A citation-based method for searching scientific literature

Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith, Emily H Turner, Ian B Stanaway, Benjamin Vernot, Maika Malig, Carl Baker, Beau Reilly, Joshua M Akey, Elhanan Borenstein, Mark J Rieder, Deborah A Nickerson, Raphael Bernier, Jay Shendure, Evan E Eichler. Nature 2012
Times Cited: 1365



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: 382




List of shared articles



Times cited

Exons as units of phenotypic impact for truncating mutations in autism.
Andrew H Chiang, Jonathan Chang, Jiayao Wang, Dennis Vitkup. Mol Psychiatry 2021
2

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

Chromatin Remodeler CHD8 in Autism and Brain Development.
Anke Hoffmann, Dietmar Spengler. J Clin Med 2021
2

Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Helen Rankin Willsey, Cameron R T Exner, Yuxiao Xu, Amanda Everitt, Nawei Sun, Belinda Wang, Jeanselle Dea, Galina Schmunk, Yefim Zaltsman, Nia Teerikorpi,[...]. Neuron 2021
1

Single-Cell Transcriptomics Supports a Role of CHD8 in Autism.
Anke Hoffmann, Dietmar Spengler. Int J Mol Sci 2021
0

The autism-associated protein CHD8 is required for cerebellar development and motor function.
Atsuki Kawamura, Yuta Katayama, Wataru Kakegawa, Daisuke Ino, Masaaki Nishiyama, Michisuke Yuzaki, Keiichi I Nakayama. Cell Rep 2021
0

Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders.
E El Khouri, J Ghoumid, D Haye, F Giuliano, L Drevillon, A Briand-Suleau, P De La Grange, V Nau, T Gaillon, T Bienvenu,[...]. Mol Psychiatry 2021
0

Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.
Veronica B Searles Quick, Belinda Wang, Matthew W State. Neuropsychopharmacology 2021
7

The autism-related protein CHD8 contributes to the stemness and differentiation of mouse hematopoietic stem cells.
Akihiro Nita, Yoshiharu Muto, Yuta Katayama, Akinobu Matsumoto, Masaaki Nishiyama, Keiichi I Nakayama. Cell Rep 2021
1

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
0

Rare and de novo coding variants in chromodomain genes in Chiari I malformation.
Brooke Sadler, Jackson Wilborn, Lilian Antunes, Timothy Kuensting, Andrew T Hale, Stephen R Gannon, Kevin McCall, Carlos Cruchaga, Matthew Harms, Norine Voisin,[...]. Am J Hum Genet 2021
0

Excitatory neuronal CHD8 in the regulation of neocortical development and sensory-motor behaviors.
Hanseul Kweon, Won Beom Jung, Geun Ho Im, Jia Ryoo, Joon-Hyuk Lee, Hogyeong Do, Yeonsoo Choi, You-Hyang Song, Hwajin Jung, Haram Park,[...]. Cell Rep 2021
0

Distinct, dosage-sensitive requirements for the autism-associated factor CHD8 during cortical development.
Shaun Hurley, Conor Mohan, Philipp Suetterlin, Robert Ellingford, Kimberley L H Riegman, Jacob Ellegood, Angela Caruso, Caterina Michetti, Olivier Brock, Romy Evans,[...]. Mol Autism 2021
0

Overexpression of CD47 is associated with brain overgrowth and 16p11.2 deletion syndrome.
Jingling Li, Thomas Brickler, Allison Banuelos, Kristopher Marjon, Anna Shcherbina, Sravani Banerjee, Jing Bian, Cyndhavi Narayanan, Irving L Weissman, Sundari Chetty. Proc Natl Acad Sci U S A 2021
1

Chromatin remodelling complexes in cerebral cortex development and neurodevelopmental disorders.
Leora D'Souza, Asha S Channakkar, Bhavana Muralidharan. Neurochem Int 2021
0

Characterizing vulnerable brain areas and circuits in mouse models of autism: Towards understanding pathogenesis and new therapeutic approaches.
Kelvin Hui, Yuta Katayama, Keiichi I Nakayama, Jun Nomura, Takeshi Sakurai. Neurosci Biobehav Rev 2020
6

Systematic phenomics analysis of autism-associated genes reveals parallel networks underlying reversible impairments in habituation.
Troy A McDiarmid, Manuel Belmadani, Joseph Liang, Fabian Meili, Eleanor A Mathews, Gregory P Mullen, Ardalan Hendi, Wan-Rong Wong, James B Rand, Kota Mizumoto,[...]. Proc Natl Acad Sci U S A 2020
11

Oligodendrocyte dysfunction due to Chd8 mutation gives rise to behavioral deficits in mice.
Atsuki Kawamura, Yuta Katayama, Masaaki Nishiyama, Hirotaka Shoji, Kota Tokuoka, Yoshifumi Ueta, Mariko Miyata, Tadashi Isa, Tsuyoshi Miyakawa, Akiko Hayashi-Takagi,[...]. Hum Mol Genet 2020
9