A citation-based method for searching scientific literature

Albert K Oh, Laura A Workman, Granger B Wong. Cleft Palate Craniofac J 2007
Times Cited: 19







List of co-cited articles
115 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
47


No justification of routine screening for 22q11 deletions in patients with overt cleft palate.
E M Ruiter, E M H F Bongers, D F C M Smeets, A M Kuijpers-Jagtman, B C J Hamel. Clin Genet 2003
18
33

Presenting phenotype in 100 children with the 22q11 deletion syndrome.
Sólveig Oskarsdóttir, Christina Persson, Bengt O Eriksson, Anders Fasth. Eur J Pediatr 2005
115
31

Prevalence of duplications and deletions of the 22q11 DiGeorge syndrome region in a population-based sample of infants with cleft palate.
Ase Sivertsen, Rolv Terje Lie, Allen J Wilcox, Frank Abyholm, Hallvard Vindenes, Bjørn Ivar Haukanes, Gunnar Houge. Am J Med Genet A 2007
27
31

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
31

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
235
31

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
821
26

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.
R J Shprintzen, R B Goldberg, M L Lewin, E J Sidoti, M D Berkman, R V Argamaso, D Young. Cleft Palate J 1978
513
26

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
D A Driscoll, J Salvin, B Sellinger, M L Budarf, D M McDonald-McGinn, E H Zackai, B S Emanuel. J Med Genet 1993
404
26

Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2.
Paula Sandrin-Garcia, Dagma V M Abramides, Lúcia R Martelli, Ester S Ramos, Antônio Richieri-Costa, Geraldo A S Passos. Mol Cell Biochem 2007
17
29

Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of DiGeorge/Velocardiofacial syndrome.
Anna Brunet, Elisabeth Gabau, Rosa Maria Perich, Laura Valdesoiro, Carme Brun, Maria Rosa Caballín, Miriam Guitart. Am J Med Genet A 2006
31
26

Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
526
26

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
274
26

Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
S Kitsiou-Tzeli, A Kolialexi, H Fryssira, A Galla-Voumvouraki, K Salavoura, M Kanariou, G Th Tsangaris, E Kanavakis, A Mavrou. In Vivo 2004
27
26

Towards earlier diagnosis of 22q11 deletions.
E S Tobias, N Morrison, M L Whiteford, J L Tolmie. Arch Dis Child 1999
39
26

22q11 Deletion in children with cleft lip and palate--is routine screening justified?
Muhammad Asim Bashir, Peter D Hodgkinson, Tara Montgomery, Miranda Splitt. J Plast Reconstr Aesthet Surg 2008
9
44

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
21

DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion.
Oliver Bartsch, Michaela Nemecková, Eduard Kocárek, Annett Wagner, Alena Puchmajerová, Maja Poppe, Katrin Ounap, Petr Goetz. Am J Med Genet A 2003
40
21

Detailed analysis of 22q11.2 with a high density MLPA probe set.
G R Jalali, J A S Vorstman, Ab Errami, R Vijzelaar, J Biegel, T Shaikh, B S Emanuel. Hum Mutat 2008
71
21

Is isolated palatal anomaly an indication to screen for 22q11 region deletion?
Orit Reish, Yehuda Finkelstein, Ronit Mesterman, Ariela Nachmani, Baruch Wolach, Moshe Fejgin, Aliza Amiel. Cleft Palate Craniofac J 2003
15
26

The search for hemizygosity at 22qll in patients with isolated cleft palate.
R Mingarelli, M C Digilio, A Mari, F Amati, L Standoli, A Giannotti, G Novelli, B Dallapiccola. J Craniofac Genet Dev Biol 1996
13
30

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
411
21


Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients.
G M Repetto, M L Guzmán, A Puga, J F Calderón, C P Astete, M Aracena, M Arriaza, T Aravena, P Sanz. Clin Genet 2009
21
21

Practical guidelines for managing patients with 22q11.2 deletion syndrome.
Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan,[...]. J Pediatr 2011
299
21

A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH.
Céline Poirsier, Justine Besseau-Ayasse, Caroline Schluth-Bolard, Jérôme Toutain, Chantal Missirian, Cédric Le Caignec, Anne Bazin, Marie Christine de Blois, Paul Kuentz, Marie Catty,[...]. Eur J Hum Genet 2016
23
21

The velo-cardio-facial syndrome: a clinical and genetic analysis.
R J Shprintzen, R B Goldberg, D Young, L Wolford. Pediatrics 1981
233
15

Craniofacial morphology in the velo-cardio-facial syndrome.
M Arvystas, R J Shprintzen. J Craniofac Genet Dev Biol 1984
79
15


Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
Adriano Carotti, Maria Cristina Digilio, Gerardo Piacentini, Claudia Saffirio, Roberto M Di Donato, Bruno Marino. Dev Disabil Res Rev 2008
80
15

Clinical features of 78 adults with 22q11 Deletion Syndrome.
Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
288
15

22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin.
S Fokstuen, U Arbenz, S Artan, F Dutly, U Bauersfeld, L Brecevic, M Fasnacht, B Röthlisberger, A Schinzel. Clin Genet 1998
64
15

Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects.
Murat Derbent, Zerrin Yilmaz, Volkan Baltaci, Arda Saygili, Birgül Varan, Kürşat Tokel. Am J Med Genet A 2003
48
15

Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India.
Ashutosh Halder, Manish Jain, Isha Chaudhary, Madhulika Kabra. BMC Med Genet 2010
13
23

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
Lorenzo D Botto, Kristin May, Paul M Fernhoff, Adolfo Correa, Karlene Coleman, Sonja A Rasmussen, Robert K Merritt, Leslie A O'Leary, Lee-Yang Wong, E Marsha Elixson,[...]. Pediatrics 2003
414
15

A population study of chromosome 22q11 deletions in infancy.
J Goodship, I Cross, J LiLing, C Wren. Arch Dis Child 1998
180
15

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
D M McDonald-McGinn, R Kirschner, E Goldmuntz, K Sullivan, P Eicher, M Gerdes, E Moss, C Solot, P Wang, I Jacobs,[...]. Genet Couns 1999
311
15



Characteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiofacial syndrome patients.
Dandan Wu, Yang Chen, Chen Xu, Ke Wang, Huijun Wang, Fengyun Zheng, Duan Ma, Guomin Wang. PLoS One 2013
16
18

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
15

Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
Anna Wozniak, Danuta Wolnik-Brzozowska, Marzena Wisniewska, Renata Glazar, Anna Materna-Kiryluk, Tomasz Moszura, Magdalena Badura-Stronka, Joanna Skolozdrzy, Maciej R Krawczynski, Joanna Zeyland,[...]. BMC Pediatr 2010
16
18

Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysis.
Rachel A Ruotolo, Nestor A Veitia, Aaron Corbin, Joseph McDonough, Cynthia B Solot, Donna McDonald-McGinn, Elaine H Zackai, Beverly S Emanuel, Avital Cnaan, Don LaRossa,[...]. Cleft Palate Craniofac J 2006
45
10

Screening of patients at risk for 22q11 deletion.
Ingeborg Barisić, Leona Morozin Pohovski, Iskra Petković, Zeljko Cvetko, Gordana Stipancić, Marijo Bagatin. Coll Antropol 2008
8
25

The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.
D M McDonald-McGinn, D LaRossa, E Goldmuntz, K Sullivan, P Eicher, M Gerdes, E Moss, P Wang, C Solot, P Schultz,[...]. Genet Test 1997
115
10

Surgical outcomes for velopharyngeal insufficiency in velocardiofacial syndrome and nonsyndromic patients.
Henry A Milczuk, Dana S Smith, Janet H Brockman. Cleft Palate Craniofac J 2007
25
10

Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2.
R Matsuoka, A Takao, M Kimura, S Imamura, C Kondo, K Joh-o, K Ikeda, M Nishibatake, M Ando, K Momma. Am J Med Genet 1994
110
10

Videonasopharyngoscopy in patients with 22q11.2 deletion syndrome (Shprintzen syndrome).
Antonio Ysunza, M C Pamplona, Elena Ramírez, Sonia Canún, M C Sierra, Andres Silva-Rojas. Int J Pediatr Otorhinolaryngol 2003
12
16

Surgical correction of velopharyngeal insufficiency in children with velocardiofacial syndrome.
Albert Losken, J Kerwin Williams, Fernando D Burstein, Deonne N Malick, John E Riski. Plast Reconstr Surg 2006
47
10


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.