| Positional cloning of the APECED gene K Nagamine, P Peterson, HS Scott, J Kudoh, S Minoshima, M Heino, ... Nature genetics 17 (4), 393-398, 1997 | 1391 | 1997 |
| Use of within-array replicate spots for assessing differential expression in microarray experiments GK Smyth, J Michaud, HS Scott Bioinformatics 21 (9), 2067-2075, 2005 | 1388 | 2005 |
| TWEAK, a new secreted ligand in the tumor necrosis factor family that weakly induces apoptosis Y Chicheportiche, PR Bourdon, H Xu, YM Hsu, H Scott, C Hession, ... Journal of Biological Chemistry 272 (51), 32401-32410, 1997 | 831 | 1997 |
| Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia CN Hahn, CE Chong, CL Carmichael, EJ Wilkins, PJ Brautigan, XC Li, ... Nature genetics 43 (10), 1012, 2011 | 497 | 2011 |
| RANK signals from CD4+3− inducer cells regulate development of Aire-expressing epithelial cells in the thymic medulla SW Rossi, MY Kim, A Leibbrandt, SM Parnell, WE Jenkinson, ... The Journal of experimental medicine 204 (6), 1267-1272, 2007 | 448 | 2007 |
| A network-biology perspective of microRNA function and dysfunction in cancer CP Bracken, HS Scott, GJ Goodall Nature Reviews Genetics 17 (12), 719-732, 2016 | 401 | 2016 |
| In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms … J Michaud, F Wu, M Osato, GM Cottles, M Yanagida, N Asou, ... Blood, The Journal of the American Society of Hematology 99 (4), 1364-1372, 2002 | 388 | 2002 |
| Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy MD Lalioti, HS Scott, C Buresi, C Rossier, A Bottani, MA Morris, ... Nature 386 (6627), 847-851, 1997 | 357 | 1997 |
| Meiotic and epigenetic defects in Dnmt3L-knockout mouse spermatogenesis KE Webster, MK O'Bryan, S Fletcher, PE Crewther, U Aapola, J Craig, ... Proceedings of the National Academy of Sciences 102 (11), 4068-4073, 2005 | 324 | 2005 |
| Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22. 3, related to the cytosine-5-methyltransferase 3 gene family U Aapola, K Shibuya, HS Scott, J Ollila, M Vihinen, M Heino, A Shintani, ... Genomics 65 (3), 293-298, 2000 | 324 | 2000 |
| Gene Dosage–limiting Role of Aire in Thymic Expression, Clonal Deletion, and Organ-specific Autoimmunity A Liston, DHD Gray, S Lesage, AL Fletcher, J Wilson, KE Webster, ... The Journal of experimental medicine 200 (8), 1015-1026, 2004 | 313 | 2004 |
| Autoimmune regulator is expressed in the cells regulating immune tolerance in thymus medulla M Heino, P Peterson, J Kudoh, K Nagamine, A Lagerstedt, V Ovod, ... Biochemical and biophysical research communications 257 (3), 821-825, 1999 | 308 | 1999 |
| A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients MC Rosatelli, A Meloni, A Meloni, M Devoto, A Cao, HS Scott, P Peterson, ... Human genetics 103 (4), 428-434, 1998 | 262 | 1998 |
| The autoimmune regulator protein has transcriptional transactivating properties and interacts with the common coactivator CREB-binding protein J Pitkänen, V Doucas, T Sternsdorf, T Nakajima, S Aratani, K Jensen, ... Journal of Biological Chemistry 275 (22), 16802-16809, 2000 | 253 | 2000 |
| A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia S Shah, KA Schrader, E Waanders, AE Timms, J Vijai, C Miething, ... Nature genetics 45 (10), 1226-1231, 2013 | 252 | 2013 |
| Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigen M Alimohammadi, P Björklund, Å Hallgren, N Pöntynen, G Szinnai, ... New England Journal of Medicine 358 (10), 1018-1028, 2008 | 240 | 2008 |
| Autoantigen-specific interactions with CD4+ thymocytes control mature medullary thymic epithelial cell cellularity M Irla, S Hugues, J Gill, T Nitta, Y Hikosaka, IR Williams, FX Hubert, ... Immunity 29 (3), 451-463, 2008 | 233 | 2008 |
| Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness HS Scott, J Kudoh, M Wattenhofer, K Shibuya, A Berry, R Chrast, ... Nature genetics 27 (1), 59-63, 2001 | 233 | 2001 |
| Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature J Kazenwadel, GA Secker, YJ Liu, JA Rosenfeld, RS Wildin, ... Blood 119 (5), 1283-1291, 2012 | 230 | 2012 |
| Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity H Mehenni, C Gehrig, J Nezu, A Oku, M Shimane, C Rossier, N Guex, ... The American Journal of Human Genetics 63 (6), 1641-1650, 1998 | 226 | 1998 |
Stylianos E. AntonarakisProfessor of Genetic Medicine, University of Geneva Medical SchoolEmail verificata su unige.ch
