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How has George C. Gabriel's publication output changed over time?
ScholarIQpublication output · 2013–2023
Output grew0% over the shown period — from 1 works in 2013 to 1 in 2023.
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2013201420152016201720182023
What are the most-cited papers on George C. Gabriel?
ScholarIQmost cited works
Global genetic analysis in mice unveils central role for cilia in congenital heart disease
You Li, Nikolai Klena, George C. Gabriel, Xiaoqin Liu, Andrew J. Kim, Kristi Lemke, Yu Chen, Bishwanath Chatterjee, William A. Devine, Rama Rao Damerla, Chien-fu Chang, Hisato Yagi, Jovenal T. San Agustin, Thahir Mohamed, Shane Anderton, Caroline Lawhead, Anita Vescovi, C. Herbert Pratt, Judy Morgan, Leslie Haynes, Cynthia L. Smith, Janan T. Eppig, Laura G. Reinholdt, Richard Francis, Linda Leatherbury, Madhavi K. Ganapathiraju, Kimimasa Tobita, Gregory J. Pazour, Cecilia Lo
Nature. 2015455 CitationsOPEN ACCESS
DYX1C1 is required for axonemal dynein assembly and ciliary motility
UK10K, Aarti Tarkar, Niki T. Loges, Christopher E. Slagle, Richard Francis, Gerard W. Dougherty, Joel V Tamayo, Brett A. Shook, Marie E. Cantino, Daniel Schwartz, Charlotte Jahnke, Heike Olbrich, Claudius Werner, Johanna Raidt, Petra Pennekamp, Marouan Abouhamed, Rim Hjeij, Gabriele Köhler, Matthias Griese, You Li, Kristi Lemke, Nikolai Klena, Xiaoqin Liu, George C. Gabriel, Kimimasa Tobita, Martine Jaspers, Lucy Morgan, Adam J. Shapiro, Stef J.F. Letteboer, Dorus A. Mans, Johnny L. Carson, Margaret W. Leigh, Whitney Wolf, Serafine Chen, Jane S. Lucas, Alexandros Onoufriadis, Vincent Plagnol, Miriam Schmidts, Karsten Boldt, Ronald Roepman, Maimoona A. Zariwala, Cecilia W. Lo, Hannah M. Mitchison, Michael R. Knowles, Rebecca D. Burdine, Joseph J. LoTurco, Heymut Omran
S137905309. 2013292 CitationsOPEN ACCESS
The complex genetics of hypoplastic left heart syndrome
Xiaoqin Liu, Hisato Yagi, Shazina Saeed, Abha Bais, George C. Gabriel, Zhaohan Chen, Kevin A. Peterson, You Li, Molly Schwartz, William Reynolds, Manush Saydmohammed, Brian Gibbs, Yijen Wu, William Devine, Bishwanath Chatterjee, Nikolai Klena, Dennis Kostka, Karen L. de Mesy Bentley, Madhavi K. Ganapathiraju, Phillip J. Dexheimer, Linda Leatherbury, Omar Khalifa, Anchit Bhagat, Maliha Zahid, William T. Pu, Simon C. Watkins, Paul Grossfeld, Stephen A. Murray, George A. Porter, Michael Tsang, Lisa J. Martin, D. Woodrow Benson, Bruce J. Aronow, Cecilia Lo
S137905309. 2017237 CitationsOPEN ACCESS
CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation
Rim Hjeij, Alexandros Onoufriadis, Christopher M. Watson, Christopher E. Slagle, Nikolai Klena, Gerard W. Dougherty, Małgorzata Kurkowiak, Niki T. Loges, Christine P. Diggle, Nicholas Morante, George C. Gabriel, Kristi Lemke, You Li, Petra Pennekamp, Tabea Menchen, Franziska Konert, June K. Marthin, Dorus A. Mans, Stef J.F. Letteboer, Claudius Werner, Thomas Burgoyne, Cordula Westermann, Andrew Rutman, Ian Carr, Christopher O’Callaghan, Eduardo Moya, Eddie M.K. Chung, Eamonn Sheridan, Kim G. Nielsen, Ronald Roepman, Kerstin Bartscherer, Rebecca D. Burdine, Cecilia Lo, Heymut Omran, Hannah M. Mitchison
S134425043. 2014174 CitationsOPEN ACCESS
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
the DDD study, Nadia Akawi, Jeremy F. McRae, Morad Ansari, Meena Balasubramanian, Moira Blyth, Angela F. Brady, Stephen Clayton, Trevor Cole, Charu Deshpande, Tomas Fitzgerald, Nicola Foulds, Richard Francis, George C. Gabriel, Sebastian S. Gerety, Judith Goodship, Emma Hobson, Wendy D. Jones, Shelagh Joss, Daniel A. King, Nikolai Klena, Ajith Kumar, Melissa Lees, Chris Lelliott, Jenny Lord, Dominic McMullan, Mary O’Regan, Deborah Osio, Virginia Piombo, Elena Prigmore, Diana Rajan, Elisabeth Rosser, Alejandro Sifrim, Audrey Smith, G. Jawahar Swaminathan, Peter D. Turnpenny, James W. Whitworth, Caroline F. Wright, Helen V. Firth, Jeffrey C. Barrett, Cecilia Lo, David Fitzpatrick, Matthew E. Hurles
S137905309. 2015167 CitationsOPEN ACCESS
Related on ScholarIQ
University of Pittsburgh
Institution
Global genetic analysis in mice unveils central role for cilia in congenital heart disease
Paper
DYX1C1 is required for axonemal dynein assembly and ciliary motility
Paper
The complex genetics of hypoplastic left heart syndrome
Paper
CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation
Paper
Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families
Paper