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Hamish S. Scott

Active 1990–2025

127
Papers
17,933
Citations
78
h-index
121
i10-index

Citations

Citations per year for Hamish S. Scott1983: 1 citations1984: 1 citations1987: 1 citations1991: 1 citations1992: 8 citations1993: 9 citations1994: 8 citations1995: 17 citations1996: 5 citations1997: 16 citations1998: 57 citations1999: 53 citations2000: 86 citations2001: 109 citations2002: 112 citations2003: 118 citations2004: 90 citations2005: 114 citations2006: 126 citations2007: 145 citations2008: 190 citations2009: 202 citations2010: 172 citations2011: 153 citations2012: 161 citations2013: 161 citations2014: 154 citations2015: 178 citations2016: 144 citations2017: 147 citations2018: 130 citations2019: 440 citations2020: 497 citations2021: 517 citations2022: 385 citations2023: 278 citations2024: 443 citations2025: 240 citations2026: 6 citations1985–1986: no citations, so these years are not shown1988–1990: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,055 citing papers, 27.1% of this breakdownUnited Kingdom: 536 citing papers, 7.1% of this breakdownChina: 528 citing papers, 7% of this breakdownGermany: 495 citing papers, 6.5% of this breakdownAustralia: 434 citing papers, 5.7% of this breakdownFrance: 351 citing papers, 4.6% of this breakdownItaly: 325 citing papers, 4.3% of this breakdownCanada: 297 citing papers, 3.9% of this breakdownJapan: 295 citing papers, 3.9% of this breakdownSwitzerland: 195 citing papers, 2.6% of this breakdownNetherlands: 186 citing papers, 2.5% of this breakdownSpain: 173 citing papers, 2.3% of this breakdown
0%27.1%Other 22.5%

Institutions

Fields

  • Medicine41.7%
  • Biochemistry, Genetics and Molecular Biology40.3%
  • Immunology and Microbiology10%
  • Neuroscience3.7%
  • Agricultural and Biological Sciences2.2%
  • Nursing0.7%
  • Other1.4%

Topics

  • Acute Myeloid Leukemia Research3.6%
  • Epigenetics and DNA Methylation3.6%
  • T-cell and B-cell Immunology3.2%
  • Immune Cell Function and Interaction2.8%
  • Adrenal Hormones and Disorders2.3%
  • MicroRNA in disease regulation2%
  • Other82.5%

Coauthors

All papers

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  1. Integrated multi-omics for rapid rare disease diagnosis on a national scale

    Authors: Sebastian Lunke, Sophie E. Bouffler, Chirag Patel, Sarah A. Sandaradura, Meredith Wilson, Jason Pinner, Matthew F. Hunter, Christopher Barnett, Mathew Wallis, Benjamin Kamien, Tiong Yang Tan, Mary‐Louise Freckmann, Belinda Chong, Dean Phelan, David Francis, Karin S. Kassahn, Thuong Ha, Song Gao, Peer Arts, Matilda R. Jackson, Hamish S. Scott, Stefanie Eggers, Simone M. Rowley, Kirsten Boggs, Ana Rakonjac, Gemma R. Brett, M. De Silva, Amanda Springer, Michelle C. Ward, Kirsty Stallard, Cas Simons, Thomas Conway, Andreas Halman, Nicole J. Van Bergen, Tim Sikora, Liana N. Semcesen, David A. Stroud, Alison G. Compton, David R. Thorburn, Katrina M. Bell, Simon Sadedin, Kathryn N. North, John Christodoulou, Zornitza Stark - Nature Medicine 2023 cited by 141

  2. MyoD-family inhibitor proteins act as auxiliary subunits of Piezo channels

    Authors: Zhigan Zhou, Xiaonuo Ma, Yiechang Lin, Delfine Cheng, Navid Bavi, Genevieve A. Secker, Jinyuan Vero Li, Vaibhao Janbandhu, Drew L. Sutton, Hamish S. Scott, Mingxi Yao, Richard P. Harvey, Natasha L. Harvey, Ben Corry, Yixiao Zhang, Charles D. Cox - Science 2023 cited by 86

  3. Use of within-array replicate spots for assessing differential expression in microarray experiments

    Authors: Gordon K. Smyth, Joëlle Michaud, Hamish S. Scott - Computer applications in the biosciences, Bioinform. 2005 cited by 1,421

  4. A network-biology perspective of microRNA function and dysfunction in cancer

    Authors: Cameron P. Bracken, Hamish S. Scott, Gregory J. Goodall - Nature Reviews Genetics 2016 cited by 692

  5. Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare

    Authors: Zornitza Stark, Tiffany Boughtwood, Matilda Haas, Jeffrey Braithwaite, Clara Gaff, Ilias Goranitis, Amanda B. Spurdle, David P. Hansen, Oliver Hofmann, Nigel G. Laing, Sylvia A. Metcalfe, Ainsley J. Newson, Hamish S. Scott, Natalie Thorne, Robyn L. Ward, Marcel E. Dinger, Stephanie Best, Janet C. Long, Sean M. Grimmond, John V. Pearson, Nicola Waddell, Christopher Barnett, Matthew Cook, Michael Field, David Fielding, Stephen B. Fox, Jozef Gécz, Adam Jaffé, Richard J. Leventer, Paul J. Lockhart, Sebastian Lunke, Andrew Mallett, Julie McGaughran, Linda Mileshkin, Kátia Nones, Tony Roscioli, Ingrid E. Scheffer, Christopher Semsarian, Cas Simons, David M. Thomas, David R. Thorburn, Richard W. Tothill, Deborah White, Sally L. Dunwoodie, Peter T. Simpson, Peta Phillips, Marie‐Jo Brion, Keri Finlay, Michael C. Quinn, Tessa Mattiske, Emma Tudini, Kirsten Boggs, Séan Murray, Kathy Wells, John Cannings, Andrew Sinclair, John Christodoulou, Kathryn N. North - The American Journal of Human Genetics 2023 cited by 72

  6. Positional cloning of the APECED gene

    Authors: Kentaro Nagamine, Pärt Peterson, Hamish S. Scott, Jun Kudoh, Shinsei Minoshima, Maarit Heino, Kai Krohn, Maria D. Lalioti, Primus E. Mullis, Stylianos E. Antonarakis, Kazuhiko Kawasaki, Shuichi Asakawa, Fumiaki Ito, Nobuyoshi Shimizu - Nature Genetics 1997 cited by 1,433

  7. GATA2 is required for lymphatic vessel valve development and maintenance

    Authors: Jan Kazenwadel, Kelly L. Betterman, Chan‐Eng Chong, Philippa H. Stokes, Young Kyung Lee, Genevieve A. Secker, Yan Agalarov, Cansaran Saygili Demir, David Lawrence, Drew L. Sutton, Sébastien P. Tabruyn, Naoyuki Miura, Marjo Salminen, Tatiana V. Petrova, Jacqueline M. Matthews, Christopher N Hahn, Hamish S. Scott, Natasha L. Harvey - Journal of Clinical Investigation 2015 cited by 231

  8. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia

    Authors: Christopher N Hahn, Chan‐Eng Chong, Catherine Carmichael, Ella Wilkins, Peter J Brautigan, Xiaochun Li, Milena Babic, Ming Lin, Amandine Carmagnac, Young Kyung Lee, Chung Hoow Kok, Lucia Gagliardi, Kathryn Friend, Paul G. Ekert, Carolyn M Butcher, Anna Brown, Ian D. Lewis, L.B. To, Andrew E. Timms, Jan Storek, Sarah Moore, Meryl Altree, Robert Escher, Peter Bardy, Graeme Suthers, Richard J. D’Andrea, Marshall S. Horwitz, Hamish S. Scott - Nature Genetics 2011 cited by 601

  9. RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML

    Authors: Anna Brown, Peer Arts, Catherine Carmichael, Milena Babic, Julia Dobbins, Chan‐Eng Chong, Andreas Schreiber, Jinghua Feng, Kerry Phillips, Paul Wang, Thuong Ha, Claire C. Homan, Sarah L. King‐Smith, Lesley Rawlings, Cassandra Vakulin, Andrew Dubowsky, Jessica Burdett, Sarah Moore, Grace McKavanagh, Denae Henry, Amanda Wells, Belinda Mercorella, Mario Nicola, Jeffrey C. Suttle, Ella Wilkins, Xiaochun Li, Joëlle Michaud, Peter J Brautigan, Ping Cannon, Meryl Altree, Louise Jaensch, Miriam Fine, Carolyn M Butcher, Richard J. D’Andrea, Ian D. Lewis, Devendra Hiwase, Elli Papaemmanuil, Marshall S. Horwitz, Georges Natsoulis, Hugh Young Rienhoff, Nigel Patton, Sally Mapp, Rachel Susman, Susan Morgan, Julian Cooney, Mark S. Currie, Uday Popat, Tilmann Bochtler, Shai Izraeli, Kenneth F. Bradstock, Lucy A. Godley, Alwin Krämer, Stefan Fröhling, Andrew H. Wei, Cecily Forsyth, Helen Mar Fan, Nicola Poplawski, Christopher N Hahn, Hamish S. Scott - Blood Advances 2020 cited by 153

  10. TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasms

    Authors: Mithun Vinod Shah, Elizabeth Ngoc Hoa Tran, Syed Shah, Rakchha Chhetri, Anmol Baranwal, Dariusz Ladon, Carl Shultz, Aref Al‐Kali, Anna Brown, Dong Chen, Hamish S. Scott, Patricia T. Greipp, Danièl Thomas, Hassan B. Alkhateeb, Deepak Singhal, Naseema Gangat, Sharad Kumar, Mrinal M. Patnaik, Christopher N Hahn, Chung Hoow Kok, Ayalew Tefferi, Devendra Hiwase - Blood Cancer Journal 2023 cited by 46

  11. ARMC5 is part of an RPB1-specific ubiquitin ligase implicated in adrenal hyperplasia

    Authors: Linjiang Lao, Isabelle Bourdeau, Lucia Gagliardi, Xiao He, Wei Shi, Bingbing Hao, Minjia Tan, Yan Hu, Junzheng Peng, Benoit Coulombe, David J. Torpy, Hamish S. Scott, André Lacroix, Hongyu Luo, Jiangping Wu - Nucleic Acids Research 2022 cited by 44

  12. Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation

    Authors: Emma Tudini, James Andrews, David Lawrence, Sarah L. King‐Smith, Naomi L. Baker, Leanne Baxter, John Beilby, Bruce Bennetts, Victoria Beshay, Michael W. Black, Tiffany Boughtwood, Kristian Brion, Pak Leng Cheong, Michael Christie, John Christodoulou, Belinda Chong, Kathy Cox, Mark R. Davis, Lucas Dejong, Marcel E. Dinger, Kenneth Doig, Evelyn Douglas, Andrew Dubowsky, Melissa Ellul, Andrew Fellowes, Katrina Fisk, Cristina Fortuño, Kathryn Friend, Renée Gallagher, Song Gao, Emma Hackett, Johanna Hadler, Michael Hipwell, Gladys Ho, Georgina E. Hollway, Amanda J. Hooper, Karin S. Kassahn, Rahul Krishnaraj, Chiyan Lau, Huong Quang Le, Huei San Leong, Ben Lundie, Sebastian Lunke, Anthony Marty, Mary McPhillips, Lan T. Nguyen, Kátia Nones, Kristen Palmer, John V. Pearson, Michael C. Quinn, Lesley Rawlings, Simon Sadedin, Louisa Sanchez, Andreas Schreiber, Emanouil Sigalas, Aygul Simsek, Julien Soubrier, Zornitza Stark, Bryony A. Thompson, U James, Cassandra G. Vakulin, Amanda V. Wells, C. Wise, Rick Woods, Andrew Ziolkowski, Marie‐Jo Brion, Hamish S. Scott, Natalie Thorne, Amanda B. Spurdle, Lauren Akesson, Richard J. N. Allcock, Katie A. Ashton, Damon A. Bell, Anna Brown, Michael Buckley, John R. Burnett, Linda Burrows, Alicia B. Byrne, Eva K.F. Chan, Corrina Cliffe, Roderick Clifton‐Bligh, S Dooley, Miriam Fanjul‐Fernández, Elizabeth Farnsworth, Thuong Ha, Denae Henry, Duncan Holds, Katherine Holman, Matilda R. Jackson, Sinlay Kang, Catherine Luxford, Sam McManus, Rachael Mehrtens, Cliff Meldrum, David Mossman, Sarah‐Jane Pantaleo, Dean Phelan, Electra Pontikinas, Anja Ravine, Tony Roscioli and 3 more - The American Journal of Human Genetics 2022 cited by 33

  13. Integrative genomic analysis reveals cancer-associated mutations at diagnosis of CML in patients with high-risk disease

    Authors: Susan Branford, Paul Wang, David T Yeung, Daniel Thomson, Adrian Purins, Carol Wadham, Nur Hezrin Shahrin, Justine E. Marum, Nathalie Nataren, Wendy T Parker, Joel Geoghegan, Jinghua Feng, Naranie Shanmuganathan, Martin Mueller, Christian Dietz, Doris Stangl, Zoe Donaldson, Haley Altamura, Jasmina Georgievski, Jodi Braley, Anna Brown, Christopher N Hahn, Ieuan Walker, Soohyun Kim, Soo-Young Choi, Sa-Hee Park, Dong-Wook Kim, Deborah L. White, Agnes S. M. Yong, David M. Ross, Hamish S. Scott, Andreas Schreiber, Timothy P. Hughes - Blood 2018 cited by 209

  14. Genomic subtyping and therapeutic targeting of acute erythroleukemia

    Authors: Ilaria Iacobucci, Ji Wen, Manja Meggendorfer, John Choi, Lei Shi, Stanley Pounds, Catherine Carmichael, Katherine E. Masih, Sarah M. Morris, R. Coleman Lindsley, Laura J. Janke, Thomas Alexander, Guangchun Song, Chunxu Qu, Yongjin Li, Debbie Payne-Turner, Daisuke Tomizawa, Nobutaka Kiyokawa, Marcus B. Valentine, Virginia Valentine, Giuseppe Basso, Franco Locatelli, Eric J. Enemark, Shirley Kow Yin Kham, Allen Eng Juh Yeoh, Xiaotu Ma, Xin Zhou, Edgar Sioson, Michael Rusch, Rhonda E. Ries, Elliot Stieglitz, Stephen P. Hunger, Andrew H. Wei, L.B. To, Ian D. Lewis, Richard J. D’Andrea, Benjamin T. Kile, Anna Brown, Hamish S. Scott, Christopher N Hahn, Paula Marlton, Deqing Pei, Cheng Cheng, Mignon L. Loh, Benjamin L. Ebert, Soheil Meshinchi, Torsten Haferlach, Charles G. Mullighan - Nature Genetics 2019 cited by 167

  15. Allogeneic hematopoietic stem cell transplant outcomes in adults with inherited myeloid malignancies

    Authors: Caner Saygin, Gregory W. Roloff, Christopher N Hahn, Rakchha Chhetri, Saar Gill, Hany Elmariah, Chetasi Talati, Emma Nunley, Guimin Gao, Aelin Kim, Michael R. Bishop, Satyajit Kosuri, Soma Das, Deepak Singhal, Parvathy Venugopal, Claire C. Homan, Anna Brown, Hamish S. Scott, Devendra Hiwase, Lucy A. Godley - Blood Advances 2022 cited by 48

  16. Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema

    Authors: Alicia B. Byrne, Pascal Brouillard, Drew L. Sutton, Jan Kazenwadel, Saba Montazaribarforoushi, Genevieve A. Secker, Anna Oszmiana, Milena Babic, Kelly L. Betterman, Peter J Brautigan, Melissa White, Sandra Piltz, Paul Q. Thomas, Christopher N Hahn, Matthias Rath, Ute Felbor, Georg-Christoph Korenke, Christopher L. Smith, Kathleen H. Wood, Sarah E. Sheppard, Denise M. Adams, Ariana Kariminejad, Raphaël Helaers, Laurence M. Boon, Nicole Revençu, Lynette Moore, Christopher Barnett, Eric Haan, Peer Arts, Miikka Vikkula, Hamish S. Scott, Natasha L. Harvey - Science Translational Medicine 2022 cited by 41

  17. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia

    Authors: Sohela Shah, Kasmintan A. Schrader, Esmé Waanders, Andrew E. Timms, Joseph Vijai, Cornelius Miething, Jeremy Wechsler, Jun J. Yang, James E. Hayes, Robert J. Klein, Jinghui Zhang, Lei Wei, Gang Wu, Michael Rusch, Panduka Nagahawatte, Jing Ma, Shann-Ching Chen, Guangchun Song, Jinjun Cheng, Paul A. Meyers, Deepa Bhojwani, Suresh C. Jhanwar, P. Maslak, Martin Fleisher, Jason Littman, Lily Offit, Rohini Rau‐Murthy, Megan Harlan Fleischut, Marina Corines, Rajmohan Murali, Xiaoni Gao, Christopher Manschreck, Thomas Kitzing, Vundavalli V. Murty, Susana C. Raimondi, Roland P. Kuiper, Annet Simons, Joshua D. Schiffman, Kenan Onel, Sharon E. Plon, David A. Wheeler, Deborah Ritter, David S. Ziegler, Kathy Tucker, Rosemary Sutton, Georgia Chenevix‐Trench, Jun Li, David G. Huntsman, Samantha Hansford, Janine Senz, Tom Walsh, Ming Lee, Christopher N Hahn, Kathryn G. Roberts, Mary‐Claire King, Sarah M. Lo, Ross L. Levine, Agnès Viale, Nicholas D. Socci, Katherine L. Nathanson, Hamish S. Scott, Mark J. Daly, Steven M. Lipkin, Scott W. Lowe, James R. Downing, David Altshuler, John T. Sandlund, Marshall S. Horwitz, Charles G. Mullighan, Kenneth Offit - Nature Genetics 2013 cited by 329

  18. HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse

    Authors: Shu Ly Lim, Zhipeng Qu, R. Daniel Kortschak, David Lawrence, Joel Geoghegan, Anna-Lena Hempfling, Martin Bergmann, Christopher C. Goodnow, Christopher J. Ormandy, Lee H. Wong, Jeff Mann, Hamish S. Scott, Duangporn Jamsai, David L. Adelson, Moira K. O’Bryan - PLoS Genetics 2015 cited by 135

  19. Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41

    Authors: Claire C. Homan, Michael W. Drazer, Kai Yu, David Lawrence, Jinghua Feng, Luis Arriola‐Martinez, Matthew Pozsgai, Kelsey E. McNeely, Thuong Ha, Parvathy Venugopal, Peer Arts, Sarah L. King‐Smith, Jesse Cheah, M. Armstrong, Paul Wang, Csaba Bödör, Alan Cantor, Mario Cazzola, Erin Degelman, Courtney D. DiNardo, Nicolas Duployez, Rémi Favier, Stefan Fröhling, Ana Rio‐Machín, Jeffery M. Klco, Alwin Krämer, Mineo Kurokawa, Joanne Lee, Luca Malcovati, Neil V. Morgan, Georges Natsoulis, Carolyn Owen, Keyur P. Patel, Claude Preudhomme, Hana Raslová, Hugh Young Rienhoff, Tim Ripperger, Rachael Schulte, Kiran Tawana, Elvira Deolinda Rodrigues Pereira Velloso, Benedict Yan, Erika Kim, Raman Sood, Amy P. Hsu, Steven M. Holland, Kerry Phillips, Nicola Poplawski, Milena Babic, Andrew H. Wei, Cecily Forsyth, Helen Mar Fan, Ian D. Lewis, Julian Cooney, Rachel Susman, Lucy C. Fox, Piers Blombery, Deepak Singhal, Devendra Hiwase, Belinda Phipson, Andreas Schreiber, Christopher N Hahn, Hamish S. Scott, Paul Liu, Lucy A. Godley, Anna Brown - Blood Advances 2023 cited by 39

  20. RANK signals from CD4+3− inducer cells regulate development of Aire-expressing epithelial cells in the thymic medulla

    Authors: Simona W. Rossi, Mi‐Yeon Kim, Andreas Leibbrandt, Sonia M. Parnell, William E. Jenkinson, Stephanie H. Glanville, Fiona M. McConnell, Hamish S. Scott, Josef Penninger, Eric J. Jenkinson, Peter J. L. Lane, Graham Anderson - The Journal of Experimental Medicine 2007 cited by 480

  21. Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions

    Authors: Christopher C. Porter, Todd E. Druley, Ayelet Erez, Roland P. Kuiper, Kenan Onel, Joshua D. Schiffman, Kami Wolfe Schneider, Sarah Scollon, Hamish S. Scott, Louise C. Strong, Michael F. Walsh, Kim E. Nichols - Clinical Cancer Research 2017 cited by 104

  22. Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26

    Authors: Claire C. Homan, Hamish S. Scott, Anna Brown - Blood 2023 cited by 55

  23. Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome–like phenotype and hyperactivated MAPK signaling in humans and mice

    Authors: Michael S. Kraft, Ion Cristian Cirstea, Anne K. Voss, Tim Thomas, Ina Goehring, Bilal N. Sheikh, Lavinia Gordon, Hamish S. Scott, Gordon K. Smyth, Mohammad Reza Ahmadian, Udo Trautmann, Martin Zenker, Marco Tartaglia, Arif B. Ekici, André Reis, Helmuth-Guenther Dörr, Anita Rauch, Christian T. Thiel - Journal of Clinical Investigation 2011 cited by 119

  24. TP53mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype

    Authors: Devendra Hiwase, Christopher N Hahn, Elizabeth Ngoc Hoa Tran, Rakchha Chhetri, Anmol Baranwal, Aref Al‐Kali, Kirsty Sharplin, Dariusz Ladon, Rachel Hollins, Patricia T. Greipp, Monika Kutyna, Hassan B. Alkhateeb, Talha Badar, Paul Wang, David M. Ross, Deepak Singhal, Naranie Shanmuganathan, Peter Bardy, Ashanka Beligaswatte, David T Yeung, Mark R. Litzow, Abhishek A. Mangaonkar, Pratyush Giri, Cindy Lee, Angie Yong, Noemi Horvath, Nimit Singhal, Raghu Gowda, William J. Hogan, Naseema Gangat, Mrinal M. Patnaik, Kebede H. Begna, Ing Soo Tiong, Andrew H. Wei, Sharad Kumar, Anna Brown, Hamish S. Scott, Danièl Thomas, Chung Hoow Kok, Ayalew Tefferi, Mithun Vinod Shah - Blood 2022 cited by 38