A citation-based method for searching scientific literature

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, Daniel J Weiner, Jason Homsy, Jonathan G Seidman, Christine E Seidman, Esben Agerbo, John J McGrath, Preben Bo Mortensen, Liselotte Petersen, Mark J Daly, Elise B Robinson. Nat Commun 2019
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


Rate of de novo mutations and the importance of father's age to disease risk.
Augustine Kong, Michael L Frigge, Gisli Masson, Soren Besenbacher, Patrick Sulem, Gisli Magnusson, Sigurjon A Gudjonsson, Asgeir Sigurdsson, Aslaug Jonasdottir, Adalbjorg Jonasdottir,[...]. Nature 2012
44

Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations.
Jacob Gratten, Naomi R Wray, Wouter J Peyrot, John J McGrath, Peter M Visscher, Michael E Goddard. Nat Genet 2016
59
38

Paternal age and psychiatric disorders: A review.
Hilde de Kluiver, Jacobine E Buizer-Voskamp, Conor V Dolan, Dorret I Boomsma. Am J Med Genet B Neuropsychiatr Genet 2017
35
33


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
27

Age-related sperm DNA methylation changes are transmitted to offspring and associated with abnormal behavior and dysregulated gene expression.
M H Milekic, Y Xin, A O'Donnell, K K Kumar, M Bradley-Moore, D Malaspina, H Moore, D Brunner, Y Ge, J Edwards,[...]. Mol Psychiatry 2015
81
27

Advanced paternal age, infertility, and reproductive risks: A review of the literature.
Justin S Brandt, Mayra A Cruz Ithier, Todd Rosen, Elena Ashkinadze. Prenat Diagn 2019
28
22

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
22

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
22

The effect of paternal factors on perinatal and paediatric outcomes: a systematic review and meta-analysis.
Nan B Oldereid, Ulla-Britt Wennerholm, Anja Pinborg, Anne Loft, Hannele Laivuori, Max Petzold, Liv Bente Romundstad, Viveca Söderström-Anttila, Christina Bergh. Hum Reprod Update 2018
63
22

Advanced paternal age effects in neurodevelopmental disorders-review of potential underlying mechanisms.
M Janecka, J Mill, M A Basson, A Goriely, H Spiers, A Reichenberg, L Schalkwyk, C Fernandes. Transl Psychiatry 2017
45
22

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
601
22

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
310
22

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
332
22

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
22

Age-associated sperm DNA methylation alterations: possible implications in offspring disease susceptibility.
Timothy G Jenkins, Kenneth I Aston, Christian Pflueger, Bradley R Cairns, Douglas T Carrell. PLoS Genet 2014
148
22

Parental influence on human germline de novo mutations in 1,548 trios from Iceland.
Hákon Jónsson, Patrick Sulem, Birte Kehr, Snaedis Kristmundsdottir, Florian Zink, Eirikur Hjartarson, Marteinn T Hardarson, Kristjan E Hjorleifsson, Hannes P Eggertsson, Sigurjon Axel Gudjonsson,[...]. Nature 2017
132
16

Timing, rates and spectra of human germline mutation.
Raheleh Rahbari, Arthur Wuster, Sarah J Lindsay, Robert J Hardwick, Ludmil B Alexandrov, Saeed Al Turki, Anna Dominiczak, Andrew Morris, David Porteous, Blair Smith,[...]. Nat Genet 2016
231
16


Parent-of-origin-specific signatures of de novo mutations.
Jakob M Goldmann, Wendy S W Wong, Michele Pinelli, Terry Farrah, Dale Bodian, Anna B Stittrich, Gustavo Glusman, Lisenka E L M Vissers, Alexander Hoischen, Jared C Roach,[...]. Nat Genet 2016
116
16

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
16

Paternal age and offspring congenital heart defects: a national cohort study.
Xiu Juan Su, Wei Yuan, Guo Ying Huang, Jørn Olsen, Jiong Li. PLoS One 2015
21
16

Advanced paternal age and childhood cancer in offspring: A nationwide register-based cohort study.
Stine Kjaer Urhoj, Ole Raaschou-Nielsen, Anne Vinkel Hansen, Laust Hvas Mortensen, Per Kragh Andersen, Anne-Marie Nybo Andersen. Int J Cancer 2017
21
16

Association of paternal age with perinatal outcomes between 2007 and 2016 in the United States: population based cohort study.
Yash S Khandwala, Valerie L Baker, Gary M Shaw, David K Stevenson, Ying Lu, Michael L Eisenberg. BMJ 2018
60
16

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.
Xin He, Stephan J Sanders, Li Liu, Silvia De Rubeis, Elaine T Lim, James S Sutcliffe, Gerard D Schellenberg, Richard A Gibbs, Mark J Daly, Joseph D Buxbaum,[...]. PLoS Genet 2013
129
16

Paternal and maternal age as risk factors for schizophrenia: a case-control study.
Konstantinos N Fountoulakis, Xenia Gonda, Melina Siamouli, Panagiotis Panagiotidis, Katerina Moutou, Ioannis Nimatoudis, Siegfried Kasper. Int J Psychiatry Clin Pract 2018
12
25

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
Daniel J Weiner, Emilie M Wigdor, Stephan Ripke, Raymond K Walters, Jack A Kosmicki, Jakob Grove, Kaitlin E Samocha, Jacqueline I Goldstein, Aysu Okbay, Jonas Bybjerg-Grauholm,[...]. Nat Genet 2017
182
16

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
16

Infantile autism: a genetic study of 21 twin pairs.
S Folstein, M Rutter. J Child Psychol Psychiatry 1977
755
16

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
16

Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks.
Elizabeth K Ruzzo, Laura Pérez-Cano, Jae-Yoon Jung, Lee-Kai Wang, Dorna Kashef-Haghighi, Chris Hartl, Chanpreet Singh, Jin Xu, Jackson N Hoekstra, Olivia Leventhal,[...]. Cell 2019
82
16

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
437
16

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.
Joon-Yong An, Kevin Lin, Lingxue Zhu, Donna M Werling, Shan Dong, Harrison Brand, Harold Z Wang, Xuefang Zhao, Grace B Schwartz, Ryan L Collins,[...]. Science 2018
79
16

Autism risk associated with parental age and with increasing difference in age between the parents.
S Sandin, D Schendel, P Magnusson, C Hultman, P Surén, E Susser, T Grønborg, M Gissler, N Gunnes, R Gross,[...]. Mol Psychiatry 2016
97
16

Recessive gene disruptions in autism spectrum disorder.
Ryan N Doan, Elaine T Lim, Silvia De Rubeis, Catalina Betancur, David J Cutler, Andreas G Chiocchetti, Lynne M Overman, Aubrie Soucy, Susanne Goetze, Christine M Freitag,[...]. Nat Genet 2019
31
16

A comprehensive assessment of parental age and psychiatric disorders.
John J McGrath, Liselotte Petersen, Esben Agerbo, Ole Mors, Preben Bo Mortensen, Carsten Bøcker Pedersen. JAMA Psychiatry 2014
129
16

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
16

Understanding the association between advanced paternal age and schizophrenia and bipolar disorder.
Mark Weiser, Daphna Fenchel, Or Frenkel, Eyal Fruchter, Shimon Burshtein, Ariel Ben Yehuda, Rinat Yoffe, Tal Bergman-Levi, Abraham Reichenberg, Michael Davidson,[...]. Psychol Med 2020
5
60

New insights into the generation and role of de novo mutations in health and disease.
Rocio Acuna-Hidalgo, Joris A Veltman, Alexander Hoischen. Genome Biol 2016
150
11

Onset of the release of spermatozoa (spermarche) in boys in relation to age, testicular growth, pubic hair, and height.
C T Nielsen, N E Skakkebaek, D W Richardson, J A Darling, W M Hunter, M Jørgensen, A Nielsen, O Ingerslev, N Keiding, J Müller. J Clin Endocrinol Metab 1986
135
11

Parent of origin, mosaicism, and recurrence risk: probabilistic modeling explains the broken symmetry of transmission genetics.
Ian M Campbell, Jonathan R Stewart, Regis A James, James R Lupski, Paweł Stankiewicz, Peter Olofsson, Chad A Shaw. Am J Hum Genet 2014
61
11

Genome-wide single-cell analysis of recombination activity and de novo mutation rates in human sperm.
Jianbin Wang, H Christina Fan, Barry Behr, Stephen R Quake. Cell 2012
301
11

New observations on maternal age effect on germline de novo mutations.
Wendy S W Wong, Benjamin D Solomon, Dale L Bodian, Prachi Kothiyal, Greg Eley, Kathi C Huddleston, Robin Baker, Dzung C Thach, Ramaswamy K Iyer, Joseph G Vockley,[...]. Nat Commun 2016
76
11

Older fathers' children have lower evolutionary fitness across four centuries and in four populations.
Ruben C Arslan, Kai P Willführ, Emma M Frans, Karin J H Verweij, Paul-Christian Bürkner, Mikko Myrskylä, Eckart Voland, Catarina Almqvist, Brendan P Zietsch, Lars Penke. Proc Biol Sci 2017
18
11

The Contribution of Mosaic Variants to Autism Spectrum Disorder.
Donald Freed, Jonathan Pevsner. PLoS Genet 2016
51
11

A Comprehensive Roadmap of Murine Spermatogenesis Defined by Single-Cell RNA-Seq.
Christopher Daniel Green, Qianyi Ma, Gabriel L Manske, Adrienne Niederriter Shami, Xianing Zheng, Simone Marini, Lindsay Moritz, Caleb Sultan, Stephen J Gurczynski, Bethany B Moore,[...]. Dev Cell 2018
112
11


High-resolution DNA methylome analysis of primordial germ cells identifies gender-specific reprogramming in mice.
Hisato Kobayashi, Takayuki Sakurai, Fumihito Miura, Misaki Imai, Kentaro Mochiduki, Eikichi Yanagisawa, Akihiko Sakashita, Takuya Wakai, Yutaka Suzuki, Takashi Ito,[...]. Genome Res 2013
163
11

Selfish mutations dysregulating RAS-MAPK signaling are pervasive in aged human testes.
Geoffrey J Maher, Hannah K Ralph, Zhihao Ding, Nils Koelling, Hana Mlcochova, Eleni Giannoulatou, Pawan Dhami, Dirk S Paul, Stefan H Stricker, Stephan Beck,[...]. Genome Res 2018
28
11

Chromosomal scan of single sperm cells by combining fluorescence-activated cell sorting and next-generation sequencing.
Quoc Ty Tran, Tatjana Jatsenko, Olev Poolamets, Olga Tšuiko, Dmitri Lubenets, Tiia Reimand, Margus Punab, Maire Peters, Andres Salumets. J Assist Reprod Genet 2019
6
33


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.