A citation-based method for searching scientific literature

Maria-Theodora Pandi, Maria Koromina, Iordanis Tsafaridis, Sotirios Patsilinakos, Evangelos Christoforou, Peter J van der Spek, George P Patrinos. Hum Genomics 2021
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity



Key challenges for next-generation pharmacogenomics: Science & Society series on Science and Drugs.
Kostas Kampourakis, Effy Vayena, Christina Mitropoulou, Ron H van Schaik, David N Cooper, Joseph Borg, George P Patrinos. EMBO Rep 2014
30
50

Integrating rare genetic variants into pharmacogenetic drug response predictions.
Magnus Ingelman-Sundberg, Souren Mkrtchian, Yitian Zhou, Volker M Lauschke. Hum Genomics 2018
105
50

Rare genetic variability in human drug target genes modulates drug response and can guide precision medicine.
Yitian Zhou, Gabriel Herras Arribas, Ainoleena Turku, Tuuli Jürgenson, Souren Mkrtchian, Kristi Krebs, Yi Wang, Barbora Svobodova, Lili Milani, Gunnar Schulte,[...]. Sci Adv 2021
8
50


Computational Methods for the Pharmacogenetic Interpretation of Next Generation Sequencing Data.
Yitian Zhou, Kohei Fujikura, Souren Mkrtchian, Volker M Lauschke. Front Pharmacol 2018
42
50


An optimized prediction framework to assess the functional impact of pharmacogenetic variants.
Yitian Zhou, Souren Mkrtchian, Masaki Kumondai, Masahiro Hiratsuka, Volker M Lauschke. Pharmacogenomics J 2019
67
50

The Ensembl Variant Effect Predictor.
William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016
33

Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network (SEAPharm).
Chakkaphan Runcharoen, Koya Fukunaga, Insee Sensorn, Nareenart Iemwimangsa, Sommon Klumsathian, Hang Tong, Nam Sy Vo, Ly Le, Tin Maung Hlaing, Myo Thant,[...]. Hum Genome Var 2021
13
33

Unveiling the guidance heterogeneity for genome-informed drug treatment interventions among regulatory bodies and research consortia.
Stefania Koutsilieri, Foteini Tzioufa, Despoina-Christina Sismanoglou, George P Patrinos. Pharmacol Res 2020
20
33

Pharmacogenomics of GPCR Drug Targets.
Alexander S Hauser, Sreenivas Chavali, Ikuo Masuho, Leonie J Jahn, Kirill A Martemyanov, David E Gloriam, M Madan Babu. Cell 2018
299
33

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
33

Clinical implementation of drug metabolizing gene-based therapeutic interventions worldwide.
Evangelia Eirini Tsermpini, Zeina N Al-Mahayri, Bassam R Ali, George P Patrinos. Hum Genet 2022
4
50



Pharmacogenetics Guidelines: Overview and Comparison of the DPWG, CPIC, CPNDS, and RNPGx Guidelines.
Heshu Abdullah-Koolmees, Antonius M van Keulen, Marga Nijenhuis, Vera H M Deneer. Front Pharmacol 2021
39
33



The global spectrum of protein-coding pharmacogenomic diversity.
G E B Wright, B Carleton, M R Hayden, C J D Ross. Pharmacogenomics J 2018
51
33

Pharmacogenomic Biomarkers for Improved Drug Therapy-Recent Progress and Future Developments.
Volker M Lauschke, Lili Milani, Magnus Ingelman-Sundberg. AAPS J 2017
78
33


Heritability of metoprolol and torsemide pharmacokinetics.
J Matthaei, J Brockmöller, M V Tzvetkov, D Sehrt, C Sachse-Seeboth, J B Hjelmborg, S Möller, U Halekoh, U Hofmann, M Schwab,[...]. Clin Pharmacol Ther 2015
41
33

Toward predicting CYP2D6-mediated variable drug response from CYP2D6 gene sequencing data.
Maaike van der Lee, William G Allard, Rolf H A M Vossen, Renée F Baak-Pablo, Roberta Menafra, Birgit A L M Deiman, Maarten J Deenen, Patrick Neven, Inger Johansson, Stefano Gastaldello,[...]. Sci Transl Med 2021
19
33

Transfer learning enables prediction of CYP2D6 haplotype function.
Gregory McInnes, Rachel Dalton, Katrin Sangkuhl, Michelle Whirl-Carrillo, Seung-Been Lee, Philip S Tsao, Andrea Gaedigk, Russ B Altman, Erica L Woodahl. PLoS Comput Biol 2020
18
33

Long-read human genome sequencing and its applications.
Glennis A Logsdon, Mitchell R Vollger, Evan E Eichler. Nat Rev Genet 2020
224
33

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people.
Matthew R Nelson, Daniel Wegmann, Margaret G Ehm, Darren Kessner, Pamela St Jean, Claudio Verzilli, Judong Shen, Zhengzheng Tang, Silviu-Alin Bacanu, Dana Fraser,[...]. Science 2012
468
33

Ethnogeographic and inter-individual variability of human ABC transporters.
Qingyang Xiao, Yitian Zhou, Volker M Lauschke. Hum Genet 2020
28
33


Genetic variation in human drug-related genes.
Charlotta Pauline Irmgard Schärfe, Roman Tremmel, Matthias Schwab, Oliver Kohlbacher, Debora Susan Marks. Genome Med 2017
62
33

Gene-Specific Variant Classifier (DPYD-Varifier) to Identify Deleterious Alleles of Dihydropyrimidine Dehydrogenase.
Shikshya Shrestha, Cheng Zhang, Calvin R Jerde, Qian Nie, Hu Li, Steven M Offer, Robert B Diasio. Clin Pharmacol Ther 2018
30
33

Evaluation of Current Regulation and Guidelines of Pharmacogenomic Drug Labels: Opportunities for Improvements.
Rawan Shekhani, Linda Steinacher, Jesse J Swen, Magnus Ingelman-Sundberg. Clin Pharmacol Ther 2020
35
33


A quantitative analysis of the mass media coverage of genomics medicine in China: a call for science journalism in the developing world.
Feifei Zhao, Yan Chen, Siqi Ge, Xinwei Yu, Shuang Shao, Michael Black, Youxin Wang, Jie Zhang, Manshu Song, Wei Wang. OMICS 2014
13
16

Realities and expectations of pharmacogenomics and personalized medicine: impact of translating genetic knowledge into clinical practice.
Alessio Squassina, Mirko Manchia, Vangelis G Manolopoulos, Mehmet Artac, Christina Lappa-Manakou, Sophia Karkabouna, Konstantinos Mitropoulos, Maria Del Zompo, George P Patrinos. Pharmacogenomics 2010
84
16

Critical appraisal of the views of healthcare professionals with respect to pharmacogenomics and personalized medicine in Greece.
Yuan Mai, Christina Mitropoulou, Xanthi E Papadopoulou, Athanassios Vozikis, David N Cooper, Ron H van Schaik, George P Patrinos. Per Med 2014
27
16


Ascertainment and critical assessment of the views of the general public and healthcare professionals on nutrigenomics in Greece.
Cristiana Pavlidis, Angeliki Karamitri, Aglaia Barakou, David N Cooper, Konstantinos Poulas, Stavros Topouzis, George P Patrinos. Per Med 2012
16
16

Genetic tests obtainable through pharmacies: the good, the bad, and the ugly.
George P Patrinos, Darrol J Baker, Fahd Al-Mulla, Vasilis Vasiliou, David N Cooper. Hum Genomics 2013
26
16

Whole genome sequencing in pharmacogenomics.
Theodora Katsila, George P Patrinos. Front Pharmacol 2015
27
16


Nutrigenomics: A controversy.
Cristiana Pavlidis, George P Patrinos, Theodora Katsila. Appl Transl Genom 2015
9
16

Assessment of the pharmacogenomics educational environment in Southeast Europe.
Claudia Pisanu, Evangelia-Eirini Tsermpini, Eirini Mavroidi, Theodora Katsila, George P Patrinos, Alessio Squassina. Public Health Genomics 2014
28
16

A critical view of the general public's awareness and physicians' opinion of the trends and potential pitfalls of genetic testing in Greece.
Yuan Mai, Theodora Koromila, Aggeliki Sagia, David N Cooper, Georgios Vlachopoulos, George Lagoumintzis, Panagoula Kollia, Konstantinos Poulas, Vlassios Stathakopoulos, George P Patrinos. Per Med 2011
36
16

Impact of biobanks on research outcomes in rare diseases: a systematic review.
Monique Garcia, Jenny Downs, Alyce Russell, Wei Wang. Orphanet J Rare Dis 2018
17
16

Current needs for human and medical genomics research infrastructure in low and middle income countries.
Diego A Forero, Ambroise Wonkam, Wei Wang, Paul Laissue, Catalina López-Correa, Juan C Fernández-López, Raja Mugasimangalam, George Perry. J Med Genet 2016
12
16

Continuous pharmacogenomics and genomic medicine education for healthcare professionals through electronic educational courses.
Evangelia-Eirini Tsermpini, Theano Stamopoulou, Zoe Kordou, Evaggelia Barba, Stavroula Siamoglou, Andreas Stathoulias, George P Patrinos. Per Med 2019
6
16

Precision Medicine and Rare Genetic Variants.
Volker M Lauschke, Magnus Ingelman-Sundberg. Trends Pharmacol Sci 2016
43
16


How to Consider Rare Genetic Variants in Personalized Drug Therapy.
Volker M Lauschke, Magnus Ingelman-Sundberg. Clin Pharmacol Ther 2018
28
16


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.