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XXX Folefac Aminkeng

rp62345

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Full Name
XXX Folefac Aminkeng
Main Affiliation
 
Faculty
 
Email
mdcfa@nus.edu.sg
 

Publications

Results 1-20 of 43 (Search time: 0.01 seconds).

Issue DateTitleAuthor(s)
116-Oct-2017Association and clinical utility of NAT2 in the prediction of isoniazid-induced liver injury in Singaporean patientsChan, Sze Ling ; Chua, Angeline Poh Gek; Aminkeng, Folefac ; Chee, Cynthia Bin Eng; Jin, Shengnan; Loh, Marie ; Gan, Suay Hong; Wang, Yee Tang ; Brunham, Liam R 
21-Nov-2017Association Between SLC16A5 Genetic Variation and Cisplatin-Induced Ototoxic Effects in Adult Patients With Testicular CancerDrogemoller, Britt I; Monzon, Jose G; Bhavsar, Amit P; Borrie, Adrienne E; Brooks, Beth; Wright, Galen EB; Liu, Geoffrey; Renouf, Daniel J; Kollmannsberger, Christian K; Bedard, Philippe L; Aminkeng, Folefac ; Amstutz, Ursula; Hildebrand, Claudette A; Gunaretnam, Erandika P; Critchley, Carol; Chen, Zhuo; Brunham, Liam R; Hayden, Michael R; Ross, Colin JD; Gelmon, Karen A; Carleton, Bruce C
325-Nov-2015Association between the rs12255372 variant of the TCF7L2 gene and obesity in a Cameroonian population ObesityNgwa, EN; Sobngwi, E; Atogho-Tiedeu, B; Noubiap, JJN; Donfack, OS; Guewo-Fokeng, M; Mofo, EPM; Fosso, PP; Djahmeni, E; Djokam-Dadjeu, R; Evehe, MS; Aminkeng, F ; Mbacham, WF; Mbanya, JC
42015Association between the TCF7L2 rs12255372 (G/T) gene polymorphism and type 2 diabetes mellitus in a Cameroonian population: a pilot study.Nanfa, Dieudonne; Sobngwi, Eugene; Atogho-Tiedeu, Barbara; Noubiap, Jean Jacques N; Donfack, Olivier Sontsa; Mofo, Edith Pascale Mato; Guewo-Fokeng, Magellan; Nguimmo Metsadjio, Aurelie; Ndonwi Ngwa, Elvis; Pokam Fosso, Priscille; Djahmeni, Eric; Djokam-Dadjeu, Rosine; Evehe, Marie-Solange; Aminkeng, Folefac ; Mbacham, Wilfred F; Mbanya, Jean Claude
51-Dec-2010Association of IL-2RA/CD25 with type 1 diabetes in the Belgian populationAminkeng, Folefac ; Weets, Ilse; Van Autreve, Jan E; Koeleman, Bobby PC; Quartier, Erik; Van Schravendijk, Chris; Gorus, Frans K; Van der Auwera, Bart JR
61-Jun-2009Association of KIR2DL2 polymorphism rs2756923 with type 1 diabetes and preliminary evidence for lack of inhibition through HLA-C1 ligand bindingRamos-Lopez, E; Scholten, F; Aminkeng, F ; Wild, C; Kalhes, H; Seidl, C; Tonn, T; Van der Auwera, B; Badenhoop, K
71-Jan-2014Clinical and biological characteristics of diabetic patients under age 40 in Cameroon: Relation to autoantibody status and comparison with Belgian patientsAsanghanwa, Milca; Gorus, Frans K; Weets, Ilse; Auwera, Bart V der; Aminkeng, Folefac ; Mbunwe, Eric; Goubert, Patrick; Verhaeghen, Katrijn; Sobngwi, Eugene; Wenzlau, Janet M; Hutton, John C; Pipeleers, Daniel G; Keymeulen, Bart; Mbanya, Jean-Claude N; van Schravendijk, Chris
81-Aug-2016Clinical Practice Recommendations for the Management and Prevention of Cisplatin-Induced Hearing Loss Using Pharmacogenetic MarkersLee, JW; Pussegoda, K; Rassekh, SR; Monzon, JG; Liu, G; Hwang, S; Bhavsar, AP; Pritchard, S; Ross, CJ; Amstutz, U; Carleton, BC; Hayden, MR; MacLeod, S; Smith, A ; Brunham, L ; Aminkeng, F ; Shear, NH; Koren, G; Ito, S; Madadi, P; Rieder, MJ; Kim, R; Maher, M; Flockhart, D
91-Sep-2015A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancerAminkeng, Folefac ; Bhavsar, Amit P; Visscher, Henk; Rassekh, Shahrad R; Li, Yuling; Lee, Jong W; Brunham, Liam R; Caron, Huib N; van Dalen, Elvira C; Kremer, Leontien C; van der Pal, Helena J; Amstutz, Ursula; Rieder, Michael J; Bernstein, Daniel; Carleton, Bruce C; Hayden, Michael R ; Ross, Colin JD
101-Aug-2018Common variation near IRF6 is associated with IFN-beta-induced liver injury in multiple sclerosisKowalec, Kaarina; Wright, Galen EB; Drogemoller, Britt I; Aminkeng, Folefac ; Bhavsar, Amit P; Kingwell, Elaine; Yoshida, Eric M; Traboulsee, Anthony; Marrie, Ruth Ann; Kremenchutzky, Marcelo; Campbell, Trudy L; Duquette, Pierre; Chalasani, Naga; Wadelius, Mia; Hallberg, Par; Xia, Zongqi; De Jager, Philip L; Denny, Joshua C; Davis, Mary F; Ross, Colin JD; Tremlett, Helen; Carleton, Bruce C
1114-Apr-2015Contribution of the TCF7L2 rs7903146 (C/T) gene polymorphism to the susceptibility to type 2 diabetes mellitus in CameroonGuewo-Fokeng, M; Sobngwi, E; Atogho-Tiedeu, B; Donfack, OS; Noubiap, JJN; Ngwa, EN; Mato-Mofo, EP; Fosso, PP; Djahmeni, E; Djokam-Dadjeu, R; Evehe, MS; Aminkeng, F ; Mbacham, WF; Mbanya, JC
121-Feb-2019CYP2D6 as a treatment decision aid for ER-positive non-metastatic breast cancer patients: a systematic review with accompanying clinical practice guidelinesDrogemoller, Britt I; Wright, Galen EB; Shih, Joanne; Monzon, Jose G; Gelmon, Karen A; Ross, Colin JD; Amstutz, Ursula; Carleton, Bruce C; Chang, Wan C; Connolly, Mary B; Dionne, Francois; Groeneweg, Gabriella; Loucks, Catrina M; MacLeod, Stuart M; Pritchard, Sheila; Rassekh, Shahrad R; Sanatani, Shubhayan; Bhavsar, Amit P; Rieder, Michael J; Shear, Neil H; Ito, Shinya; Liu, Geoffrey; Khayat, Philip; Bernstein, Daniel; Lesko, Lawrence J; Aminkeng, Folefac 
1328-Jan-2022Cytokine Release Syndrome in Cancer Patients Receiving Immune Checkpoint Inhibitors: A Case Series of 25 Patients and Review of the LiteratureTay, Sen Hee ; Toh, Michelle Min Xuan ; Thian, Yee Liang ; Vellayappan, Balamurugan A ; Fairhurst, Anna-Marie ; Chan, Yiong Huak ; Aminkeng, Folefac ; Bharwani, Lavina D; Huang, Yiqing; Mak, Anselm ; Wong, Alvin Seng Cheong
141-Dec-2015DLL4 loss-of-function heterozygous mutations cause Adams-Oliver syndromeAminkeng, F 
151-Sep-2014EIF2AK4 genetic mutations cause a recessive form of rare and deadly lung disease, pulmonary veno-occlusive diseaseAminkeng, F 
161-Jul-2014The emerging era of pharmacogenomics: current successes, future potential, and challengesLee, JW; Aminkeng, F ; Bhavsar, AP; Shaw, K; Carleton, BC; Hayden, MR; Ross, CJD
171-Nov-2017Genetic Variation in SLC16A5 Confers Protection from Cisplatin-Induced Ototoxicity in Adult Testicular Cancer PatientsDrogemoller, Britt; Monzon, Jose; Bhavsar, Amit; Borrie, Adrienne; Brooks, Beth; Wright, Galen; Liu, Geoffrey; Fadhel, Ehab; Renouf, Daniel; Kollmannsberger, Christian; Bedard, Philippe; Aminkeng, Folefac ; Hildebrand, Claudette; Gunaretnam, Erandika; Critchley, Carol; Chen, Zhou; Brunham, Liam; Hayden, Michael; Ross, Colin; Gelmon, Karen; Carleton, Bruce
181-Nov-2017Genome-wide Scan Identifies Association Between an Interferon Regulatory Factor Variant and Interferon-beta Induced Liver Injury in Multiple Sclerosis PatientsKowalec, Kaarina; Wright, Galen EB; Drogemoller, Britt I; Aminkeng, Folefac ; Bhavsar, Amit P; Kingwell, Elaine; Yoshida, Eric M; Traboulsee, Anthony; Marrie, Ruth Ann; Kremenchutzky, Marcelo; Campbell, Trudy L; Duquette, Pierre; Chalasani, Naga; Wadelius, Mia; Hallberg, Par; Xia, Zongqi; De Jager, Philip; Ross, Colin; Tremlett, Helen; Carleton, Bruce
191-Jun-2014GFI1B mutation causes autosomal dominant gray platelet syndromeAminkeng, F 
201-Jan-2013HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotoniaAminkeng, F