A citation-based method for searching scientific literature

Carolina Sanchez-Jimeno, Fiona Blanco-Kelly, Fermina López-Grondona, Rebeca Losada-Del Pozo, Beatriz Moreno, María Rodrigo-Moreno, Elena Martinez-Cayuelas, Rosa Riveiro-Alvarez, María Fenollar-Cortés, Carmen Ayuso, Marta Rodríguez de Alba, Isabel Lorda-Sanchez, Berta Almoguera. Genes (Basel) 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: a case report and literature review.
Alexandra Jolley, Mark Corbett, Lesley McGregor, Wendy Waters, Susan Brown, Jillian Nicholl, Sui Yu. Am J Med Genet A 2013
24
100

Ring1B compacts chromatin structure and represses gene expression independent of histone ubiquitination.
Ragnhild Eskeland, Martin Leeb, Graeme R Grimes, Clémence Kress, Shelagh Boyle, Duncan Sproul, Nick Gilbert, Yuhong Fan, Arthur I Skoultchi, Anton Wutz,[...]. Mol Cell 2010
367
100


Transcriptional Complexity and Distinct Expression Patterns of auts2 Paralogs in Danio rerio.
Igor Kondrychyn, Lena Robra, Vatsala Thirumalai. G3 (Bethesda) 2017
7
100

Polycomb-dependent histone H2A ubiquitination links developmental disorders with cancer.
Simone Tamburri, Eric Conway, Diego Pasini. Trends Genet 2021
2
100


Regulation of gene transcription by Polycomb proteins.
Sergi Aranda, Gloria Mas, Luciano Di Croce. Sci Adv 2015
171
100

Cytoskeletal regulation by AUTS2 in neuronal migration and neuritogenesis.
Kei Hori, Taku Nagai, Wei Shan, Asami Sakamoto, Shinichiro Taya, Ryoya Hashimoto, Takashi Hayashi, Manabu Abe, Maya Yamazaki, Keiko Nakao,[...]. Cell Rep 2014
71
100

Polycomb group-mediated histone H2A monoubiquitination in epigenome regulation and nuclear processes.
Haithem Barbour, Salima Daou, Michael Hendzel, El Bachir Affar. Nat Commun 2020
11
100

On the retention of gene duplicates prone to dominant deleterious mutations.
Giulia Malaguti, Param Priya Singh, Hervé Isambert. Theor Popul Biol 2014
7
100

A case of autism spectrum disorder with cleft lip and palate carrying a mutation in exon 8 of AUTS2.
Saki Saeki, Takashi Enokizono, Kazuo Imagawa, Hiroko Fukushima, Daigo Kajikawa, Aiko Sakai, Mai Tanaka, Tatsuyuki Ohto, Hisato Suzuki, Tomoko Uehara,[...]. Clin Case Rep 2019
4
100

Role of Polycomb Complexes in Normal and Malignant Plasma Cells.
Emmanuel Varlet, Sara Ovejero, Anne-Marie Martinez, Giacomo Cavalli, Jerome Moreaux. Int J Mol Sci 2020
5
100

NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain.
Sanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, Takae Kiyama, Mitali Dave, Hanna K McNamara, Wukui Zhao, James M Stafford, Nicolas Descostes, Pedro Lee,[...]. Mol Cell 2021
1
100

Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
Jeroen H Roelfsema, Stefan J White, Yavuz Ariyürek, Deborah Bartholdi, Dunja Niedrist, Francesco Papadia, Carlos A Bacino, Johan T den Dunnen, Gert-Jan B van Ommen, Martijn H Breuning,[...]. Am J Hum Genet 2005
285
100

On the expansion of "dangerous" gene repertoires by whole-genome duplications in early vertebrates.
Param Priya Singh, Séverine Affeldt, Ilaria Cascone, Rasim Selimoglu, Jacques Camonis, Hervé Isambert. Cell Rep 2012
30
100

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
212
100

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP.
F Petrij, R H Giles, H G Dauwerse, J J Saris, R C Hennekam, M Masuno, N Tommerup, G J van Ommen, R H Goodman, D J Peters. Nature 1995
890
100

De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome.
Roser Ufartes, Hanna Berger, Katharina Till, Gabriela Salinas, Marc Sturm, Janine Altmüller, Peter Nürnberg, Holger Thiele, Rudolf Funke, Neophytos Apeshiotis,[...]. Hum Genet 2020
5
100

Role of histone H2A ubiquitination in Polycomb silencing.
Hengbin Wang, Liangjun Wang, Hediye Erdjument-Bromage, Miguel Vidal, Paul Tempst, Richard S Jones, Yi Zhang. Nature 2004
100

A de novo balanced translocation breakpoint truncating the autism susceptibility candidate 2 (AUTS2) gene in a patient with autism.
Xin-Li Huang, Ying S Zou, Tom A Maher, Stephanie Newton, Jeff M Milunsky. Am J Med Genet A 2010
39
100

Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus.
Gea Beunders, Els Voorhoeve, Christelle Golzio, Luba M Pardo, Jill A Rosenfeld, Michael E Talkowski, Ingrid Simonic, Anath C Lionel, Sarah Vergult, Robert E Pyatt,[...]. Am J Hum Genet 2013
98
100

Assessing predictors for new post translational modification sites: A case study on hydroxylation.
Damiano Piovesan, Andras Hatos, Giovanni Minervini, Federica Quaglia, Alexander Miguel Monzon, Silvio C E Tosatto. PLoS Comput Biol 2020
4
100

The role of AUTS2 in neurodevelopment and human evolution.
Nir Oksenberg, Nadav Ahituv. Trends Genet 2013
74
100

PCGF homologs, CBX proteins, and RYBP define functionally distinct PRC1 family complexes.
Zhonghua Gao, Jin Zhang, Roberto Bonasio, Francesco Strino, Ayana Sawai, Fabio Parisi, Yuval Kluger, Danny Reinberg. Mol Cell 2012
504
100

Polycomb and Trithorax Group Genes in Drosophila.
Judith A Kassis, James A Kennison, John W Tamkun. Genetics 2017
70
100


Neuronal Migration and AUTS2 Syndrome.
Kei Hori, Mikio Hoshino. Brain Sci 2017
36
100

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
Betul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, Abha R Gupta, Jesse F Abelson, Thomas M Morgan, Katarzyna Chawarska, Ami Klin, A Gulhan Ercan-Sencicek, Althea A Stillman,[...]. Am J Hum Genet 2008
382
100

Function and regulation of AUTS2, a gene implicated in autism and human evolution.
Nir Oksenberg, Laurie Stevison, Jeffrey D Wall, Nadav Ahituv. PLoS Genet 2013
89
100

Ohnologs are overrepresented in pathogenic copy number mutations.
Aoife McLysaght, Takashi Makino, Hannah M Grayton, Maria Tropeano, Kevin J Mitchell, Evangelos Vassos, David A Collier. Proc Natl Acad Sci U S A 2014
36
100

Untangle the Multi-Facet Functions of Auts2 as an Entry Point to Understand Neurodevelopmental Disorders.
Wenbin Pang, Xinan Yi, Ling Li, Liyan Liu, Wei Xiang, Le Xiao. Front Psychiatry 2021
1
100

Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
Razia Sultana, Chang-En Yu, Jun Yu, Jeffery Munson, Donghui Chen, Wenhui Hua, Annette Estes, Fanny Cortes, Flora de la Barra, Dongmei Yu,[...]. Genomics 2002
129
100

Molecular architecture of polycomb repressive complexes.
Emily C Chittock, Sebastian Latwiel, Thomas C R Miller, Christoph W Müller. Biochem Soc Trans 2017
92
100


AUTS2 isoforms control neuronal differentiation.
Galya Monderer-Rothkoff, Nitzan Tal, Marina Risman, Odem Shani, Malka Nissim-Rafinia, Laura Malki-Feldman, Vera Medvedeva, Matthias Groszer, Eran Meshorer, Sagiv Shifman. Mol Psychiatry 2021
9
100

Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.
Vera M Kalscheuer, David FitzPatrick, Niels Tommerup, Merete Bugge, Erik Niebuhr, Luitgard M Neumann, Andreas Tzschach, Sarah A Shoichet, Corinna Menzel, Fikret Erdogan,[...]. Hum Genet 2007
91
100

De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review.
Yi Liu, Dongmei Zhao, Rui Dong, Xiaomeng Yang, Yanqing Zhang, Kristiina Tammimies, Mohammed Uddin, Stephen W Scherer, Zhongtao Gai. Am J Med Genet A 2015
25
100

Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology.
Francesco Bedogni, Rebecca D Hodge, Branden R Nelson, Erika A Frederick, Naoko Shiba, Ray A Daza, Robert F Hevner. Gene Expr Patterns 2010
81
100

A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype.
Gea Beunders, Jiddeke van de Kamp, Pradeep Vasudevan, Jenny Morton, Katrien Smets, Tjitske Kleefstra, Sonja A de Munnik, Janneke Schuurs-Hoeijmakers, Berten Ceulemans, Marcella Zollino,[...]. J Med Genet 2016
24
100

Heterozygous Disruption of Autism susceptibility candidate 2 Causes Impaired Emotional Control and Cognitive Memory.
Kei Hori, Taku Nagai, Wei Shan, Asami Sakamoto, Manabu Abe, Maya Yamazaki, Kenji Sakimura, Kiyofumi Yamada, Mikio Hoshino. PLoS One 2015
15
100

On the origins of Mendelian disease genes in man: the impact of gene duplication.
Jonathan E Dickerson, David L Robertson. Mol Biol Evol 2012
33
100

An AUTS2-Polycomb complex activates gene expression in the CNS.
Zhonghua Gao, Pedro Lee, James M Stafford, Melanie von Schimmelmann, Anne Schaefer, Danny Reinberg. Nature 2014
153
100

Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.
Sandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, Moshe Frydman, Susan Winter, Robert Zeller, Dima El-Khechen, Luis Escobar, Pawel Stankiewicz, Ankita Patel,[...]. Eur J Hum Genet 2013
44
100


Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder.
Julien Van Gils, Frederique Magdinier, Patricia Fergelot, Didier Lacombe. Genes (Basel) 2021
2
100

Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation.
Mariana de Napoles, Jacqueline E Mermoud, Rika Wakao, Y Amy Tang, Mitusuhiro Endoh, Ruth Appanah, Tatyana B Nesterova, Jose Silva, Arie P Otte, Miguel Vidal,[...]. Dev Cell 2004
625
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.