PDGFRB mutation causes autosomal-dominant Penttinen syndrome

by Aminkeng, F
Published 2022

DLL4 loss-of-function heterozygous mutations cause Adams-Oliver syndrome

by Aminkeng, F
Published 2022

EIF2AK4 genetic mutations cause a recessive form of rare and deadly lung disease, pulmonary veno-occlusive disease

by Aminkeng, F
Published 2022

Using pharmacogenetics in real time to guide therapy: the warfarin example

by Aminkeng, F
Published 2022

GFI1B mutation causes autosomal dominant gray platelet syndrome

by Aminkeng, F
Published 2022

WDR45 mutations define a novel disease entity - Static Encephalopathy of Childhood with Neurodegeneration in Adulthood

by Aminkeng, F
Published 2022

KCNT1 mutations in ADNFLE and MMPSI: a new driver in the etiology and pathophysiology of early-onset epileptic syndromes

by Aminkeng, F
Published 2022

Mutations in ATP1A3 cause alternating hemiplegia of childhood

by Aminkeng, F
Published 2022

HINT1 mutations define a novel disease entity - autosomal recessive axonal neuropathy with neuromyotonia

by Aminkeng, F
Published 2022

The emerging era of pharmacogenomics: current successes, future potential, and challenges

by Lee, JW, Aminkeng, F, Bhavsar, AP, Shaw, K, Carleton, BC, Hayden, MR, Ross, CJD
Published 2022

Risk Factors for Immune-Related Adverse Events from Anti-PD-1/PD-L1 Treatment in an Asian Cohort of NSCLC Patients

by Huang, Y, Soon, YY, Aminkeng, F, Tay, SH, Ang, Y, Goh, BC, Wong, A, Soo, RA
Published 2023

Association of KIR2DL2 polymorphism rs2756923 with type 1 diabetes and preliminary evidence for lack of inhibition through HLA-C1 ligand binding

by Ramos-Lopez, E, Scholten, F, Aminkeng, F, Wild, C, Kalhes, H, Seidl, C, Tonn, T, Van der Auwera, B, Badenhoop, K
Published 2022

Factors Predictive of Primary Resistance to Immune Checkpoint Inhibitors in Asian Patients with Advanced NSCLC

by Huang, Y, Zhao, JJ, Soon, YY, Kee, A, Tay, SH, Aminkeng, F, Ang, Y, Wong, A, Goh, BC, Soo, R
Published 2023

Neither an intronic CA repeat within the CD48 gene nor the HERV-K18 polymorphisms are associated with type 1 diabetes

by Ramos-Lopez, E, Ghebru, S, Van Autreve, J, Aminkeng, F, Herwig, J, Seifried, E, Seidl, C, Van der Auwera, B, Badenhoop, K
Published 2022

Association between the rs12255372 variant of the TCF7L2 gene and obesity in a Cameroonian population Obesity

by Ngwa, 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
Published 2022

Contribution of the TCF7L2 rs7903146 (C/T) gene polymorphism to the susceptibility to type 2 diabetes mellitus in Cameroon

by Guewo-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
Published 2022

Pharmacogenomic diversity in Singaporean populations and Europeans

by Brunham, LR, Chan, SL, Li, R, Aminkeng, F, Liu, X, Saw, WY, Ong, RTH, Pillai, EN, Carleton, BC, Toh, D, Tan, SH, Koo, SH, Lee, EJD, Chia, KS, Ross, CJD, Hayden, MR, Sung, C, Teo, YY
Published 2022

Unbiased Profiling of Isogenic Huntington Disease hPSC-Derived CNS and Peripheral Cells Reveals Strong Cell-Type Specificity of CAG Length Effects

by Ooi, J., Langley, S.R., Xu, X., Utami, K.H., Sim, B., Huang, Y., Harmston, N.P., Tay, Y.L., Ziaei, A., Zeng, R., Low, D., Aminkeng, F., Sobota, R.M., Ginhoux, F., Petretto, E., Pouladi, M.A.
Published 2021

Clinical Practice Recommendations for the Management and Prevention of Cisplatin-Induced Hearing Loss Using Pharmacogenetic Markers

by Lee, 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
Published 2022