A citation-based method for searching scientific literature

S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban, E Antoniou, E Kelleher, C O'Brien, G Donohoe, M Gill, D W Morris, W R McCombie, A Corvin. Mol Psychiatry 2014
Times Cited: 229



Neelroop N Parikshak, Rui Luo, Alice Zhang, Hyejung Won, Jennifer K Lowe, Vijayendran Chandran, Steve Horvath, Daniel H Geschwind. Cell 2013
Times Cited: 562




List of shared articles



Times cited

Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders.
Yijia Zhang, Ruochen Wang, Zhenwei Liu, Shan Jiang, Lifeng Du, Kairui Qiu, Fengxia Li, Qiongdan Wang, Jing Jin, Xiaomin Chen,[...]. Am J Med Genet B Neuropsychiatr Genet 2021
0

Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.
Jennifer K Forsyth, Daniel Nachun, Michael J Gandal, Daniel H Geschwind, Ariana E Anderson, Giovanni Coppola, Carrie E Bearden. Biol Psychiatry 2020
14


A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.
Else Eising, Amaia Carrion-Castillo, Arianna Vino, Edythe A Strand, Kathy J Jakielski, Thomas S Scerri, Michael S Hildebrand, Richard Webster, Alan Ma, Bernard Mazoyer,[...]. Mol Psychiatry 2019
48

Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency.
A Ayanna Wade, Kenneth Lim, Rinaldo Catta-Preta, Alex S Nord. Front Mol Neurosci 2019
13


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
44

Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders.
Julie Chow, Matthew Jensen, Hajar Amini, Farhad Hormozdiari, Osnat Penn, Sagiv Shifman, Santhosh Girirajan, Fereydoun Hormozdiari. Genome Med 2019
7

Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.
Zi-Bing Jin, Zhongshan Li, Zhenwei Liu, Yi Jiang, Xue-Bi Cai, Jinyu Wu. Biol Rev Camb Philos Soc 2018
17