A citation-based method for searching scientific literature

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
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


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
60

Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia.
Milena Simioni, Társis Paiva Vieira, Ilária Cristina Sgardioli, Erika Lopes Freitas, Carla Rosenberg, Cláudia Vianna Maurer-Morelli, Iscia Lopes-Cendes, Agnes Cristina Fett-Conte, Vera Lúcia Gil-da-Silva-Lopes. Am J Med Genet A 2012
11
40

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
286
40

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
40


Clinical Features in Patients With 22q11.2 Deletion Syndrome Ascertained by Palatal Abnormalities.
Társis P Vieira, Fabíola P Monteiro, Ilária C Sgardioli, Josiane Souza, Agnes C Fett-Conte, Isabella L Monlleó, Marshall B Fontes, Têmis M Félix, Gabriela F Leal, Erlane Marques Ribeiro,[...]. Cleft Palate Craniofac J 2015
7
40

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
40

Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.
F Greenberg, F F Elder, P Haffner, H Northrup, D H Ledbetter. Am J Hum Genet 1988
157
20

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
Margaret J Wat, Oleg A Shchelochkov, Ashley M Holder, Amy M Breman, Aditi Dagli, Carlos Bacino, Fernando Scaglia, Roberto T Zori, Sau Wai Cheung, Daryl A Scott,[...]. Am J Med Genet A 2009
102
20

Distal 8p deletion (8p23.1----8pter): a common deletion?
R Hutchinson, M Wilson, L Voullaire. J Med Genet 1992
83
20


A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8.
I Claeys, M Holvoet, B Eyskens, P Adriaensens, M Gewillig, J P Fryns, K Devriendt. Am J Med Genet 1997
42
20


Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks.
Mauro Longoni, Kasper Lage, Meaghan K Russell, Maria Loscertales, Omar A Abdul-Rahman, Gareth Baynam, Steven B Bleyl, Paul D Brady, Jeroen Breckpot, Chih P Chen,[...]. Am J Med Genet A 2012
30
20

Genotype-phenotype correlations in a new case of 8p23.1 deletion and review of the literature.
Lucia Ballarati, Anna Cereda, Rossella Caselli, Angelo Selicorni, Maria P Recalcati, Silvia Maitz, Palma Finelli, Lidia Larizza, Daniela Giardino. Eur J Med Genet 2011
33
20

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.
Kayoko Hirayama-Yamada, Mitsuhiro Kamisago, Kaoru Akimoto, Hiroyuki Aotsuka, Yoshihide Nakamura, Hideshi Tomita, Michiko Furutani, Shin-ichiro Imamura, Atsuyoshi Takao, Makoto Nakazawa,[...]. Am J Med Genet A 2005
150
20



High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome.
Tracy Busse, John M Graham, Gerald Feldman, Juan Perin, Anne Catherwood, Robert Knowlton, Eric F Rappaport, Beverly Emanuel, Deborah A Driscoll, Sulagna C Saitta. Hum Mutat 2011
15
20


Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects.
Patrick Y Jay, Malgorzata Bielinska, Jonathan M Erlich, Susanna Mannisto, William T Pu, Markku Heikinheimo, David B Wilson. Dev Biol 2007
118
20

Prenatal diagnosis of deletion 17p13 associated with DiGeorge anomaly.
F Greenberg, K B Courtney, R A Wessels, J Huhta, R J Carpenter, D C Rich, D H Ledbetter. Am J Med Genet 1988
45
20

SoxF genes: Key players in the development of the cardio-vascular system.
Mathias Francois, Peter Koopman, Monica Beltrame. Int J Biochem Cell Biol 2010
105
20

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot.
Georges Nemer, Fatimah Fadlalah, Julnar Usta, Mona Nemer, Ghassan Dbaibo, Mounir Obeid, Fadi Bitar. Hum Mutat 2006
119
20

SOX7 transcription factor: sequence, chromosomal localisation, expression, transactivation and interference with Wnt signalling.
W Takash, J Cañizares, N Bonneaud, F Poulat, M G Mattéi, P Jay, P Berta. Nucleic Acids Res 2001
132
20

Noncompaction of the left ventricular myocardium in a boy with a novel chromosome 8p23.1 deletion.
Joshua J Blinder, Hugo R Martinez, William J Craigen, John Belmont, Ricardo H Pignatelli, John L Jefferies. Am J Med Genet A 2011
16
20

Nonrandom association of atrioventricular canal and del (8p) syndrome.
B Marino, A Reale, A Giannotti, M C Digilio, B Dallapiccola. Am J Med Genet 1992
51
20

Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects.
Isabel López, Juan A Bafalliu, M Carmen Bernabé, Francisco García, Miguel Costa, Encarna Guillén-Navarro. Prenat Diagn 2006
31
20

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
E A Lindsay, F Vitelli, H Su, M Morishima, T Huynh, T Pramparo, V Jurecic, G Ogunrinu, H F Sutherland, P J Scambler,[...]. Nature 2001
677
20

Isolation and characterization of a mouse SRY-related cDNA, mSox7.
K Taniguchi, Y Hiraoka, M Ogawa, Y Sakai, S Kido, S Aiso. Biochim Biophys Acta 1999
35
20


Cardiomyocyte GATA4 functions as a stress-responsive regulator of angiogenesis in the murine heart.
Joerg Heineke, Mannix Auger-Messier, Jian Xu, Toru Oka, Michelle A Sargent, Allen York, Raisa Klevitsky, Sachin Vaikunth, Stephen A Duncan, Bruce J Aronow,[...]. J Clin Invest 2007
162
20

Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome.
S A Yatsenko, A N Yatsenko, K Szigeti, W J Craigen, P Stankiewicz, S W Cheung, J R Lupski. Clin Genet 2004
33
20

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.
S Giglio, S L Graw, G Gimelli, B Pirola, P Varone, L Voullaire, F Lerzo, E Rossi, C Dellavecchia, M C Bonaglia,[...]. Circulation 2000
60
20

T-box genes in vertebrate development.
L A Naiche, Zachary Harrelson, Robert G Kelly, Virginia E Papaioannou. Annu Rev Genet 2005
311
20

Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.
K Devriendt, G Matthijs, R Van Dael, M Gewillig, B Eyskens, H Hjalgrim, B Dolmer, J McGaughran, K Bröndum-Nielsen, P Marynen,[...]. Am J Hum Genet 1999
96
20

Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.
K Devriendt, K De Mars, P De Cock, M Gewillig, J P Fryns. Ann Genet 1995
25
20

GATA4 transcription factor is required for ventral morphogenesis and heart tube formation.
C T Kuo, E E Morrisey, R Anandappa, K Sigrist, M M Lu, M S Parmacek, C Soudais, J M Leiden. Genes Dev 1997
782
20

[Subvalvular aortic stenosis associated with 8p23 deletion].
Patrício Aguiar, Diogo Cruz, Rita Ferro Rodrigues, Francisco Araújo, José Luís Ducla Soares. Rev Port Cardiol 2013
1
100

Complex low-copy repeats associated with a common polymorphic inversion at human chromosome 8p23.
Hirobumi Sugawara, Naoki Harada, Tomoko Ida, Takafumi Ishida, David H Ledbetter, Ko-ichiro Yoshiura, Tohru Ohta, Tatsuya Kishino, Norio Niikawa, Naomichi Matsumoto. Genomics 2003
61
20

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
S Merscher, B Funke, J A Epstein, J Heyer, A Puech, M M Lu, R J Xavier, M B Demay, R G Russell, S Factor,[...]. Cell 2001
650
20

A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects.
Fei Long, Xike Wang, Shaohai Fang, Yuejuan Xu, Kun Sun, Sun Chen, Rang Xu. PLoS One 2013
7
20


Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities.
Seema R Lalani, Chad Shaw, Xueqing Wang, Ankita Patel, Lance W Patterson, Katarzyna Kolodziejska, Przemyslaw Szafranski, Zhishuo Ou, Qi Tian, Sung-Hae L Kang,[...]. Eur J Hum Genet 2013
34
20

SOX7 and SOX18 are essential for cardiogenesis in Xenopus.
Chi Zhang, Tamara Basta, Michael W Klymkowsky. Dev Dyn 2005
65
20

An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14.
P Lichtner, R König, T Hasegawa, H Van Esch, T Meitinger, S Schuffenhauer. J Med Genet 2000
69
20

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Vidu Garg, Irfan S Kathiriya, Robert Barnes, Marie K Schluterman, Isabelle N King, Cheryl A Butler, Caryn R Rothrock, Reenu S Eapen, Kayoko Hirayama-Yamada, Kunitaka Joo,[...]. Nature 2003
797
20

Two patients with atypical interstitial deletions of 8p23.1: mapping of phenotypical traits.
Marco T Páez, Toshiyuki Yamamoto, Ken-ichi Hayashi, Toshiyuki Yasuda, Naoki Harada, Naomichi Matsumoto, Kenji Kurosawa, Yoshiyuki Furutani, Shuichi Asakawa, Nobuyoshi Shimizu,[...]. Am J Med Genet A 2008
26
20

[Analysis of genomic copy number variations in two unrelated neonates with 8p deletion and duplication associated with congenital heart disease].
Mei Mei, Lin Yang, Guodong Zhan, Huijun Wang, Duan Ma, Wenhao Zhou, Guoying Huang. Zhonghua Er Ke Za Zhi 2014
4
25

Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion.
Luis Fernández, Pablo Lapunzina, Isidora López Pajares, María Palomares, Isabel Martínez, Blanca Fernández, José Quero, Luis García-Guereta, Alfredo García-Alix, Margarita Burgueros,[...]. Am J Med Genet A 2008
13
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.