A citation-based method for searching scientific literature

Ivan K Chinn, Alice Y Chan, Karin Chen, Janet Chou, Morna J Dorsey, Joud Hajjar, Artemio M Jongco, Michael D Keller, Lisa J Kobrynski, Attila Kumanovics, Monica G Lawrence, Jennifer W Leiding, Patricia L Lugar, Jordan S Orange, Kiran Patel, Craig D Platt, Jennifer M Puck, Nikita Raje, Neil Romberg, Maria A Slack, Kathleen E Sullivan, Teresa K Tarrant, Troy R Torgerson, Jolan E Walter. J Allergy Clin Immunol 2020
Times Cited: 23







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



Times Cited
  Times     Co-cited
Similarity


Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee.
Stuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, Talal Chatila, Charlotte Cunningham-Rundles, Amos Etzioni, Jose Luis Franco, Steven M Holland, Christoph Klein, Tomohiro Morio,[...]. J Clin Immunol 2020
350
60

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
52

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
143
43

Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.
Aziz Bousfiha, Leila Jeddane, Capucine Picard, Waleed Al-Herz, Fatima Ailal, Talal Chatila, Charlotte Cunningham-Rundles, Amos Etzioni, Jose Luis Franco, Steven M Holland,[...]. J Clin Immunol 2020
182
30

International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity.
Capucine Picard, H Bobby Gaspar, Waleed Al-Herz, Aziz Bousfiha, Jean-Laurent Casanova, Talal Chatila, Yanick J Crow, Charlotte Cunningham-Rundles, Amos Etzioni, Jose Luis Franco,[...]. J Clin Immunol 2018
421
26

Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing.
Vera Gallo, Laura Dotta, Giuliana Giardino, Emilia Cirillo, Vassilios Lougaris, Roberta D'Assante, Alberto Prandini, Rita Consolini, Emily G Farrow, Isabelle Thiffault,[...]. Front Immunol 2016
40
21

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
140
21

Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies.
Isaac J Nijman, Joris M van Montfrans, Marlous Hoogstraat, Marianne L Boes, Lisette van de Corput, Ellen D Renner, Patrick van Zon, Stef van Lieshout, Martin G Elferink, Mirjam van der Burg,[...]. J Allergy Clin Immunol 2014
95
21

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
68
17

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
60
17

Sanger Confirmation Is Required to Achieve Optimal Sensitivity and Specificity in Next-Generation Sequencing Panel Testing.
Wenbo Mu, Hsiao-Mei Lu, Jefferey Chen, Shuwei Li, Aaron M Elliott. J Mol Diagn 2016
96
17

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
101
17

Targeted NGS: A Cost-Effective Approach to Molecular Diagnosis of PIDs.
Jennifer L Stoddard, Julie E Niemela, Thomas A Fleisher, Sergio D Rosenzweig. Front Immunol 2014
62
17

Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
James E D Thaventhiran, Hana Lango Allen, Oliver S Burren, William Rae, Daniel Greene, Emily Staples, Zinan Zhang, James H R Farmery, Ilenia Simeoni, Elizabeth Rivers,[...]. Nature 2020
48
17

Diagnostic Yield of Next Generation Sequencing in Genetically Undiagnosed Patients with Primary Immunodeficiencies: a Systematic Review.
Hemmo A F Yska, Kim Elsink, Taco W Kuijpers, Geert W J Frederix, Mariëlle E van Gijn, Joris M van Montfrans. J Clin Immunol 2019
25
17

Use of Genetic Testing for Primary Immunodeficiency Patients.
Jennifer R Heimall, David Hagin, Joud Hajjar, Sarah E Henrickson, Hillary S Hernandez-Trujillo, Yuval Tan, Lisa Kobrynski, Kenneth Paris, Troy R Torgerson, James W Verbsky,[...]. J Clin Immunol 2018
40
17



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
464
13

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
13

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
334
13

Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency.
Karin Chen, Emily M Coonrod, Attila Kumánovics, Zechariah F Franks, Jacob D Durtschi, Rebecca L Margraf, Wilfred Wu, Nahla M Heikal, Nancy H Augustine, Perry G Ridge,[...]. Am J Hum Genet 2013
140
13

Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4.
Hye Sun Kuehn, Weiming Ouyang, Bernice Lo, Elissa K Deenick, Julie E Niemela, Danielle T Avery, Jean-Nicolas Schickel, Dat Q Tran, Jennifer Stoddard, Yu Zhang,[...]. Science 2014
490
13

Diagnostics of primary immunodeficiency diseases: a sequencing capture approach.
Lotte N Moens, Elin Falk-Sörqvist, A Charlotta Asplund, Ewa Bernatowska, C I Edvard Smith, Mats Nilsson. PLoS One 2014
50
13

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.
Qiang Pan-Hammarström, Ulrich Salzer, Likun Du, Janne Björkander, Charlotte Cunningham-Rundles, David L Nelson, Chiara Bacchelli, H Bobby Gaspar, Steven Offer, Timothy W Behrens,[...]. Nat Genet 2007
152
13

Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency.
Hassan Abolhassani, Asghar Aghamohammadi, Mingyan Fang, Nima Rezaei, Chongyi Jiang, Xiao Liu, Qiang Pan-Hammarström, Lennart Hammarström. Genet Med 2019
55
13

Guidelines for genetic studies in single patients: lessons from primary immunodeficiencies.
Jean-Laurent Casanova, Mary Ellen Conley, Stephen J Seligman, Laurent Abel, Luigi D Notarangelo. J Exp Med 2014
140
13

AUTOIMMUNE DISEASE. Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy.
Bernice Lo, Kejian Zhang, Wei Lu, Lixin Zheng, Qian Zhang, Chrysi Kanellopoulou, Yu Zhang, Zhiduo Liu, Jill M Fritz, Rebecca Marsh,[...]. Science 2015
334
13

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity.
Markus G Seidel, Gerhard Kindle, Benjamin Gathmann, Isabella Quinti, Matthew Buckland, Joris van Montfrans, Raphael Scheible, Stephan Rusch, Lukas M Gasteiger, Bodo Grimbacher,[...]. J Allergy Clin Immunol Pract 2019
140
13

Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.
Hamoud Al-Mousa, Mohamed Abouelhoda, Dorota M Monies, Nada Al-Tassan, Abdulaziz Al-Ghonaium, Bandar Al-Saud, Hasan Al-Dhekri, Rand Arnaout, Saleh Al-Muhsen, Nazema Ades,[...]. J Allergy Clin Immunol 2016
73
13

Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies.
Peer Arts, Annet Simons, Mofareh S AlZahrani, Elanur Yilmaz, Eman AlIdrissi, Koen J van Aerde, Njood Alenezi, Hamza A AlGhamdi, Hadeel A AlJubab, Abdulrahman A Al-Hussaini,[...]. Genome Med 2019
20
15

Expanding the Clinical and Genetic Spectra of Primary Immunodeficiency-Related Disorders With Clinical Exome Sequencing: Expected and Unexpected Findings.
Francesc Rudilla, Clara Franco-Jarava, Mónica Martínez-Gallo, Marina Garcia-Prat, Andrea Martín-Nalda, Jacques Rivière, Aina Aguiló-Cucurull, Laura Mongay, Francisco Vidal, Xavier Solanich,[...]. Front Immunol 2019
17
17

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
261
13

Inborn Errors of Immunity With Immune Dysregulation: From Bench to Bedside.
Ottavia Maria Delmonte, Riccardo Castagnoli, Enrica Calzoni, Luigi Daniele Notarangelo. Front Pediatr 2019
29
13

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
13

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.
Keith Nykamp, Michael Anderson, Martin Powers, John Garcia, Blanca Herrera, Yuan-Yuan Ho, Yuya Kobayashi, Nila Patil, Janita Thusberg, Marjorie Westbrook,[...]. Genet Med 2017
246
13

Uses of Next-Generation Sequencing Technologies for the Diagnosis of Primary Immunodeficiencies.
Michael Seleman, Rodrigo Hoyos-Bachiloglu, Raif S Geha, Janet Chou. Front Immunol 2017
42
13


A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.
Qing Zhou, Geun-Shik Lee, Jillian Brady, Shrimati Datta, Matilda Katan, Afzal Sheikh, Marta S Martins, Tom D Bunney, Brian H Santich, Susan Moir,[...]. Am J Hum Genet 2012
193
8

Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
Aziz Belkadi, Alexandre Bolze, Yuval Itan, Aurélie Cobat, Quentin B Vincent, Alexander Antipenko, Lei Shang, Bertrand Boisson, Jean-Laurent Casanova, Laurent Abel. Proc Natl Acad Sci U S A 2015
265
8

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.
Ulrich Salzer, Chiara Bacchelli, Sylvie Buckridge, Qiang Pan-Hammarström, Stephanie Jennings, Vassilis Lougaris, Astrid Bergbreiter, Tina Hagena, Jennifer Birmelin, Alessandro Plebani,[...]. Blood 2009
168
8

Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency.
Bodo Grimbacher, Andreas Hutloff, Michael Schlesier, Erik Glocker, Klaus Warnatz, Ruth Dräger, Hermann Eibel, Beate Fischer, Alejandro A Schäffer, Hans W Mages,[...]. Nat Immunol 2003
513
8

A human immunodeficiency caused by mutations in the PIK3R1 gene.
Marie-Céline Deau, Lucie Heurtier, Pierre Frange, Felipe Suarez, Christine Bole-Feysot, Patrick Nitschke, Marina Cavazzana, Capucine Picard, Anne Durandy, Alain Fischer,[...]. J Clin Invest 2014
146
8

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.
Paul Tuijnenburg, Hana Lango Allen, Siobhan O Burns, Daniel Greene, Machiel H Jansen, Emily Staples, Jonathan Stephens, Keren J Carss, Daniele Biasci, Helen Baxendale,[...]. J Allergy Clin Immunol 2018
82
8

Effective "activated PI3Kδ syndrome"-targeted therapy with the PI3Kδ inhibitor leniolisib.
V Koneti Rao, Sharon Webster, Virgil A S H Dalm, Anna Šedivá, P Martin van Hagen, Steven Holland, Sergio D Rosenzweig, Andreas D Christ, Birgitte Sloth, Maciej Cabanski,[...]. Blood 2017
129
8

Inborn errors of human STAT1: allelic heterogeneity governs the diversity of immunological and infectious phenotypes.
Stephanie Boisson-Dupuis, Xiao-Fei Kong, Satoshi Okada, Sophie Cypowyj, Anne Puel, Laurent Abel, Jean-Laurent Casanova. Curr Opin Immunol 2012
169
8

Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis.
Luyan Liu, Satoshi Okada, Xiao-Fei Kong, Alexandra Y Kreins, Sophie Cypowyj, Avinash Abhyankar, Julie Toubiana, Yuval Itan, Magali Audry, Patrick Nitschke,[...]. J Exp Med 2011
495
8

Use of whole exome and genome sequencing in the identification of genetic causes of primary immunodeficiencies.
Janet Chou, Toshiro K Ohsumi, Raif S Geha. Curr Opin Allergy Clin Immunol 2012
43
8

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.
U Salzer, H M Chapel, A D B Webster, Q Pan-Hammarström, A Schmitt-Graeff, M Schlesier, H H Peter, J K Rockstroh, P Schneider, A A Schäffer,[...]. Nat Genet 2005
455
8

Burden of copy number variation in common variable immunodeficiency.
M Keller, J Glessner, E Resnick, E Perez, H Chapel, M Lucas, K E Sullivan, C Cunningham-Rundles, J S Orange, H Hakonarson. Clin Exp Immunol 2014
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.