A citation-based method for searching scientific literature

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, Damien Sanlaville, William Andrews, Vasi Sundaresan, Weimin Bi, Jiong Yan, Jacques C Giltay, Cisca Wijmenga, Tom P V M de Jong, Sally A Feather, Adrian S Woolf, Yi Rao, James R Lupski, Michael R Eccles, Bradley J Quade, James F Gusella, Cynthia C Morton, Richard L Maas. Am J Hum Genet 2007
Times Cited: 139







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



Times Cited
  Times     Co-cited
Similarity


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
278
41

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
48
60

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
139
23

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
123
23

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
126
22

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
494
21

Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1.
S A Feather, S Malcolm, A S Woolf, V Wright, D Blaydon, C J Reid, F A Flinter, W Proesmans, K Devriendt, J Carter,[...]. Am J Hum Genet 2000
91
19

De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure.
Dagan Jenkins, Maria Bitner-Glindzicz, Sue Malcolm, Chih-Chi A Hu, Jennifer Allison, Paul J D Winyard, Ambrose M Gullett, David F M Thomas, Rachel A Belk, Sally A Feather,[...]. J Am Soc Nephrol 2005
83
21

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
110
18


Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance.
K Brose, K S Bland, K H Wang, D Arnott, W Henzel, C S Goodman, M Tessier-Lavigne, T Kidd. Cell 1999
894
18


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
218
16

Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric reflux.
Heather J Cordell, Rebecca Darlay, Pimphen Charoen, Aisling Stewart, Ambrose M Gullett, Heather J Lambert, Sue Malcolm, Sally A Feather, Timothy H J Goodship, Adrian S Woolf,[...]. J Am Soc Nephrol 2010
40
40

Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract.
Stefania Gimelli, Gianluca Caridi, Silvana Beri, Kyle McCracken, Renata Bocciardi, Paola Zordan, Monica Dagnino, Patrizia Fiorio, Luisa Murer, Elisa Benetti,[...]. Hum Mutat 2010
44
36

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
126
15

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
38
39

Role of the angiotensin type 2 receptor gene in congenital anomalies of the kidney and urinary tract, CAKUT, of mice and men.
H Nishimura, E Yerkes, K Hohenfellner, Y Miyazaki, J Ma, T E Hunley, H Yoshida, T Ichiki, D Threadgill, J A Phillips,[...]. Mol Cell 1999
264
14

A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13.
Patricia L Weng, Simone Sanna-Cherchi, Terry Hensle, Ellen Shapiro, Alan Werzberger, Gianluca Caridi, Claudia Izzi, Anita Konka, Adam C Reese, Rong Cheng,[...]. J Am Soc Nephrol 2009
33
42

Vesicoureteral reflux.
Gabrielle Williams, Jeffery T Fletcher, Stephen I Alexander, Jonathan C Craig. J Am Soc Nephrol 2008
88
15


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
259
13

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
110
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
30

RET Gly691Ser mutation is associated with primary vesicoureteral reflux in the French-Canadian population from Quebec.
Yaoming Yang, Anne-Marie Houle, Julien Letendre, Andrea Richter. Hum Mutat 2008
32
37

Vesico-ureteric reflux and urinary tract development in the Pax2 1Neu+/- mouse.
Inga J Murawski, David B Myburgh, Jack Favor, Indra R Gupta. Am J Physiol Renal Physiol 2007
47
25

Bone morphogenetic protein 4 regulates the budding site and elongation of the mouse ureter.
Y Miyazaki, K Oshima, A Fogo, B L Hogan, I Ichikawa. J Clin Invest 2000
296
12

A genome-wide scan for genes involved in primary vesicoureteric reflux.
H Kelly, C M Molony, J M Darlow, M E Pirker, A Yoneda, A J Green, P Puri, D E Barton. J Med Genet 2007
33
36

Conserved roles for Slit and Robo proteins in midline commissural axon guidance.
Hua Long, Christelle Sabatier, Le Ma, Andrew Plump, Wenlin Yuan, David M Ornitz, Atsushi Tamada, Fujio Murakami, Corey S Goodman, Marc Tessier-Lavigne. Neuron 2004
327
12

Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors.
T Kidd, K Brose, K J Mitchell, R D Fetter, M Tessier-Lavigne, C S Goodman, G Tear. Cell 1998
688
12

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
74
16

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
59
20

Ablation of uroplakin III gene results in small urothelial plaques, urothelial leakage, and vesicoureteral reflux.
P Hu, F M Deng, F X Liang, C M Hu, A B Auerbach, E Shapiro, X R Wu, B Kachar, T T Sun. J Cell Biol 2000
183
11

Distal ureter morphogenesis depends on epithelial cell remodeling mediated by vitamin A and Ret.
Ekatherina Batourina, Christopher Choi, Neal Paragas, Natalie Bello, Terry Hensle, Frank D Costantini, Anita Schuchardt, Robert L Bacallao, Cathy L Mendelsohn. Nat Genet 2002
112
11

Tbx18 regulates the development of the ureteral mesenchyme.
Rannar Airik, Markus Bussen, Manvendra K Singh, Marianne Petry, Andreas Kispert. J Clin Invest 2006
106
11

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
112
11

High incidence of vesicoureteral reflux in mice with Fgfr2 deletion in kidney mesenchyma.
David S Hains, Sunder Sims-Lucas, Ashley Carpenter, Monalee Saha, Inga Murawski, Kayle Kish, Indra Gupta, Kirk McHugh, Carlton M Bates. J Urol 2010
39
28

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
53
20

Inhibitory effects of Robo2 on nephrin: a crosstalk between positive and negative signals regulating podocyte structure.
Xueping Fan, Qinggang Li, Anna Pisarek-Horowitz, Hila Milo Rasouly, Xiangling Wang, Ramon G Bonegio, Hang Wang, Margaret McLaughlin, Steve Mangos, Raghu Kalluri,[...]. Cell Rep 2012
42
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
102
11

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
126
11

The development of the bladder trigone, the center of the anti-reflux mechanism.
Renata Viana, Ekatherina Batourina, Hongying Huang, Gregory R Dressler, Akio Kobayashi, Richard R Behringer, Ellen Shapiro, Terry Hensle, Sarah Lambert, Cathy Mendelsohn. Development 2007
49
20

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein.
Lesley McGregor, Ville Makela, Susan M Darling, Sofia Vrontou, Georges Chalepakis, Catherine Roberts, Nicola Smart, Paul Rutland, Natalie Prescott, Jason Hopkins,[...]. Nat Genet 2003
165
10

Roles of uroplakins in plaque formation, umbrella cell enlargement, and urinary tract diseases.
Xiang-Tian Kong, Fang-Ming Deng, Ping Hu, Feng-Xia Liang, Ge Zhou, Anna B Auerbach, Nancy Genieser, Peter K Nelson, Edith S Robbins, Ellen Shapiro,[...]. J Cell Biol 2004
126
10

Sibling vesicoureteral reflux in multiple gestation births.
M Kaefer, M Curran, S T Treves, S Bauer, W H Hendren, C A Peters, A Atala, D Diamond, A Retik. Pediatrics 2000
57
17

Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.
J Kohlhase, A Wischermann, H Reichenbach, U Froster, W Engel. Nat Genet 1998
331
10

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
160
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
348
10

Reduction of BMP4 activity by gremlin 1 enables ureteric bud outgrowth and GDNF/WNT11 feedback signalling during kidney branching morphogenesis.
Odyssé Michos, Alexandre Gonçalves, Javier Lopez-Rios, Eva Tiecke, Florence Naillat, Konstantin Beier, Antonella Galli, Seppo Vainio, Rolf Zeller. Development 2007
136
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
485
10


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.