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



Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall, Anthony Leotta, Deepa Pai, Ray Zhang, Yoon-Ha Lee, James Hicks, Sarah J Spence, Annette T Lee, Kaija Puura, Terho Lehtimäki, David Ledbetter, Peter K Gregersen, Joel Bregman, James S Sutcliffe, Vaidehi Jobanputra, Wendy Chung, Dorothy Warburton, Mary-Claire King, David Skuse, Daniel H Geschwind, T Conrad Gilliam, Kenny Ye, Michael Wigler. Science 2007
Times Cited: 1774




List of shared articles



Times cited

Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms.
Devanand S Manoli, Matthew W State. Am J Psychiatry 2021
4

Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.
Veronica B Searles Quick, Belinda Wang, Matthew W State. Neuropsychopharmacology 2021
6

Genomic Variation, Evolvability, and the Paradox of Mental Illness.
Camillo Thomas Gualtieri. Front Psychiatry 2021
0

16p11.2 deletion syndrome.
Wendy K Chung, Timothy Pl Roberts, Elliott H Sherr, LeeAnne Green Snyder, John E Spiro. Curr Opin Genet Dev 2021
0

Mapping and characterization of structural variation in 17,795 human genomes.
Haley J Abel, David E Larson, Allison A Regier, Colby Chiang, Indraniel Das, Krishna L Kanchi, Ryan M Layer, Benjamin M Neale, William J Salerno, Catherine Reeves,[...]. Nature 2020
26

Phenotypes Associated with 16p11.2 Copy Number Gains and Losses at a Single Institution.
Caleb Chu, Haotian Wu, Fangling Xu, Joseph W Ray, Allison Britt, Sally S Robinson, Pamela J Lupo, Christine R C Murphy, Charles F Dreyer, Phillip D K Lee,[...]. Lab Med 2020
0

Language characterization in 16p11.2 deletion and duplication syndromes.
So Hyun Kim, LeeAnne Green-Snyder, Catherine Lord, Somer Bishop, Kyle J Steinman, Raphael Bernier, Ellen Hanson, Robin P Goin-Kochel, Wendy K Chung. Am J Med Genet B Neuropsychiatr Genet 2020
4

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



Rare copy number variations of planar cell polarity genes are associated with human neural tube defects.
Tian Tian, Yunping Lei, Yongyan Chen, Yinnan Guo, Lei Jin, Richard H Finnell, Linlin Wang, Aiguo Ren. Neurogenetics 2020
0

Genetic Risk Profiling in Parkinson's Disease and Utilizing Genetics to Gain Insight into Disease-Related Biological Pathways.
Ashley Hall, Sara Bandres-Ciga, Monica Diez-Fairen, John P Quinn, Kimberley J Billingsley. Int J Mol Sci 2020
5

A Bibliometric Insight of Genetic Factors in ASD: Emerging Trends and New Developments.
Kang Wang, Weicheng Duan, Yijie Duan, Yuxin Yu, Xiuyi Chen, Yinhui Xu, Haihong Chen, Hongzhi Huang, Bo Xiong. Brain Sci 2020
0