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: 143



Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong, Arthur P Goldberg, Cai Jinlu, John F Keaney, Lambertus Klei, Jeffrey D Mandell, Daniel Moreno-De-Luca, Christopher S Poultney, Elise B Robinson, Louw Smith, Tor Solli-Nowlan, Mack Y Su, Nicole A Teran, Michael F Walker, Donna M Werling, Arthur L Beaudet, Rita M Cantor, Eric Fombonne, Daniel H Geschwind, Dorothy E Grice, Catherine Lord, Jennifer K Lowe, Shrikant M Mane, Donna M Martin, Eric M Morrow, Michael E Talkowski, James S Sutcliffe, Christopher A Walsh, Timothy W Yu, David H Ledbetter, Christa Lese Martin, Edwin H Cook, Joseph D Buxbaum, Mark J Daly, Bernie Devlin, Kathryn Roeder, Matthew W State. Neuron 2015
Times Cited: 632




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


Large mosaic copy number variations confer autism risk.
Maxwell A Sherman, Rachel E Rodin, Giulio Genovese, Caroline Dias, Alison R Barton, Ronen E Mukamel, Bonnie Berger, Peter J Park, Christopher A Walsh, Po-Ru Loh. Nat Neurosci 2021
4

Genetic contributions to autism spectrum disorder.
A Havdahl, M Niarchou, A Starnawska, M Uddin, C van der Merwe, V Warrier. Psychol Med 2021
2




Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
Evin M Padhi, Tristan J Hayeck, Zhang Cheng, Sumantra Chatterjee, Brandon J Mannion, Marta Byrska-Bishop, Marjolaine Willems, Lucile Pinson, Sylvia Redon, Caroline Benech,[...]. Hum Genomics 2021
0

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

Rates of contributory de novo mutation in high and low-risk autism families.
Seungtai Yoon, Adriana Munoz, Boris Yamrom, Yoon-Ha Lee, Peter Andrews, Steven Marks, Zihua Wang, Catherine Reeves, Lara Winterkorn, Abba M Krieger,[...]. Commun Biol 2021
0

Genetic counseling as preventive intervention: toward individual specification of transgenerational autism risk.
Natasha Marrus, Tychele N Turner, Elizabeth Forsen, Drew Bolster, Alison Marvin, Andrew Whitehouse, Laura Klinger, Christina A Gurnett, J N Constantino. J Neurodev Disord 2021
0

Molecular Dysregulation in Autism Spectrum Disorder.
Pritmohinder S Gill, Jeffery L Clothier, Aravindhan Veerapandiyan, Harsh Dweep, Patricia A Porter-Gill, G Bradley Schaefer. J Pers Med 2021
0

Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.
Behrang Mahjani, Silvia De Rubeis, Christina Gustavsson Mahjani, Maureen Mulhern, Xinyi Xu, Lambertus Klei, F Kyle Satterstrom, Jack Fu, Michael E Talkowski, Abraham Reichenberg,[...]. Mol Autism 2021
1

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

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

Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes.
Kensuke Matsumura, Kaoru Seiriki, Shota Okada, Masashi Nagase, Shinya Ayabe, Ikuko Yamada, Tamio Furuse, Hirotoshi Shibuya, Yuka Yasuda, Hidenaga Yamamori,[...]. Nat Commun 2020
17

Forecasting risk gene discovery in autism with machine learning and genome-scale data.
Leo Brueggeman, Tanner Koomar, Jacob J Michaelson. Sci Rep 2020
5

Genetic landscape of autism spectrum disorder in Vietnamese children.
Kien Trung Tran, Vinh Sy Le, Hoa Thi Phuong Bui, Duong Huy Do, Ha Thi Thanh Ly, Hieu Thi Nguyen, Lan Thi Mai Dao, Thanh Hong Nguyen, Duc Minh Vu, Lien Thi Ha,[...]. Sci Rep 2020
3

Recent Advances in Understanding the Genetic Architecture of Autism.
Caroline M Dias, Christopher A Walsh. Annu Rev Genomics Hum Genet 2020
7

The Genetic Control of Stoichiometry Underlying Autism.
Robert B Darnell. Annu Rev Neurosci 2020
4

Autism spectrum disorder genomics: The progress and potential of genomic technologies.
Fiana Ní Ghrálaigh, Louise Gallagher, Lorna M Lopez. Genomics 2020
2

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

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck,[...]. Genet Med 2019
61

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

Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.
Hui Guo, Michael H Duyzend, Bradley P Coe, Carl Baker, Kendra Hoekzema, Jennifer Gerdts, Tychele N Turner, Michael C Zody, Jennifer S Beighley, Shwetha C Murali,[...]. Genet Med 2019
37

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
104

Copy number variants in autism spectrum disorders.
Stefano Vicari, Eleonora Napoli, Viviana Cordeddu, Deny Menghini, Viola Alesi, Sara Loddo, Antonio Novelli, Marco Tartaglia. Prog Neuropsychopharmacol Biol Psychiatry 2019
10

Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.
Jian Zhou, Christopher Y Park, Chandra L Theesfeld, Aaron K Wong, Yuan Yuan, Claudia Scheckel, John J Fak, Julien Funk, Kevin Yao, Yoko Tajima,[...]. Nat Genet 2019
81

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