A citation-based method for searching scientific literature

Emily E Groopman, Gundula Povysil, David B Goldstein, Ali G Gharavi. Nat Rev Nephrol 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Mutations in PAX2 associate with adult-onset FSGS.
Moumita Barua, Emilia Stellacci, Lorenzo Stella, Astrid Weins, Giulio Genovese, Valentina Muto, Viviana Caputo, Hakan R Toka, Victoria T Charoonratana, Marco Tartaglia,[...]. J Am Soc Nephrol 2014
53
66

Diagnostic Utility of Exome Sequencing for Kidney Disease.
Emily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, Slavé Petrovski, Vimla S Aggarwal, Hila Milo-Rasouly, Yifu Li, Junying Zhang, Jordan Nestor, Priya Krithivasan,[...]. N Engl J Med 2019
144
66

Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
Nina Mann, Daniela A Braun, Kassaundra Amann, Weizhen Tan, Shirlee Shril, Dervla M Connaughton, Makiko Nakayama, Ronen Schneider, Thomas M Kitzler, Amelie T van der Ven,[...]. J Am Soc Nephrol 2019
35
66

Exploring the genetic basis of early-onset chronic kidney disease.
Asaf Vivante, Friedhelm Hildebrandt. Nat Rev Nephrol 2016
134
66

Monogenic causes of chronic kidney disease in adults.
Dervla M Connaughton, Claire Kennedy, Shirlee Shril, Nina Mann, Susan L Murray, Patrick A Williams, Eoin Conlon, Makiko Nakayama, Amelie T van der Ven, Hadas Ityel,[...]. Kidney Int 2019
47
66

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Jillian K Warejko, Weizhen Tan, Ankana Daga, David Schapiro, Jennifer A Lawson, Shirlee Shril, Svjetlana Lovric, Shazia Ashraf, Jia Rao, Tobias Hermle,[...]. Clin J Am Soc Nephrol 2018
72
66

Forecasting life expectancy, years of life lost, and all-cause and cause-specific mortality for 250 causes of death: reference and alternative scenarios for 2016-40 for 195 countries and territories.
Kyle J Foreman, Neal Marquez, Andrew Dolgert, Kai Fukutaki, Nancy Fullman, Madeline McGaughey, Martin A Pletcher, Amanda E Smith, Kendrick Tang, Chun-Wei Yuan,[...]. Lancet 2018
409
66

Insights into genetics, human biology and disease gleaned from family based genomic studies.
Jennifer E Posey, Anne H O'Donnell-Luria, Jessica X Chong, Tamar Harel, Shalini N Jhangiani, Zeynep H Coban Akdemir, Steven Buyske, Davut Pehlivan, Claudia M B Carvalho, Samantha Baxter,[...]. Genet Med 2019
59
33

Dent's disease complicated by nephrotic syndrome: A case report.
Guohua He, Hongwen Zhang, Shanshan Cao, Huijie Xiao, Yong Yao. Intractable Rare Dis Res 2016
5
33

Genetic testing can resolve diagnostic confusion in Alport syndrome.
Jennifer Adam, Thomas M F Connor, Katrina Wood, David Lewis, Ramesh Naik, Daniel P Gale, John A Sayer. Clin Kidney J 2014
14
33

Diagnosis of monogenic chronic kidney diseases.
Margaret E Armstrong, Christie P Thomas. Curr Opin Nephrol Hypertens 2019
11
33

COL4A3 mutations cause focal segmental glomerulosclerosis.
Jingyuan Xie, Xiaoxi Wu, Hong Ren, Weiming Wang, Zhaohui Wang, Xiaoxia Pan, Xu Hao, Jun Tong, Jun Ma, Zhibin Ye,[...]. J Mol Cell Biol 2014
31
33

Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome.
Anja K Büscher, Bodo B Beck, Anette Melk, Julia Hoefele, Birgitta Kranz, Daniel Bamborschke, Sabrina Baig, Bärbel Lange-Sperandio, Theresa Jungraithmayr, Lutz T Weber,[...]. Clin J Am Soc Nephrol 2016
54
33

An updated review on phenocopies of primary immunodeficiency diseases.
Ankita Singh, Ankur K Jindal, Vibhu Joshi, Gummadi Anjani, Amit Rawat. Genes Dis 2019
8
33

Renal replacement therapy for rare diseases affecting the kidney: an analysis of the ERA-EDTA Registry.
Elke Wühl, Karlijn J van Stralen, Christoph Wanner, Gema Ariceta, James Goya Heaf, Anna K Bjerre, Runolfur Palsson, Gabrielle Duneau, Andries J Hoitsma, Pietro Ravani,[...]. Nephrol Dial Transplant 2014
31
33

Complete Remission in the Nephrotic Syndrome Study Network.
Debbie S Gipson, Jonathan P Troost, Richard A Lafayette, Michelle A Hladunewich, Howard Trachtman, Crystal A Gadegbeku, John R Sedor, Lawrence B Holzman, Marva M Moxey-Mims, Kalyani Perumal,[...]. Clin J Am Soc Nephrol 2016
34
33

Diagnostic Clues for the Diagnosis of Nonsarcomeric Hypertrophic Cardiomyopathy (Phenocopies): Amyloidosis, Fabry Disease, and Mitochondrial Disease.
Giuseppe Limongelli, Daniele Masarone, Marina Verrengia, Rita Gravino, Gemma Salerno, Silvia Castelletti, Marta Rubino, Tommaso Marrazzo, Antonio Pisani, Franco Cecchi,[...]. J Cardiovasc Echogr 2018
5
33


Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.
Murim Choi, Ute I Scholl, Weizhen Ji, Tiewen Liu, Irina R Tikhonova, Paul Zumbo, Ahmet Nayir, Ayşin Bakkaloğlu, Seza Ozen, Sami Sanjad,[...]. Proc Natl Acad Sci U S A 2009
833
33

Parkinson Disease from Mendelian Forms to Genetic Susceptibility: New Molecular Insights into the Neurodegeneration Process.
Amin Karimi-Moghadam, Saeid Charsouei, Benjamin Bell, Mohammad Reza Jabalameli. Cell Mol Neurobiol 2018
55
33

What's up in the ALPS.
Frédéric Rieux-Laucat. Curr Opin Immunol 2017
13
33

Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.
Tamás Szabó, Petronella Orosz, Eszter Balogh, Eszter Jávorszky, István Máttyus, Csaba Bereczki, Zoltán Maróti, Tibor Kalmár, Attila J Szabó, George Reusz,[...]. Pediatr Nephrol 2018
12
33

Human teratogens and genetic phenocopies. Understanding pathogenesis through human genes mutation.
Matteo Cassina, Giulia A Cagnoli, Daniela Zuccarello, Elena Di Gianantonio, Maurizio Clementi. Eur J Med Genet 2017
11
33

Glomerular Pathology in Dent Disease and Its Association with Kidney Function.
Xiangling Wang, Franca Anglani, Lada Beara-Lasic, Anila J Mehta, Lisa E Vaughan, Loren Herrera Hernandez, Andrea Cogal, Steven J Scheinman, Gema Ariceta, Robert Isom,[...]. Clin J Am Soc Nephrol 2016
26
33

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
Andrew F Malone, Paul J Phelan, Gentzon Hall, Umran Cetincelik, Alison Homstad, Andrea S Alonso, Ruiji Jiang, Thomas B Lindsey, Guanghong Wu, Matthew A Sparks,[...]. Kidney Int 2014
109
33

Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
Gemma Bullich, Daniel Trujillano, Sheila Santín, Stephan Ossowski, Santiago Mendizábal, Gloria Fraga, Álvaro Madrid, Gema Ariceta, José Ballarín, Roser Torra,[...]. Eur J Hum Genet 2015
52
33

A case of adult Dent disease in Japan with advanced chronic kidney disease.
Ken Saida, Yuji Kamijo, Daisuke Matsuoka, Shunsuke Noda, Yoshihiko Hidaka, Tetsuo Mori, Hisashi Shimojo, Takashi Ehara, Kenichiro Miura, Junko Takita,[...]. CEN Case Rep 2014
3
33

Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
Agnes Trautmann, Monica Bodria, Fatih Ozaltin, Alaleh Gheisari, Anette Melk, Marta Azocar, Ali Anarat, Salim Caliskan, Francesco Emma, Jutta Gellermann,[...]. Clin J Am Soc Nephrol 2015
133
33

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation.
Bénédicte Neven, Aude Magerus-Chatinet, Benoit Florkin, Delphine Gobert, Olivier Lambotte, Lien De Somer, Nina Lanzarotti, Marie-Claude Stolzenberg, Brigitte Bader-Meunier, Nathalie Aladjidi,[...]. Blood 2011
82
33

Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidney disease from focal segmental glomerulosclerosis.
Alkis Pierides, Konstantinos Voskarides, Yiannis Athanasiou, Kyriacos Ioannou, Loukas Damianou, Maria Arsali, Michalis Zavros, Michael Pierides, Vasilios Vargemezis, Charalambos Patsias,[...]. Nephrol Dial Transplant 2009
82
33

Autoantibody-mediated acquired deficiency of C1 inhibitor.
J Alsenz, K Bork, M Loos. N Engl J Med 1987
169
33

A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases.
Gemma Bullich, Andrea Domingo-Gallego, Iván Vargas, Patricia Ruiz, Laura Lorente-Grandoso, Mónica Furlano, Gloria Fraga, Álvaro Madrid, Gema Ariceta, Mar Borregán,[...]. Kidney Int 2018
39
33

Brugada phenocopy: new terminology and proposed classification.
Adrian Baranchuk, Timothy Nguyen, Min Hyung Ryu, Francisco Femenía, Wojciech Zareba, Arthur A M Wilde, Wataru Shimizu, Pedro Brugada, Andrés R Pérez-Riera. Ann Noninvasive Electrocardiol 2012
133
33


Propofol infusion syndrome and Brugada syndrome electrocardiographic phenocopy.
Andrés Ricardo Pérez Riera, Augusto Hiroshi Uchida, Edgardo Schapachnik, Sergio Dubner, Celso Ferreira Filho, Celso Ferreira. Cardiol J 2010
23
33

Phenocopies.
W Lenz. J Med Genet 1973
13
33


Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
Beata S Lipska, Paraskevas Iatropoulos, Ramona Maranta, Gianluca Caridi, Fatih Ozaltin, Ali Anarat, Ayse Balat, Jutta Gellermann, Agnes Trautmann, Ozlem Erdogan,[...]. Kidney Int 2013
53
33

DNA sequencing with chain-terminating inhibitors.
F Sanger, S Nicklen, A R Coulson. Proc Natl Acad Sci U S A 1977
33

Chronic kidney disease: global dimension and perspectives.
Vivekanand Jha, Guillermo Garcia-Garcia, Kunitoshi Iseki, Zuo Li, Saraladevi Naicker, Brett Plattner, Rajiv Saran, Angela Yee-Moon Wang, Chih-Wei Yang. Lancet 2013
33

Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies.
Korbinian M Riedhammer, Matthias C Braunisch, Roman Günthner, Matias Wagner, Clara Hemmer, Tim M Strom, Christoph Schmaderer, Lutz Renders, Velibor Tasic, Zoran Gucev,[...]. Am J Kidney Dis 2020
8
33

Phenocopy--a strategy to qualify chemical compounds during hit-to-lead and/or lead optimization.
Patrick Baum, Ramona Schmid, Carina Ittrich, Werner Rust, Katrin Fundel-Clemens, Susanne Siewert, Martin Baur, Lisa Mara, Lore Gruenbaum, Armin Heckel,[...]. PLoS One 2010
6
33

Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.
Mev Dominguez-Valentin, D Gareth R Evans, Sigve Nakken, Hélène Tubeuf, Daniel Vodak, Per Olaf Ekstrøm, Anke M Nissen, Monika Morak, Elke Holinski-Feder, Alexandra Martins,[...]. Hered Cancer Clin Pract 2018
7
33

Genome sequencing: a systematic review of health economic evidence.
Martin Frank, Anne Prenzler, Roland Eils, J-Matthias Graf von der Schulenburg. Health Econ Rev 2013
35
33

Diagnostic Yield of Next-Generation Sequencing in Patients With Chronic Kidney Disease of Unknown Etiology.
Amber de Haan, Mark Eijgelsheim, Liffert Vogt, Nine V A M Knoers, Martin H de Borst. Front Genet 2019
6
33

Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies.
Heon Yung Gee, Edgar A Otto, Toby W Hurd, Shazia Ashraf, Moumita Chaki, Andrew Cluckey, Virginia Vega-Warner, Pawaree Saisawat, Katrina A Diaz, Humphrey Fang,[...]. Kidney Int 2014
50
33

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.
Ankana Daga, Amar J Majmundar, Daniela A Braun, Heon Yung Gee, Jennifer A Lawson, Shirlee Shril, Tilman Jobst-Schwan, Asaf Vivante, David Schapiro, Weizhen Tan,[...]. Kidney Int 2018
57
33

Podocytopathies.
Jeffrey B Kopp, Hans-Joachim Anders, Katalin Susztak, Manuel A Podestà, Giuseppe Remuzzi, Friedhelm Hildebrandt, Paola Romagnani. Nat Rev Dis Primers 2020
23
33

Rare-disease genetics in the era of next-generation sequencing: discovery to translation.
Kym M Boycott, Megan R Vanstone, Dennis E Bulman, Alex E MacKenzie. Nat Rev Genet 2013
414
33

Advances in renal genetic diagnosis.
Carsten Bergmann. Cell Tissue Res 2017
8
33


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.