A citation-based method for searching scientific literature

Ilária C Sgardioli, Elaine Lustosa-Mendes, Ana P Dos Santos, Társis P Vieira, Vera L Gil-da-Silva-Lopes. Cytogenet Genome Res 2018
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Associated anomalies among infants with oral clefts at birth and during a 1-year follow-up.
Monica Rittler, Viviana Cosentino, Jorge S López-Camelo, Jeffrey C Murray, George Wehby, Eduardo E Castilla. Am J Med Genet A 2011
37
100

Speech-Language Disorders in 22q11.2 Deletion Syndrome: Best Practices for Diagnosis and Management.
Cynthia B Solot, Debbie Sell, Anne Mayne, Adriane L Baylis, Christina Persson, Oksana Jackson, Donna M McDonald-McGinn. Am J Speech Lang Pathol 2019
7
100

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.
Satoshi Suzuki, Mary L Marazita, Margaret E Cooper, Nobutomo Miwa, Anne Hing, Astanand Jugessur, Nagato Natsume, Kazuo Shimozato, Naofumi Ohbayashi, Yasushi Suzuki,[...]. Am J Hum Genet 2009
140
100

Associated anomalies in multi-malformed infants with cleft lip and palate: An epidemiologic study of nearly 6 million births in 23 EUROCAT registries.
Elisa Calzolari, Anna Pierini, Gianni Astolfi, Fabrizio Bianchi, Amanda J Neville, Francesca Rivieri. Am J Med Genet A 2007
128
100

Delivering genetic education and genetic counseling for rare diseases in rural Brazil.
A X Acosta, K Abé-Sandes, R Giugliani, A H Bittles. J Genet Couns 2013
8
100

Wound complications after cleft repair in children with Van der Woude syndrome.
Jodi L P Jones, John W Canady, James T Brookes, George L Wehby, Jamie L'Heureux, Brian C Schutte, Jeffrey C Murray, Martine Dunnwald. J Craniofac Surg 2010
34
100

Current concepts in the embryology and genetics of cleft lip and cleft palate.
Mary L Marazita, Mark P Mooney. Clin Plast Surg 2004
74
100

Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
Mirta Basha, Bénédicte Demeer, Nicole Revencu, Raphael Helaers, Stephanie Theys, Sami Bou Saba, Odile Boute, Bernard Devauchelle, Geneviève Francois, Bénédicte Bayet,[...]. J Med Genet 2018
30
100

Fostering international collaboration in birth defects research and prevention: a perspective from the International Clearinghouse for Birth Defects Surveillance and Research.
Lorenzo D Botto, Elisabeth Robert-Gnansia, Csaba Siffel, John Harris, Barry Borman, Pierpaolo Mastroiacovo. Am J Public Health 2006
27
100

Associated malformations in infants with cleft lip and palate: a prospective, population-based study.
Josef Milerad, Ola Larson, Catherina Hagberg, Margareta Ideberg. Pediatrics 1997
143
100

Planning the human variome project: the Spain report.
Jim Kaput, Richard G H Cotton, Lauren Hardman, Michael Watson, Aida I Al Aqeel, Jumana Y Al-Aama, Fahd Al-Mulla, Santos Alonso, Stefan Aretz, Arleen D Auerbach,[...]. Hum Mutat 2009
37
100

CranFlow: An Application for Record-Taking and Management Through the Brazilian Database on Craniofacial Anomalies.
Roberta M Volpe-Aquino, Isabella L Monlleó, Elaine Lustosa-Mendes, Amanda F Mora, Agnes C Fett-Conte, Têmis M Félix, Ana C Xavier, Rita Tonocchi, Erlane M Ribeiro, Rui Pereira,[...]. Birth Defects Res 2018
4
100

8p23.1 Interstitial Deletion in a Patient with Congenital Cardiopathy, Neurobehavioral Disorders, and Minor Signs Suggesting 22q11.2 Deletion Syndrome.
Miriam C Molck, Fabíola P Monteiro, Milena Simioni, Vera L Gil-da-Silva-Lopes. J Dev Behav Pediatr 2015
5
100

A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population.
Tânia Kawasaki de Araujo, Rodrigo Secolin, Têmis Maria Félix, Liliane Todeschini de Souza, Marshall Ítalo Barros Fontes, Isabella Lopes Monlleó, Josiane de Souza, Agnes Cristina Fett-Conte, Erlane Marques Ribeiro, Ana Carolina Xavier,[...]. J Craniomaxillofac Surg 2016
27
100

Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health.
Ilária Cristina Sgardioli, Fabíola Paoli Monteiro, Paulo Fanti, Társis Paiva Vieira, Vera Lúcia Gil-da-Silva-Lopes. Orphanet J Rare Dis 2019
2
100

[Craniofacial anomalies: description and evaluation of treatment under the Brazilian Unified Health System].
Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes. Cad Saude Publica 2006
14
100

Polymorphisms associated with oral clefts as potential susceptibility markers for oral and breast cancer.
Edimilson Martins de Freitas, Renato Assis Machado, Edilmar de Moura Santos, Felipe Rodrigues de Matos, Hébel Cavalcanti Galvão, Priscila Bernardina Miranda Soares, Roseana de Almeida Freitas, Hercílio Martelli-Júnior. Arch Oral Biol 2019
6
100

Global oral health inequalities: challenges in the prevention and management of orofacial clefts and potential solutions.
P A Mossey, W C Shaw, R G Munger, J C Murray, J Murthy, J Little. Adv Dent Res 2011
57
100

A boy with partial dup(18q)/del(18p) due to a maternal pericentric inversion: Genotype-phenotype correlation and risk of recombinant chromosomes based on systematic review of the literature.
Elaine Lustosa-Mendes, Ana Paula Dos Santos, Nilma Lúcia Viguetti-Campos, Társis Paiva Vieira, Vera Lúcia Gil-da-Silva-Lopes. Am J Med Genet A 2017
7
100

Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources.
Sebastian Köhler, Leigh Carmody, Nicole Vasilevsky, Julius O B Jacobsen, Daniel Danis, Jean-Philippe Gourdine, Michael Gargano, Nomi L Harris, Nicolas Matentzoglu, Julie A McMurry,[...]. Nucleic Acids Res 2019
208
100

Implementing the brazilian database on orofacial clefts.
Isabella Lopes Monlleó, Marshall Ítalo Barros Fontes, Erlane Marques Ribeiro, Josiane de Souza, Gabriela Ferraz Leal, Têmis Maria Félix, Agnes Cristina Fett-Conte, Bruna Henrique Bueno, Luis Alberto Magna, Peter Anthony Mossey,[...]. Plast Surg Int 2013
9
100


Neonatal care of infants with cleft lip and/or palate: feeding orientation and evolution of weight gain in a nonspecialized Brazilian hospital.
Lívia Gobby Amstalden-Mendes, Luis Alberto Magna, Vera Lúcia Gil-da-Silva-Lopes. Cleft Palate Craniofac J 2007
23
100

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.
K Osoegawa, G M Vessere, K H Utami, M A Mansilla, M K Johnson, B M Riley, J L'Heureux, R Pfundt, J Staaf, W A van der Vliet,[...]. J Med Genet 2008
70
100

Association of bone morphogenetic protein 4 gene polymorphisms with nonsyndromic cleft lip with or without cleft palate in Chinese children.
Jian-Yan Lin, Yong-Juan Chen, Yuan-lu Huang, Guang-Peng Tang, Li Zhang, Bing Deng, Ming Li, Hong Ma, Rong-Sheng Luan. DNA Cell Biol 2008
36
100

Brazil's Craniofacial Project: genetic evaluation and counseling in the Reference Network for Craniofacial Treatment.
Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes. Cleft Palate Craniofac J 2006
14
100

Genotype-phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literature.
Marshall I B Fontes, Ana P Santos, Miriam C Molck, Milena Simioni, Diogo L L Nascimento, Ana K M Andrade, Carla Rosenberg, Ana C V Krepischi, Simone Appenzeller, Isabella L Monlleó,[...]. Am J Med Genet A 2016
4
100

Genetic services and testing in Brazil.
Dafne Dain Gandelman Horovitz, Victor Evangelista de Faria Ferraz, Sulamis Dain, Antonia Paula Marques-de-Faria. J Community Genet 2013
38
100

Distal 22q11.2 microduplication combined with typical 22q11.2 proximal deletion: a case report.
Miriam Coelho Molck, Társis Paiva Vieira, Milena Simioni, Ilária Cristina Sgardioli, Ana Paula dos Santos, Ana Carolina Xavier, Vera Lúcia Gil-da-Silva-Lopes. Am J Med Genet A 2015
5
100

22q11.2 Deletion Syndrome: Laboratory Diagnosis and TBX1 and FGF8 Mutation Screening.
Ilária C Sgardioli, Társis P Vieira, Milena Simioni, Fabíola P Monteiro, Vera L Gil-da-Silva-Lopes. J Pediatr Genet 2015
7
100

Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.
Fabíola P Monteiro, Társis P Vieira, Ilária C Sgardioli, Miriam C Molck, Ana Paula Damiano, Josiane Souza, Isabella L Monlleó, Marshall I B Fontes, Agnes C Fett-Conte, Têmis M Félix,[...]. Eur J Pediatr 2013
35
100

An epidemiologic study of orofacial clefts with other birth defects in Victoria, Australia.
Linda D Vallino-Napoli, Merilyn M Riley, Jane L Halliday. Cleft Palate Craniofac J 2006
30
100

A New Case of the Rare 10q22.3q23.2 Microdeletion Flanked by Low-Copy Repeats 3/4.
Miriam Coelho Molck, Milena Simioni, Társis Paiva Vieira, Fabíola Paoli Monteiro, Vera L Gil-da-Silva-Lopes. Mol Syndromol 2017
2
100

17p13.3 Microdeletion: Insights on Genotype-Phenotype Correlation.
Marshall I Barros Fontes, Ana P Dos Santos, Fábio Rossi Torres, Iscia Lopes-Cendes, Fernando Cendes, Simone Appenzeller, Tânia Kawasaki de Araujo, Isabella Lopes Monlleó, Vera L Gil-da-Silva-Lopes. Mol Syndromol 2017
8
100

Diagnostic Approach to Microdeletion Syndromes Based on 22q11.2 Investigation: Challenges in Four Cases.
Ilária C Sgardioli, Matheus de Mello Copelli, Fabíola P Monteiro, Ana P Dos Santos, Elaine Lustosa Mendes, Társis Paiva Vieira, Vera L Gil-da-Silva-Lopes. Mol Syndromol 2017
4
100

Study of IRF6 and 8q24 region in non-syndromic oral clefts in the Brazilian population.
L T de Souza, T W Kowalski, J Ferrari, I L Monlléo, E M Ribeiro, J de Souza, A C Fett-Conte, T K de Araujo, V L Gil-da-Silva-Lopes, Â K C Ribeiro-Dos-Santos,[...]. Oral Dis 2016
9
100

A 35-year experience with syndromic cleft palate repair: operative outcomes and long-term speech function.
Marten N Basta, Jason Silvestre, Carrie Stransky, Cynthia Solot, Marilyn Cohen, Donna McDonald-McGinn, Elaine Zackai, Richard Kirschner, David W Low, Peter Randall,[...]. Ann Plast Surg 2014
27
100

Brazil's unified health system: the first 30 years and prospects for the future.
Marcia C Castro, Adriano Massuda, Gisele Almeida, Naercio Aquino Menezes-Filho, Monica Viegas Andrade, Kenya Valéria Micaela de Souza Noronha, Rudi Rocha, James Macinko, Thomas Hone, Renato Tasca,[...]. Lancet 2019
109
100

Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.
George P Patrinos, Jumana Al Aama, Aida Al Aqeel, Fahd Al-Mulla, Joseph Borg, Andrew Devereux, Alex E Felice, Finlay Macrae, Makia J Marafie, Michael B Petersen,[...]. Hum Mutat 2011
15
100

Disease-specific databases: why we need them and some recommendations from the Human Variome Project Meeting, May 28, 2011.
Heather J Howard, Arthur Beaudet, Vera Gil-da-Silva Lopes, Mike Lyne, Graeme Suthers, Peter Van den Akker, Katarzyna Wertheim-Tysarowska, Patrick Willems, Finlay Macrae. Am J Med Genet A 2012
7
100

Genetics and genomics in Brazil: a promising future.
Maria Rita Passos-Bueno, Debora Bertola, Dafne Dain Gandelman Horovitz, Victor Evangelista de Faria Ferraz, Luciano Abreu Brito. Mol Genet Genomic Med 2014
21
100

Preliminary Analysis of the Nonsynonymous Polymorphism rs17563 in BMP4 Gene in Brazilian Population Suggests Protection for Nonsyndromic Cleft Lip and Palate.
Tânia Kawasaki Araújo, Milena Simioni, Têmis Maria Félix, Liliane Todeschini de Souza, Marshall Ítalo Barros Fontes, Isabella Lopes Monlleó, Josiane Souza, Agnes Cristina Fett-Conte, Rodrigo Secolin, Iscia Lopes-Cendes,[...]. Plast Surg Int 2012
12
100

Atypical copy number abnormalities in 22q11.2 region: report of three cases.
Miriam Coelho Molck, Társis Paiva Vieira, Ilária Cristina Sgardioli, Milena Simioni, Ana Paula Dos Santos, Josiane Souza, Fabíola Paoli Monteiro, Vera Lúcia Gil-da-Silva-Lopes. Eur J Med Genet 2013
14
100

A Pure 2-Mb 3q26.2 Duplication Proximal to the Critical Region of 3q Duplication Syndrome.
Miriam Coelho Molck, Milena Simioni, Társis Paiva Vieira, Fabíola Paoli Monteiro, Vera L Gil-da-Silva-Lopes. Mol Syndromol 2018
1
100

Feeding Infants With Cleft Lip and/or Palate in Brazil: Suggestions to Improve Health Policy and Research.
Vera Lúcia Gil-da-Silva-Lopes, Ana Carolina Xavier, Denise Klein-Antunes, Ana Carolina R G Ferreira, Rita Tonocchi, Agnes C Fett-Conte, Raquel N Silva, Vera H V Leirião, Lázara P C Caramori, Luiz A Magna,[...]. Cleft Palate Craniofac J 2013
12
100


Variants in members of the cadherin-catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome.
Anneke Kievit, Federico Tessadori, Hannie Douben, Ingrid Jordens, Madelon Maurice, Jeannette Hoogeboom, Raoul Hennekam, Sheela Nampoothiri, Hülya Kayserili, Marco Castori,[...]. Eur J Hum Genet 2018
13
100

Identification of genomic imbalances in oral clefts.
Elaine Lustosa-Mendes, Ana P Dos Santos, Társis P Vieira, Erlane M Ribeiro, Adriana A Rezende, Agnes C Fett-Conte, Denise P Cavalcanti, Têmis M Félix, Isabella L Monlleó, Vera Lúcia Gil-da-Silva-Lopes. J Pediatr (Rio J) 2021
1
100

Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome.
Lisa D Palmer, Nancy J Butcher, Erik Boot, Kathleen A Hodgkinson, Tracy Heung, Eva W C Chow, Alina Guna, T Blaine Crowley, Elaine Zackai, Donna M McDonald-McGinn,[...]. Am J Med Genet A 2018
16
100

Time of diagnosis of oral clefts: a multicenter study.
Lívia G Amstalden-Mendes, Ana Carolina Xavier, Denise K Antunes, Ana Carolina R G Ferreira, Rita Tonocchi, Agnes C Fett-Conte, Raquel N Silva, Vera H V Leirião, Lázara P C Caramori, Luiz A Magna,[...]. J Pediatr (Rio J) 2011
7
100


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.