A citation-based method for searching scientific literature

Verneri Anttila, Hreinn Stefansson, Mikko Kallela, Unda Todt, Gisela M Terwindt, M Stella Calafato, Dale R Nyholt, Antigone S Dimas, Tobias Freilinger, Bertram Müller-Myhsok, Ville Artto, Michael Inouye, Kirsi Alakurtti, Mari A Kaunisto, Eija Hämäläinen, Boukje de Vries, Anine H Stam, Claudia M Weller, Axel Heinze, Katja Heinze-Kuhn, Ingrid Goebel, Guntram Borck, Hartmut Göbel, Stacy Steinberg, Christiane Wolf, Asgeir Björnsson, Gretar Gudmundsson, Malene Kirchmann, Anne Hauge, Thomas Werge, Jean Schoenen, Johan G Eriksson, Knut Hagen, Lars Stovner, H-Erich Wichmann, Thomas Meitinger, Michael Alexander, Susanne Moebus, Stefan Schreiber, Yurii S Aulchenko, Monique M B Breteler, Andre G Uitterlinden, Albert Hofman, Cornelia M van Duijn, Päivi Tikka-Kleemola, Salli Vepsäläinen, Susanne Lucae, Federica Tozzi, Pierandrea Muglia, Jeffrey Barrett, Jaakko Kaprio, Markus Färkkilä, Leena Peltonen, Kari Stefansson, John-Anker Zwart, Michel D Ferrari, Jes Olesen, Mark Daly, Maija Wessman, Arn M J M van den Maagdenberg, Martin Dichgans, Christian Kubisch, Emmanouil T Dermitzakis, Rune R Frants, Aarno Palotie. Nat Genet 2010
Times Cited: 250







List of co-cited articles
1239 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Genome-wide association study reveals three susceptibility loci for common migraine in the general population.
Daniel I Chasman, Markus Schürks, Verneri Anttila, Boukje de Vries, Ulf Schminke, Lenore J Launer, Gisela M Terwindt, Arn M J M van den Maagdenberg, Konstanze Fendrich, Henry Völzke,[...]. Nat Genet 2011
251
71

Genome-wide association analysis identifies susceptibility loci for migraine without aura.
Tobias Freilinger, Verneri Anttila, Boukje de Vries, Rainer Malik, Mikko Kallela, Gisela M Terwindt, Patricia Pozo-Rosich, Bendik Winsvold, Dale R Nyholt, Willebrordus P J van Oosterhout,[...]. Nat Genet 2012
210
63

Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Verneri Anttila, Bendik S Winsvold, Padhraig Gormley, Tobias Kurth, Francesco Bettella, George McMahon, Mikko Kallela, Rainer Malik, Boukje de Vries, Gisela Terwindt,[...]. Nat Genet 2013
245
63

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Padhraig Gormley, Verneri Anttila, Bendik S Winsvold, Priit Palta, Tonu Esko, Tune H Pers, Kai-How Farh, Ester Cuenca-Leon, Mikko Muona, Nicholas A Furlotte,[...]. Nat Genet 2016
310
39


Migraine pathophysiology: lessons from mouse models and human genetics.
Michel D Ferrari, Roselin R Klever, Gisela M Terwindt, Cenk Ayata, Arn M J M van den Maagdenberg. Lancet Neurol 2015
211
29

Genetic and environmental influences on migraine: a twin study across six countries.
Elles J Mulder, Caroline Van Baal, David Gaist, Mikko Kallela, Jaakko Kaprio, Dan A Svensson, Dale R Nyholt, Nicholas G Martin, Alex J MacGregor, Lynn F Cherkas,[...]. Twin Res 2003
219
24

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans, Tobias Freilinger, Gertrud Eckstein, Elena Babini, Bettina Lorenz-Depiereux, Saskia Biskup, Michel D Ferrari, Jürgen Herzog, Arn M J M van den Maagdenberg, Michael Pusch,[...]. Lancet 2005
545
24

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
R A Ophoff, G M Terwindt, M N Vergouwe, R van Eijk, P J Oefner, S M Hoffman, J E Lamerdin, H W Mohrenweiser, D E Bulman, M Ferrari,[...]. Cell 1996
23

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2.
Maurizio De Fusco, Roberto Marconi, Laura Silvestri, Luigia Atorino, Luca Rampoldi, Letterio Morgante, Andrea Ballabio, Paolo Aridon, Giorgio Casari. Nat Genet 2003
650
23

Meta-analysis of genome-wide association for migraine in six population-based European cohorts.
Lannie Ligthart, Boukje de Vries, Albert V Smith, M Arfan Ikram, Najaf Amin, Jouke-Jan Hottenga, Stephany C Koelewijn, V Mathijs Kattenberg, Marleen H M de Moor, A Cecile J W Janssens,[...]. Eur J Hum Genet 2011
62
27

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.
Ronald G Lafrenière, M Zameel Cader, Jean-François Poulin, Isabelle Andres-Enguix, Maryse Simoneau, Namrata Gupta, Karine Boisvert, François Lafrenière, Shannon McLaughlan, Marie-Pierre Dubé,[...]. Nat Med 2010
232
16


Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies.
Dale R Nyholt, Verneri Anttila, Bendik S Winsvold, Tobias Kurth, Hreinn Stefansson, Mikko Kallela, Rainer Malik, Boukje de Vries, Gisela M Terwindt, M Arfan Ikram,[...]. Cephalalgia 2015
27
55

Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants.
Rainer Malik, Tobias Freilinger, Bendik S Winsvold, Verneri Anttila, Jason Vander Heiden, Matthew Traylor, Boukje de Vries, Elizabeth G Holliday, Gisela M Terwindt, Jonathan Sturm,[...]. Neurology 2015
63
23


Molecular genetics of migraine.
Boukje de Vries, Rune R Frants, Michel D Ferrari, Arn M J M van den Maagdenberg. Hum Genet 2009
193
14



Systematic re-evaluation of genes from candidate gene association studies in migraine using a large genome-wide association data set.
Boukje de Vries, Verneri Anttila, Tobias Freilinger, Maija Wessman, Mari A Kaunisto, Mikko Kallela, Ville Artto, Lisanne S Vijfhuizen, Hartmut Göbel, Martin Dichgans,[...]. Cephalalgia 2016
25
52

Casein kinase iδ mutations in familial migraine and advanced sleep phase.
K C Brennan, Emily A Bates, Robert E Shapiro, Jekaterina Zyuzin, William C Hallows, Yong Huang, Hsien-Yang Lee, Christopher R Jones, Ying-Hui Fu, Andrew C Charles,[...]. Sci Transl Med 2013
127
13


Selectivity in genetic association with sub-classified migraine in women.
Daniel I Chasman, Verneri Anttila, Julie E Buring, Paul M Ridker, Markus Schürks, Tobias Kurth. PLoS Genet 2014
32
37

Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010.
Theo Vos, Abraham D Flaxman, Mohsen Naghavi, Rafael Lozano, Catherine Michaud, Majid Ezzati, Kenji Shibuya, Joshua A Salomon, Safa Abdalla, Victor Aboyans,[...]. Lancet 2012
12

Genetic analysis for a shared biological basis between migraine and coronary artery disease.
Bendik S Winsvold, Christopher P Nelson, Rainer Malik, Padhraig Gormley, Verneri Anttila, Jason Vander Heiden, Katherine S Elliott, Line M Jacobsen, Priit Palta, Najaf Amin,[...]. Neurol Genet 2015
40
30

A replication study of GWAS findings in migraine identifies association in a Swedish case-control sample.
Caroline Ran, Lisette Graae, Patrik K E Magnusson, Nancy L Pedersen, Lars Olson, Andrea C Belin. BMC Med Genet 2014
22
54

Gene-based pleiotropy across migraine with aura and migraine without aura patient groups.
Huiying Zhao, Else Eising, Boukje de Vries, Lisanne S Vijfhuizen, Verneri Anttila, Bendik S Winsvold, Tobias Kurth, Hreinn Stefansson, Mikko Kallela, Rainer Malik,[...]. Cephalalgia 2016
34
35

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
11

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities.
Dale R Nyholt, Nathan G Gillespie, Andrew C Heath, Kathleen R Merikangas, David L Duffy, Nicholas G Martin. Genet Epidemiol 2004
90
12


A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.
Arn M J M van den Maagdenberg, Daniela Pietrobon, Tommaso Pizzorusso, Simon Kaja, Ludo A M Broos, Tiziana Cesetti, Rob C G van de Ven, Angelita Tottene, Jos van der Kaa, Jaap J Plomp,[...]. Neuron 2004
470
11

Increased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.
Loredana Leo, Lisa Gherardini, Virginia Barone, Maurizio De Fusco, Daniela Pietrobon, Tommaso Pizzorusso, Giorgio Casari. PLoS Genet 2011
134
11

The relative role of genetic and environmental factors in migraine without aura.
M Gervil, V Ulrich, J Kaprio, J Olesen, M B Russell. Neurology 1999
111
11


A high-density association screen of 155 ion transport genes for involvement with common migraine.
Dale R Nyholt, K Steven LaForge, Mikko Kallela, Kirsi Alakurtti, Verneri Anttila, Markus Färkkilä, Eija Hämaläinen, Jaakko Kaprio, Mari A Kaunisto, Andrew C Heath,[...]. Hum Mol Genet 2008
67
14

Association of the C677T polymorphism in the MTHFR gene with migraine: a meta-analysis.
E Rubino, M Ferrero, I Rainero, E Binello, G Vaula, L Pinessi. Cephalalgia 2009
69
14

Spreading depression triggers headache by activating neuronal Panx1 channels.
Hulya Karatas, Sefik Evren Erdener, Yasemin Gursoy-Ozdemir, Sevda Lule, Emine Eren-Koçak, Zümrüt Duygu Sen, Turgay Dalkara. Science 2013
280
10


Replication of migraine GWAS susceptibility loci in Chinese Han population.
Xiaoping Fan, Jing Wang, Wen Fan, Lixue Chen, Bei Gui, Ge Tan, Jiying Zhou. Headache 2014
25
40

The association between candidate migraine susceptibility loci and severe migraine phenotype in a clinical sample.
Ann-Louise Esserlind, Anne Francke Christensen, Stacy Steinberg, Niels Grarup, Oluf Pedersen, Torben Hansen, Thomas Werge, Thomas Folkmann Hansen, Lise Lotte N Husemoen, Allan Linneberg,[...]. Cephalalgia 2016
22
45

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility.
Hannah C Cox, Rod A Lea, Claire Bellis, Melanie Carless, Thomas D Dyer, Joanne Curran, Jac Charlesworth, Stuart Macgregor, Dale Nyholt, Daniel Chasman,[...]. Neurogenetics 2012
26
38

Migraine and concomitant symptoms among 8167 adult twin pairs.
M L Honkasalo, J Kaprio, T Winter, K Heikkilä, M Sillanpää, M Koskenvuo. Headache 1995
122
10

Pathophysiology of migraine.
Daniela Pietrobon, Michael A Moskowitz. Annu Rev Physiol 2013
374
10

Meta-analysis of the heritability of human traits based on fifty years of twin studies.
Tinca J C Polderman, Beben Benyamin, Christiaan A de Leeuw, Patrick F Sullivan, Arjen van Bochoven, Peter M Visscher, Danielle Posthuma. Nat Genet 2015
762
10

Pathophysiology of Migraine: A Disorder of Sensory Processing.
Peter J Goadsby, Philip R Holland, Margarida Martins-Oliveira, Jan Hoffmann, Christoph Schankin, Simon Akerman. Physiol Rev 2017
641
10

Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura.
M A Kaunisto, M Kallela, E Hämäläinen, R Kilpikari, H Havanka, H Harno, M Nissilä, E Säkö, M Ilmavirta, J Liukkonen,[...]. Cephalalgia 2006
75
12

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders.
Lannie Ligthart, Jouke-Jan Hottenga, Cathryn M Lewis, Anne E Farmer, Ian W Craig, Gerome Breen, Gonneke Willemsen, Jacqueline M Vink, Christel M Middeldorp, Enda M Byrne,[...]. Hum Genet 2014
44
20

Migraine without aura and migraine with aura are distinct disorders. A population-based twin survey.
Michael Bjørn Russell, Vibeke Ulrich, Morten Gervil, Jes Olesen. Headache 2002
76
11

Defective membrane expression of the Na(+)-HCO(3)(-) cotransporter NBCe1 is associated with familial migraine.
Masashi Suzuki, Wim Van Paesschen, Ingeborg Stalmans, Shoko Horita, Hideomi Yamada, Bruno A Bergmans, Eric Legius, Florence Riant, Peter De Jonghe, Yuehong Li,[...]. Proc Natl Acad Sci U S A 2010
103
9

Methylenetetrahydrofolate reductase gene variant (MTHFR C677T) and migraine: a case control study and meta-analysis.
Zainab Samaan, Daria Gaysina, Sarah Cohen-Woods, Nick Craddock, Lisa Jones, Ania Korszun, Mike Owen, Andrew Mente, Peter McGuffin, Anne Farmer. BMC Neurol 2011
32
28


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.