PICO Portalanswers from OpenAlex & ORCID
Martin C. Frith
ResearcherPublications, citations & collaboration network
Martin C. Frith is a researcher indexed in PICO Portal from OpenAlex & ORCID.
How many works does Martin C. Frith have?
PICO Portalindexed works
Martin C. Frith has 168 works in the PICO Portal index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Martin C. Frith have?
PICO Portalcitation count
Martin C. Frith has 32,564 citations in the OpenAlex counts PICO Portal stores.
What is the h-index of Martin C. Frith?
PICO Portalh-index
Martin C. Frith has an h-index of 51 in OpenAlex.
What is the i10-index of Martin C. Frith?
PICO Portali10-index
Martin C. Frith has an i10-index of 82 in OpenAlex.
What is the ORCID of Martin C. Frith?
PICO Portalorcid
The ORCID for Martin C. Frith is on the source record.
What is the OpenAlex record for Martin C. Frith?
PICO Portalopenalex
The OpenAlex for Martin C. Frith is on the source record.
What are the most-cited papers on Martin C. Frith?
PICO Portalmost cited works
The Transcriptional Landscape of the Mammalian Genome
Piero Carninci, Takeya Kasukawa, Shintaro Katayama, Julian Gough, Martin C. Frith, Norihiro Maeda, Rieko Oyama, Timothy Ravasi, Boris Lenhard, Christine A. Wells, Rimantas Kodzius, Koya Shimokawa, Vladimir B. Bajić, Steven E. Brenner, Serge Batalov, Alistair R. R. Forrest, Mihaela Zavolan, Melissa J. Davis, Laurens Wilming, Vassilis Aidinis, Jonathan Allen, Alberto Ambesi‐Impiombato, Rolf Apweiler, Rajith Aturaliya, Timothy L. Bailey, Mukul S. Bansal, Laura L. Baxter, Kirk W. Beisel, Tom Bersano, Hidemasa Bono, Alistair M. Chalk, Kuo Ping Chiu, Vijayata Choudhary, Alan Christoffels, D. R. Clutterbuck, Mark L. Crowe, Emiliano Dalla, Brian P. Dalrymple, Bernard de Bono, Giusy Della Gatta, Diego di Bernardo, Thomas A. Down, Pär G. Engström, Michela Fagiolini, Geoffrey J. Faulkner, Colin Fletcher, Tatsuya Fukushima, Masaaki Furuno, Sugiko Futaki, Manuela Gariboldi, Patrik Georgii‐Hemming, T Gingeras, Takashi Gojobori, Richard E. Green, Stefano Gustincich, Matthias Harbers, Yoshitaka Hayashi, Takao K. Hensch, Nobutaka Hirokawa, David E. Hill, Łukasz Huminiecki, Michele Iacono, Kazuho Ikeo, Atsushi Iwama, Takanori Ishikawa, Lars Martin Jakt, Alexander Kanapin, Masaru Katoh, Yuka Imamura Kawasawa, Janet Kelso, Hiroshi Kitamura, Hiroaki Kitano, George Kollias, Sivanand Krishnan, Adéle Kruger, Sarah Kummerfeld, Igor V. Kurochkin, Liana F. Lareau, Dejan Lazarević, Leonard Lipovich, Jinfeng Liu, Sabino Liuni, Sean McWilliam, M. Madan Babu, Martin Madera, Luigi Marchionni, Hideo Matsuda, Shu‐ichi Matsuzawa, Hiroaki Miki, Flavio Mignone, S. Miyake, Ken A. Morris, Salim Mottagui‐Tabar, Nicola Mulder, Norio Nakano, Hiromitsu Nakauchi, Patrick Ng, Roland Nilsson, Seiji Nishiguchi, Shigemichi Nishikawa
Antisense Transcription in the Mammalian Transcriptome
Shintaro Katayama, Yuji Tomaru, Takeya Kasukawa, Kazunori Waki, Misato Nakanishi, Mari Nakamura, Hiromi Nishida, Chui-Sun Yap, Masanori Suzuki, Jun Kawai, Harukazu Suzuki, Piero Carninci, Yoshihide Hayashizaki, Christine A. Wells, Martin C. Frith, Timothy Ravasi, Ken C. Pang, Jennifer Hallinan, John S. Mattick, David Hume, Leonard Lipovich, Serge Batalov, Pär G. Engström, Yosuke Mizuno, Mohammad Ali Faghihi, Albin Sandelin, Alistair M. Chalk, Salim Mottagui‐Tabar, Z. Liang, Boris Lenhard, Claes Wahlestedt
Rapid evolution of noncoding RNAs: lack of conservation does not mean lack of function
Ken C. Pang, Martin C. Frith, John S. Mattick
Experimental validation of the regulated expression of large numbers of non-coding RNAs from the mouse genome
Timothy Ravasi, Harukazu Suzuki, Ken C. Pang, Shintaro Katayama, Masaaki Furuno, Rie Okunishi, Shiro Fukuda, Kelin Ru, Martin C. Frith, Milena Gongora, Sean M. Grimmond, David Hume, Yoshihide Hayashizaki, John S. Mattick