A citation-based method for searching scientific literature

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
Times Cited: 24







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



Times Cited
  Times     Co-cited
Similarity


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
97
54

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
50

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
45

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
45

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
69
45


Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome.
Gea Beunders, Sonja A de Munnik, Nathalie Van der Aa, Berten Ceulemans, Els Voorhoeve, Alexander J Groffen, Willy M Nillesen, Elizabeth J Meijers-Heijboer, R Frank Kooy, Helger G Yntema,[...]. Eur J Hum Genet 2015
15
60

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
37

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
43
37

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
88
37

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
J Elia, X Gai, H M Xie, J C Perin, E Geiger, J T Glessner, M D'arcy, R deBerardinis, E Frackelton, C Kim,[...]. Mol Psychiatry 2010
355
33

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
33

The role of AUTS2 in neurodevelopment and human evolution.
Nir Oksenberg, Nadav Ahituv. Trends Genet 2013
73
33

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
80
33

Genome-wide distribution of Auts2 binding localizes with active neurodevelopmental genes.
N Oksenberg, G D E Haliburton, W L Eckalbar, I Oren, S Nishizaki, K Murphy, K S Pollard, R Y Birnbaum, N Ahituv. Transl Psychiatry 2014
31
29

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
381
25

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies.
Heather C Mefford, Hiltrud Muhle, Philipp Ostertag, Sarah von Spiczak, Karen Buysse, Carl Baker, Andre Franke, Alain Malafosse, Pierre Genton, Pierre Thomas,[...]. PLoS Genet 2010
333
25

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
210
25

Exonic deletions of AUTS2 in Chinese patients with developmental delay and intellectual disability.
Yanjie Fan, Wenjuan Qiu, Lili Wang, Xuefan Gu, Yongguo Yu. Am J Med Genet A 2016
8
75

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
25

The clinical significance of small copy number variants in neurodevelopmental disorders.
Reza Asadollahi, Beatrice Oneda, Pascal Joset, Silvia Azzarello-Burri, Deborah Bartholdi, Katharina Steindl, Marie Vincent, Joana Cobilanschi, Heinrich Sticht, Rosa Baldinger,[...]. J Med Genet 2014
57
20

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption.
Gunter Schumann, Lachlan J Coin, Anbarasu Lourdusamy, Pimphen Charoen, Karen H Berger, David Stacey, Sylvane Desrivières, Fazil A Aliev, Anokhi A Khan, Najaf Amin,[...]. Proc Natl Acad Sci U S A 2011
195
20

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.
Michael E Talkowski, Jill A Rosenfeld, Ian Blumenthal, Vamsee Pillalamarri, Colby Chiang, Adrian Heilbut, Carl Ernst, Carrie Hanscom, Elizabeth Rossin, Amelia M Lindgren,[...]. Cell 2012
381
20

Neuronal Migration and AUTS2 Syndrome.
Kei Hori, Mikio Hoshino. Brain Sci 2017
35
20

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
16

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
16

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
16

Association study identifying a new susceptibility gene (AUTS2) for schizophrenia.
Bao Zhang, Yue-Hong Xu, Shu-Guang Wei, Hong-Bo Zhang, Dong-Ke Fu, Zu-Fei Feng, Fang-Lin Guan, Yong-Sheng Zhu, Sheng-Bin Li. Int J Mol Sci 2014
23
17

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
26

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
44

PAX5-AUTS2: a recurrent fusion gene in childhood B-cell precursor acute lymphoblastic leukemia.
Dagmar Denk, Karin Nebral, Jutta Bradtke, Gertrud Pass, Anja Möricke, Andishe Attarbaschi, Sabine Strehl. Leuk Res 2012
19
15

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder.
A M Persico, L D'Agruma, N Maiorano, A Totaro, R Militerni, C Bravaccio, T H Wassink, C Schneider, R Melmed, S Trillo,[...]. Mol Psychiatry 2001
249
12

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
12

An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.
Ye Cheng, Jeffrey Francis Quinn, Lauren Anne Weiss. Hum Mol Genet 2013
38
12

How does Reelin control neuronal migration and layer formation in the developing mammalian neocortex?
Katsutoshi Sekine, Ken-ichiro Kubo, Kazunori Nakajima. Neurosci Res 2014
81
12

The involvement of Reelin in neurodevelopmental disorders.
Timothy D Folsom, S Hossein Fatemi. Neuropharmacology 2013
162
12

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban,[...]. Mol Psychiatry 2014
230
12

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex.
Francesco Bedogni, Rebecca D Hodge, Gina E Elsen, Branden R Nelson, Ray A M Daza, Richard P Beyer, Theo K Bammler, John L R Rubenstein, Robert F Hevner. Proc Natl Acad Sci U S A 2010
208
12

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
Olga Peñagarikano, Brett S Abrahams, Edward I Herman, Kellen D Winden, Amos Gdalyahu, Hongmei Dong, Lisa I Sonnenblick, Robin Gruver, Joel Almajano, Anatol Bragin,[...]. Cell 2011
577
12

Patches of disorganization in the neocortex of children with autism.
Rich Stoner, Maggie L Chow, Maureen P Boyle, Susan M Sunkin, Peter R Mouton, Subhojit Roy, Anthony Wynshaw-Boris, Sophia A Colamarino, Ed S Lein, Eric Courchesne. N Engl J Med 2014
384
12

The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes.
Jerzy Wegiel, Izabela Kuchna, Krzysztof Nowicki, Humi Imaki, Jarek Wegiel, Elaine Marchi, Shuang Yong Ma, Abha Chauhan, Ved Chauhan, Teresa Wierzba Bobrowicz,[...]. Acta Neuropathol 2010
344
12


Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept.
M L Hamshere, E K Green, I R Jones, L Jones, V Moskvina, G Kirov, D Grozeva, I Nikolov, D Vukcevic, S Caesar,[...]. Br J Psychiatry 2009
73
12

Reelin signaling is impaired in autism.
S Hossein Fatemi, Anne V Snow, Joel M Stary, Mohsen Araghi-Niknam, Teri J Reutiman, Suzanne Lee, Andrew I Brooks, David A Pearce. Biol Psychiatry 2005
160
12

Loss of δ-catenin function in severe autism.
Tychele N Turner, Kamal Sharma, Edwin C Oh, Yangfan P Liu, Ryan L Collins, Maria X Sosa, Dallas R Auer, Harrison Brand, Stephan J Sanders, Daniel Moreno-De-Luca,[...]. Nature 2015
92
12


A clinicopathological study of autism.
A Bailey, P Luthert, A Dean, B Harding, I Janota, M Montgomery, M Rutter, P Lantos. Brain 1998
687
12

Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.
Eyal Ben-David, Einat Granot-Hershkovitz, Galya Monderer-Rothkoff, Elad Lerer, Shlomit Levi, Maya Yaari, Richard P Ebstein, Nurit Yirmiya, Sagiv Shifman. Hum Mol Genet 2011
43
12

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
A Jeremy Willsey, Stephan J Sanders, Mingfeng Li, Shan Dong, Andrew T Tebbenkamp, Rebecca A Muhle, Steven K Reilly, Leon Lin, Sofia Fertuzinhos, Jeremy A Miller,[...]. Cell 2013
499
12

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
534
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.