A citation-based method for searching scientific literature

Valentina P Capone, William Morello, Francesca Taroni, Giovanni Montini. Int J Mol Sci 2017
Times Cited: 32







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



Times Cited
  Times     Co-cited
Similarity


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
40

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
122
28

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
97
21

Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
Amelie T van der Ven, Asaf Vivante, Friedhelm Hildebrandt. J Am Soc Nephrol 2018
48
21

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
213
21

Genetic kidney diseases.
Friedhelm Hildebrandt. Lancet 2010
169
18

Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT).
Maria M Rodriguez. Fetal Pediatr Pathol 2014
39
18


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
122
15

An illustrated anatomical ontology of the developing mouse lower urogenital tract.
Kylie M Georgas, Jane Armstrong, Janet R Keast, Christine E Larkins, Kirk M McHugh, E Michelle Southard-Smith, Martin J Cohn, Ekatherina Batourina, Hanbin Dan, Kerry Schneider,[...]. Development 2015
74
15

Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney.
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,[...]. Kidney Int 2015
41
12


HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.
Makiko Nakayama, Kandai Nozu, Yuki Goto, Koichi Kamei, Shuichi Ito, Hidenori Sato, Mitsuru Emi, Koichi Nakanishi, Shigeru Tsuchiya, Kazumoto Iijima. Pediatr Nephrol 2010
52
12

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
12

Congenital anomalies of the kidney and urinary tract: an embryogenetic review.
Augusto Cesar Soares dos Santos Junior, Debora Marques de Miranda, Ana Cristina Simões e Silva. Birth Defects Res C Embryo Today 2014
20
20


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

Renal branching morphogenesis: morphogenetic and signaling mechanisms.
Joshua Blake, Norman D Rosenblum. Semin Cell Dev Biol 2014
36
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
138
12

SLIT2-mediated ROBO2 signaling restricts kidney induction to a single site.
Uta Grieshammer, Le Ma, Andrew S Plump, Fan Wang, Marc Tessier-Lavigne, Gail R Martin. Dev Cell 2004
274
12

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
Laurence Heidet, Vincent Morinière, Charline Henry, Lara De Tomasi, Madeline Louise Reilly, Camille Humbert, Olivier Alibeu, Cécile Fourrage, Christine Bole-Feysot, Patrick Nitschké,[...]. J Am Soc Nephrol 2017
44
9

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
47
9

Targeted gene sequencing and whole-exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies.
M Rasmussen, L Sunde, M L Nielsen, M Ramsing, A Petersen, T D Hjortshøj, T E Olsen, A Tabor, J M Hertz, I Johnsen,[...]. Clin Genet 2018
23
13

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
9

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
109
9

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
71
9

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
9


Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT).
Kirsten Y Renkema, Paul J Winyard, Ilya N Skovorodkin, Elena Levtchenko, An Hindryckx, Cécile Jeanpierre, Stefanie Weber, Rémi Salomon, Corinne Antignac, Seppo Vainio,[...]. Nephrol Dial Transplant 2011
40
9

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
9

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
10

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
485
9

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret.
A Schuchardt, V D'Agati, L Larsson-Blomberg, F Costantini, V Pachnis. Nature 1994
9

Maternal risk factors involved in specific congenital anomalies of the kidney and urinary tract: A case-control study.
Sander Groen In 't Woud, Kirsten Y Renkema, Michiel F Schreuder, Charlotte H W Wijers, Loes F M van der Zanden, Nine V A M Knoers, Wout F J Feitz, Ernie M H F Bongers, Nel Roeleveld, Iris A L M van Rooij. Birth Defects Res A Clin Mol Teratol 2016
18
16

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
9

Renal agenesis and the absence of enteric neurons in mice lacking GDNF.
M P Sánchez, I Silos-Santiago, J Frisén, B He, S A Lira, M Barbacid. Nature 1996
969
9

Conserved and Divergent Features of Human and Mouse Kidney Organogenesis.
Nils O Lindström, Jill A McMahon, Jinjin Guo, Tracy Tran, Qiuyu Guo, Elisabeth Rutledge, Riana K Parvez, Gohar Saribekyan, Robert E Schuler, Christopher Liao,[...]. J Am Soc Nephrol 2018
87
9

Global quantification of tissue dynamics in the developing mouse kidney.
Kieran M Short, Alexander N Combes, James Lefevre, Adler L Ju, Kylie M Georgas, Timothy Lamberton, Oliver Cairncross, Bree A Rumballe, Andrew P McMahon, Nicholas A Hamilton,[...]. Dev Cell 2014
147
9


Kidney development in the absence of Gdnf and Spry1 requires Fgf10.
Odyssé Michos, Cristina Cebrian, Deborah Hyink, Uta Grieshammer, Linda Williams, Vivette D'Agati, Jonathan D Licht, Gail R Martin, Frank Costantini. PLoS Genet 2010
101
9

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, Nina Mann, Makiko Nakayama, Jing Chen, Asaf Vivante, Daw-Yang Hwang, Julian Schulz, Daniela A Braun,[...]. J Am Soc Nephrol 2018
55
9

Apoptosis induced by vitamin A signaling is crucial for connecting the ureters to the bladder.
Ekatherina Batourina, Sheaumei Tsai, Sarah Lambert, Preston Sprenkle, Renata Viana, Sonia Dutta, Terry Hensle, Fengwei Wang, Karen Niederreither, Andrew P McMahon,[...]. Nat Genet 2005
108
9

Ret-dependent cell rearrangements in the Wolffian duct epithelium initiate ureteric bud morphogenesis.
Xuan Chi, Odyssé Michos, Reena Shakya, Paul Riccio, Hideki Enomoto, Jonathan D Licht, Naoya Asai, Masahide Takahashi, Nobutaka Ohgami, Masashi Kato,[...]. Dev Cell 2009
145
9

Congenital anomalies of kidney and urinary tract.
Hakan R Toka, Okan Toka, Ali Hariri, Hiep T Nguyen. Semin Nephrol 2010
51
9

Whole-exome sequencing for prenatal diagnosis of fetuses with congenital anomalies of the kidney and urinary tract.
Ting-Ying Lei, Fang Fu, Ru Li, Dan Wang, Rong-Yue Wang, Xiang-Yi Jing, Qiong Deng, Zhou-Zhou Li, Ze-Qun Liu, Xin Yang,[...]. Nephrol Dial Transplant 2017
28
10

Molecular diagnostics for autosomal dominant polycystic kidney disease.
Peter C Harris, Sandro Rossetti. Nat Rev Nephrol 2010
90
9

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
9


Lower urinary tract development and disease.
Hila Milo Rasouly, Weining Lu. Wiley Interdiscip Rev Syst Biol Med 2013
35
9


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.