A citation-based method for searching scientific literature

Anna Maria Pinto, Francesca Ariani, Laura Bianciardi, Sergio Daga, Alessandra Renieri. Expert Rev Mol Diagn 2016
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity




Asthma Genetics in the Post-GWAS Era.
Carole Ober. Ann Am Thorac Soc 2016
43
20


Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide.
Stephen T Turner, Eric Boerwinkle, Jeffrey R O'Connell, Kent R Bailey, Yan Gong, Arlene B Chapman, Caitrin W McDonough, Amber L Beitelshees, Gary L Schwartz, John G Gums,[...]. Hypertension 2013
70
20


Defining the role of common variation in the genomic and biological architecture of adult human height.
Andrew R Wood, Tonu Esko, Jian Yang, Sailaja Vedantam, Tune H Pers, Stefan Gustafsson, Audrey Y Chu, Karol Estrada, Jian'an Luan, Zoltán Kutalik,[...]. Nat Genet 2014
975
20

Genome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a).
Harshal A Deshmukh, Helen M Colhoun, Toby Johnson, Paul M McKeigue, D John Betteridge, Paul N Durrington, John H Fuller, Shona Livingstone, Valentine Charlton-Menys, Andrew Neil,[...]. J Lipid Res 2012
69
20

Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA study.
Francesca Frau, Roberta Zaninello, Erika Salvi, Maria Francesca Ortu, Daniele Braga, Dinesh Velayutham, Giuseppe Argiolas, Giovanni Fresu, Chiara Troffa, Emanuela Bulla,[...]. Pharmacogenomics 2014
21
20

The clinical pharmacogenetics implementation consortium guideline for SLCO1B1 and simvastatin-induced myopathy: 2014 update.
L B Ramsey, S G Johnson, K E Caudle, C E Haidar, D Voora, R A Wilke, W D Maxwell, H L McLeod, R M Krauss, D M Roden,[...]. Clin Pharmacol Ther 2014
210
20

Genome-based prediction of common diseases: advances and prospects.
A Cecile J W Janssens, Cornelia M van Duijn. Hum Mol Genet 2008
209
20


Polymorphic hydroxylation of Debrisoquine in man.
A Mahgoub, J R Idle, L G Dring, R Lancaster, R L Smith. Lancet 1977
20

Genome-wide association studies in pharmacogenomics: successes and lessons.
Alison A Motsinger-Reif, Eric Jorgenson, Mary V Relling, Deanna L Kroetz, Richard Weinshilboum, Nancy J Cox, Dan M Roden. Pharmacogenet Genomics 2013
90
20



Management and monitoring recommendations for the use of eliglustat in adults with type 1 Gaucher disease in Europe.
Nadia Belmatoug, Maja Di Rocco, Cristina Fraga, Pilar Giraldo, Derralynn Hughes, Elena Lukina, Pierre Maison-Blanche, Martin Merkel, Claus Niederau, Ursula Plӧckinger,[...]. Eur J Intern Med 2017
39
20

Genetic studies of body mass index yield new insights for obesity biology.
Adam E Locke, Bratati Kahali, Sonja I Berndt, Anne E Justice, Tune H Pers, Felix R Day, Corey Powell, Sailaja Vedantam, Martin L Buchkovich, Jian Yang,[...]. Nature 2015
20

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.
Kouichi Ozaki, Yozo Ohnishi, Aritoshi Iida, Akihiko Sekine, Ryo Yamada, Tatsuhiko Tsunoda, Hiroshi Sato, Hideyuki Sato, Masatsugu Hori, Yusuke Nakamura,[...]. Nat Genet 2002
627
20

Pharmacogenomics of human OATP transporters.
Jörg König, Annick Seithel, Ulrike Gradhand, Martin F Fromm. Naunyn Schmiedebergs Arch Pharmacol 2006
256
20

HLA-B*5701 screening for hypersensitivity to abacavir.
Simon Mallal, Elizabeth Phillips, Giampiero Carosi, Jean-Michel Molina, Cassy Workman, Janez Tomazic, Eva Jägel-Guedes, Sorin Rugina, Oleg Kozyrev, Juan Flores Cid,[...]. N Engl J Med 2008
20

A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin.
Giovanna D'Andrea, Rosa Lucia D'Ambrosio, Pasquale Di Perna, Massimiliano Chetta, Rosa Santacroce, Vincenzo Brancaccio, Elvira Grandone, Maurizio Margaglione. Blood 2005
535
20


Common variants in ACYP2 influence susceptibility to cisplatin-induced hearing loss.
Heng Xu, Giles W Robinson, Jie Huang, Joshua Yew-Suang Lim, Hui Zhang, Johnnie K Bass, Alberto Broniscer, Murali Chintagumpala, Ute Bartels, Sri Gururangan,[...]. Nat Genet 2015
71
20

Genotypic Context and Epistasis in Individuals and Populations.
Timothy B Sackton, Daniel L Hartl. Cell 2016
54
20

Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C.
Yasuhito Tanaka, Nao Nishida, Masaya Sugiyama, Masayuki Kurosaki, Kentaro Matsuura, Naoya Sakamoto, Mina Nakagawa, Masaaki Korenaga, Keisuke Hino, Shuhei Hige,[...]. Nat Genet 2009
20

Using principal components of genetic variation for robust and powerful detection of gene-gene interactions in case-control and case-only studies.
Samsiddhi Bhattacharjee, Zhaoming Wang, Julia Ciampa, Peter Kraft, Stephen Chanock, Kai Yu, Nilanjan Chatterjee. Am J Hum Genet 2010
32
20


Common genetic variation and human traits.
David B Goldstein. N Engl J Med 2009
609
20

Hints of hidden heritability in GWAS.
Greg Gibson. Nat Genet 2010
177
20

A gene variant near ATM is significantly associated with metformin treatment response in type 2 diabetes: a replication and meta-analysis of five cohorts.
N van Leeuwen, G Nijpels, M L Becker, H Deshmukh, K Zhou, B H C Stricker, A G Uitterlinden, A Hofman, E van 't Riet, C N A Palmer,[...]. Diabetologia 2012
78
20


Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic.
Stephen T Turner, Kent R Bailey, Brooke L Fridley, Arlene B Chapman, Gary L Schwartz, High Seng Chai, Hugues Sicotte, Jean-Pierre Kocher, Andréi S Rodin, Eric Boerwinkle. Hypertension 2008
80
20


A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.
Gregory M Cooper, Julie A Johnson, Taimour Y Langaee, Hua Feng, Ian B Stanaway, Ute I Schwarz, Marylyn D Ritchie, C Michael Stein, Dan M Roden, Joshua D Smith,[...]. Blood 2008
310
20

Genome-wide association study of warfarin maintenance dose in a Brazilian sample.
Esteban J Parra, Mariana R Botton, Jamila A Perini, S Krithika, Stephane Bourgeois, Todd A Johnson, Tatsuhiko Tsunoda, Munir Pirmohamed, Mia Wadelius, Nita A Limdi,[...]. Pharmacogenomics 2015
19
20

CYP2D6 phenotype-specific codeine population pharmacokinetics.
Oscar A Linares, Jeffrey Fudin, William E Schiesser, Annemarie L Daly Linares, Raymond C Boston. J Pain Palliat Care Pharmacother 2015
15
20

Personalized medicine: temper expectations.
D W Nebert, G Zhang. Science 2012
3
33

Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.
Rudolf Uher, Nader Perroud, Mandy Y M Ng, Joanna Hauser, Neven Henigsberg, Wolfgang Maier, Ole Mors, Anna Placentino, Marcella Rietschel, Daniel Souery,[...]. Am J Psychiatry 2010
235
20



Recovery of divergent avian bornaviruses from cases of proventricular dilatation disease: identification of a candidate etiologic agent.
Amy L Kistler, Ady Gancz, Susan Clubb, Peter Skewes-Cox, Kael Fischer, Katherine Sorber, Charles Y Chiu, Avishai Lublin, Sara Mechani, Yigal Farnoushi,[...]. Virol J 2008
184
20

Defective N-oxidation of sparteine in man: a new pharmacogenetic defect.
M Eichelbaum, N Spannbrucker, B Steincke, H J Dengler. Eur J Clin Pharmacol 1979
591
20

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium.
Megan L Grove, Bing Yu, Barbara J Cochran, Talin Haritunians, Joshua C Bis, Kent D Taylor, Mark Hansen, Ingrid B Borecki, L Adrienne Cupples, Myriam Fornage,[...]. PLoS One 2013
179
20



Characterization of the common genetic defect in humans deficient in debrisoquine metabolism.
F J Gonzalez, R C Skoda, S Kimura, M Umeno, U M Zanger, D W Nebert, H V Gelboin, J P Hardwick, U A Meyer. Nature 1988
644
20


Comprehensive genome-wide evaluation of lapatinib-induced liver injury yields a single genetic signal centered on known risk allele HLA-DRB1*07:01.
L R Parham, L P Briley, L Li, J Shen, P J Newcombe, K S King, A J Slater, A Dilthey, Z Iqbal, G McVean,[...]. Pharmacogenomics J 2016
36
20



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.