| 1-31-24 Immune system genes in multiple sclerosis: Genetic association and linkage analyses on TCRβ, IGH, IL-1ra/IL-1β and IFN-γ loci PJ Tienari, K Wansen, T Pastinen, S Kuokkanen, J Wikström, L Peltonen, ... Journal of the Neurological Sciences, S51, 1997 | | 1997 |
| 18. Dysregulation of Non-Cg Methylation by Child Abuse PE Lutz, MA Chay, JF Théroux, T Kwan, A Redensek, N Mechawar, ... Biological Psychiatry 83 (9), S7, 2018 | | 2018 |
| 41 Disclosure of individual genetic data to research participants: the debate reconsidered 48 The cooperative amoeba: Dictyostelium as a model for social evolution JX Zhou, S Huang, PJ Wijchers, W de Laat, J Majewski, T Pastinen | | |
| A cis-acting regulatory variant in the IL2RA locus HQ Qu, DJ Verlaan, B Ge, Y Lu, KCL Lam, R Grabs, E Harmsen, ... The Journal of Immunology 183 (8), 5158-5162, 2009 | 29 | 2009 |
| A common flanking variant is associated with enhanced meiotic stability of the FGF14-SCA27B locus D Pellerin, GD Gobbo, M Couse, E Dolzhenko, MJ Dicaire, A Rebelo, ... Biorxiv, 2023.05. 11.540430, 2023 | 7 | 2023 |
| A common STAT4 risk haplotype for Systemic Lupus Erythematosus is over-expressed, correlates with anti-dsDNA production and shows additive effects with two IRF5 risk alleles GA Eriksson, HHH Göring11, T Pastinen, AC Syvänen, L Rönnblom | | 2008 |
| A fluorescent, multiplex solid-phase minisequencing method for genotyping Cytochrome P450 genes T Pastinen, AC Syvänen, C Moberg, G Sitbon, J Lönngren PCR applications, 521-535, 1999 | 2 | 1999 |
| A genome scan and array-based candidate gene analysis identify loci for hand osteoarthritis. J Leppavuori, T Pastinen, U Kujala, J Kaprio, J Lohiniva, L Ala-Kokko, ... AMERICAN JOURNAL OF HUMAN GENETICS 65 (4), A44-A44, 1999 | | 1999 |
| A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels JB Richards, D Waterworth, S O'Rahilly, MF Hivert, RJF Loos, JRB Perry, ... PLoS genetics 5 (12), e1000768, 2009 | 210 | 2009 |
| A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. C Willenborg, JM Egan, SE Epstein, CM Van Duijn, J Witteman, B Glaser, ... | 1 | 2010 |
| A hidden Markov model for identifying differentially methylated sites in bisulfite sequencing data F Shokoohi, DA Stephens, G Bourque, T Pastinen, CMT Greenwood, ... Biometrics 75 (1), 210-221, 2019 | 16 | 2019 |
| A large-scale whole genome sequence-based analysis discovered novel genetic variants influencing bone mineral density: Results from the GEFOS and UK10K Consortia HF Zheng, V Forgetta, YH Hsu, K Estrada, P Leo, J Tobias, C Kooperberg, ... 29. Annual Meeting of the American-Society-for-Bone-and-Mineral-Research 29, 2014 | 1 | 2014 |
| A low-cost open-source SNP genotyping platform for association mapping applications SJ Macdonald, T Pastinen, A Genissel, TW Cornforth, AD Long Genome biology 6, 1-11, 2005 | 42 | 2005 |
| A mutation map of Finland: Array-based screening of Finnish mutations in population based samples. T Pastinen, P Tainola, AC Syvänen, L Peltonen AMERICAN JOURNAL OF HUMAN GENETICS 65 (4), A45-A45, 1999 | 1 | 1999 |
| A novel and comprehensive testing strategy to identify the genetic etiology of neonatal hypotonia phenotypes JA McQuerry, M Gibson, ST Younger, T Pastinen, EG Farrow | | 2023 |
| A novel statistical method for modeling covariate effects in bisulfite sequencing derived measures of DNA methylation K Zhao, K Oualkacha, L Lakhal-Chaieb, A Labbe, K Klein, A Ciampi, ... Biometrics 77 (2), 424-438, 2021 | 6 | 2021 |
| A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients JL Guéant, C Chéry, A Oussalah, J Nadaf, D Coelho, T Josse, J Flayac, ... Nature Communications 9 (1), 67, 2018 | 84 | 2018 |
| A probabilistic approach for SNP discovery in high-throughput human resequencing data R Hoberman, J Dias, B Ge, E Harmsen, M Mayhew, DJ Verlaan, T Kwan, ... Genome Research 19 (9), 1542-1552, 2009 | 58 | 2009 |
| A Recurrent De Novo Variant in EIF2AK2 Causes a Hypomyelinating Leukodystrophy J Macintosh, I Thiffault, T Pastinen, L Sztriha, G Bernard Child Neurology Open 10, 2329048X231176673, 2023 | | 2023 |
| A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of … S Sigurdsson, G Nordmark, S Garnier, E Grundberg, T Kwan, O Nilsson, ... Human molecular genetics 17 (18), 2868-2876, 2008 | 245 | 2008 |
