A citation-based method for searching scientific literature

Christopher Taylor, Ian Crosby, Vincent Yip, Peter Maguire, Munir Pirmohamed, Richard M Turner. Genes (Basel) 2020
Times Cited: 37







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



Times Cited
  Times     Co-cited
Similarity


Metabolism, variability and risk assessment.
J L C M Dorne. Toxicology 2010
49
5

CYP2D6 polymorphism and its impact on the clinical response to metoprolol: A systematic review and meta-analysis.
Maxime Meloche, Michael Khazaka, Imad Kassem, Amina Barhdadi, Marie-Pierre Dubé, Simon de Denus. Br J Clin Pharmacol 2020
12
16

CYP2D6 Genotype-Based Dose Recommendations for Risperidone in Asian People.
Yuanxia Cui, Hao Yan, Yi Su, Lifang Wang, Tianlan Lu, Dai Zhang, Weihua Yue. Front Pharmacol 2020
5
40

CYP2D6 genotype and adjuvant tamoxifen: meta-analysis of heterogeneous study populations.
M A Province, M P Goetz, H Brauch, D A Flockhart, J M Hebert, R Whaley, V J Suman, W Schroth, S Winter, H Zembutsu,[...]. Clin Pharmacol Ther 2014
121
5



Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring.
Alexander Kolevzon, Benjamin Angarita, Lauren Bush, A Ting Wang, Yitzchak Frank, Amy Yang, Robert Rapaport, Jeffrey Saland, Shubhika Srivastava, Cristina Farrell,[...]. J Neurodev Disord 2014
79
5

Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations.
Silvia De Rubeis, Paige M Siper, Allison Durkin, Jordana Weissman, François Muratet, Danielle Halpern, Maria Del Pilar Trelles, Yitzchak Frank, Reymundo Lozano, A Ting Wang,[...]. Mol Autism 2018
75
5

Interstitial 22q13 deletions not involving SHANK3 gene: a new contiguous gene syndrome.
Vittoria Disciglio, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Mafalda Mucciolo, Annabella Marozza, Chiara Di Marco, Antonio Massarelli, Valentina Canocchi, Margherita Baldassarri, Enea Ndoni,[...]. Am J Med Genet A 2014
34
5

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
Latha Soorya, Alexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, Lily Schwartz, Yitzchak Frank, A Ting Wang, Guiqing Cai, Elena Parkhomenko,[...]. Mol Autism 2013
173
5

A framework to identify contributing genes in patients with Phelan-McDermid syndrome.
Anne-Claude Tabet, Thomas Rolland, Marie Ducloy, Jonathan Lévy, Julien Buratti, Alexandre Mathieu, Damien Haye, Laurence Perrin, Céline Dupont, Sandrine Passemard,[...]. NPJ Genom Med 2017
31
6

Clinical Pharmacogenetics Implementation Consortium Guideline for HLA Genotype and Use of Carbamazepine and Oxcarbazepine: 2017 Update.
Elizabeth J Phillips, Chonlaphat Sukasem, Michelle Whirl-Carrillo, Daniel J Müller, Henry M Dunnenberger, Wasun Chantratita, Barry Goldspiel, Yuan-Tsong Chen, Bruce C Carleton, Alfred L George,[...]. Clin Pharmacol Ther 2018
115
5

Clinical and genomic evaluation of 201 patients with Phelan-McDermid syndrome.
Sara M Sarasua, Luigi Boccuto, Julia L Sharp, Alka Dwivedi, Chin-Fu Chen, Jonathan D Rollins, R Curtis Rogers, Katy Phelan, Barbara R DuPont. Hum Genet 2014
93
5

Mitochondrial Dysfunction may explain symptom variation in Phelan-McDermid Syndrome.
Richard E Frye, Devin Cox, John Slattery, Marie Tippett, Stephen Kahler, Doreen Granpeesheh, Shirish Damle, Agustin Legido, Michael J Goldenthal. Sci Rep 2016
30
6

Identification of 22q13 genes most likely to contribute to Phelan McDermid syndrome.
Andrew R Mitz, Travis J Philyaw, Luigi Boccuto, Aleksandr Shcheglovitov, Sara M Sarasua, Walter E Kaufmann, Audrey Thurm. Eur J Hum Genet 2018
29
6

Variability in Phelan-McDermid syndrome: The impact of the PNPLA3 p.I148M polymorphism.
Luigi Boccuto, Ludovico Abenavoli, Lauren Cascio, Sujata Srikanth, Barbara DuPont, Andrew R Mitz, Roger Curtis Rogers, Katy Phelan. Clin Genet 2018
7
28

DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome.
L C Schenkel, E Aref-Eshghi, K Rooney, J Kerkhof, M A Levy, H McConkey, R C Rogers, K Phelan, S M Sarasua, L Jain,[...]. Clin Epigenetics 2021
9
22

Development of a PCR-based strategy for CYP2D6 genotyping including gene multiplication of worldwide potential use.
Pedro Dorado, Macarena Cáceres, Eulalia Pozo-Guisado, Ma-Li Wong, Julio Licinio, Adrián Llerena. Biotechniques 2005
52
5

Targeted Next-Generation Sequencing for Comprehensive Genetic Profiling of Pharmacogenes.
S M Han, J Park, J H Lee, S S Lee, H Kim, H Han, Y Kim, S Yi, J-Y Cho, I-J Jang,[...]. Clin Pharmacol Ther 2017
33
6

A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort.
Kathrin Klein, Roman Tremmel, Stefan Winter, Sarah Fehr, Florian Battke, Tim Scheurenbrand, Elke Schaeffeler, Saskia Biskup, Matthias Schwab, Ulrich M Zanger. Front Genet 2019
23
8

Copy number variants in pharmacogenetic genes.
Yijing He, Janelle M Hoskins, Howard L McLeod. Trends Mol Med 2011
60
5

Population Diversity in Pharmacogenetics: A Latin American Perspective.
Guilherme Suarez-Kurtz, Esteban J Parra. Adv Pharmacol 2018
13
15

DMET™ (Drug Metabolism Enzymes and Transporters): a pharmacogenomic platform for precision medicine.
Mariamena Arbitrio, Maria Teresa Di Martino, Francesca Scionti, Giuseppe Agapito, Pietro Hiram Guzzi, Mario Cannataro, Pierfrancesco Tassone, Pierosandro Tagliaferri. Oncotarget 2016
39
5


PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation.
Adam S Gordon, Robert S Fulton, Xiang Qin, Elaine R Mardis, Deborah A Nickerson, Steve Scherer. Pharmacogenet Genomics 2016
76
5

Pharmacogenetics: from bench to byte--an update of guidelines.
J J Swen, M Nijenhuis, A de Boer, L Grandia, A H Maitland-van der Zee, H Mulder, G A P J M Rongen, R H N van Schaik, T Schalekamp, D J Touw,[...]. Clin Pharmacol Ther 2011
628
5

Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study.
Iris Cohn, Tara A Paton, Christian R Marshall, Raveen Basran, Dimitri J Stavropoulos, Peter N Ray, Nasim Monfared, Robin Z Hayeems, M Stephen Meyn, Sarah Bowdin,[...]. NPJ Genom Med 2017
24
8

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
58
5

Targeted next generation sequencing as a tool for precision medicine.
Markus Gulilat, Tyler Lamb, Wendy A Teft, Jian Wang, Jacqueline S Dron, John F Robinson, Rommel G Tirona, Robert A Hegele, Richard B Kim, Ute I Schwarz. BMC Med Genomics 2019
28
7

Clinical Pharmacogenetics Implementation Consortium guideline for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants.
J K Hicks, J J Swen, C F Thorn, K Sangkuhl, E D Kharasch, V L Ellingrod, T C Skaar, D J Müller, A Gaedigk, J C Stingl. Clin Pharmacol Ther 2013
287
5

CYP450 phenotyping and accurate mass identification of metabolites of the 8-aminoquinoline, anti-malarial drug primaquine.
Brandon S Pybus, Jason C Sousa, Xiannu Jin, James A Ferguson, Robert E Christian, Rebecca Barnhart, Chau Vuong, Richard J Sciotti, Gregory A Reichard, Michael P Kozar,[...]. Malar J 2012
80
5


Determinants of Primaquine and Carboxyprimaquine Exposures in Children and Adults with Plasmodium vivax Malaria.
Cindy S Chu, James A Watson, Aung Pyae Phyo, Htun Htun Win, Widi Yotyingaphiram, Suradet Thinraow, Nay Lin Soe, Aye Aye Aung, Pornpimon Wilaisrisak, Kanokpich Kraft,[...]. Antimicrob Agents Chemother 2021
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
24
8

PharmVar GeneFocus: CYP2C19.
Mariana R Botton, Michelle Whirl-Carrillo, Andria L Del Tredici, Katrin Sangkuhl, Larisa H Cavallari, José A G Agúndez, Jorge Duconge, Ming Ta Michael Lee, Erica L Woodahl, Karla Claudio-Campos,[...]. Clin Pharmacol Ther 2021
27
7

Pharmacogene Variation Consortium: A Global Resource and Repository for Pharmacogene Variation.
Andrea Gaedigk, Scott T Casey, Michelle Whirl-Carrillo, Neil A Miller, Teri E Klein. Clin Pharmacol Ther 2021
10
20

Pharmacogenetics of antidepressants and antipsychotics: the contribution of allelic variations to the phenotype of drug response.
J Kirchheiner, K Nickchen, M Bauer, M-L Wong, J Licinio, I Roots, J Brockmöller. Mol Psychiatry 2004
498
5

What is precision medicine?
Inke R König, Oliver Fuchs, Gesine Hansen, Erika von Mutius, Matthias V Kopp. Eur Respir J 2017
124
5

Cancer Statistics, 2021.
Rebecca L Siegel, Kimberly D Miller, Hannah E Fuchs, Ahmedin Jemal. CA Cancer J Clin 2021
5

Distribution of CYP2D6 alleles and phenotypes in the Brazilian population.
Deise C Friedrich, Júlia P Genro, Vinicius A Sortica, Guilherme Suarez-Kurtz, Maria Elizabete de Moraes, Sergio D J Pena, Andrea K Ribeiro dos Santos, Marco A Romano-Silva, Mara H Hutz. PLoS One 2014
37
5

Tafenoquine versus Primaquine to Prevent Relapse of Plasmodium vivax Malaria.
Alejandro Llanos-Cuentas, Marcus V G Lacerda, Tran T Hien, Iván D Vélez, Chayadol Namaik-Larp, Cindy S Chu, Maria F Villegas, Fernando Val, Wuelton M Monteiro, Marcelo A M Brito,[...]. N Engl J Med 2019
101
5


A review of the metabolism and pharmacokinetics of paroxetine in man.
C M Kaye, R E Haddock, P F Langley, G Mellows, T C Tasker, B D Zussman, W H Greb. Acta Psychiatr Scand Suppl 1989
220
2

The expanding GRK interactome: Implications in cardiovascular disease and potential for therapeutic development.
Jonathan Hullmann, Christopher J Traynham, Ryan C Coleman, Walter J Koch. Pharmacol Res 2016
45
2

Crystal structure of human cytochrome P450 2D6.
Paul Rowland, Frank E Blaney, Martin G Smyth, Jo J Jones, Vaughan R Leydon, Amanda K Oxbrow, Ceri J Lewis, Mike G Tennant, Sandeep Modi, Drake S Eggleston,[...]. J Biol Chem 2006
338
2


G protein-coupled receptor kinase 2 ablation in cardiac myocytes before or after myocardial infarction prevents heart failure.
Philip W Raake, Leif E Vinge, Erhe Gao, Matthieu Boucher, Giuseppe Rengo, Xiongwen Chen, Brent R DeGeorge, Scot Matkovich, Steven R Houser, Patrick Most,[...]. Circ Res 2008
170
2

Paroxetine: current status in psychiatry.
Chi-Un Pae, Ashwin A Patkar. Expert Rev Neurother 2007
28
3


Ebola outbreak in Western Africa 2014: what is going on with Ebola virus?
Woonsung Na, Nanuri Park, Minju Yeom, Daesub Song. Clin Exp Vaccine Res 2015
24
4


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.