A citation-based method for searching scientific literature

Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H Zackai, Paige Kaplan, Jaya Ganesh, Ian D Krantz, Nancy B Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B Lakshmi, Anthony Leotta, Jude Kendall, Yoon-Ha Lee, Vladimir Vacic, Sydney Gary, Lilia M Iakoucheva, Timothy J Crow, Susan L Christian, Jeffrey A Lieberman, T Scott Stroup, Terho Lehtimäki, Kaija Puura, Chad Haldeman-Englert, Justin Pearl, Meredith Goodell, Virginia L Willour, Pamela Derosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J McMahon, Anil K Malhotra, James B Potash, Thomas G Schulze, Markus M Nöthen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara M Lajonchere, James S Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R Mendell, Nick Craddock, Michael J Owen, Michael C O'Donovan, Tamim H Shaikh, Ezra Susser, Lynn E Delisi, Patrick F Sullivan, Curtis K Deutsch, Judith Rapoport, Deborah L Levy, Mary-Claire King, Jonathan Sebat. Nat Genet 2009
Times Cited: 472



Christine Ochoa Escamilla, Irina Filonova, Angela K Walker, Zhong X Xuan, Roopashri Holehonnur, Felipe Espinosa, Shunan Liu, Summer B Thyme, Isabel A López-García, Dorian B Mendoza, Noriyoshi Usui, Jacob Ellegood, Amelia J Eisch, Genevieve Konopka, Jason P Lerch, Alexander F Schier, Haley E Speed, Craig M Powell. Nature 2017
Times Cited: 44




List of shared articles



Times cited

Behavioral, circuitry, and molecular aberrations by region-specific deficiency of the high-risk autism gene Cul3.
Maximiliano Rapanelli, Tao Tan, Wei Wang, Xue Wang, Zi-Jun Wang, Ping Zhong, Luciana Frick, Luye Qin, Kaijie Ma, Jun Qu,[...]. Mol Psychiatry 2021
15

Functional Genomics Identify a Regulatory Risk Variation rs4420550 in the 16p11.2 Schizophrenia-Associated Locus.
Hong Chang, Xin Cai, Hui-Juan Li, Wei-Peng Liu, Li-Juan Zhao, Chu-Yi Zhang, Jun-Yang Wang, Jie-Wei Liu, Xiao-Lei Ma, Lu Wang,[...]. Biol Psychiatry 2021
2

Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models.
Sandra Martin Lorenzo, Valérie Nalesso, Claire Chevalier, Marie-Christine Birling, Yann Herault. Mol Autism 2021
0

Expression of Genes in the 16p11.2 Locus during Development of the Human Fetal Cerebral Cortex.
Sarah Morson, Yifei Yang, David J Price, Thomas Pratt. Cereb Cortex 2021
0

16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro.
Maria Sundberg, Hannah Pinson, Richard S Smith, Kellen D Winden, Pooja Venugopal, Derek J C Tai, James F Gusella, Michael E Talkowski, Christopher A Walsh, Max Tegmark,[...]. Nat Commun 2021
0

CRISPR/Cas9-mediated Knockout of the Neuropsychiatric Risk Gene KCTD13 Causes Developmental Deficits in Human Cortical Neurons Derived from Induced Pluripotent Stem Cells.
Valeria Kizner, Maximilian Naujock, Sandra Fischer, Stefan Jäger, Selina Reich, Ines Schlotthauer, Kai Zuckschwerdt, Tobias Geiger, Tobias Hildebrandt, Nathan Lawless,[...]. Mol Neurobiol 2020
6


16p11.2 Copy Number Variations and Neurodevelopmental Disorders.
Benjamin Rein, Zhen Yan. Trends Neurosci 2020
3

16p11.2 microdeletion imparts transcriptional alterations in human iPSC-derived models of early neural development.
Julien G Roth, Kristin L Muench, Aditya Asokan, Victoria M Mallett, Hui Gai, Yogendra Verma, Stephen Weber, Carol Charlton, Jonas L Fowler, Kyle M Loh,[...]. Elife 2020
3

Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions.
Thomas Arbogast, Parisa Razaz, Jacob Ellegood, Spencer U McKinstry, Serkan Erdin, Benjamin Currall, Tanya Aneichyk, Jason P Lerch, Lily R Qiu, Ramona M Rodriguiz,[...]. Hum Mol Genet 2019
11

KCTD: A new gene family involved in neurodevelopmental and neuropsychiatric disorders.
Xinchen Teng, Abdel Aouacheria, Loïc Lionnard, Kyle A Metz, Lucian Soane, Atsushi Kamiya, J Marie Hardwick. CNS Neurosci Ther 2019
16

Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.
Yuqi Qiu, Thomas Arbogast, Sandra Martin Lorenzo, Hongying Li, Shih C Tang, Ellen Richardson, Oanh Hong, Shawn Cho, Omar Shanta, Timothy Pang,[...]. Cell Rep 2019
11

Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.
Rebecca L Walker, Gokul Ramaswami, Christopher Hartl, Nicholas Mancuso, Michael J Gandal, Luis de la Torre-Ubieta, Bogdan Pasaniuc, Jason L Stein, Daniel H Geschwind. Cell 2019
36

Zebrafish Models of Neurodevelopmental Disorders: Past, Present, and Future.
Catalina Sakai, Sundas Ijaz, Ellen J Hoffman. Front Mol Neurosci 2018
35