A citation-based method for searching scientific literature

E Ferda Percin, L A Ploder, J J Yu, K Arici, D J Horsford, A Rutherford, B Bapat, D W Cox, A M Duncan, V I Kalnins, A Kocak-Altintas, J C Sowden, E Traboulsi, M Sarfarazi, R R McInnes. Nat Genet 2000
Times Cited: 209







List of co-cited articles
1027 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
39

Heterozygous mutations of OTX2 cause severe ocular malformations.
Nicola K Ragge, Alison G Brown, Charlotte M Poloschek, Birgit Lorenz, R Alex Henderson, Michael P Clarke, Isabelle Russell-Eggitt, Alistair Fielder, Dianne Gerrelli, Juan Pedro Martinez-Barbera,[...]. Am J Hum Genet 2005
216
36

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
417
33

Mutations in SOX2 cause anophthalmia.
Judy Fantes, Nicola K Ragge, Sally-Ann Lynch, Niolette I McGill, J Richard O Collin, Patricia N Howard-Peebles, Caroline Hayward, Anthony J Vivian, Kathy Williamson, Veronica van Heyningen,[...]. Nat Genet 2003
381
31

National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology.
D Morrison, D FitzPatrick, I Hanson, K Williamson, V van Heyningen, B Fleck, I Jones, J Chalmers, H Campbell. J Med Genet 2002
181
29


Anophthalmia and microphthalmia.
Amit S Verma, David R Fitzpatrick. Orphanet J Rare Dis 2007
221
26

SOX2 anophthalmia syndrome.
Nicola K Ragge, Birgit Lorenz, Adele Schneider, Kate Bushby, Luisa de Sanctis, Ugo de Sanctis, Alison Salt, J Richard O Collin, Anthony J Vivian, Samantha L Free,[...]. Am J Med Genet A 2005
166
22


CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindreds.
Udy Bar-Yosef, Izzeldin Abuelaish, Tamar Harel, Neta Hendler, Rivka Ofir, Ohad S Birk. Hum Genet 2004
54
40

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.
Preeti Bakrania, Maria Efthymiou, Johannes C Klein, Alison Salt, David J Bunyan, Alex Wyatt, Chris P Ponting, Angela Martin, Steven Williams, Victoria Lindley,[...]. Am J Hum Genet 2008
185
20

Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar.
M Faiyaz-Ul-Haque, S H E Zaidi, M S Al-Mureikhi, I Peltekova, L-C Tsui, A S Teebi. Clin Genet 2007
21
80

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
16

Chx10 is required to block photoreceptor differentiation but is dispensable for progenitor proliferation in the postnatal retina.
Izzy Livne-Bar, Marek Pacal, Melissa C Cheung, Mark Hankin, Judy Trogadis, Danian Chen, Kimberley M Dorval, Rod Bremner. Proc Natl Acad Sci U S A 2006
72
22

Eye morphogenesis and patterning of the optic vesicle.
Sabine Fuhrmann. Curr Top Dev Biol 2010
223
16

Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy.
Sibel Ugur Iseri, Alexander W Wyatt, Gudrun Nürnberg, Christian Kluck, Peter Nürnberg, Graham E Holder, Ed Blair, Alison Salt, Nicola K Ragge. Hum Genet 2010
24
66

The Rx homeobox gene is essential for vertebrate eye development.
P H Mathers, A Grinberg, K A Mahon, M Jamrich. Nature 1997
541
15

SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions.
P Bakrania, D O Robinson, D J Bunyan, A Salt, A Martin, J A Crolla, A Wyatt, A Fielder, J Ainsworth, A Moore,[...]. Br J Ophthalmol 2007
81
18

Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma.
Alexander Wyatt, Preeti Bakrania, David J Bunyan, Robert J Osborne, John A Crolla, Alison Salt, Carmen Ayuso, Ruth Newbury-Ecob, Y Abou-Rayyah, J Richard O Collin,[...]. Hum Mutat 2008
78
19

Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans.
Sophie Valleix, Florence Niel, Brigitte Nedelec, Marie-Paule Algros, Claire Schwartz, Bernard Delbosc, Marc Delpech, Bernadette Kantelip. Am J Hum Genet 2006
68
22

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
56
26

GDF6, a novel locus for a spectrum of ocular developmental anomalies.
Mika Asai-Coakwell, Curtis R French, Karyn M Berry, Ming Ye, Ron Koss, Martin Somerville, Rosemary Mueller, Veronica van Heyningen, Andrew J Waskiewicz, Ordan J Lehmann. Am J Hum Genet 2007
80
17

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
144
14

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
14

Mutations of the PAX6 gene detected in patients with a variety of optic-nerve malformations.
Noriyuki Azuma, Yuki Yamaguchi, Hiroshi Handa, Keiko Tadokoro, Atsuko Asaka, Eriko Kawase, Masao Yamada. Am J Hum Genet 2003
174
13

Confirmation of RAX gene involvement in human anophthalmia.
L Lequeux, M Rio, A Vigouroux, M Titeux, H Etchevers, F Malecaze, N Chassaing, P Calvas. Clin Genet 2008
32
40


Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation.
Francesca Pasutto, Heinrich Sticht, Gerhard Hammersen, Gabriele Gillessen-Kaesbach, David R Fitzpatrick, Gudrun Nürnberg, Frank Brasch, Heidemarie Schirmer-Zimmermann, John L Tolmie, David Chitayat,[...]. Am J Hum Genet 2007
250
13

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies.
Ming Ye, Karyn M Berry-Wynne, Mika Asai-Coakwell, Periasamy Sundaresan, Tim Footz, Curtis R French, Marc Abitbol, Valerie C Fleisch, Nathan Corbett, W Ted Allison,[...]. Hum Mol Genet 2010
99
13

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
75
17

Novel SOX2 mutations and genotype-phenotype correlation in anophthalmia and microphthalmia.
Adele Schneider, Tanya Bardakjian, Linda M Reis, Rebecca C Tyler, Elena V Semina. Am J Med Genet A 2009
77
16

VSX2 mutations in autosomal recessive microphthalmia.
Linda M Reis, Ayesha Khan, Ariana Kariminejad, Farhad Ebadi, Rebecca C Tyler, Elena V Semina. Mol Vis 2011
20
65


Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma.
Robyn V Jamieson, Rahat Perveen, Bronwyn Kerr, Martin Carette, Jill Yardley, Elise Heon, M Gabriela Wirth, Veronica van Heyningen, Di Donnai, Francis Munier,[...]. Hum Mol Genet 2002
198
12


Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein.
Olof H Sundin, Gregory S Leppert, Eduardo D Silva, Jun-Ming Yang, Sharola Dharmaraj, Irene H Maumenee, Luisa Coutinho Santos, Cameron F Parsa, Elias I Traboulsi, Karl W Broman,[...]. Proc Natl Acad Sci U S A 2005
127
12

The descriptive epidemiology of anophthalmia and microphthalmia.
B Källén, E Robert, J Harris. Int J Epidemiol 1996
95
12

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
73
16

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
11

Negative regulation of Vsx1 by its paralog Chx10/Vsx2 is conserved in the vertebrate retina.
Anna M Clark, Sanghee Yun, Eric S Veien, Yuan Y Wu, Robert L Chow, Richard I Dorsky, Edward M Levine. Brain Res 2008
48
22

Transcriptional activity of the paired-like homeodomain proteins CHX10 and VSX1.
Kimberley M Dorval, Brian P Bobechko, K Farid Ahmad, Rod Bremner. J Biol Chem 2005
44
25

Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.
David Ng, Nalin Thakker, Connie M Corcoran, Dian Donnai, Rahat Perveen, Adele Schneider, Donald W Hadley, Cynthia Tifft, Liqun Zhang, Andrew O M Wilkie,[...]. Nat Genet 2004
215
11


Pax2 contributes to inner ear patterning and optic nerve trajectory.
M Torres, E Gómez-Pardo, P Gruss. Development 1996
450
10

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Lisenka E L M Vissers, Conny M A van Ravenswaaij, Ronald Admiraal, Jane A Hurst, Bert B A de Vries, Irene M Janssen, Walter A van der Vliet, Erik H L P G Huys, Pieter J de Jong, Ben C J Hamel,[...]. Nat Genet 2004
779
10


Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.
E V Semina, I Brownell, H A Mintz-Hittner, J C Murray, M Jamrich. Hum Mol Genet 2001
146
10

Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.
Sibel Ugur Iseri, Robert J Osborne, Martin Farrall, Alexander William Wyatt, Ghazala Mirza, Gudrun Nürnberg, Christian Kluck, Helen Herbert, Angela Martin, Muhammad Sajid Hussain,[...]. Hum Mutat 2009
65
15

VSX2 in microphthalmia: a novel splice site mutation producing a severe microphthalmia phenotype.
Emma M M Burkitt Wright, Rahat Perveen, Naomi Bowers, Simon Ramsden, Emma McCann, Mary O'Driscoll, I Chris Lloyd, Jill Clayton-Smith, Graeme C M Black. Br J Ophthalmol 2010
13
76

Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2.
A M Hever, K A Williamson, V van Heyningen. Clin Genet 2006
126
10


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.