A citation-based method for searching scientific literature

Todd Lencz, Jin Yu, Raiyan Rashid Khan, Erin Flaherty, Shai Carmi, Max Lam, Danny Ben-Avraham, Nir Barzilai, Susan Bressman, Ariel Darvasi, Judy H Cho, Lorraine N Clark, Zeynep H Gümüş, Joseph Vijai, Robert J Klein, Steven Lipkin, Kenneth Offit, Harry Ostrer, Laurie J Ozelius, Inga Peter, Anil K Malhotra, Tom Maniatis, Gil Atzmon, Itsik Pe'er. Neuron 2021
Times Cited: 2

List of co-cited articles
articles co-cited >1

Times Cited
  Times     Co-cited

Pcdhαc2 is required for axonal tiling and assembly of serotonergic circuitries in mice.
Weisheng V Chen, Chiamaka L Nwakeze, Christine A Denny, Sean O'Keeffe, Michael A Rieger, George Mountoufaris, Amy Kirner, Joseph D Dougherty, René Hen, Qiang Wu,[...]. Science 2017

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L Nimgaonkar, Rodney C P Go,[...]. Cell 2013

Calcium Channels, Synaptic Plasticity, and Neuropsychiatric Disease.
Evanthia Nanou, William A Catterall. Neuron 2018

Genetics of schizophrenia in the South African Xhosa.
S Gulsuner, D J Stein, E S Susser, G Sibeko, A Pretorius, T Walsh, L Majara, M M Mndini, S G Mqulwana, O A Ntola,[...]. Science 2020

A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014

Dysregulated protocadherin-pathway activity as an intrinsic defect in induced pluripotent stem cell-derived cortical interneurons from subjects with schizophrenia.
Zhicheng Shao, Haneul Noh, Woong Bin Kim, Peiyan Ni, Christine Nguyen, Sarah E Cote, Elizabeth Noyes, Joyce Zhao, Teagan Parsons, James M Park,[...]. Nat Neurosci 2019

Evolution and functional impact of rare coding variation from deep sequencing of human exomes.
Jacob A Tennessen, Abigail W Bigham, Timothy D O'Connor, Wenqing Fu, Eimear E Kenny, Simon Gravel, Sean McGee, Ron Do, Xiaoming Liu, Goo Jun,[...]. Science 2012

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
Giulio Genovese, Menachem Fromer, Eli A Stahl, Douglas M Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L Moran, Shaun M Purcell, Pamela Sklar, Patrick F Sullivan,[...]. Nat Neurosci 2016

Genetic heterogeneity in human disease.
Jon McClellan, Mary-Claire King. Cell 2010

Low-Level Brain Somatic Mutations Are Implicated in Schizophrenia.
Myeong-Heui Kim, Il Bin Kim, Junehawk Lee, Do Hyeon Cha, Sang Min Park, Ja Hye Kim, Ryunhee Kim, Jun Sung Park, Yohan An, Kyungdeok Kim,[...]. Biol Psychiatry 2021

Brain somatic mutations observed in Alzheimer's disease associated with aging and dysregulation of tau phosphorylation.
Jun Sung Park, Junehawk Lee, Eun Sun Jung, Myeong-Heui Kim, Il Bin Kim, Hyeonju Son, Sangwoo Kim, Sanghyeon Kim, Young Mok Park, Inhee Mook-Jung,[...]. Nat Commun 2019

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.
Eric Larsen, Idan Menashe, Mark N Ziats, Wayne Pereanu, Alan Packer, Sharmila Banerjee-Basu. Mol Autism 2016

Inhibitory regulation of calcium transients in prefrontal dendritic spines is compromised by a nonsense Shank3 mutation.
Farhan Ali, Ling-Xiao Shao, Danielle M Gerhard, Katherine Sweasy, Santosh Pothula, Christopher Pittenger, Ronald S Duman, Alex C Kwan. Mol Psychiatry 2021

Human GRIN2B variants in neurodevelopmental disorders.
Chun Hu, Wenjuan Chen, Scott J Myers, Hongjie Yuan, Stephen F Traynelis. J Pharmacol Sci 2016

Putative Blood Somatic Mutations in Post-Traumatic Stress Disorder-Symptomatic Soldiers: High Impact of Cytoskeletal and Inflammatory Proteins.
Shlomo Sragovich, Michael Gershovits, Jacqueline C K Lam, Victor O K Li, Illana Gozes. J Alzheimers Dis 2021

Autophagy has a key role in the pathophysiology of schizophrenia.
A Merenlender-Wagner, A Malishkevich, Z Shemer, M Udawela, A Gibbons, E Scarr, B Dean, J Levine, G Agam, I Gozes. Mol Psychiatry 2015

Long genes are more frequently affected by somatic mutations and show reduced expression in Alzheimer's disease: Implications for disease etiology.
Sourena Soheili-Nezhad, Robert J van der Linden, Marcel Olde Rikkert, Emma Sprooten, Geert Poelmans. Alzheimers Dement 2021

Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.