A citation-based method for searching scientific literature

Gerald D Fischbach, Catherine Lord. Neuron 2010
Times Cited: 358



Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov, Paz Polak, Seungtai Yoon, Jared Maguire, Emily L Crawford, Nicholas G Campbell, Evan T Geller, Otto Valladares, Chad Schafer, Han Liu, Tuo Zhao, Guiqing Cai, Jayon Lihm, Ruth Dannenfelser, Omar Jabado, Zuleyma Peralta, Uma Nagaswamy, Donna Muzny, Jeffrey G Reid, Irene Newsham, Yuanqing Wu, Lora Lewis, Yi Han, Benjamin F Voight, Elaine Lim, Elizabeth Rossin, Andrew Kirby, Jason Flannick, Menachem Fromer, Khalid Shakir, Tim Fennell, Kiran Garimella, Eric Banks, Ryan Poplin, Stacey Gabriel, Mark DePristo, Jack R Wimbish, Braden E Boone, Shawn E Levy, Catalina Betancur, Shamil Sunyaev, Eric Boerwinkle, Joseph D Buxbaum, Edwin H Cook, Bernie Devlin, Richard A Gibbs, Kathryn Roeder, Gerard D Schellenberg, James S Sutcliffe, Mark J Daly. Nature 2012
Times Cited: 1138




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

Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms.
Devanand S Manoli, Matthew W State. Am J Psychiatry 2021
7

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

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

Prioritizing de novo autism risk variants with calibrated gene- and variant-scoring models.
Yuxiang Jiang, Jorge Urresti, Kymberleigh A Pagel, Akula Bala Pramod, Lilia M Iakoucheva, Predrag Radivojac. Hum Genet 2021
0

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

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
19

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

Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
Lin Wang, Yi Zhang, Kuokuo Li, Zheng Wang, Xiaomeng Wang, Bin Li, Guihu Zhao, Zhenghuan Fang, Zhengbao Ling, Tengfei Luo,[...]. Mol Autism 2020
2

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

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

Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation.
Daniel Duran, Xue Zeng, Sheng Chih Jin, Jungmin Choi, Carol Nelson-Williams, Bogdan Yatsula, Jonathan Gaillard, Charuta Gavankar Furey, Qiongshi Lu, Andrew T Timberlake,[...]. Neuron 2019
23