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Stanley F. Nelson

Active 1993–2025

164
Papers
38,687
Citations
104
h-index
161
i10-index

Citations

Citations per year for Stanley F. Nelson1928: 1 citations1967: 2 citations1993: 1 citations1994: 4 citations1995: 7 citations1996: 2 citations1997: 12 citations1998: 20 citations1999: 51 citations2000: 56 citations2001: 71 citations2002: 71 citations2003: 97 citations2004: 120 citations2005: 142 citations2006: 184 citations2007: 195 citations2008: 315 citations2009: 445 citations2010: 502 citations2011: 613 citations2012: 750 citations2013: 794 citations2014: 723 citations2015: 693 citations2016: 571 citations2017: 551 citations2018: 492 citations2019: 1,210 citations2020: 1,205 citations2021: 1,063 citations2022: 790 citations2023: 504 citations2024: 717 citations2025: 287 citations2026: 10 citations1929–1966: no citations, so these years are not shown1968–1992: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 6,470 citing papers, 32% of this breakdownUnited Kingdom: 1,546 citing papers, 7.6% of this breakdownChina: 1,354 citing papers, 6.7% of this breakdownGermany: 1,137 citing papers, 5.6% of this breakdownCanada: 843 citing papers, 4.2% of this breakdownFrance: 780 citing papers, 3.9% of this breakdownNetherlands: 695 citing papers, 3.4% of this breakdownItaly: 690 citing papers, 3.4% of this breakdownAustralia: 621 citing papers, 3.1% of this breakdownSpain: 470 citing papers, 2.3% of this breakdownSwitzerland: 447 citing papers, 2.2% of this breakdownJapan: 447 citing papers, 2.2% of this breakdown
0%32%Other 23.4%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology52.3%
  • Medicine24.6%
  • Neuroscience10.5%
  • Computer Science4.6%
  • Agricultural and Biological Sciences2.7%
  • Immunology and Microbiology2.3%
  • Other3%

Topics

  • Genomic variations and chromosomal abnormalities3.2%
  • Genetics and Neurodevelopmental Disorders3.1%
  • Genomics and Rare Diseases3.1%
  • Autism Spectrum Disorder Research2.7%
  • Cancer Genomics and Diagnostics2.2%
  • Epigenetics and DNA Methylation2.2%
  • Other83.5%

Coauthors

All papers

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  1. Targeted Therapy Resistance Mediated by Dynamic Regulation of Extrachromosomal Mutant EGFR DNA

    Authors: David A. Nathanson, Beatrice Gini, Jack Mottahedeh, Koppany Visnyei, Tomoyuki Koga, German G. Gomez, Ascia Eskin, Kiwook Hwang, Jun Wang, Kenta Masui, Andres A. Paucar, Huijun Yang, Minori Ohashi, Shaojun Zhu, Jill Wykosky, Rachel Reed, Stanley F. Nelson, Timothy F. Cloughesy, C. David James, P. Nagesh Rao, Harley I. Kornblum, James R. Heath, Webster K. Cavenee, Frank B. Furnari, Paul S. Mischel - Science 2013 cited by 708

  2. Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation

    Authors: Ramin Nazarian, Hubing Shi, Qi Wang, Xiangju Kong, Richard C. Koya, Hane Lee, Zugen Chen, Mi‐Kyung Lee, Narsis Attar, Hooman Sazegar, Thinle Chodon, Stanley F. Nelson, Grant A. McArthur, Jeffrey A. Sosman, Antoni Ribas, Roger S. Lo - Nature 2010 cited by 2,174

  3. Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays

    Authors: Nils Homer, Szabolcs Szelinger, Margot Redman, David Duggan, Waibhav Tembe, Jill Muehling, John V. Pearson, Dietrich A. Stephan, Stanley F. Nelson, David W. Craig - PLoS Genetics 2008 cited by 1,258

  4. Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning

    Authors: Shawn Cokus, Suhua Feng, Xiaoyu Zhang, Zugen Chen, Barry Merriman, Christian Haudenschild, Sriharsa Pradhan, Stanley F. Nelson, Matteo Pellegrini, Steven E. Jacobsen - Nature 2008 cited by 2,333

  5. Functional impact of global rare copy number variation in autism spectrum disorders

    Authors: Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R. Magalhães, Catarina Correia, Brett S. Abrahams, Joana Almeida, Elena Bacchelli, Gary D. Bader, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Sven Bölte, Patrick Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, Susan E. Bryson, Andrew R. Carson, Guillermo Casallo, Jillian P. Casey, Brian Hon‐Yin Chung, Lynne Cochrane, Christina Corsello, Emily L. Crawford, Andrew Crossett, Cheryl Cytrynbaum, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Håkon Håkonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, A lexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Anath C. Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge and 77 more - Nature 2010 cited by 2,066

  6. Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease

    Authors: Kimberly Splinter, David R. Adams, Carlos A. Bacino, Hugo J. Bellen, Jonathan A. Bernstein, Alys M. Cheatle Jarvela, Christine M. Eng, Cecilia Esteves, William A. Gahl, Rizwan Hamid, Howard J. Jacob, Bijal Kikani, David M. Koeller, Isaac S. Kohane, Brendan Lee, Joseph Loscalzo, Xi Luo, Alexa T. McCray, Thomas Metz, John J. Mulvihill, Stanley F. Nelson, Christina G.S. Palmer, John A. Phillips, Leslie Pick, John H. Postlethwait, Chloe M. Reuter, Vandana Shashi, David A. Sweetser, Cynthia J. Tifft, Nicole M. Walley, Michael F. Wangler, Monte Westerfield, Matthew T. Wheeler, Anastasia L. Wise, Elizabeth A. Worthey, Shinya Yamamoto, Euan A. Ashley - New England Journal of Medicine 2018 cited by 374

  7. Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

    Authors: Tom Walsh, Jon McClellan, Shane McCarthy, Anjené Addington, Sarah B. Pierce, Gregory M. Cooper, Alex S. Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari, Sunday M. Stray, Caitlin Rippey, Patricia Roccanova, Vlad Makarov, B. Lakshmi, Robert L. Findling, Linmarie Sikich, T Stromberg, Barry Merriman, Nitin Gogtay, Philip Butler, Kristen Eckstrand, Laila Noory, Peter Gochman, Robert T. Long, Zugen Chen, Sean Davis, Carl Baker, Evan E. Eichler, Paul S. Meltzer, Stanley F. Nelson, Andrew Singleton, Ming K. Lee, Judith L. Rapoport, Mary‐Claire King, Jonathan Sebat - Science 2008 cited by 1,832

  8. Diagnostic utility of transcriptome sequencing for rare Mendelian diseases

    Authors: Hane Lee, Alden Huang, Lee-kai Wang, Amanda J. Yoon, Genecee Renteria, Ascia Eskin, Rebecca Signer, Naghmeh Dorrani, Shirley Nieves‐Rodriguez, Jijun Wan, Emilie D. Douine, Jeremy D. Woods, Esteban C. Dell’Angelica, Brent L. Fogel, Martín G. Martín, Manish J. Butte, Neil H. Parker, Richard T. Wang, Perry B. Shieh, Derek A. Wong, Natalie M. Gallant, Kathryn Singh, Yael Asher, Janet S. Sinsheimer, Deborah Krakow, Sandra K. Loo, Patrick Allard, Jeanette C. Papp, Christina G.S. Palmer, Julián A. Martínez-Agosto, Stanley F. Nelson - Genetics in Medicine 2019 cited by 221

  9. Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

    Authors: Hane Lee, Joshua L. Deignan, Naghmeh Dorrani, Samuel P. Strom, Sibel Kantarci, Fabiola Quintero‐Rivera, Kingshuk Das, Traci L. Toy, Bret Harry, Michael Yourshaw, Michelle Fox, Brent L. Fogel, Julián A. Martínez-Agosto, Derek A. Wong, Vivian Y. Chang, Perry B. Shieh, Christina G.S. Palmer, Katrina M. Dipple, Wayne W. Grody, Éric Vilain, Stanley F. Nelson - JAMA 2014 cited by 981

  10. Genome Sequencing Highlights the Dynamic Early History of Dogs

    Authors: Adam H. Freedman, Ilan Gronau, Rena M. Schweizer, Diego Ortega‐Del Vecchyo, Eunjung Han, Pedro Silva, Marco Galaverni, Zhenxin Fan, Péter Marx, Belén Lorente-Galdós, Holly C. Beale, Óscar Ramírez, Farhad Hormozdiari, Can Alkan, Carles Vilà, Kevin Squire, Eli Geffen, Josip Kusak, Adam R. Boyko, Heidi G. Parker, Clarence Lee, Vasisht Tadigotla, Adam Siepel, Carlos D. Bustamante, Timothy T. Harkins, Stanley F. Nelson, Elaine A. Ostrander, Tomàs Marquès‐Bonet, Robert K. Wayne, John Novembre - PLoS Genetics 2014 cited by 649

  11. Melanoma whole-exome sequencing identifies V600EB-RAF amplification-mediated acquired B-RAF inhibitor resistance

    Authors: Hubing Shi, Gatien Moriceau, Xiangju Kong, Mi‐Kyung Lee, Hane Lee, Richard C. Koya, Charles Ng, Thinle Chodon, Richard A. Scolyer, Kimberly B. Dahlman, Jeffrey A. Sosman, Richard Kefford, Georgina V. Long, Stanley F. Nelson, Antoni Ribas, Roger S. Lo - Nature Communications 2012 cited by 620

  12. C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

    Authors: Anna Richards, Arn M. J. M. van den Maagdenberg, Joanna C. Jen, David Kavanagh, Paula Bertram, Dirk Spitzer, M. Kathryn Liszewski, Maria Louise Barilla-Labarca, Gisela M. Terwindt, Yumi Kasai, Mike McLellan, M. Gilbert Grand, Kaate R. J. Vanmolkot, Boukje de Vries, Jijun Wan, Michael J. Kane, Hafsa Mamsa, R Schäfer, Anine H Stam, Joost Haan, Paulus T.V.M. de Jong, Caroline W. J. M. Storimans, Mary J. van Schooneveld, J.A. Oosterhuis, Andreas Gschwendter, Martin Dichgans, Katya Kotschet, Suzanne Hodgkinson, Todd A. Hardy, Martin B. Delatycki, Rula A. Hajj‐Ali, Parul H. Kothari, Stanley F. Nelson, Rune R. Frants, Robert W. Baloh, Michel D. Ferrari, John P. Atkinson - Nature Genetics 2007 cited by 452

  13. Gene Expression Profile Correlates with T-Cell Infiltration and Relative Survival in Glioblastoma Patients Vaccinated with Dendritic Cell Immunotherapy

    Authors: Robert M. Prins, Horacio Soto, Vera Konkankit, Sylvia K. Odesa, Ascia Eskin, William H. Yong, Stanley F. Nelson, Linda M. Liau - Clinical Cancer Research 2010 cited by 457

  14. A Single CRISPR-Cas9 Deletion Strategy that Targets the Majority of DMD Patients Restores Dystrophin Function in hiPSC-Derived Muscle Cells

    Authors: Courtney S. Young, Michael R. Hicks, Natalia Ermolova, Haruko Nakano, Majib Jan, Shahab Younesi, Saravanan Karumbayaram, Chino Kumagai-Cresse, Derek Wang, Jerome A. Zack, Donald B. Kohn, Atsushi Nakano, Stanley F. Nelson, M. Carrie Miceli, Melissa J. Spencer, April D. Pyle - Cell stem cell 2016 cited by 382

  15. Epidermal Growth Factor Receptor Activation in Glioblastoma through Novel Missense Mutations in the Extracellular Domain

    Authors: Jeffrey C. Lee, Igor Vivanco, Rameen Beroukhim, Julie H. Huang, Whei Feng, Ralph DeBiasi, Koji Yoshimoto, Jennifer C. King, Phioanh L. Nghiemphu, Yuki Yuza, Qing Xu, Heidi Greulich, Roman K. Thomas, J. Guillermo Paez, Timothy C. Peck, David Linhart, Karen A. Glatt, Gad Getz, Robert C. Onofrio, Liuda Ziaugra, Ross L. Levine, Stacey Gabriel, Tomohiro Kawaguchi, Keith O'Neill, Haumith Khan, Linda M. Liau, Stanley F. Nelson, P. Nagesh Rao, Paul S. Mischel, Russell O. Pieper, Tim Cloughesy, Daniel J. Leahy, William R. Sellers, Charles L. Sawyers, Matthew Meyerson, Ingo K. Mellinghoff - PLoS Medicine 2006 cited by 369

  16. EGFR Mutation-Induced Alternative Splicing of Max Contributes to Growth of Glycolytic Tumors in Brain Cancer

    Authors: Ivan Babić, Erik S. Anderson, Kazuhiro Tanaka, Deliang Guo, Kenta Masui, Bing Li, Shaojun Zhu, Yuchao Gu, Genaro R. Villa, David Akhavan, David A. Nathanson, Beatrice Gini, Sergey Mareninov, Rui Li, Carolina Espindola Camacho, Siavash K. Kurdistani, Ascia Eskin, Stanley F. Nelson, William H. Yong, Webster K. Cavenee, Timothy F. Cloughesy, Heather R. Christofk, Douglas L. Black, Paul S. Mischel - Cell Metabolism 2013 cited by 165

  17. Gene Expression Profiling of Gliomas Strongly Predicts Survival

    Authors: William A. Freije, F. Edmundo Castro-Vargas, Zixing Fang, Steve Horvath, Timothy F. Cloughesy, Linda M. Liau, Paul S. Mischel, Stanley F. Nelson - Cancer Research 2004 cited by 740

  18. Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

    Authors: Marcello Scala, Masashi Nishikawa, Hidenori Ito, Hidenori Tabata, Tayyaba Khan, Andrea Accogli, Laura Davids, Anna Ruiz, Pietro Chiurazzi, Gabriella Cericola, Björn Schulte, Kristin G. Monaghan, Amber Begtrup, Annalaura Torella, Michele Pinelli, Anne‐Sophie Denommé‐Pichon, Antonio Vitobello, Caroline Racine, Maria Margherita Mancardi, Courtney Kiss, Andrea Guerin, Wendy Wu, Elisabeth Gabau Vila, Bryan C. Mak, Julián A. Martínez-Agosto, Michael B. Gorin, Bugrahan Duz, Yavuz Bayram, Claudia M.B. Carvalho, Jaime E Vengoechea, David Chitayat, Tiong Yang Tan, Bert Callewaert, Bernd Kruse, Lynne M. Bird, Laurence Faivre, Marcella Zollino, Saskia Biskup, Undiagnosed Diseases Network, Gabrielle Brown, Manish J. Butte, Esteban C. Dell’Angelica, Naghmeh Dorrani, Emilie D. Douine, Brent L. Fogel, Irma Gutierrez, Alden Huang, Deborah Krakow, Hane Lee, Sandra K. Loo, Bryan C. Mak, Martín G. Martín, Julián A. Martínez-Agosto, Elisabeth McGee, Stanley F. Nelson, Shirley Nieves‐Rodriguez, Christina G.S. Palmer, Jeanette C. Papp, Neil H. Parker, Genecee Renteria, Janet S. Sinsheimer, Jijun Wan, Lee-kai Wang, Katherine Wesseling Perry, Telethon Undiagnosed Diseases Program, Vincenzo Nigro, Nicola Brunetti‐Pierri, Giorgio Casari, Gerarda Cappuccio, Annalaura Torella, Michele Pinelli, Francesco Musacchia, Margherita Mutarelli, Diego Carrella, Giuseppina Vitiello, Valeria Capra, Giancarlo Parenti, Vincenzo Leuzzi, Angelo Selicorni, Silvia Maitz, Sandro Banfi, Marcella Zollino, Mario Montomoli, Donatelli Milani, Corrado Romano, Albina Tummolo, Daniele De Brasi, Antonietta Coppola, Claudia Santoro, Angela Peron, Chiara Pantaleoni, Raffaele Castello, Stefano D’Arrigo, Pasquale Striano, Vincenzo Nigro, Mariasavina Severino, Valeria Capra, Gregory Costain, Koh Nagata - Brain 2022 cited by 51

  19. Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration

    Authors: Jijun Wan, Michael Yourshaw, Hafsa Mamsa, Sabine Rudnik‐Schöneborn, Manoj P. Menezes, Ji Eun Hong, Derek W. Leong, Jan Senderek, Michael S. Salman, David Chitayat, Pavel Seeman, Arpad von Moers, Luitgard Graul‐Neumann, Andrew J. Kornberg, Manuel Castro‐Gago, María Jesús Sobrido, Masafumi Sanefuji, Perry B. Shieh, Noriko Salamon, Ronald C. Kim, Harry V. Vinters, Zugen Chen, Klaus Zerres, Monique M. Ryan, Stanley F. Nelson, Joanna C. Jen - Nature Genetics 2012 cited by 262

  20. Identification of EpCAM as the Gene for Congenital Tufting Enteropathy

    Authors: Mamata Sivagnanam, James L. Mueller, Hane Lee, Zugen Chen, Stanley F. Nelson, Dan Turner, Stanley Zlotkin, Paul B. Pencharz, Bo‐Yee Ngan, Ondrej Libiger, Nicholas J. Schork, Joel E. Lavine, Sharon Taylor, Robert Newbury, Richard D. Kolodner, Hal M. Hoffman - Gastroenterology 2008 cited by 222

  21. ERBB3 and NGFR mark a distinct skeletal muscle progenitor cell in human development and hPSCs

    Authors: Michael R. Hicks, Julia Hiserodt, Katrina I. Paras, Wakana Fujiwara, Ascia Eskin, Majib Jan, Haibin Xi, Courtney S. Young, Denis Evseenko, Stanley F. Nelson, Melissa J. Spencer, Ben Van Handel, April D. Pyle - Nature Cell Biology 2017 cited by 210

  22. High-throughput profiling of influenza A virus hemagglutinin gene at single-nucleotide resolution

    Authors: Nicholas C. Wu, Arthur P. Young, Laith Q. Al‐Mawsawi, C. Anders Olson, Jun Feng, Hangfei Qi, Shu-Hwa Chen, I-Hsuan Lu, Chung‐Yen Lin, Robert Chin, Harding H. Luan, Nguyen Thanh Nguyen, Stanley F. Nelson, Xinmin Li, Ting-Ting Wu, Ren Sun - Scientific Reports 2014 cited by 169

  23. KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants

    Authors: Joanna Kennedy, David Goudie, Edward Blair, Kate Chandler, Shelagh Joss, Victoria McKay, Andrew Green, Ruth Armstrong, Melissa Lees, Benjamin Kamien, Bruce Hopper, Tiong Yang Tan, Patrick Yap, Zornitza Stark, Nobuhiko Okamoto, Noriko Miyake, Naomichi Matsumoto, Ellen F. Macnamara, Jennifer L. Murphy, Elizabeth M. McCormick, Håkon Håkonarson, Marni J. Falk, Dong Li, Patrick R. Blackburn, Eric W. Klee, Dusica Babovic‐Vuksanovic, Susan Schelley, Louanne Hudgins, Sarina G. Kant, Bertrand Isidor, Benjamin Cogné, Kimberley Bradbury, Mark Williams, Chirag Patel, Helen Heussler, Celia Duff‐Farrier, Phillis Lakeman, Ingrid Scurr, Usha Kini, Mariet Elting, Margot R.F. Reijnders, Janneke Schuurs-Hoeijmakers, Mohamed Wafik, Anne Blomhoff, Claudia Ruivenkamp, Esther Nibbeling, Alexander J.M. Dingemans, Emilie D. Douine, Stanley F. Nelson, Maja Hempel, Tatjana Bierhals, Davor Lessel, Jessika Johannsen, Valerie A. Arboleda, Ruth Newbury‐Ecob - Genetics in Medicine 2018 cited by 111

  24. INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex

    Authors: Lauren G. Mascibroda, Mohammad Shboul, Nathan D. Elrod, Laurence Colleaux, Hanan Hamamy, Kai-Lieh Huang, Natoya Peart, Moirangthem Kiran Singh, Hane Lee, Barry Merriman, Jeanne N. Jodoin, Poojitha Sitaram, Laura A. Lee, Raja Fathalla, Baeth Al‐Rawashdeh, Osama H. Ababneh, Mohammad El-Khateeb, Nathalie Escande‐Beillard, Stanley F. Nelson, Yixuan Wu, Liang Tong, Linda J. Kenney, Sudipto Roy, William K. Russell, Jeanne Amiel, Bruno Reversade, Eric J. Wagner - Nature Communications 2022 cited by 35