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Gill Bejerano

Active 1999–2025

87
Papers
23,733
Citations
51
h-index
78
i10-index

Citations

Citations per year for Gill Bejerano1976: 1 citations1990: 1 citations1993: 1 citations1996: 2 citations2000: 6 citations2001: 13 citations2002: 34 citations2003: 39 citations2004: 52 citations2005: 117 citations2006: 217 citations2007: 352 citations2008: 269 citations2009: 239 citations2010: 224 citations2011: 233 citations2012: 261 citations2013: 297 citations2014: 298 citations2015: 295 citations2016: 302 citations2017: 288 citations2018: 365 citations2019: 898 citations2020: 858 citations2021: 917 citations2022: 829 citations2023: 598 citations2024: 853 citations2025: 443 citations2026: 27 citations1977–1989: no citations, so these years are not shown1991–1992: no citations, so these years are not shown1994–1995: no citations, so these years are not shown1997–1999: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,791 citing papers, 30.8% of this breakdownUnited Kingdom: 1,181 citing papers, 7.6% of this breakdownChina: 1,129 citing papers, 7.3% of this breakdownGermany: 1,042 citing papers, 6.7% of this breakdownCanada: 630 citing papers, 4% of this breakdownFrance: 556 citing papers, 3.6% of this breakdownAustralia: 493 citing papers, 3.2% of this breakdownSpain: 475 citing papers, 3% of this breakdownItaly: 449 citing papers, 2.9% of this breakdownNetherlands: 391 citing papers, 2.5% of this breakdownJapan: 352 citing papers, 2.3% of this breakdownSwitzerland: 328 citing papers, 2.1% of this breakdown
0%30.8%Other 24%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology72.2%
  • Medicine10.5%
  • Computer Science4.7%
  • Agricultural and Biological Sciences4.3%
  • Immunology and Microbiology3.1%
  • Neuroscience2.6%
  • Other2.6%

Topics

  • Genomics and Chromatin Dynamics6.4%
  • Genomics and Phylogenetic Studies5.1%
  • RNA and protein synthesis mechanisms4.7%
  • RNA Research and Splicing4.6%
  • RNA modifications and cancer4.3%
  • Epigenetics and DNA Methylation4.1%
  • Other70.8%

Coauthors

All papers

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  1. GREAT improves functional interpretation of cis-regulatory regions

    Authors: Cory Y. McLean, Dave Bristor, Michael Hiller, Shoa L. Clarke, Bruce T. Schaar, Craig B. Lowe, Aaron M. Wenger, Gill Bejerano - Nature Biotechnology 2010 cited by 5,003

  2. Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

    Authors: Adam Siepel, Gill Bejerano, Jakob Skou Pedersen, Angie S. Hinrichs, Minmei Hou, Kate R. Rosenbloom, Hiram Clawson, John Spieth, LaDeana W. Hillier, Stephen Richards, George M. Weinstock, Richard K. Wilson, Richard A. Gibbs, W. James Kent, Webb Miller, David Haussler - Genome Research 2005 cited by 4,310

  3. The UCSC Genome Browser Database: update 2006

    Authors: Angela S. Hinrichs, Donna Karolchik, Robert Baertsch, Galt P. Barber, Gill Bejerano, Hiram Clawson, Mark Diekhans, Terrence S. Furey, Rachel A. Harte, Fan Hsu, Jennifer Hillman-Jackson, Robert M. Kuhn, Jakob Skou Pedersen, Andy Pohl, Brian J. Raney, Kate R. Rosenbloom, Adam C. Siepel, Kayla E. Smith, Charles W. Sugnet, A. Sultan-Qurraie, Daryl J. Thomas, Heather Trumbower, Ryan J. Weber, M. Weirauch, Ann S. Zweig, David Haussler, W. James Kent - Nucleic Acids Research, Nucleic Acids Res. 2005 cited by 1,799

  4. M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity

    Authors: Karthik A. Jagadeesh, Aaron M. Wenger, Mark J. Berger, Harendra Guturu, Peter D. Stenson, D.N. Cooper, Jonathan A. Bernstein, Gill Bejerano - Nature Genetics 2016 cited by 917

  5. A comparative genomics multitool for scientific discovery and conservation

    Authors: Diane P. Genereux, Aitor Serres, Joel Armstrong, Jeremy Johnson, Voichita D. Marinescu, Eva Murén, David Juan, Gill Bejerano, Nicholas R. Casewell, Leona G. Chemnick, Joana Damas, Federica Di Palma, Mark Diekhans, Ian T. Fiddes, Manuel Garber, Vadim N. Gladyshev, Linda Goodman, Wilfried Haerty, Marlys L. Houck, Robert Hubley, Teemu Kivioja, Klaus-Peter Koepfli, Lukas F. K. Kuderna, Eric S. Lander, Jennifer R. S. Meadows, William J. Murphy, Will Nash, Hyun Ji Noh, Martin Nweeia, Andreas R. Pfenning, Katherine S. Pollard, David A. Ray, Beth Shapiro, Arian F. A. Smit, Mark S. Springer, Cynthia C. Steiner, Ross Swofford, Jussi Taipale, Emma C. Teeling, Jason Turner-Maier, Jessica Alfoldi, Bruce Birren, Oliver A. Ryder, Harris A. Lewin, Benedict Paten, Tomas Marques-Bonet, Kerstin Lindblad-Toh, Elinor K. Karlsson - Nature 2020 cited by 444

  6. Ultraconserved Elements in the Human Genome

    Authors: Gill Bejerano, Michael Pheasant, Igor V. Makunin, Stuart Stephen, W. James Kent, John S. Mattick, David Haussler - Science 2004 cited by 1,774

  7. Enhancers: five essential questions

    Authors: L Pennacchio, Wendy A. Bickmore, Ann Dean, Marcelo A. Nóbrega, Gill Bejerano - Nature Reviews Genetics 2013 cited by 647

  8. Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts

    Authors: Undiagnosed Diseases Network, Laure Frésard, Craig Smail, Nicole M. Ferraro, Nicole A. Teran, Xin Li, Kevin S. Smith, Devon Bonner, Kristin D. Kernohan, Shruti Marwaha, Zachary Zappala, Brunilda Balliu, Joe R. Davis, Boxiang Liu, Cameron J. Prybol, Jennefer N. Kohler, Diane B. Zastrow, Chloe M. Reuter, Dianna G. Fisk, Megan E. Grove, Jean M. Davidson, Taila Hartley, Ruchi Joshi, Benjamin J. Strober, Sowmithri Utiramerur, Lars Lind, Erik Ingelsson, Alexis Battle, Gill Bejerano, Jonathan A. Bernstein, Euan A. Ashley, Kym M. Boycott, Jason D. Merker, Matthew T. Wheeler, Stephen B. Montgomery - Nature Medicine 2019 cited by 355

  9. Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

    Authors: Monica H. Wojcik, Chloe M. Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan, Bo Yuan, Philip M. Boone, Emily Groopman, Emmanuèle C. Délot, Deepti Jain, Alba Sanchis‐Juan, Siwaar Abouhala, Jessica Albert, Miguel Almalvez, Raquel Alvarez, Mutaz Amin, Peter Anderson, Swaroop Aradhya, Euan A. Ashley, Themistocles L. Assimes, Light Auriga, Christina Austin‐Tse, Mike Bamshad, Hayk Barseghyan, Samantha Baxter, Sairam Behera, Shaghayegh Beheshti, Gill Bejerano, Seth Berger, Jon Bernstein, Sabrina Best, Benjamin Blankenmeister, Elizabeth Blue, Eric Boerwinkle, Emily Bonkowski, Devon Bonner, Philip Boone, Miriam Bornhorst, Tugce Bozkurt‐Yozgatli, Harrison Brand, Kati J. Buckingham, Daniel G. Calame, Silvia Casadei, Lisa H. Chadwick, Clarisa Chavez, Ziwei Chen, Iván K. Chinn, Jessica X. Chong, Zeynep Coban‐Akdemir, Andrea J. Cohen, Sarah J. Conner, Matthew P. Conomos, Karen J. Coveler, Ya Allen Cui, Sara Currin, Robert Daber, Zain Dardas, Colleen Davis, Moez Dawood, Ivan De Dios, Celine de Esch, Meghan Delaney, Emmanuèle C. Délot, Stephanie DiTroia, HarshaVardhan Doddapaneni, Haowei Du, Ruizhi Duan, Shannon Dugan‐Perez, Nhat Duong, Michael Duyzend, Evan E. Eichler, Sara Emami, Jawid M. Fatih, Jamie L. Fraser, Vincent A. Fusaro, Miranda Galey, Vijay Ganesh, Kiran Garimella, Richard A. Gibbs, Casey A. Gifford, Amy Ginsburg, Pagé C. Goddard, Stephanie M. Gogarten, Nikhita Gogate, William Gordon, John E. Gorzynski, William J. Greenleaf, Christopher M. Grochowski, Emily Groopman, Rodrigo Guarischi Sousa, Sanna Gudmundsson, Ashima Gulati, Daniel Guo, Walker Hale, Stacey Hall, William T. Harvey, Megan Hawley, Ben Heavner, Isabella Herman and 151 more - The American Journal of Human Genetics 2023 cited by 122

  10. Forces Shaping the Fastest Evolving Regions in the Human Genome

    Authors: Katherine S. Pollard, Sofie R. Salama, Bryan H. King, Andrew D. Kern, Timothy R. Dreszer, Sol Katzman, Adam Siepel, Jakob Skou Pedersen, Gill Bejerano, Robert Baertsch, Kate R. Rosenbloom, Jim Kent, David Haussler - PLoS Genetics 2006 cited by 548

  11. AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature

    Authors: Johannes Birgmeier, Maximilian Haeussler, Cole A. Deisseroth, Ethan Steinberg, Karthik A. Jagadeesh, Alexander Ratner, Harendra Guturu, Aaron M. Wenger, Mark Diekhans, Peter D. Stenson, D.N. Cooper, Christopher Ré, Alan H. Beggs, Jonathan A. Bernstein, Gill Bejerano - Science Translational Medicine 2020 cited by 125

  12. Systematic reanalysis of clinical exome data yields additional diagnoses: implications for providers

    Authors: Aaron M. Wenger, Harendra Guturu, Jonathan A. Bernstein, Gill Bejerano - Genetics in Medicine 2016 cited by 329

  13. Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification

    Authors: Elena‐Raluca Nicoli, Mary Weston, Mary E. Hackbarth, Alissa J. Becerril, Austin Larson, Wadih M. Zein, Peter R. Baker, John D. Burke, Heidi Dorward, Mariska Davids, Yan Huang, David R. Adams, Patricia M. Zerfas, Dong Chen, Thomas C. Markello, Camilo Toro, Tim Wood, Gene Elliott, Mylinh Vu, Maria T. Acosta, David R. Adams, Pankaj B. Agrawal, Mercedes E. Alejandro, Patrick Allard, Justin Alvey, Ashley Andrews, Euan A. Ashley, Mahshid S. Azamian, Carlos A. Bacino, Güney Bademci, Eva H. Baker, Ashok Balasubramanyam, Dustin Baldridge, Jim Bale, Deborah Barbouth, Gabriel F. Batzli, Pinar Bayrak‐Toydemir, Alan H. Beggs, Gill Bejerano, Hugo J. Bellen, Jonathan A. Bernstein, Gerard T. Berry, Anna Bican, David Bick, Camille L. Birch, Stephanie Bivona, John Bohnsack, Carsten Bonnenmann, Devon Bonner, Braden Boone, Bret L. Bostwick, Lorenzo D. Botto, Lauren C. Briere, Elly Brokamp, Donna M. Brown, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Manish J. Butte, John C. Carey, Olveen Carrasquillo, Ta Chen Chang, Hsiao‐Tuan Chao, Gary Clark, Terra R. Coakley, Laurel A. Cobban, Joy D. Cogan, F. Sessions Cole, Heather A. Colley, Cynthia M. Cooper, Heidi Cope, William J. Craigen, Precilla D’Souza, Surendra Dasari, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Naghmeh Dorrani, Daniel C. Dorset, Emilie D. Douine, David D. Draper, Laura Duncan, David J. Eckstein, Lisa Emrick, Christine M. Eng, Cecilia Esteves, Tyra Estwick, Liliana Fernández, Carlos R. Ferreira, Elizabeth L. Fieg, Paul G. Fisher, Brent L. Fogel, Irman Forghani, Laure Frésard, William A. Gahl, Rena A. Godfrey, Alica M. Goldman, David B. Goldstein, Jean‐Philippe F. Gourdine and 175 more - The American Journal of Human Genetics 2019 cited by 97

  14. Emergent high fatality lung disease in systemic juvenile arthritis

    Authors: Vivian E Saper, Guangbo Chen, Gail Deutsch, R. Paul Guillerman, Johannes Birgmeier, Karthik A. Jagadeesh, Scott Canna, Grant S. Schulert, Robin R. Deterding, Jianpeng Xu, Ann N. Leung, Layla Bouzoubaa, Khalid Abulaban, Kevin Baszis, Edward M. Behrens, James Birmingham, Alicia Casey, Michal Cidon, Randy Q. Cron, Aliva De, Fabrizio De Benedetti, Ian Ferguson, Martha P. Fishman, Steven I. Goodman, T. Brent Graham, Alexei A. Grom, Kathleen Haines, Melissa M. Hazen, Lauren A. Henderson, Assunta CH Ho, Maria Ibarra, C. Inman, Rita Jerath, Khulood Khawaja, D. Kingsbury, Marisa Klein‐Gitelman, Khanh Lai, Sivia Lapidus, Clara Lin, Jenny Lin, Deborah R. Liptzin, Diana Milojevic, Joy Mombourquette, Karen Onel, Seza Özen, Marı́a Pérez-Vázquez, K. Phillippi, Sampath Prahalad, Suhas M. Radhakrishna, Adam Reinhardt, Mona Riskalla, Natalie Rosenwasser, Johannes Roth, Rayfel Schneider, Dieneke Schonenberg‐Meinema, Susan Shenoi, Judith A. Smith, Hafize Emine Sönmez, Matthew L. Stoll, C. Towe, Sara O. Vargas, Richard K. Vehe, Lisa R. Young, Jacqueline Yang, Tushar Desai, Raymond R. Balise, Ying Lü, Lü Tian, Gill Bejerano, Mark M. Davis, Purvesh Khatri, Elizabeth Mellins - Annals of the Rheumatic Diseases 2019 cited by 216

  15. Human-specific loss of regulatory DNA and the evolution of human-specific traits

    Authors: Cory Y. McLean, Philip L. Reno, Alex A. Pollen, Abraham I. Bassan, Terence D. Capellini, Catherine Guenther, Vahan B. Indjeian, Xinhong Lim, Douglas B. Menke, Bruce T. Schaar, Aaron M. Wenger, Gill Bejerano, David M. Kingsley - Nature 2011 cited by 562

  16. ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis

    Authors: Cole A. Deisseroth, Johannes Birgmeier, Ethan E. Bodle, Jennefer N. Kohler, Dena R. Matalon, Yelena Nazarenko, Casie A. Genetti, Donna M. Brown, Klaus Schmitz‐Abe, Kelly Schoch, Heidi Cope, Rebecca Signer, Julián A. Martínez-Agosto, Vandana Shashi, Alan H. Beggs, Matthew T. Wheeler, Jonathan A. Bernstein, Gill Bejerano - Genetics in Medicine 2018 cited by 111

  17. Darwin: A Genomics Co-processor Provides up to 15, 000X Acceleration on Long Read Assembly

    Authors: Yatish Turakhia, Gill Bejerano, William J. Dally - ACM SIGPLAN Notices 2018 cited by 112

  18. Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans

    Authors: Victoria E. Rael, Julian A. Yano, John Huizar, Leianna C. Slayden, Madeleine A. Weiss, Elizabeth A Turcotte, J M Terry, Wenqi Zuo, Isabelle Thiffault, Tomi Pastinen, Emily Farrow, Janda Jenkins, Mara L. Becker, Stephen C. Wong, Anne M. Stevens, Catherine Otten, Eric J. Allenspach, Devon Bonner, Jonathan A. Bernstein, Matthew T. Wheeler, Robert A. Saxton, Undiagnosed Diseases Network, Maria T. Acosta, David R. Adams, Raquel L. Alvarez, Justin Alvey, Aimee Allworth, Ashley Andrews, Euan A. Ashley, Ben Afzali, Carlos A. Bacino, Güney Bademci, Ashok Balasubramanyam, Dustin Baldridge, Jim Bale, Michael J. Bamshad, Deborah Barbouth, Pınar Bayrak‐Toydemir, Anita E. Beck, Alan H. Beggs, Edward M. Behrens, Gill Bejerano, Hugo J. Bellen, Jimmy Bennett, Jonathan A. Bernstein, Gerard T. Berry, Anna Bican, Stephanie Bivona, Elizabeth Blue, John Bohnsack, Devon Bonner, Lorenzo D. Botto, Lauren C. Briere, Gabrielle Brown, Elizabeth A. Burke, Lindsay C. Burrage, Manish J. Butte, Peter H. Byers, William E. Byrd, John M. Carey, Thomas Cassini, Sirisak Chanprasert, Hsiao‐Tuan Chao, Iván K. Chinn, Gary Clark, Terra R. Coakley, Laurel A. Cobban, Joy D. Cogan, Matthew Coggins, F. Sessions Cole, Heather A. Colley, Rosario I. Corona, William J. Craigen, Andrew B. Crouse, Michael L. Cunningham, Precilla D’Souza, Hongzheng Dai, Surendra Dasari, Joie Davis, Jyoti G. Dayal, Margaret Delgado, Esteban C. Dell’Angelica, Katrina M. Dipple, Daniel Doherty, Naghmeh Dorrani, Argenia L. Doss, Emilie D. Douine, Dawn Earl, David J. Eckstein, Lisa Emrick, Christine M. Eng, Marni J. Falk, Elizabeth L. Fieg, Paul G. Fisher, Brent L. Fogel, Jiayu Fu, William A. Gahl, I. S. Glass, Pagé C. Goddard, Rena A. Godfrey and 163 more - The Journal of Experimental Medicine 2024 cited by 37

  19. Microbiota modulate transcription in the intestinal epithelium without remodeling the accessible chromatin landscape

    Authors: J. Gray Camp, Christopher L. Frank, Colin R. Lickwar, Harendra Guturu, Tomas Rube, Aaron M. Wenger, Jenny Chen, Gill Bejerano, Gregory E. Crawford, John F. Rawls - Genome Research 2014 cited by 166

  20. Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome

    Authors: Christina Torres Kozycki, Shilpa Kodati, Laryssa A. Huryn, Hongying Wang, Blake M. Warner, Priyam Jani, Dima A. Hammoud, Mones Abu‐Asab, Yingyos Jittayasothorn, Mary J. Mattapallil, Wanxia Li Tsai, Ehsan Ullah, Ping‐Kun Zhou, Xiaoying Tian, Ariane Soldatos, Niki M. Moutsopoulos, Marie Kao-Hsieh, Theo Heller, Edward W. Cowen, Chyi‐Chia Richard Lee, Camilo Toro, Shelley S. Kalsi, Zohreh Khavandgar, Alan N. Baer, Margaret Beach, Debra Long Priel, Michele Nehrebecky, Sofia Rosenzweig, Tina Romeo, Natalie Deuitch, Laurie Brenchley, Eileen Pelayo, Wadih M. Zein, Nida Sen, Alexander H. Yang, Gary L. Farley, David A. Sweetser, Lauren C. Briere, Janine Yang, Fabiano de Oliveira Poswar, Ida Vanessa Döederlein Schwartz, Tamires Silva Alves, Perrine Dusser, Isabelle Koné‐Paut, Isabelle Touitou, Salah Mohamed Titah, P. Martin van Hagen, Rogier T. A. van Wijck, Peter J. van der Spek, Hiromi YANO, Andreas Benneche, Ellen M. Apalset, Ragnhild Wivestad Jansson, Rachel R Caspi, Douglas B. Kuhns, Massimo Gadina, Hidetoshi Takada, Hiroaki Ida, Ryuta Nishikomori, Elena Verrecchia, Eugenio Sangiorgi, Raffaele Manna, Brian P. Brooks, Lucia Sobrin, Robert B. Hufnagel, David B. Beck, Feng Shao, Amanda K. Ombrello, Ivona Aksentijevich, Daniel L. Kastner, Maria T. Acosta, Margaret Adam, David R. Adams, Justin Alvey, Laura Amendola, Ashley Andrews, Euan A. Ashley, Mahshid S. Azamian, Carlos A. Bacino, Guney Bademci, Ashok Balasubramanyam, Dustin Baldridge, Jim Bale, Michael Bamshad, Deborah Barbouth, Pinar Bayrak-Toydemir, Anita Beck, Alan H. Beggs, Edward Behrens, Gill Bejerano, Jimmy Bennet, Beverly Berg-Rood, Jonathan A. Bernstein, Gerard T. Berry, Anna Bican, Stephanie Bivona, Elizabeth Blue, John Bohnsack, Devon Bonner, Lorenzo Botto and 233 more - Annals of the Rheumatic Diseases 2022 cited by 70

  21. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

    Authors: Dongxue Mao, Chloe M. Reuter, Maura Ruzhnikov, Anita E. Beck, Emily Farrow, Lisa Emrick, Jill A. Rosenfeld, Katherine M. Mackenzie, Laurie Robak, Matthew T. Wheeler, Lindsay C. Burrage, Mahim Jain, Pengfei Liu, Daniel G. Calame, Sébastien Küry, Martin Sillesen, Klaus Schmitz‐Abe, Davide Tonduti, Luigina Spaccini, Maria Iascone, Casie A. Genetti, Mary Kay Koenig, Madeline Graf, Alyssa A. Tran, Mercedes E. Alejandro, Maria T. Acosta, Margaret P Adam, David R. Adams, Pankaj B. Agrawal, Mercedes E. Alejandro, Patrick Allard, Justin Alvey, Laura M. Amendola, Ashley Andrews, Euan A. Ashley, Mahshid S. Azamian, Carlos A. Bacino, Güney Bademci, Eva H. Baker, Ashok Balasubramanyam, Dustin Baldridge, Jim Bale, Michael Bamshad, Deborah Barbouth, Gabriel F. Batzli, Pınar Bayrak‐Toydemir, Anita E. Beck, Alan H. Beggs, Gill Bejerano, Hugo J. Bellen, Jimmy Bennet, Beverly Berg-Rood, Raphael Bernier, Jonathan A. Bernstein, Gerard T. Berry, Anna Bican, Stephanie Bivona, Elizabeth Blue, John F. Bohnsack, Carsten Bonnenmann, Devon Bonner, Lorenzo D. Botto, Lauren C. Briere, Elly Brokamp, Elizabeth A. Burke, Lindsay C. Burrage, Manish J. Butte, Peter H. Byers, John C. Carey, Olveen Carrasquillo, Ta Chen Chang, Sirisak Chanprasert, Hsiao-Tuan Chao, Gary Clark, Terra R. Coakley, Laurel A. Cobban, Joy D. Cogan, F. Sessions Cole, Heather A. Colley, Cynthia M. Cooper, Heidi Cope, William J. Craigen, Michael L. Cunningham, Precilla D’Souza, Hongzheng Dai, Surendra Dasari, Mariska Davids, Jyoti G. Dayal, Esteban C. Dell’Angelica, Shweta U. Dhar, Katrina M. Dipple, Daniel Doherty, Naghmeh Dorrani, Emilie D. Douine, David D. Draper, Laura Duncan, Dawn Earl, David J. Eckstein, Lisa Emrick, Christine M. Eng and 195 more - The American Journal of Human Genetics 2020 cited by 69

  22. Darwin-WGA: A Co-processor Provides Increased Sensitivity in Whole Genome Alignments with High Speedup

    Authors: Yatish Turakhia, Sneha D. Goenka, Gill Bejerano, William J. Dally - IEEE International Symposium on High Performance Computer Architecture (HPCA) 2019 cited by 39

  23. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

    Authors: Burak Tepe, Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers, Yuri A. Zárate, G. Bradley Schaefer, Jorge Luis Granadillo De Luque, Daniel Wegner, Benjamin Cogné, Brigitte Gilbert‐Dussardier, Xavier Le Guillou, Eric J. Wagner, Lynn Pais, Jennifer E. Neil, Ganeshwaran H. Mochida, Christopher A. Walsh, Nurit Magal, Valerie Drasinover, Mordechai Shohat, Tanya L. Schwab, C Schmitz, Karl J. Clark, Anthony L. Fine, Brendan C. Lanpher, Ralitza H. Gavrilova, Pierre Blanc, Lydie Bürglen, Alexandra Afenjar, Dora Steel, Manju A. Kurian, Prab Prabhakar, Sophie Gößwein, Nataliya Di Donato, Enrico Bertini, Maria T. Acosta, Margaret P Adam, David R. Adams, Justin Alvey, Laura M. Amendola, Ashley Andrews, Euan A. Ashley, Mahshid S. Azamian, Carlos A. Bacino, Güney Bademci, Ashok Balasubramanyam, Dustin Baldridge, Jim Bale, Michael J. Bamshad, Deborah Barbouth, Pınar Bayrak‐Toydemir, Anita E. Beck, Alan H. Beggs, Edward M. Behrens, Gill Bejerano, Hugo J. Bellen, Jimmy Bennet, Beverly Berg-Rood, Jonathan A. Bernstein, Gerard T. Berry, Anna Bican, Stephanie Bivona, Elizabeth Blue, John F. Bohnsack, Devon Bonner, Lorenzo D. Botto, Brenna Boyd, Lauren C. Briere, Elly Brokamp, Gabrielle Brown, Elizabeth A. Burke, Lindsay C. Burrage, Manish J. Butte, Peter H. Byers, William E. Byrd, John C. Carey, Olveen Carrasquillo, Thomas Cassini, Ta Chen Chang, Sirisak Chanprasert, Hsiao‐Tuan Chao, Gary Clark, Terra R. Coakley, Laurel A. Cobban, Joy D. Cogan, Matthew Coggins, F. Sessions Cole, Heather A. Colley, Cynthia M. Cooper, Heidi Cope, William J. Craigen, Andrew B. Crouse, Michael L. Cunningham, Precilla D’Souza, Hongzheng Dai, Surendra Dasari, Joie Davis, Jyoti G. Dayal, Matthew A. Deardorff and 208 more - The American Journal of Human Genetics 2023 cited by 37

  24. Novel small RNA-encoding genes in the intergenic regions of Escherichia coli

    Authors: Liron Argaman, Ruth Hershberg, Jörg Vogel, Gill Bejerano, E. Gerhart H. Wagner, Hanah Margalit, Shoshy Altuvia - Current Biology 2001 cited by 762