, Gabriela David, Tongchao Li, Kuchuan Chen, Upasana Gala, Tamar Harel, Davut Pehli̇van, Samantha Penney, Lisenka E.L.M. Vissers, Joep de Ligt, Shalini N. Jhangiani, Ya‐Jing Xie, Stephen H. Tsang, Yeşim Parman, Merve Sivaci, Esra Battaloğlu, Donna M. Muzny, Ying-Wooi Wan, Zhandong Liu, Alexander T. Lin-Moore, Robin D. Clark, Cynthia J. Curry, Nichole Link, Karen L. Schulze, Eric Boerwinkle, William B. Dobyns, Rando Allikmets, Richard A. Gibbs, Rui Chen, James R. Lupski, Michael F. Wangler, Hugo J. Bellen - Cell 2014 cited by 401

  12. Mapping the cis -regulatory architecture of the human retina reveals noncoding genetic variation in disease

    Authors: Timothy J. Cherry, Marty G. Yang, David A. Harmin, Peter Tao, Andrew E. Timms, Miriam Bauwens, Rando Allikmets, Evan Jones, Rui Chen, Elfride De Baere, Michael E. Greenberg - National Academy of Sciences, Proceedings of the National Academy of Sciences 2020 cited by 121

  13. Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degeneration

    Authors: Jana Zernant, Winston Lee, Frederick T. Collison, Gerald A. Fishman, Yuri V. Sergeev, Kaspar Schuerch, Janet R. Sparrow, Stephen H. Tsang, Rando Allikmets - Journal of Medical Genetics 2017 cited by 192

  14. Identification and Rescue of Splice Defects Caused by Two Neighboring Deep-Intronic ABCA4 Mutations Underlying Stargardt Disease

    Authors: Sílvia Albert, Alejandro Garanto, Riccardo Sangermano, Mubeen Khan, Nathalie M. Bax, Carel B. Hoyng, Jana Zernant, Winston Lee, Rando Allikmets, Rob W.J. Collin, Frans P.M. Cremers - The American Journal of Human Genetics 2018 cited by 136

  15. Genetic Restriction of HIV-1 Infection and Progression to AIDS by a Deletion Allele of the CKR5 Structural Gene

    Authors: Michael Dean, Mary Carrington, Cheryl A. Winkler, Gavin Huttley, Michael W. Smith, Rando Allikmets, James J. Goedert, Susan Buchbinder, Eric Vittinghoff, Edward D. Gomperts, Sharyne Donfield, David Vlahov, Richard A. Kaslow, Alfred J. Saah, Charles R. Rinaldo, Roger Detels, Stephen J. O’Brien - Science 1996 cited by 2,503

  16. Quantitative Fundus Autofluorescence in Recessive Stargardt Disease

    Authors: Tomas R. Burke, Tobias Duncker, Russell L. Woods, Jonathan P. Greenberg, Jana Zernant, Stephen H. Tsang, R. Theodore Smith, Rando Allikmets, Janet R. Sparrow, François C. Delori - Investigative Ophthalmology & Visual Science 2014 cited by 184

  17. Systems genomics in age-related macular degeneration

    Authors: Anneke I. den Hollander, Robert F. Mullins, Luz D. Orozco, Andrew P. Voigt, Hsu-Hsin Chen, Tobias Strunz, Felix Graßmann, Jonathan L. Haines, Jonas J. W. Kuiper, Santa J. Tumminia, Rando Allikmets, Gregory S. Hageman, Dwight Stambolian, Caroline C. W. Klaver, Jef D. Boeke, Hao Chen, Lee Honigberg, Suresh Katti, Kelly A. Frazer, Bernhard H. F. Weber, Michael B. Gorin - Experimental Eye Research 2022 cited by 40

  18. Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease

    Authors: Winston Lee, Jana Zernant, Takayuki Nagasaki, Laurie L. Molday, Pei-Yin Su, Gerald A. Fishman, Stephen H. Tsang, Robert S. Molday, Rando Allikmets - Human Molecular Genetics 2021 cited by 56

  19. Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease

    Authors: Kaoru Fujinami, Jana Zernant, Ravinder Chana, Genevieve Wright, Kazushige Tsunoda, Yoko Ozawa, Kazuo Tsubota, Anthony G. Robson, Graham E. Holder, Rando Allikmets, Michel Michaelides, Anthony T. Moore - Ophthalmology 2014 cited by 190

  20. A genotype-phenotype correlation matrix for ABCA4 disease based on long-term prognostic outcomes

    Authors: Winston Lee, Jana Zernant, Pei-Yin Su, Takayuki Nagasaki, Stephen H. Tsang, Rando Allikmets - JCI Insight 2021 cited by 55

  21. Mutation of the Stargardt Disease Gene ( ABCR ) in Age-Related Macular Degeneration

    Authors: Rando Allikmets, Noah F. Shroyer, Nanda Singh, Johanna M. Seddon, Richard A. Lewis, Paul S. Bernstein, Andy Peiffer, Norman A. Zabriskie, Yixin Li, Amy Hutchinson, Michael Dean, James R. Lupski, Mark Leppert - Science 1997 cited by 878

  22. Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption

    Authors: Mi‐Hye Lee, Kangmo Lu, Star Hazard, Hongwei Yu, Sergey Shulenin, Hideki Hidaka, Hideto Kojima, Rando Allikmets, Nagahiko SAKUMA, R.J. Pegoraro, Anand K. Srivastava, Gerald Salen, Michael Dean, Shailendra B. Patel - Nature Genetics 2001 cited by 688

  23. In SilicoFunctional Meta-Analysis of 5,962ABCA4Variants in 3,928 Retinal Dystrophy Cases

    Authors: Stéphanie S. Cornelis, Nathalie M. Bax, Jana Zernant, Rando Allikmets, Lars G. Fritsche, Johan T. den Dunnen, Muhammad Ajmal, Carel B. Hoyng, Frans P.M. Cremers - Human Mutation 2017 cited by 135

  24. Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes

    Authors: J. Claiborne Stephens, David Reich, David Goldstein, Hyoung Doo Shin, Michael W. Smith, Mary Carrington, Cheryl A. Winkler, Gavin Huttley, Rando Allikmets, Lynn M. Schriml, Bernard Gerrard, Michael Malasky, María Dolores Burguete Ramos, Susanne Morlot, Maria Tzetis, Carole Oddoux, Francesco S. di Giovine, George Nasioulas, David Chandler, Michael Aseev, Matthew Hanson, Luba Kalaydjieva, Damjan Glavač, Paolo Gasparini, Emmanouel Kanavakis, Mireille Claustres, Marios Kambouris, Harry Ostrer, Gordon W. Duff, В. С. Баранов, Hiljar Sibul, Andres Metspalu, David Goldman, Nick Martin, David L. Duffy, Jörg Schmidtke, Xavier Estivill, Stephen J. O’Brien, Michael Dean - The American Journal of Human Genetics 1998 cited by 525