A citation-based method for searching scientific literature

Bipan K Deb, Helen S Bateup. Front Mol Neurosci 2022
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Aging and neurodegeneration are associated with increased mutations in single human neurons.
Michael A Lodato, Rachel E Rodin, Craig L Bohrson, Michael E Coulter, Alison R Barton, Minseok Kwon, Maxwell A Sherman, Carl M Vitzthum, Lovelace J Luquette, Chandri N Yandava,[...]. Science 2018
245
50

Epilepsy in patients with brain tumours: epidemiology, mechanisms, and management.
Melanie S M van Breemen, Erik B Wilms, Charles J Vecht. Lancet Neurol 2007
510
50

Somatic TARDBP variants as a cause of semantic dementia.
Jeroen van Rooij, Merel O Mol, Shamiram Melhem, Pelle van der Wal, Pascal Arp, Francesca Paron, Laura Donker Kaat, Harro Seelaar, Suzanne S M Miedema, Takuya Oshima,[...]. Brain 2020
6
50

Somatic retrotransposition alters the genetic landscape of the human brain.
J Kenneth Baillie, Mark W Barnett, Kyle R Upton, Daniel J Gerhardt, Todd A Richmond, Fioravante De Sapio, Paul M Brennan, Patrizia Rizzu, Sarah Smith, Mark Fell,[...]. Nature 2011
457
50

Cerebrospinal fluid liquid biopsy for detecting somatic mosaicism in brain.
Zimeng Ye, Zac Chatterton, Jahnvi Pflueger, John A Damiano, Lara McQuillan, Anthony Simon Harvey, Stephen Malone, Hongdo Do, Wirginia Maixner, Amy Schneider,[...]. Brain Commun 2021
23
50

Neural stem cells: historical perspective and future prospects.
Joshua J Breunig, Tarik F Haydar, Pasko Rakic. Neuron 2011
104
50

Dissecting the genetic basis of focal cortical dysplasia: a large cohort study.
Sara Baldassari, Théo Ribierre, Elise Marsan, Homa Adle-Biassette, Sarah Ferrand-Sorbets, Christine Bulteau, Nathalie Dorison, Martine Fohlen, Marc Polivka, Sarah Weckhuysen,[...]. Acta Neuropathol 2019
97
50

Second-hit mosaic mutation in mTORC1 repressor DEPDC5 causes focal cortical dysplasia-associated epilepsy.
Théo Ribierre, Charlotte Deleuze, Alexandre Bacq, Sara Baldassari, Elise Marsan, Mathilde Chipaux, Giuseppe Muraca, Delphine Roussel, Vincent Navarro, Eric Leguern,[...]. J Clin Invest 2018
99
50

Somatic mutations in the human brain: implications for psychiatric research.
Masaki Nishioka, Miki Bundo, Kazuya Iwamoto, Tadafumi Kato. Mol Psychiatry 2019
20
50

Somatic activation of AKT3 causes hemispheric developmental brain malformations.
Annapurna Poduri, Gilad D Evrony, Xuyu Cai, Princess Christina Elhosary, Rameen Beroukhim, Maria K Lehtinen, L Benjamin Hills, Erin L Heinzen, Anthony Hill, R Sean Hill,[...]. Neuron 2012
304
50

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Conceição Bettencourt, Davina Hensman-Moss, Michael Flower, Sarah Wiethoff, Alexis Brice, Cyril Goizet, Giovanni Stevanin, Georgios Koutsis, Georgia Karadima, Marios Panas,[...]. Ann Neurol 2016
129
50

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs.
S Hong Lee, Teresa R DeCandia, Stephan Ripke, Jian Yang, Patrick F Sullivan, Michael E Goddard, Matthew C Keller, Peter M Visscher, Naomi R Wray. Nat Genet 2012
401
50

Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.
Alissa M D'Gama, Sirisha Pochareddy, Mingfeng Li, Saumya S Jamuar, Rachel E Reiff, Anh-Thu N Lam, Nenad Sestan, Christopher A Walsh. Neuron 2015
92
50

Stem cell divisions, somatic mutations, cancer etiology, and cancer prevention.
Cristian Tomasetti, Lu Li, Bert Vogelstein. Science 2017
468
50



Modeling genetic epileptic encephalopathies using brain organoids.
Daniel J Steinberg, Srinivasarao Repudi, Afifa Saleem, Irina Kustanovich, Sergey Viukov, Baraa Abudiab, Ehud Banne, Muhammad Mahajnah, Jacob H Hanna, Shani Stern,[...]. EMBO Mol Med 2021
6
50

Improving and accelerating drug development for nervous system disorders.
Diana E Pankevich, Bruce M Altevogt, John Dunlop, Fred H Gage, Steve E Hyman. Neuron 2014
115
50

Somatic mutations in neurodegeneration: An update.
Christos Proukakis. Neurobiol Dis 2020
11
50


Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia.
Jae Seok Lim, Ramu Gopalappa, Se Hoon Kim, Suresh Ramakrishna, Minji Lee, Woo-Il Kim, Junho Kim, Sang Min Park, Junehawk Lee, Jung-Hwa Oh,[...]. Am J Hum Genet 2017
100
50

Neural stem cells and the origin of gliomas.
Nader Sanai, Arturo Alvarez-Buylla, Mitchel S Berger. N Engl J Med 2005
721
50

The atlas of RNase H antisense oligonucleotide distribution and activity in the CNS of rodents and non-human primates following central administration.
Paymaan Jafar-Nejad, Berit Powers, Armand Soriano, Hien Zhao, Daniel A Norris, John Matson, Beatrice DeBrosse-Serra, Jamie Watson, Padmakumar Narayanan, Seung J Chun,[...]. Nucleic Acids Res 2021
16
50

The mutational landscape of human somatic and germline cells.
Luiza Moore, Alex Cagan, Tim H H Coorens, Matthew D C Neville, Rashesh Sanghvi, Mathijs A Sanders, Thomas R W Oliver, Daniel Leongamornlert, Peter Ellis, Ayesha Noorani,[...]. Nature 2021
37
50

Convulsive seizures from experimental focal cortical dysplasia occur independently of cell misplacement.
Lawrence S Hsieh, John H Wen, Kumiko Claycomb, Yuegao Huang, Felicia A Harrsch, Janice R Naegele, Fahmeed Hyder, Gordon F Buchanan, Angelique Bordey. Nat Commun 2016
49
50

Brain Somatic Mutations in MTOR Disrupt Neuronal Ciliogenesis, Leading to Focal Cortical Dyslamination.
Sang Min Park, Jae Seok Lim, Suresh Ramakrishina, Se Hoon Kim, Woo Kyeong Kim, Junehawk Lee, Hoon-Chul Kang, Jeremy F Reiter, Dong Seok Kim, Hyongbum Henry Kim,[...]. Neuron 2018
54
50

Analysis of LINE-1 Elements in DNA from Postmortem Brains of Individuals with Schizophrenia.
Glenn A Doyle, Richard C Crist, Emre T Karatas, Matthew J Hammond, Adam D Ewing, Thomas N Ferraro, Chang-Gyu Hahn, Wade H Berrettini. Neuropsychopharmacology 2017
39
50

Assessment of the genetic variance of late-onset Alzheimer's disease.
Perry G Ridge, Kaitlyn B Hoyt, Kevin Boehme, Shubhabrata Mukherjee, Paul K Crane, Jonathan L Haines, Richard Mayeux, Lindsay A Farrer, Margaret A Pericak-Vance, Gerard D Schellenberg,[...]. Neurobiol Aging 2016
122
50


Assessment of somatic single-nucleotide variation in brain tissue of cases with schizophrenia.
John F Fullard, Alexander W Charney, Georgios Voloudakis, Andrew V Uzilov, Vahram Haroutunian, Panos Roussos. Transl Psychiatry 2019
10
50

Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder.
Deidre R Krupp, Rebecca A Barnard, Yannis Duffourd, Sara A Evans, Ryan M Mulqueen, Raphael Bernier, Jean-Baptiste Rivière, Eric Fombonne, Brian J O'Roak. Am J Hum Genet 2017
90
50

Brain pharmacology of intrathecal antisense oligonucleotides revealed through multimodal imaging.
Curt Mazur, Berit Powers, Kenneth Zasadny, Jenna M Sullivan, Hemi Dimant, Fredrik Kamme, Jacob Hesterman, John Matson, Michael Oestergaard, Marc Seaman,[...]. JCI Insight 2019
27
50

The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Rachel E Rodin, Yanmei Dou, Minseok Kwon, Maxwell A Sherman, Alissa M D'Gama, Ryan N Doan, Lariza M Rento, Kelly M Girskis, Craig L Bohrson, Sonia N Kim,[...]. Nat Neurosci 2021
27
50

m-TOR inhibitors and risk of Pneumocystis pneumonia after solid organ transplantation: a systematic review and meta-analysis.
Maryam Ghadimi, Zinat Mohammadpour, Simin Dashti-Khavidaki, Alireza Milajerdi. Eur J Clin Pharmacol 2019
11
50

Antisense oligonucleotides increase Scn1a expression and reduce seizures and SUDEP incidence in a mouse model of Dravet syndrome.
Zhou Han, Chunling Chen, Anne Christiansen, Sophina Ji, Qian Lin, Charles Anumonwo, Chante Liu, Steven C Leiser, Meena, Isabel Aznarez,[...]. Sci Transl Med 2020
80
50

Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease.
Gaël Nicolas, Rocío Acuña-Hidalgo, Michael J Keogh, Olivier Quenez, Marloes Steehouwer, Stefan Lelieveld, Stéphane Rousseau, Anne-Claire Richard, Manon S Oud, Florent Marguet,[...]. Alzheimers Dement 2018
31
50

Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE).
Thomas Bonduelle, Till Hartlieb, Sara Baldassari, Nam Suk Sim, Se Hoon Kim, Hoon-Chul Kang, Katja Kobow, Roland Coras, Mathilde Chipaux, Georg Dorfmüller,[...]. Acta Neuropathol Commun 2021
26
50


APP gene copy number changes reflect exogenous contamination.
Junho Kim, Boxun Zhao, August Yue Huang, Michael B Miller, Michael A Lodato, Christopher A Walsh, Eunjung Alice Lee. Nature 2020
11
50

On the identification of low allele frequency mosaic mutations in the brains of Alzheimer's disease patients.
Carlo Sala Frigerio, Pierre Lau, Claire Troakes, Vincent Deramecourt, Patrick Gele, Peter Van Loo, Thierry Voet, Bart De Strooper. Alzheimers Dement 2015
48
50

Antisense oligonucleotide therapy in a humanized mouse model of MECP2 duplication syndrome.
Yingyao Shao, Yehezkel Sztainberg, Qi Wang, Sameer S Bajikar, Alexander J Trostle, Ying-Wooi Wan, Paymaan Jafar-Nejad, Frank Rigo, Zhandong Liu, Jianrong Tang,[...]. Sci Transl Med 2021
9
50

MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.
Michael Flower, Vilija Lomeikaite, Marc Ciosi, Sarah Cumming, Fernando Morales, Kitty Lo, Davina Hensman Moss, Lesley Jones, Peter Holmans, Darren G Monckton,[...]. Brain 2019
56
50

An estimation of the number of cells in the human body.
Eva Bianconi, Allison Piovesan, Federica Facchin, Alina Beraudi, Raffaella Casadei, Flavia Frabetti, Lorenza Vitale, Maria Chiara Pelleri, Simone Tassani, Francesco Piva,[...]. Ann Hum Biol 2013
399
50


Precise detection of low-level somatic mutation in resected epilepsy brain tissue.
Nam Suk Sim, Ara Ko, Woo Kyeong Kim, Se Hoon Kim, Ju Seong Kim, Kyu-Won Shim, Eleonora Aronica, Caroline Mijnsbergen, Wim G M Spliet, Hyun Yong Koh,[...]. Acta Neuropathol 2019
49
50

Gene therapy for ALS: A review.
Defne A Amado, Beverly L Davidson. Mol Ther 2021
25
50

ALS antisense drug falters in phase III.
Asher Mullard. Nat Rev Drug Discov 2021
5
50

Increased l1 retrotransposition in the neuronal genome in schizophrenia.
Miki Bundo, Manabu Toyoshima, Yohei Okada, Wado Akamatsu, Junko Ueda, Taeko Nemoto-Miyauchi, Fumiko Sunaga, Michihiro Toritsuka, Daisuke Ikawa, Akiyoshi Kakita,[...]. Neuron 2014
196
50

The druggable genome.
Andrew L Hopkins, Colin R Groom. Nat Rev Drug Discov 2002
50

Human glioblastoma arises from subventricular zone cells with low-level driver mutations.
Joo Ho Lee, Jeong Eun Lee, Jee Ye Kahng, Se Hoon Kim, Jun Sung Park, Seon Jin Yoon, Ji-Yong Um, Woo Kyeong Kim, June-Koo Lee, Junseong Park,[...]. Nature 2018
260
50


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.