A citation-based method for searching scientific literature

Christelle Golzio, Nicholas Katsanis. Curr Opin Genet Dev 2013
Times Cited: 32







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



Times Cited
  Times     Co-cited
Similarity


KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant.
Christelle Golzio, Jason Willer, Michael E Talkowski, Edwin C Oh, Yu Taniguchi, Sébastien Jacquemont, Alexandre Reymond, Mei Sun, Akira Sawa, James F Gusella,[...]. Nature 2012
240
43

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
820
31

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
28

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
Nicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, John Belmont, Carlos A Bacino, Trilochan Sahoo, Seema R Lalani, Brett Graham, Brendan Lee, Marwan Shinawi,[...]. Nat Genet 2008
396
28

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D Beckmann,[...]. Nature 2011
268
25

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
21

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
815
21

Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
21

Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
487
21

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
Marwan Shinawi, Pengfei Liu, Sung-Hae L Kang, Joseph Shen, John W Belmont, Daryl A Scott, Frank J Probst, William J Craigen, Brett H Graham, Amber Pursley,[...]. J Med Genet 2010
324
21

Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.
K Osoegawa, G M Vessere, K H Utami, M A Mansilla, M K Johnson, B M Riley, J L'Heureux, R Pfundt, J Staaf, W A van der Vliet,[...]. J Med Genet 2008
71
18

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Steven C Greenway, Alexandre C Pereira, Jennifer C Lin, Steven R DePalma, Samuel J Israel, Sonia M Mesquita, Emel Ergul, Jessie H Conta, Joshua M Korn, Steven A McCarroll,[...]. Nat Genet 2009
297
18

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
129
18

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, Ellen Hanson, Anne M Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari, Zoltán Kutalik, Joris Andrieux,[...]. J Med Genet 2012
155
18

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
521
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
18

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
18


Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
Guy Horev, Jacob Ellegood, Jason P Lerch, Young-Eun E Son, Lakshmi Muthuswamy, Hannes Vogel, Abba M Krieger, Andreas Buja, R Mark Henkelman, Michael Wigler,[...]. Proc Natl Acad Sci U S A 2011
176
15

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
15

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
15

Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.
Thomas Portmann, Mu Yang, Rong Mao, Georgia Panagiotakos, Jacob Ellegood, Gul Dolen, Patrick L Bader, Brad A Grueter, Carleton Goold, Elaine Fisher,[...]. Cell Rep 2014
119
15


CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
385
15

Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
15

Genetic approaches to human renal agenesis/hypoplasia and dysplasia.
Simone Sanna-Cherchi, Gianluca Caridi, Patricia L Weng, Francesco Scolari, Francesco Perfumo, Ali G Gharavi, Gian Marco Ghiggeri. Pediatr Nephrol 2007
63
15

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
358
15

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
15

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
186
15

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.
A M Maillard, A Ruef, F Pizzagalli, E Migliavacca, L Hippolyte, S Adaszewski, J Dukart, C Ferrari, P Conus, K Männik,[...]. Mol Psychiatry 2015
98
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
43
15

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
50
15

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
15

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
421
15

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
205
15

Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
12

Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
466
12

Large-scale copy number polymorphism in the human genome.
Jonathan Sebat, B Lakshmi, Jennifer Troge, Joan Alexander, Janet Young, Pär Lundin, Susanne Månér, Hillary Massa, Megan Walker, Maoyen Chi,[...]. Science 2004
12

SCRIB and PUF60 are primary drivers of the multisystemic phenotypes of the 8q24.3 copy-number variant.
Andrew Dauber, Christelle Golzio, Cécile Guenot, Francine M Jodelka, Maria Kibaek, Susanne Kjaergaard, Bruno Leheup, Danielle Martinet, Malgorzata J M Nowaczyk, Jill A Rosenfeld,[...]. Am J Hum Genet 2013
49
12

Clinical implications of the solitary functioning kidney.
Rik Westland, Michiel F Schreuder, Johannes B van Goudoever, Simone Sanna-Cherchi, Joanna A E van Wijk. Clin J Am Soc Nephrol 2014
53
12

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
37
12

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
175
12

The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1.
Anna Materna-Kiryluk, Krzysztof Kiryluk, Katelyn E Burgess, Arkadiusz Bieleninik, Simone Sanna-Cherchi, Ali G Gharavi, Anna Latos-Bielenska. Pediatr Nephrol 2014
13
30

Timing and outcome of renal replacement therapy in patients with congenital malformations of the kidney and urinary tract.
Elke Wühl, Karlijn J van Stralen, Enrico Verrina, Anna Bjerre, Christoph Wanner, James Goya Heaf, Oscar Zurriaga, Andries Hoitsma, Patrick Niaudet, Runolfur Palsson,[...]. Clin J Am Soc Nephrol 2013
108
12


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
77
12

Coordinating early kidney development: lessons from gene targeting.
Seppo Vainio, Yanfeng Lin. Nat Rev Genet 2002
169
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
48
12

Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
Debra D'Angelo, Sébastien Lebon, Qixuan Chen, Sandra Martin-Brevet, LeeAnne Green Snyder, Loyse Hippolyte, Ellen Hanson, Anne M Maillard, W Andrew Faucett, Aurélien Macé,[...]. JAMA Psychiatry 2016
107
12

Opposing brain differences in 16p11.2 deletion and duplication carriers.
Abid Y Qureshi, Sophia Mueller, Abraham Z Snyder, Pratik Mukherjee, Jeffrey I Berman, Timothy P L Roberts, Srikantan S Nagarajan, John E Spiro, Wendy K Chung, Elliott H Sherr,[...]. J Neurosci 2014
94
12


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.