A citation-based method for searching scientific literature


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
50

[Nasolacrimal ducts and the dry eye].
F Paulsen, A Thale, U Schaudig. Ophthalmologe 2002
13
50


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
50

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
50

Identifying an appropriate animal model for the nasolacrimal drainage system.
Nicholas J Frame, Cat Nguyen Burkat. Ophthalmic Plast Reconstr Surg 2009
11
50

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
50

The Wnt signaling pathway in development and disease.
Catriona Y Logan, Roel Nusse. Annu Rev Cell Dev Biol 2004
50


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
50


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
50

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
50


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
25
50

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
25
50

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
50

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
50


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
23
50


Hereditary disorders affecting the lacrimal system.
Richard C Allen. Curr Opin Ophthalmol 2014
6
50

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
27
50

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
50

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
80
50

Endoscopic-assisted probing for congenital nasolacrimal duct obstruction.
E J Wallace, A Cox, P White, C J Macewen. Eye (Lond) 2006
34
50

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
50

Prickle1 stunts limb growth through alteration of cell polarity and gene expression.
Tian Yang, Alexander G Bassuk, Bernd Fritzsch. Dev Dyn 2013
20
50

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
50

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
50

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
50

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
215
50

Ocular surface pathogenesis associated with precocious eyelid opening and necrotic autologous tissue in mouse with disruption of Prickle 1 gene.
Dianlei Guo, Mengke Li, Bin Zou, Xinyu Gu, Zhaohui Yuan, Michael Liu, Fuxiang Mao, Hong Ouyang, Kaili Wu, Lai Wei,[...]. Exp Eye Res 2019
1
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
50


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
372
50

Frizzled6 controls hair patterning in mice.
Nini Guo, Charles Hawkins, Jeremy Nathans. Proc Natl Acad Sci U S A 2004
208
50


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
125
50

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
50

Signaling Networks in Epithelial Tube Formation.
Ilenia Bernascone, Mariam Hachimi, Fernando Martin-Belmonte. Cold Spring Harb Perspect Biol 2017
9
50

Validation of digital pathology imaging for primary histopathological diagnosis.
David R J Snead, Yee-Wah Tsang, Aisha Meskiri, Peter K Kimani, Richard Crossman, Nasir M Rajpoot, Elaine Blessing, Klaus Chen, Kishore Gopalakrishnan, Paul Matthews,[...]. Histopathology 2016
95
50

Genetic dissection of retinal inputs to brainstem nuclei controlling image stabilization.
Onkar S Dhande, Maureen E Estevez, Lauren E Quattrochi, Rana N El-Danaf, Phong L Nguyen, David M Berson, Andrew D Huberman. J Neurosci 2013
97
50

Orbital fibrosis in a mouse model of Graves' disease induced by genetic immunization of thyrotropin receptor cDNA.
Shuang-Xia Zhao, Shanli Tsui, Anthony Cheung, Raymond S Douglas, Terry J Smith, J Paul Banga. J Endocrinol 2011
48
50


Understanding the retinal basis of vision across species.
Tom Baden, Thomas Euler, Philipp Berens. Nat Rev Neurosci 2020
37
50

Hematoxylin and eosin staining of intact tissues via delipidation and ultrasound.
Yawu Li, Ning Li, Xiang Yu, Kai Huang, Ting Zheng, Xiaofeng Cheng, Shaoqun Zeng, Xiuli Liu. Sci Rep 2018
8
50


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.