A citation-based method for searching scientific literature

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, Velibor Tasic, Friedhelm Hildebrandt. Kidney Int 2014
Times Cited: 119







List of co-cited articles
873 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
113
34

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
119
33

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
95
33

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
50

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
209
28

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
22

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
44
47

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
135
20

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
27

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
47


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
72
25

Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.
Daw-Yang Hwang, Stefan Kohl, Xueping Fan, Asaf Vivante, Stefanie Chan, Gabriel C Dworschak, Julian Schulz, Albertien M van Eerde, Alina C Hilger, Heon Yung Gee,[...]. Hum Genet 2015
33
54

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
270
18

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
17

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
107
17

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
22

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
30

Genetic kidney diseases.
Friedhelm Hildebrandt. Lancet 2010
167
15

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
28

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
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
36

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
32

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
40
35

ROBO2 gene variants are associated with familial vesicoureteral reflux.
Aida M Bertoli-Avella, Maria Luisa Conte, Francesca Punzo, Bianca M de Graaf, Giuliana Lama, Angela La Manna, Cesare Polito, Carolina Grassia, Bruno Nobili, Pier Francesco Rambaldi,[...]. J Am Soc Nephrol 2008
47
27

Epidemiology of chronic kidney disease in children.
Jérôme Harambat, Karlijn J van Stralen, Jon Jin Kim, E Jane Tizard. Pediatr Nephrol 2012
360
13

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
36

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
13

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
137
12

A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Carolin E Sadowski, Svjetlana Lovric, Shazia Ashraf, Werner L Pabst, Heon Yung Gee, Stefan Kohl, Susanne Engelmann, Virginia Vega-Warner, Humphrey Fang, Jan Halbritter,[...]. J Am Soc Nephrol 2015
282
12

Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis.
Pawaree Saisawat, Velibor Tasic, Virginia Vega-Warner, Elijah O Kehinde, Barbara Günther, Rannar Airik, Jeffrey W Innis, Bethan E Hoskins, Julia Hoefele, Edgar A Otto,[...]. Kidney Int 2012
52
23

Exploring the genetic basis of early-onset chronic kidney disease.
Asaf Vivante, Friedhelm Hildebrandt. Nat Rev Nephrol 2016
127
12

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
26

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
27

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
50
24

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
46
26


Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome.
Bethan E Hoskins, Carl H Cramer, Derek Silvius, Dan Zou, Richard M Raymond, Dana J Orten, William J Kimberling, Richard J H Smith, Dominique Weil, Christine Petit,[...]. Am J Hum Genet 2007
107
11

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
180
11

Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans.
Camille Humbert, Flora Silbermann, Bharti Morar, Mélanie Parisot, Mohammed Zarhrate, Cécile Masson, Frédéric Tores, Patricia Blanchet, Marie-José Perez, Yuliya Petrov,[...]. Am J Hum Genet 2014
48
22

Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signaling.
Asaf Vivante, Michal Mark-Danieli, Miriam Davidovits, Orit Harari-Steinberg, Dorit Omer, Yehudit Gnatek, Roxana Cleper, Daniel Landau, Yael Kovalski, Irit Weissman,[...]. J Am Soc Nephrol 2013
32
34

FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man.
Hila Barak, Sung-Ho Huh, Shuang Chen, Cécile Jeanpierre, Jelena Martinovic, Mélanie Parisot, Christine Bole-Feysot, Patrick Nitschké, Rémi Salomon, Corinne Antignac,[...]. Dev Cell 2012
163
11

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
Rainer G Ruf, Pin-Xian Xu, Derek Silvius, Edgar A Otto, Frank Beekmann, Ulla T Muerb, Shrawan Kumar, Thomas J Neuhaus, Markus J Kemper, Richard M Raymond,[...]. Proc Natl Acad Sci U S A 2004
249
10

GATA3 haplo-insufficiency causes human HDR syndrome.
H Van Esch, P Groenen, M A Nesbit, S Schuffenhauer, P Lichtner, G Vanderlinden, B Harding, R Beetz, R W Bilous, I Holdaway,[...]. Nature 2000
342
10


Six2 is required for suppression of nephrogenesis and progenitor renewal in the developing kidney.
Michelle Self, Oleg V Lagutin, Beth Bowling, Jaime Hendrix, Yi Cai, Gregory R Dressler, Guillermo Oliver. EMBO J 2006
302
10

Six2 defines and regulates a multipotent self-renewing nephron progenitor population throughout mammalian kidney development.
Akio Kobayashi, M Todd Valerius, Joshua W Mugford, Thomas J Carroll, Michelle Self, Guillermo Oliver, Andrew P McMahon. Cell Stem Cell 2008
566
10

Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia.
P X Xu, J Adams, H Peters, M C Brown, S Heaney, R Maas. Nat Genet 1999
475
10

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
43
23

Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.
Y Horikawa, N Iwasaki, M Hara, H Furuta, Y Hinokio, B N Cockburn, T Lindner, K Yamagata, M Ogata, O Tomonaga,[...]. Nat Genet 1997
631
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.