Erica E Davis

Citado por

	Total	Desde 2019
Citas	11089	4908
Índice h	57	43
Índice i10	96	91

1000

500

250

750

200620072008200920102011201220132014201520162017201820192020202120222023202461 134 158 254 371 537 541 609 614 585 706 728 753 803 883 992 955 932 341

Acceso público

Ver todo

103 artículos

2 artículos

disponibles

no disponibles

Basado en requisitos de financiación

Coautores

Nicholas KatsanisGalatea BioDirección de correo verificada de galatea.bio
Michel LerouxSimon Fraser UniversityDirección de correo verificada de sfu.ca
Heather C. EtcheversScientist, INSERM, Aix-Marseille UniversitéDirección de correo verificada de inserm.fr
Jean MullerAssociate Professor of Genetics, Strasbourg University, Inserm, UMR_S 1112Dirección de correo verificada de unistra.fr
Edgar Otto, PhDAssociate Research Scientist, Internal Medicine-Nephrology, University of MichiganDirección de correo verificada de umich.edu
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUDirección de correo verificada de igbmc.fr
Blair R. AndersonGraduate Student, Program in Genetics and Genomics, Duke UniversityDirección de correo verificada de duke.edu
Hulya KayseriliProfessor of medical genetics, Koc university School of MedicineDirección de correo verificada de kuh.ku.edu.tr
Aysegul OzanturkDuke University Medical CenterDirección de correo verificada de duke.edu
Frédéric FarnirUniversité de LiègeDirección de correo verificada de ulg.ac.be
Jacek MajewskiProfessor of Human Genetics, McGill UniversityDirección de correo verificada de mcgill.ca
Daniel JordanPostdoctoral Fellow, Icahn School of Medicine at Mt. SinaiDirección de correo verificada de mssm.edu
Karsten BoldtSenior staff Scientist, Medical bioanalytics TuebingenDirección de correo verificada de uni-tuebingen.de
Jeremy C McIntyreAssistant Professor, University of FloridaDirección de correo verificada de ufl.edu
oliver blacqueUniversity College DublinDirección de correo verificada de ucd.ie
Zhou WeibinIcahn School of Medicine at Mount SinaiDirección de correo verificada de mssm.edu
Moumita ChakiField Medical DirectorDirección de correo verificada de tayshagtx.com
A Micheil InnesUniversity of CalgaryDirección de correo verificada de albertahealthservices.ca
Fowzan S Alkuraya, MDProfessor of Human Genetics, Alfaisal University and KFSHRC, Riyadh, Saudi ArabiaDirección de correo verificada de kfshrc.edu.sa
Albert E. ChudleyProfessor Emeritus, Paediatrics and Child Health, University of ManitobaDirección de correo verificada de umanitoba.ca

Seguir

Erica E Davis

Lurie Children's Hospital and Northwestern University

Dirección de correo verificada de luriechildrens.org

Genetics Zebrafish Ciliopathy Neurodevelopment


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
The vertebrate primary cilium in development, homeostasis, and disease JM Gerdes, EE Davis, N Katsanis Cell 137 (1), 32-45, 2009	841	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	470	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	415	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	409	2011
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	366	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	354	2006
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	345	2006
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	323	2010
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	308	2009
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	293	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	264	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	252	2011
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), 11491, 2016	243	2016
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	236	2013
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	226	2011
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	184	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	175	2006
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	173	2013
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome ND Shaw, H Brand, ZA Kupchinsky, H Bengani, L Plummer, TI Jones, ... Nature genetics 49 (2), 238-248, 2017	166	2017
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	163	2010

El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.

Artículos 1–20

Citas por año

Citas duplicadas

Citas combinadas

Añadir coautoresCoautores

Seguir

Citado por

Coautores