| Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ... Cell 180 (3), 568-584. e23, 2020 | 1741 | 2020 |
| Coordinate linkage of HIV evolution reveals regions of immunological vulnerability V Dahirel, K Shekhar, F Pereyra, T Miura, M Artyomov, S Talsania, ... Proceedings of the National Academy of Sciences 108 (28), 11530-11535, 2011 | 221 | 2011 |
| Rare coding variation provides insight into the genetic architecture and phenotypic context of autism JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ... Nature genetics 54 (9), 1320-1331, 2022 | 218* | 2022 |
| Gender disparity and mutation burden in metastatic melanoma S Gupta, M Artomov, W Goggins, M Daly, H Tsao Journal of the National Cancer Institute 107 (11), djv221, 2015 | 137 | 2015 |
| Haplotype sharing provides insights into fine-scale population history and disease in Finland AR Martin, KJ Karczewski, S Kerminen, MI Kurki, AP Sarin, M Artomov, ... The American Journal of Human Genetics 102 (5), 760-775, 2018 | 76 | 2018 |
| A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis H Yu, M Artomov, S Brähler, MC Stander, G Shamsan, MG Sampson, ... The Journal of clinical investigation 126 (3), 1067-1078, 2016 | 69 | 2016 |
| Germline Lysine-Specific Demethylase 1 (LSD1/KDM1A) Mutations Confer Susceptibility to Multiple Myeloma X Wei, MN Calvo-Vidal, S Chen, G Wu, MV Revuelta, J Sun, J Zhang, ... Cancer research 78 (10), 2747-2759, 2018 | 68 | 2018 |
| Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy HO Heyne, M Artomov, F Battke, C Bianchini, DR Smith, N Liebmann, ... Genetics in Medicine 21 (11), 2496-2503, 2019 | 53 | 2019 |
| Burden of unique and low prevalence somatic mutations correlates with cancer survival N Klebanov, M Artomov, WB Goggins, E Daly, MJ Daly, H Tsao Scientific reports 9 (1), 4848, 2019 | 51 | 2019 |
| Enhanced epigenetic profiling of classical human monocytes reveals a specific signature of healthy aging in the DNA methylome I Shchukina, J Bagaitkar, O Shpynov, E Loginicheva, S Porter, ... Nature aging 1 (1), 124-141, 2021 | 38* | 2021 |
| Rare variant, gene-based association study of hereditary melanoma using whole-exome sequencing M Artomov, AJ Stratigos, I Kim, R Kumar, M Lauss, BY Reddy, B Miao, ... JNCI: Journal of the National Cancer Institute 109 (12), djx083, 2017 | 30 | 2017 |
| Use of targeted next-generation sequencing to identify activating hot spot mutations in cherry angiomas N Klebanov, WM Lin, M Artomov, M Shaughnessy, CN Njauw, R Bloom, ... JAMA dermatology 155 (2), 211-215, 2019 | 29 | 2019 |
| Prioritization of disease genes from GWAS using ensemble-based positive-unlabeled learning N Kolosov, MJ Daly, M Artomov European Journal of Human Genetics 29 (10), 1527-1535, 2021 | 25 | 2021 |
| The 22q11. 2 region regulates presynaptic gene-products linked to schizophrenia R Nehme, O Pietiläinen, M Artomov, M Tegtmeyer, V Valakh, L Lehtonen, ... Nature Communications 13 (1), 3690, 2022 | 21 | 2022 |
| Classifying melanoma by TERT promoter mutational status M Shaughnessy, CN Njauw, M Artomov, H Tsao Journal of Investigative Dermatology 140 (2), 390-394. e1, 2020 | 20 | 2020 |
| Cancer risks associated with the germline MITF (E318K) variant SM Guhan, M Artomov, S McCormick, CN Njauw, AJ Stratigos, K Shannon, ... Scientific Reports 10 (1), 17051, 2020 | 19 | 2020 |
| Assessment of genetic variant burden in epilepsy-associated brain lesions LM Niestroj, P May, M Artomov, K Kobow, R Coras, E Pérez-Palma, ... European Journal of Human Genetics 27 (11), 1738-1744, 2019 | 15 | 2019 |
| Mosaic mutations in blood DNA sequence are associated with solid tumor cancers M Artomov, MA Rivas, G Genovese, MJ Daly NPJ Genomic Medicine 2 (1), 22, 2017 | 10 | 2017 |
| Genetic variant in SPDL1 reveals novel mechanism linking pulmonary fibrosis risk and cancer protection JT Koskela, P Häppölä, A Liu, FinnGen, J Partanen, G Genovese, ... medRxiv, 2021.05. 07.21255988, 2021 | 9 | 2021 |
| Case–control analysis identifies shared properties of rare germline variation in cancer predisposing genes M Artomov, V Joseph, G Tiao, T Thomas, K Schrader, RJ Klein, A Kiezun, ... European Journal of Human Genetics 27 (5), 824-828, 2019 | 8* | 2019 |
