A citation-based method for searching scientific literature

Gerald D Fischbach, Catherine Lord. Neuron 2010
Times Cited: 360



Raphael Bernier, Christelle Golzio, Bo Xiong, Holly A Stessman, Bradley P Coe, Osnat Penn, Kali Witherspoon, Jennifer Gerdts, Carl Baker, Anneke T Vulto-van Silfhout, Janneke H Schuurs-Hoeijmakers, Marco Fichera, Paolo Bosco, Serafino Buono, Antonino Alberti, Pinella Failla, Hilde Peeters, Jean Steyaert, Lisenka E L M Vissers, Ludmila Francescatto, Heather C Mefford, Jill A Rosenfeld, Trygve Bakken, Brian J O'Roak, Matthew Pawlus, Randall Moon, Jay Shendure, David G Amaral, Ed Lein, Julia Rankin, Corrado Romano, Bert B A de Vries, Nicholas Katsanis, Evan E Eichler. Cell 2014
Times Cited: 394




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

Exons as units of phenotypic impact for truncating mutations in autism.
Andrew H Chiang, Jonathan Chang, Jiayao Wang, Dennis Vitkup. Mol Psychiatry 2021
3

Brief Report: Associations Between Self-injurious Behaviors and Abdominal Pain Among Individuals with ASD-Associated Disruptive Mutations.
Evangeline C Kurtz-Nelson, See Wan Tham, Kaitlyn Ahlers, Daniel Cho, Arianne S Wallace, Evan E Eichler, Raphael A Bernier, Rachel K Earl. J Autism Dev Disord 2021
1

Sleep Problems in Children with ASD and Gene Disrupting Mutations.
Rachel K Earl, Tracey Ward, Jennifer Gerdts, Evan E Eichler, Raphael A Bernier, Caitlin M Hudac. J Genet Psychol 2021
0

The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defects.
Mireia Coll-Tané, Naihua N Gong, Samuel J Belfer, Lara V van Renssen, Evangeline C Kurtz-Nelson, Milan Szuperak, Ilse Eidhof, Boyd van Reijmersdal, Isabel Terwindt, Jaclyn Durkin,[...]. Sci Adv 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

How rare and common risk variation jointly affect liability for autism spectrum disorder.
Lambertus Klei, Lora Lee McClain, Behrang Mahjani, Klea Panayidou, Silvia De Rubeis, Anna-Carin Säll Grahnat, Gun Karlsson, Yangyi Lu, Nadine Melhem, Xinyi Xu,[...]. Mol Autism 2021
0

A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder.
Livia O Loureiro, Jennifer L Howe, Miriam S Reuter, Alana Iaboni, Kristina Calli, Delnaz Roshandel, Iva Pritišanac, Alan Moses, Julie D Forman-Kay, Brett Trost,[...]. NPJ Genom Med 2021
0

Clinical Phenotypes of Carriers of Mutations in CHD8 or Its Conserved Target Genes.
Jennifer S Beighley, Caitlin M Hudac, Anne B Arnett, Jessica L Peterson, Jennifer Gerdts, Arianne S Wallace, Heather C Mefford, Kendra Hoekzema, Tychele N Turner, Brian J O'Roak,[...]. Biol Psychiatry 2020
12

De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.
Carolina Cappi, Melody E Oliphant, Zsanett Péter, Gwyneth Zai, Maria Conceição do Rosário, Catherine A W Sullivan, Abha R Gupta, Ellen J Hoffman, Manmeet Virdee, Emily Olfson,[...]. Biol Psychiatry 2020
20

Transcriptional subtyping explains phenotypic variability in genetic subtypes of autism spectrum disorder.
Sandy Trinh, Anne Arnett, Evangeline Kurtz-Nelson, Jennifer Beighley, Marta Picoto, Raphael Bernier. Dev Psychopathol 2020
1

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

Co-occurring medical conditions among individuals with ASD-associated disruptive mutations.
Evangeline C Kurtz-Nelson, Jennifer S Beighley, Caitlin M Hudac, Jennifer Gerdts, Arianne S Wallace, Kendra Hoekzema, Evan E Eichler, Raphael A Bernier. Child Health Care 2020
1

A comparative study of the genetic components of three subcategories of autism spectrum disorder.
Jinchen Li, Shanshan Hu, Kun Zhang, Leisheng Shi, Yi Zhang, Tingting Zhao, Lin Wang, Xin He, Kun Xia, Chunyu Liu,[...]. Mol Psychiatry 2019
17