A citation-based method for searching scientific literature

Thomas Arbogast, Abdel-Mouttalib Ouagazzal, Claire Chevalier, Maksym Kopanitsa, Nurudeen Afinowi, Eugenia Migliavacca, Belinda S Cowling, Marie-Christine Birling, Marie-France Champy, Alexandre Reymond, Yann Herault. PLoS Genet 2016
Times Cited: 55



Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong, Arthur P Goldberg, Cai Jinlu, John F Keaney, Lambertus Klei, Jeffrey D Mandell, Daniel Moreno-De-Luca, Christopher S Poultney, Elise B Robinson, Louw Smith, Tor Solli-Nowlan, Mack Y Su, Nicole A Teran, Michael F Walker, Donna M Werling, Arthur L Beaudet, Rita M Cantor, Eric Fombonne, Daniel H Geschwind, Dorothy E Grice, Catherine Lord, Jennifer K Lowe, Shrikant M Mane, Donna M Martin, Eric M Morrow, Michael E Talkowski, James S Sutcliffe, Christopher A Walsh, Timothy W Yu, David H Ledbetter, Christa Lese Martin, Edwin H Cook, Joseph D Buxbaum, Mark J Daly, Bernie Devlin, Kathryn Roeder, Matthew W State. Neuron 2015
Times Cited: 624




List of shared articles



Times cited

CNV biology in neurodevelopmental disorders.
Toru Takumi, Kota Tamada. Curr Opin Neurobiol 2018
44

Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model.
Denise Haslinger, Regina Waltes, Afsheen Yousaf, Silvia Lindlar, Ines Schneider, Chai K Lim, Meng-Miao Tsai, Boyan K Garvalov, Amparo Acker-Palmer, Nicolas Krezdorn,[...]. Mol Autism 2018
13

Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.
Timothy P Rutkowski, Jason P Schroeder, Georgette M Gafford, Stephen T Warren, David Weinshenker, Tamara Caspary, Jennifer G Mulle. J Neurosci Res 2017
22

The 16p11.2 homologs fam57ba and doc2a generate certain brain and body phenotypes.
Jasmine M McCammon, Alicia Blaker-Lee, Xiao Chen, Hazel Sive. Hum Mol Genet 2017
12

Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism.
Jorge Urresti, Pan Zhang, Patricia Moran-Losada, Nam-Kyung Yu, Priscilla D Negraes, Cleber A Trujillo, Danny Antaki, Megha Amar, Kevin Chau, Akula Bala Pramod,[...]. Mol Psychiatry 2021
2

The abiding relevance of mouse models of rare mutations to psychiatric neuroscience and therapeutics.
Joseph A Gogos, Gregg Crabtree, Anastasia Diamantopoulou. Schizophr Res 2020
4

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?
Chelsea Lowther, Gregory Costain, Danielle A Baribeau, Anne S Bassett. Curr Psychiatry Rep 2017
19