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







List of shared articles



Times cited

Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.
Yasser Al-Sarraj, Eman Al-Dous, Rowaida Z Taha, Dina Ahram, Fouad Alshaban, Mohammed Tolfat, Hatem El-Shanti, Omar M E Albagha. Genes (Basel) 2021
0


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

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
0

Genome-wide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders.
Lu Xia, Jianjun Ou, Kuokuo Li, Hui Guo, Zhengmao Hu, Ting Bai, Jingping Zhao, Kun Xia, Fengyu Zhang. Autism Res 2020
4

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

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
13

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
2

Recent Advances in Understanding the Genetic Architecture of Autism.
Caroline M Dias, Christopher A Walsh. Annu Rev Genomics Hum Genet 2020
5

Genetic pathways involved in human speech disorders.
Joery den Hoed, Simon E Fisher. Curr Opin Genet Dev 2020
4

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

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
36

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


Insights into genetics, human biology and disease gleaned from family based genomic studies.
Jennifer E Posey, Anne H O'Donnell-Luria, Jessica X Chong, Tamar Harel, Shalini N Jhangiani, Zeynep H Coban Akdemir, Steven Buyske, Davut Pehlivan, Claudia M B Carvalho, Samantha Baxter,[...]. Genet Med 2019
67

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

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
79