A citation-based method for searching scientific literature

Isabella Lopes Monlleó, Vera Lúcia Gil-da-Silva-Lopes. Cleft Palate Craniofac J 2006
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Evaluation of craniofacial care outside the Brazilian reference network for craniofacial treatment.
Isabella Lopes Monlleo, Peter Anthony Mossey, Vera Lucia Gil-da-Silva-Lopes. Cleft Palate Craniofac J 2009
7
85

[Birth defects in Brazil and health care: proposals for public policies in clinical genetics].
Dafne Dain Gandelman Horovitz, Maria Helena Cabral de Almeida Cardoso, Juan Clinton Llerena, Ruben Araújo de Mattos. Cad Saude Publica 2006
16
35

[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
35

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
58
35


Clinical genetics in developing countries: the case of Brazil.
Antonia Paula Marques-de-Faria, Victor E Faria Ferraz, Angelina Xavier Acosta, Décio Brunoni. Community Genet 2004
25
28

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
28

Associated malformations in infants with cleft lip and palate: a prospective, population-based study.
Josef Milerad, Ola Larson, Catherina Hagberg, Margareta Ideberg. Pediatrics 1997
144
28


Cleft lip and palate: understanding genetic and environmental influences.
Michael J Dixon, Mary L Marazita, Terri H Beaty, Jeffrey C Murray. Nat Rev Genet 2011
855
28

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
44

Anomalies associated with cleft lip, cleft palate, or both.
R J Shprintzen, V L Siegel-Sadewitz, J Amato, R B Goldberg. Am J Med Genet 1985
179
21

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
21

Local strategies to address health needs of individuals with orofacial clefts in alagoas, Brazil.
Marshall Ítalo Barros Fontes, Lanusia Nunes Almeida, Gilberto de Oliveira Reis Junior, José Ivam Vieira Filho, Kathleen Moura Dos Santos, Filipe Silveira Dos Anjos, Ana Karolina Maia de Andrade, Carlos Guilherme Gaelzer Porciuncula, Michelline Costa de Oliveira, Rui Manoel Pereira,[...]. Cleft Palate Craniofac J 2013
5
60

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
21

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
42

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
21

Cleft lip and palate.
Peter A Mossey, Julian Little, Ron G Munger, Mike J Dixon, William C Shaw. Lancet 2009
744
21

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
42

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
21


Health reform in Brazil: lessons to consider.
Paulo Eduardo M Elias, Amelia Cohn. Am J Public Health 2003
37
14


The Eurocleft project 1996-2000: overview.
W C Shaw, G Semb, P Nelson, V Brattström, K Mølsted, B Prahl-Andersen, K K Gundlach. J Craniomaxillofac Surg 2001
163
14


Classification and birth prevalence of orofacial clefts.
M M Tolarová, J Cervenka. Am J Med Genet 1998
233
14



Congenital malformations in births with orofacial clefts among 3.6 million California births, 1983-1997.
Gary M Shaw, Suzan L Carmichael, Wei Yang, John A Harris, Edward J Lammer. Am J Med Genet A 2004
38
14

Oral clefts with associated anomalies: methodological issues.
Diego F Wyszynski, Andrea Sárközi, Andrew E Czeizel. Cleft Palate Craniofac J 2006
46
14

Ten years recording common oral clefts with a new descriptive system.
Antonius J M Luijsterburg, Christl Vermeij-Keers. Cleft Palate Craniofac J 2011
33
14

Racial and ethnic variations in the prevalence of orofacial clefts in California, 1983-1992.
L A Croen, G M Shaw, C R Wasserman, M M Tolarová. Am J Med Genet 1998
150
14

Cleft lip and palate: association with other congenital malformations.
Soraya Beriaghi, Sandra L Myers, Scott A Jensen, Shanti Kaimal, Cynthia M Chan, G Bradley Schaefer. J Clin Pediatr Dent 2009
28
14

Orofacial clefts in the National Birth Defects Prevention Study, 1997-2004.
Alicia E Genisca, Jaime L Frías, Cheryl S Broussard, Margaret A Honein, Edward J Lammer, Cynthia A Moore, Gary M Shaw, Jeffrey C Murray, Wei Yang, Sonja A Rasmussen. Am J Med Genet A 2009
95
14

Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries.
Fernanda Sarquis Jehee, Jean Tetsuo Takamori, Paula F Vasconcelos Medeiros, Ana Carolina B Pordeus, Flavia Roche M Latini, Débora Romeo Bertola, Chong Ae Kim, Maria Rita Passos-Bueno. Eur J Med Genet 2011
31
14

Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome.
L Fernández, P Lapunzina, D Arjona, I López Pajares, L García-Guereta, D Elorza, M Burgueros, M L De Torres, M A Mori, M Palomares,[...]. Clin Genet 2005
61
14

How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.
Maija R J Kohonen-Corish, Jumana Y Al-Aama, Arleen D Auerbach, Myles Axton, Carol Isaacson Barash, Inge Bernstein, Christophe Béroud, John Burn, Fiona Cunningham, Garry R Cutting,[...]. Hum Mutat 2010
31
14

Brazil: public health genomics.
E E Castilla, D V Luquetti. Public Health Genomics 2009
8
25


How can developing countries harness biotechnology to improve health?
Abdallah S Daar, Kathryn Berndtson, Deepa L Persad, Peter A Singer. BMC Public Health 2007
20
14

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
227
14

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
28

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
14

Parental age as a risk factor for non-syndromic oral clefts: a meta-analysis.
Ana Paula Corrêa de Queiroz Herkrath, Fernando José Herkrath, Maria Augusta Bessa Rebelo, Mario Vianna Vettore. J Dent 2012
55
14

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
14

A cohort study of recurrence patterns among more than 54,000 relatives of oral cleft cases in Denmark: support for the multifactorial threshold model of inheritance.
Dorthe Grosen, Cécile Chevrier, Axel Skytthe, Camilla Bille, Kirsten Mølsted, Ase Sivertsen, Jeffrey C Murray, Kaare Christensen. J Med Genet 2010
104
14

Risk, medicine and women: a case study on prenatal genetic counselling in Brazil.
Maria Cristina R Guilam, Marilena C D V Corrêa. Dev World Bioeth 2007
5
40

Genetic counselling in tribals in India.
Dipika Mohanty, Kishalaya Das. Indian J Med Res 2011
17
14

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
16

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
35
14


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.