| Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study R Guerreiro, OA Ross, C Kun-Rodrigues, DG Hernandez, T Orme, ... The Lancet Neurology 17 (1), 64-74, 2018 | 267 | 2018 |
| Human induced pluripotent stem cell-derived microglia-like cells harboring TREM2 missense mutations show specific deficits in phagocytosis P Garcia-Reitboeck, A Phillips, TM Piers, C Villegas-Llerena, M Butler, ... Cell Reports 24 (9), 2300-2311, 2018 | 159 | 2018 |
| Habitat fragmentation and genetic diversity in natural populations of the Bornean elephant: Implications for conservation B Goossens, R Sharma, N Othman, C Kun-Rodrigues, R Sakong, ... Biological Conservation 196, 80-92, 2016 | 74 | 2016 |
| New density estimates of a threatened sifaka species (Propithecus coquereli) in Ankarafantsika National Park C Kun‐Rodrigues, J Salmona, A Besolo, E Rasolondraibe, C Rabarivola, ... American Journal of Primatology 76 (6), 515-528, 2014 | 52 | 2014 |
| A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease C Kun-Rodrigues, C Ganos, R Guerreiro, SA Schneider, C Schulte, ... Human Molecular Genetics 24 (23), 6711-6720, 2015 | 50 | 2015 |
| Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies T Orme, D Hernandez, OA Ross, C Kun-Rodrigues, L Darwent, ... Acta Neuropathologica Communications 8, 1-11, 2020 | 45 | 2020 |
| Genetic architecture of common non-Alzheimer’s disease dementias R Guerreiro, E Gibbons, M Tábuas-Pereira, C Kun-Rodrigues, GC Santo, ... Neurobiology of disease 142, 104946, 2020 | 43 | 2020 |
| The Chihuahua dog: A new animal model for neuronal ceroid lipofuscinosis CLN7 disease? KME Faller, J Bras, SJ Sharpe, GW Anderson, L Darwent, ... Journal of Neuroscience Research 94 (4), 339-347, 2016 | 39 | 2016 |
| Heritability and genetic variance of dementia with Lewy bodies R Guerreiro, V Escott-Price, DG Hernandez, C Kun-Rodrigues, OA Ross, ... Neurobiology of disease 127, 492-501, 2019 | 35 | 2019 |
| Two different high throughput sequencing approaches identify thousands of de novo genomic markers for the genetically depleted Bornean elephant R Sharma, B Goossens, C Kun-Rodrigues, T Teixeira, N Othman, ... PLoS One 7 (11), e49533, 2012 | 32 | 2012 |
| Clinical, ocular motor, and imaging profile of Niemann-Pick type C heterozygosity T Bremova-Ertl, C Sztatecsny, M Brendel, M Moser, B Möller, DA Clevert, ... Neurology 94 (16), e1702-e1715, 2020 | 29 | 2020 |
| Genetic Differentiation and Demographic History of the Northern Rufous Mouse Lemur (Microcebus tavaratra) Across a Fragmented Landscape in Northern … GM Sgarlata, J Salmona, I Aleixo-Pais, A Rakotonanahary, AP Sousa, ... International Journal of Primatology 39, 65-89, 2018 | 24 | 2018 |
| The genetic structure of a mouse lemur living in a fragmented habitat in Northern Madagascar I Aleixo-Pais, J Salmona, GM Sgarlata, A Rakotonanahary, AP Sousa, ... Conservation Genetics 20, 229-243, 2019 | 20 | 2019 |
| A comprehensive screening of copy number variability in dementia with Lewy bodies C Kun-Rodrigues, T Orme, S Carmona, DG Hernandez, OA Ross, ... Neurobiology of aging 75, 223. e1-223. e10, 2019 | 20 | 2019 |
| Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies C Kun-Rodrigues, OA Ross, T Orme, C Shepherd, L Parkkinen, L Darwent, ... Neurobiology of aging 49, 214. e13-214. e15, 2017 | 20 | 2017 |
| LRP10 in α-synucleinopathies DA Kia, MS Sabir, S Ahmed, J Trinh, S Bandres-Ciga, AJ Noyce, ... The Lancet Neurology 17 (12), 1032, 2018 | 18 | 2018 |
| Genetic Diversity, Population Size, and Conservation of the Critically Endangered Perrier’s Sifaka (Propithecus perrieri) J Salmona, H Teixeira, E Rasolondraibe, I Aleixo-Pais, C Kun-Rodrigues, ... International Journal of Primatology 36, 1132-1153, 2015 | 17 | 2015 |
| CYLD variants in frontotemporal dementia associated with severe memory impairment in a Portuguese cohort M Tábuas-Pereira, I Santana, C Kun-Rodrigues, J Bras, R Guerreiro Brain 143 (8), e67-e67, 2020 | 14 | 2020 |
| Whole-exome sequencing of Finnish patients with vascular cognitive impairment S Mönkäre, L Kuuluvainen, C Kun-Rodrigues, S Carmona, J Schleutker, ... European Journal of Human Genetics 29 (4), 663-671, 2021 | 11 | 2021 |
| Mutations in TYROBP are not a common cause of dementia in a Turkish cohort L Darwent, S Carmona, E Lohmann, G Guven, C Kun-Rodrigues, B Bilgic, ... Neurobiology of aging 58, 240. e1-240. e3, 2017 | 11 | 2017 |
