A citation-based method for searching scientific literature

Maxwell A Sherman, Rachel E Rodin, Giulio Genovese, Caroline Dias, Alison R Barton, Ronen E Mukamel, Bonnie Berger, Peter J Park, Christopher A Walsh, Po-Ru Loh. Nat Neurosci 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Monogenic and polygenic inheritance become instruments for clonal selection.
Po-Ru Loh, Giulio Genovese, Steven A McCarroll. Nature 2020
25
75

Neurons with Complex Karyotypes Are Rare in Aged Human Neocortex.
William D Chronister, Ian E Burbulis, Margaret B Wierman, Matthew J Wolpert, Mark F Haakenson, Aiden C B Smith, Joel E Kleinman, Thomas M Hyde, Daniel R Weinberger, Stefan Bekiranov,[...]. Cell Rep 2019
21
75

Mosaic copy number variation in human neurons.
Michael J McConnell, Michael R Lindberg, Kristen J Brennand, Julia C Piper, Thierry Voet, Chris Cowing-Zitron, Svetlana Shumilina, Roger S Lasken, Joris R Vermeesch, Ira M Hall,[...]. Science 2013
320
75

Chromosomal alterations among age-related haematopoietic clones in Japan.
Chikashi Terao, Akari Suzuki, Yukihide Momozawa, Masato Akiyama, Kazuyoshi Ishigaki, Kazuhiko Yamamoto, Koichi Matsuda, Yoshinori Murakami, Steven A McCarroll, Michiaki Kubo,[...]. Nature 2020
21
75

Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations.
Po-Ru Loh, Giulio Genovese, Robert E Handsaker, Hilary K Finucane, Yakir A Reshef, Pier Francesco Palamara, Brenda M Birmann, Michael E Talkowski, Samuel F Bakhoum, Steven A McCarroll,[...]. Nature 2018
99
75

Mosaic structural variation in children with developmental disorders.
Daniel A King, Wendy D Jones, Yanick J Crow, Anna F Dominiczak, Nicola A Foster, Tom R Gaunt, Jade Harris, Stephen W Hellens, Tessa Homfray, Josie Innes,[...]. Hum Mol Genet 2015
32
50

Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence.
Giulio Genovese, Anna K Kähler, Robert E Handsaker, Johan Lindberg, Samuel A Rose, Samuel F Bakhoum, Kimberly Chambert, Eran Mick, Benjamin M Neale, Menachem Fromer,[...]. N Engl J Med 2014
50

Physiologic brain activity causes DNA double-strand breaks in neurons, with exacerbation by amyloid-β.
Elsa Suberbielle, Pascal E Sanchez, Alexxai V Kravitz, Xin Wang, Kaitlyn Ho, Kirsten Eilertson, Nino Devidze, Anatol C Kreitzer, Lennart Mucke. Nat Neurosci 2013
236
50

Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.
Xuyu Cai, Gilad D Evrony, Hillel S Lehmann, Princess C Elhosary, Bhaven K Mehta, Annapurna Poduri, Christopher A Walsh. Cell Rep 2014
154
50

Single cell sequencing reveals low levels of aneuploidy across mammalian tissues.
Kristin A Knouse, Jie Wu, Charles A Whittaker, Angelika Amon. Proc Natl Acad Sci U S A 2014
156
50

Constitutional aneuploidy in the normal human brain.
Stevens K Rehen, Yun C Yung, Matthew P McCreight, Dhruv Kaushal, Amy H Yang, Beatriz S V Almeida, Marcy A Kingsbury, Kátia M S Cabral, Michael J McConnell, Brigitte Anliker,[...]. J Neurosci 2005
207
50

Mosaic loss of human Y chromosome: what, how and why.
Xihan Guo, Xueqin Dai, Tao Zhou, Han Wang, Juan Ni, Jinglun Xue, Xu Wang. Hum Genet 2020
12
50

Mosaicism, aging and cancer.
Mitchell J Machiela. Curr Opin Oncol 2019
9
50

Detectable clonal mosaicism from birth to old age and its relationship to cancer.
Cathy C Laurie, Cecelia A Laurie, Kenneth Rice, Kimberly F Doheny, Leila R Zelnick, Caitlin P McHugh, Hua Ling, Kurt N Hetrick, Elizabeth W Pugh, Chris Amos,[...]. Nat Genet 2012
351
50

Genetic Interleukin 6 Signaling Deficiency Attenuates Cardiovascular Risk in Clonal Hematopoiesis.
Alexander G Bick, James P Pirruccello, Gabriel K Griffin, Namrata Gupta, Stacey Gabriel, Danish Saleheen, Peter Libby, Sekar Kathiresan, Pradeep Natarajan. Circulation 2020
75
50

Genetic predisposition to mosaic Y chromosome loss in blood.
Deborah J Thompson, Giulio Genovese, Jonatan Halvardson, Jacob C Ulirsch, Daniel J Wright, Chikashi Terao, Olafur B Davidsson, Felix R Day, Patrick Sulem, Yunxuan Jiang,[...]. Nature 2019
50
50


Chromosome Mis-segregation Generates Cell-Cycle-Arrested Cells with Complex Karyotypes that Are Eliminated by the Immune System.
Stefano Santaguida, Amelia Richardson, Divya Ramalingam Iyer, Ons M'Saad, Lauren Zasadil, Kristin A Knouse, Yao Liang Wong, Nicholas Rhind, Arshad Desai, Angelika Amon. Dev Cell 2017
110
50

GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation.
Chikashi Terao, Yukihide Momozawa, Kazuyoshi Ishigaki, Eiryo Kawakami, Masato Akiyama, Po-Ru Loh, Giulio Genovese, Hiroki Sugishita, Tazro Ohta, Makoto Hirata,[...]. Nat Commun 2019
14
50

Clonal hematopoiesis in human aging and disease.
Siddhartha Jaiswal, Benjamin L Ebert. Science 2019
143
50

Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis.
Henne Holstege, Wayne Pfeiffer, Daoud Sie, Marc Hulsman, Thomas J Nicholas, Clarence C Lee, Tristen Ross, Jue Lin, Mark A Miller, Bauke Ylstra,[...]. Genome Res 2014
91
50

Aging of hematopoietic stem cells.
Gerald de Haan, Seka Simone Lazare. Blood 2018
100
50

Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome.
Mitchell J Machiela, Weiyin Zhou, Eric Karlins, Joshua N Sampson, Neal D Freedman, Qi Yang, Belynda Hicks, Casey Dagnall, Christopher Hautman, Kevin B Jacobs,[...]. Nat Commun 2016
43
50

Detectable clonal mosaicism and its relationship to aging and cancer.
Kevin B Jacobs, Meredith Yeager, Weiyin Zhou, Sholom Wacholder, Zhaoming Wang, Benjamin Rodriguez-Santiago, Amy Hutchinson, Xiang Deng, Chenwei Liu, Marie-Josephe Horner,[...]. Nat Genet 2012
352
50

Age-related remodelling of oesophageal epithelia by mutated cancer drivers.
Akira Yokoyama, Nobuyuki Kakiuchi, Tetsuichi Yoshizato, Yasuhito Nannya, Hiromichi Suzuki, Yasuhide Takeuchi, Yusuke Shiozawa, Yusuke Sato, Kosuke Aoki, Soo Ki Kim,[...]. Nature 2019
183
50

Large-scale analysis of acquired chromosomal alterations in non-tumor samples from patients with cancer.
Y A Jakubek, K Chang, S Sivakumar, Y Yu, M R Giordano, J Fowler, C D Huff, H Kadara, E Vilar, P Scheet. Nat Biotechnol 2020
9
50

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
181
25

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
G Kirov, A J Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, J Moran, K Chambert, D Toncheva, L Georgieva,[...]. Mol Psychiatry 2012
515
25

Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.
Elaine T Lim, Mohammed Uddin, Silvia De Rubeis, Yingleong Chan, Anne S Kamumbu, Xiaochang Zhang, Alissa M D'Gama, Sonia N Kim, Robert Sean Hill, Arthur P Goldberg,[...]. Nat Neurosci 2017
110
25

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban,[...]. Mol Psychiatry 2014
226
25

Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males.
J Clayton-Smith, P Watson, S Ramsden, G C Black. Lancet 2000
117
25

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
25

An Organismal CNV Mutator Phenotype Restricted to Early Human Development.
Pengfei Liu, Bo Yuan, Claudia M B Carvalho, Arthur Wuster, Klaudia Walter, Ling Zhang, Tomasz Gambin, Zechen Chong, Ian M Campbell, Zeynep Coban Akdemir,[...]. Cell 2017
41
25

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
278
25

Ontogenetic de novo copy number variations (CNVs) as a source of genetic individuality: studies on two families with MZD twins for schizophrenia.
Sujit Maiti, Kiran Halagur Bhoge Gowda Kumar, Christina A Castellani, Richard O'Reilly, Shiva M Singh. PLoS One 2011
48
25

De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly.
Jeong Ho Lee, My Huynh, Jennifer L Silhavy, Sangwoo Kim, Tracy Dixon-Salazar, Andrew Heiberg, Eric Scott, Vineet Bafna, Kiley J Hill, Adrienne Collazo,[...]. Nat Genet 2012
399
25

The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1.
Yuri B Yurov, Ivan Y Iourov, Svetlana G Vorsanova, Irina A Demidova, Viktor S Kravetz, Alphia K Beresheva, Alexei D Kolotii, Viktor V Monakchov, Natalia A Uranova, Viktor M Vostrikov,[...]. Schizophr Res 2008
60
25

Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay.
Katja Kobow, Samir Jabari, Tom Pieper, Manfred Kudernatsch, Tilman Polster, Friedrich G Woermann, Thilo Kalbhenn, Hajo Hamer, Karl Rössler, Angelika Mühlebner,[...]. Acta Neuropathol 2020
3
33

Deep sequencing reveals variations in somatic cell mosaic mutations between monozygotic twins with discordant psychiatric disease.
Yoshiro Morimoto, Shinji Ono, Akira Imamura, Yuji Okazaki, Akira Kinoshita, Hiroyuki Mishima, Hideyuki Nakane, Hiroki Ozawa, Koh-Ichiro Yoshiura, Naohiro Kurotaki. Hum Genome Var 2017
10
25

Long Neural Genes Harbor Recurrent DNA Break Clusters in Neural Stem/Progenitor Cells.
Pei-Chi Wei, Amelia N Chang, Jennifer Kao, Zhou Du, Robin M Meyers, Frederick W Alt, Bjoern Schwer. Cell 2016
134
25

Microarray Analyses Reveal Marked Differences in Growth Factor and Receptor Expression Between 8-Cell Human Embryos and Pluripotent Stem Cells.
Antonis Vlismas, Ritsa Bletsa, Despina Mavrogianni, Georgina Mamali, Maria Pergamali, Vasiliki Dinopoulou, George Partsinevelos, Peter Drakakis, Dimitris Loutradis, Ann A Kiessling. Stem Cells Dev 2016
4
25

Mosaic Brain Aneuploidy in Mental Illnesses: An Association of Low-level Post-zygotic Aneuploidy with Schizophrenia and Comorbid Psychiatric Disorders.
Yuri B Yurov, Svetlana G Vorsanova, Irina A Demidova, Alexei D Kolotii, Ilia V Soloviev, Ivan Y Iourov. Curr Genomics 2018
10
25

Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations.
Yanmei Dou, Xiaoxu Yang, Ziyi Li, Sheng Wang, Zheng Zhang, Adam Yongxin Ye, Linlin Yan, Changhong Yang, Qixi Wu, Jiarui Li,[...]. Hum Mutat 2017
27
25

Failure to Identify Somatic Mutations in Monozygotic Twins Discordant for Schizophrenia by Whole Exome Sequencing.
Nan Lyu, Li-Li Guan, Hong Ma, Xi-Jin Wang, Bao-Ming Wu, Fan-Hong Shang, Dan Wang, Hong Wen, Xin Yu. Chin Med J (Engl) 2016
3
33

Chromosome instability is common in human cleavage-stage embryos.
Evelyne Vanneste, Thierry Voet, Cédric Le Caignec, Michèle Ampe, Peter Konings, Cindy Melotte, Sophie Debrock, Mustapha Amyere, Miikka Vikkula, Frans Schuit,[...]. Nat Med 2009
495
25

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
Itaru Kushima, Branko Aleksic, Masahiro Nakatochi, Teppei Shimamura, Takashi Okada, Yota Uno, Mako Morikawa, Kanako Ishizuka, Tomoko Shiino, Hiroki Kimura,[...]. Cell Rep 2018
77
25

Chromosome Segregation Fidelity in Epithelia Requires Tissue Architecture.
Kristin A Knouse, Kristina E Lopez, Marc Bachofner, Angelika Amon. Cell 2018
53
25

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
25

Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including the AKT3 gene.
V Conti, M Pantaleo, C Barba, G Baroni, D Mei, A M Buccoliero, S Giglio, F Giordano, S T Baek, J G Gleeson,[...]. Clin Genet 2015
32
25

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.
Lauren M McGrath, Dongmei Yu, Christian Marshall, Lea K Davis, Bhooma Thiruvahindrapuram, Bingbin Li, Carolina Cappi, Gloria Gerber, Aaron Wolf, Frederick A Schroeder,[...]. J Am Acad Child Adolesc Psychiatry 2014
70
25


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.