A citation-based method for searching scientific literature

Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren, Bhooma Thiruvahindrapduram, Andreas Fiebig, Stefan Schreiber, Jan Friedman, Cees E J Ketelaars, Yvonne J Vos, Can Ficicioglu, Susan Kirkpatrick, Rob Nicolson, Leon Sloman, Anne Summers, Clare A Gibbons, Ahmad Teebi, David Chitayat, Rosanna Weksberg, Ann Thompson, Cathy Vardy, Vicki Crosbie, Sandra Luscombe, Rebecca Baatjes, Lonnie Zwaigenbaum, Wendy Roberts, Bridget Fernandez, Peter Szatmari, Stephen W Scherer. Am J Hum Genet 2008
Times Cited: 1182



Peter Szatmari, Andrew D Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, Xiao-Qing Liu, John B Vincent, Jennifer L Skaug, Ann P Thompson, Lili Senman, Lars Feuk, Cheng Qian, Susan E Bryson, Marshall B Jones, Christian R Marshall, Stephen W Scherer, Veronica J Vieland, Christopher Bartlett, La Vonne Mangin, Rhinda Goedken, Alberto Segre, Margaret A Pericak-Vance, Michael L Cuccaro, John R Gilbert, Harry H Wright, Ruth K Abramson, Catalina Betancur, Thomas Bourgeron, Christopher Gillberg, Marion Leboyer, Joseph D Buxbaum, Kenneth L Davis, Eric Hollander, Jeremy M Silverman, Joachim Hallmayer, Linda Lotspeich, James S Sutcliffe, Jonathan L Haines, Susan E Folstein, Joseph Piven, Thomas H Wassink, Val Sheffield, Daniel H Geschwind, Maja Bucan, W Ted Brown, Rita M Cantor, John N Constantino, T Conrad Gilliam, Martha Herbert, Clara Lajonchere, David H Ledbetter, Christa Lese-Martin, Janet Miller, Stan Nelson, Carol A Samango-Sprouse, Sarah Spence, Matthew State, Rudolph E Tanzi, Hilary Coon, Geraldine Dawson, Bernie Devlin, Annette Estes, Pamela Flodman, Lambertus Klei, William M McMahon, Nancy Minshew, Jeff Munson, Elena Korvatska, Patricia M Rodier, Gerard D Schellenberg, Moyra Smith, M Anne Spence, Chris Stodgell, Ping Guo Tepper, Ellen M Wijsman, Chang-En Yu, Bernadette Rogé, Carine Mantoulan, Kerstin Wittemeyer, Annemarie Poustka, Bärbel Felder, Sabine M Klauck, Claudia Schuster, Fritz Poustka, Sven Bölte, Sabine Feineis-Matthews, Evelyn Herbrecht, Gabi Schmötzer, John Tsiantis, Katerina Papanikolaou, Elena Maestrini, Elena Bacchelli, Francesca Blasi, Simona Carone, Claudio Toma, Herman Van Engeland, Maretha de Jonge, Chantal Kemner, Frederieke Koop, Marjolein Langemeijer, Channa Hijmans, Wouter G Staal, Gillian Baird, Patrick F Bolton, Michael L Rutter, Emma Weisblatt, Jonathan Green, Catherine Aldred, Julie-Anne Wilkinson, Andrew Pickles, Ann Le Couteur, Tom Berney, Helen McConachie, Anthony J Bailey, Kostas Francis, Gemma Honeyman, Aislinn Hutchinson, Jeremy R Parr, Simon Wallace, Anthony P Monaco, Gabrielle Barnby, Kazuhiro Kobayashi, Janine A Lamb, Ines Sousa, Nuala Sykes, Edwin H Cook, Stephen J Guter, Bennett L Leventhal, Jeff Salt, Catherine Lord, Christina Corsello, Vanessa Hus, Daniel E Weeks, Fred Volkmar, Maïté Tauber, Eric Fombonne, Andy Shih, Kacie J Meyer. Nat Genet 2007
Times Cited: 949




List of shared articles



Times cited


Copy number variations in Japanese children with autism spectrum disorder.
Yui Sakamoto, Shuji Shimoyama, Tomonori Furukawa, Masaki Adachi, Michio Takahashi, Tamaki Mikami, Michito Kuribayashi, Ayako Osato, Daiki Tsushima, Manabu Saito,[...]. Psychiatr Genet 2021
0

Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review.
Paola Castronovo, Marco Baccarin, Arianna Ricciardello, Chiara Picinelli, Pasquale Tomaiuolo, Francesca Cucinotta, Myriam Frittoli, Carla Lintas, Roberto Sacco, Antonio M Persico. Clin Genet 2020
13

ELMOD3-SH2D6 gene fusion as a possible co-star actor in autism spectrum disorder scenario.
Eleonora Loi, Loredana Moi, Sylvain Blois, Elena Bacchelli, Ana Florencia Vega Benedetti, Cinzia Cameli, Roberta Fadda, Elena Maestrini, Marinella Carta, Giuseppe Doneddu,[...]. J Cell Mol Med 2020
4

Refining critical regions in 15q24 microdeletion syndrome pertaining to autism.
Yi Liu, Yanqing Zhang, Mehdi Zarrei, Rui Dong, Xiaomeng Yang, Dongmei Zhao, Stephen W Scherer, Zhongtao Gai. Am J Med Genet B Neuropsychiatr Genet 2020
0

Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
Lin Wang, Yi Zhang, Kuokuo Li, Zheng Wang, Xiaomeng Wang, Bin Li, Guihu Zhao, Zhenghuan Fang, Zhengbao Ling, Tengfei Luo,[...]. Mol Autism 2020
1

Assessing the developmental trajectory of mouse models of neurodevelopmental disorders: Social and communication deficits in mice with Neurexin 1α deletion.
Emily C Armstrong, Angela Caruso, Michela Servadio, Laura C Andreae, Viviana Trezza, Maria L Scattoni, Cathy Fernandes. Genes Brain Behav 2020
3

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Afsheen Yousaf, Regina Waltes, Denise Haslinger, Sabine M Klauck, Eftichia Duketis, Michael Sachse, Anette Voran, Monica Biscaldi, Martin Schulte-Rüther, Sven Cichon,[...]. Transl Psychiatry 2020
5

Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia.
Kanako Ishizuka, Tomoyuki Yoshida, Takeshi Kawabata, Ayako Imai, Hisashi Mori, Hiroki Kimura, Toshiya Inada, Yuko Okahisa, Jun Egawa, Masahide Usami,[...]. J Neurodev Disord 2020
0

A Bibliometric Insight of Genetic Factors in ASD: Emerging Trends and New Developments.
Kang Wang, Weicheng Duan, Yijie Duan, Yuxin Yu, Xiuyi Chen, Yinhui Xu, Haihong Chen, Hongzhi Huang, Bo Xiong. Brain Sci 2020
0

IPSC Models of Chromosome 15Q Imprinting Disorders: From Disease Modeling to Therapeutic Strategies.
Noelle D Germain, Eric S Levine, Stormy J Chamberlain. Adv Neurobiol 2020
0

A comparative study of the genetic components of three subcategories of autism spectrum disorder.
Jinchen Li, Shanshan Hu, Kun Zhang, Leisheng Shi, Yi Zhang, Tingting Zhao, Lin Wang, Xin He, Kun Xia, Chunyu Liu,[...]. Mol Psychiatry 2019
17

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders.
Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, Ming Li. Mol Psychiatry 2019
24