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Rune R. Frants

ResearcherPublications, citations & collaboration network

Rune R. Frants is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Rune R. Frants have?

ScholarIQindexed works

Rune R. Frants has 392 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Rune R. Frants have?

ScholarIQcitation count

Rune R. Frants has 32,383 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Rune R. Frants?

ScholarIQh-index

Rune R. Frants has an h-index of 90 in OpenAlex.

What is the i10-index of Rune R. Frants?

ScholarIQi10-index

Rune R. Frants has an i10-index of 302 in OpenAlex.

What is the OpenAlex record for Rune R. Frants?

ScholarIQopenalex

The OpenAlex for Rune R. Frants is on the source record.

What are the most-cited papers on Rune R. Frants?

ScholarIQmost cited works
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe, Ronald van Eijk, Peter J. Oefner, Susan M.G. Hoffman, Jane E. Lamerdin, Harvey W. Mohrenweiser, Dennis E. Bulman, Maurizio Ferrari, Joost Haan, Dick Lindhout, Gert‐Jan B. van Ommen, Marten H. Hofker, Michel D. Ferrari, Rune R. Frants
Cell. 19962,343 CitationsOPEN ACCESS
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Josée Dupuis, the MAGIC investigators, Claudia Langenberg, Inga Prokopenko, Richa Saxena, Nicole Soranzo, Anne Jackson, Eleanor Wheeler, Nicole L. Glazer, Nabila Bouatia‐Naji, Anna L. Gloyn, Cecilia M. Lindgren, Reedik Mägi, Andrew P. Morris, Joshua C. Randall, Toby Johnson, Paul Elliott, Denis Rybin, Guðmar Þorleifsson, Valgerður Steinthórsdóttir, Peter Henneman, Harald Grallert, Abbas Dehghan, Jouke‐Jan Hottenga, C. Franklin, Pau Navarro, Kijoung Song, Anuj Goel, John R. B. Perry, Josephine M. Egan, Taina K. Lajunen, Niels Grarup, Thomas Sparsø, Alex S. F. Doney, Benjamin F. Voight, Heather M. Stringham, Man Li, Stavroula Kanoni, Peter Shrader, Christine Cavalcanti-Proença, Meena Kumari, Lu Qi, Nicholas J. Timpson, Christian Gieger, Katja K.H. Aben, Ghislain Rocheleau, Erik Ingelsson, Ping An, Jeffrey R. O’Connell, Jian’an Luan, Amanda Elliott, Steven A. McCarroll, Felicity Payne, Rosa Maria Roccasecca, François Pattou, Praveen Sethupathy, Kristin Ardlie, Yavuz Ariyürek, Beverley Balkau, Philip J. Barter, John Beilby, Yoav Ben‐Shlomo, Rafn Benediktsson, Amanda J. Bennett, Richard N. Bergman, Murielle Bochud, Eric Boerwinkle, Amélie Bonnefond, Lori L. Bonnycastle, Knut Borch‐Johnsen, Yvonne Böttcher, Eric J. Brunner, Suzannah J. Bumpstead, G. Charpentier, Yii‐Der Ida Chen, Peter S. Chines, Robert Clarke, Lachlan Coin, Matthew N. Cooper, Marilyn C. Cornelis, Gabe Crawford, Laura Crisponi, Ian N.M. Day, Eco J. C. de Geus, Jérôme Delplanque, Christian Dina, Michael R. Erdos, Annette C. Fedson, Antje Fischer‐Rosinsky, Nita G. Forouhi, Caroline S. Fox, Rune R. Frants, Maria Grazia Franzosi, Pilar Galán, Mark O. Goodarzi, J. Graessler, Christopher J. Groves, Scott M. Grundy, Rhian Gwilliam, Ulf Gyllensten
Nature Genetics. 20102,239 CitationsOPEN ACCESS
C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy
Anna Richards, Arn M. J. M. van den Maagdenberg, Joanna C. Jen, David Kavanagh, Paula Bertram, Dirk Spitzer, M. Kathryn Liszewski, Maria Louise Barilla-Labarca, Gisela M. Terwindt, Yumi Kasai, Mike McLellan, M. Gilbert Grand, Kaate R. J. Vanmolkot, Boukje de Vries, Jijun Wan, Michael J. Kane, Hafsa Mamsa, R Schäfer, Anine H Stam, Joost Haan, Paulus T.V.M. de Jong, Caroline W. J. M. Storimans, Mary J. van Schooneveld, J.A. Oosterhuis, Andreas Gschwendter, Martin Dichgans, Katya Kotschet, Suzanne Hodgkinson, Todd A. Hardy, Martin B. Delatycki, Rula A. Hajj‐Ali, Parul H. Kothari, Stanley F. Nelson, Rune R. Frants, Robert W. Baloh, Michel D. Ferrari, John P. Atkinson
Nature Genetics. 2007454 Citations
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element
Jan Gabriëls, M.-C. Beckers, Hao Ding, An S. De Vriese, Stéphane Plaisance, Silvère M. van der Maarel, George W. Padberg, Rune R. Frants, Jane Hewitt, Désiré Collen, Alexandra Belayew
Gene. 1999352 Citations

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