A citation-based method for searching scientific literature

Dianlei Guo, Mengke Li, Bin Zou, Xinyu Gu, Zhaohui Yuan, Michael Liu, Fuxiang Mao, Hong Ouyang, Kaili Wu, Lai Wei, Yizhi Liu, Chunqiao Liu. Exp Eye Res 2019
Times Cited: 1







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



What happens to tears inside the efferent lacrimal passage? An animal experimental study.
F Paulsen, A Thale, R Mentlein. Graefes Arch Clin Exp Ophthalmol 2000
13
100

[Nasolacrimal ducts and the dry eye].
F Paulsen, A Thale, U Schaudig. Ophthalmologe 2002
13
100


Morphogenesis of the human excretory lacrimal system.
C de la Cuadra-Blanco, M D Peces-Peña, L Jáñez-Escalada, J R Mérida-Velasco. J Anat 2006
30
100

Development of the nasolacrimal apparatus in the Mongolian gerbil (Meriones unguiculatus), with notes on network topology and function.
Susan J Rehorek, Jayna Cunningham, Amanda E Bruening, Jessica L Johnson, Kunwar P Bhatnagar, Timothy D Smith, Willem J Hillenius. J Morphol 2015
4
100

Identifying an appropriate animal model for the nasolacrimal drainage system.
Nicholas J Frame, Cat Nguyen Burkat. Ophthalmic Plast Reconstr Surg 2009
11
100

Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction.
J Foster, S Kapoor, O Diaz-Horta, A Singh, C Abad, A Rastogi, R Moharana, O Tekeli, K Walz, M Tekin. Clin Genet 2014
7
100

The Wnt signaling pathway in development and disease.
Catriona Y Logan, Roel Nusse. Annu Rev Cell Dev Biol 2004
100


Prickle1 is expressed in distinct cell populations of the central nervous system and contributes to neuronal morphogenesis.
Chunqiao Liu, Chen Lin, D Thad Whitaker, Hirva Bakeri, Oleg V Bulgakov, Pinghu Liu, Jingqi Lei, Lijin Dong, Tiansen Li, Anand Swaroop. Hum Mol Genet 2013
31
100


Disruption of Core Planar Cell Polarity Signaling Regulates Renal Tubule Morphogenesis but Is Not Cystogenic.
Koshi Kunimoto, Roy D Bayly, Eszter K Vladar, Tyson Vonderfecht, Anna-Rachel Gallagher, Jeffrey D Axelrod. Curr Biol 2017
25
100

Ocular abnormalities in Apert syndrome: genotype/phenotype correlations with fibroblast growth factor receptor type 2 mutations.
Suzanne K Jadico, David A Young, Alexandra Huebner, Jane C Edmond, Avrum N Pollock, Donna M McDonald-McGinn, Yi-Ju Li, Elaine H Zackai, Terri L Young. J AAPOS 2006
14
100


Null and hypomorph Prickle1 alleles in mice phenocopy human Robinow syndrome and disrupt signaling downstream of Wnt5a.
Chunqiao Liu, Chen Lin, Chun Gao, Helen May-Simera, Anand Swaroop, Tiansen Li. Biol Open 2014
26
100

Apoptosis as a creative agent of embryonic development of bucca, mentum and nasolacrimal duct. An in vivo study in rats.
Kristina Lotz, Peter Proff, Volker Bienengraeber, Jochen Fanghaenel, Tomas Gedrange, Jens Weingaertner. J Craniomaxillofac Surg 2006
26
100

Animal model for the absorption of lipophilic substances from tear fluid by the epithelium of the nasolacrimal ducts.
Friedrich P Paulsen, Marc Föge, Andreas B Thale, Bernhard N Tillmann, Rolf Mentlein. Invest Ophthalmol Vis Sci 2002
30
100

Ontogenesis of the tear drainage system requires Prickle1-driven polarized basement membrane deposition.
Dianlei Guo, Jiali Ru, Fuxiang Mao, Hong Ouyang, Rong Ju, Kaili Wu, Yizhi Liu, Chunqiao Liu. Development 2020
1
100

Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature.
M M van Genderen, G F Kinds, F C Riemslag, R C Hennekam. Br J Ophthalmol 2000
41
100


Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.
Brian C Gibbs, Rama Rao Damerla, Eszter K Vladar, Bishwanath Chatterjee, Yong Wan, Xiaoqin Liu, Cheng Cui, George C Gabriel, Maliha Zahid, Hisato Yagi,[...]. Biol Open 2016
24
100


Hereditary disorders affecting the lacrimal system.
Richard C Allen. Curr Opin Ophthalmol 2014
6
100

Characteristics of lacrimo-auriculo-dento-digital (LADD) syndrome: case report of a family and literature review.
Umit Ubeyt Inan, Mustafa Deniz Yilmaz, Yavuz Demir, Bumin Degirmenci, Sitki Samet Ermis, Faruk Ozturk. Int J Pediatr Otorhinolaryngol 2006
28
100

Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutations.
Suzanne K Jadico, Alexandra Huebner, Donna M McDonald-McGinn, Elaine H Zackai, Terri L Young. J AAPOS 2006
16
100

Mouse prickle1, the homolog of a PCP gene, is essential for epiblast apical-basal polarity.
Hirotaka Tao, Makoto Suzuki, Hiroshi Kiyonari, Takaya Abe, Toshikuni Sasaoka, Naoto Ueno. Proc Natl Acad Sci U S A 2009
81
100

Endoscopic-assisted probing for congenital nasolacrimal duct obstruction.
E J Wallace, A Cox, P White, C J Macewen. Eye (Lond) 2006
34
100

Mutant p63 causes defective expansion of ectodermal progenitor cells and impaired FGF signalling in AEC syndrome.
Giustina Ferone, Helen A Thomason, Dario Antonini, Laura De Rosa, Bing Hu, Marica Gemei, Huiqing Zhou, Raffaele Ambrosio, David P Rice, Dario Acampora,[...]. EMBO Mol Med 2012
57
100

Prickle1 stunts limb growth through alteration of cell polarity and gene expression.
Tian Yang, Alexander G Bassuk, Bernd Fritzsch. Dev Dyn 2013
21
100

Development of the Lacrimal Apparatus in the Rabbit (Oryctolagus cuniculus) and Its Potential Role as an Animal Model for Humans.
S J Rehorek, J R Holland, J L Johnson, J M Caprez, J Cray, M P Mooney, W J Hillenius, T D Smith. Anat Res Int 2011
13
100

A Spatiotemporal Requirement for Prickle 1-Mediated PCP Signaling in Eyelid Morphogenesis and Homeostasis.
Dianlei Guo, Zhaohui Yuan, Jiali Ru, Xinyu Gu, Wang Zhang, Fuxiang Mao, Hong Ouyang, Kaili Wu, Yizhi Liu, Chunqiao Liu. Invest Ophthalmol Vis Sci 2018
4
100

Congenital Nasolacrimal Duct Obstruction (CNLDO): A Review.
Aldo Vagge, Lorenzo Ferro Desideri, Paolo Nucci, Massimiliano Serafino, Giuseppe Giannaccare, Andrea Lembo, Carlo Enrico Traverso. Diseases 2018
16
100

A new nomenclature for int-1 and related genes: the Wnt gene family.
R Nusse, A Brown, J Papkoff, P Scambler, G Shackleford, A McMahon, R Moon, H Varmus. Cell 1991
217
100



Familial Wolf-Hirschhorn syndrome associated with Rieger anomaly of the eye.
C Kozma, M Hunt, J Meck, E Traboulsi, N Scribanu. Ophthalmic Paediatr Genet 1990
10
100


Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease.
Sakura Saburi, Ian Hester, Evelyne Fischer, Marco Pontoglio, Vera Eremina, Manfred Gessler, Sue E Quaggin, Robert Harrison, Richard Mount, Helen McNeill. Nat Genet 2008
375
100

Frizzled6 controls hair patterning in mice.
Nini Guo, Charles Hawkins, Jeremy Nathans. Proc Natl Acad Sci U S A 2004
209
100


Mutations in different components of FGF signaling in LADD syndrome.
Edyta Rohmann, Han G Brunner, Hülya Kayserili, Oya Uyguner, Gudrun Nürnberg, Erin D Lew, Angus Dobbie, Veraragavan P Eswarakumar, Abdullah Uzumcu, Melike Ulubil-Emeroglu,[...]. Nat Genet 2006
126
100

p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities.
A Yang, M Kaghad, Y Wang, E Gillett, M D Fleming, V Dötsch, N C Andrews, D Caput, F McKeon. Mol Cell 1998
100

Signaling Networks in Epithelial Tube Formation.
Ilenia Bernascone, Mariam Hachimi, Fernando Martin-Belmonte. Cold Spring Harb Perspect Biol 2017
11
100


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.