ScholarIQanswers from OpenAlex
Institute of Genetics and Cancer
InstitutionResearch output, impact & collaborations
Institute of Genetics and Cancer is a institution indexed in ScholarIQ from OpenAlex.
What is known about Institute of Genetics and Cancer?
ScholarIQrecord summary
Institute of Genetics and Cancer is a research organisation in Edinburgh, GB. OpenAlex records 5,957 works and 1,516,376 citations for it. 758 researchers list it as their most recent affiliation.
How many works does Institute of Genetics and Cancer have?
ScholarIQindexed works
Institute of Genetics and Cancer has 5,957 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Institute of Genetics and Cancer have?
ScholarIQcitation count
Institute of Genetics and Cancer has 1,516,376 citations in the OpenAlex counts ScholarIQ stores.
How many researchers are at Institute of Genetics and Cancer?
ScholarIQresearcher count
Institute of Genetics and Cancer has 758 researchers in the ScholarIQ index.
What is the average h-index at Institute of Genetics and Cancer?
ScholarIQavg h-index
Institute of Genetics and Cancer has an average h-index of 75.9 in OpenAlex.
What is the ROR of Institute of Genetics and Cancer?
ScholarIQror
The ROR for Institute of Genetics and Cancer is on the source record.
What is the OpenAlex record for Institute of Genetics and Cancer?
ScholarIQopenalex
The OpenAlex for Institute of Genetics and Cancer is on the source record.
Who are the most-cited researchers behind Institute of Genetics and Cancer?
ScholarIQtop researchers by citations
What are the most-cited papers on Institute of Genetics and Cancer?
ScholarIQmost cited works
A promoter-level mammalian expression atlas
Alistair R. R. Forrest, Hideya Kawaji, Michiel de Hoon, Timo Lassmann, Marina Lizio, Masayoshi Itoh, Nicolas Bertin, Erik Arner, Charles Plessy, Morana Vitezic, Jessica Severin, Yuri Ishizu, Takahiro Arakawa, Alessandro Bonetti, A. Maxwell Burroughs, Shiro Fukuda, Masaaki Furuno, Matthias Harbers, Jayson Harshbarger, Akira Hasegawa, Yuki Hasegawa, Takehiro Hashimoto, Fumi Hori, Bogumił Kaczkowski, Kaoru Kaida, Ai Kaiho, Kazuhiro Kajiyama, Mutsumi Kanamori-Katayama, Shintaro Katayama, Sachi Kato, T Kawashima, Miki Kojima, Naoto Kondo, Atsutaka Kubosaki, Andrew Tae-Jun Kwon, Ri‐Ichiroh Manabe, Efthymios Motakis, Mitsuyoshi Murata, Sayaka Nagao-Sato, Kenichi Nakazato, Noriko Ninomiya, Hiromi Nishiyori, Shohei Noma, Hiroko Ohmiya, Jordan A. Ramilowski, Sugata Roy, Eri Saijyo, Akiko Saka, Mizuho Sakai, Alka Saxena, Thierry Sengstag, Hisashi Shimoji, Jay W. Shin, Christophe Simon, Masanori Suzuki, Naoko Suzuki, Michihira Tagami, Naoko Takahashi, Shoko Watanabe, Shigehiro Yoshida, Harukazu Suzuki, C Daub, J Kawai, Piero Carninci, Yoshihide Hayashizaki, Takeya Kasukawa, Michael Rehli, Christian Schmidl, Matthias Edinger, J. Kenneth Baillie, Lynsey Fairbairn, Malcolm E Fisher, Anagha Joshi, Kim Summers, Tom C. Freeman, David A. Hume, Vanja Haberle, Boris Lenhard, Ivan V. Kulakovskiy, Vsevolod J. Makeev, Yulia A. Medvedeva, Alexander V. Favorov, Artem S. Kasianov, Ilya E. Vorontsov, Robin Andersson, Mette Jørgensen, Yun Chen, Ilka Hoof, Kang Li, Berit Lilje, Xiaobei Zhao, Albin Sandelin, Chris Mungall, Terrence F. Meehan, Sebastian Schmeier, Ulf Schaefer, Intikhab Alam, John A. C. Archer, Boris R. Janković, Benoı̂t Marchand
Resolving the fibrotic niche of human liver cirrhosis at single-cell level
Prakash Ramachandran, Ross Dobie, John R. Wilson‐Kanamori, Elena Dorà, Beth E. P. Henderson, N. Thin Luu, Jordan R. Portman, Kylie P. Matchett, Madara Brice, John A. Marwick, Richard S. Taylor, Mirjana Efremova, Roser Vento‐Tormo, Neil O. Carragher, Timothy J. Kendall, Jonathan Fallowfield, Ewen M. Harrison, Damian J. Mole, Stephen J. Wigmore, Philip N. Newsome, Chris J. Weston, John P. Iredale, Frank Tacke, Jeffrey W. Pollard, Chris P. Ponting, John C. Marioni, Sarah A. Teichmann, Neil C. Henderson
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
Kimberly A. McAllister, K.M. Grogg, David W. Johnson, Carol J. Gallione, Melanie A. Baldwin, Charles E. Jackson, E.A. Helmbold, Dorene S. Markel, Wendy McKinnon, J. Murrel, Mary Kay McCormick, M. A. Pericak‐Vance, Peter Heutink, Ben A. Oostra, T. Haitjema, C.J.J. Westerman, Mary Porteous, Alan E. Guttmacher, Michelle Letarte, Douglas A. Marchuk
Runs of Homozygosity in European Populations
Ruth McQuillan, Anne‐Louise Leutenegger, Rehab Abdel-Rahman, Christopher S. Franklin, Marijana Peričić, Lovorka Barac-Lauc, Nina Smolej‐Narančić, Branka Janičijević, Ozren Polašek, Albert Tenesa, Andrew K. MacLeod, Susan M. Farrington, Pavao Rudan, Caroline Hayward, Véronique Vitart, Igor Rudan, Sarah H. Wild, Malcolm G. Dunlop, Alan F. Wright, Harry Campbell, James F. Wilson
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
David W. Johnson, Jonathan Berg, Melanie A. Baldwin, Carol J. Gallione, Ivonne Marondel, Sang-Heon Yoon, Timothy T. Stenzel, Marcy C. Speer, M. A. Pericak‐Vance, Austin G. Diamond, Alan E. Guttmacher, Charles E. Jackson, Liliana Attisano, Raju Kucherlapati, Mary Porteous, Douglas A. Marchuk
How much of the research on Institute of Genetics and Cancer is open access?
ScholarIQopen access share
67%OPEN ACCESS