A citation-based method for searching scientific literature

Colleen A Morris, Carolyn B Mervis, Alex P Paciorkowski, Omar Abdul-Rahman, Sarah L Dugan, Alan F Rope, Patricia Bader, Laura G Hendon, Shelley L Velleman, Bonita P Klein-Tasman, Lucy R Osborne. Am J Med Genet A 2015
Times Cited: 37







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



Times Cited
  Times     Co-cited
Similarity


Children with 7q11.23 duplication syndrome: psychological characteristics.
Carolyn B Mervis, Bonita P Klein-Tasman, Myra J Huffman, Shelley L Velleman, C Holley Pitts, Danielle R Henderson, Janet Woodruff-Borden, Colleen A Morris, Lucy R Osborne. Am J Med Genet A 2015
27
55

Williams-Beuren syndrome.
Barbara R Pober. N Engl J Med 2010
439
32

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
806
32

Severe expressive-language delay related to duplication of the Williams-Beuren locus.
Martin J Somerville, Carolyn B Mervis, Edwin J Young, Eul-Ju Seo, Miguel del Campo, Stephen Bamforth, Ella Peregrine, Wayne Loo, Margaret Lilley, Luis A Pérez-Jurado,[...]. N Engl J Med 2005
204
27

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer, Jenneke van den Ende, Edwin Reyniers, Marco Fichera, Corrado Romano, Barbara Delle Chiaie, Geert Mortier, Björn Menten,[...]. Eur J Med Genet 2009
114
27

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.
Jonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, Sung-Hae L Kang, Chin-to Fong, Jessica Salamone, Debra Freedenberg, Vickie L Hannig, Lisa Albers Prock, David T Miller,[...]. Genet Med 2007
134
24


Copy number variants at Williams-Beuren syndrome 7q11.23 region.
Giuseppe Merla, Nicola Brunetti-Pierri, Lucia Micale, Carmela Fusco. Hum Genet 2010
96
21

7q11.23 Microduplication: a recognizable phenotype.
A Dixit, S McKee, S Mansour, S G Mehta, G A Tanteles, V Anastasiadou, P C Patsalis, K Martin, S McCullough, M Suri,[...]. Clin Genet 2013
23
34

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia.
Jennifer Gladys Mulle, Ann E Pulver, John A McGrath, Paula S Wolyniec, Anne F Dodd, David J Cutler, Jonathan Sebat, Dheeraj Malhotra, Gerald Nestadt, Donald F Conrad,[...]. Biol Psychiatry 2014
47
18

Aortopathy in the 7q11.23 microduplication syndrome.
Ashley Parrott, Jeanne James, Paula Goldenberg, Robert B Hinton, Erin Miller, Amy Shikany, Arthur S Aylsworth, Kathleen Kaiser-Rogers, Sunita J Ferns, Seema R Lalani,[...]. Am J Med Genet A 2015
19
36

Duplication of GTF2I results in separation anxiety in mice and humans.
Carolyn B Mervis, Joana Dida, Emily Lam, Nicole A Crawford-Zelli, Edwin J Young, Danielle R Henderson, Tuncer Onay, Colleen A Morris, Janet Woodruff-Borden, John Yeomans,[...]. Am J Hum Genet 2012
48
18

Autism, language delay and mental retardation in a patient with 7q11 duplication.
C Depienne, D Heron, C Betancur, B Benyahia, O Trouillard, D Bouteiller, A Verloes, E LeGuern, M Leboyer, A Brice. J Med Genet 2007
64
16

Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: phenotypic expansion and review of the literature.
Yuri A Zarate, Tiffany Lepard, Elizabeth Sellars, Julie A Kaylor, Maria P Alfaro, Charles Sailey, G Bradley Schaefer, R Thomas Collins. Am J Med Genet A 2014
18
33

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Kyle J Steinman, Sarah J Spence, Melissa B Ramocki, Monica B Proud, Sudha K Kessler, Elysa J Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K Chung,[...]. Am J Med Genet A 2016
70
16

Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Raphael Bernier, Kyle J Steinman, Beau Reilly, Arianne Stevens Wallace, Elliott H Sherr, Nicholas Pojman, Heather C Mefford, Jennifer Gerdts, Rachel Earl, Ellen Hanson,[...]. Genet Med 2016
74
16

Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23.
Emma Strong, Darci T Butcher, Rajat Singhania, Carolyn B Mervis, Colleen A Morris, Daniel De Carvalho, Rosanna Weksberg, Lucy R Osborne. Am J Hum Genet 2015
38
16

Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits.
Carmela Fusco, Lucia Micale, Bartolomeo Augello, Maria Teresa Pellico, Deny Menghini, Paolo Alfieri, Maria Cristina Digilio, Barbara Mandriani, Massimo Carella, Orazio Palumbo,[...]. Eur J Hum Genet 2014
40
13

Recurrent distal 7q11.23 deletion including HIP1 and YWHAG identified in patients with intellectual disabilities, epilepsy, and neurobehavioral problems.
Melissa B Ramocki, Magdalena Bartnik, Przemyslaw Szafranski, Katarzyna E Kołodziejska, Zhilian Xia, Jaclyn Bravo, G Steve Miller, Diana L Rodriguez, Charles A Williams, Patricia I Bader,[...]. Am J Hum Genet 2010
41
13

Rare de novo and transmitted copy-number variation in autistic spectrum disorders.
Dan Levy, Michael Ronemus, Boris Yamrom, Yoon-ha Lee, Anthony Leotta, Jude Kendall, Steven Marks, B Lakshmi, Deepa Pai, Kenny Ye,[...]. Neuron 2011
437
13

Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders.
Patrick Malenfant, Xudong Liu, Melissa L Hudson, Ying Qiao, Monica Hrynchak, Noémie Riendeau, M Jeannette Hildebrand, Ira L Cohen, Albert E Chudley, Cynthia Forster-Gibson,[...]. J Autism Dev Disord 2012
45
13

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
515
13

Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.
Takeshi Sakurai, Nathan P Dorr, Nagahide Takahashi, L Alison McInnes, Gregory A Elder, Joseph D Buxbaum. Autism Res 2011
69
13

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.
A K Ewart, C A Morris, D Atkinson, W Jin, K Sternes, P Spallone, A D Stock, M Leppert, M T Keating. Nat Genet 1993
761
13

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
405
13

Autism Spectrum Symptomatology in Children with Williams Syndrome Who Have Phrase Speech or Fluent Language.
Bonita P Klein-Tasman, Faye van der Fluit, Carolyn B Mervis. J Autism Dev Disord 2018
17
29

Autism Spectrum Symptomatology Among Children with Duplication 7q11.23 Syndrome.
Bonita P Klein-Tasman, Carolyn B Mervis. J Autism Dev Disord 2018
10
50

Mutational mechanisms of Williams-Beuren syndrome deletions.
Mònica Bayés, Luis F Magano, Núria Rivera, Raquel Flores, Luis A Pérez Jurado. Am J Hum Genet 2003
238
10

Prevalence estimation of Williams syndrome.
Petter Strømme, Per G Bjørnstad, Kjersti Ramstad. J Child Neurol 2002
421
10

Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion.
Claudia Torniero, Bernardo Dalla Bernardina, Francesca Novara, Roberto Cerini, Clara Bonaglia, Tiziano Pramparo, Roberto Ciccone, Renzo Guerrini, Orsetta Zuffardi. Eur J Hum Genet 2008
37
10

Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype.
Marilee A Martens, Sarah J Wilson, David C Reutens. J Child Psychol Psychiatry 2008
246
10

ELN gene triplication responsible for familial supravalvular aortic aneurysm.
Anne-Sophie Guemann, Joris Andrieux, Florence Petit, Emmanuel Halimi, Sonia Bouquillon, Sylvie Manouvrier-Hanu, Jiddeke Van De Kamp, Catherine Boileau, Nadine Hanna, Guillaume Jondeau,[...]. Cardiol Young 2015
13
30

Brief report: functional MRI of a patient with 7q11.23 duplication syndrome and autism spectrum disorder.
Paolo Prontera, Domenico Serino, Bernardo Caldini, Laura Scarponi, Giuseppe Merla, Giuseppe Testa, Marco Muti, Valerio Napolioni, Giovanni Mazzotta, Massimo Piccirilli,[...]. J Autism Dev Disord 2014
13
30

Familial 7q11.23 duplication with variable phenotype.
Siddaramappa J Patil, Smrithi Salian, Venkaraman Bhat, Katta Mohan Girisha, Yash Shrivastava, Kiran Vs, Anilkumar Sapare. Am J Med Genet A 2015
5
80

Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
221
10

Partial 7q11.23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams-Beuren syndrome neurocognitive profile.
A Antonell, M Del Campo, L F Magano, L Kaufmann, J Martínez de la Iglesia, F Gallastegui, R Flores, U Schweigmann, C Fauth, D Kotzot,[...]. J Med Genet 2010
74
10

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
128
10

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
614
10

Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
Megan R Glassford, Jill A Rosenfeld, Alexa A Freedman, Michael E Zwick, Jennifer G Mulle. Am J Med Genet A 2016
39
10


Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome.
Ovsanna T Leyfer, Janet Woodruff-Borden, Bonita P Klein-Tasman, Johanna S Fricke, Carolyn B Mervis. Am J Med Genet B Neuropsychiatr Genet 2006
179
10

Perioperative morbidity in children with elastin arteriopathy.
Gregory J Latham, Faith J Ross, Michael J Eisses, Michael J Richards, Jeremy M Geiduschek, Denise C Joffe. Paediatr Anaesth 2016
19
21


Social interaction behaviors discriminate young children with autism and Williams syndrome.
Alan J Lincoln, Yvonne M Searcy, Wendy Jones, Catherine Lord. J Am Acad Child Adolesc Psychiatry 2007
57
10

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.
Andreas Meyer-Lindenberg, Carolyn B Mervis, Karen Faith Berman. Nat Rev Neurosci 2006
252
10

Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior.
Li Dai, C Sue Carter, Jian Ying, Ursula Bellugi, Hossein Pournajafi-Nazarloo, Julie R Korenberg. PLoS One 2012
57
10

Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome.
Cristina Borralleras, Ignasi Sahun, Luis A Pérez-Jurado, Victoria Campuzano. Mol Ther 2015
19
21

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
390
10

Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays.
L Dai, U Bellugi, X-N Chen, A M Pulst-Korenberg, A Järvinen-Pasley, T Tirosh-Wagner, P S Eis, J Graham, D Mills, Y Searcy,[...]. Am J Med Genet A 2009
76
10

Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region.
Francesco Nicita, Giacomo Garone, Alberto Spalice, Salvatore Savasta, Pasquale Striano, Chiara Pantaleoni, Maria Valentina Spartà, Gerhard Kluger, Giuseppe Capovilla, Dario Pruna,[...]. Am J Med Genet A 2016
17
23


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.