Erica E Davis

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Nicholas KatsanisNorthwestern U and Rescindo TherapeuticsAdresse e-mail validée de rescindorx.com
Michel LerouxSimon Fraser UniversityAdresse e-mail validée de sfu.ca
Heather EtcheversScientist, INSERM, Aix-Marseille UniversitéAdresse e-mail validée de inserm.fr
Jean MullerLaboratoire de Génétique Médicale U1112Adresse e-mail validée de unistra.fr
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUAdresse e-mail validée de igbmc.fr
Edgar Otto, PhDAssociate Research Scientist, Internal Medicine-Nephrology, University of MichiganAdresse e-mail validée de umich.edu
Blair R. AndersonGraduate Student, Program in Genetics and Genomics, Duke UniversityAdresse e-mail validée de duke.edu
Hulya KayseriliProfessor of medical genetics, Koc university School of MedicineAdresse e-mail validée de kuh.ku.edu.tr
Aysegul OzanturkDuke University Medical CenterAdresse e-mail validée de duke.edu
Frédéric FarnirUniversité de LiègeAdresse e-mail validée de ulg.ac.be
Jacek MajewskiProfessor of Human Genetics, McGill UniversityAdresse e-mail validée de mcgill.ca
Daniel JordanPostdoctoral Fellow, Icahn School of Medicine at Mt. SinaiAdresse e-mail validée de mssm.edu
Karsten BoldtSenior staff Scientist, Medical bioanalytics TuebingenAdresse e-mail validée de uni-tuebingen.de
Jim MullikinDirector NIH Intramural Sequencing Center, NHGRI, NIHAdresse e-mail validée de mail.nih.gov
Jeremy C McIntyreAssistant Professor, University of FloridaAdresse e-mail validée de ufl.edu
oliver blacqueUniversity College DublinAdresse e-mail validée de ucd.ie
Zhou WeibinIcahn School of Medicine at Mount SinaiAdresse e-mail validée de mssm.edu
Moumita ChakiField Medical DirectorAdresse e-mail validée de tayshagtx.com
A Micheil InnesUniversity of CalgaryAdresse e-mail validée de albertahealthservices.ca
Fowzan S Alkuraya, MDProfessor of Human Genetics, Alfaisal University and KFSHRC, Riyadh, Saudi ArabiaAdresse e-mail validée de kfshrc.edu.sa

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Erica E Davis

Lurie Children's Hospital and Northwestern University

Adresse e-mail validée de luriechildrens.org

Genetics Zebrafish Ciliopathy Neurodevelopment


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
The vertebrate primary cilium in development, homeostasis, and disease JM Gerdes, EE Davis, N Katsanis Cell 137 (1), 32-45, 2009	752	2009
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome CC Leitch, NA Zaghloul, EE Davis, C Stoetzel, A Diaz-Font, S Rix, ... Nature genetics 40 (4), 443-448, 2008	427	2008
RNAi-mediated allelic trans-interaction at the imprinted Rtl1/Peg11 locus E Davis, F Caiment, X Tordoir, J Cavaillé, A Ferguson-Smith, N Cockett, ... Current Biology 15 (8), 743-749, 2005	382	2005
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum EE Davis, Q Zhang, Q Liu, BH Diplas, LM Davey, J Hartley, C Stoetzel, ... Nature genetics 43 (3), 189-196, 2011	360	2011
The ciliary proteome database: an integrated community resource for the genetic and functional dissection of cilia A Gherman, EE Davis, N Katsanis Nature genetics 38 (9), 961-962, 2006	336	2006
CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs AC Merveille, EE Davis, A Becker-Heck, M Legendre, I Amirav, G Bataille, ... Nature genetics 43 (1), 72-78, 2011	324	2011
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus C Stoetzel, V Laurier, EE Davis, J Muller, S Rix, JL Badano, CC Leitch, ... Nature genetics 38 (5), 521-524, 2006	315	2006
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies H Khanna, EE Davis, CA Murga-Zamalloa, A Estrada-Cuzcano, I Lopez, ... Nature genetics 41 (6), 739-745, 2009	292	2009
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes EM Valente, CV Logan, S Mougou-Zerelli, JH Lee, JL Silhavy, F Brancati, ... Nature genetics 42 (7), 619-625, 2010	285	2010
Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome C Stoetzel, J Muller, V Laurier, EE Davis, NA Zaghloul, S Vicaire, ... The American Journal of Human Genetics 80 (1), 1-11, 2007	271	2007
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290 NT Gorden, HH Arts, MA Parisi, KLM Coene, SJF Letteboer, ... The American Journal of Human Genetics 83 (5), 559-571, 2008	238	2008
KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes A Putoux, S Thomas, KLM Coene, EE Davis, Y Alanay, G Ogur, E Uz, ... Nature genetics 43 (6), 601-606, 2011	220	2011
TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone L Huang, K Szymanska, VL Jensen, AR Janecke, AM Innes, EE Davis, ... The American Journal of Human Genetics 89 (6), 713-730, 2011	199	2011
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans J Halbritter, AA Bizet, M Schmidts, JD Porath, DA Braun, HY Gee, ... The American Journal of Human Genetics 93 (5), 915-925, 2013	191	2013
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms K Boldt, J Van Reeuwijk, Q Lu, K Koutroumpas, TMT Nguyen, Y Texier, ... Nature communications 7 (1), 1-13, 2016	174	2016
The ciliopathies: a transitional model into systems biology of human genetic disease EE Davis, N Katsanis Current opinion in genetics & development 22 (3), 290-303, 2012	167	2012
The emerging complexity of the vertebrate cilium: new functional roles for an ancient organelle EE Davis, M Brueckner, N Katsanis Developmental cell 11 (1), 9-19, 2006	164	2006
Ectopic expression of DLK1 protein in skeletal muscle of padumnal heterozygotes causes the callipyge phenotype E Davis, CH Jensen, HD Schroder, F Farnir, T Shay-Hadfield, A Kliem, ... Current Biology 14 (20), 1858-1862, 2004	153	2004
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry R Hjeij, A Lindstrand, R Francis, MA Zariwala, X Liu, Y Li, R Damerla, ... The American Journal of Human Genetics 93 (2), 357-367, 2013	151	2013
Pitchfork regulates primary cilia disassembly and left-right asymmetry D Kinzel, K Boldt, EE Davis, I Burtscher, D Trümbach, B Diplas, ... Developmental cell 19 (1), 66-77, 2010	146	2010

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