A citation-based method for searching scientific literature

J L Zagozewski, Q Zhang, D D Eisenstat. Clin Genet 2014
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


Specification of the vertebrate eye by a network of eye field transcription factors.
Michael E Zuber, Gaia Gestri, Andrea S Viczian, Giuseppina Barsacchi, William A Harris. Development 2003
336
22

An eye on eye development.
Rebecca Sinn, Joachim Wittbrodt. Mech Dev 2013
67
18

Early eye development in vertebrates.
R L Chow, R A Lang. Annu Rev Cell Dev Biol 2001
443
18

The genetic architecture of microphthalmia, anophthalmia and coloboma.
Kathleen A Williamson, David R FitzPatrick. Eur J Med Genet 2014
134
18

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
18

The Rx homeobox gene is essential for vertebrate eye development.
P H Mathers, A Grinberg, K A Mahon, M Jamrich. Nature 1997
534
18

Pax6 is required for the multipotent state of retinal progenitor cells.
T Marquardt, R Ashery-Padan, N Andrejewski, R Scardigli, F Guillemot, P Gruss. Cell 2001
672
18

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
18

Intrinsic control of mammalian retinogenesis.
Mengqing Xiang. Cell Mol Life Sci 2013
57
18

Eye morphogenesis and patterning of the optic vesicle.
Sabine Fuhrmann. Curr Top Dev Biol 2010
215
18

Eye development and retinogenesis.
Whitney Heavner, Larysa Pevny. Cold Spring Harb Perspect Biol 2012
111
13

Lhx2 links the intrinsic and extrinsic factors that control optic cup formation.
Sanghee Yun, Yukio Saijoh, Karla E Hirokawa, Daniel Kopinke, L Charles Murtaugh, Edwin S Monuki, Edward M Levine. Development 2009
62
13

Regulation of vertebrate eye development by Rx genes.
Travis J Bailey, Heithem El-Hodiri, Li Zhang, Rina Shah, Peter H Mathers, Milan Jamrich. Int J Dev Biol 2004
127
13

Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.
Joe Rainger, Davut Pehlivan, Stefan Johansson, Hemant Bengani, Luis Sanchez-Pulido, Kathleen A Williamson, Mehmet Ture, Heather Barker, Karen Rosendahl, Jürgen Spranger,[...]. Am J Hum Genet 2014
57
13


The cellular and molecular mechanisms of vertebrate lens development.
Aleš Cvekl, Ruth Ashery-Padan. Development 2014
108
13

Mouse small eye results from mutations in a paired-like homeobox-containing gene.
R E Hill, J Favor, B L Hogan, C C Ton, G F Saunders, I M Hanson, J Prosser, T Jordan, N D Hastie, V van Heyningen. Nature 1991
13

Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development.
F D Porter, J Drago, Y Xu, S S Cheema, C Wassif, S P Huang, E Lee, A Grinberg, J S Massalas, D Bodine,[...]. Development 1997
353
13

Haploinsufficiency of Six3 fails to activate Sonic hedgehog expression in the ventral forebrain and causes holoprosencephaly.
Xin Geng, Christina Speirs, Oleg Lagutin, Adi Inbal, Wei Liu, Lilianna Solnica-Krezel, Yongsu Jeong, Douglas J Epstein, Guillermo Oliver. Dev Cell 2008
120
13

Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development.
Oleg V Lagutin, Changqi C Zhu, Daisuke Kobayashi, Jacek Topczewski, Kenji Shimamura, Luis Puelles, Helen R C Russell, Peter J McKinnon, Lilianna Solnica-Krezel, Guillermo Oliver. Genes Dev 2003
339
13

Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia.
N Chassaing, A Causse, A Vigouroux, A Delahaye, J-L Alessandri, O Boespflug-Tanguy, O Boute-Benejean, H Dollfus, B Duban-Bedu, B Gilbert-Dussardier,[...]. Clin Genet 2014
71
13

Timing and topography of cell genesis in the rat retina.
David H Rapaport, Lily L Wong, Eric D Wood, Douglas Yasumura, Matthew M LaVail. J Comp Neurol 2004
266
13

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation.
M Burmeister, J Novak, M Y Liang, S Basu, L Ploder, N L Hawes, D Vidgen, F Hoover, D Goldman, V I Kalnins,[...]. Nat Genet 1996
410
13

Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development.
Akihiro Nishida, Akiko Furukawa, Chieko Koike, Yasuo Tano, Shinichi Aizawa, Isao Matsuo, Takahisa Furukawa. Nat Neurosci 2003
404
13

Mutational screening of CHX10, GDF6, OTX2, RAX and SOX2 genes in 50 unrelated microphthalmia-anophthalmia-coloboma (MAC) spectrum cases.
J Gonzalez-Rodriguez, E L Pelcastre, J L Tovilla-Canales, J E Garcia-Ortiz, M Amato-Almanza, C Villanueva-Mendoza, Z Espinosa-Mattar, J C Zenteno. Br J Ophthalmol 2010
54
13

Math5 is required for retinal ganglion cell and optic nerve formation.
N L Brown, S Patel, J Brzezinski, T Glaser. Development 2001
363
13

From progenitors to differentiated cells in the vertebrate retina.
Michalis Agathocleous, William A Harris. Annu Rev Cell Dev Biol 2009
172
13

Vertebrate neural cell-fate determination: lessons from the retina.
F J Livesey, C L Cepko. Nat Rev Neurosci 2001
692
13

Foxn4 controls the genesis of amacrine and horizontal cells by retinal progenitors.
Shengguo Li, Zeqian Mo, Xuejie Yang, Sandy M Price, Michael M Shen, Mengqing Xiang. Neuron 2004
178
13

Developmental eye disorders.
David R Fitzpatrick, Veronica van Heyningen. Curr Opin Genet Dev 2005
66
13

Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina.
Anand Swaroop, Douglas Kim, Douglas Forrest. Nat Rev Neurosci 2010
329
13

Generation of three-dimensional retinal tissue with functional photoreceptors from human iPSCs.
Xiufeng Zhong, Christian Gutierrez, Tian Xue, Christopher Hampton, M Natalia Vergara, Li-Hui Cao, Ann Peters, Tea Soon Park, Elias T Zambidis, Jason S Meyer,[...]. Nat Commun 2014
427
13


Math5 is required for both early retinal neuron differentiation and cell cycle progression.
Tien T Le, Emily Wroblewski, Sima Patel, Amy N Riesenberg, Nadean L Brown. Dev Biol 2006
79
13

The role of homeobox genes in retinal development and disease.
Jamie L Zagozewski, Qi Zhang, Vanessa I Pinto, Jeffrey T Wigle, David D Eisenstat. Dev Biol 2014
31
13

Anophthalmos, microphthalmos, and typical coloboma in the United Kingdom: a prospective study of incidence and risk.
Shaheen P Shah, Amy E Taylor, Jane C Sowden, Nicola K Ragge, Isabelle Russell-Eggitt, Jugnoo S Rahi, Clare E Gilbert. Invest Ophthalmol Vis Sci 2011
63
13

Organoid technology for retinal repair.
Sílvia Llonch, Madalena Carido, Marius Ader. Dev Biol 2018
73
13

Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia.
J Plaisancié, F Ceroni, R Holt, C Zazo Seco, P Calvas, N Chassaing, Nicola K Ragge. Hum Genet 2019
24
13

Transdifferentiation of the retina into pigmented cells in ocular retardation mice defines a new function of the homeodomain gene Chx10.
Sheldon Rowan, C-M Amy Chen, Tracy L Young, David E Fisher, Constance L Cepko. Development 2004
120
13

Chx10 repression of Mitf is required for the maintenance of mammalian neuroretinal identity.
D Jonathan Horsford, Minh-Thanh T Nguyen, Grant C Sellar, Rashmi Kothary, Heinz Arnheiter, Roderick R McInnes. Development 2005
142
13

Stimulation of functional neuronal regeneration from Müller glia in adult mice.
Nikolas L Jorstad, Matthew S Wilken, William N Grimes, Stefanie G Wohl, Leah S VandenBosch, Takeshi Yoshimatsu, Rachel O Wong, Fred Rieke, Thomas A Reh. Nature 2017
185
13


New functions for old genes: Pax6 and Mitf in eye pigment biogenesis.
Florencia Cavodeassi, Paola Bovolenta. Pigment Cell Melanoma Res 2014
6
33

Regulation of neuronal diversity in the Xenopus retina by Delta signalling.
R I Dorsky, W S Chang, D H Rapaport, W A Harris. Nature 1997
222
9

Retinal stem cells and regeneration.
Ala Moshiri, Jennie Close, Thomas A Reh. Int J Dev Biol 2004
121
9

Molecular regulation of vertebrate retina cell fate.
Massimiliano Andreazzoli. Birth Defects Res C Embryo Today 2009
30
9

Xrx1 controls proliferation and multipotency of retinal progenitors.
Simona Casarosa, Marcos A Amato, Massimiliano Andreazzoli, Gaia Gestri, Giuseppina Barsacchi, Federico Cremisi. Mol Cell Neurosci 2003
53
9

Early steps in the development of the forebrain.
Stephen W Wilson, Corinne Houart. Dev Cell 2004
301
9

Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.
Kathleen A Williamson, Joe Rainger, James A B Floyd, Morad Ansari, Alison Meynert, Kishan V Aldridge, Jacqueline K Rainger, Carl A Anderson, Anthony T Moore, Matthew E Hurles,[...]. Am J Hum Genet 2014
63
9

A secreted WNT-ligand-binding domain of FZD5 generated by a frameshift mutation causes autosomal dominant coloboma.
Chunqiao Liu, Sonya A Widen, Kathleen A Williamson, Rinki Ratnapriya, Christina Gerth-Kahlert, Joe Rainger, Ramakrishna P Alur, Erin Strachan, Souparnika H Manjunath, Archana Balakrishnan,[...]. Hum Mol Genet 2016
26
9


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.