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



Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta, Jude Kendall, Ewa Grabowska, Beicong Ma, Steven Marks, Linda Rodgers, Asya Stepansky, Jennifer Troge, Peter Andrews, Mitchell Bekritsky, Kith Pradhan, Elena Ghiban, Melissa Kramer, Jennifer Parla, Ryan Demeter, Lucinda L Fulton, Robert S Fulton, Vincent J Magrini, Kenny Ye, Jennifer C Darnell, Robert B Darnell, Elaine R Mardis, Richard K Wilson, Michael C Schatz, W Richard McCombie, Michael Wigler. Neuron 2012
Times Cited: 899




List of shared articles



Times cited

Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms.
Devanand S Manoli, Matthew W State. Am J Psychiatry 2021
4

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

Cell Type-Specific Predictive Models Perform Prioritization of Genes and Gene Sets Associated With Autism.
Jinting Guan, Yang Wang, Yiping Lin, Qingyang Yin, Yibo Zhuang, Guoli Ji. Front Genet 2021
1

De novo variants in neurodevelopmental disorders-experiences from a tertiary care center.
Theresa Brunet, Robert Jech, Melanie Brugger, Reka Kovacs, Bader Alhaddad, Gloria Leszinski, Korbinian M Riedhammer, Dominik S Westphal, Isabella Mahle, Katharina Mayerhanser,[...]. Clin Genet 2021
1

A white paper on a neurodevelopmental framework for drug discovery in autism and other neurodevelopmental disorders.
C M Díaz-Caneja, M W State, R J Hagerman, S Jacquemont, O Marín, C Bagni, D Umbricht, E Simonoff, F de Andrés-Trelles, A Kaale,[...]. Eur Neuropsychopharmacol 2021
2

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

Targeted sequencing and integrative analysis of 3,195 Chinese patients with neurodevelopmental disorders prioritized 26 novel candidate genes.
Tao Wang, Yi Zhang, Liqui Liu, Yan Wang, Huiqian Chen, Tianda Fan, Jinchen Li, Kun Xia, Zhongsheng Sun. J Genet Genomics 2021
0

Alternative splicing and gene co-expression network-based analysis of dizygotic twins with autism-spectrum disorder and their parents.
Kaan Okay, Pelin Ünal Varış, Süha Miral, Burcu Ekinci, Tutku Yaraş, Gökhan Karakülah, Yavuz Oktay. Genomics 2021
0

The Monash Autism-ADHD genetics and neurodevelopment (MAGNET) project design and methodologies: a dimensional approach to understanding neurobiological and genetic aetiology.
Rachael Knott, Beth P Johnson, Jeggan Tiego, Olivia Mellahn, Amy Finlay, Kathryn Kallady, Maria Kouspos, Vishnu Priya Mohanakumar Sindhu, Ziarih Hawi, Aurina Arnatkeviciute,[...]. Mol Autism 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

A method to delineate de novo missense variants across pathways prioritizes genes linked to autism.
Amanda Koire, Panagiotis Katsonis, Young Won Kim, Christie Buchovecky, Stephen J Wilson, Olivier Lichtarge. Sci Transl Med 2021
0

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

Abnormal neocortex arealization and Sotos-like syndrome-associated behavior in Setd2 mutant mice.
Lichao Xu, Yue Zheng, Xuejing Li, Andi Wang, Dawei Huo, Qinglan Li, Shikang Wang, Zhiyuan Luo, Ying Liu, Fuqiang Xu,[...]. Sci Adv 2021
0


A Whole-Exome Sequencing Study of Tourette Disorder in a Chinese Population.
Xin Zhao, Sheng Wang, Juanjuan Hao, Pengcheng Zhu, Xin Zhang, Min Wu. DNA Cell Biol 2020
4

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.
Daniel P Howrigan, Samuel A Rose, Kaitlin E Samocha, Menachem Fromer, Felecia Cerrato, Wei J Chen, Claire Churchhouse, Kimberly Chambert, Sharon D Chandler, Mark J Daly,[...]. Nat Neurosci 2020
31

Paternal age is affected by genetic abnormalities, perinatal complications and mental health of the offspring.
Dominika Janeczko, Magdalena Hołowczuk, Anna Orzeł, Barbara Klatka, Andrzej Semczuk. Biomed Rep 2020
5

Genetic evidence of gender difference in autism spectrum disorder supports the female-protective effect.
Yi Zhang, Na Li, Chao Li, Ze Zhang, Huajing Teng, Yan Wang, Tingting Zhao, Leisheng Shi, Kun Zhang, Kun Xia,[...]. Transl Psychiatry 2020
13

Gene Expression in Patient-Derived Neural Progenitors Implicates WNT5A Signaling in the Etiology of Schizophrenia.
Oleg V Evgrafov, Chris Armoskus, Bozena B Wrobel, Valeria N Spitsyna, Tade Souaiaia, Jennifer S Herstein, Christopher P Walker, Joseph D Nguyen, Adrian Camarena, Jonathan R Weitz,[...]. Biol Psychiatry 2020
4

Are Steroid Hormones Dysregulated in Autistic Girls?
Benedikt Andreas Gasser, Johann Kurz, Bernhard Dick, Markus Georg Mohaupt. Diseases 2020
3