A citation-based method for searching scientific literature

Cruz Morenilla-Palao, María Teresa López-Cascales, José P López-Atalaya, Diana Baeza, Luís Calvo-Díaz, Angel Barco, Eloísa Herrera. Sci Adv 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Zic2 patterns binocular vision by specifying the uncrossed retinal projection.
Eloísa Herrera, Lucia Brown, Jun Aruga, Rivka A Rachel, Gül Dolen, Katsuhiko Mikoshiba, Stephen Brown, Carol A Mason. Cell 2003
182
66

Biallelic UFM1 and UFC1 mutations expand the essential role of ufmylation in brain development.
Michael S Nahorski, Sateesh Maddirevula, Ryosuke Ishimura, Saud Alsahli, Angela F Brady, Anaïs Begemann, Tsunehiro Mizushima, Francisco J Guzmán-Vega, Miki Obata, Yoshinobu Ichimura,[...]. Brain 2018
32
33

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
33

Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation.
Alex R Paciorkowski, Judy Weisenberg, Joshua B Kelley, Adam Spencer, Emily Tuttle, Dalia Ghoneim, Liu Lin Thio, Susan L Christian, William B Dobyns, Bryce M Paschal. Eur J Hum Genet 2014
18
33

Phenotype and genotype in 17 patients with Goltz-Gorlin syndrome.
S M Maas, M P Lombardi, A J van Essen, E L Wakeling, B Castle, I K Temple, V K A Kumar, K Writzl, Raoul C M Hennekam. J Med Genet 2009
50
33

Hemorrhagic stroke and renovascular hypertension with Grange syndrome arising from a novel pathogenic variant in YY1AP1.
Ken Saida, Chong Ae Kim, José Ricardo Magliocco Ceroni, Debora Romeo Bertola, Rachel Sayuri Honjo, Satomi Mitsuhashi, Atsushi Takata, Takeshi Mizuguchi, Satoko Miyatake, Noriko Miyake,[...]. J Hum Genet 2019
5
33

Effect of inbreeding on intellectual disability revisited by trio sequencing.
Kimia Kahrizi, Hao Hu, Masoumeh Hosseini, Vera M Kalscheuer, Zohreh Fattahi, Maryam Beheshtian, Vanessa Suckow, Marzieh Mohseni, Bettina Lipkowitz, Sepideh Mehvari,[...]. Clin Genet 2019
26
33

WLS-dependent secretion of WNT3A requires Ser209 acylation and vacuolar acidification.
Gary S Coombs, Jia Yu, Claire A Canning, Charles A Veltri, Tracy M Covey, Jit K Cheong, Velani Utomo, Nikhil Banerjee, Zong Hong Zhang, Raquel C Jadulco,[...]. J Cell Sci 2010
133
33

Small molecule-mediated disruption of Wnt-dependent signaling in tissue regeneration and cancer.
Baozhi Chen, Michael E Dodge, Wei Tang, Jianming Lu, Zhiqiang Ma, Chih-Wei Fan, Shuguang Wei, Wayne Hao, Jessica Kilgore, Noelle S Williams,[...]. Nat Chem Biol 2009
33

Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum.
Roser Urreizti, Estrella Lopez-Martin, Antonio Martinez-Monseny, Montse Pujadas, Laura Castilla-Vallmanya, Luis Alberto Pérez-Jurado, Mercedes Serrano, Daniel Natera-de Benito, Beatriz Martínez-Delgado, Manuel Posada-de-la-Paz,[...]. Orphanet J Rare Dis 2020
7
33




Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.
Eric M Scott, Anason Halees, Yuval Itan, Emily G Spencer, Yupeng He, Mostafa Abdellateef Azab, Stacey B Gabriel, Aziz Belkadi, Bertrand Boisson, Laurent Abel,[...]. Nat Genet 2016
160
33

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, Nabil Moghrabi, Rafiullah Rafiullah, Naif Almontashiri, Mohammed Alowain, Hamad Alzaidan, Moeen Alsayed, Shazia Subhani,[...]. Am J Hum Genet 2019
15
33

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
33

Focal dermal hypoplasia syndrome. An update.
R W Goltz. Arch Dermatol 1992
94
33

Identification of pathogenic YY1AP1 splice variants in siblings with Grange syndrome by whole exome sequencing.
Matthias Rath, Stefanie Spiegler, Tim M Strom, Johannes Trenkler, Peter Michael Kroisel, Ute Felbor. Am J Med Genet A 2019
3
33

Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis.
Carol-Anne Martin, Jennie E Murray, Paula Carroll, Andrea Leitch, Karen J Mackenzie, Mihail Halachev, Ahmed E Fetit, Charlotte Keith, Louise S Bicknell, Adeline Fluteau,[...]. Genes Dev 2016
60
33

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
33

Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease.
Dong-Chuan Guo, Xue-Yan Duan, Ellen S Regalado, Lauren Mellor-Crummey, Callie S Kwartler, Dong Kim, Kenneth Lieberman, Bert B A de Vries, Rolph Pfundt, Albert Schinzel,[...]. Am J Hum Genet 2017
31
33


Goltz-Gorlin Syndrome: Revisiting the Clinical Spectrum.
Dhanya Yesodharan, Uta Meyer Zum Büschenfelde, Kerstin Kutsche, K Mohandas Nair, Sheela Nampoothiri. Indian J Pediatr 2018
1
100

VarAFT: a variant annotation and filtration system for human next generation sequencing data.
Jean-Pierre Desvignes, Marc Bartoli, Valérie Delague, Martin Krahn, Morgane Miltgen, Christophe Béroud, David Salgado. Nucleic Acids Res 2018
62
33


Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling.
Erich Roessler, Ping Hu, Juliana Marino, Sungkook Hong, Rachel Hart, Seth Berger, Ariel Martinez, Yu Abe, Paul Kruszka, James W Thomas,[...]. Hum Mutat 2018
16
33

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
33

Post-translational palmitoylation and glycosylation of Wnt-5a are necessary for its signalling.
Manabu Kurayoshi, Hideki Yamamoto, Shunsuke Izumi, Akira Kikuchi. Biochem J 2007
159
33

PORCN mutations in focal dermal hypoplasia: coping with lethality.
Dorothea Bornholdt, Frank Oeffner, Arne König, Rudolf Happle, Yasemin Alanay, Jeffrey Ascherman, Paul J Benke, María del Carmen Boente, Ineke van der Burgt, Nicolas Chassaing,[...]. Hum Mutat 2009
52
33

Zic2 regulates the kinetics of neurulation.
T Nagai, J Aruga, O Minowa, T Sugimoto, Y Ohno, T Noda, K Mikoshiba. Proc Natl Acad Sci U S A 2000
179
33

Transcription factor Zic2 inhibits Wnt/β-catenin protein signaling.
Rasoul Pourebrahim, Rob Houtmeyers, Stephen Ghogomu, Sylvie Janssens, Aurore Thelie, Hong Thi Tran, Tobias Langenberg, Kris Vleminckx, Eric Bellefroid, Jean-Jacques Cassiman,[...]. J Biol Chem 2011
61
33

Single-Cell Analysis of Human Retina Identifies Evolutionarily Conserved and Species-Specific Mechanisms Controlling Development.
Yufeng Lu, Fion Shiau, Wenyang Yi, Suying Lu, Qian Wu, Joel D Pearson, Alyssa Kallman, Suijuan Zhong, Thanh Hoang, Zhentao Zuo,[...]. Dev Cell 2020
42
33




Recurrent DCC gene losses during bird evolution.
François Friocourt, Anne-Gaelle Lafont, Clémence Kress, Bertrand Pain, Marie Manceau, Sylvie Dufour, Alain Chédotal. Sci Rep 2017
13
33

Massive increase in visual range preceded the origin of terrestrial vertebrates.
Malcolm A MacIver, Lars Schmitz, Ugurcan Mugan, Todd D Murphey, Curtis D Mobley. Proc Natl Acad Sci U S A 2017
31
33

Overlapping visual fields and ipsilateral retinal projections in turtles.
S Hergueta, R Ward, M Lemire, J P Rio, J Reperant, C Weidner. Brain Res Bull 1992
10
33

Spatiotemporal expression patterns of slit and robo genes in the rat brain.
Valérie Marillat, Oliver Cases, Kim Tuyen Nguyen-Ba-Charvet, Marc Tessier-Lavigne, Constantino Sotelo, Alain Chédotal. J Comp Neurol 2002
204
33


The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons.
Ingo Braasch, Andrew R Gehrke, Jeramiah J Smith, Kazuhiko Kawasaki, Tereza Manousaki, Jeremy Pasquier, Angel Amores, Thomas Desvignes, Peter Batzel, Julian Catchen,[...]. Nat Genet 2016
287
33


Single-cell transcriptional logic of cell-fate specification and axon guidance in early-born retinal neurons.
Quentin Lo Giudice, Marion Leleu, Gioele La Manno, Pierre J Fabre. Development 2019
21
33

Signaling switch of the axon guidance receptor Robo3 during vertebrate evolution.
Pavol Zelina, Heike Blockus, Yvrick Zagar, Amélie Péres, François Friocourt, Zhuhao Wu, Nicolas Rama, Coralie Fouquet, Erhard Hohenester, Marc Tessier-Lavigne,[...]. Neuron 2014
95
33

Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype.
Olivier Jaillon, Jean-Marc Aury, Frédéric Brunet, Jean-Louis Petit, Nicole Stange-Thomann, Evan Mauceli, Laurence Bouneau, Cécile Fischer, Catherine Ozouf-Costaz, Alain Bernot,[...]. Nature 2004
33

Three-dimensional evaluation of retinal ganglion cell axon regeneration and pathfinding in whole mouse tissue after injury.
Xueting Luo, Yadira Salgueiro, Samuel R Beckerman, Vance P Lemmon, Pantelis Tsoulfas, Kevin K Park. Exp Neurol 2013
88
33

SoxC Transcription Factors Promote Contralateral Retinal Ganglion Cell Differentiation and Axon Guidance in the Mouse Visual System.
Takaaki Kuwajima, Célia A Soares, Austen A Sitko, Véronique Lefebvre, Carol Mason. Neuron 2017
41
33


The genetic factors of bilaterian evolution.
Peter Heger, Wen Zheng, Anna Rottmann, Kristen A Panfilio, Thomas Wiehe. Elife 2020
6
33



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.