A citation-based method for searching scientific literature

Clarice Pagani Savastano, Kênia Balbi El-Jaick, Marcelo Aguiar Costa-Lima, Cristina Maria Batista Abath, Sebastiano Bianca, Denise Pontes Cavalcanti, Têmis Maria Félix, Gioacchino Scarano, Juan Clinton Llerena, Fernando Regla Vargas, Miguel Ângelo Martins Moreira, Hector N Seuánez, Eduardo Enrique Castilla, Iêda Maria Orioli. Genet Mol Biol 2014
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
301
33

Computed tomography of a cyclotocephalic neonate.
S Louryan, N Vanmuylder, M Rooze. Surg Radiol Anat 2002
4
50

Holoprosencephaly and agnathia spectrum: Presentation of two new patients and review of the literature.
Emily F Kauvar, Benjamin D Solomon, Cynthia J R Curry, Anthonie J van Essen, Nicole Janssen, Amalia Dutra, Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
27
33


OTX2 mutations contribute to the otocephaly-dysgnathia complex.
Nicolas Chassaing, Susanna Sorrentino, Erica E Davis, Dominique Martin-Coignard, Anthony Iacovelli, William Paznekas, Bryn D Webb, Ona Faye-Petersen, Férechté Encha-Razavi, Leopoldine Lequeux,[...]. J Med Genet 2012
39
33

The homeobox gene Otx2 in development and disease.
Francis Beby, Thomas Lamonerie. Exp Eye Res 2013
76
33

Back to the future: museum specimens in population genetics.
Peter Wandeler, Paquita E A Hoeck, Lukas F Keller. Trends Ecol Evol 2007
230
16

The mammalian twisted gastrulation gene functions in foregut and craniofacial development.
Anna Petryk, Ryan M Anderson, Michael P Jarcho, Irina Leaf, Cathy S Carlson, John Klingensmith, William Shawlot, Michael B O'Connor. Dev Biol 2004
87
16

Agnathia-otocephaly complex: a case report and examination of the OTX2 and PRRX1 genes.
Sean Herman, Maria Delio, Bernice Morrow, Joy Samanich. Gene 2012
16
16

Familial agnathia-holoprosencephaly.
R M Pauli, J C Pettersen, S Arya, E F Gilbert. Am J Med Genet 1983
75
16


Genomics and museum specimens.
Michael W Nachman. Mol Ecol 2013
11
16

PRRX1 is mutated in a fetus with agnathia-otocephaly.
C Sergi, D Kamnasaran. Clin Genet 2011
26
16

Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects.
Jennifer F Dennis, Hiroshi Kurosaka, Angelo Iulianella, Jennifer Pace, Nancy Thomas, Sharon Beckham, Trevor Williams, Paul A Trainor. PLoS Genet 2012
41
16

DNA damage in preserved specimens and tissue samples: a molecular assessment.
Juergen Zimmermann, Mehrdad Hajibabaei, David C Blackburn, James Hanken, Elizabeth Cantin, Janos Posfai, Thomas C Evans. Front Zool 2008
73
16

Current perspectives on the etiology of agnathia-otocephaly.
Jean Gekas, Bin Li, Deepak Kamnasaran. Eur J Med Genet 2010
36
16

Mouse Otx2 functions in the formation and patterning of rostral head.
I Matsuo, S Kuratani, C Kimura, N Takeda, S Aizawa. Genes Dev 1995
553
16


Functional anatomy of the premaxillary area.
H C Hafkamp, T D Bruintjes, E H Huizing. Rhinology 1999
2
50


Congenital nasal pyriform aperture stenosis.
O E Brown, C M Myer, S C Manning. Laryngoscope 1989
133
16

Osteogenesis of the human upper jaw: proof of the non-existence of a separate premaxillary centre.
N K Wood, L E Wragg, O H Stuteville, R J Oglesby. Arch Oral Biol 1969
28
16


Vomero-premaxillary joint: A marker of evolution of the species.
S Botti, C Rumeau, P Gallet, R Jankowski. Eur Ann Otorhinolaryngol Head Neck Dis 2017
6
16

Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes.
Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Wen Pan, Wayseen Wang. Gene 2013
13
16

The human incisal suture and premaxillary area studied on archaeologic material.
B Sejrsen, I Kjaer, J Jakobsen. Acta Odontol Scand 1993
14
16


[The growth of the maxilla in humans. What place for the premaxilla?].
C Vacher, J P Onolfo, J P Lézy, H Copin. Rev Stomatol Chir Maxillofac 2001
6
16

Relationship of premaxillary bone and its sutures to deciduous dentition in nonhuman primates.
K A Carmody, M P Mooney, G M Cooper, C J Bonar, M I Siegel, E R Dumont, T D Smith. Cleft Palate Craniofac J 2008
6
16

The Fate of the Human Premaxilla.
F Wood-Jones. J Anat 1938
1
100

A re-evaluation of the premaxillary bone in humans.
K Barteczko, M Jacob. Anat Embryol (Berl) 2004
33
16

Cleft lip, cleft palate, and other fusion disorders.
N R Pashley, C J Krause. Otolaryngol Clin North Am 1981
3
33


Dental and skeletal maturity- a biological indicator of chronologic age.
Vivek Rai, Sonali Saha, Gunjan Yadav, Abhay Mani Tripathi, Kavita Grover. J Clin Diagn Res 2014
10
16

Assessment of congenital bony nasal obstruction by 3-dimensional CT volume rendering.
R A Faust, C D Phillips. Int J Pediatr Otorhinolaryngol 2001
16
16





Location of alveolar clefts relative to the incisive fissure.
J A Lisson, I Kjaer. Cleft Palate Craniofac J 1997
21
16

[Growth and development of the maxillary complex].
A Björk, V Skieller. Inf Orthod Kieferorthop 1984
9
16

A computer-based assessment of structural and displacement asymmetries of the mandible.
W Schmid, F Mongini, A Felisio. Am J Orthod Dentofacial Orthop 1991
59
16


Magnetic versus mechanical expansion with different force thresholds and points of force application.
A D Vardimon, T M Graber, L R Voss, E Verrusio. Am J Orthod Dentofacial Orthop 1987
43
16

Cancer risks attributable to low doses of ionizing radiation: assessing what we really know.
David J Brenner, Richard Doll, Dudley T Goodhead, Eric J Hall, Charles E Land, John B Little, Jay H Lubin, Dale L Preston, R Julian Preston, Jerome S Puskin,[...]. Proc Natl Acad Sci U S A 2003
16

Congenital nasal pyriform aperture stenosis.
José V Tagliarini, Victor Nakajima, Emanuel C Castilho. Braz J Otorhinolaryngol 2005
6
16

[Anthropological and anatomical characteristics of the bony palate].
D Kadanoff, S Mutafov, J Jordanov. Gegenbaurs Morphol Jahrb 1969
1
100

More on premaxillary-maxillary suture.
T J Spahl. Am J Orthod Dentofacial Orthop 1991
2
50



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.