A citation-based method for searching scientific literature

Christelle M Durand, Catalina Betancur, Tobias M Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Rastam, I Carina Gillberg, Henrik Anckarsäter, Eili Sponheim, Hany Goubran-Botros, Richard Delorme, Nadia Chabane, Marie-Christine Mouren-Simeoni, Philippe de Mas, Eric Bieth, Bernadette Rogé, Delphine Héron, Lydie Burglen, Christopher Gillberg, Marion Leboyer, Thomas Bourgeron. Nat Genet 2007
Times Cited: 949



Julie Gauthier, Dan Spiegelman, Amélie Piton, Ronald G Lafrenière, Sandra Laurent, Judith St-Onge, Line Lapointe, Fadi F Hamdan, Patrick Cossette, Laurent Mottron, Eric Fombonne, Ridha Joober, Claude Marineau, Pierre Drapeau, Guy A Rouleau. Am J Med Genet B Neuropsychiatr Genet 2009
Times Cited: 218




List of shared articles



Times cited


CaMKIIα-driven, phosphatase-checked postsynaptic plasticity via phase separation.
Qixu Cai, Menglong Zeng, Xiandeng Wu, Haowei Wu, Yumeng Zhan, Ruijun Tian, Mingjie Zhang. Cell Res 2021
7

Perinatal Exposure to Diesel Exhaust-Origin Secondary Organic Aerosol Induces Autism-Like Behavior in Rats.
Tin-Tin Win-Shwe, Chaw Kyi-Tha-Thu, Yuji Fujitani, Shinji Tsukahara, Seishiro Hirano. Int J Mol Sci 2021
1

Genetic influences of autism candidate genes on circuit wiring and olfactory decoding.
Renée Hartig, David Wolf, Michael J Schmeisser, Wolfgang Kelsch. Cell Tissue Res 2021
1

Autism-associated SHANK3 missense point mutations impact conformational fluctuations and protein turnover at synapses.
Michael Bucher, Stephan Niebling, Yuhao Han, Dmitry Molodenskiy, Fatemeh Hassani Nia, Hans-Jürgen Kreienkamp, Dmitri Svergun, Eunjoon Kim, Alla S Kostyukova, Michael R Kreutz,[...]. Elife 2021
0

Truncating variants in the SHANK1 gene are associated with a spectrum of neurodevelopmental disorders.
Halie J May, Jaehoon Jeong, Anya Revah-Politi, Julie S Cohen, Anna Chassevent, Julia Baptista, Evan H Baugh, Louise Bier, Armand Bottani, Maria Teresa Carminho A Rodrigues,[...]. Genet Med 2021
0

Social Deficits and Repetitive Behaviors Are Improved by Early Postnatal Low-Dose VPA Intervention in a Novel shank3-Deficient Zebrafish Model.
Chunxue Liu, Yi Wang, Jingxin Deng, Jia Lin, Chunchun Hu, Qiang Li, Xiu Xu. Front Neurosci 2021
0


Association of SHANK Family with Neuropsychiatric Disorders: An Update on Genetic and Animal Model Discoveries.
Lily Wan, Du Liu, Wen-Biao Xiao, Bo-Xin Zhang, Xiao-Xin Yan, Zhao-Hui Luo, Bo Xiao. Cell Mol Neurobiol 2021
2


Genetic Findings as the Potential Basis of Personalized Pharmacotherapy in Phelan-McDermid Syndrome.
Brianna Dyar, Erika Meaddough, Sara M Sarasua, Curtis Rogers, Katy Phelan, Luigi Boccuto. Genes (Basel) 2021
0

Sam Domains in Multiple Diseases.
Marian Vincenzi, Flavia Anna Mercurio, Marilisa Leone. Curr Med Chem 2020
3

Shank3 Binds to and Stabilizes the Active Form of Rap1 and HRas GTPases via Its NTD-ANK Tandem with Distinct Mechanisms.
Qixu Cai, Tomohisa Hosokawa, Menglong Zeng, Yasunori Hayashi, Mingjie Zhang. Structure 2020
6

Genetic and Epigenetic Etiology Underlying Autism Spectrum Disorder.
Sang Hoon Yoon, Joonhyuk Choi, Won Ji Lee, Jeong Tae Do. J Clin Med 2020
18

Targeting of δ-catenin to postsynaptic sites through interaction with the Shank3 N-terminus.
Fatemeh Hassani Nia, Daniel Woike, Victoria Martens, Malte Klüssendorf, Hans-Hinrich Hönck, Sönke Harder, Hans-Jürgen Kreienkamp. Mol Autism 2020
1


Shank3 mutation in a mouse model of autism leads to changes in the S-nitroso-proteome and affects key proteins involved in vesicle release and synaptic function.
Haitham Amal, Boaz Barak, Vadiraja Bhat, Guanyu Gong, Brian A Joughin, Xin Wang, John S Wishnok, Guoping Feng, Steven R Tannenbaum. Mol Psychiatry 2020
31