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Colin A. Johnson

ResearcherPublications, citations & collaboration network

Colin A. Johnson is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Colin A. Johnson have?

ScholarIQindexed works

Colin A. Johnson has 652 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Colin A. Johnson have?

ScholarIQcitation count

Colin A. Johnson has 21,919 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Colin A. Johnson?

ScholarIQh-index

Colin A. Johnson has an h-index of 78 in OpenAlex.

What is the i10-index of Colin A. Johnson?

ScholarIQi10-index

Colin A. Johnson has an i10-index of 145 in OpenAlex.

What is the ORCID of Colin A. Johnson?

ScholarIQorcid

The ORCID for Colin A. Johnson is on the source record.

What is the OpenAlex record for Colin A. Johnson?

ScholarIQopenalex

The OpenAlex for Colin A. Johnson is on the source record.

What are the most-cited papers on Colin A. Johnson?

ScholarIQmost cited works
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
Marion Delous, Lekbir Baala, Rémi Salomon, Christine Laclef, Jeanette Vierkotten, Kálmán Tory, Christelle Golzio, Tiphanie Lacoste, Laurianne Besse, Catherine Ozilou, Imane Moutkine, Nathan E. Hellman, Isabelle Anselme, Flora Silbermann, Christine Vesque, Christoph Gerhardt, Eleanor Rattenberry, Matthias T. F. Wolf, Marie-Claire Gübler, Jéléna Martinovic, Férechté Encha‐Razavi, Nathalie Boddaert, Marie Gonzalès, Marie Alice Macher, Hubert Nivet, Gérard Champion, Jean Pierre Berthélémé, Patrick Niaudet, Fiona McDonald, Friedhelm Hildebrandt, Colin A. Johnson, Michel Vekemans, Corinne Antignac, Ulrich Rüther, Sylvie Schneider‐Maunoury, Tania Attié‐Bitach, Sophie Saunier
Nature Genetics. 2007497 Citations
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling
Moumita Chaki, Rannar Airik, Amiya K. Ghosh, Rachel H. Giles, Rui Chen, Gisela G. Slaats, Hui Wang, Toby W. Hurd, Weibin Zhou, Andrew Cluckey, Heon Yung Gee, Gokul Ramaswami, Chen‐Jei Hong, Bruce A. Hamilton, Igor Červenka, Ranjani Sri Ganji, Vı́tězslav Bryja, Heleen H. Arts, Jeroen van Reeuwijk, Machteld M. Oud, Stef J.F. Letteboer, Ronald Roepman, Hervé Husson, Oxana Ibraghimov‐Beskrovnaya, Takayuki Yasunaga, Gerd Walz, Lorraine Eley, John A. Sayer, Bernhard Schermer, Max C. Liebau, Thomas Benzing, Stéphanie Le Corre, Iain A. Drummond, Sabine Janssen, Susan J. Allen, S. Natarajan, John F. O’Toole, Massimo Attanasio, Sophie Saunier, Corinne Antignac, Robert K. Koenekoop, Huanan Ren, Irma López, Ahmet Nayır, Corinne Stoetzel, Hélène Dollfus, Rustin Massoudi, Joseph G. Gleeson, Sharon Andreoli, D Doherty, Anna Lindstrad, Christelle Golzio, Nicholas Katsanis, Lars Pape, Emad B. Abboud, Ali A. Al‐Rajhi, Richard A. Lewis, Heymut Omran, Eva Y.-H.P. Lee, Shaohui Wang, JoAnn Sekiguchi, Rudel A. Saunders, Colin A. Johnson, Elizabeth Garner, Katja Vanselow, Jens Andersen, Joseph Shlomai, Gudrun Nürnberg, Peter Nürnberg, Shawn Levy, Agata Smogorzewska, Edgar A. Otto, Friedhelm Hildebrandt
Cell. 2012398 CitationsOPEN ACCESS
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
NISC Comparative Sequencing Program, Erica E. Davis, Qi Zhang, Qin Liu, Bill H. Diplas, Lisa Davey, Jane Hartley, Corinne Stoetzel, Katarzyna Szymańska, Gokul Ramaswami, Clare V. Logan, Donna M. Muzny, Alice Young, David A. Wheeler, Pedro Cruz, Margaret Morgan, Lora Lewis, Praveen F. Cherukuri, Baishali Maskeri, Nancy F. Hansen, James C. Mullikin, Robert W. Blakesley, Gerard G. Bouffard, Gàbor Gyapay, Susanne Rieger, Burkhard Tönshoff, Ilse Kern, Neveen A. Soliman, Thomas J. Neuhaus, Kathryn J. Swoboda, Hülya Kayserili, Tomas E Gallagher, Richard A. Lewis, Carsten Bergmann, Edgar A. Otto, Sophie Saunier, Peter Scambler, Philip L. Beales, Joseph G. Gleeson, Eamonn R. Maher, Tania Attié‐Bitach, Hélène Dollfus, Colin A. Johnson, Eric D. Green, Richard A. Gibbs, Friedhelm Hildebrandt, Eric A. Pierce, Nicholas Katsanis
Nature Genetics. 2011381 CitationsOPEN ACCESS
IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy
Philip L. Beales, Elizabeth Bland, Jonathan L. Tobin, Chiara Bacchelli, Beyhan Tüysüz, Josephine Hill, Suzanne Rix, Chad G. Pearson, Masatake Kai, Jane Hartley, Colin A. Johnson, Melita Irving, Nursel Elçioğlu, Mark Winey, Masazumi Tada, Peter Scambler
Nature Genetics. 2007342 CitationsOPEN ACCESS
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
Hemant Khanna, Erica E. Davis, Carlos Murga‐Zamalloa, Alejandro Estrada‐Cuzcano, Irma López, Anneke I. den Hollander, Marijke N. Zonneveld, Mohammad Othman, Naushin Waseem, Christina Chakarova, C. Maubaret, Anna Dı́az-Font, Ian M. MacDonald, Donna M. Muzny, David A. Wheeler, Margaret Morgan, Lora Lewis, Clare V. Logan, Perciliz L. Tan, M Beer, Chris F. Inglehearn, Richard A. Lewis, Samuel G. Jacobson, Carsten Bergmann, Philip L. Beales, Tania Attié‐Bitach, Colin A. Johnson, Edgar A. Otto, Shomi S. Bhattacharya, Friedhelm Hildebrandt, Richard A. Gibbs, Robert K. Koenekoop, Anand Swaroop, Nicholas Katsanis
Nature Genetics. 2009272 Citations

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