ScholarIQanswers from OpenAlex & ORCID
Joseph G. Gleeson
ResearcherPublications, citations & collaboration network
Joseph G. Gleeson is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Joseph G. Gleeson have?
ScholarIQindexed works
Joseph G. Gleeson has 294 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Joseph G. Gleeson have?
ScholarIQcitation count
Joseph G. Gleeson has 21,775 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Joseph G. Gleeson?
ScholarIQh-index
Joseph G. Gleeson has an h-index of 81 in OpenAlex.
What is the i10-index of Joseph G. Gleeson?
ScholarIQi10-index
Joseph G. Gleeson has an i10-index of 177 in OpenAlex.
What is the ORCID of Joseph G. Gleeson?
ScholarIQorcid
The ORCID for Joseph G. Gleeson is on the source record.
What is the OpenAlex record for Joseph G. Gleeson?
ScholarIQopenalex
The OpenAlex for Joseph G. Gleeson is on the source record.
What are the most-cited papers on Joseph G. Gleeson?
ScholarIQmost cited works
doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein
Joseph G. Gleeson, Kristina M. Allen, Jeremy W. Fox, Edward D. Lamperti, Samuel F. Berkovic, Ingrid E. Scheffer, Edward C. Cooper, William B. Dobyns, Sharon Minnerath, M. Elizabeth Ross, Christopher A. Walsh
Aberrant methylation of tRNAs links cellular stress to neuro‐developmental disorders
Sandra Blanco, Sabine Dietmann, Joana V. Flores, Shobbir Hussain, Claudia Kutter, Peter Humphreys, Margus Lukk, Patrick Lombard, Lucas Treps, Martyna Popis, Stefanie Kellner, Sabine M. Hölter, Lillian Garrett, Wolfgang Wurst, Lore Becker, Thomas Klopstock, Helmut Fuchs, Valérie Gailus‐Durner, Martin Hrabě de Angelis, Ragnhildur Thóra Káradóttir, Mark Helm, Jernej Ule, Joseph G. Gleeson, Duncan T. Odom, Michaela Frye
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
CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration
Ashleigh E. Schaffer, Veerle Rc Eggens, Ahmet Okay Çağlayan, Miriam S. Reuter, Eric Scott, Nicole G. Coufal, Jennifer L. Silhavy, Yuanchao Xue, Hülya Kayserili, Katsuhito Yasuno, Rasim Özgür Rosti, Mostafa Abdellateef, Caner Çağlar, Paul R. Kasher, J. Leonie Cazemier, Marian A. J. Weterman, Vincent Cantagrel, Na Cai, Christiane Zweier, Umut Altunoğlu, N. Bilge Satkin, Fesih Aktar, Beyhan Tüysüz, Cengiz Yalçınkaya, Hüseyîn Çaksen, Kaya Bilgüvar, Xiang‐Dong Fu, Christopher R. Trotta, Stacey Gabriel, André Reis, Murat Günel, Frank Baas, Joseph G. Gleeson