A citation-based method for searching scientific literature

Kathleen E Sullivan, Evanette Burrows, Donna M McDonald McGinn. Am J Med Genet A 2016
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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
66

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
66

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
180
50

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
65
50


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
344
50

Risk Factors and Clinical Significance of Lymphopenia in Survivors of the Fontan Procedure for Single-Ventricle Congenital Cardiac Disease.
Megan M Morsheimer, Jack Rychik, Lisa Forbes, Kathryn Dodds, David J Goldberg, Kathleen Sullivan, Jennifer R Heimall. J Allergy Clin Immunol Pract 2016
15
50

Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing.
J Helgeson, J Wardrop, T Boomer, E Almasri, W B Paxton, J S Saldivar, N Dharajiya, T J Monroe, D H Farkas, D S Grosu,[...]. Prenat Diagn 2015
79
33

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
33

Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease.
Aoy Tomita-Mitchell, Donna K Mahnke, Joshua M Larson, Sujana Ghanta, Ying Feng, Pippa M Simpson, Ulrich Broeckel, Kelly Duffy, James S Tweddell, William J Grossman,[...]. Physiol Genomics 2010
25
33

Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Donna M McDonald-McGinn, Kathleen E Sullivan. Medicine (Baltimore) 2011
235
33

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
33

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
33

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
33

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
33

Bone marrow transplantation in DiGeorge syndrome.
A B Goldsobel, A Haas, E R Stiehm. J Pediatr 1987
52
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
33

Live viral vaccines in patients with partial DiGeorge syndrome: clinical experience and cellular immunity.
Edina H Moylett, Anita N Wasan, Lenora M Noroski, William T Shearer. Clin Immunol 2004
33
33

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
33

Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
C A Smith, D A Driscoll, B S Emanuel, D M McDonald-McGinn, E H Zackai, K E Sullivan. Clin Diagn Lab Immunol 1998
53
33

Thrombocytopenia in patients with chromosome 22q11.2 deletion syndrome.
Scott Lawrence, Donna M McDonald-McGinn, Elaine Zackai, Kathleen E Sullivan. J Pediatr 2003
52
33

Characterization of immune function and analysis of RAG gene mutations in Omenn syndrome and related disorders.
T Wada, K Takei, M Kudo, S Shimura, Y Kasahara, S Koizumi, K Kawa-Ha, Y Ishida, S Imashuku, H Seki,[...]. Clin Exp Immunol 2000
32
33

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
33

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
33

Long-term results of bone marrow transplantation in complete DiGeorge syndrome.
Michael H Land, Maria I Garcia-Lloret, Michael S Borzy, P Nagesh Rao, Najib Aziz, Sean A McGhee, Karin Chen, Jack Gorski, E Richard Stiehm. J Allergy Clin Immunol 2007
29
33

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
33

Safety of live viral vaccines in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).
Elena E Perez, Aleksandra Bokszczanin, Donna McDonald-McGinn, Elaine H Zackai, Kathleen E Sullivan. Pediatrics 2003
51
33

Lymphopenic mice reconstituted with limited repertoire T cells develop severe, multiorgan, Th2-associated inflammatory disease.
Joshua D Milner, Jerrold M Ward, Andrea Keane-Myers, William E Paul. Proc Natl Acad Sci U S A 2007
77
33

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
33

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
33


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
33

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
33

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.
T H Shaikh, H Kurahashi, S C Saitta, A M O'Hare, P Hu, B A Roe, D A Driscoll, D M McDonald-McGinn, E H Zackai, M L Budarf,[...]. Hum Mol Genet 2000
377
33

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
33

Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome.
Evelyn Ning Man Cheung, Susan R George, Danielle M Andrade, Eva W C Chow, Candice K Silversides, Anne S Bassett. Genet Med 2014
46
33

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
743
33

Pediatric healthcare costs for patients with 22q11.2 deletion syndrome.
Peter Benn, Sushma Iyengar, Terrence Blaine Crowley, Elaine H Zackai, Evanette K Burrows, Solomon Moshkevich, Donna M McDonald-McGinn, Kathleen E Sullivan, Zachary Demko. Mol Genet Genomic Med 2017
3
66

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
664
16

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
Diana W Bianchi, Lawrence D Platt, James D Goldberg, Alfred Z Abuhamad, Amy J Sehnert, Richard P Rava. Obstet Gynecol 2012
456
16

Association of copy number variants with specific ultrasonographically detected fetal anomalies.
Jennifer C Donnelly, Lawrence D Platt, Andrei Rebarber, Julia Zachary, William A Grobman, Ronald J Wapner. Obstet Gynecol 2014
86
16

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing.
Desheng Liang, Weigang Lv, Hua Wang, Liangpu Xu, Jing Liu, Haoxian Li, Liang Hu, Ying Peng, Lingqian Wu. Prenat Diagn 2013
108
16

Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins.
Sebastian Grömminger, Erbil Yagmur, Sanli Erkan, Sándor Nagy, Ulrike Schöck, Joachim Bonnet, Patricia Smerdka, Mathias Ehrich, Rolf-Dieter Wegner, Wera Hofmann,[...]. J Clin Med 2014
55
16



Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing.
Frédéric Amant, Magali Verheecke, Iwona Wlodarska, Luc Dehaspe, Paul Brady, Nathalie Brison, Kris Van Den Bogaert, Daan Dierickx, Vincent Vandecaveye, Thomas Tousseyn,[...]. JAMA Oncol 2015
116
16

Noninvasive prenatal diagnosis of a fetal microdeletion syndrome.
David Peters, Tianjiao Chu, Svetlana A Yatsenko, Nancy Hendrix, W Allen Hogge, Urvashi Surti, Kimberly Bunce, Mary Dunkel, Patricia Shaw, Aleksandar Rajkovic. N Engl J Med 2011
92
16

Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA.
Ai-hua Yin, Chun-fang Peng, Xin Zhao, Bennett A Caughey, Jie-xia Yang, Jian Liu, Wei-wei Huang, Chang Liu, Dong-hong Luo, Hai-liang Liu,[...]. Proc Natl Acad Sci U S A 2015
74
16

Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma.
Anupama Srinivasan, Diana W Bianchi, Hui Huang, Amy J Sehnert, Richard P Rava. Am J Hum Genet 2013
172
16

Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
Andrew B Sparks, Eric T Wang, Craig A Struble, Wade Barrett, Renee Stokowski, Celeste McBride, Jacob Zahn, Kevin Lee, Naiping Shen, Jigna Doshi,[...]. Prenat Diagn 2012
178
16


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.