A citation-based method for searching scientific literature

Tychele N Turner, Bradley P Coe, Diane E Dickel, Kendra Hoekzema, Bradley J Nelson, Michael C Zody, Zev N Kronenberg, Fereydoun Hormozdiari, Archana Raja, Len A Pennacchio, Robert B Darnell, Evan E Eichler. Cell 2017
Times Cited: 141



Kaitlin E Samocha, Elise B Robinson, Stephan J Sanders, Christine Stevens, Aniko Sabo, Lauren M McGrath, Jack A Kosmicki, Karola Rehnström, Swapan Mallick, Andrew Kirby, Dennis P Wall, Daniel G MacArthur, Stacey B Gabriel, Mark DePristo, Shaun M Purcell, Aarno Palotie, Eric Boerwinkle, Joseph D Buxbaum, Edwin H Cook, Richard A Gibbs, Gerard D Schellenberg, James S Sutcliffe, Bernie Devlin, Kathryn Roeder, Benjamin M Neale, Mark J Daly. Nat Genet 2014
Times Cited: 521




List of shared articles



Times cited

Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.
Veronica B Searles Quick, Belinda Wang, Matthew W State. Neuropsychopharmacology 2021
8

The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Rachel E Rodin, Yanmei Dou, Minseok Kwon, Maxwell A Sherman, Alissa M D'Gama, Ryan N Doan, Lariza M Rento, Kelly M Girskis, Craig L Bohrson, Sonia N Kim,[...]. Nat Neurosci 2021
8

Patterns of de novo tandem repeat mutations and their role in autism.
Ileena Mitra, Bonnie Huang, Nima Mousavi, Nichole Ma, Michael Lamkin, Richard Yanicky, Sharona Shleizer-Burko, Kirk E Lohmueller, Melissa Gymrek. Nature 2021
11

Recent ultra-rare inherited variants implicate new autism candidate risk genes.
Amy B Wilfert, Tychele N Turner, Shwetha C Murali, PingHsun Hsieh, Arvis Sulovari, Tianyun Wang, Bradley P Coe, Hui Guo, Kendra Hoekzema, Trygve E Bakken,[...]. Nat Genet 2021
3

Developmental and temporal characteristics of clonal sperm mosaicism.
Xiaoxu Yang, Martin W Breuss, Xin Xu, Danny Antaki, Kiely N James, Valentina Stanley, Laurel L Ball, Renee D George, Sara A Wirth, Beibei Cao,[...]. Cell 2021
0

Nonrandom occurrence of multiple de novo coding variants in a proband indicates the existence of an oligogenic model in autism.
Yaoqiang Du, Zhongshan Li, Zhenwei Liu, Na Zhang, Ruochen Wang, Fengxia Li, Tao Zhang, Yi Jiang, Xiao Zhi, Zhen Wang,[...]. Genet Med 2020
8

Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.
Huidan Wu, Honghui Li, Ting Bai, Lin Han, Jianjun Ou, Guanglei Xun, Yu Zhang, Yazhe Wang, Guiqin Duan, Ningxia Zhao,[...]. Clin Genet 2020
8

Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
Eduarda Morgana da Silva Montenegro, Claudia Samogy Costa, Gabriele Campos, Marília Scliar, Tatiana Ferreira de Almeida, Elaine Cristina Zachi, Isabela Maya Wahys Silva, Ada J S Chan, Mehdi Zarrei, Naila C V Lourenço,[...]. Autism Res 2020
5

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios.
Madison R Bishop, Kimberly K Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay, Jacqueline B Hetmanski, Margaret A Taub, Lina M Moreno-Uribe, Luz Consuelo Valencia-Ramirez,[...]. Am J Hum Genet 2020
5

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Tianyun Wang, Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P Coe, Madelyn A Gillentine, Amy B Wilfert, Luis A Perez-Jurado, Malin Kvarnung,[...]. Nat Commun 2020
17

A Machine Learning Approach to Predicting Autism Risk Genes: Validation of Known Genes and Discovery of New Candidates.
Ying Lin, Shiva Afshar, Anjali M Rajadhyaksha, James B Potash, Shizhong Han. Front Genet 2020
3

Next-Generation Sequencing in Autism Spectrum Disorder.
Stephan J Sanders. Cold Spring Harb Perspect Med 2019
9

A map of constrained coding regions in the human genome.
James M Havrilla, Brent S Pedersen, Ryan M Layer, Aaron R Quinlan. Nat Genet 2019
77

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.
Bradley P Coe, Holly A F Stessman, Arvis Sulovari, Madeleine R Geisheker, Trygve E Bakken, Allison M Lake, Joseph D Dougherty, Ed S Lein, Fereydoun Hormozdiari, Raphael A Bernier,[...]. Nat Genet 2019
99

Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder.
Susan M Hiatt, Michelle L Thompson, Jeremy W Prokop, James M J Lawlor, David E Gray, E Martina Bebin, Tuula Rinne, Marlies Kempers, Rolph Pfundt, Bregje W van Bon,[...]. Am J Hum Genet 2019
3

Recent genetic and functional insights in autism spectrum disorder.
Moe Nakanishi, Matthew P Anderson, Toru Takumi. Curr Opin Neurol 2019
1