A citation-based method for searching scientific literature

Maire A Conrad, Judith R Kelsen. Pediatr Dev Pathol 2019
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Inflammatory skin and bowel disease linked to ADAM17 deletion.
Diana C Blaydon, Paolo Biancheri, Wei-Li Di, Vincent Plagnol, Rita M Cabral, Matthew A Brooke, David A van Heel, Franz Ruschendorf, Mark Toynbee, Amanda Walne,[...]. N Engl J Med 2011
208
40

Congenital alterations of NEMO glutamic acid 223 result in hypohidrotic ectodermal dysplasia and immunodeficiency with normal serum IgG levels.
Gital Karamchandani-Patel, Eric P Hanson, Rushani Saltzman, C Eve Kimball, Ricardo U Sorensen, Jordan S Orange. Ann Allergy Asthma Immunol 2011
11
40

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Luke Jostins, Stephan Ripke, Rinse K Weersma, Richard H Duerr, Dermot P McGovern, Ken Y Hui, James C Lee, L Philip Schumm, Yashoda Sharma, Carl A Anderson,[...]. Nature 2012
40

Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.
Erik-Oliver Glocker, Daniel Kotlarz, Kaan Boztug, E Michael Gertz, Alejandro A Schäffer, Fatih Noyan, Mario Perro, Jana Diestelhorst, Anna Allroth, Dhaarini Murugan,[...]. N Engl J Med 2009
887
40

Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.
Federica Barzaghi, Laura Cristina Amaya Hernandez, Benedicte Neven, Silvia Ricci, Zeynep Yesim Kucuk, Jack J Bleesing, Zohreh Nademi, Mary Anne Slatter, Erlinda Rose Ulloa, Anna Shcherbina,[...]. J Allergy Clin Immunol 2018
105
40

Distinct Histopathological Features at Diagnosis of Very Early Onset Inflammatory Bowel Disease.
Máire A Conrad, Chrystalle Katte Carreon, Noor Dawany, Pierre Russo, Judith R Kelsen. J Crohns Colitis 2019
11
40

Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome.
Eleonora Gambineri, Sara Ciullini Mannurita, David Hagin, Marina Vignoli, Stephanie Anover-Sombke, Stacey DeBoer, Gesmar R S Segundo, Eric J Allenspach, Claudio Favre, Hans D Ochs,[...]. Front Immunol 2018
58
40

Statewide newborn screening for severe T-cell lymphopenia.
John M Routes, William J Grossman, James Verbsky, Ronald H Laessig, Gary L Hoffman, Charles D Brokopp, Mei W Baker. JAMA 2009
136
20

The EUROclass trial: defining subgroups in common variable immunodeficiency.
Claudia Wehr, Teemu Kivioja, Christian Schmitt, Berne Ferry, Torsten Witte, Efrem Eren, Marcela Vlkova, Manuel Hernandez, Drahomira Detkova, Philip R Bos,[...]. Blood 2008
508
20

Immune deficiency caused by impaired expression of nuclear factor-kappaB essential modifier (NEMO) because of a mutation in the 5' untranslated region of the NEMO gene.
Jana L Mooster, Caterina Cancrini, Alessandra Simonetti, Paolo Rossi, Gigliola Di Matteo, Maria Luisa Romiti, Silvia Di Cesare, Luigi Notarangelo, Raif S Geha, Douglas R McDonald. J Allergy Clin Immunol 2010
27
20

Long-term efficacy of enzyme replacement therapy for adenosine deaminase (ADA)-deficient severe combined immunodeficiency (SCID).
Belinda Chan, Diane Wara, John Bastian, Michael S Hershfield, John Bohnsack, Colleen G Azen, Robertson Parkman, Kenneth Weinberg, Donald B Kohn. Clin Immunol 2005
104
20

Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency.
Carrie L Lucas, Hye Sun Kuehn, Fang Zhao, Julie E Niemela, Elissa K Deenick, Umaimainthan Palendira, Danielle T Avery, Leen Moens, Jennifer L Cannons, Matthew Biancalana,[...]. Nat Immunol 2014
368
20

Update on gene therapy for adenosine deaminase-deficient severe combined immunodeficiency.
Francesca Ferrua, Immacolata Brigida, Alessandro Aiuti. Curr Opin Allergy Clin Immunol 2010
40
20

Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q.
Alejandro A Schäffer, Jessica Pfannstiel, A David B Webster, Alessandro Plebani, Lennart Hammarström, Bodo Grimbacher. Hum Genet 2006
29
20

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders.
Francisco A Bonilla, Isil Barlan, Helen Chapel, Beatriz T Costa-Carvalho, Charlotte Cunningham-Rundles, M Teresa de la Morena, Francisco J Espinosa-Rosales, Lennart Hammarström, Shigeaki Nonoyama, Isabella Quinti,[...]. J Allergy Clin Immunol Pract 2016
313
20

The overlap between allergy and immunodeficiency.
Kristin Sokol, Joshua D Milner. Curr Opin Pediatr 2018
7
20

A Practical Approach to Newborn Screening for Severe Combined Immunodeficiency Using the T Cell Receptor Excision Circle Assay.
Monica S Thakar, Mary K Hintermeyer, Miranda G Gries, John M Routes, James W Verbsky. Front Immunol 2017
19
20

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations.
Desirée Schubert, Claudia Bode, Rupert Kenefeck, Tie Zheng Hou, James B Wing, Alan Kennedy, Alla Bulashevska, Britt-Sabina Petersen, Alejandro A Schäffer, Björn A Grüning,[...]. Nat Med 2014
445
20

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
Asbjørg Stray-Pedersen, Hanne Sørmo Sorte, Pubudu Samarakoon, Tomasz Gambin, Ivan K Chinn, Zeynep H Coban Akdemir, Hans Christian Erichsen, Lisa R Forbes, Shen Gu, Bo Yuan,[...]. J Allergy Clin Immunol 2017
137
20

Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency.
Manfred Fliegauf, Vanessa L Bryant, Natalie Frede, Charlotte Slade, See-Tarn Woon, Klaus Lehnert, Sandra Winzer, Alla Bulashevska, Thomas Scerri, Euphemia Leung,[...]. Am J Hum Genet 2015
122
20

Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.
Ricardo C Ferreira, Qiang Pan-Hammarström, Robert R Graham, Vesela Gateva, Gumersindo Fontán, Annette T Lee, Ward Ortmann, Elena Urcelay, Miguel Fernández-Arquero, Concepción Núñez,[...]. Nat Genet 2010
101
20

A Markov model to analyze cost-effectiveness of screening for severe combined immunodeficiency (SCID).
Kee Chan, Joie Davis, Sung-Yun Pai, Francisco A Bonilla, Jennifer M Puck, Michael Apkon. Mol Genet Metab 2011
66
20

Screening of Newborns for Disorders with High Benefit-Risk Ratios Should Be Mandatory.
Nicole Kelly, Dalia Chehayeb Makarem, Melissa P Wasserstein. J Law Med Ethics 2016
16
20

Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.
Guillem de Valles-Ibáñez, Ana Esteve-Solé, Mònica Piquer, E Azucena González-Navarro, Jessica Hernandez-Rodriguez, Hafid Laayouni, Eva González-Roca, Ana María Plaza-Martin, Ángela Deyà-Martínez, Andrea Martín-Nalda,[...]. Front Immunol 2018
61
20

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.
Anemone Finck, Jos W M Van der Meer, Alejandro A Schäffer, Jessica Pfannstiel, Claire Fieschi, Alessandro Plebani, A David B Webster, Lennart Hammarström, Bodo Grimbacher. Eur J Hum Genet 2006
36
20


Changes in thymic function with age and during the treatment of HIV infection.
D C Douek, R D McFarland, P H Keiser, E A Gage, J M Massey, B F Haynes, M A Polis, A T Haase, M B Feinberg, J L Sullivan,[...]. Nature 1998
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
333
20

Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.
Pauline A van Schouwenburg, Emma E Davenport, Anne-Kathrin Kienzler, Ishita Marwah, Benjamin Wright, Mary Lucas, Tomas Malinauskas, Hilary C Martin, Helen E Lockstone, Jean-Baptiste Cazier,[...]. Clin Immunol 2015
59
20

Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing.
Rohan Ameratunga, Klaus Lehnert, See-Tarn Woon, David Gillis, Vanessa L Bryant, Charlotte A Slade, Richard Steele. Clin Rev Allergy Immunol 2018
42
20

Abatacept alleviates severe autoimmune symptoms in a patient carrying a de novo variant in CTLA-4.
Sangmoon Lee, Jin Soo Moon, Cho-Rong Lee, Hye-Eun Kim, Sun-Mi Baek, Solha Hwang, Gyeong Hoon Kang, Jeong Kee Seo, Choong Ho Shin, Hyoung Jin Kang,[...]. J Allergy Clin Immunol 2016
74
20

V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations.
A Villa, C Sobacchi, L D Notarangelo, F Bozzi, M Abinun, T G Abrahamsen, P D Arkwright, M Baniyash, E G Brooks, M E Conley,[...]. Blood 2001
241
20

Mutation of unique region of Bruton's tyrosine kinase in immunodeficient XID mice.
D J Rawlings, D C Saffran, S Tsukada, D A Largaespada, J C Grimaldi, L Cohen, R N Mohr, J F Bazan, M Howard, N G Copeland. Science 1993
765
20


Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
Delfien J A Bogaert, Melissa Dullaers, Bart N Lambrecht, Karim Y Vermaelen, Elfride De Baere, Filomeen Haerynck. J Med Genet 2016
131
20

Colocalization of X-linked agammaglobulinemia and X-linked immunodeficiency genes.
J D Thomas, P Sideras, C I Smith, I Vorechovský, V Chapman, W E Paul. Science 1993
576
20

DiGeorge syndrome/chromosome 22q11.2 deletion syndrome.
K E Sullivan. Curr Allergy Asthma Rep 2001
9
20

GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome.
Amy P Hsu, Kirby D Johnson, E Liana Falcone, Rajendran Sanalkumar, Lauren Sanchez, Dennis D Hickstein, Jennifer Cuellar-Rodriguez, Jacob E Lemieux, Christa S Zerbe, Emery H Bresnick,[...]. Blood 2013
142
20

Exome and genome sequencing for inborn errors of immunity.
Isabelle Meyts, Barbara Bosch, Alexandre Bolze, Bertrand Boisson, Yuval Itan, Aziz Belkadi, Vincent Pedergnana, Leen Moens, Capucine Picard, Aurélie Cobat,[...]. J Allergy Clin Immunol 2016
94
20

Genetic Diagnosis Using Whole Exome Sequencing in Common Variable Immunodeficiency.
Patrick Maffucci, Charles A Filion, Bertrand Boisson, Yuval Itan, Lei Shang, Jean-Laurent Casanova, Charlotte Cunningham-Rundles. Front Immunol 2016
136
20


Radiosensitive severe combined immunodeficiency disease.
Christopher C Dvorak, Morton J Cowan. Immunol Allergy Clin North Am 2010
40
20

Clinical efficacy of a next-generation sequencing gene panel for primary immunodeficiency diagnostics.
W Rae, D Ward, C Mattocks, R J Pengelly, E Eren, S V Patel, S N Faust, D Hunt, A P Williams. Clin Genet 2018
27
20

Common Variable Immunodeficiency with Genetic Defects Identified by Whole Exome Sequencing.
Ran Li, Yali Zheng, Yuqian Li, Rongbao Zhang, Fang Wang, Donghong Yang, Yanliang Ma, Xinlin Mu, Zhaolong Cao, Zhancheng Gao. Biomed Res Int 2018
13
20

Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature.
Katharina Schwarze, James Buchanan, Jenny C Taylor, Sarah Wordsworth. Genet Med 2018
183
20

Using ClinVar as a Resource to Support Variant Interpretation.
Steven M Harrison, Erin R Riggs, Donna R Maglott, Jennifer M Lee, Danielle R Azzariti, Annie Niehaus, Erin M Ramos, Christa L Martin, Melissa J Landrum, Heidi L Rehm. Curr Protoc Hum Genet 2016
56
20

Single-cell transcriptomics to explore the immune system in health and disease.
Michael J T Stubbington, Orit Rozenblatt-Rosen, Aviv Regev, Sarah A Teichmann. Science 2017
187
20

Clinical application of whole-genome sequencing in patients with primary immunodeficiency.
Talal Mousallem, Thomas J Urban, K Melodi McSweeney, Sarah E Kleinstein, Mingfu Zhu, Mehdi Adeli, Roberta E Parrott, Joseph L Roberts, Brian Krueger, Rebecca H Buckley,[...]. J Allergy Clin Immunol 2015
15
20

Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage.
Ivan Angulo, Oscar Vadas, Fabien Garçon, Edward Banham-Hall, Vincent Plagnol, Timothy R Leahy, Helen Baxendale, Tanya Coulter, James Curtis, Changxin Wu,[...]. Science 2013
350
20



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.