A citation-based method for searching scientific literature

Florencia Cavodeassi, Sophie Creuzet, Heather C Etchevers. Hum Genet 2019
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies.
Fabiola Ceroni, Domingo Aguilera-Garcia, Nicolas Chassaing, Dorine Arjanne Bax, Fiona Blanco-Kelly, Patricia Ramos, Maria Tarilonte, Cristina Villaverde, Luciana Rodrigues Jacy da Silva, Maria Juliana Ballesta-Martínez,[...]. Hum Genet 2019
20
20

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
20

Identification of PITX3 mutations in individuals with various ocular developmental defects.
Celia Zazo Seco, Julie Plaisancié, Tatiana Lupasco, Caroline Michot, Jacmine Pechmeja, Julian Delanne, Edouard Cottereau, Carmen Ayuso, Marta Corton, Patrick Calvas,[...]. Ophthalmic Genet 2018
11
27

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
376
20

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
20

Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia.
Dominique Brémond-Gignac, Pierre Bitoun, Linda M Reis, Henri Copin, Jeffrey C Murray, Elena V Semina. Mol Vis 2010
38
13

Novel and recurrent PITX3 mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics.
Hannah Verdin, Elena A Sorokina, Françoise Meire, Ingele Casteels, Thomy de Ravel, Elena V Semina, Elfride De Baere. Orphanet J Rare Dis 2014
23
13

Novel mutations in PAX6, OTX2 and NDP in anophthalmia, microphthalmia and coloboma.
Brett Deml, Linda M Reis, Emmanuelle Lemyre, Robin D Clark, Ariana Kariminejad, Elena V Semina. Eur J Hum Genet 2016
44
13

Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies.
Marcello Niceta, Emilia Stellacci, Karen W Gripp, Giuseppe Zampino, Maria Kousi, Massimiliano Anselmi, Alice Traversa, Andrea Ciolfi, Deborah Stabley, Alessandro Bruselles,[...]. Am J Hum Genet 2015
67
13

Peroxidasin is essential for eye development in the mouse.
Xiaohe Yan, Sibylle Sabrautzki, Marion Horsch, Helmut Fuchs, Valerie Gailus-Durner, Johannes Beckers, Martin Hrabě de Angelis, Jochen Graw. Hum Mol Genet 2014
37
13

FOXE3 plays a significant role in autosomal recessive microphthalmia.
Linda M Reis, Rebecca C Tyler, Adele Schneider, Tanya Bardakjian, Joan M Stoler, Serge B Melancon, Elena V Semina. Am J Med Genet A 2010
41
13


Genetic investigation of 93 families with microphthalmia or posterior microphthalmos.
N Patel, A O Khan, S Alsahli, G Abdel-Salam, S R Nowilaty, A M Mansour, A Nabil, M Al-Owain, S Sogati, M A Salih,[...]. Clin Genet 2018
21
13

Novel recessive BFSP2 and PITX3 mutations: insights into mutational mechanisms from consanguineous populations.
Mohammed A Aldahmesh, Arif O Khan, Jawahir Mohamed, Fowzan S Alkuraya. Genet Med 2011
40
13

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
184
13

Eye development genes and known syndromes.
Anne M Slavotinek. Mol Genet Metab 2011
73
13

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
164
13

FOXE3 mutations: genotype-phenotype correlations.
J Plaisancié, N K Ragge, H Dollfus, J Kaplan, D Lehalle, C Francannet, G Morin, H Colineaux, P Calvas, N Chassaing. Clin Genet 2018
14
14

Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma.
Shazia Micheal, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Aftab Iqbal, Muhammad Imran Khan, Anneke I den Hollander. PLoS One 2016
13
15


Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network.
Nicolas Chassaing, Erica E Davis, Kelly L McKnight, Adrienne R Niederriter, Alexandre Causse, Véronique David, Annaïck Desmaison, Sophie Lamarre, Catherine Vincent-Delorme, Laurent Pasquier,[...]. Genome Res 2016
23
13

Epidemiology of anophthalmia and microphthalmia: Prevalence and patterns in Texas, 1999-2009.
Tiffany M Chambers, A J Agopian, Richard A Lewis, Peter H Langlois, Heather E Danysh, Kari A Weber, Gary M Shaw, Laura E Mitchell, Philip J Lupo. Am J Med Genet A 2018
12
16

Novel mutations in PXDN cause microphthalmia and anterior segment dysgenesis.
Alex Choi, Richard Lao, Paul Ling-Fung Tang, Eunice Wan, Wasima Mayer, Tanya Bardakjian, Gary M Shaw, Pui-Yan Kwok, Adele Schneider, Anne Slavotinek. Eur J Hum Genet 2015
23
13

BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning.
G Luo, C Hofmann, A L Bronckers, M Sohocki, A Bradley, G Karsenty. Genes Dev 1995
799
13

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
13

The Rx homeobox gene is essential for vertebrate eye development.
P H Mathers, A Grinberg, K A Mahon, M Jamrich. Nature 1997
534
13


Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing.
Alan S Ma, John R Grigg, Gladys Ho, Ivan Prokudin, Elizabeth Farnsworth, Katherine Holman, Anson Cheng, Frank A Billson, Frank Martin, Clare Fraser,[...]. Hum Mutat 2016
72
13

Eye morphogenesis and patterning of the optic vesicle.
Sabine Fuhrmann. Curr Top Dev Biol 2010
215
13

Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Kamron Khan, Adam Rudkin, David A Parry, Kathryn P Burdon, Martin McKibbin, Clare V Logan, Zakia I A Abdelhamed, James S Muecke, Narcis Fernandez-Fuentes, Kate J Laurie,[...]. Am J Hum Genet 2011
51
13

The genetic architecture of aniridia and Gillespie syndrome.
Hildegard Nikki Hall, Kathleen A Williamson, David R FitzPatrick. Hum Genet 2019
20
13



Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase.
P S Danielian, D Muccino, D H Rowitch, S K Michael, A P McMahon. Curr Biol 1998
999
13

Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis.
Y Chai, X Jiang, Y Ito, P Bringas, J Han, D H Rowitch, P Soriano, A P McMahon, H M Sucov. Development 2000
937
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





WNT/β-Catenin Signaling in Vertebrate Eye Development.
Naoko Fujimura. Front Cell Dev Biol 2016
47
13

Sonic hedgehog mutations are an uncommon cause of developmental eye anomalies.
Preeti Bakrania, Sibel A Ugur Iseri, Alexander W Wyatt, Dave J Bunyan, Wayne W K Lam, Alison Salt, Jacqueline Ramsay, David O Robinson, Nicola K Ragge. Am J Med Genet A 2010
24
13


Indian hedgehog signaling from endothelial cells is required for sclera and retinal pigment epithelium development in the mouse eye.
Gabriel D Dakubo, Chantal Mazerolle, Marosh Furimsky, Chuan Yu, Benoit St-Jacques, Andrew P McMahon, Valerie A Wallace. Dev Biol 2008
32
13

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
13

Genes and molecular pathways underpinning ciliopathies.
Jeremy F Reiter, Michel R Leroux. Nat Rev Mol Cell Biol 2017
497
13

Genetics of anterior segment dysgenesis disorders.
Linda M Reis, Elena V Semina. Curr Opin Ophthalmol 2011
77
13

Co-occurrence of distinct ciliopathy diseases in single families suggests genetic modifiers.
Maha S Zaki, Shifteh Sattar, Rustin A Massoudi, Joseph G Gleeson. Am J Med Genet A 2011
30
13

Hedgehog signaling regulates cell motility and optic fissure and stalk formation during vertebrate eye morphogenesis.
Hannah B Gordon, Sarah Lusk, Keith R Carney, Emily O Wirick, Brooke Froelich Murray, Kristen M Kwan. Development 2018
16
13

Separate and coincident expression of Hes1 and Hes5 in the developing mouse eye.
Amy N Riesenberg, Kevin W Conley, Tien T Le, Nadean L Brown. Dev Dyn 2018
10
20


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.