A citation-based method for searching scientific literature

D Timothy Bishop, Florence Demenais, Mark M Iles, Mark Harland, John C Taylor, Eve Corda, Juliette Randerson-Moor, Joanne F Aitken, Marie-Francoise Avril, Esther Azizi, Bert Bakker, Giovanna Bianchi-Scarrà, Brigitte Bressac-de Paillerets, Donato Calista, Lisa A Cannon-Albright, Thomas Chin-A-Woeng, Tadeusz Debniak, Gilli Galore-Haskel, Paola Ghiorzo, Ivo Gut, Johan Hansson, Marko Hocevar, Veronica Höiom, John L Hopper, Christian Ingvar, Peter A Kanetsky, Richard F Kefford, Maria Teresa Landi, Julie Lang, Jan Lubiński, Rona Mackie, Josep Malvehy, Graham J Mann, Nicholas G Martin, Grant W Montgomery, Frans A van Nieuwpoort, Srdjan Novakovic, Håkan Olsson, Susana Puig, Marjan Weiss, Wilbert van Workum, Diana Zelenika, Kevin M Brown, Alisa M Goldstein, Elizabeth M Gillanders, Anne Boland, Pilar Galan, David E Elder, Nelleke A Gruis, Nicholas K Hayward, G Mark Lathrop, Jennifer H Barrett, Julia A Newton Bishop. Nat Genet 2009
Times Cited: 324







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



Times Cited
  Times     Co-cited
Similarity


Genome-wide association study identifies three new melanoma susceptibility loci.
Jennifer H Barrett, Mark M Iles, Mark Harland, John C Taylor, Joanne F Aitken, Per Arne Andresen, Lars A Akslen, Bruce K Armstrong, Marie-Francoise Avril, Esther Azizi,[...]. Nat Genet 2011
173
36

Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
Mario Falchi, Veronique Bataille, Nicholas K Hayward, David L Duffy, Julia A Newton Bishop, Tomi Pastinen, Alessandra Cervino, Zhen Z Zhao, Panos Deloukas, Nicole Soranzo,[...]. Nat Genet 2009
163
23

Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
Christopher I Amos, Li-E Wang, Jeffrey E Lee, Jeffrey E Gershenwald, Wei V Chen, Shenying Fang, Roman Kosoy, Mingfeng Zhang, Abrar A Qureshi, Selina Vattathil,[...]. Hum Mol Genet 2011
148
23

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
Matthew H Law, D Timothy Bishop, Jeffrey E Lee, Myriam Brossard, Nicholas G Martin, Eric K Moses, Fengju Song, Jennifer H Barrett, Rajiv Kumar, Douglas F Easton,[...]. Nat Genet 2015
137
23

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
Stuart Macgregor, Grant W Montgomery, Jimmy Z Liu, Zhen Zhen Zhao, Anjali K Henders, Mitchell Stark, Helen Schmid, Elizabeth A Holland, David L Duffy, Mingfeng Zhang,[...]. Nat Genet 2011
108
19

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.
Daniel F Gudbjartsson, Patrick Sulem, Simon N Stacey, Alisa M Goldstein, Thorunn Rafnar, Bardur Sigurgeirsson, Kristrun R Benediktsdottir, Kristin Thorisdottir, Rafn Ragnarsson, Steinunn G Sveinsdottir,[...]. Nat Genet 2008
231
17

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
Jiali Han, Peter Kraft, Hongmei Nan, Qun Guo, Constance Chen, Abrar Qureshi, Susan E Hankinson, Frank B Hu, David L Duffy, Zhen Zhen Zhao,[...]. PLoS Genet 2008
321
17

Genome-wide association study identifies five susceptibility loci for glioma.
Sanjay Shete, Fay J Hosking, Lindsay B Robertson, Sara E Dobbins, Marc Sanson, Beatrice Malmer, Matthias Simon, Yannick Marie, Blandine Boisselier, Jean-Yves Delattre,[...]. Nat Genet 2009
585
16

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.
David L Duffy, Zhen Z Zhao, Richard A Sturm, Nicholas K Hayward, Nicholas G Martin, Grant W Montgomery. J Invest Dermatol 2010
126
16

Common sequence variants on 20q11.22 confer melanoma susceptibility.
Kevin M Brown, Stuart Macgregor, Grant W Montgomery, David W Craig, Zhen Zhen Zhao, Kelly Iyadurai, Anjali K Henders, Nils Homer, Megan J Campbell, Mitchell Stark,[...]. Nat Genet 2008
159
16

MC1R variants, melanoma and red hair color phenotype: a meta-analysis.
Sara Raimondi, Francesco Sera, Sara Gandini, Simona Iodice, Saverio Caini, Patrick Maisonneuve, Maria Concetta Fargnoli. Int J Cancer 2008
226
13

Genome-wide association study of tanning phenotype in a population of European ancestry.
Hongmei Nan, Peter Kraft, Abrar A Qureshi, Qun Guo, Constance Chen, Susan E Hankinson, Frank B Hu, Gilles Thomas, Robert N Hoover, Stephen Chanock,[...]. J Invest Dermatol 2009
97
13

Genetic determinants of hair, eye and skin pigmentation in Europeans.
Patrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, Agnar Helgason, Thorunn Rafnar, Kristinn P Magnusson, Andrei Manolescu, Ari Karason, Arnar Palsson, Gudmar Thorleifsson,[...]. Nat Genet 2007
451
13

A common variant on chromosome 9p21 affects the risk of myocardial infarction.
Anna Helgadottir, Gudmar Thorleifsson, Andrei Manolescu, Solveig Gretarsdottir, Thorarinn Blondal, Aslaug Jonasdottir, Adalbjorg Jonasdottir, Asgeir Sigurdsson, Adam Baker, Arnar Palsson,[...]. Science 2007
11

Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a.
Kyoko L Yap, Side Li, Ana M Muñoz-Cabello, Selina Raguz, Lei Zeng, Shiraz Mujtaba, Jesús Gil, Martin J Walsh, Ming-Ming Zhou. Mol Cell 2010
946
11

Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene.
Y Kotake, T Nakagawa, K Kitagawa, S Suzuki, N Liu, M Kitagawa, Y Xiong. Oncogene 2011
706
11

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.
Corine Bertolotto, Fabienne Lesueur, Sandy Giuliano, Thomas Strub, Mahaut de Lichy, Karine Bille, Philippe Dessen, Benoit d'Hayer, Hamida Mohamdi, Audrey Remenieras,[...]. Nature 2011
310
11

Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
Mingfeng Zhang, Fengju Song, Liming Liang, Hongmei Nan, Jiangwen Zhang, Hongliang Liu, Li-E Wang, Qingyi Wei, Jeffrey E Lee, Christopher I Amos,[...]. Hum Mol Genet 2013
74
14

Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma.
Hongmei Nan, Mousheng Xu, Peter Kraft, Abrar A Qureshi, Constance Chen, Qun Guo, Frank B Hu, Gary Curhan, Christopher I Amos, Li-E Wang,[...]. Hum Mol Genet 2011
68
16

Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.
Fan Liu, Mijke Visser, David L Duffy, Pirro G Hysi, Leonie C Jacobs, Oscar Lao, Kaiyin Zhong, Susan Walsh, Lakshmi Chaitanya, Andreas Wollstein,[...]. Hum Genet 2015
71
15

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.
Anna Helgadottir, Gudmar Thorleifsson, Kristinn P Magnusson, Solveig Grétarsdottir, Valgerdur Steinthorsdottir, Andrei Manolescu, Gregory T Jones, Gabriel J E Rinkel, Jan D Blankensteijn, Antti Ronkainen,[...]. Nat Genet 2008
524
10

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.
Michael S Cunnington, Mauro Santibanez Koref, Bongani M Mayosi, John Burn, Bernard Keavney. PLoS Genet 2010
274
10

New common variants affecting susceptibility to basal cell carcinoma.
Simon N Stacey, Patrick Sulem, Gisli Masson, Sigurjon A Gudjonsson, Gudmar Thorleifsson, Margret Jakobsdottir, Asgeir Sigurdsson, Daniel F Gudbjartsson, Bardur Sigurgeirsson, Kristrun R Benediktsdottir,[...]. Nat Genet 2009
246
10

A variant in FTO shows association with melanoma risk not due to BMI.
Mark M Iles, Matthew H Law, Simon N Stacey, Jiali Han, Shenying Fang, Ruth Pfeiffer, Mark Harland, Stuart Macgregor, John C Taylor, Katja K Aben,[...]. Nat Genet 2013
75
13

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
Satoru Yokoyama, Susan L Woods, Glen M Boyle, Lauren G Aoude, Stuart MacGregor, Victoria Zismann, Michael Gartside, Anne E Cust, Rizwan Haq, Mark Harland,[...]. Nature 2011
263
10

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.
Thorunn Rafnar, Patrick Sulem, Simon N Stacey, Frank Geller, Julius Gudmundsson, Asgeir Sigurdsson, Margret Jakobsdottir, Hafdis Helgadottir, Steinunn Thorlacius, Katja K H Aben,[...]. Nat Genet 2009
458
10

An ultraviolet-radiation-independent pathway to melanoma carcinogenesis in the red hair/fair skin background.
Devarati Mitra, Xi Luo, Ann Morgan, Jin Wang, Mai P Hoang, Jennifer Lo, Candace R Guerrero, Jochen K Lennerz, Martin C Mihm, Jennifer A Wargo,[...]. Nature 2012
262
10

Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
Margaret Wrensch, Robert B Jenkins, Jeffrey S Chang, Ru-Fang Yeh, Yuanyuan Xiao, Paul A Decker, Karla V Ballman, Mitchel Berger, Jan C Buckner, Susan Chang,[...]. Nat Genet 2009
359
9

TERT promoter mutations in familial and sporadic melanoma.
Susanne Horn, Adina Figl, P Sivaramakrishna Rachakonda, Christine Fischer, Antje Sucker, Andreas Gast, Stephanie Kadel, Iris Moll, Eduardo Nagore, Kari Hemminki,[...]. Science 2013
9

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes.
David L Duffy, Neil F Box, Wei Chen, James S Palmer, Grant W Montgomery, Michael R James, Nicholas K Hayward, Nicholas G Martin, Richard A Sturm. Hum Mol Genet 2004
191
9

Web-based, participant-driven studies yield novel genetic associations for common traits.
Nicholas Eriksson, J Michael Macpherson, Joyce Y Tung, Lawrence S Hon, Brian Naughton, Serge Saxonov, Linda Avey, Anne Wojcicki, Itsik Pe'er, Joanna Mountain. PLoS Genet 2010
272
9

Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma.
Maryam M Asgari, Wei Wang, Nilah M Ioannidis, Jacqueline Itnyre, Thomas Hoffmann, Eric Jorgenson, Alice S Whittemore. J Invest Dermatol 2016
56
16

Two newly identified genetic determinants of pigmentation in Europeans.
Patrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, Agnar Helgason, Thorunn Rafnar, Margret Jakobsdottir, Stacy Steinberg, Sigurjon A Gudjonsson, Arnar Palsson, Gudmar Thorleifsson,[...]. Nat Genet 2008
239
9

Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma.
Harvind S Chahal, Wenting Wu, Katherine J Ransohoff, Lingyao Yang, Haley Hedlin, Manisha Desai, Yuan Lin, Hong-Ji Dai, Abrar A Qureshi, Wen-Qing Li,[...]. Nat Commun 2016
53
16

Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.
Katherine J Ransohoff, Wenting Wu, Hyunje G Cho, Harvind C Chahal, Yuan Lin, Hong-Ji Dai, Christopher I Amos, Jeffrey E Lee, Jean Y Tang, David A Hinds,[...]. Oncotarget 2017
30
30

Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus.
Olga Jarinova, Alexandre F R Stewart, Robert Roberts, George Wells, Paulina Lau, Thet Naing, Christine Buerki, Bradley W McLean, Richard C Cook, Joel S Parker,[...]. Arterioscler Thromb Vasc Biol 2009
278
8


Genome-wide association study identifies five new breast cancer susceptibility loci.
Clare Turnbull, Shahana Ahmed, Jonathan Morrison, David Pernet, Anthony Renwick, Mel Maranian, Sheila Seal, Maya Ghoussaini, Sarah Hines, Catherine S Healey,[...]. Nat Genet 2010
523
8

Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.
Jennifer H Barrett, John C Taylor, Chloe Bright, Mark Harland, Alison M Dunning, Lars A Akslen, Per A Andresen, Marie-Françoise Avril, Esther Azizi, Giovanna Bianchi Scarrà,[...]. Int J Cancer 2015
21
38

A landscape of driver mutations in melanoma.
Eran Hodis, Ian R Watson, Gregory V Kryukov, Stefan T Arold, Marcin Imielinski, Jean-Philippe Theurillat, Elizabeth Nickerson, Daniel Auclair, Liren Li, Chelsea Place,[...]. Cell 2012
8

IRF4 variants have age-specific effects on nevus count and predispose to melanoma.
David L Duffy, Mark M Iles, Dan Glass, Gu Zhu, Jennifer H Barrett, Veronica Höiom, Zhen Z Zhao, Richard A Sturm, Nicole Soranzo, Chris Hammond,[...]. Am J Hum Genet 2010
89
8


A genomewide association study of skin pigmentation in a South Asian population.
Renee P Stokowski, P V Krishna Pant, Tony Dadd, Amelia Fereday, David A Hinds, Carl Jarman, Wendy Filsell, Rebecca S Ginger, Martin R Green, Frans J van der Ouderaa,[...]. Am J Hum Genet 2007
183
8

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
8

INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis.
Yan Liu, Hanna K Sanoff, Hyunsoon Cho, Christin E Burd, Chad Torrice, Karen L Mohlke, Joseph G Ibrahim, Nancy E Thomas, Norman E Sharpless. PLoS One 2009
195
7

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.
Eleftheria Zeggini, Michael N Weedon, Cecilia M Lindgren, Timothy M Frayling, Katherine S Elliott, Hana Lango, Nicholas J Timpson, John R B Perry, Nigel W Rayner, Rachel M Freathy,[...]. Science 2007
7

Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk.
Christin E Burd, William R Jeck, Yan Liu, Hanna K Sanoff, Zefeng Wang, Norman E Sharpless. PLoS Genet 2010
595
7

ANRIL, a long, noncoding RNA, is an unexpected major hotspot in GWAS.
Eric Pasmant, Audrey Sabbagh, Michel Vidaud, Ivan Bièche. FASEB J 2011
321
7

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color.
Richard A Sturm, David L Duffy, Zhen Zhen Zhao, Fabio P N Leite, Mitchell S Stark, Nicholas K Hayward, Nicholas G Martin, Grant W Montgomery. Am J Hum Genet 2008
223
7

Melanoma genetics: recent findings take us beyond well-traveled pathways.
Matthew H Law, Stuart Macgregor, Nicholas K Hayward. J Invest Dermatol 2012
57
12


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.