A citation-based method for searching scientific literature

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
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
145
85

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
66
57

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
92
57

Neuronal Migration and AUTS2 Syndrome.
Kei Hori, Mikio Hoshino. Brain Sci 2017
31
57

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
83
57

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
125
57

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
77
57

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
14
57

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
352
42


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
22
42

The role of AUTS2 in neurodevelopment and human evolution.
Nir Oksenberg, Nadav Ahituv. Trends Genet 2013
68
42

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
88
42

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
194
42

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
29
42

Functional Landscape of PCGF Proteins Reveals Both RING1A/B-Dependent-and RING1A/B-Independent-Specific Activities.
Andrea Scelfo, Daniel Fernández-Pérez, Simone Tamburri, Marika Zanotti, Elisa Lavarone, Monica Soldi, Tiziana Bonaldi, Karin Johanna Ferrari, Diego Pasini. Mol Cell 2019
37
28

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
28

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
375
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
42
28

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
375
28

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
28

Glycosphingolipid metabolic reprogramming drives neural differentiation.
Domenico Russo, Floriana Della Ragione, Riccardo Rizzo, Eiji Sugiyama, Francesco Scalabrì, Kei Hori, Serena Capasso, Lucia Sticco, Salvatore Fioriniello, Roberto De Gregorio,[...]. EMBO J 2018
20
28

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
327
28

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
28

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
205
28

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
22
28

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
20
28


Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene.
Blanca E Himes, Keith Sheppard, Annerose Berndt, Adriana S Leme, Rachel A Myers, Christopher R Gignoux, Albert M Levin, W James Gauderman, James J Yang, Rasika A Mathias,[...]. PLoS One 2013
24
14

Three candidate genes and angiotensin-converting enzyme inhibitor-related cough: a pharmacogenetic analysis.
R Y Zee, V S Rao, R Z Paster, C S Sweet, K Lindpaintner. Hypertension 1998
34
14

Improved whole-chromosome phasing for disease and population genetic studies.
Olivier Delaneau, Jean-Francois Zagury, Jonathan Marchini. Nat Methods 2013
740
14

Chemistry and pharmacology of Angiotensin-converting enzyme inhibitors.
Milosz Regulski, Katarzyna Regulska, Beata J Stanisz, Marek Murias, Paulina Gieremek, Anna Wzgarda, Bartlomiej Niznik. Curr Pharm Des 2015
15
14

Association between genetic polymorphisms and angiotensin-converting enzyme inhibitor-induced cough: a systematic review and meta-analysis.
Guangyan Mu, Qian Xiang, Shuang Zhou, Qiufen Xie, Zhiyan Liu, Zhuo Zhang, Yimin Cui. Pharmacogenomics 2019
5
20

Meta-analysis of genome-wide association studies on the intolerance of angiotensin-converting enzyme inhibitors.
Seyed H Mahmoudpour, Abirami Veluchamy, Moneeza K Siddiqui, Folkert W Asselbergs, Patrick C Souverein, Catherine E de Keyser, Albert Hofman, Chim C Lang, Alexander S F Doney, Bruno H Stricker,[...]. Pharmacogenet Genomics 2017
9
14

Genome wide identification and expression profile in epithelial cells exposed to TiO₂ particles.
Tae-Hoon Kim, Seung-Woo Shin, Jong-Sook Park, Choon-Sik Park. Environ Toxicol 2015
13
14

PNPASE regulates RNA import into mitochondria.
Geng Wang, Hsiao-Wen Chen, Yavuz Oktay, Jin Zhang, Eric L Allen, Geoffrey M Smith, Kelly C Fan, Jason S Hong, Samuel W French, J Michael McCaffery,[...]. Cell 2010
215
14


Complexin cross-links prefusion SNAREs into a zigzag array.
Daniel Kümmel, Shyam S Krishnakumar, Daniel T Radoff, Feng Li, Claudio G Giraudo, Frederic Pincet, James E Rothman, Karin M Reinisch. Nat Struct Mol Biol 2011
105
14

[Study on candidate genes of benazepril related cough in Chinese hypertensives].
Jun Lu, Li-ming Li, Si-yan Zhan, Hui-ying Yang, Xiao-hui Li, Wei-hua Cao, Yong-hua Hu. Zhonghua Liu Xing Bing Xue Za Zhi 2003
8
14

Complexin facilitates exocytosis and synchronizes vesicle release in two secretory model systems.
Ming-Yi Lin, Joyce G Rohan, Haijiang Cai, Kerstin Reim, Chien-Ping Ko, Robert H Chow. J Physiol 2013
23
14

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
14


Association of B2 receptor polymorphisms and ACE activity with ACE inhibitor-induced angioedema in black and mixed-race South Africans.
Retsilisitsoe R Moholisa, Brian R Rayner, E Patricia Owen, Sylva L U Schwager, Joalice S Stark, Motassim Badri, Clint L Cupido, Edward D Sturrock. J Clin Hypertens (Greenwich) 2013
20
14

Efficacy of folic acid therapy in primary prevention of stroke among adults with hypertension in China: the CSPPT randomized clinical trial.
Yong Huo, Jianping Li, Xianhui Qin, Yining Huang, Xiaobin Wang, Rebecca F Gottesman, Genfu Tang, Binyan Wang, Dafang Chen, Mingli He,[...]. JAMA 2015
377
14

MiR-532-5p suppresses renal cancer cell proliferation by disrupting the ETS1-mediated positive feedback loop with the KRAS-NAP1L1/P-ERK axis.
Wei Zhai, Junjie Ma, Rujian Zhu, Chen Xu, Jin Zhang, Yonghui Chen, Zhiguo Chen, Dongkui Gong, Jiayi Zheng, Chen Chen,[...]. Br J Cancer 2018
34
14

Identification of genetic factors associated with susceptibility to angiotensin-converting enzyme inhibitors-induced cough.
Antonio Grilo, María P Sáez-Rosas, Juan Santos-Morano, Elena Sánchez, Concha Moreno-Rey, Luis M Real, Reposo Ramírez-Lorca, María E Sáez. Pharmacogenet Genomics 2011
33
14

CC chemokine ligand 18(CCL18) promotes migration and invasion of lung cancer cells by binding to Nir1 through Nir1-ELMO1/DOC180 signaling pathway.
Lihong Shi, Baogang Zhang, Xiuning Sun, Xiurong Zhang, Shijun Lv, Hongli Li, Xuejian Wang, Chunzhen Zhao, Heng Zhang, Xinpeng Xie,[...]. Mol Carcinog 2016
30
14

Angiotensin converting enzyme inhibitors and risk of lung cancer: population based cohort study.
Blánaid M Hicks, Kristian B Filion, Hui Yin, Lama Sakr, Jacob A Udell, Laurent Azoulay. BMJ 2018
75
14


Association of polymorphisms of the renin-angiotensin system and bradykinin B2 receptor with ACE-inhibitor-related cough.
S Mukae, S Itoh, S Aoki, T Iwata, K Nishio, R Sato, T Katagiri. J Hum Hypertens 2002
44
14


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.