A citation-based method for searching scientific literature

Rik Westland, Miguel Verbitsky, Katarina Vukojevic, Brittany J Perry, David A Fasel, Petra J G Zwijnenburg, Arend Bökenkamp, Johan J P Gille, Mirna Saraga-Babic, Gian Marco Ghiggeri, Vivette D D'Agati, Michiel F Schreuder, Ali G Gharavi, Joanna A E van Wijk, Simone Sanna-Cherchi. Kidney Int 2015
Times Cited: 41







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



Times Cited
  Times     Co-cited
Similarity


Copy-number disorders are a common cause of congenital kidney malformations.
Simone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, Monica Bodria, Matthew G Sampson, Dexter Hadley, Shannon N Nees, Miguel Verbitsky, Brittany J Perry, Roel Sterken,[...]. Am J Hum Genet 2012
121
70

Genetic, environmental, and epigenetic factors involved in CAKUT.
Nayia Nicolaou, Kirsten Y Renkema, Ernie M H F Bongers, Rachel H Giles, Nine V A M Knoers. Nat Rev Nephrol 2015
115
39

Genomic imbalances in pediatric patients with chronic kidney disease.
Miguel Verbitsky, Simone Sanna-Cherchi, David A Fasel, Brynn Levy, Krzysztof Kiryluk, Matthias Wuttke, Alison G Abraham, Frederick Kaskel, Anna Köttgen, Bradley A Warady,[...]. J Clin Invest 2015
46
39

Copy-number variation associated with congenital anomalies of the kidney and urinary tract.
Georgina Caruana, Milagros N Wong, Amanda Walker, Yves Heloury, Nathalie Webb, Lilian Johnstone, Paul A James, Trent Burgess, John F Bertram. Pediatr Nephrol 2015
36
41

Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.
Daw-Yang Hwang, Gabriel C Dworschak, Stefan Kohl, Pawaree Saisawat, Asaf Vivante, Alina C Hilger, Heiko M Reutter, Neveen A Soliman, Radovan Bogdanovic, Elijah O Kehinde,[...]. Kidney Int 2014
120
36

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study.
Stefanie Weber, Vincent Moriniere, Tanja Knüppel, Marina Charbit, Jirí Dusek, Gian Marco Ghiggeri, Augustina Jankauskiené, Sevgi Mir, Giovanni Montini, Amira Peco-Antic,[...]. J Am Soc Nephrol 2006
211
31

Renal outcome in patients with congenital anomalies of the kidney and urinary tract.
Simone Sanna-Cherchi, Pietro Ravani, Valentina Corbani, Stefano Parodi, Riccardo Haupt, Giorgio Piaggio, Maria L Degli Innocenti, Danio Somenzi, Antonella Trivelli, Gianluca Caridi,[...]. Kidney Int 2009
182
31


Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT.
Nayia Nicolaou, Sara L Pulit, Isaac J Nijman, Glen R Monroe, Wout F J Feitz, Michiel F Schreuder, Albertien M van Eerde, Tom P V M de Jong, Jacques C Giltay, Bert van der Zwaag,[...]. Kidney Int 2016
46
26

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
Esther Lopez-Rivera, Yangfan P Liu, Miguel Verbitsky, Blair R Anderson, Valentina P Capone, Edgar A Otto, Zhonghai Yan, Adele Mitrotti, Jeremiah Martino, Nicholas J Steers,[...]. N Engl J Med 2017
62
26

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
Asaf Vivante, Stefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak, Friedhelm Hildebrandt. Pediatr Nephrol 2014
96
24

HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.
Rosemary Thomas, Simone Sanna-Cherchi, Bradley A Warady, Susan L Furth, Frederick J Kaskel, Ali G Gharavi. Pediatr Nephrol 2011
74
24

Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development.
Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, Stefan Kohl, Amita Sharma, Jing Chen, Shirlee Shril, Daw-Yang Hwang, Anna-Carina Weiss, Michael M Kaminski,[...]. Am J Hum Genet 2015
40
22

Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridization.
Stefanie Weber, Christina Landwehr, Miriam Renkert, Alexander Hoischen, Elke Wühl, Jonas Denecke, Bernhard Radlwimmer, Dieter Haffner, Franz Schaefer, Ruthild G Weber. Nephrol Dial Transplant 2011
43
21

Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
Stefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak, Alina C Hilger, Pawaree Saisawat, Asaf Vivante, Natasa Stajic, Radovan Bogdanovic, Heiko M Reutter, Elijah O Kehinde,[...]. J Am Soc Nephrol 2014
57
21

Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene.
Mir Reza Bekheirnia, Nasim Bekheirnia, Matthew N Bainbridge, Shen Gu, Zeynep Hande Coban Akdemir, Tomek Gambin, Nicolette K Janzen, Shalini N Jhangiani, Donna M Muzny, Mini Michael,[...]. Genet Med 2017
41
21

Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
Leire Madariaga, Vincent Morinière, Cécile Jeanpierre, Raymonde Bouvier, Philippe Loget, Jelena Martinovic, Pierre Dechelotte, Nathalie Leporrier, Christel Thauvin-Robinet, Uffe Birk Jensen,[...]. Clin J Am Soc Nephrol 2013
50
19

Mutations in DSTYK and dominant urinary tract malformations.
Simone Sanna-Cherchi, Rosemary V Sampogna, Natalia Papeta, Katelyn E Burgess, Shannon N Nees, Brittany J Perry, Murim Choi, Monica Bodria, Yan Liu, Patricia L Weng,[...]. N Engl J Med 2013
71
19

Renal aplasia in humans is associated with RET mutations.
Michael A Skinner, Shawn D Safford, Justin G Reeves, Margaret E Jackson, Alex J Freemerman. Am J Hum Genet 2008
108
19

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.
P Sanyanusin, L A Schimmenti, L A McNoe, T A Ward, M E Pierpont, M J Sullivan, W B Dobyns, M R Eccles. Nat Genet 1995
483
19

Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy.
Heather C Mefford, Severine Clauin, Andrew J Sharp, Rikke S Moller, Reinhard Ullmann, Raj Kapur, Dan Pinkel, Gregory M Cooper, Mario Ventura, H Hilger Ropers,[...]. Am J Hum Genet 2007
174
17

Renal injury in children with a solitary functioning kidney--the KIMONO study.
Rik Westland, Michiel F Schreuder, Arend Bökenkamp, Marieke D Spreeuwenberg, Joanna A E van Wijk. Nephrol Dial Transplant 2011
77
17

Clinical implications of the solitary functioning kidney.
Rik Westland, Michiel F Schreuder, Johannes B van Goudoever, Simone Sanna-Cherchi, Joanna A E van Wijk. Clin J Am Soc Nephrol 2014
48
17


American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
511
14


HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.
Shazia Adalat, Adrian S Woolf, Karen A Johnstone, Andrea Wirsing, Lorna W Harries, David A Long, Raoul C Hennekam, Sarah E Ledermann, Lesley Rees, William van't Hoff,[...]. J Am Soc Nephrol 2009
136
14

High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT.
Burcu Bulum, Z Birsin Ozçakar, Evren Ustüner, Ebru Düşünceli, Aslı Kavaz, Duygu Duman, Katherina Walz, Suat Fitoz, Mustafa Tekin, Fatoş Yalçınkaya. Pediatr Nephrol 2013
28
21

SIX2 and BMP4 mutations associate with anomalous kidney development.
Stefanie Weber, Jaclyn C Taylor, Paul Winyard, Kari F Baker, Jessica Sullivan-Brown, Raphael Schild, Tanja Knüppel, Aleksandra M Zurowska, Alberto Caldas-Alfonso, Mieczyslaw Litwin,[...]. J Am Soc Nephrol 2008
136
14

Paradigm shift from classic anatomic theories to contemporary cell biological views of CAKUT.
Iekuni Ichikawa, Fumiyo Kuwayama, John C Pope, F Douglas Stephens, Yoichi Miyazaki. Kidney Int 2002
120
14

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
14

Genomic Disorders and Neurocognitive Impairment in Pediatric CKD.
Miguel Verbitsky, Amy J Kogon, Matthew Matheson, Stephen R Hooper, Craig S Wong, Bradley A Warady, Susan L Furth, Ali G Gharavi. J Am Soc Nephrol 2017
18
33


Traditional and targeted exome sequencing reveals common, rare and novel functional deleterious variants in RET-signaling complex in a cohort of living US patients with urinary tract malformations.
Rajshekhar Chatterjee, Enrique Ramos, Mary Hoffman, Jessica VanWinkle, Daniel R Martin, Thomas K Davis, Masato Hoshi, Stanley P Hmiel, Anne Beck, Keith Hruska,[...]. Hum Genet 2012
52
12

TNXB mutations can cause vesicoureteral reflux.
Rasheed A Gbadegesin, Patrick D Brophy, Adebowale Adeyemo, Gentzon Hall, Indra R Gupta, David Hains, Bartlomeij Bartkowiak, C Egla Rabinovich, Settara Chandrasekharappa, Alison Homstad,[...]. J Am Soc Nephrol 2013
43
12

Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux.
Weining Lu, Albertien M van Eerde, Xueping Fan, Fabiola Quintero-Rivera, Shashikant Kulkarni, Heather Ferguson, Hyung-Goo Kim, Yanli Fan, Qiongchao Xi, Qing-Gang Li,[...]. Am J Hum Genet 2007
137
12

Hepatocyte nuclear factor 1β controls nephron tubular development.
Filippo Massa, Serge Garbay, Raymonde Bouvier, Yoshinobu Sugitani, Tetsuo Noda, Marie-Claire Gubler, Laurence Heidet, Marco Pontoglio, Evelyne Fischer. Development 2013
69
12

Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases.
Laurence Heidet, Stéphane Decramer, Audrey Pawtowski, Vincent Morinière, Flavio Bandin, Bertrand Knebelmann, Anne-Sophie Lebre, Stanislas Faguer, Vincent Guigonis, Corinne Antignac,[...]. Clin J Am Soc Nephrol 2010
139
12

Pbx1 regulates nephrogenesis and ureteric branching in the developing kidney.
Catherine A Schnabel, Robert E Godin, Michael L Cleary. Dev Biol 2003
74
12

Genetic architecture of reciprocal CNVs.
Christelle Golzio, Nicholas Katsanis. Curr Opin Genet Dev 2013
32
15

Genetic approaches to human renal agenesis/hypoplasia and dysplasia.
Simone Sanna-Cherchi, Gianluca Caridi, Patricia L Weng, Francesco Scolari, Francesco Perfumo, Ali G Gharavi, Gian Marco Ghiggeri. Pediatr Nephrol 2007
62
12

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Steven C Greenway, Alexandre C Pereira, Jennifer C Lin, Steven R DePalma, Samuel J Israel, Sonia M Mesquita, Emel Ergul, Jessie H Conta, Joshua M Korn, Steven A McCarroll,[...]. Nat Genet 2009
295
12

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.
Pawaree Saisawat, Stefan Kohl, Alina C Hilger, Daw-Yang Hwang, Heon Yung Gee, Gabriel C Dworschak, Velibor Tasic, Tracie Pennimpede, Sivakumar Natarajan, Ethan Sperry,[...]. Kidney Int 2014
69
12

Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort.
Tim Ulinski, Sandra Lescure, Sandrine Beaufils, Vincent Guigonis, Stéphane Decramer, Denis Morin, Séverine Clauin, Georges Deschênes, François Bouissou, Albert Bensman,[...]. J Am Soc Nephrol 2006
155
12

Epidemiology of chronic kidney disease in children.
Jérôme Harambat, Karlijn J van Stralen, Jon Jin Kim, E Jane Tizard. Pediatr Nephrol 2012
362
12

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
799
12

Epidemiology of chronic renal failure in children: data from the ItalKid project.
Gianluigi Ardissino, Valeria Daccò, Sara Testa, Roberto Bonaudo, Aldo Claris-Appiani, Emanuela Taioli, Giuseppina Marra, Alberto Edefonti, Fabio Sereni. Pediatrics 2003
289
12

Risk factors for renal injury in children with a solitary functioning kidney.
Rik Westland, Roel A J Kurvers, Joanna A E van Wijk, Michiel F Schreuder. Pediatrics 2013
68
12

Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract.
Asaf Vivante, Daw-Yang Hwang, Stefan Kohl, Jing Chen, Shirlee Shril, Julian Schulz, Amelie van der Ven, Ghaleb Daouk, Neveen A Soliman, Aravind Selvin Kumar,[...]. J Am Soc Nephrol 2017
43
12

Timing and outcome of renal replacement therapy in patients with congenital malformations of the kidney and urinary tract.
Elke Wühl, Karlijn J van Stralen, Enrico Verrina, Anna Bjerre, Christoph Wanner, James Goya Heaf, Oscar Zurriaga, Andries Hoitsma, Patrick Niaudet, Runolfur Palsson,[...]. Clin J Am Soc Nephrol 2013
106
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.