A citation-based method for searching scientific literature

Augustine Kong, Michael L Frigge, Gisli Masson, Soren Besenbacher, Patrick Sulem, Gisli Magnusson, Sigurjon A Gudjonsson, Asgeir Sigurdsson, Aslaug Jonasdottir, Adalbjorg Jonasdottir, Wendy S W Wong, Gunnar Sigurdsson, G Bragi Walters, Stacy Steinberg, Hannes Helgason, Gudmar Thorleifsson, Daniel F Gudbjartsson, Agnar Helgason, Olafur Th Magnusson, Unnur Thorsteinsdottir, Kari Stefansson. Nature 2012
Times Cited: 1052







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



Times Cited
  Times     Co-cited
Similarity


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
129
28

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
227
19

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
113
19

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
14


A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
13

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
12

Overlooked roles of DNA damage and maternal age in generating human germline mutations.
Ziyue Gao, Priya Moorjani, Thomas A Sasani, Brent S Pedersen, Aaron R Quinlan, Lynn B Jorde, Guy Amster, Molly Przeworski. Proc Natl Acad Sci U S A 2019
41
29

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
127
11

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
11


Genome-wide patterns and properties of de novo mutations in humans.
Laurent C Francioli, Paz P Polak, Amnon Koren, Androniki Menelaou, Sung Chun, Ivo Renkens, Cornelia M van Duijn, Morris Swertz, Cisca Wijmenga, Gertjan van Ommen,[...]. Nat Genet 2015
186
10

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
10

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
76
11

Reproductive Longevity Predicts Mutation Rates in Primates.
Gregg W C Thomas, Richard J Wang, Arthi Puri, R Alan Harris, Muthuswamy Raveendran, Daniel S T Hughes, Shwetha C Murali, Lawrence E Williams, Harsha Doddapaneni, Donna M Muzny,[...]. Curr Biol 2018
28
32

Tissue-specific mutation accumulation in human adult stem cells during life.
Francis Blokzijl, Joep de Ligt, Myrthe Jager, Valentina Sasselli, Sophie Roerink, Nobuo Sasaki, Meritxell Huch, Sander Boymans, Ewart Kuijk, Pjotr Prins,[...]. Nature 2016
387
8

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
75
10

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
328
8

Differences between germline and somatic mutation rates in humans and mice.
Brandon Milholland, Xiao Dong, Lei Zhang, Xiaoxiao Hao, Yousin Suh, Jan Vijg. Nat Commun 2017
131
8

Analysis of genetic inheritance in a family quartet by whole-genome sequencing.
Jared C Roach, Gustavo Glusman, Arian F A Smit, Chad D Huff, Robert Hubley, Paul T Shannon, Lee Rowen, Krishna P Pant, Nathan Goodman, Michael Bamshad,[...]. Science 2010
680
8

Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation.
Thomas A Sasani, Brent S Pedersen, Ziyue Gao, Lisa Baird, Molly Przeworski, Lynn B Jorde, Aaron R Quinlan. Elife 2019
26
30

Determinants of mutation rate variation in the human germline.
Laure Ségurel, Minyoung J Wyman, Molly Przeworski. Annu Rev Genomics Hum Genet 2014
140
8

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
8

Paternal age at childbearing and offspring psychiatric and academic morbidity.
Brian M D'Onofrio, Martin E Rickert, Emma Frans, Ralf Kuja-Halkola, Catarina Almqvist, Arvid Sjölander, Henrik Larsson, Paul Lichtenstein. JAMA Psychiatry 2014
139
7


Germline de novo mutation clusters arise during oocyte aging in genomic regions with high double-strand-break incidence.
Jakob M Goldmann, Vladimir B Seplyarskiy, Wendy S W Wong, Thierry Vilboux, Pieter B Neerincx, Dale L Bodian, Benjamin D Solomon, Joris A Veltman, John F Deeken, Christian Gilissen,[...]. Nat Genet 2018
23
30

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
145
7

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
57
12

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
7

Multiple transmissions of de novo mutations in families.
Hákon Jónsson, Patrick Sulem, Gudny A Arnadottir, Gunnar Pálsson, Hannes P Eggertsson, Snaedis Kristmundsdottir, Florian Zink, Birte Kehr, Kristjan E Hjorleifsson, Brynjar Ö Jensson,[...]. Nat Genet 2018
34
20

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
7

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
147
7

Signatures of mutational processes in human cancer.
Ludmil B Alexandrov, Serena Nik-Zainal, David C Wedge, Samuel A J R Aparicio, Sam Behjati, Andrew V Biankin, Graham R Bignell, Niccolò Bolli, Ake Borg, Anne-Lise Børresen-Dale,[...]. Nature 2013
7

Genomic Patterns of De Novo Mutation in Simplex Autism.
Tychele N Turner, Bradley P Coe, Diane E Dickel, Kendra Hoekzema, Bradley J Nelson, Michael C Zody, Zev N Kronenberg, Fereydoun Hormozdiari, Archana Raja, Len A Pennacchio,[...]. Cell 2017
134
7

Variation in genome-wide mutation rates within and between human families.
Donald F Conrad, Jonathan E M Keebler, Mark A DePristo, Sarah J Lindsay, Yujun Zhang, Ferran Casals, Youssef Idaghdour, Chris L Hartl, Carlos Torroja, Kiran V Garimella,[...]. Nat Genet 2011
343
7

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
7

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios.
Søren Besenbacher, Siyang Liu, José M G Izarzugaza, Jakob Grove, Kirstine Belling, Jette Bork-Jensen, Shujia Huang, Thomas D Als, Shengting Li, Rachita Yadav,[...]. Nat Commun 2015
91
7

Consistent age-dependent declines in human semen quality: a systematic review and meta-analysis.
Sheri L Johnson, Jessica Dunleavy, Neil J Gemmell, Shinichi Nakagawa. Ageing Res Rev 2015
130
7

Nonhuman genetics. Strong male bias drives germline mutation in chimpanzees.
Oliver Venn, Isaac Turner, Iain Mathieson, Natasja de Groot, Ronald Bontrop, Gil McVean. Science 2014
73
9

Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals.
Simon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, Marc-André Legault, Amina Barhdadi, Amirthagowri Ambalavanan, Mara Brendgen, Frank Vitaro, Anne Noreau, Ginette Dionne,[...]. PLoS One 2016
18
33

Advanced paternal age: how old is too old?
Isabelle Bray, David Gunnell, George Davey Smith. J Epidemiol Community Health 2006
125
6

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
Jacob J Michaelson, Yujian Shi, Madhusudan Gujral, Hancheng Zheng, Dheeraj Malhotra, Xin Jin, Minghan Jian, Guangming Liu, Douglas Greer, Abhishek Bhandari,[...]. Cell 2012
328
6

De novo mutations in human genetic disease.
Joris A Veltman, Han G Brunner. Nat Rev Genet 2012
435
6

Characterizing mutagenic effects of recombination through a sequence-level genetic map.
Bjarni V Halldorsson, Gunnar Palsson, Olafur A Stefansson, Hakon Jonsson, Marteinn T Hardarson, Hannes P Eggertsson, Bjarni Gunnarsson, Asmundur Oddsson, Gisli H Halldorsson, Florian Zink,[...]. Science 2019
56
10

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans.
Jedidiah Carlson, Adam E Locke, Matthew Flickinger, Matthew Zawistowski, Shawn Levy, Richard M Myers, Michael Boehnke, Hyun Min Kang, Laura J Scott, Jun Z Li,[...]. Nat Commun 2018
36
16

Advancing paternal age and autism.
Abraham Reichenberg, Raz Gross, Mark Weiser, Michealine Bresnahan, Jeremy Silverman, Susan Harlap, Jonathan Rabinowitz, Cory Shulman, Dolores Malaspina, Gad Lubin,[...]. Arch Gen Psychiatry 2006
356
6

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
894
6

Effects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspring.
Rakesh Sharma, Ashok Agarwal, Vikram K Rohra, Mourad Assidi, Muhammad Abu-Elmagd, Rola F Turki. Reprod Biol Endocrinol 2015
124
6

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Jason Homsy, Samir Zaidi, Yufeng Shen, James S Ware, Kaitlin E Samocha, Konrad J Karczewski, Steven R DePalma, David McKean, Hiroko Wakimoto, Josh Gorham,[...]. Science 2015
328
6

Similarities and differences in patterns of germline mutation between mice and humans.
Sarah J Lindsay, Raheleh Rahbari, Joanna Kaplanis, Thomas Keane, Matthew E Hurles. Nat Commun 2019
16
37


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.