| The genetic architecture of type 1 diabetes mellitus DM Nyaga, MH Vickers, C Jefferies, JK Perry, JM O'Sullivan Molecular and cellular endocrinology 477, 70-80, 2018 | 92 | 2018 |
| Type 1 diabetes mellitus-associated genetic variants contribute to overlapping immune regulatory networks DM Nyaga, MH Vickers, C Jefferies, JK Perry, JM O’Sullivan Frontiers in genetics 9, 535, 2018 | 60 | 2018 |
| Assigning function to SNPs: considerations when interpreting genetic variation T Fadason, S Farrow, S Gokuladhas, E Golovina, D Nyaga, JM O’Sullivan, ... Seminars in Cell & Developmental Biology 121, 135-142, 2022 | 25 | 2022 |
| A transcription regulatory network within the ACE2 locus may promote a pro-viral environment for SARS-CoV-2 by modulating expression of host factors T Fadason, S Gokuladhas, E Golovina, D Ho, S Farrow, D Nyaga, H Pan, ... bioRxiv, 2020.04. 14.042002, 2020 | 13 | 2020 |
| Untangling the genetic link between type 1 and type 2 diabetes using functional genomics DM Nyaga, MH Vickers, C Jefferies, T Fadason, JM O’Sullivan Scientific Reports 11 (1), 13871, 2021 | 10 | 2021 |
| Identifying the lungs as a susceptible site for allele-specific regulatory changes associated with type 1 diabetes risk D Ho, DM Nyaga, W Schierding, R Saffery, JK Perry, JA Taylor, ... Communications Biology 4 (1), 1072, 2021 | 4 | 2021 |
| A de novo ACTB gene pathogenic variant in identical twins with phenotypic variation for hydrops and jejunal atresia K Sibbin, P Yap, D Nyaga, R Heller, S Evans, K Strachan, S Alburaiky, ... American Journal of Medical Genetics Part A 188 (4), 1299-1306, 2022 | 3 | 2022 |
| Diagnostic Utility of Genome-wide DNA Methylation Analysis in Genetically Unsolved Developmental and Epileptic Encephalopathies and Refinement of a CHD2 Episignature CW LaFlamme, C Rastin, S Sengupta, HE Pennington, SJ Russ-Hall, ... medRxiv, 2023.10. 11.23296741, 2023 | 2 | 2023 |
| Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy E Banks, V Francis, SJ Lin, F Kharfallah, V Fonov, M Levesque, C Han, ... medRxiv, 2022 | 1 | 2022 |
| SCN8A self‐limited infantile epilepsy: Does epilepsy resolve? E Young, R Harris, N Lieffering, G de Valles‐Ibáñez, D Nyaga, ... Epilepsia, 2024 | | 2024 |
| Leveraging multiple approaches for the detection of pathogenic deep intronic variants in developmental and epileptic encephalopathies: A case report DM Nyaga, MS Hildebrand, G de Valles‐Ibáñez, NF Keenan, Z Ye, ... Epilepsia Open 9 (2), 758-764, 2024 | | 2024 |
| Benchmarking and quality control for nanopore sequencing and feasibility of rapid genomics in New Zealand: validation phase at a single quaternary hospital DM Nyaga, P Tsai, C Gebbie, HH Phua, P Yap, PLQ Stabej, S Farrow, ... medRxiv, 2024.06. 13.24307636, 2024 | | 2024 |
| DENND5A-related developmental and epileptic encephalopathy driven by loss of symmetric cell division of apical neural progenitors E Banks McGill University, 2024 | | 2024 |
| Regulatory networks for single nucleotide polymorphisms in type 1 diabetes mellitus DM Nyaga PhD Thesis-University of Auckland, 2020 | | 2020 |
