A citation-based method for searching scientific literature

Can Kosukcu, Ekim Z Taskiran, Ezgi Deniz Batu, Erdal Sag, Yelda Bilginer, Mehmet Alikasifoglu, Seza Ozen. Rheumatology (Oxford) 2021
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
42

Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease.
Najoua Lalaoui, Steven E Boyden, Hirotsugu Oda, Geryl M Wood, Deborah L Stone, Diep Chau, Lin Liu, Monique Stoffels, Tobias Kratina, Kate E Lawlor,[...]. Nature 2020
89
28

A dominant autoinflammatory disease caused by non-cleavable variants of RIPK1.
Panfeng Tao, Jinqiao Sun, Zheming Wu, Shihao Wang, Jun Wang, Wanjin Li, Heling Pan, Renkui Bai, Jiahui Zhang, Ying Wang,[...]. Nature 2020
64
28

New workflow for classification of genetic variants' pathogenicity applied to hereditary recurrent fevers by the International Study Group for Systemic Autoinflammatory Diseases (INSAID).
Marielle E Van Gijn, Isabella Ceccherini, Yael Shinar, Ellen C Carbo, Mariska Slofstra, Juan I Arostegui, Guillaume Sarrabay, Dorota Rowczenio, Ebun Omoyımnı, Banu Balci-Peynircioglu,[...]. J Med Genet 2018
56
28

Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis.
Ebun Omoyinmi, Ariane Standing, Annette Keylock, Fiona Price-Kuehne, Sonia Melo Gomes, Dorota Rowczenio, Sira Nanthapisal, Thomas Cullup, Rodney Nyanhete, Emma Ashton,[...]. PLoS One 2017
41
28

Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study.
Carlo De Pieri, Josef Vuch, Eleonora De Martino, Anna M Bianco, Luca Ronfani, Emmanouil Athanasakis, Barbara Bortot, Sergio Crovella, Andrea Taddio, Giovanni M Severini,[...]. Pediatr Rheumatol Online J 2015
16
28

Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes.
Berk Ozyilmaz, Ozgur Kirbiyik, Altug Koc, Taha R Ozdemir, Ozge Kaya Ozer, Yasar B Kutbay, Kadri M Erdogan, Merve Saka Guvenc, Can Ozturk. Int J Immunogenet 2019
3
66

Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases.
Nienke M Ter Haar, Charlotte Eijkelboom, Luca Cantarini, Riccardo Papa, Paul A Brogan, Isabelle Kone-Paut, Consuelo Modesto, Michael Hofer, Nicolae Iagaru, Sárka Fingerhutová,[...]. Ann Rheum Dis 2019
17
28

Classification criteria for autoinflammatory recurrent fevers.
Marco Gattorno, Michael Hofer, Silvia Federici, Federica Vanoni, Francesca Bovis, Ivona Aksentijevich, Jordi Anton, Juan Ignacio Arostegui, Karyl Barron, Eldad Ben-Cherit,[...]. Ann Rheum Dis 2019
103
28

Genetic panel screening in patients with clinically unclassified systemic autoinflammatory diseases.
Ferhat Demir, Özlem Akgün Doğan, Yasemin Kendir Demirkol, Kübra Ermiş Tekkuş, Sezin Canbek, Şerife Gül Karadağ, Hafize Emine Sönmez, Nuray Aktay Ayaz, Hamdi Levent Doğanay, Betül Sözeri. Clin Rheumatol 2020
2
100

Next-generation sequencing and its initial applications for molecular diagnosis of systemic auto-inflammatory diseases.
Marta Rusmini, Silvia Federici, Francesco Caroli, Alice Grossi, Maurizia Baldi, Laura Obici, Antonella Insalaco, Alberto Tommasini, Roberta Caorsi, Eleonora Gallo,[...]. Ann Rheum Dis 2016
40
28

Periodic fever syndrome in children.
K T Thomas, H M Feder, A R Lawton, K M Edwards. J Pediatr 1999
277
28

Presence of Genetic Variants Among Young Men With Severe COVID-19.
Caspar I van der Made, Annet Simons, Janneke Schuurs-Hoeijmakers, Guus van den Heuvel, Tuomo Mantere, Simone Kersten, Rosanne C van Deuren, Marloes Steehouwer, Simon V van Reijmersdal, Martin Jaeger,[...]. JAMA 2020
264
28

The roles of two IkappaB kinase-related kinases in lipopolysaccharide and double stranded RNA signaling and viral infection.
Hiroaki Hemmi, Osamu Takeuchi, Shintaro Sato, Masahiro Yamamoto, Tsuneyasu Kaisho, Hideki Sanjo, Taro Kawai, Katsuaki Hoshino, Kiyoshi Takeda, Shizuo Akira. J Exp Med 2004
428
28

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.
Qian Zhang, Paul Bastard, Zhiyong Liu, Jérémie Le Pen, Marcela Moncada-Velez, Jie Chen, Masato Ogishi, Ira K D Sabli, Stephanie Hodeib, Cecilia Korol,[...]. Science 2020
755
28

Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals.
Jack A Kosmicki, Julie E Horowitz, Nilanjana Banerjee, Rouel Lanche, Anthony Marcketta, Evan Maxwell, Xiaodong Bai, Dylan Sun, Joshua D Backman, Deepika Sharma,[...]. Am J Hum Genet 2021
12
28

Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.
Gundula Povysil, Guillaume Butler-Laporte, Ning Shang, Chen Wang, Atlas Khan, Manal Alaamery, Tomoko Nakanishi, Sirui Zhou, Vincenzo Forgetta, Robert Jm Eveleigh,[...]. J Clin Invest 2021
17
28

Characteristics and Outcomes of US Children and Adolescents With Multisystem Inflammatory Syndrome in Children (MIS-C) Compared With Severe Acute COVID-19.
Leora R Feldstein, Mark W Tenforde, Kevin G Friedman, Margaret Newhams, Erica Billig Rose, Heda Dapul, Vijaya L Soma, Aline B Maddux, Peter M Mourani, Cindy Bowens,[...]. JAMA 2021
124
28

Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.
Anja Brehm, Yin Liu, Afzal Sheikh, Bernadette Marrero, Ebun Omoyinmi, Qing Zhou, Gina Montealegre, Angelique Biancotto, Adam Reinhardt, Adriana Almeida de Jesus,[...]. J Clin Invest 2015
139
14

Exome sequencing has higher diagnostic yield compared to simulated disease-specific panels in children with suspected monogenic disorders.
Oliver James Dillon, Sebastian Lunke, Zornitza Stark, Alison Yeung, Natalie Thorne, Clara Gaff, Susan M White, Tiong Yang Tan. Eur J Hum Genet 2018
51
14

Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome.
Antonio Torrelo, Sapna Patel, Isabel Colmenero, Dolores Gurbindo, Francisco Lendínez, Angela Hernández, Juan Carlos López-Robledillo, Ali Dadban, Luis Requena, Amy S Paller. J Am Acad Dermatol 2010
109
14

DNA polymerase-α regulates the activation of type I interferons through cytosolic RNA:DNA synthesis.
Petro Starokadomskyy, Terry Gemelli, Jonathan J Rios, Chao Xing, Richard C Wang, Haiying Li, Vladislav Pokatayev, Igor Dozmorov, Shaheen Khan, Naoteru Miyata,[...]. Nat Immunol 2016
70
14

Activated STING in a vascular and pulmonary syndrome.
Y Liu, A A Jesus, B Marrero, D Yang, S E Ramsey, G A Montealegre Sanchez, K Tenbrock, H Wittkowski, O Y Jones, H S Kuehn,[...]. N Engl J Med 2014
624
14

Brief Report: Association of Tumor Necrosis Factor Receptor-Associated Periodic Syndrome With Gonosomal Mosaicism of a Novel 24-Nucleotide TNFRSF1A Deletion.
Dorota M Rowczenio, Hadija Trojer, Ebun Omoyinmi, Juan I Aróstegui, Grigor Arakelov, Anna Mensa-Vilaro, Anna Baginska, Caroline Silva Pilorz, Guosu Wang, Thirusha Lane,[...]. Arthritis Rheumatol 2016
30
14

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.
Anath C Lionel, Gregory Costain, Nasim Monfared, Susan Walker, Miriam S Reuter, S Mohsen Hosseini, Bhooma Thiruvahindrapuram, Daniele Merico, Rebekah Jobling, Thomas Nalpathamkalam,[...]. Genet Med 2018
192
14

Human protein-coding genes and gene feature statistics in 2019.
Allison Piovesan, Francesca Antonaros, Lorenza Vitale, Pierluigi Strippoli, Maria Chiara Pelleri, Maria Caracausi. BMC Res Notes 2019
32
14

Updated recommendation for the benign stand-alone ACMG/AMP criterion.
Rajarshi Ghosh, Steven M Harrison, Heidi L Rehm, Sharon E Plon, Leslie G Biesecker. Hum Mutat 2018
30
14

Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
Laura M Amendola, Gail P Jarvik, Michael C Leo, Heather M McLaughlin, Yassmine Akkari, Michelle D Amaral, Jonathan S Berg, Sawona Biswas, Kevin M Bowling, Laura K Conlin,[...]. Am J Hum Genet 2016
239
14

Somatic Variants: New Kids on the Block in Human Immunogenetics.
L Van Horebeek, B Dubois, A Goris. Trends Genet 2019
13
14

A novel Pyrin-Associated Autoinflammation with Neutrophilic Dermatosis mutation further defines 14-3-3 binding of pyrin and distinction to Familial Mediterranean Fever.
Fiona Moghaddas, Rafael Llamas, Dominic De Nardo, Helios Martinez-Banaclocha, Juan J Martinez-Garcia, Pablo Mesa-Del-Castillo, Paul J Baker, Vanessa Gargallo, Anna Mensa-Vilaro, Scott Canna,[...]. Ann Rheum Dis 2017
64
14

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
14

Blood-based test for diagnosis and functional subtyping of familial Mediterranean fever.
Hanne Van Gorp, Linyan Huang, Pedro Saavedra, Marnik Vuylsteke, Tomoko Asaoka, Giusi Prencipe, Antonella Insalaco, Benson Ogunjimi, Jerold Jeyaratnam, Ilaria Cataldo,[...]. Ann Rheum Dis 2020
14
14

Heterozygous Truncating Variants in POMP Escape Nonsense-Mediated Decay and Cause a Unique Immune Dysregulatory Syndrome.
M Cecilia Poli, Frédéric Ebstein, Sarah K Nicholas, Marietta M de Guzman, Lisa R Forbes, Ivan K Chinn, Emily M Mace, Tiphanie P Vogel, Alexandre F Carisey, Felipe Benavides,[...]. Am J Hum Genet 2018
65
14

Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases.
Anna Mensa-Vilaró, María Bravo García-Morato, Oscar de la Calle-Martin, Clara Franco-Jarava, María Teresa Martínez-Saavedra, Luis I González-Granado, Eva González-Roca, Jose Luis Fuster, Laia Alsina, Osvaldo M Mutchinick,[...]. J Allergy Clin Immunol 2019
24
14

Benefits and limitations of genome-wide association studies.
Vivian Tam, Nikunj Patel, Michelle Turcotte, Yohan Bossé, Guillaume Paré, David Meyre. Nat Rev Genet 2019
324
14


Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification framework.
Sean V Tavtigian, Marc S Greenblatt, Steven M Harrison, Robert L Nussbaum, Snehit A Prabhu, Kenneth M Boucher, Leslie G Biesecker. Genet Med 2018
118
14

Dominant familial Mediterranean fever.
Guillaume Sarrabay, Isabelle Touitou. Rheumatology (Oxford) 2017
7
14

Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature.
Dorota M Rowczenio, Hadija Trojer, Tonia Russell, Anna Baginska, Thirusha Lane, Nicola M Stewart, Julian D Gillmore, Philip N Hawkins, Patricia Woo, Bozena Mikoluc,[...]. Arthritis Res Ther 2013
37
14

Monogenic autoinflammatory diseases.
Ricardo A G Russo, Paul A Brogan. Rheumatology (Oxford) 2014
15
14

Evidence-based provisional clinical classification criteria for autoinflammatory periodic fevers.
Silvia Federici, Maria Pia Sormani, Seza Ozen, Helen J Lachmann, Gayane Amaryan, Patricia Woo, Isabelle Koné-Paut, Natacha Dewarrat, Luca Cantarini, Antonella Insalaco,[...]. Ann Rheum Dis 2015
136
14

A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry.
Riccardo Papa, Matteo Doglio, Helen J Lachmann, Seza Ozen, Joost Frenkel, Anna Simon, Bénédicte Neven, Jasmin Kuemmerle-Deschner, Huri Ozgodan, Roberta Caorsi,[...]. Orphanet J Rare Dis 2017
30
14

The musculoskeletal system manifestations in children with familial Mediterranean fever.
Ferhat Demir, Gizem Leyla Bolac, Tuba Merter, Sezin Canbek, Ozlem Akgun Dogan, Yasemin Kendir Demirkol, Jale Yildiz, Hamdi Levent Doganay, Betul Sozeri. North Clin Istanb 2020
1
100

Profile of new referrals to a single pediatric rheumatology center in Turkey.
Şerife Gül Karadağ, Hafize Emine Sönmez, Ayşe Tanatar, Figen Çakmak, Mustafa Çakan, Nuray Aktay Ayaz. Rheumatol Int 2020
5
20

Old Dogs, New Tricks: Monogenic Autoinflammatory Disease Unleashed.
Monique Stoffels, Daniel L Kastner. Annu Rev Genomics Hum Genet 2016
28
14

Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes.
Isabelle Jéru, Gaëlle Le Borgne, Emmanuelle Cochet, Hasmik Hayrapetyan, Philippe Duquesnoy, Gilles Grateau, Alain Morali, Tamara Sarkisian, Serge Amselem. Arthritis Rheum 2011
64
14

Profile of a pediatric rheumatology practice in Israel.
P J Hashkes. Clin Exp Rheumatol 2003
5
20

Criteria for the diagnosis of familial Mediterranean fever.
A Livneh, P Langevitz, D Zemer, N Zaks, S Kees, T Lidar, A Migdal, S Padeh, M Pras. Arthritis Rheum 1997
14

Role of Colchicine Treatment in Tumor Necrosis Factor Receptor Associated Periodic Syndrome (TRAPS): Real-Life Data from the AIDA Network.
Antonio Vitale, Jurgen Sota, Laura Obici, Nicola Ricco, Maria Cristina Maggio, Marco Cattalini, Piero Ruscitti, Francesco Caso, Raffaele Manna, Ombretta Viapiana,[...]. Mediators Inflamm 2020
4
25

Colchicine in the treatment of AA and AL amyloidosis.
A Livneh, D Zemer, P Langevitz, J Shemer, E Sohar, M Pras. Semin Arthritis Rheum 1993
52
14


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.