A citation-based method for searching scientific literature

S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban, E Antoniou, E Kelleher, C O'Brien, G Donohoe, M Gill, D W Morris, W R McCombie, A Corvin. Mol Psychiatry 2014
Times Cited: 229



Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson, Joshua D Smith, Bryan Paeper, Deborah A Nickerson, Jeanselle Dea, Shan Dong, Luis E Gonzalez, Jeffrey D Mandell, Shrikant M Mane, Michael T Murtha, Catherine A Sullivan, Michael F Walker, Zainulabedin Waqar, Liping Wei, A Jeremy Willsey, Boris Yamrom, Yoon-ha Lee, Ewa Grabowska, Ertugrul Dalkic, Zihua Wang, Steven Marks, Peter Andrews, Anthony Leotta, Jude Kendall, Inessa Hakker, Julie Rosenbaum, Beicong Ma, Linda Rodgers, Jennifer Troge, Giuseppe Narzisi, Seungtai Yoon, Michael C Schatz, Kenny Ye, W Richard McCombie, Jay Shendure, Evan E Eichler, Matthew W State, Michael Wigler. Nature 2014
Times Cited: 1193




List of shared articles



Times cited

Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome.
Joost Kummeling, Diante E Stremmelaar, Nicholas Raun, Margot R F Reijnders, Marjolein H Willemsen, Martina Ruiterkamp-Versteeg, Marga Schepens, Calvin C O Man, Christian Gilissen, Megan T Cho,[...]. Mol Psychiatry 2021
5

Genetic association of FMRP targets with psychiatric disorders.
Nicholas E Clifton, Elliott Rees, Peter A Holmans, Antonio F Pardiñas, Janet C Harwood, Arianna Di Florio, George Kirov, James T R Walters, Michael C O'Donovan, Michael J Owen,[...]. Mol Psychiatry 2021
1

Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.
Jennifer K Forsyth, Daniel Nachun, Michael J Gandal, Daniel H Geschwind, Ariana E Anderson, Giovanni Coppola, Carrie E Bearden. Biol Psychiatry 2020
14

Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.
Guihu Zhao, Kuokuo Li, Bin Li, Zheng Wang, Zhenghuan Fang, Xiaomeng Wang, Yi Zhang, Tengfei Luo, Qiao Zhou, Lin Wang,[...]. Nucleic Acids Res 2020
17

Multiple rare inherited variants in a four generation schizophrenia family offer leads for complex mode of disease inheritance.
Jibin John, Upasana Bhattacharyya, Navneesh Yadav, Prachi Kukshal, Triptish Bhatia, V L Nimgaonkar, Smita N Deshpande, B K Thelma. Schizophr Res 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
36

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families.
Andreas J Forstner, Sascha B Fischer, Lorena M Schenk, Jana Strohmaier, Anna Maaser-Hecker, Céline S Reinbold, Sugirthan Sivalingam, Julian Hecker, Fabian Streit, Franziska Degenhardt,[...]. Transl Psychiatry 2020
5

Machine learning analysis of exome trios to contrast the genomic architecture of autism and schizophrenia.
Sameer Sardaar, Bill Qi, Alexandre Dionne-Laporte, Guy A Rouleau, Reihaneh Rabbany, Yannis J Trakadis. BMC Psychiatry 2020
1

A Caenorhabditis elegans Model for Integrating the Functions of Neuropsychiatric Risk Genes Identifies Components Required for Normal Dendritic Morphology.
Cristina Aguirre-Chen, Natalia Stec, Olivia Mendivil Ramos, Nuri Kim, Melissa Kramer, Shane McCarthy, Jesse Gillis, W Richard McCombie, Christopher M Hammell. G3 (Bethesda) 2020
5

Emerging role of NIK/IKK2-binding protein (NIBP)/trafficking protein particle complex 9 (TRAPPC9) in nervous system diseases.
Brittany Bodnar, Arianna DeGruttola, Yuanjun Zhu, Yuan Lin, Yonggang Zhang, Xianming Mo, Wenhui Hu. Transl Res 2020
5


Genes regulated by BCL11B during T-cell development are enriched for de novo mutations found in schizophrenia patients.
Laura Fahey, Gary Donohoe, Pilib Ó Broin, Derek W Morris. Am J Med Genet B Neuropsychiatr Genet 2020
0

Postzygotic Somatic Mutations in the Human Brain Expand the Threshold-Liability Model of Schizophrenia.
Shiva M Singh, Christina A Castellani, Kathleen A Hill. Front Psychiatry 2020
1

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2.
Vikas Pejaver, Jorge Urresti, Jose Lugo-Martinez, Kymberleigh A Pagel, Guan Ning Lin, Hyun-Jun Nam, Matthew Mort, David N Cooper, Jonathan Sebat, Lilia M Iakoucheva,[...]. Nat Commun 2020
32

Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder.
Hidekazu Kato, Itaru Kushima, Daisuke Mori, Akira Yoshimi, Branko Aleksic, Yoshihiro Nawa, Miho Toyama, Sho Furuta, Yanjie Yu, Kanako Ishizuka,[...]. Transl Psychiatry 2020
1

Assessment of de novo copy-number variations in Italian patients with schizophrenia: Detection of putative mutations involving regulatory enhancer elements.
Giulio Piluso, Palmiero Monteleone, Silvana Galderisi, Teresa Giugliano, Alessandro Bertolino, Paola Rocca, Alessandro Rossi, Armida Mucci, Eugenio Aguglia, Ileana Andriola,[...]. World J Biol Psychiatry 2019
7

The ubiquitin proteasome pathway in neuropsychiatric disorders.
Solmi Cheon, Milan Dean, Maria Chahrour. Neurobiol Learn Mem 2019
12

A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.
Else Eising, Amaia Carrion-Castillo, Arianna Vino, Edythe A Strand, Kathy J Jakielski, Thomas S Scerri, Michael S Hildebrand, Richard Webster, Alan Ma, Bernard Mazoyer,[...]. Mol Psychiatry 2019
48

Regulatory genes and pathways disrupted in autism spectrum disorders.
Fatma Ayhan, Genevieve Konopka. Prog Neuropsychopharmacol Biol Psychiatry 2019
10

Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of CHD8 Haploinsufficiency.
A Ayanna Wade, Kenneth Lim, Rinaldo Catta-Preta, Alex S Nord. Front Mol Neurosci 2019
13


Essential genetic findings in neurodevelopmental disorders.
Ana R Cardoso, Mónica Lopes-Marques, Raquel M Silva, Catarina Serrano, António Amorim, Maria J Prata, Luísa Azevedo. Hum Genomics 2019
12

Paternal-age-related de novo mutations and risk for five disorders.
Jacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, Emilie M Wigdor, Henrike O Heyne, Dennis Lal, Daniel P Howrigan, Alex Bloemendal, Janne T Larsen, Jack A Kosmicki,[...]. Nat Commun 2019
23

Genetic Causes and Modifiers of Autism Spectrum Disorder.
Lauren Rylaarsdam, Alicia Guemez-Gamboa. Front Cell Neurosci 2019
54

Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms.
Rebecca L Walker, Gokul Ramaswami, Christopher Hartl, Nicholas Mancuso, Michael J Gandal, Luis de la Torre-Ubieta, Bogdan Pasaniuc, Jason L Stein, Daniel H Geschwind. Cell 2019
44

Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders.
Julie Chow, Matthew Jensen, Hajar Amini, Farhad Hormozdiari, Osnat Penn, Sagiv Shifman, Santhosh Girirajan, Fereydoun Hormozdiari. Genome Med 2019
7


Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.
Zi-Bing Jin, Zhongshan Li, Zhenwei Liu, Yi Jiang, Xue-Bi Cai, Jinyu Wu. Biol Rev Camb Philos Soc 2018
17

A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency.
Sandra Jansen, Alexander Hoischen, Bradley P Coe, Gemma L Carvill, Hilde Van Esch, Daniëlle G M Bosch, Ulla A Andersen, Carl Baker, Marijke Bauters, Raphael A Bernier,[...]. Eur J Hum Genet 2018
15



Damaging de novo mutations diminish motor skills in children on the autism spectrum.
Andreas Buja, Natalia Volfovsky, Abba M Krieger, Catherine Lord, Alex E Lash, Michael Wigler, Ivan Iossifov. Proc Natl Acad Sci U S A 2018
28

Advanced Whole-Genome Sequencing and Analysis of Fetal Genomes from Amniotic Fluid.
Qing Mao, Robert Chin, Weiwei Xie, Yuqing Deng, Wenwei Zhang, Huixin Xu, Rebecca Yu Zhang, Quan Shi, Erin E Peters, Natali Gulbahce,[...]. Clin Chem 2018
4

Identification of somatic mutations in monozygotic twins discordant for psychiatric disorders.
Masaki Nishioka, Miki Bundo, Junko Ueda, Akane Yoshikawa, Fumichika Nishimura, Tsukasa Sasaki, Chihiro Kakiuchi, Kiyoto Kasai, Tadafumi Kato, Kazuya Iwamoto. NPJ Schizophr 2018
7