A citation-based method for searching scientific literature

Leyre Pernaute-Lau, Ayola Akim Adegnika, Yitian Zhou, Jeannot F Zinsou, Jose Pedro Gil, Sanjeev Krishna, Peter G Kremsner, Volker M Lauschke, Thirumalaisamy P Velavan. Antimicrob Agents Chemother 2021
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity





Prediction of CYP2D6 phenotype from genotype across world populations.
Andrea Gaedigk, Katrin Sangkuhl, Michelle Whirl-Carrillo, Teri Klein, J Steven Leeder. Genet Med 2017
280
50

Genetic variation in the human cytochrome P450 supergene family.
Kohei Fujikura, Magnus Ingelman-Sundberg, Volker M Lauschke. Pharmacogenet Genomics 2015
97
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



A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics.
Clint Mizzi, Eleni Dalabira, Judit Kumuthini, Nduna Dzimiri, Istvan Balogh, Nazli Başak, Ruwen Böhm, Joseph Borg, Paola Borgiani, Nada Bozina,[...]. PLoS One 2016
66
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

Frequencies of clinically important CYP2C19 and CYP2D6 alleles are graded across Europe.
Jelena Petrović, Vesna Pešić, Volker M Lauschke. Eur J Hum Genet 2020
45
33


G6PD Namoru (208 T--> C) is the major polymorphic variant in the tribal populations in southern India.
R Chalvam, M B Mukherjee, R B Colah, D Mohanty, K Ghosh. Br J Haematol 2007
11
33

G6PD deficiency assessment in Freetown, Sierra Leone, reveals further insight into the molecular heterogeneity of G6PD A-.
Amadu Jalloh, Muctarr Jalloh, Idrissa Gamanga, David Baion, Foday Sahr, Aiah Gbakima, Victor R Willoughby, Hiroyuki Matsuoka. J Hum Genet 2008
14
33


ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants.
Najmeh Alirezaie, Kristin D Kernohan, Taila Hartley, Jacek Majewski, Toby Dylan Hocking. Am J Hum Genet 2018
75
33

Prevalence and spectrum of mutations causing G6PD deficiency in Indian populations.
Rati Devendra, Vinodkumar Gupta, Rajasubramaniam Shanmugam, M P S S Singh, Purushottam Patel, Neena Valecha, Neelima Mishra, Naseem Ahmed, S L Hoti, Harsha V Hegde,[...]. Infect Genet Evol 2020
6
33

CADD-Splice-improving genome-wide variant effect prediction using deep learning-derived splice scores.
Philipp Rentzsch, Max Schubach, Jay Shendure, Martin Kircher. Genome Med 2021
128
33

Impact of the method of G6PD deficiency assessment on genetic association studies of malaria susceptibility.
Marla K Johnson, Tamara D Clark, Denise Njama-Meya, Philip J Rosenthal, Sunil Parikh. PLoS One 2009
50
33


Understanding human genetic factors influencing primaquine safety and efficacy to guide primaquine roll-out in a pre-elimination setting in southern Africa.
Shehu S Awandu, Jaishree Raman, Takalani I Makhanthisa, Philip Kruger, John Frean, Teun Bousema, Jandeli Niemand, Lyn-Marie Birkholtz. Malar J 2018
9
33

Red cell glucose-6-phosphate dehydrogenase status and pyruvate kinase activity in a Nigerian population.
J May, C G Meyer, L Grossterlinden, O G Ademowo, F P Mockenhaupt, P E Olumese, A G Falusi, L Luzzatto, U Bienzle. Trop Med Int Health 2000
42
33

The role of the G6PD AEth376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the seerer population of Senegal.
Carla De Araujo, Florence Migot-Nabias, Juliette Guitard, Stéphane Pelleau, Tom Vulliamy, Rolande Ducrocq. Haematologica 2006
43
33

A population survey of the glucose-6-phosphate dehydrogenase (G6PD) 563C>T (Mediterranean) mutation in Afghanistan.
Natsuda Jamornthanyawat, Ghulam R Awab, Naowarat Tanomsing, Sasithon Pukrittayakamee, Fazel Yamin, Arjen M Dondorp, Nicholas P J Day, Nicholas J White, Charles J Woodrow, Mallika Imwong. PLoS One 2014
10
33

Glucose-6-phosphate dehydrogenase (G6PD) mutations in Cambodia: G6PD Viangchan (871G>A) is the most common variant in the Cambodian population.
Hiroyuki Matsuoka, Chea Nguon, Toshio Kanbe, Amadu Jalloh, Hiroko Sato, Shigeto Yoshida, Makoto Hirai, Meiji Arai, Duong Socheat, Fumihiko Kawamoto. J Hum Genet 2005
45
33

Spatial distribution of G6PD deficiency variants across malaria-endemic regions.
Rosalind E Howes, Mewahyu Dewi, Frédéric B Piel, Wuelton M Monteiro, Katherine E Battle, Jane P Messina, Anavaj Sakuntabhai, Ari W Satyagraha, Thomas N Williams, J Kevin Baird,[...]. Malar J 2013
105
33

Prevalence and distribution of glucose-6-phosphate dehydrogenase (G6PD) variants in Thai and Burmese populations in malaria endemic areas of Thailand.
Papichaya Phompradit, Jiraporn Kuesap, Wanna Chaijaroenkul, Ronnatrai Rueangweerayut, Yaowaluck Hongkaew, Rujira Yamnuan, Kesara Na-Bangchang. Malar J 2011
49
33

Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Females from Previously Malaria Endemic Regions in Northeastern Thailand and Identification of a Novel G6PD Variant.
Sumalai Dechyotin, Kittipong Sakunthai, Noppmats Khemtonglang, Supawadee Yamsri, Kanokwan Sanchaisuriya, Kriengkrai Kitcharoen, Suttiphan Kitcharoen. Mediterr J Hematol Infect Dis 2021
4
50

Primaquine-induced haemolysis in females heterozygous for G6PD deficiency.
Cindy S Chu, Germana Bancone, François Nosten, Nicholas J White, Lucio Luzzatto. Malar J 2018
56
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

Genotypes and phenotypes of G6PD deficiency among Indonesian females across diagnostic thresholds of G6PD activity guiding safe primaquine therapy of latent malaria.
Ari Winasti Satyagraha, Arkasha Sadhewa, Lydia Visita Panggalo, Decy Subekti, Iqbal Elyazar, Saraswati Soebianto, Nunung Mahpud, Alida Rosita Harahap, J Kevin Baird. PLoS Negl Trop Dis 2021
5
40

DANN: a deep learning approach for annotating the pathogenicity of genetic variants.
Daniel Quang, Yifei Chen, Xiaohui Xie. Bioinformatics 2015
502
33

Prevalence and molecular characterization of Glucose-6-Phosphate dehydrogenase deficient variants among the Kurdish population of Northern Iraq.
Nasir Al-Allawi, Adil A Eissa, Jaladet Ms Jubrael, Shakir Ar Jamal, Hanan Hamamy. BMC Blood Disord 2010
15
33


Molecular characterization of G6PD mutations reveals the high frequency of G6PD Aures in the Lao Theung population.
Amkha Sanephonasa, Chalisa Louicharoen Cheepsunthorn, Naly Khaminsou, Onekham Savongsy, Issarang Nuchprayoon, Kamonlak Leecharoenkiat. Malar J 2021
6
33

Glucose-6-phosphate dehydrogenase (G6PD) mutations in Myanmar: G6PD Mahidol (487G>A) is the most common variant in the Myanmar population.
Hiroyuki Matsuoka, Jichun Wang, Makoto Hirai, Meiji Arai, Shigeto Yoshida, Tamaki Kobayashi, Amadu Jalloh, Khin Lin, Fumihiko Kawamoto. J Hum Genet 2004
48
33

SIFT: Predicting amino acid changes that affect protein function.
Pauline C Ng, Steven Henikoff. Nucleic Acids Res 2003
33

A DPYD variant (Y186C) in individuals of african ancestry is associated with reduced DPD enzyme activity.
S M Offer, A M Lee, L K Mattison, C Fossum, N J Wegner, R B Diasio. Clin Pharmacol Ther 2013
62
33

Meta-analysis of probability estimates of worldwide variation of CYP2D6 and CYP2C19.
Anne B Koopmans, Mario H Braakman, David J Vinkers, Hans W Hoek, Peter N van Harten. Transl Psychiatry 2021
18
33

Genetic polymorphism of CYP2D6 and CYP2C19 in east- and southern African populations including psychiatric patients.
C Dandara, C M Masimirembwa, A Magimba, J Sayi, S Kaaya, D K Sommers, J R Snyman, J A Hasler. Eur J Clin Pharmacol 2001
64
33

Characterization of the CYP2D6*29 allele commonly present in a black Tanzanian population causing reduced catalytic activity.
A Wennerholm, I Johansson, M Hidestrand, L Bertilsson, L L Gustafsson, M Ingelman-Sundberg. Pharmacogenetics 2001
67
33

Frequent distribution of ultrarapid metabolizers of debrisoquine in an ethiopian population carrying duplicated and multiduplicated functional CYP2D6 alleles.
E Aklillu, I Persson, L Bertilsson, I Johansson, F Rodrigues, M Ingelman-Sundberg. J Pharmacol Exp Ther 1996
307
33

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
33

Pharmacogenetic comparison of CYP2D6 predictive and measured phenotypes in a South African cohort.
T M Dodgen, C De J Labuschagne, A van Schalkwyk, F E Steffens, A Gaedigk, A D Cromarty, M Alessandrini, M S Pepper. Pharmacogenomics J 2016
11
33



Novel Deleterious Dihydropyrimidine Dehydrogenase Variants May Contribute to 5-Fluorouracil Sensitivity in an East African Population.
T Elraiyah, C R Jerde, S Shrestha, R Wu, Q Nie, N H Giama, V Sarangi, L R Roberts, S M Offer, R B Diasio. Clin Pharmacol Ther 2017
26
33

CYP2D6 worldwide genetic variation shows high frequency of altered activity variants and no continental structure.
Johanna Sistonen, Antti Sajantila, Oscar Lao, Jukka Corander, Guido Barbujani, Silvia Fuselli. Pharmacogenet Genomics 2007
274
33

Genetic contribution to variable human CYP3A-mediated metabolism.
Jatinder K Lamba, Yvonne S Lin, Erin G Schuetz, Kenneth E Thummel. Adv Drug Deliv Rev 2002
737
33

Human genetic variation is associated with Plasmodium falciparum drug resistance.
Giacomo M Paganotti, Baba C Gallo, Federica Verra, Bienvenu S Sirima, Issa Nebié, Amidou Diarra, Mario Coluzzi, David Modiano. J Infect Dis 2011
36
33


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.