A citation-based method for searching scientific literature

Patricia A Gongal, Curtis R French, Andrew J Waskiewicz. Biochim Biophys Acta 2011
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


Midline signalling is required for Pax gene regulation and patterning of the eyes.
R Macdonald, K A Barth, Q Xu, N Holder, I Mikkola, S W Wilson. Development 1995
359
47

Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia.
Lisa A Schimmenti, June de la Cruz, Richard Alan Lewis, J D Karkera, Glenda S Manligas, Erich Roessler, Maximilian Muenke. Am J Med Genet A 2003
112
35

Patterning activities of vertebrate hedgehog proteins in the developing eye and brain.
S C Ekker, A R Ungar, P Greenstein, D P von Kessler, J A Porter, R T Moon, P A Beachy. Curr Biol 1995
470
35

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
365
29

Hedgehog signalling maintains the optic stalk-retinal interface through the regulation of Vax gene activity.
Masaya Take-uchi, Jonathan D W Clarke, Stephen W Wilson. Development 2003
123
29

Stages of embryonic development of the zebrafish.
C B Kimmel, W W Ballard, S R Kimmel, B Ullmann, T F Schilling. Dev Dyn 1995
29


The Pax protein Noi is required for commissural axon pathway formation in the rostral forebrain.
R Macdonald, J Scholes, U Strähle, C Brennan, N Holder, M Brand, S W Wilson. Development 1997
143
23

The eye organizes neural crest cell migration.
Tobias Langenberg, Alon Kahana, Joseph A Wszalek, Mary C Halloran. Dev Dyn 2008
59
23

Impairing retinoic acid signalling in the neural crest cells is sufficient to alter entire eye morphogenesis.
Nicolas Matt, Norbert B Ghyselinck, Isabelle Pellerin, Valérie Dupé. Dev Biol 2008
73
23

A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrum.
Daniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, Joan Z Balog, Donald W Hadley, Wadih M Zein, Casey K Hadsall, Brian P Brooks, Maximilian Muenke. Am J Med Genet A 2011
26
23

Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.
L Y Brown, S Odent, V David, M Blayau, C Dubourg, C Apacik, M A Delgado, B D Hall, J F Reynolds, A Sommer,[...]. Hum Mol Genet 2001
138
23

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
L Nanni, J E Ming, M Bocian, K Steinhaus, D W Bianchi, C Die-Smulders, A Giannotti, K Imaizumi, K L Jones, M D Campo,[...]. Hum Mol Genet 1999
259
23

Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation.
Jin S Hahn, Patrick D Barnes. Am J Med Genet C Semin Med Genet 2010
93
23

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
843
23

Sox11 is required to maintain proper levels of Hedgehog signaling during vertebrate ocular morphogenesis.
Lakshmi Pillai-Kastoori, Wen Wen, Stephen G Wilson, Erin Strachan, Adriana Lo-Castro, Marco Fichera, Sebastiano A Musumeci, Ordan J Lehmann, Ann C Morris. PLoS Genet 2014
31
23

Ocular coloboma: a reassessment in the age of molecular neuroscience.
C Y Gregory-Evans, M J Williams, S Halford, K Gregory-Evans. J Med Genet 2004
147
23

Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibres and eye coloboma.
Anna Maria Barbieri, Vania Broccoli, Paola Bovolenta, Giovanna Alfano, Anna Marchitiello, Cristina Mocchetti, Luca Crippa, Alessandro Bulfone, Valeria Marigo, Andrea Ballabio,[...]. Development 2002
104
23

Retinoic acid is necessary for development of the ventral retina in zebrafish.
N Marsh-Armstrong, P McCaffery, W Gilbert, J E Dowling, U C Dräger. Proc Natl Acad Sci U S A 1994
158
17

Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes.
Mika Asai-Coakwell, Curtis R French, Ming Ye, Kamal Garcha, Karin Bigot, Anoja G Perera, Karen Staehling-Hampton, Silvina C Mema, Bhaskar Chanda, Arcady Mushegian,[...]. Hum Mol Genet 2009
74
17

The Rx homeobox gene is essential for vertebrate eye development.
P H Mathers, A Grinberg, K A Mahon, M Jamrich. Nature 1997
534
17

Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea.
Vera A Voronina, Elena A Kozhemyakina, Christina M O'Kernick, Natan D Kahn, Sharon L Wenger, John V Linberg, Adele S Schneider, Peter H Mathers. Hum Mol Genet 2004
149
17

Retinoic acid receptor signaling regulates choroid fissure closure through independent mechanisms in the ventral optic cup and periocular mesenchyme.
Giuseppe Lupo, Gaia Gestri, Matthew O'Brien, Ross M Denton, Roshantha A S Chandraratna, Steven V Ley, William A Harris, Stephen W Wilson. Proc Natl Acad Sci U S A 2011
57
17

Neurogenesis in the fish retina.
Deborah L Stenkamp. Int Rev Cytol 2007
85
17

Uveal coloboma: clinical and basic science update.
Lan Chang, Delphine Blain, Stefano Bertuzzi, Brian P Brooks. Curr Opin Ophthalmol 2006
83
17


Eye development genes and known syndromes.
Anne M Slavotinek. Mol Genet Metab 2011
73
17


Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
Benjamin D Solomon, Felicitas Lacbawan, Sandra Mercier, Nancy J Clegg, Mauricio R Delgado, Kenneth Rosenbaum, Christèle Dubourg, Veronique David, Ann Haskins Olney, Lars-Erik Wehner,[...]. J Med Genet 2010
57
17

Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation.
Nicholas Warr, Nicola Powles-Glover, Anna Chappell, Joan Robson, Dominic Norris, Ruth M Arkell. Hum Mol Genet 2008
68
17

The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism.
Erich Roessler, Felicitas Lacbawan, Christèle Dubourg, Aimee Paulussen, Jos Herbergs, Ute Hehr, Claude Bendavid, Nan Zhou, Maia Ouspenskaia, Sherri Bale,[...]. Hum Mutat 2009
49
17


Holoprosencephaly due to numeric chromosome abnormalities.
Benjamin D Solomon, Kenneth N Rosenbaum, Jeanne M Meck, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
41
17

Regionalization of the prosencephalic neural plate.
J L Rubenstein, K Shimamura, S Martinez, L Puelles. Annu Rev Neurosci 1998
396
17

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
17

Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome.
C A Wassif, C Maslen, S Kachilele-Linjewile, D Lin, L M Linck, W E Connor, R D Steiner, F D Porter. Am J Hum Genet 1998
305
17

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
157
17


The mechanisms of Hedgehog signalling and its roles in development and disease.
James Briscoe, Pascal P Thérond. Nat Rev Mol Cell Biol 2013
979
17

Proper patterning of the optic fissure requires the sequential activity of BMP7 and SHH.
Julian Morcillo, Juan Ramon Martínez-Morales, Françoise Trousse, Yasmin Fermin, Jane C Sowden, Paola Bovolenta. Development 2006
100
17

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
D E Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, G Gillessen-Kaesbach, E H Zackai, J Rommens, M Muenke. Nat Genet 1999
283
17

Fate maps of neural crest and mesoderm in the mammalian eye.
Philip J Gage, William Rhoades, Sandra K Prucka, Tord Hjalt. Invest Ophthalmol Vis Sci 2005
240
17

Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway.
Christèle Dubourg, Wilfrid Carré, Houda Hamdi-Rozé, Charlotte Mouden, Joëlle Roume, Benmansour Abdelmajid, Daniel Amram, Clarisse Baumann, Nicolas Chassaing, Christine Coubes,[...]. Hum Mutat 2016
38
17

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome.
E V Semina, R Reiter, N J Leysens, W L Alward, K W Small, N A Datson, J Siegel-Bartelt, D Bierke-Nelson, P Bitoun, B U Zabel,[...]. Nat Genet 1996
690
17


Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
F Lacbawan, B D Solomon, E Roessler, K El-Jaick, S Domené, J I Vélez, N Zhou, D Hadley, J Z Balog, R Long,[...]. J Med Genet 2009
65
11

Eye development.
Jochen Graw. Curr Top Dev Biol 2010
143
11

Retinoic acid-dependent eye morphogenesis is orchestrated by neural crest cells.
Nicolas Matt, Valérie Dupé, Jean-Marie Garnier, Christine Dennefeld, Pierre Chambon, Manuel Mark, Norbert B Ghyselinck. Development 2005
183
11

Mutations affecting development of the zebrafish retina.
J Malicki, S C Neuhauss, A F Schier, L Solnica-Krezel, D L Stemple, D Y Stainier, S Abdelilah, F Zwartkruis, Z Rangini, W Driever. Development 1996
239
11

A complex regulatory network of transcription factors critical for ocular development and disease.
Moulinath Acharya, Lijia Huang, Valerie C Fleisch, W Ted Allison, Michael A Walter. Hum Mol Genet 2011
33
11


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.