A citation-based method for searching scientific literature

Solrun Melkorka Maggadottir, Kathleen E Sullivan. J Allergy Clin Immunol Pract 2013
Times Cited: 26







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



Times Cited
  Times     Co-cited
Similarity


Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
235
30

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
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
411
26

Prevalence of 22q11 microdeletion.
S Tézenas Du Montcel, H Mendizabai, S Aymé, A Lévy, N Philip. J Med Genet 1996
194
19

Clinical features and follow-up in patients with 22q11.2 deletion syndrome.
Caterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, Annarosa Soresina, Silvana Martino, Roberto Rondelli, Rita Consolini, Ezia Maria Ruga, Fabio Cardinale, Andrea Finocchi,[...]. J Pediatr 2014
80
19

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
19

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
161
19

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


Immunological aspects of 22q11.2 deletion syndrome.
A R Gennery. Cell Mol Life Sci 2012
66
15

Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromes.
K E Sullivan, A F Jawad, P Randall, D A Driscoll, B S Emanuel, D M McDonald-McGinn, E H Zackai. Clin Immunol Immunopathol 1998
75
15

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
202
15


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
69
15

Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome.
Shan Gao, Xiao Li, Brad A Amendt. Curr Allergy Asthma Rep 2013
20
15

Practical guidelines for managing adults with 22q11.2 deletion syndrome.
Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, Danielle M Andrade, Erik Boot, Eva W C Chow, Brian Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman,[...]. Genet Med 2015
117
11

Screening newborn blood spots for 22q11.2 deletion syndrome using multiplex droplet digital PCR.
Dalyir Pretto, Dianna Maar, Carolyn M Yrigollen, Jack Regan, Flora Tassone. Clin Chem 2015
21
14



Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome.
Beverly A Karpinski, Thomas M Maynard, Matthew S Fralish, Samer Nuwayhid, Irene E Zohn, Sally A Moody, Anthony-S LaMantia. Dis Model Mech 2014
35
11

Case fatality rate and associated factors in patients with 22q11 microdeletion syndrome: a retrospective cohort study.
Gabriela M Repetto, M Luisa Guzmán, Iris Delgado, Hugo Loyola, Mirta Palomares, Guillermo Lay-Son, Cecilia Vial, Felipe Benavides, Karena Espinoza, Patricia Alvarez. BMJ Open 2014
22
13

Live vaccine use and safety in DiGeorge syndrome.
Annika M Hofstetter, Kathleen Jakob, Nicola P Klein, Cornelia L Dekker, Kathryn M Edwards, Neal A Halsey, Roger Baxter, S Elizabeth Williams, Philip L Graham, Philip LaRussa. Pediatrics 2014
22
13

Perioperative risk factors in patients with 22q11.2 deletion syndrome requiring surgery for velopharyngeal dysfunction.
Carrie Stransky, Marten Basta, Donna M McDonald-McGinn, Cynthia B Solot, Denis Drummond, Elaine Zackai, Don LaRossa, Richard Kirschner, Oksana Jackson. Cleft Palate Craniofac J 2015
12
25


Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
274
11

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
11

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
11

Otolaryngologic manifestations of the 22q11.2 deletion syndrome.
Orville Dyce, Donna McDonald-McGinn, Richard E Kirschner, Elaine Zackai, Kathleen Young, Ian N Jacobs. Arch Otolaryngol Head Neck Surg 2002
72
11

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
687
11

Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/velo-cardio-facial chromosomal region in 22q11.2.
M L Budarf, B A Konkle, L B Ludlow, D Michaud, M Li, D J Yamashiro, D McDonald-McGinn, E H Zackai, D A Driscoll. Hum Mol Genet 1995
117
11


Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome.
Deborah L Guris, Gregg Duester, Virginia E Papaioannou, Akira Imamoto. Dev Cell 2006
135
11

Molecular mechanisms of functional natural killer deficiency in patients with partial DiGeorge syndrome.
Peilin Zheng, Lenora M Noroski, Imelda C Hanson, Yuhui Chen, Michelle E Lee, Yu Huang, Michael X Zhu, Pinaki P Banerjee, George Makedonas, Jordan S Orange,[...]. J Allergy Clin Immunol 2015
16
18



T-cell homeostasis in humans with thymic hypoplasia due to chromosome 22q11.2 deletion syndrome.
Lisa M Piliero, Amy N Sanford, Donna M McDonald-McGinn, Elaine H Zackai, Kathleen E Sullivan. Blood 2004
89
11

A population study of chromosome 22q11 deletions in infancy.
J Goodship, I Cross, J LiLing, C Wren. Arch Dis Child 1998
180
11

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
662
11

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
11

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
408
7

Spinal deformity in patients with DiGeorge syndrome.
Athanasios I Tsirikos, Lukman Ahmed Kashif Khan, Michael J McMaster. J Spinal Disord Tech 2010
6
33

Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?
Kate Baker, Jacob A S Vorstman. Curr Opin Neurol 2012
45
7

Presenting symptoms in adults with the 22q11 deletion syndrome.
Annick Vogels, Sara Schevenels, Richard Cayenberghs, Eddy Weyts, Griet Van Buggenhout, Ann Swillen, Hilde Van Esch, Thomy de Ravel, Pieter Corveleyn, Koen Devriendt. Eur J Med Genet 2014
11
18


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
7

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Maria Delio, Tingwei Guo, Donna M McDonald-McGinn, Elaine Zackai, Sean Herman, Mark Kaminetzky, Anne Marie Higgins, Karlene Coleman, Carolyn Chow, Maria Jalbrzikowski,[...]. Am J Hum Genet 2013
32
7

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Grégory Raux, Emilie Bumsel, Bernadette Hecketsweiler, Therese van Amelsvoort, Janneke Zinkstok, Sylvie Manouvrier-Hanu, Carole Fantini, Georges-Marie M Brévière, Gabriella Di Rosa, Giuseppina Pustorino,[...]. Hum Mol Genet 2007
109
7

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
343
7


Facial features in children with the 22q11 deletion syndrome.
S Oskarsdóttir, E Holmberg, A Fasth, K Strömland. Acta Paediatr 2008
16
12


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.