A citation-based method for searching scientific literature

Anke Hoffmann, Michael Ziller, Dietmar Spengler. Cells 2020
Times Cited: 7







List of co-cited articles
40 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
42

Progress in iPSC-Based Modeling of Psychiatric Disorders.
Anke Hoffmann, Michael Ziller, Dietmar Spengler. Int J Mol Sci 2019
17
42



New considerations for hiPSC-based models of neuropsychiatric disorders.
Gabriel E Hoffman, Nadine Schrode, Erin Flaherty, Kristen J Brennand. Mol Psychiatry 2019
35
28

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
506
28

The CHD8 overgrowth syndrome: A detailed evaluation of an emerging overgrowth phenotype in 27 patients.
Philip J Ostrowski, Anna Zachariou, Chey Loveday, Ana Beleza-Meireles, Marta Bertoli, John Dean, Andrew G L Douglas, Ian Ellis, Alison Foster, John M Graham,[...]. Am J Med Genet C Semin Med Genet 2019
10
28

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
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,[...]. Nature 2012
28

Chromatin remodelers: We are the drivers!!
Monica Tyagi, Nasir Imam, Kirtika Verma, Ashok K Patel. Nucleus 2016
44
28

De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth.
Yu An, Linna Zhang, Wenwen Liu, Yunyun Jiang, Xue Chen, Xiaoping Lan, Gan Li, Qiang Hang, Jian Wang, James F Gusella,[...]. Hum Genet 2020
8
28

Early nutrition influences developmental myelination and cognition in infants and young children.
Sean Deoni, Douglas Dean, Sarah Joelson, Jonathan O'Regan, Nora Schneider. Neuroimage 2018
35
28

Disruptive CHD8 mutations define a subtype of autism early in development.
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,[...]. Cell 2014
382
28

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.
Holly A F Stessman, Bo Xiong, Bradley P Coe, Tianyun Wang, Kendra Hoekzema, Michaela Fenckova, Malin Kvarnung, Jennifer Gerdts, Sandy Trinh, Nele Cosemans,[...]. Nat Genet 2017
219
28

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
28

Structure and mechanism of helicases and nucleic acid translocases.
Martin R Singleton, Mark S Dillingham, Dale B Wigley. Annu Rev Biochem 2007
804
28

The contribution of de novo coding mutations to autism spectrum disorder.
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,[...]. Nature 2014
28

Genetic variation in the epigenetic machinery and mental health.
Chris Murgatroyd, Dietmar Spengler. Curr Psychiatry Rep 2012
26
28

A de novo convergence of autism genetics and molecular neuroscience.
Niklas Krumm, Brian J O'Roak, Jay Shendure, Evan E Eichler. Trends Neurosci 2014
272
28

Oligodendrocyte precursor survival and differentiation requires chromatin remodeling by Chd7 and Chd8.
Corentine Marie, Adrien Clavairoly, Magali Frah, Hatem Hmidan, Jun Yan, Chuntao Zhao, Juliette Van Steenwinckel, Romain Daveau, Bernard Zalc, Bassem Hassan,[...]. Proc Natl Acad Sci U S A 2018
42
28

De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012
899
28

The clinical presentation caused by truncating CHD8 variants.
Sofia Douzgou, Hui Wen Liang, Kay Metcalfe, Suresh Somarathi, Marc Tischkowitz, Wafik Mohamed, Usha Kini, Shane McKee, Laura Yates, Marta Bertoli,[...]. Clin Genet 2019
15
28


Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.
Huidan Wu, Honghui Li, Ting Bai, Lin Han, Jianjun Ou, Guanglei Xun, Yu Zhang, Yazhe Wang, Guiqin Duan, Ningxia Zhao,[...]. Clin Genet 2020
9
28


A proton spectroscopy study of white matter in children with autism.
Antonio Y Hardan, Lawrence K Fung, Thomas Frazier, Sean W Berquist, Nancy J Minshew, Matcheri S Keshavan, Jeffrey A Stanley. Prog Neuropsychopharmacol Biol Psychiatry 2016
14
28

A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8.
Heba Yasin, William T Gibson, Sylvie Langlois, Robert M Stowe, Erica S Tsang, Leora Lee, Jenny Poon, Grant Tran, Christine Tyson, Chi Kin Wong,[...]. J Hum Genet 2019
15
28

Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits.
Randall J Platt, Yang Zhou, Ian M Slaymaker, Ashwin S Shetty, Niels R Weisbach, Jin-Ah Kim, Jitendra Sharma, Mitul Desai, Sabina Sood, Hannah R Kempton,[...]. Cell Rep 2017
86
28

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.
Michael E Talkowski, Jill A Rosenfeld, Ian Blumenthal, Vamsee Pillalamarri, Colby Chiang, Adrian Heilbut, Carl Ernst, Carrie Hanscom, Elizabeth Rossin, Amelia M Lindgren,[...]. Cell 2012
375
28

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
28

De novo genic mutations among a Chinese autism spectrum disorder cohort.
Tianyun Wang, Hui Guo, Bo Xiong, Holly A F Stessman, Huidan Wu, Bradley P Coe, Tychele N Turner, Yanling Liu, Wenjing Zhao, Kendra Hoekzema,[...]. Nat Commun 2016
147
28

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
28

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
12
28

Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology.
Rebecca A Barnard, Matthew B Pomaville, Brian J O'Roak. Front Neurosci 2015
40
28

Gene hunting in autism spectrum disorder: on the path to precision medicine.
Daniel H Geschwind, Matthew W State. Lancet Neurol 2015
240
28

Recurrent de novo mutations implicate novel genes underlying simplex autism risk.
B J O'Roak, H A Stessman, E A Boyle, K T Witherspoon, B Martin, C Lee, L Vives, C Baker, J B Hiatt, D A Nickerson,[...]. Nat Commun 2014
182
28

Sexually dimorphic behavior, neuronal activity, and gene expression in Chd8-mutant mice.
Hwajin Jung, Haram Park, Yeonsoo Choi, Hyojin Kang, Eunee Lee, Hanseul Kweon, Junyeop Daniel Roh, Jacob Ellegood, Woochul Choi, Jaeseung Kang,[...]. Nat Neurosci 2018
55
28

Dual Requirement of CHD8 for Chromatin Landscape Establishment and Histone Methyltransferase Recruitment to Promote CNS Myelination and Repair.
Chuntao Zhao, Chen Dong, Magali Frah, Yaqi Deng, Corentine Marie, Feng Zhang, Lingli Xu, Zhixing Ma, Xinran Dong, Yifeng Lin,[...]. Dev Cell 2018
45
28

Transcription regulation by CHD proteins to control plant development.
Yongfeng Hu, Yan Lai, Deyan Zhu. Front Plant Sci 2014
13
28

In vivo Perturb-Seq reveals neuronal and glial abnormalities associated with autism risk genes.
Xin Jin, Sean K Simmons, Amy Guo, Ashwin S Shetty, Michelle Ko, Lan Nguyen, Vahbiz Jokhi, Elise Robinson, Paul Oyler, Nathan Curry,[...]. Science 2020
15
28

The biology of chromatin remodeling complexes.
Cedric R Clapier, Bradley R Cairns. Annu Rev Biochem 2009
28


Chondrogenic Differentiation from Induced Pluripotent Stem Cells Using Non-Viral Minicircle Vectors.
Yeri Alice Rim, Yoojun Nam, Narae Park, Hyerin Jung, Kijun Lee, Jennifer Lee, Ji Hyeon Ju. Cells 2020
9
14

Pipeline for the Generation and Characterization of Transgenic Human Pluripotent Stem Cells Using the CRISPR/Cas9 Technology.
Joffrey Mianné, Chloé Bourguignon, Chloé Nguyen Van, Mathieu Fieldès, Amel Nasri, Said Assou, John De Vos. Cells 2020
2
50

Pre-clinical study of induced pluripotent stem cell-derived dopaminergic progenitor cells for Parkinson's disease.
Daisuke Doi, Hiroaki Magotani, Tetsuhiro Kikuchi, Megumi Ikeda, Satoe Hiramatsu, Kenji Yoshida, Naoki Amano, Masaki Nomura, Masafumi Umekage, Asuka Morizane,[...]. Nat Commun 2020
48
14


Stem Cell Secretome and Its Effect on Cellular Mechanisms Relevant to Wound Healing.
Se-Ra Park, Jae-Wan Kim, Hee-Sook Jun, Joo Young Roh, Hwa-Yong Lee, In-Sun Hong. Mol Ther 2018
58
14

Human Organoids: Tools for Understanding Biology and Treating Diseases.
Frans Schutgens, Hans Clevers. Annu Rev Pathol 2020
72
14



Mesenchymal Stem Cell Immunomodulation: Mechanisms and Therapeutic Potential.
Na Song, Martijn Scholtemeijer, Khalid Shah. Trends Pharmacol Sci 2020
32
14


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.