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Murim Choi

Active 2004–2025

93
Papers
22,335
Citations
56
h-index
89
i10-index

Citations

Citations per year for Murim Choi1955: 2 citations1987: 1 citations1994: 3 citations2003: 1 citations2005: 11 citations2006: 7 citations2007: 13 citations2008: 12 citations2009: 23 citations2010: 76 citations2011: 155 citations2012: 277 citations2013: 381 citations2014: 439 citations2015: 414 citations2016: 409 citations2017: 371 citations2018: 357 citations2019: 892 citations2020: 923 citations2021: 925 citations2022: 669 citations2023: 490 citations2024: 689 citations2025: 304 citations2026: 7 citations1956–1986: no citations, so these years are not shown1988–1993: no citations, so these years are not shown1995–2002: no citations, so these years are not shown2004: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,601 citing papers, 27.8% of this breakdownChina: 985 citing papers, 7.6% of this breakdownUnited Kingdom: 900 citing papers, 6.9% of this breakdownGermany: 759 citing papers, 5.9% of this breakdownItaly: 644 citing papers, 5% of this breakdownFrance: 604 citing papers, 4.7% of this breakdownCanada: 504 citing papers, 3.9% of this breakdownJapan: 409 citing papers, 3.2% of this breakdownNetherlands: 394 citing papers, 3% of this breakdownAustralia: 347 citing papers, 2.7% of this breakdownSpain: 324 citing papers, 2.5% of this breakdownSouth Korea: 302 citing papers, 2.3% of this breakdown
0%27.8%Other 24.5%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology46%
  • Medicine36.7%
  • Neuroscience9.8%
  • Immunology and Microbiology5.1%
  • Psychology0.6%
  • Nursing0.4%
  • Other1.4%

Topics

  • Genetics and Neurodevelopmental Disorders3.8%
  • Genomics and Rare Diseases3.1%
  • Autism Spectrum Disorder Research2.8%
  • Genomic variations and chromosomal abnormalities2.4%
  • Congenital heart defects research2.3%
  • Renal Diseases and Glomerulopathies2.3%
  • Other83.3%

Coauthors

All papers

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  1. Co-occurring Genomic Alterations Define Major Subsets of KRAS -Mutant Lung Adenocarcinoma with Distinct Biology, Immune Profiles, and Therapeutic Vulnerabilities

    Authors: Ferdinandos Skoulidis, Lauren A. Byers, Lixia Diao, Vassiliki A. Papadimitrakopoulou, Pan Tong, Julie Izzo, Carmen Behrens, Humam Kadara, Edwin R. Parra, Jaime Rodriguez Canales, Jianjun Zhang, Uma Giri, Jayanthi Gudikote, María Angélica Cortez, Chao Yang, You-Hong Fan, Michael Peyton, Luc Girard, Kevin R. Coombes, Carlo Toniatti, Timothy P. Heffernan, Murim Choi, Garrett M. Frampton, Vincent A. Miller, John N. Weinstein, Roy S. Herbst, Kwok‐Kin Wong, Jianhua Zhang, Padmanee Sharma, Gordon B. Mills, Waun Ki Hong, John D. Minna, James P. Allison, P. Andrew Futreal, Jing Wang, Ignacio I. Wistuba, John V. Heymach - Cancer Discovery 2015 cited by 916

  2. De novo mutations revealed by whole-exome sequencing are strongly associated with autism

    Authors: Stephan Sanders, Michael T. Murtha, Abha R. Gupta, John D. Murdoch, Melanie J. Raubeson, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Nicholas M. DiLullo, Neelroop Parikshak, Jason L. Stein, Michael F. Walker, G Ober, Nicole A. Teran, Youeun Song, Paul El-Fishawy, Ryan Murtha, Murim Choi, John D. Overton, Robert Bjornson, Nicholas Carriero, Kyle A. Meyer, Kaya Bilgüvar, Shrikant Mane, Nenad Šestan, Richard P. Lifton, Murat Günel, Kathryn Roeder, Daniel H. Geschwind, Bernie Devlin, Matthew W. State - Nature 2012 cited by 2,183

  3. A logical network-based drug-screening platform for Alzheimer’s disease representing pathological features of human brain organoids

    Authors: Jong‐Chan Park, So‐Yeong Jang, Dongjoon Lee, Jeong-Ha Lee, Uiryong Kang, Hongjun Chang, Haeng Jun Kim, Sun-Ho Han, Jinsoo Seo, Murim Choi, Dong Young Lee, Min Soo Byun, Dahyun Yi, Kwang‐Hyun Cho, Inhee Mook‐Jung - Nature Communications 2021 cited by 218

  4. De novo mutations in histone-modifying genes in congenital heart disease

    Authors: Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D. Overton, Angela Romano-Adesman, Robert Bjornson, Roger E. Breitbart, Kerry K. Brown, Nicholas Carriero, Yee Him Cheung, John Deanfield, Steven R. DePalma, Khalid A. Fakhro, Joseph Glessner, Håkon Håkonarson, Michael J. Italia, Jonathan R. Kaltman, Juan Pablo Kaski, Richard Kim, Jennie Kline, Teresa Lee, Jeremy Leipzig, Alexander Lopez, Shrikant Mane, Laura E. Mitchell, Jane W. Newburger, Michael Parfenov, Itsik Pe’er, George A. Porter, Amy E. Roberts, Ravi Sachidanandam, Stephan Sanders, Howard Seiden, Mathew W. State, Sai Lakshmi Subramanian, Irina R. Tikhonova, Wei Wang, Dorothy Warburton, Peter S. White, Ismée A. Williams, Hongyu Zhao, Jonathan G. Seidman, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Christine E. Seidman, Richard P. Lifton - Nature 2013 cited by 968

  5. Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

    Authors: Krzysztof Kiryluk, Yifu Li, Francesco Scolari, Simone Sanna‐Cherchi, Murim Choi, Miguel Verbitsky, David Fasel, Sneh Lata, Sindhuri Prakash, Samantha L. Shapiro, Clara Fischman, Holly J. Snyder, Gerald B. Appel, Claudia Izzi, Battista Fabio Viola, Nadia Dallera, Lucia Del Vecchio, Cristina Barlassina, Erika Salvi, Francesca Bertinetto, Antonio Amoroso, Silvana Savoldi, Marcella Rocchietti, Alessandro Amore, Licia Peruzzi, Rosanna Coppo, Maurizio Salvadori, Pietro Ravani, Riccardo Magistroni, Gian Marco Ghiggeri, Gianluca Caridi, Monica Bodria, Francesca Lugani, Landino Allegri, Marco Delsante, Mariarosa Maiorana, Andrea Magnano, Giovanni M. Frascà, Emanuela Boer, Giuliano Boscutti, Claudio Ponticelli, Renzo Mignani, Carmelita Marcantoni, Domenico Di Landro, Domenico Santoro, Antonello Pani, Rosaria Polci, Sandro Feriozzi, Silvana Chicca, Marco Galliani, Maddalena Gigante, Loreto Gesualdo, Pasquale Zamboli, Giovanni Giorgio Battaglia, Maurizio Garozzo, Dita Maixnerová, Vladimı́r Tesař, Frank Eitner, Thomas Rauen, Jürgen Floege, Tibor Kovács, Judit Nagy, Krzysztof Mucha, Leszek Pączek, Marcin Zaniew, Małgorzata Mizerska-Wasiak, Maria Roszkowska–Blaim, Krzysztof Pawlaczyk, Daniel P. Gale, Jonathan Barratt, Lise Thibaudin, F. Berthoux, Guillaume Canaud, Anne Boland, Marie Metzger, Ulf Panzer, Hitoshi Suzuki, Shin Goto, Ichiei Narita, Yaşar Çalışkan, Jingyuan Xie, Ping Hou, Nan Chen, Hong Zhang, Robert Wyatt, Jan Novák, Bruce A. Julian, John Feehally, Bénédicte Stengel, Daniele Cusi, Richard P. Lifton, Ali G. Gharavi - Nature Genetics 2014 cited by 626

  6. Genomic Analysis of Non- NF2 Meningiomas Reveals Mutations in TRAF7 , KLF4 , AKT1 , and SMO

    Authors: Victoria Clark, E. Zeynep Erson‐Omay, Akdes Serin, Jun Yin, Justin Cotney, Koray Özduman, Timuçin Avşar, Jie Li, Phillip B. Murray, Octavian Henegariu, Saliha Yılmaz, Jennifer Moliterno Günel, Geneive Carrión-Grant, Baran Yılmaz, Conor Grady, Bahattin Tanrıkulu, Mehmet Bakırcıoğlu, Hande Kaymakçalan, Ahmet Okay Çağlayan, Leman Sencar, Emre Ceyhun, Ahmet Atik, Yaşar Bayri, Hanwen Bai, Luis Kolb, Ryan Hebert, Sacit Bulent Omay, Ketu Mishra-Gorur, Murim Choi, John D. Overton, Eric C. Holland, Shrikant Mane, Matthew W. State, Kaya Bilgüvar, Joachim M. Baehring, Philip H. Gutin, Joseph M. Piepmeier, Alexander O. Vortmeyer, Cameron Brennan, M. Necmettin Pamir, Türker Kılıç, Richard P. Lifton, James P. Noonan, Katsuhito Yasuno, Murat Günel - Science 2013 cited by 904

  7. Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

    Authors: Neil Romberg, Khatoun Al Moussawi, Carol Nelson‐Williams, Amy L. Stiegler, Erin Loring, Murim Choi, John D. Overton, Eric Meffre, Mustafa K. Khokha, Anita Hüttner, Brian L. West, Nikolai A. Podoltsev, Titus J. Boggon, Barbara I. Kazmierczak, Richard P. Lifton - Nature Genetics 2014 cited by 510

  8. Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma

    Authors: Michael Krauthammer, Yong Kong, Byung Hak Ha, Perry Evans, Antonella Bacchiocchi, Jamie P. McCusker, Elaine Cheng, Matthew J. Davis, Gerald Goh, Murim Choi, Stephan Ariyan, Deepak Narayan, Ken Dutton‐Regester, Ana Capatana, Edna C. Holman, Marcus Bosenberg, Mario Sznol, Harriet M. Kluger, Douglas E. Brash, David F. Stern, Miguel A. Materin, Roger S. Lo, Shrikant Mane, Shuangge Ma, Kenneth K. Kídd, Nicholas K. Hayward, Richard P. Lifton, Joseph Schlessinger, Titus J. Boggon, Ruth Halaban - Nature Genetics 2012 cited by 1,192

  9. Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

    Authors: Hyung-Lok Chung, Michael F. Wangler, Paul C. Marcogliese, Ju-Yeon Jo, Thomas A. Ravenscroft, Zhongyuan Zuo, Lita Duraine, Sina Sadeghzadeh, David Li‐Kroeger, Robert E. Schmidt, Alan Pestronk, Jill A. Rosenfeld, Lindsay C. Burrage, Mitchell J. Herndon, Shan Chen, Amelle Shillington, Marissa Vawter‐Lee, Robert J. Hopkin, Jackeline Rodriguez‐Smith, Michael Henrickson, Brendan Lee, Ann B. Moser, Richard O. Jones, Paul A. Watkins, Taekyeong Yoo, Soe Mar, Murim Choi, Robert C. Bucelli, Shinya Yamamoto, Hyun Kyoung Lee, Carlos E. Prada, Jong‐Hee Chae, Tiphanie P. Vogel, Hugo J. Bellen - Neuron 2020 cited by 163

  10. Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

    Authors: Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Rui Luo, Michael T. Murtha, Daniel Moreno‐De‐Luca, Su H. Chu, Michael Moreau, Abha R. Gupta, Susanne Thomson, Christopher E. Mason, Kaya Bilgüvar, Patrícia B. S. Celestino-Soper, Murim Choi, Emily L. Crawford, Lea K. Davis, Nicole R. Davis Wright, Rahul M. Dhodapkar, Michael DiCola, Nicholas M. DiLullo, Thomas Fernandez, Vikram Fielding‐Singh, Daniel O. Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K. Lowe, Sabata C. Lund, Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State - Neuron 2011 cited by 1,292

  11. K + Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

    Authors: Murim Choi, Ute I. Scholl, Peng Yue, Peyman Björklund, Bixiao Zhao, Carol Nelson‐Williams, Weizhen Ji, Yoonsang Cho, Aniruddh P. Patel, Clara J. Men, Elias Lolis, Max Wisgerhof, David S. Geller, Shrikant Mane, Per Hellman, Gunnar Westin, Göran Åkerström, Wen‐Hui Wang, Tobias Carling, Richard P. Lifton - Science 2011 cited by 991

  12. A database of 5305 healthy Korean individuals reveals genetic and clinical implications for an East Asian population

    Authors: J. Lee, Jean Lee, Sungwon Jeon, Jeong-Ha Lee, Insu Jang, Jin Ok Yang, Soojin Park, Byung-Wook Lee, Jinwook Choi, Byung‐Ok Choi, Heon Yung Gee, Jaeseong Oh, In‐Jin Jang, Sanghyuk Lee, Daehyun Baek, Youngil Koh, Sung‐Soo Yoon, Young-Joon Kim, Jong‐Hee Chae, Woong‐Yang Park, Jong Bhak, Murim Choi - Experimental & Molecular Medicine 2022 cited by 59

  13. Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

    Authors: Ute I. Scholl, Gerald Goh, Gabriel Stölting, Regina Campos de Oliveira, Murim Choi, John D. Overton, Annabelle L. Fonseca, Reju Korah, Lee F. Starker, John W. Kunstman, Manju L. Prasad, Erum A. Hartung, Nelly Mauras, Matthew Benson, Tammy M. Brady, Jay R. Shapiro, Erin Loring, Carol Nelson‐Williams, Steven K. Libutti, Shrikant Mane, Per Hellman, Gunnar Westin, Göran Åkerström, Peyman Björklund, Tobias Carling, Christoph Fahlke, Patricia Hidalgo, Richard P. Lifton - Nature Genetics 2013 cited by 619

  14. Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis

    Authors: Krzysztof Kiryluk, Yifu Li, Simone Sanna‐Cherchi, Mersedeh Rohanizadegan, Hitoshi Suzuki, Frank Eitner, Holly J. Snyder, Murim Choi, Ping Hou, Francesco Scolari, Claudia Izzi, Maddalena Gigante, Loreto Gesualdo, Silvana Savoldi, Antonio Amoroso, Daniele Cusi, Pasquale Zamboli, Bruce A. Julian, Jan Novák, Robert Wyatt, Krzysztof Mucha, Markus Perola, Kati Kristiansson, Alexander Viktorin, Patrik K. E. Magnusson, Guðmar Þorleifsson, Unnur Þorsteinsdóttir, Kāri Stefánsson, Anne Boland, Marie Metzger, Lise Thibaudin, Christoph Wanner, Kitty J. Jager, Shin Goto, Dita Maixnerová, Hussein H. Karnib, Judit Nagy, Ulf Panzer, Jingyuan Xie, Nan Chen, Vladimı́r Tesař, Ichiei Narita, F. Berthoux, Jürgen Floege, Bénédicte Stengel, Hong Zhang, Richard P. Lifton, Ali G. Gharavi - PLoS Genetics 2012 cited by 387

  15. Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

    Authors: John W. Kunstman, C. Christofer Juhlin, Gerald Goh, T Brown, Adam Stenman, James M. Healy, Jill C. Rubinstein, Murim Choi, Nimrod Kiss, Carol Nelson‐Williams, Shrikant Mane, David L. Rimm, Manju L. Prasad, Anders Höög, Jan Zedenius, Catharina Larsson, Reju Korah, Richard P. Lifton, Tobias Carling - Human Molecular Genetics 2015 cited by 362

  16. Landscape of somatic single-nucleotide and copy-number mutations in uterine serous carcinoma

    Authors: Siming Zhao, Murim Choi, John D. Overton, Stefania Bellone, Dana M. Roque, Emiliano Cocco, Federica Guzzo, Diana P. English, Joyce Varughese, Sara Gasparrini, Ileana Bortolomai, Natália Buza, Pei Hui, Maysa Abu‐Khalaf, Antonella Ravaggi, Eliana Bignotti, Elisabetta Bandiera, Chiara Romani, Paola Todeschini, Renata Tassi, Laura Zanotti, Luisa Carrara, Sërgio Pecorelli, Dan‐Arin Silasi, Elena Ratner, Masoud Azodi, Peter E. Schwartz, Thomas Rutherford, Amy L. Stiegler, Shrikant Mane, Titus J. Boggon, Joseph Schlessinger, Richard P. Lifton, Alessandro D. Santin - National Academy of Sciences, Proceedings of the National Academy of Sciences 2013 cited by 337

  17. Defining the phenotypic spectrum of SLC6A1 mutations

    Authors: Katrine M. Johannesen, Elena Gardella, Tarja Linnankivi, Carolina Courage, Anne de Saint Martin, Anna‐Elina Lehesjoki, Cyril Mignot, Alexandra Afenjar, Gaëtan Lesca, Marie‐Thérèse Abi‐Warde, Jamel Chelly, Amélie Piton, J. Lawrence Merritt, Lance H. Rodan, Wen‐Hann Tan, Lynne M. Bird, Mark Nespeca, Joseph G. Gleeson, Yongjin Yoo, Murim Choi, Jong‐Hee Chae, Desiree Czapansky-Beilman, Sara Reichert, Manuela Pendziwiat, Judith Verhoeven, Helenius J. Schelhaas, Orrin Devinsky, Jakob Christensen, Nicola Specchio, Marina Trivisano, Yvonne Weber, Caroline Nava, Boris Keren, Diane Doummar, Élise Schaefer, Sarah Hopkins, Holly Dubbs, Jessica Shaw, Laura Rosa Pisani, Candace T. Myers, Sha Tang, Shan Tang, Deb K. Pal, J Gordon Millichap, Gemma L. Carvill, Kathrine L. Helbig, Oriano Mecarelli, Pasquale Striano, Ingo Helbig, Guido Rubboli, Heather C. Mefford, Rikke S. Møller - Epilepsia 2018 cited by 152

  18. Microglia Gravitate toward Amyloid Plaques Surrounded by Externalized Phosphatidylserine via TREM2

    Authors: Jong‐Chan Park, Jong Won Han, Woochan Lee, Jieun Kim, Sang‐Eun Lee, Dongjoon Lee, Hayoung Choi, Jihui Han, You Jung Kang, Yen N. Diep, Hansang Cho, Rian Kang, Won Jong Yu, Jean Lee, Murim Choi, Sun-Wha Im, Jong‐Il Kim, Inhee Mook‐Jung - Advanced Science 2024 cited by 31

  19. Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

    Authors: Lynn M. Boyden, Murim Choi, Keith A. Choate, Carol Nelson‐Williams, Anita Farhi, Hakan R. Toka, Irina R. Tikhonova, Robert Bjornson, Shrikant Mane, Giacomo Colussi, Marcel Lebel, Richard D. Gordon, Ben A. Semmekrot, A. Poujol, Matti Välimäki, Maria Elisabetta De Ferrari, Sami A. Sanjad, Michael Gutkin, Fiona E. Karet, Joseph Tucci, Jim Stockigt, Kim M. Keppler‐Noreuil, Craig Porter, Sudhir Anand, Margo L. Whiteford, Ira D. Davis, Stephanie Dewar, Alberto Bettinelli, Jeffrey J. Fadrowski, Craig W. Belsha, Tracy E. Hunley, Raoul D. Nelson, Howard Trachtman, Trevor Cole, Maury Pinsk, Detlef Böckenhauer, Mohan Shenoy, Priya Vaidyanathan, John W. Foreman, Majid Rasoulpour, Farook Thameem, Hania Z. Al-Shahrouri, Jai Radhakrishnan, Ali G. Gharavi, Béatrice Goilav, Richard P. Lifton - Nature 2012 cited by 638

  20. Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

    Authors: Ute I. Scholl, Gabriel Stölting, Carol Nelson‐Williams, Alfred A. Vichot, Murim Choi, Erin Loring, Manju L. Prasad, Gerald Goh, Tobias Carling, C. Christofer Juhlin, Ivo Quack, Lars Christian Rump, Anne Thiel, Marc B. Lande, Britney G Frazier, Majid Rasoulpour, David L Bowlin, Christine B. Sethna, Howard Trachtman, Christoph Fahlke, Richard P. Lifton - eLife 2015 cited by 355

  21. CLCN2 chloride channel mutations in familial hyperaldosteronism type II

    Authors: Ute I. Scholl, Gabriel Stölting, Julia Schewe, Anne Thiel, Hua Tan, Carol Nelson‐Williams, Alfred A. Vichot, Sheng Chih Jin, Erin Loring, Verena Untiet, Taekyeong Yoo, Jungmin Choi, Shengxin Xu, Aihua Wu, Marieluise Kirchner, Philipp Mertins, Lars Christian Rump, Ali Mirza Onder, Cory Gamble, Daniel W. McKenney, Robert W. Lash, Deborah P. Jones, G. Chune, Priscila Gagliardi, Murim Choi, Richard D. Gordon, Michael Stowasser, Christoph Fahlke, Richard P. Lifton - Nature Genetics 2018 cited by 267

  22. Korean Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer's Disease: Methodology and Baseline Sample Characteristics

    Authors: Min Soo Byun, Dahyun Yi, Jun Ho Lee, Young Min Choe, Bo Kyung Sohn, Jun‐Young Lee, Hyo Jung Choi, Hyewon Baek, Yu Kyeong Kim, Yun‐Sang Lee, Chul‐Ho Sohn, Inhee Mook‐Jung, Murim Choi, Yu Jin Lee, Dong Woo Lee, Seung‐Ho Ryu, Shin Gyeom Kim, Jee Wook Kim, Jong Inn Woo, Dong Young Lee - Psychiatry Investigation 2017 cited by 134

  23. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

    Authors: Murim Choi, Ute I. Scholl, Weizhen Ji, Tiewen Liu, Irina R. Tikhonova, Paul Zumbo, Ahmet Nayır, Ayşı̇n Bakkaloğlu, Seza Özen, Sami A. Sanjad, Carol Nelson‐Williams, Anita Farhi, Shrikant Mane, Richard P. Lifton - National Academy of Sciences, Proceedings of the National Academy of Sciences 2009 cited by 1,342

  24. Multi‐Omics‐Based Autophagy‐Related Untypical Subtypes in Patients with Cerebral Amyloid Pathology

    Authors: Jong‐Chan Park, Natalia Barahona‐Torres, So‐Yeong Jang, Kin Y. Mok, Haeng Jun Kim, Sun‐Ho Han, Kwang‐Hyun Cho, Xiaopu Zhou, Amy K.Y. Fu, Nancy Y. Ip, Jieun Seo, Murim Choi, Hyobin Jeong, Daehee Hwang, Dong Young Lee, Min Soo Byun, Dahyun Yi, Jong Won Han, Inhee Mook‐Jung, John Hardy - Advanced Science 2022 cited by 28