A citation-based method for searching scientific literature

Kathleen E Sullivan. Immunol Rev 2019
Times Cited: 32







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



Times Cited
  Times     Co-cited
Similarity


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
446
40

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
310
28

The immune deficiency of chromosome 22q11.2 deletion syndrome.
Megan Morsheimer, Terri F Brown Whitehorn, Jennifer Heimall, Kathleen E Sullivan. Am J Med Genet A 2017
38
25

Thymic Epithelium Abnormalities in DiGeorge and Down Syndrome Patients Contribute to Dysregulation in T Cell Development.
Genni Enza Marcovecchio, Ileana Bortolomai, Francesca Ferrua, Elena Fontana, Luisa Imberti, Erika Conforti, Donato Amodio, Sonia Bergante, Giulia Macchiarulo, Veronica D'Oria,[...]. Front Immunol 2019
31
19

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
242
15

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
423
15

Molecular genetics of 22q11.2 deletion syndrome.
Bernice E Morrow, Donna M McDonald-McGinn, Beverly S Emanuel, Joris R Vermeesch, Peter J Scambler. Am J Med Genet A 2018
37
15

Immunological aspects of 22q11.2 deletion syndrome.
A R Gennery. Cell Mol Life Sci 2012
68
15

Velo-cardio-facial syndrome: 30 Years of study.
Robert J Shprintzen. Dev Disabil Res Rev 2008
276
12

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
126
12

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
294
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
533
12

22q11.2 deletion syndrome in diverse populations.
Paul Kruszka, Yonit A Addissie, Daniel E McGinn, Antonio R Porras, Elijah Biggs, Matthew Share, T Blaine Crowley, Brian H Y Chung, Gary T K Mok, Christopher C Y Mak,[...]. Am J Med Genet A 2017
56
12


In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
83
12

Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
R Zemble, E Luning Prak, K McDonald, D McDonald-McGinn, E Zackai, K Sullivan. Clin Immunol 2010
54
12

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
665
12


Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion Syndrome.
Davide Montin, Agostina Marolda, Francesco Licciardi, Francesca Robasto, Silvia Di Cesare, Emanuela Ricotti, Francesca Ferro, Giacomo Scaioli, Carmela Giancotta, Donato Amodio,[...]. J Allergy Clin Immunol Pract 2019
21
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
82
12

What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia.
Ian M Campbell, Sarah E Sheppard, T Blaine Crowley, Daniel E McGinn, Alice Bailey, Michael J McGinn, Marta Unolt, Jelle F Homans, Erin Y Chen, Harold I Salmons,[...]. Am J Med Genet A 2018
37
12

CD4(+) CD25(+) T-cell production in healthy humans and in patients with thymic hypoplasia.
Kathleen E Sullivan, Donna McDonald-McGinn, Elaine H Zackai. Clin Diagn Lab Immunol 2002
65
12

Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome.
Blaine Crowley, Melanie Ruffner, Donna M McDonald McGinn, Kathleen E Sullivan. Am J Med Genet A 2018
26
15

Microduplication 22q11.2: a new chromosomal syndrome.
Marie-France Portnoï. Eur J Med Genet 2009
151
9


Retinoic acid embryopathy.
E J Lammer, D T Chen, R M Hoar, N D Agnish, P J Benke, J T Braun, C J Curry, P M Fernhoff, A W Grix, I T Lott. N Engl J Med 1985
9

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
692
9

Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?
Veronica Bertini, Alessia Azzarà, Annalisa Legitimo, Roberta Milone, Roberta Battini, Rita Consolini, Angelo Valetto. Front Genet 2017
9
33

Neurobiological perspective of 22q11.2 deletion syndrome.
Janneke R Zinkstok, Erik Boot, Anne S Bassett, Noboru Hiroi, Nancy J Butcher, Claudia Vingerhoets, Jacob A S Vorstman, Therese A M J van Amelsvoort. Lancet Psychiatry 2019
27
11

Rebalancing gene haploinsufficiency in vivo by targeting chromatin.
Filomena Gabriella Fulcoli, Monica Franzese, Xiangyang Liu, Zhen Zhang, Claudia Angelini, Antonio Baldini. Nat Commun 2016
36
9

Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions.
Christiane Zweier, Heinrich Sticht, Inci Aydin-Yaylagül, Christine E Campbell, Anita Rauch. Am J Hum Genet 2007
144
9

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
690
9

A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency.
I Paganini, R Sestini, G L Capone, A L Putignano, E Contini, I Giotti, F Gensini, A Marozza, A Barilaro, B Porfirio,[...]. Clin Genet 2017
23
13

A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome.
Esther Pohl, Ayca Aykut, Filippo Beleggia, Emin Karaca, Burak Durmaz, Katharina Keupp, Esra Arslan, Melis Palamar, Gökhan Yigit, Ferda Özkinay,[...]. Hum Genet 2013
34
9

Signature MicroRNA expression patterns identified in humans with 22q11.2 deletion/DiGeorge syndrome.
M Teresa de la Morena, Jennifer L Eitson, Igor M Dozmorov, Serkan Belkaya, Ashley R Hoover, Esperanza Anguiano, M Virginia Pascual, Nicolai S C van Oers. Clin Immunol 2013
42
9

Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.
Alina Guna, Nancy J Butcher, Anne S Bassett. J Neurodev Disord 2015
55
9

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.
Elisabeth E Mlynarski, Molly B Sheridan, Michael Xie, Tingwei Guo, Silvia E Racedo, Donna M McDonald-McGinn, Xiaowu Gai, Eva W C Chow, Jacob Vorstman, Ann Swillen,[...]. Am J Hum Genet 2015
47
9


Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients.
Luis E León, Felipe Benavides, Karena Espinoza, Cecilia Vial, Patricia Alvarez, Mirta Palomares, Guillermo Lay-Son, Macarena Miranda, Gabriela M Repetto. Sci Rep 2017
18
16

Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH.
D C Bittel, S Yu, H Newkirk, N Kibiryeva, A Holt, M G Butler, L D Cooley. Cytogenet Genome Res 2009
48
9

Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.
Daniel W Meechan, Thomas M Maynard, Eric S Tucker, Alejandra Fernandez, Beverly A Karpinski, Lawrence A Rothblat, Anthony-S LaMantia. Prog Neurobiol 2015
51
9

The regional pattern of retinoic acid synthesis by RALDH2 is essential for the development of posterior pharyngeal arches and the enteric nervous system.
Karen Niederreither, Julien Vermot, Isabelle Le Roux, Brigitte Schuhbaur, Pierre Chambon, Pascal Dollé. Development 2003
158
9

Decreased levels of embryonic retinoic acid synthesis accelerate recovery from arterial growth delay in a mouse model of DiGeorge syndrome.
Lucile Ryckebüsch, Nicolas Bertrand, Karim Mesbah, Fanny Bajolle, Karen Niederreither, Robert G Kelly, Stéphane Zaffran. Circ Res 2010
56
9

The diverse clinical features of chromosome 22q11.2 deletion syndrome (DiGeorge syndrome).
Solrun Melkorka Maggadottir, Kathleen E Sullivan. J Allergy Clin Immunol Pract 2013
28
10

In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
Zahra Motahari, Sally Ann Moody, Thomas Michael Maynard, Anthony-Samuel LaMantia. J Neurodev Disord 2019
27
11

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
93
9

Clinical and immunological features in a cohort of patients with partial DiGeorge syndrome followed at a single center.
Giuliana Giardino, Nesrine Radwan, Patra Koletsi, Deborah M Morrogh, Stuart Adams, Winnie Ip, Austen Worth, Alison Jones, Imke Meyer-Parsonson, H Bobby Gaspar,[...]. Blood 2019
14
21

Chromosome 22q11.2 microdeletion in children with conotruncal heart defects: frequency, associated cardiovascular anomalies, and outcome following cardiac surgery.
Lidia Ziolkowska, Wanda Kawalec, Anna Turska-Kmiec, Malgorzata Krajewska-Walasek, Grazyna Brzezinska-Rajszys, Jadwiga Daszkowska, Bogdan Maruszewski, Piotr Burczynski. Eur J Pediatr 2008
48
9



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.