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Bruce D. Gelb

Active 1991–2025

182
Papers
30,791
Citations
91
h-index
171
i10-index

Citations

Citations per year for Bruce D. Gelb1951: 1 citations1955: 7 citations1964: 1 citations1987: 2 citations1992: 2 citations1993: 4 citations1994: 10 citations1995: 14 citations1996: 16 citations1997: 30 citations1998: 32 citations1999: 48 citations2000: 56 citations2001: 60 citations2002: 79 citations2003: 93 citations2004: 114 citations2005: 164 citations2006: 166 citations2007: 168 citations2008: 246 citations2009: 168 citations2010: 245 citations2011: 312 citations2012: 208 citations2013: 241 citations2014: 246 citations2015: 253 citations2016: 230 citations2017: 223 citations2018: 263 citations2019: 816 citations2020: 901 citations2021: 1,099 citations2022: 907 citations2023: 546 citations2024: 1,015 citations2025: 418 citations2026: 20 citations1952–1954: no citations, so these years are not shown1956–1963: no citations, so these years are not shown1965–1986: no citations, so these years are not shown1988–1991: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,294 citing papers, 30.1% of this breakdownUnited Kingdom: 772 citing papers, 7.1% of this breakdownGermany: 670 citing papers, 6.1% of this breakdownChina: 639 citing papers, 5.8% of this breakdownItaly: 580 citing papers, 5.3% of this breakdownCanada: 534 citing papers, 4.9% of this breakdownNetherlands: 430 citing papers, 3.9% of this breakdownFrance: 422 citing papers, 3.9% of this breakdownAustralia: 318 citing papers, 2.9% of this breakdownJapan: 310 citing papers, 2.8% of this breakdownSpain: 236 citing papers, 2.2% of this breakdownBelgium: 223 citing papers, 2% of this breakdown
0%30.1%Other 23%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology53.2%
  • Medicine38.8%
  • Neuroscience2.2%
  • Immunology and Microbiology2%
  • Engineering1.1%
  • Computer Science0.7%
  • Other2%

Topics

  • Congenital heart defects research4.5%
  • Protein Tyrosine Phosphatases3.8%
  • Congenital Heart Disease Studies3%
  • Genomics and Rare Diseases2.9%
  • Cardiomyopathy and Myosin Studies2.1%
  • Galectins and Cancer Biology2%
  • Other81.7%

Coauthors

All papers

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  1. Enabling Technologies for Personalized and Precision Medicine

    Authors: Dean Ho, Stephen R. Quake, Edward R.B. McCabe, Wee Joo Chng, Edward Kai‐Hua Chow, Xianting Ding, Bruce D. Gelb, Geoffrey S. Ginsburg, Jason Hassenstab, Chih‐Ming Ho, William C. Mobley, Garry P. Nolan, Steven T. Rosen, Patrick Tan, Yun Yen, Ali Zarrinpar - Trends in biotechnology 2020 cited by 484

  2. Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

    Authors: Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah U. Morton, Steven R. DePalma, Xue Zeng, Hongjian Qi, Wen-I Chang, Michael C. Sierant, Wei-Chien Hung, Shozeb Haider, Junhui Zhang, James Knight, Robert Bjornson, Christopher Castaldi, Irina R Tikhonoa, Kaya Bilgüvar, Shrikant Mane, Stephan Sanders, Seema Mital, Mark W. Russell, J. William Gaynor, John Deanfield, Anna Giardini, George A. Porter, Deepak Srivastava, Cecilia Lo, Yufeng Shen, W. Scott Watkins, Mark Yandell, H. Joseph Yost, Martin Tristani‐Firouzi, Jane W. Newburger, Amy E. Roberts, Richard Kim, Hongyu Zhao, Jonathan R. Kaltman, Elizabeth Goldmuntz, Wendy K. Chung, Jonathan G. Seidman, Bruce D. Gelb, Christine E. Seidman, Richard P. Lifton, Martina Brueckner - Nature Genetics 2017 cited by 928

  3. De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

    Authors: Jason Homsy, Samir Zaidi, Yufeng Shen, James S. Ware, Kaitlin E. Samocha, Konrad J. Karczewski, Steven R. DePalma, David McKean, Hiroko Wakimoto, Josh Gorham, Sheng Chih Jin, John Deanfield, Anna Giardini, George A. Porter, Richard Kim, Kaya Bilgüvar, Francesc López‐Giráldez, Irina Tikhonova, Shrikant Mane, Angela Romano-Adesman, Hongjian Qi, Badri N. Vardarajan, Lijiang Ma, Mark J. Daly, Amy E. Roberts, Mark W. Russell, Seema Mital, Jane W. Newburger, J. William Gaynor, Roger E. Breitbart, Ivan Iossifov, Michael Ronemus, Stephan Sanders, Jonathan R. Kaltman, Jonathan G. Seidman, Martina Brueckner, Bruce D. Gelb, Elizabeth Goldmuntz, Richard P. Lifton, Christine E. Seidman, Wendy K. Chung - Science 2015 cited by 910

  4. Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

    Authors: Mary Ella Pierpont, Martina Brueckner, Wendy K. Chung, Vidu Garg, Ronald V. Lacro, Amy L. McGuire, Seema Mital, James R. Priest, William T. Pu, Amy E. Roberts, Stephanie M. Ware, Bruce D. Gelb, Mark W. Russell - Circulation 2018 cited by 650

  5. 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

  6. Noonan syndrome

    Authors: Amy E. Roberts, Judith Allanson, Marco Tartaglia, Bruce D. Gelb - The Lancet 2013 cited by 769

  7. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

    Authors: Marco Tartaglia, Ernest L. Mehler, Rosalie Goldberg, Giuseppe Zampino, Han G. Brunner, Hannie Kremer, Ineke van der Burgt, Andrew H. Crosby, Andra Ion, Steve Jeffery, Kamini Kalidas, Michael A. Patton, Raju Kucherlapati, Bruce D. Gelb - Nature Genetics 2001 cited by 1,735

  8. Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-Inhibition

    Authors: Grégor Andelfinger, Christopher Marquis, Marie‐Josée Raboisson, Yves Théorêt, Stephan Waldmüller, G. Wiegand, Bruce D. Gelb, Martin Zenker, Marie‐Ange Delrue, Michael Hofbeck - Journal of the American College of Cardiology 2019 cited by 179

  9. Mapping Systemic Inflammation and Antibody Responses in Multisystem Inflammatory Syndrome in Children (MIS-C)

    Authors: Conor Gruber, Roosheel S. Patel, Rebecca Trachtman, Lauren Lepow, Fatima Amanat, Florian Krammer, Karen M. Wilson, Kenan Onel, Daniel Geanon, Kevin Tuballes, Manishkumar Patel, Konstantinos Mouskas, Timothy J. O’Donnell, Elliot Merritt, Nicole W. Simons, Vanessa Barcessat, Diane M. Del Valle, Samantha Udondem, Gurpawan Kang, Charuta Agashe, Neha Karekar, Joanna Grabowska, Kai Nie, Jessica Le Bérichel, Hui Xie, Noam D. Beckmann, Sandeep Gangadharan, George Ofori‐Amanfo, Uri Laserson, Adeeb Rahman, Seunghee Kim‐Schulze, Alexander W. Charney, Sacha Gnjatic, Bruce D. Gelb, Miriam Mérad, Dusan Bogunovic - Cell 2020 cited by 562

  10. Complex Autoinflammatory Syndrome Unveils Fundamental Principles of JAK1 Kinase Transcriptional and Biochemical Function

    Authors: Conor Gruber, Jorg J. A. Calis, Sofija Buta, Gilad D. Evrony, J.P. Martin, Skyler Uhl, Rachel Caron, Lauren Jarchin, David Dunkin, Robert Phelps, Bryn D. Webb, Jeffrey M. Saland, Miriam Mérad, Jordan S. Orange, Emily M. Mace, Brad R. Rosenberg, Bruce D. Gelb, Dusan Bogunovic - Immunity 2020 cited by 127

  11. Genetic association analysis of 77,539 genomes reveals rare disease etiologies

    Authors: Daniel Greene, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al‐Owain, Arnaud P. J. Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D. Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Østergaard, Bart Loeys, Hiroko Morisaki, Zubair M. Ahmed, Graeme M. Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro - Nature Medicine 2023 cited by 80

  12. Genetics of Congenital Heart Disease

    Authors: Akl C. Fahed, Bruce D. Gelb, J. G. Seidman, Christine E. Seidman - Circulation Research 2013 cited by 587

  13. Molecular states during acute COVID-19 reveal distinct etiologies of long-term sequelae

    Authors: Ryan C. Thompson, Nicole W. Simons, Lillian Wilkins, Esther Cheng, Diane M. Del Valle, Gabriel E. Hoffman, Carlo Cervia, Brian Fennessy, Konstantinos Mouskas, Nancy Francoeur, Jessica Johnson, Lauren Lepow, Jessica Le Bérichel, Christie Chang, Aviva G. Beckmann, Ying‐Chih Wang, Kai Nie, Nicholas Zaki, Kevin Tuballes, Vanessa Barcessat, Mario A. Cedillo, Dan Yuan, Laura M. Huckins, Panos Roussos, Thomas U. Marron, The Mount Sinai COVID-19 Biobank Team, Charuta Agashe, Priyal Agrawal, Alara Akyatan, Kasey Alesso-Carra, Eziwoma Alibo, Kelvin Alvarez, Angelo Amabile, Carmen Argmann, Kimberly Argueta, Steven Ascolillo, Rasheed Bailey, Craig Batchelor, Noam D. Beckmann, Priya Begani, Dusan Bogunovic, Swaroop Bose, Cansu Cimen Bozkus, Paloma Bravo, Stacey-Ann Whittaker Brown, Mark Buckup, Larissa Burka, Sharlene Calorossi, Lena Cambron, Guillermo Carbonell, Gina Carrara, Mario A. Cedillo, Christie Chang, Serena Chang, Steven T. Chen, Jonathan Chien, Mashkura Chowdhury, Jonathan Chung, Phillip Comella, Dana Cosgrove, Francesca Cossarini, Liam Cotter, Arpit Dave, Travis Dawson, Bheesham D. Dayal, Maxime Dhainaut, Rebecca Dornfeld, Katie Dul, Melody Eaton, Nissan Eber, Cordelia Elaiho, Ethan Ellis, Frank Fabris, Jeremiah J. Faith, Dominique Falci, Susie Feng, Marie Fernandes, Nataly Fishman, Nancy Francoeur, Sandeep Gangadharan, Daniel Geanon, Bruce D. Gelb, Benjamin S. Glicksberg, Sacha Gnjatic, Edgar Gonzalez‐Kozlova, Joanna Grabowska, Gavin Gyimesi, Maha Hamdani, Diana Handler, Jocelyn Harris, Matthew Hartnett, Sandra Hatem, Manon Herbinet, Elva Herrera, Arielle Hochman, Gabriel E. Hoffman, Jaime L. Hook, Laila Horta, Étienne Humblin, Suraj K. Jaladanki and 115 more - Nature Medicine 2022 cited by 73

  14. Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy

    Authors: Bhaswati Pandit, Anna Sárközy, L Pennacchio, Claudio Carta, Kimihiko Oishi, Simone Martinelli, Edgar A. Pogna, Wendy Schackwitz, Anna Ustaszewska, Andrew P. Landstrom, J. Martijn Bos, Steve R. Ommen, Giorgia Esposito, Francesca Romana Lepri, Christian Faul, Peter Mündel, Juan Pedro López Siguero, Romano Tenconi, Angelo Selicorni, Cesare Rossi, Laura Mazzanti, Isabella Torrente, Bruno Marino, M. Cristina Digilio, Giuseppe Zampino, Michael J. Ackerman, Bruno Dallapiccola, Marco Tartaglia, Bruce D. Gelb - Nature Genetics 2007 cited by 702

  15. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia

    Authors: Marco Tartaglia, Charlotte M. Niemeyer, Alessandra Fragale, Xiaoling Song, Jochen Buechner, Andreas Jung, Karel Hählen, Henrik Hasle, Jonathan D. Licht, Bruce D. Gelb - Nature Genetics 2003 cited by 1,039

  16. Genomic analyses implicate noncoding de novo variants in congenital heart disease

    Authors: Felix Richter, Sarah U. Morton, Seong Won Kim, Alexander Kitaygorodsky, Lauren K. Wasson, Kathleen Chen, Jian Zhou, Hongjian Qi, Nihir Patel, Steven R. DePalma, Michael Parfenov, Jason Homsy, Joshua Gorham, Kathryn B. Manheimer, Matthew Velinder, Andrew Farrell, Gábor Marth, Eric E. Schadt, Jonathan R. Kaltman, Jane W. Newburger, Anna Giardini, Elizabeth Goldmuntz, Martina Brueckner, Richard Kim, George A. Porter, Daniel Bernstein, Wendy K. Chung, Deepak Srivastava, Martin Tristani‐Firouzi, Olga G. Troyanskaya, Diane E. Dickel, Yufeng Shen, Jonathan G. Seidman, Christine E. Seidman, Bruce D. Gelb - Nature Genetics 2020 cited by 177

  17. Genetic Testing for Heritable Cardiovascular Diseases in Pediatric Patients: A Scientific Statement From the American Heart Association

    Authors: Andrew P. Landstrom, Jeffrey J. Kim, Bruce D. Gelb, Benjamin M. Helm, Prince J. Kannankeril, Christopher Semsarian, Amy C. Sturm, Martin Tristani‐Firouzi, Stephanie M. Ware - Circulation Genomic and Precision Medicine 2021 cited by 112

  18. Myopathic Cardiac Genotypes Increase Risk for Myocarditis

    Authors: Amy Kontorovich, Nihir Patel, Arden Moscati, Felix Richter, Inga Peter, Enkhsaikhan Purevjav, Simina Selejan, Ingrid Kindermann, Jeffrey A. Towbin, Michael Böhm, Karin Klingel, Bruce D. Gelb - JACC Basic to Translational Science 2021 cited by 86

  19. SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype

    Authors: Marialetizia Motta, Giulia Fasano, Sina Gredy, Julia Brinkmann, Adeline Bonnard, Pelin Özlem Şimşek‐Kiper, Elif Yılmaz Güleç, L. Essaddam, Gülen Eda Ütine, Ingrid G. Prandi, Martina Venditti, Francesca Pantaleoni, Francesca Clementina Radio, Andrea Ciolfi, Stefania Petrini, Federica Consoli, Cédric Vignal, Denis Hepbasli, Melanie Ullrich, Elke de Boer, Lisenka E.L.M. Vissers, Sami Gritli, Cesare Rossi, Alessandro De Luca, S. Ben Bêcher, Bruce D. Gelb, Bruno Dallapiccola, Antonella Lauri, Giovanni Chillemi, Kai Schuh, Hélène Cavé, Martin Zenker, Marco Tartaglia - The American Journal of Human Genetics 2021 cited by 80

  20. Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic Disorder

    Authors: Jill L. Maron, Stephen F. Kingsmore, Bruce D. Gelb, Jerry Vockley, Kristen Wigby, Jennifer Bragg, Annemarie Stroustrup, Brenda B. Poindexter, Kristen Suhrie, Jae H. Kim, Thomas G. Diacovo, Cynthia M. Powell, Andrea Trembath, Lucia Guidugli, Katarzyna A. Ellsworth, Dallas Reed, Anne Kurfiss, Janis L. Breeze, Ludovic Trinquart, Jonathan M. Davis - JAMA 2023 cited by 72

  21. Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines

    Authors: Alicia Romanò, Judith Allanson, Jovanna Dahlgren, Bruce D. Gelb, Bryan D. Hall, Mary Ella Pierpont, Amy E. Roberts, Wanda Robinson, Clifford M. Takemoto, Jacqueline A. Noonan - PEDIATRICS 2010 cited by 619

  22. Distinct epigenetic programs regulate cardiac myocyte development and disease in the human heart in vivo

    Authors: Ralf Gilsbach, Martin Schwaderer, Sebastian Preißl, Björn Grüning, David Kranzhöfer, Pedro Schneider, Thomas Nührenberg, Sonia Mulero‐Navarro, Dieter Weichenhan, Christian Braun, Martina Dreßen, Adam R. Jacobs, Harald Lahm, Torsten Doenst, Rolf Backofen, Markus Krane, Bruce D. Gelb, Lutz Hein - Nature Communications 2018 cited by 249

  23. MEK inhibitors for neurofibromatosis type 1 manifestations: Clinical evidence and consensus

    Authors: Peter de Blank, Andrea M. Gross, Srivandana Akshintala, Jaishri O. Blakeley, Gideon Bollag, Ashley Cannon, Eva Dombi, Jason Fangusaro, Bruce D. Gelb, Darren Hargrave, AeRang Kim, Laura J. Klesse, Mignon L. Loh, Staci Martin, Christopher L. Moertel, Roger J. Packer, Jonathan M. Payne, Katherine A. Rauen, Jonathan J. Rios, Nathan Robison, Elizabeth K. Schorry, Kevin Shannon, David A. Stevenson, Elliot Stieglitz, Nicole J. Ullrich, Karin S. Walsh, Brian Weiss, Pamela L. Wolters, Kaleb Yohay, Marielle E. Yohe, Brigitte C. Widemann, Michael J. Fisher - Neuro-Oncology 2022 cited by 101

  24. PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

    Authors: Marco Tartaglia, Kamini Kalidas, Adam Shaw, Xiaoling Song, Dan L. Musat, Ineke van der Burgt, Han G. Brunner, Débora Romeo Bertola, Andrew H. Crosby, Andra Ion, Raju Kucherlapati, Steve Jeffery, Michael A. Patton, Bruce D. Gelb - The American Journal of Human Genetics 2002 cited by 797