A citation-based method for searching scientific literature

Megan Morsheimer, Terri F Brown Whitehorn, Jennifer Heimall, Kathleen E Sullivan. Am J Med Genet A 2017
Times Cited: 35







List of co-cited articles
259 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
397
37


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
22
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
294
22


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
18
44

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
87
20

Newborn screening for severe combined immunodeficiency in 11 screening programs in the United States.
Antonia Kwan, Roshini S Abraham, Robert Currier, Amy Brower, Karen Andruszewski, Jordan K Abbott, Mei Baker, Mark Ballow, Louis E Bartoshesky, Francisco A Bonilla,[...]. JAMA 2014
339
20

Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.
Lauren Staple, Timothy Andrews, Donna McDonald-McGinn, Elaine Zackai, Kathleen E Sullivan. Pediatr Allergy Immunol 2005
31
22

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
20

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
230
20

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
820
17

B cell development in chromosome 22q11.2 deletion syndrome.
Beata Derfalvi, Kelly Maurer, Donna M McDonald McGinn, Elaine Zackai, Wenzhao Meng, Eline T Luning Prak, Kathleen E Sullivan. Clin Immunol 2016
14
42

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
53
17

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
25
24


Low thymic output, peripheral homeostasis deregulation, and hastened regulatory T cells differentiation in children with 22q11.2 deletion syndrome.
Sara Ferrando-Martínez, Raquel Lorente, Dolores Gurbindo, Ma Isabel De José, Manuel Leal, Ma Angeles Muñoz-Fernández, Rafael Correa-Rocha. J Pediatr 2014
24
20

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
411
14

Autoimmunity in a cohort of 130 pediatric patients with partial DiGeorge syndrome.
Brian E Tison, Sarah K Nicholas, Stuart L Abramson, Imelda C Hanson, Mary E Paul, Filiz O Seeborg, William T Shearer, Maria D Perez, Lenora M Noroski, Javier Chinen. J Allergy Clin Immunol 2011
32
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
14

Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants.
M Louise Markert, Blythe H Devlin, Marilyn J Alexieff, Jie Li, Elizabeth A McCarthy, Stephanie E Gupton, Ivan K Chinn, Laura P Hale, Thomas B Kepler, Min He,[...]. Blood 2007
137
14

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
155
14

Immunological aspects of 22q11.2 deletion syndrome.
A R Gennery. Cell Mol Life Sci 2012
63
14

Immunoglobulin deficiencies: the B-lymphocyte side of DiGeorge Syndrome.
Kiran Patel, Javeed Akhter, Lisa Kobrynski, M A Benjamin Gathmann, Onika Davis, Kathleen E Sullivan. J Pediatr 2012
38
11

Humoral immune responses and CD27+ B cells in children with DiGeorge syndrome (22q11.2 deletion syndrome).
A Finocchi, S Di Cesare, M L Romiti, C Capponi, P Rossi, R Carsetti, C Cancrini. Pediatr Allergy Immunol 2006
52
11

Congenital heart disease in mice deficient for the DiGeorge syndrome region.
E A Lindsay, A Botta, V Jurecic, S Carattini-Rivera, Y C Cheah, H M Rosenblatt, A Bradley, A Baldini. Nature 1999
299
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
681
11

Antibody deficiency and autoimmunity in 22q11.2 deletion syndrome.
A R Gennery, D Barge, J J O'Sullivan, T J Flood, M Abinun, A J Cant. Arch Dis Child 2002
103
11

Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency.
Jessica C Barry, Terrence Blaine Crowley, Soma Jyonouchi, Jennifer Heimall, Elaine H Zackai, Kathleen E Sullivan, Donna M McDonald-McGinn. J Clin Immunol 2017
19
21

A prospective study of influenza vaccination and a comparison of immunologic parameters in children and adults with chromosome 22q11.2 deletion syndrome (digeorge syndrome/velocardiofacial syndrome).
Abbas F Jawad, Eline Luning Prak, Jean Boyer, Donna M McDonald-McGinn, Elaine Zackai, Kenyetta McDonald, Kathleen E Sullivan. J Clin Immunol 2011
24
16

Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.
S J Gross, M Stosic, D M McDonald-McGinn, A S Bassett, A Norvez, R Dhamankar, K Kobara, E Kirkizlar, B Zimmermann, N Wayham,[...]. Ultrasound Obstet Gynecol 2016
64
11

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
738
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
654
11

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
46
11

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
11

Microduplication 22q11.2: a new chromosomal syndrome.
Marie-France Portnoï. Eur J Med Genet 2009
147
11

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
78
11

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
524
11

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Marta Unolt, Paolo Versacci, Silvia Anaclerio, Caterina Lambiase, Giulio Calcagni, Matteo Trezzi, Adriano Carotti, Terrence Blaine Crowley, Elaine H Zackai, Elizabeth Goldmuntz,[...]. Am J Med Genet A 2018
17
23

The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
Aziz Bousfiha, Leïla Jeddane, Capucine Picard, Fatima Ailal, H Bobby Gaspar, Waleed Al-Herz, Talal Chatila, Yanick J Crow, Charlotte Cunningham-Rundles, Amos Etzioni,[...]. J Clin Immunol 2018
252
11


Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies.
Alain Fischer, Johan Provot, Jean-Philippe Jais, Alexandre Alcais, Nizar Mahlaoui. J Allergy Clin Immunol 2017
99
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
35
11

In vivo response to high-resolution variation of Tbx1 mRNA dosage.
Zhen Zhang, Antonio Baldini. Hum Mol Genet 2008
83
11

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
39
11

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
10
40

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
64
8

Thymic and bone marrow output in individuals with 22q11.2 deletion syndrome.
Nina Dar, Doron Gothelf, David Korn, Amos Frisch, Abraham Weizman, Elena Michaelovsky, Miri Carmel, Yonatan Yeshayahu, Gal Dubnov-Raz, Itai M Pessach,[...]. Pediatr Res 2015
9
33

Long-term assessment of T-cell populations in DiGeorge syndrome.
Javier Chinen, Howard M Rosenblatt, E O'Brian Smith, William T Shearer, Lenora M Noroski. J Allergy Clin Immunol 2003
55
8


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.