A citation-based method for searching scientific literature

Glenda M Beaman, Adrian S Woolf, Raimondo M Cervellione, David Keene, Imran Mushtaq, Jill E Urquhart, Helen M Stuart, William G Newman. Am J Med Genet A 2019
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
Markus Draaken, Heiko Reutter, Charlotte Schramm, Enrika Bartels, Thomas M Boemers, Anne-Karoline Ebert, Wolfgang Rösch, Annette Schröder, Raimund Stein, Susanne Moebus,[...]. Eur J Med Genet 2010
35
100

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney.
J Favor, R Sandulache, A Neuhäuser-Klaus, W Pretsch, B Chatterjee, E Senft, W Wurst, V Blanquet, P Grimes, R Spörle,[...]. Proc Natl Acad Sci U S A 1996
309
50

Primary vesicoureteral reflux detected in neonates with a history of fetal renal pelvis dilatation: a prospective clinical and imaging study.
Khalid Ismaili, Michelle Hall, Amy Piepsz, Karl M Wissing, Frank Collier, Claude Schulman, Fred E Avni. J Pediatr 2006
43
50

LRIG2 mutations cause urofacial syndrome.
Helen M Stuart, Neil A Roberts, Berk Burgu, Sarah B Daly, Jill E Urquhart, Sanjeev Bhaskar, Jonathan E Dickerson, Murat Mermerkaya, Mesrur Selcuk Silay, Malcolm A Lewis,[...]. Am J Hum Genet 2013
39
50

DNA copy number variants: A potentially useful predictor of early onset renal failure in boys with posterior urethral valves.
A Faure, A Bouty, G Caruana, L Williams, T Burgess, M N Wong, P A James, M O'Brien, A Walker, J F Bertram,[...]. J Pediatr Urol 2016
6
50

Genetics of human congenital urinary bladder disease.
Adrian S Woolf, Helen M Stuart, William G Newman. Pediatr Nephrol 2014
8
50

Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome.
Stefanie Weber, Holger Thiele, Sevgi Mir, Mohammad Reza Toliat, Betül Sozeri, Heiko Reutter, Markus Draaken, Michael Ludwig, Janine Altmüller, Peter Frommolt,[...]. Am J Hum Genet 2011
44
50

A mouse model of urofacial syndrome with dysfunctional urination.
Chunming Guo, Satoshi Kaneko, Ye Sun, Yichen Huang, Israel Vlodavsky, Xiaokun Li, Zhong-Rong Li, Xue Li. Hum Mol Genet 2015
18
50

Urinary bladder-urethral sphincter dysfunction in mice with targeted disruption of neuronal nitric oxide synthase models idiopathic voiding disorders in humans.
A L Burnett, D C Calvin, S L Chamness, J X Liu, R J Nelson, S L Klein, V L Dawson, T M Dawson, S H Snyder. Nat Med 1997
111
50

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
137
50

A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.
J Schalkwijk, M C Zweers, P M Steijlen, W B Dean, G Taylor, I M van Vlijmen, B van Haren, W L Miller, J Bristow. N Engl J Med 2001
257
50

Contemporary epidemiology and characterization of newborn males with prune belly syndrome.
Jonathan C Routh, Lin Huang, Alan B Retik, Caleb P Nelson. Urology 2010
49
50

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
50

Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype.
Abeer Fadda, Fiza Butt, Sara Tomei, Sara Deola, Bernice Lo, Amal Robay, Alya Al-Shakaki, Noor Al-Hajri, Ronald Crystal, Marios Kambouris,[...]. BMC Med Genet 2016
12
50

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
50

TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons.
Xavier Caubit, Paolo Gubellini, Joris Andrieux, Pierre L Roubertoux, Mehdi Metwaly, Bernard Jacq, Ahmed Fatmi, Laurence Had-Aissouni, Kenneth Y Kwan, Pascal Salin,[...]. Nat Genet 2016
31
50

Role of the LF-SINE-Derived Distal ISL1 Enhancer in Patients with Classic Bladder Exstrophy.
Rong Zhang, Michael Knapp, Franziska Kause, Heiko Reutter, Michael Ludwig. J Pediatr Genet 2017
1
100

Requirement for a uroplakin 3a-like protein in the development of zebrafish pronephric tubule epithelial cell function, morphogenesis, and polarity.
Shalini Mitra, Stefan Lukianov, Wily G Ruiz, Chiara Cianciolo Cosentino, Subramaniam Sanker, Linton M Traub, Neil A Hukriede, Gerard Apodaca. PLoS One 2012
15
50

Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development.
Elizabeth J Bhoj, Purita Ramos, Linda A Baker, Vidu Garg, Nicholas Cost, Agneta Nordenskjöld, Frederick F Elder, Steven B Bleyl, Neil E Bowles, Cammon B Arrington,[...]. Eur J Hum Genet 2011
19
50


Kidney-specific expression of GFP by in-utero delivery of pseudotyped adeno-associated virus 9.
Jason L Picconi, Melissa A Muff-Luett, Di Wu, Erik Bunchman, Franz Schaefer, Patrick D Brophy. Mol Ther Methods Clin Dev 2014
11
50


A novel clinical syndrome revealing a deficiency of the muscarinic M3 receptor.
J K Pomper, H Wilhelm, S K Tayebati, F Asmus, R Schüle, K-D Sievert, C-A Haensch, A Melms, T Haarmeier. Neurology 2011
7
50

First HPSE2 missense mutation in urofacial syndrome.
S Mahmood, C Beetz, M M Tahir, M Imran, R Mumtaz, I Bassmann, A Jahic, M Malik, G Nürnberg, S A A Hassan,[...]. Clin Genet 2012
16
50




A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome.
Julie Gauthier, Bouchra Ouled Amar Bencheikh, Fadi F Hamdan, Steven M Harrison, Linda A Baker, Françoise Couture, Isabelle Thiffault, Reda Ouazzani, Mark E Samuels, Grant A Mitchell,[...]. Eur J Hum Genet 2015
44
50

Genetic basis of prune belly syndrome: screening for HNF1β gene.
Candace F Granberg, Steven M Harrison, Daniel Dajusta, Shaohua Zhang, Sachin Hajarnis, Peter Igarashi, Linda A Baker. J Urol 2012
32
50

Direct Reprogramming of Fibroblasts Into Smooth Muscle-Like Cells With Defined Transcription Factors-Brief Report.
Hiroyuki Hirai, Bo Yang, Minerva T Garcia-Barrio, Oren Rom, Peter X Ma, Jifeng Zhang, Y Eugene Chen. Arterioscler Thromb Vasc Biol 2018
12
50

Vesicoureteral reflux.
Gabrielle Williams, Jeffery T Fletcher, Stephen I Alexander, Jonathan C Craig. J Am Soc Nephrol 2008
84
50

ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development.
Rong Zhang, Michael Knapp, Kentaro Suzuki, Daiki Kajioka, Johanna M Schmidt, Jonas Winkler, Öznur Yilmaz, Michael Pleschka, Jia Cao, Christina Clementson Kockum,[...]. Sci Rep 2017
15
50


Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction.
Dagan Jenkins, Xavier Caubit, Aleksandar Dimovski, Nadica Matevska, Claire M Lye, Feryal Cabuk, Zoran Gucev, Velibor Tasic, Laurent Fasano, Adrian S Woolf. Nephrol Dial Transplant 2010
19
50


A classic twin study of lower urinary tract obstruction: Report of 3 cases and literature review.
Sandra Frese, Alexander Weigert, Bernd Hoppe, Markus Feldkötter, Michael Ludwig, Stefanie Weber, Katarzyna Kiliś-Pstrusińska, Marcin Zaniew, Heiko Reutter, Alina C Hilger. Low Urin Tract Symptoms 2019
2
50

Evaluation of the ISL1 gene in the pathogenesis of bladder exstrophy in a Swedish cohort.
Samara Arkani, Jia Cao, Johanna Lundin, Daniel Nilsson, Thomas Källman, Gillian Barker, Gundela Holmdahl, Christina Clementsson Kockum, Hans Matsson, Agneta Nordenskjöld. Hum Genome Var 2018
7
50

Malformations among infants of mothers with insulin-dependent diabetes: Is there a recognizable pattern of abnormalities?
Hanah Z Nasri, Kara Houde Ng, Marie-Noel Westgate, Anne-Therese Hunt, Lewis B Holmes. Birth Defects Res 2018
11
50

Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region.
Markus Draaken, Friederike Baudisch, Bernd Timmermann, Heiner Kuhl, Martin Kerick, Judith Proske, Lars Wittler, Tracie Pennimpede, Anne-Karoline Ebert, Wolfgang Rösch,[...]. Birth Defects Res A Clin Mol Teratol 2014
13
50

Mutations in HPSE2 cause urofacial syndrome.
Sarah B Daly, Jill E Urquhart, Emma Hilton, Edward A McKenzie, Richard A Kammerer, Malcolm Lewis, Bronwyn Kerr, Helen Stuart, Dian Donnai, David A Long,[...]. Am J Hum Genet 2010
58
50

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
50

The LRIG family: enigmatic regulators of growth factor receptor signaling.
Catalina Simion, Maria Elvira Cedano-Prieto, Colleen Sweeney. Endocr Relat Cancer 2014
28
50

Epidemiology and demography of recently diagnosed cases of posterior urethral valves.
Devesh Thakkar, Anirudh V Deshpande, Sean E Kennedy. Pediatr Res 2014
20
50

LRIG2 promotes the proliferation and cell cycle progression of glioblastoma cells in vitro and in vivo through enhancing PDGFRβ signaling.
Qungen Xiao, Minhai Dong, Fangling Cheng, Feng Mao, Weifeng Zong, Kang Wu, Heping Wang, Ruifan Xie, Baofeng Wang, Ting Lei,[...]. Int J Oncol 2018
4
50

Deletion of hepatocyte nuclear factor-1-beta in an infant with prune belly syndrome.
Sina Haeri, Patricia L Devers, Kathleen A Kaiser-Rogers, Vincent J Moylan, Beth S Torchia, Amanda L Horton, Honor M Wolfe, Arthur S Aylsworth. Am J Perinatol 2010
32
50

Multiple functional defects in peripheral autonomic organs in mice lacking muscarinic acetylcholine receptor gene for the M3 subtype.
M Matsui, D Motomura, H Karasawa, T Fujikawa, J Jiang, Y Komiya, S Takahashi, M M Taketo. Proc Natl Acad Sci U S A 2000
325
50

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
50

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
124
50

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
50

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
81
50


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.