| Population genomics of picophytoplankton unveils novel chromosome hypervariability R Blanc-Mathieu, M Krasovec, M Hebrard, S Yau, E Desgranges, J Martin, ... Science Advances 3 (7), e1700239, 2017 | 86 | 2017 |
| Mutations in IMPG1 cause vitelliform macular dystrophies G Manes, I Meunier, A Avila-Fernández, S Banfi, G Le Meur, X Zanlonghi, ... The American Journal of Human Genetics 93 (3), 571-578, 2013 | 80 | 2013 |
| Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations B Bocquet, N al Dain Marzouka, M Hebrard, G Manes, A Sénéchal, ... Molecular vision 19, 2487, 2013 | 64 | 2013 |
| Recessive mutations in RTN4IP1 cause isolated and syndromic optic neuropathies C Angebault, PO Guichet, Y Talmat-Amar, M Charif, S Gerber, ... The American Journal of Human Genetics 97 (5), 754-760, 2015 | 61 | 2015 |
| Relative frequencies of inherited retinal dystrophies and optic neuropathies in Southern France: assessment of 21-year data management B Bocquet, A Lacroux, MO Surget, C Baudoin, V Marquette, G Manes, ... Ophthalmic epidemiology 20 (1), 13-25, 2013 | 61 | 2013 |
| Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability C Angebault, M Charif, N Guegen, C Piro-Megy, B Mousson de Camaret, ... Human molecular genetics 24 (14), 3948-3955, 2015 | 48 | 2015 |
| Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families M Hebrard, G Manes, B Bocquet, I Meunier, D Coustes-Chazalette, ... European journal of human genetics 19 (12), 1256-1263, 2011 | 30 | 2011 |
| Transcriptomic study of Salmonella enterica subspecies enterica serovar Typhi biofilm KCJ Chin, TD Taylor, M Hebrard, K Anbalagan, MG Dashti, KK Phua BMC genomics 18, 1-9, 2017 | 24 | 2017 |
| ScripTree: scripting phylogenetic graphics F Chevenet, O Croce, M Hebrard, R Christen, V Berry Bioinformatics 26 (8), 1125-1126, 2010 | 19 | 2010 |
| The Singapore national precision medicine strategy E Wong, N Bertin, M Hebrard, R Tirado-Magallanes, C Bellis, WK Lim, ... Nature Genetics 55 (2), 178-186, 2023 | 18 | 2023 |
| Analysis of clinically relevant variants from ancestrally diverse Asian genomes SH Chan, Y Bylstra, JX Teo, JL Kuan, N Bertin, M Gonzalez-Porta, ... Nature Communications 13 (1), 6694, 2022 | 17 | 2022 |
| EHMT2 epigenetically suppresses Wnt signaling and is a potential target in embryonal rhabdomyosarcoma A Pal, JY Leung, GCK Ang, VK Rao, L Pignata, HJ Lim, M Hebrard, ... Elife 9, e57683, 2020 | 17 | 2020 |
| A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1 G Manes, M Hebrard, B Bocquet, I Meunier, D Coustes-Chazalette, ... BMC Medical Genetics 12, 1-8, 2011 | 9 | 2011 |
| Metatreemap: An alternative visualization method for displaying metagenomic phylogenic trees M Hebrard, TD Taylor PloS one 11 (6), e0158261, 2016 | 6 | 2016 |
| SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasion G Leuzzi, A Vasciaveo, A Taglialatela, X Chen, TM Firestone, ... Cell 187 (4), 861-881. e32, 2024 | 2 | 2024 |
| A five-safes approach to a secure and scalable genomics data repository CC Shih, J Chen, AS Lee, N Bertin, M Hebrard, CC Khor, Z Li, JHJ Tan, ... Iscience 26 (4), 2023 | 1 | 2023 |
| Abstract PR009: SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasion G Leuzzi, A Vasciaveo, A Taglialatela, X Chen, TM Firestone, ... Cancer Research 84 (1_Supplement), PR009-PR009, 2024 | | 2024 |
| A Catalogue of Structural Variation across Ancestrally Diverse Asian Genomes N Bertin, J Tan, Z Li, M Gonzalez-Porta, R Rajaby, R Jimenez, WK Lim, ... | | 2023 |
| Genomic landscape of drug binding and pharmacogenetic variation across diverse populations using SNPdrug3D S Maurer-Stroh, A Malik, D Kenanov, CS Chong, MB Ozturk, M Hebrard, ... | | 2023 |
| RAPTOR: A Five-Safes approach to a secure, cloud native and serverless genomics data repository CC Shih, J Chen, AS Lee, N Bertin, M Hebrard, CC Khor, Z Li, ... bioRxiv, 2022.10. 27.514127, 2022 | | 2022 |
