A citation-based method for searching scientific literature

Farah Qaiser, Yue Yin, Carolyn B Mervis, Colleen A Morris, Bonita P Klein-Tasman, Elaine Tam, Lucy R Osborne, Ryan K C Yuen. Orphanet J Rare Dis 2021
Times Cited: 1







List of co-cited articles
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
100

Mild macrocytosis in Williams-Beuren syndrome.
Eric Yu, Richard Feinn, Robert Bona, Benjamin Brink, Sampat Sindhar, Beth A Kozel, Barbara R Pober. Eur J Med Genet 2020
3
100

The 7q11.23 Protein DNAJC30 Interacts with ATP Synthase and Links Mitochondria to Brain Development.
Andrew T N Tebbenkamp, Luis Varela, Jinmyung Choi, Miguel I Paredes, Alice M Giani, Jae Eun Song, Matija Sestan-Pesa, Daniel Franjic, André M M Sousa, Zhong-Wu Liu,[...]. Cell 2018
16
100


High-throughput screening identifies histone deacetylase inhibitors that modulate GTF2I expression in 7q11.23 microduplication autism spectrum disorder patient-derived cortical neurons.
Francesca Cavallo, Flavia Troglio, Giovanni Fagà, Daniele Fancelli, Reinald Shyti, Sebastiano Trattaro, Matteo Zanella, Giuseppe D'Agostino, James M Hughes, Maria Rosaria Cera,[...]. Mol Autism 2020
1
100

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
802
100

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
46
100

Social, neurodevelopmental, endocrine, and head size differences associated with atypical deletions in Williams-Beuren syndrome.
Michael Lugo, Zoë C Wong, Charles J Billington, Phoebe C R Parrish, Glennis Muldoon, Delong Liu, Barbara R Pober, Beth A Kozel. Am J Med Genet A 2020
4
100


Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.
Christian R Marshall, Edwin J Young, Ariel M Pani, Mary-Louise Freckmann, Yves Lacassie, Cédric Howald, Kristi K Fitzgerald, Maarit Peippo, Colleen A Morris, Kate Shane,[...]. Am J Hum Genet 2008
84
100

Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome.
Shahryar Khattak, Elise Brimble, Wenbo Zhang, Kirill Zaslavsky, Emma Strong, P Joel Ross, Jason Hendry, Seema Mital, Michael W Salter, Lucy R Osborne,[...]. Mol Brain 2015
19
100


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
203
100

Do microdeletions lead to immune deficiency?
Sait Karaman, Filiz Hazan, Semiha Bahçeci Erdem, Nesrin Gülez, Ferah Genel. Cent Eur J Immunol 2020
1
100

Divergent functions of hematopoietic transcription factors in lineage priming and differentiation during erythro-megakaryopoiesis.
Maxim Pimkin, Andrew V Kossenkov, Tejaswini Mishra, Christapher S Morrissey, Weisheng Wu, Cheryl A Keller, Gerd A Blobel, Dongwon Lee, Michael A Beer, Ross C Hardison,[...]. Genome Res 2014
58
100

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
56
100


Serotonergic innervation of the amygdala is increased in autism spectrum disorder and decreased in Williams syndrome.
C H Lew, K M Groeniger, K L Hanson, D Cuevas, D M Z Greiner, B Hrvoj-Mihic, U Bellugi, C M Schumann, K Semendeferi. Mol Autism 2020
4
100

Genome-wide Analysis of the Role of Copy Number Variation in Schizophrenia Risk in Chinese.
Zhiqiang Li, Jianhua Chen, Yifeng Xu, Qizhong Yi, Weidong Ji, Peng Wang, Jiawei Shen, Zhijian Song, Meng Wang, Ping Yang,[...]. Biol Psychiatry 2016
36
100

Williams Syndrome, Human Self-Domestication, and Language Evolution.
Amy Niego, Antonio Benítez-Burraco. Front Psychol 2019
6
100

Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndrome.
Marta Codina-Sola, Mar Costa-Roger, Debora Pérez-García, Raquel Flores, Maria Gabriela Palacios-Verdú, Ivon Cusco, Luis Alberto Pérez-Jurado. J Med Genet 2019
4
100

TFII-I/Gtf2i and Erythro-Megakaryopoiesis.
Aishwarya Gurumurthy, Qiong Wu, Rukiye Nar, Kimberly Paulsen, Alexis Trumbull, Ryan C Fishman, Marjorie Brand, John Strouboulis, Zhijian Qian, Jörg Bungert. Front Physiol 2020
1
100

The sociability spectrum: evidence from reciprocal genetic copy number variations.
Alejandro López-Tobón, Sebastiano Trattaro, Giuseppe Testa. Mol Autism 2020
2
100



Impaired adult myelination in the prefrontal cortex of socially isolated mice.
Jia Liu, Karen Dietz, Jacqueline M DeLoyht, Xiomara Pedre, Dipti Kelkar, Jasbir Kaur, Vincent Vialou, Mary Kay Lobo, David M Dietz, Eric J Nestler,[...]. Nat Neurosci 2012
367
100

A comparison of methods to measure central and peripheral oxytocin concentrations in human and non-human primates.
Arthur Lefevre, Raphaëlle Mottolese, Manon Dirheimer, Carmine Mottolese, Jean-René Duhamel, Angela Sirigu. Sci Rep 2017
38
100

Williams-Beuren Syndrome as a Potential Risk Factor for Burkitt Lymphoma.
Ryo Kimura, Yuko Ishii, Kiyotaka Tomiwa, Tomonari Awaya, Masatoshi Nakata, Takeo Kato, Shin Okazaki, Toshio Heike, Masatoshi Hagiwara. Front Genet 2018
5
100

A specific missense mutation in GTF2I occurs at high frequency in thymic epithelial tumors.
Iacopo Petrini, Paul S Meltzer, In-Kyu Kim, Marco Lucchi, Kang-Seo Park, Gabriella Fontanini, James Gao, Paolo A Zucali, Fiorella Calabrese, Adolfo Favaretto,[...]. Nat Genet 2014
102
100

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.
Colleen A Morris, Carolyn B Mervis, Holly H Hobart, Ronald G Gregg, Jacquelyn Bertrand, Gregory J Ensing, Annemarie Sommer, Cynthia A Moore, Robert J Hopkin, Patricia A Spallone,[...]. Am J Med Genet A 2003
114
100

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development.
Badam Enkhmandakh, Aleksandr V Makeyev, Lkhamsuren Erdenechimeg, Frank H Ruddle, Nyam-Osor Chimge, Maria Isabel Tussie-Luna, Ananda L Roy, Dashzeveg Bayarsaihan. Proc Natl Acad Sci U S A 2009
78
100

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
100

Transcription Factor 2I Regulates Neuronal Development via TRPC3 in 7q11.23 Disorder Models.
Marielle H S Deurloo, Ekaterina Turlova, Wen-Liang Chen, You Wei Lin, Elaine Tam, Nardos G Tassew, Michael Wu, Ya-Chi Huang, Jacqueline N Crawley, Philippe P Monnier,[...]. Mol Neurobiol 2019
7
100

Heat shock protein 27 gene: chromosomal and molecular location and relationship to Williams syndrome.
A Dean Stock, Patricia A Spallone, Thomas R Dennis, Dale Netski, Colleen A Morris, Carolyn B Mervis, Holly H Hobart. Am J Med Genet A 2003
26
100


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
16
100

Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug.
Boaz Barak, Zicong Zhang, Yuanyuan Liu, Ariel Nir, Sari S Trangle, Michaela Ennis, Kirsten M Levandowski, Dongqing Wang, Kathleen Quast, Gabriella L Boulting,[...]. Nat Neurosci 2019
32
100

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
760
100

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis.
M E Curran, D L Atkinson, A K Ewart, C A Morris, M F Leppert, M T Keating. Cell 1993
296
100

Autism Spectrum Symptomatology Among Children with Duplication 7q11.23 Syndrome.
Bonita P Klein-Tasman, Carolyn B Mervis. J Autism Dev Disord 2018
10
100

Functions of Gtf2i and Gtf2ird1 in the developing brain: transcription, DNA binding and long-term behavioral consequences.
Nathan D Kopp, Kayla R Nygaard, Yating Liu, Katherine B McCullough, Susan E Maloney, Harrison W Gabel, Joseph D Dougherty. Hum Mol Genet 2020
3
100

Social cognition in williams syndrome: genotype/phenotype insights from partial deletion patients.
Annette Karmiloff-Smith, Hannah Broadbent, Emily K Farran, Elena Longhi, Dean D'Souza, Kay Metcalfe, May Tassabehji, Rachel Wu, Atsushi Senju, Francesca Happé,[...]. Front Psychol 2012
23
100

Williams-Beuren syndrome in diverse populations.
Paul Kruszka, Antonio R Porras, Deise Helena de Souza, Angélica Moresco, Victoria Huckstadt, Ashleigh D Gill, Alec P Boyle, Tommy Hu, Yonit A Addissie, Gary T K Mok,[...]. Am J Med Genet A 2018
33
100

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
100

7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages.
Antonio Adamo, Sina Atashpaz, Pierre-Luc Germain, Matteo Zanella, Giuseppe D'Agostino, Veronica Albertin, Josh Chenoweth, Lucia Micale, Carmela Fusco, Christian Unger,[...]. Nat Genet 2015
75
100

Cognitive, Behavioral, and Adaptive Profiles in Williams Syndrome With and Without Loss of GTF2IRD2.
Carlos Alberto Serrano-Juárez, Carlos Alberto Venegas-Vega, Ma Guillermina Yáñez-Téllez, Mario Rodríguez-Camacho, Juan Silva-Pereyra, Hermelinda Salgado-Ceballos, Belén Prieto-Corona. J Int Neuropsychol Soc 2018
5
100

Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication.
Matteo Zanella, Alessandro Vitriolo, Alejandro Andirko, Pedro Tiago Martins, Stefanie Sturm, Thomas O'Rourke, Magdalena Laugsch, Natascia Malerba, Adrianos Skaros, Sebastiano Trattaro,[...]. Sci Adv 2019
16
100

Action of TFII-I outside the nucleus as an inhibitor of agonist-induced calcium entry.
Gabriela Caraveo, Damian B van Rossum, Randen L Patterson, Solomon H Snyder, Stephen Desiderio. Science 2006
69
100

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
47
100

Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder.
Julie Masson, Caroline Demily, Nicolas Chatron, Audrey Labalme, Pierre-Antoine Rollat-Farnier, Caroline Schluth-Bolard, Brigitte Gilbert-Dussardier, Fabienne Giuliano, Renaud Touraine, Sylvie Tordjman,[...]. Orphanet J Rare Dis 2019
5
100


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.