A citation-based method for searching scientific literature

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, Vladimir J Lozanovski, Anna Materna-Kiryluk, Cristina Barlassina, Akshata Kini, Valentina Corbani, Alba Carrea, Danio Somenzi, Corrado Murtas, Nadica Ristoska-Bojkovska, Claudia Izzi, Beatrice Bianco, Marcin Zaniew, Hana Flogelova, Patricia L Weng, Nilgun Kacak, Stefania Giberti, Maddalena Gigante, Adela Arapovic, Kristina Drnasin, Gianluca Caridi, Simona Curioni, Franca Allegri, Anita Ammenti, Stefania Ferretti, Vinicio Goj, Luca Bernardo, Vaidehi Jobanputra, Wendy K Chung, Richard P Lifton, Stephan Sanders, Matthew State, Lorraine N Clark, Marijan Saraga, Sandosh Padmanabhan, Anna F Dominiczak, Tatiana Foroud, Loreto Gesualdo, Zoran Gucev, Landino Allegri, Anna Latos-Bielenska, Daniele Cusi, Francesco Scolari, Velibor Tasic, Hakon Hakonarson, Gian Marco Ghiggeri, Ali G Gharavi. Am J Hum Genet 2012
Times Cited: 119







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



Times Cited
  Times     Co-cited
Similarity


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
119
39

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
31

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
65

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
80

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
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
113
26

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
35

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
43

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
26


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
29

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
28

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
40

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
17

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
61
27

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
16

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

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
37

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
26

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
14

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

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

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
172
13

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
504
13

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
13

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
13

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
13

Genetic kidney diseases.
Friedhelm Hildebrandt. Lancet 2010
167
13

Exploring the genetic basis of early-onset chronic kidney disease.
Asaf Vivante, Friedhelm Hildebrandt. Nat Rev Nephrol 2016
127
13

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
794
12

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
27

Epidemiology of chronic kidney disease in children.
Jérôme Harambat, Karlijn J van Stralen, Jon Jin Kim, E Jane Tizard. Pediatr Nephrol 2012
360
12

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
12

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Andrew Kirby, Andreas Gnirke, David B Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel, Chun Ye, Daniel Aird, Christine Stevens, James T Robinson,[...]. Nat Genet 2013
129
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
135
12

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
23

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

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Priya Krithivasan, Adele Mitrotti, David A Fasel, Ekaterina Batourina, Matthew G Sampson,[...]. Nat Genet 2019
43
27

Guidelines for investigating causality of sequence variants in human disease.
D G MacArthur, T A Manolio, D P Dimmock, H L Rehm, J Shendure, G R Abecasis, D R Adams, R B Altman, S E Antonarakis, E A Ashley,[...]. Nature 2014
752
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
11

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
22

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
11

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
79
12

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
31

High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation sequencing.
Jan Halbritter, Katrina Diaz, Moumita Chaki, Jonathan D Porath, Brendan Tarrier, Clementine Fu, Jamie L Innis, Susan J Allen, Robert H Lyons, Constantinos J Stefanidis,[...]. J Med Genet 2012
85
11

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
35


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
23

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
20


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.