A citation-based method for searching scientific literature

Orville Dyce, Donna McDonald-McGinn, Richard E Kirschner, Elaine Zackai, Kathleen Young, Ian N Jacobs. Arch Otolaryngol Head Neck Surg 2002
Times Cited: 72







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



Times Cited
  Times     Co-cited
Similarity


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
819
36


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
289
29


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
26

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
381
20

Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow.
P S Eicher, D M McDonald-Mcginn, C A Fox, D A Driscoll, B S Emanuel, E H Zackai. J Pediatr 2000
67
20


Communication issues in 22q11.2 deletion syndrome: children at risk.
C B Solot, M Gerdes, R E Kirschner, D M McDonald-McGinn, E Moss, M Woodin, D Aleman, E H Zackai, P P Wang. Genet Med 2001
50
24

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
408
16

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
270
16

Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome).
M C Digilio, C Pacifico, L Tieri, B Marino, A Giannotti, B Dallapiccola. Br J Audiol 1999
51
23

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
512
15

The annual incidence of DiGeorge/velocardiofacial syndrome.
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
257
15


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
24

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
285
15

Hearing loss and otitis media in velo-cardio-facial syndrome.
M R Reyes, E M LeBlanc, M K Bassila. Int J Pediatr Otorhinolaryngol 1999
35
31

Speech and hearing in adults with 22q11.2 deletion syndrome.
Christina Persson, Vanda Friman, Sólveig Óskarsdóttir, Radi Jönsson. Am J Med Genet A 2012
18
61

Defining the clinical spectrum of deletion 22q11.2.
Nathaniel H Robin, Robert J Shprintzen. J Pediatr 2005
152
13

Middle and inner ear malformations in velocardiofacial syndrome.
Koenraad Devriendt, Ann Swillen, Isabelle Schatteman, Marc Lemmerling, Ingeborg Dhooge. Am J Med Genet A 2004
15
66

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!
D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, B Finucane, D A Driscoll, B S Emanuel, E H Zackai. Genet Med 2001
199
13

Prevalence of 22q11 microdeletion.
S Tézenas Du Montcel, H Mendizabai, S Aymé, A Lévy, N Philip. J Med Genet 1996
193
13

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
21

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.
Sulagna C Saitta, Stacy E Harris, Ann P Gaeth, Deborah A Driscoll, Donna M McDonald-McGinn, Melissa K Maisenbacher, Jill M Yersak, Prabir K Chakraborty, April M Hacker, Elaine H Zackai,[...]. Hum Mol Genet 2004
102
13

Chromosomal and cardiovascular anomalies associated with congenital laryngeal web.
Doff B McElhinney, Ian Jacobs, Donna M McDonald-McGinn, Elaine H Zackai, Elizabeth Goldmuntz. Int J Pediatr Otorhinolaryngol 2002
33
27

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
341
12

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.
M Gerdes, C Solot, P P Wang, E Moss, D LaRossa, P Randall, E Goldmuntz, B J Clark, D A Driscoll, A Jawad,[...]. Am J Med Genet 1999
197
12

The velo-cardio-facial syndrome: the otorhinolaryngeal manifestations and implications.
G Vantrappen, N Rommel, C W Cremers, K Devriendt, J P Frijns. Int J Pediatr Otorhinolaryngol 1998
22
40

Upper airway asymmetry in velo-cardio-facial syndrome.
Burke E Chegar, Sherard A Tatum, Eileen Marrinan, Robert J Shprintzen. Int J Pediatr Otorhinolaryngol 2006
32
28

A population study of chromosome 22q11 deletions in infancy.
J Goodship, I Cross, J LiLing, C Wren. Arch Dis Child 1998
178
12

Communication disorders in the 22Q11.2 microdeletion syndrome.
C B Solot, C Knightly, S D Handler, M Gerdes, D M McDonald-McGinn, E Moss, P Wang, M Cohen, P Randall, D Larossa,[...]. J Commun Disord 2000
38
23

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
227
12

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega,[...]. Prenat Diagn 2015
154
12

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
523
11

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus.
P J Scambler, D Kelly, E Lindsay, R Williamson, R Goldberg, R Shprintzen, D I Wilson, J A Goodship, I E Cross, J Burn. Lancet 1992
362
11

Association of anterior glottic webs with velocardiofacial syndrome (chromosome 22q11.2 deletion).
R Christopher Miyamoto, Robin T Cotton, Alan F Rope, Robert J Hopkin, Aliza P Cohen, Sally R Shott, Michael J Rutter. Otolaryngol Head Neck Surg 2004
45
17

Velopharyngoplasty for noncleft velopharyngeal insufficiency: results in relation to 22q11 microdeletion.
Isabelle Rouillon, Nicolas Leboulanger, Gilles Roger, Michel Maulet, Sandrine Marlin, Natalie Loundon, Marie France Portnoï, Francoise Denoyelle, Erea Noel Garabédian. Arch Otolaryngol Head Neck Surg 2009
24
33

A comparative study of hearing loss in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.
Omer Zarchi, Josef Attias, Eyal Raveh, Lina Basel-Vanagaite, Liron Saporta, Doron Gothelf. J Pediatr 2011
17
47

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
736
9

Velo-cardio-facial syndrome.
Robert J Shprintzen, Anne Marie Higgins, Kevin Antshel, Wanda Fremont, Nancy Roizen, Wendy Kates. Curr Opin Pediatr 2005
70
10

Velocardiofacial syndrome.
R J Shprintzen. Otolaryngol Clin North Am 2000
44
15

Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: report of three patients.
S Fokstuen, A Bottani, P F Medeiros, S E Antonarakis, C Stoll, A Schinzel. Am J Med Genet 1997
45
15

Presenting phenotype in 100 children with the 22q11 deletion syndrome.
Sólveig Oskarsdóttir, Christina Persson, Bengt O Eriksson, Anders Fasth. Eur J Pediatr 2005
114
9

Sphincter pharyngoplasty: speech outcome and complications.
K C Sie, D A Tampakopoulou, L M de Serres, J S Gruss, L E Eblen, T Yonick. Laryngoscope 1998
45
15

Pharyngeal flap and obstructive apnea: maximizing speech outcome while limiting complications.
Burke E Chegar, Robert J Shprintzen, Michael S Curtis, Sherard A Tatum. Arch Facial Plast Surg 2007
47
14

Chiari malformation, cervical spine anomalies, and neurologic deficits in velocardiofacial syndrome.
C S Hultman, J E Riski, S R Cohen, F D Burstein, W R Boydston, R J Hudgins, D Grattan-Smith, K Uhas, C Simms. Plast Reconstr Surg 2000
42
16

Speech outcomes following pharyngeal flap in patients with velocardiofacial syndrome.
Edward W Swanson, Stephen R Sullivan, Emily B Ridgway, Eileen M Marrinan, John B Mulliken. Plast Reconstr Surg 2011
26
26

An outcome evaluation of sphincter pharyngoplasty for the management of velopharyngeal insufficiency.
Albert Losken, J Kerwin Williams, Fernando D Burstein, Deonne Malick, John E Riski. Plast Reconstr Surg 2003
48
14

Analysis of speech characteristics in children with velocardiofacial syndrome (VCFS) and children with phenotypic overlap without VCFS.
L L D'Antonio, N J Scherer, L L Miller, J H Kalbfleisch, J A Bartley. Cleft Palate Craniofac J 2001
38
18


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.