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: 1173



Thomas Bourgeron. Nat Rev Neurosci 2015
Times Cited: 403




List of shared articles



Times cited

A white paper on a neurodevelopmental framework for drug discovery in autism and other neurodevelopmental disorders.
C M Díaz-Caneja, M W State, R J Hagerman, S Jacquemont, O Marín, C Bagni, D Umbricht, E Simonoff, F de Andrés-Trelles, A Kaale,[...]. Eur Neuropsychopharmacol 2021
1

Novel missense mutations in PTCHD1 alter its plasma membrane subcellular localization and cause intellectual disability and autism spectrum disorder.
Judith Halewa, Sylviane Marouillat, Manon Dixneuf, Rose-Anne Thépault, Dévina C Ung, Nicolas Chatron, Bénédicte Gérard, Jamal Ghoumid, Gaëtan Lesca, Marianne Till,[...]. Hum Mutat 2021
0

Regulation of Neural Circuit Development by Cadherin-11 Provides Implications for Autism.
Jeannine A Frei, Robert F Niescier, Morgan S Bridi, Madel Durens, Jonathan E Nestor, Michaela B C Kilander, Xiaobing Yuan, Derek M Dykxhoorn, Michael W Nestor, Shiyong Huang,[...]. eNeuro 2021
0

Synaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-AS.
P Joel Ross, Wen-Bo Zhang, Rebecca S F Mok, Kirill Zaslavsky, Eric Deneault, Lia D'Abate, Deivid C Rodrigues, Ryan K C Yuen, Muhammad Faheem, Marat Mufteev,[...]. Biol Psychiatry 2020
22

Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
Eduarda Morgana da Silva Montenegro, Claudia Samogy Costa, Gabriele Campos, Marília Scliar, Tatiana Ferreira de Almeida, Elaine Cristina Zachi, Isabela Maya Wahys Silva, Ada J S Chan, Mehdi Zarrei, Naila C V Lourenço,[...]. Autism Res 2020
4

Genome-wide detection of tandem DNA repeats that are expanded in autism.
Brett Trost, Worrawat Engchuan, Charlotte M Nguyen, Bhooma Thiruvahindrapuram, Egor Dolzhenko, Ian Backstrom, Mila Mirceta, Bahareh A Mojarad, Yue Yin, Alona Dov,[...]. Nature 2020
28

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

Clinical correlates in children with autism spectrum disorder and CNVs: Systematic investigation in a clinical setting.
Rita Barone, Mariangela Gulisano, Renata Amore, Carla Domini, Maria Chiara Milana, Sabrina Giglio, Francesca Madia, Teresa Mattina, Antonino Casabona, Marco Fichera,[...]. Int J Dev Neurosci 2020
3

Genetic association of DNMT variants can play a critical role in defining the methylation patterns in autism.
Ann Mary Alex, Korammannil R Saradalekshmi, Neena Shilen, Poovathinal A Suresh, Moinak Banerjee. IUBMB Life 2019
6