A citation-based method for searching scientific literature

Sandesh C S Nagamani, Ayelet Erez, Bruria Ben-Zeev, Moshe Frydman, Susan Winter, Robert Zeller, Dima El-Khechen, Luis Escobar, Pawel Stankiewicz, Ankita Patel, Sau Wai Cheung. Eur J Hum Genet 2013
Times Cited: 42







List of co-cited articles
284 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
95
64

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
127
59

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
332
45

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
379
45

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
90
45

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
38
44

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
35

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
23
65

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
353
33

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
208
33


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
85
28

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
26

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
79
26

The role of AUTS2 in neurodevelopment and human evolution.
Nir Oksenberg, Nadav Ahituv. Trends Genet 2013
71
26

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
151
26

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
21

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
21

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
14
64

A draft sequence of the Neandertal genome.
Richard E Green, Johannes Krause, Adrian W Briggs, Tomislav Maricic, Udo Stenzel, Martin Kircher, Nick Patterson, Heng Li, Weiwei Zhai, Markus Hsi-Yang Fritz,[...]. Science 2010
19

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
929
19

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
23
34

Whole genome association scan for genetic polymorphisms influencing information processing speed.
Michelle Luciano, Narelle K Hansell, Jari Lahti, Gail Davies, Sarah E Medland, Katri Räikkönen, Albert Tenesa, Elisabeth Widen, Kevin A McGhee, Aarno Palotie,[...]. Biol Psychol 2011
54
16

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
16

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
16

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
67
16

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
30
23

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
14

Possible association between suicide committed under influence of ethanol and a variant in the AUTS2 gene.
Izabela Chojnicka, Krzysztof Gajos, Katarzyna Strawa, Grażyna Broda, Sylwia Fudalej, Marcin Fudalej, Piotr Stawiński, Aleksandra Pawlak, Paweł Krajewski, Marcin Wojnar,[...]. PLoS One 2013
14
42

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
14

Neuronal Migration and AUTS2 Syndrome.
Kei Hori, Mikio Hoshino. Brain Sci 2017
33
18

Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder.
Michael E Talkowski, Sureni V Mullegama, Jill A Rosenfeld, Bregje W M van Bon, Yiping Shen, Elena A Repnikova, Julie Gastier-Foster, Devon Lamb Thrush, Sekar Kathiresan, Douglas M Ruderfer,[...]. Am J Hum Genet 2011
140
11

Accelerated evolution of conserved noncoding sequences in humans.
Shyam Prabhakar, James P Noonan, Svante Pääbo, Edward M Rubin. Science 2006
245
11

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
207
11

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
811
11

Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.
Maria Tropeano, Joo Wook Ahn, Richard J B Dobson, Gerome Breen, James Rucker, Abhishek Dixit, Deb K Pal, Peter McGuffin, Anne Farmer, Peter S White,[...]. PLoS One 2013
73
11

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.
Kevin A Strauss, Erik G Puffenberger, Matthew J Huentelman, Steven Gottlieb, Seth E Dobrin, Jennifer M Parod, Dietrich A Stephan, D Holmes Morton. N Engl J Med 2006
418
11

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
21

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
807
9

In vivo enhancer analysis of human conserved non-coding sequences.
Len A Pennacchio, Nadav Ahituv, Alan M Moses, Shyam Prabhakar, Marcelo A Nobrega, Malak Shoukry, Simon Minovitsky, Inna Dubchak, Amy Holt, Keith D Lewis,[...]. Nature 2006
812
9


Tbr1 regulates differentiation of the preplate and layer 6.
R F Hevner, L Shi, N Justice, Y Hsueh, M Sheng, S Smiga, A Bulfone, A M Goffinet, A T Campagnoni, J L Rubenstein. Neuron 2001
626
9

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
9

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
439
9

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
769
9

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
Maja Bucan, Brett S Abrahams, Kai Wang, Joseph T Glessner, Edward I Herman, Lisa I Sonnenblick, Ana I Alvarez Retuerto, Marcin Imielinski, Dexter Hadley, Jonathan P Bradfield,[...]. PLoS Genet 2009
283
9

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
9

[Twins with autism and mental retardation associated with balanced (7;20) chromosomal translocation].
F de la Barra, V Skoknic, A Alliende, E Raimann, F Cortés, Y Lacassie. Rev Chil Pediatr 1986
11
36

A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.
Heon-Jeong Lee, Hyun Goo Woo, Tiffany A Greenwood, Daniel F Kripke, John R Kelsoe. J Affect Disord 2013
31
12

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
493
9


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.