Joseph G. Gleeson - Concepedia

Author

Joseph G. Gleeson

University of California San Diego

Also Known As

JOSEPH G GLEESON, Joseph G Gleeson, Joseph G. Gleeson, Joseph Gerard Gleeson, Joseph Gleeson, Joseph G. Gleeson

Publications

3.5K

Citations

H-Index

Concepts

All Affiliations

University of California San Diego Howard Hughes Medical Institute National Research Centre University of Washington Harvard University

About

Joseph G. Gleeson is an author at University of California San Diego specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	14	1.9K
2	Cell Biology	4	4	701
3	Natural Sciences	2	2	162
4	Public Health	1	1	92
5	Molecular Biology	1	1	126

Joseph G. Gleeson

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
Functional genomic screen for modulators of ciliogenesis and cilium length Joon Kim, Ji Eun Lee, Susanne Heynen‐Genel, Nature Functional GenomicsDevelopmental BiologyCilium LengthGeneticsGenomic Mechanism	2010	537
CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium Joon Kim, Suguna Rani Krishnaswami, Joseph G. Gleeson Human Molecular Genetics	2008	289
The NPHP1 Gene Deletion Associated with Juvenile Nephronophthisis Is Present in a Subset of Individuals with Joubert Syndrome Melissa A. Parisi, Craig L. Bennett, Melissa Eckert, The American Journal of Human Genetics Developmental BiologyMendelian DisorderJoubert SyndromeGenetic DisorderGenetics	2004	255
Molar tooth sign of the midbrain–hindbrain junction: Occurrence in multiple distinct syndromes Joseph G. Gleeson, Lesley C. Keeler, Melissa A. Parisi, American Journal of Medical Genetics Part A	2003	240
Impaired Wnt–β-catenin signaling disrupts adult renal homeostasis and leads to cystic kidney ciliopathy Madeline A. Lancaster, Carrie M Louie, Jennifer L. Silhavy, Nature Medicine Signal TransductionMolecular PhysiologyMedicineKidney CiliopathyPhysiology	2009	169
CCDC41 is required for ciliary vesicle docking to the mother centriole Kwangsic Joo, Chang Gun Kim, Mi‐Sun Lee, Proceedings of the National Academy of Sciences	2013	158
A Homozygous<i>PDE6D</i>Mutation in Joubert Syndrome Impairs Targeting of Farnesylated INPP5E Protein to the Primary Cilium Sophie Thomas, Kevin J. Wright, Stéphanie Le Corre, Human Mutation NeurogenomicsJoubert SyndromeLysosomal Storage DiseaseGeneticsMolecular Biology	2013	126
Mutations in the Glycosylphosphatidylinositol Gene PIGL Cause CHIME Syndrome Bobby G. Ng, Karl Hackmann, Melanie A. Jones, The American Journal of Human Genetics Molecular PhysiologyMendelian DisorderGenetic DisorderGeneticsPathogenesis	2012	124
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy John F. O’Toole, Yangjian Liu, Erica E. Davis, Journal of Clinical Investigation GeneticsRenal PathologyPathologyMitochondrial Localization SignalMolecular Genetics	2010	118
Mutations in LAMB1 Cause Cobblestone Brain Malformation without Muscular or Ocular Abnormalities Farid Radmanesh, Ahmet Okay Çağlayan, Jennifer L. Silhavy, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderOcular AbnormalitiesNeuroanatomy	2013	110

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