A citation-based method for searching scientific literature

Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green, Orah S Platt, Douglas M Ruderfer, Christopher A Walsh, David Altshuler, Aravinda Chakravarti, Rudolph E Tanzi, Kari Stefansson, Susan L Santangelo, James F Gusella, Pamela Sklar, Bai-Lin Wu, Mark J Daly. N Engl J Med 2008
Times Cited: 1079



Ian Blumenthal, Ashok Ragavendran, Serkan Erdin, Lambertus Klei, Aarathi Sugathan, Jolene R Guide, Poornima Manavalan, Julian Q Zhou, Vanessa C Wheeler, Joshua Z Levin, Carl Ernst, Kathryn Roeder, Bernie Devlin, James F Gusella, Michael E Talkowski. Am J Hum Genet 2014
Times Cited: 65




List of shared articles



Times cited

Three case reports of patients indicating the diversity of molecular and clinical features of 16p11.2 microdeletion anomaly.
Monika Szelest, Martyna Stefaniak, Gabriela Ręka, Ilona Jaszczuk, Monika Lejman. BMC Med Genomics 2021
0

Transcriptome analysis of human neural cells derived from isogenic embryonic stem cells with 16p11.2 deletion.
Yoshiko Nomura, Jun Nomura, Hiroyuki Kamiguchi, Toru Nishikawa, Toru Takumi. Neurosci Res 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

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice.
Xiaojun Ren, Nan Yang, Nan Wu, Ximing Xu, Weisheng Chen, Ling Zhang, Yingping Li, Ren-Qian Du, Shuangshuang Dong, Sen Zhao,[...]. J Med Genet 2020
8

Reversal of synaptic and behavioral deficits in a 16p11.2 duplication mouse model via restoration of the GABA synapse regulator Npas4.
Benjamin Rein, Tao Tan, Fengwei Yang, Wei Wang, Jamal Williams, Freddy Zhang, Alea Mills, Zhen Yan. Mol Psychiatry 2020
9

Understanding the clinical manifestations of 16p11.2 deletion syndrome: a series of developmental case reports in children.
Rana Fetit, David J Price, Stephen M Lawrie, Mandy Johnstone. Psychiatr Genet 2020
1

Neurodevelopmental trajectory and modifiers of 16p11.2 microdeletion: A follow-up study of four Chinese children carriers.
Hua Xie, Fang Liu, Yu Zhang, Qian Chen, Shaofang Shangguan, Zhijie Gao, Nan Wu, Jian Wang, Xiaodai Cui, Lin Wang,[...]. Mol Genet Genomic Med 2020
0

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

16p11 Duplication Disrupts Hippocampal-Orbitofrontal-Amygdala Connectivity, Revealing a Neural Circuit Endophenotype for Schizophrenia.
Greg C Bristow, David M Thomson, Rebecca L Openshaw, Emma J Mitchell, Judith A Pratt, Neil Dawson, Brian J Morris. Cell Rep 2020
6

16p11.2 Copy Number Variations and Neurodevelopmental Disorders.
Benjamin Rein, Zhen Yan. Trends Neurosci 2020
4