| Pituitary Adenoma Predisposition Caused by Germline Mutations in the AIP Gene O Vierimaa, M Georgitsi, R Lehtonen, P Vahteristo, A Kokko, A Raitila, ... Science 312 (5777), 1228-1230, 2006 | 672 | 2006 |
| Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin J Borg, P Papadopoulos, M Georgitsi, L Gutiérrez, G Grech, P Fanis, ... Nature genetics 42 (9), 801-805, 2010 | 449 | 2010 |
| Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study AF Daly, MA Tichomirowa, P Petrossians, E Heliovaara, ML Jaffrain-Rea, ... The Journal of Clinical Endocrinology & Metabolism 95 (11), E373-E383, 2010 | 396 | 2010 |
| Germline CDKN1B/p27Kip1 Mutation in Multiple Endocrine Neoplasia M Georgitsi, A Raitila, A Karhu, RB van der Luijt, CM Aalfs, T Sane, ... The Journal of Clinical Endocrinology & Metabolism 92 (8), 3321-3325, 2007 | 324 | 2007 |
| Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations M Georgitsi, A Raitila, A Karhu, K Tuppurainen, MJ Mäkinen, O Vierimaa, ... Proceedings of the National Academy of Sciences 104 (10), 4101-4105, 2007 | 196 | 2007 |
| Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach B Giardine, J Borg, DR Higgs, KR Peterson, S Philipsen, D Maglott, ... Nature genetics 43 (4), 295-301, 2011 | 185 | 2011 |
| De novo sequence and copy number variants are strongly associated with tourette disorder and implicate cell polarity in pathogenesis S Wang, JD Mandell, Y Kumar, N Sun, MT Morris, J Arbelaez, C Nasello, ... Cell reports 24 (13), 3441-3454. e12, 2018 | 117 | 2018 |
| Evidence for association of an ACCN1 gene variant with response to lithium treatment in Sardinian patients with bipolar disorder A Squassina, M Manchia, J Borg, D Congiu, M Costa, M Georgitsi, ... Pharmacogenomics 12 (11), 1559-1569, 2011 | 107 | 2011 |
| Aryl hydrocarbon receptor interacting protein (AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas M Georgitsi, E De Menis, S Cannavò, MJ Mäkinen, K Tuppurainen, ... Clinical endocrinology 69 (4), 621-627, 2008 | 99 | 2008 |
| Large Genomic Deletions in AIP in Pituitary Adenoma Predisposition M Georgitsi, E Heliovaara, R Paschke, AVK Kumar, M Tischkowitz, ... The Journal of Clinical Endocrinology & Metabolism 93 (10), 4146-4151, 2008 | 98 | 2008 |
| Mice with inactivation of aryl hydrocarbon receptor-interacting protein (Aip) display complete penetrance of pituitary adenomas with aberrant ARNT expression A Raitila, HJ Lehtonen, J Arola, E Heliövaara, M Ahlsten, M Georgitsi, ... The American journal of pathology 177 (4), 1969-1976, 2010 | 92 | 2010 |
| MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27Kip1 and p18INK4C) mutations M Georgitsi Best practice & research Clinical endocrinology & metabolism 24 (3), 425-437, 2010 | 77 | 2010 |
| Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers M Georgitsi, A Karhu, R Winqvist, T Visakorpi, K Waltering, P Vahteristo, ... British Journal of Cancer 96 (2), 352-356, 2007 | 73 | 2007 |
| No evidence of somatic aryl hydrocarbon receptor interacting protein mutations in sporadic endocrine neoplasia A Raitila, M Georgitsi, A Karhu, K Tuppurainen, MJ Makinen, ... Endocrine-Related Cancer 14 (3), 901-906, 2007 | 66 | 2007 |
| Somatostatin analogues increase AIP expression in somatotropinomas, irrespective of Gsp mutations ML Jaffrain-Rea, S Rotondi, A Turchi, G Occhi, A Barlier, E Peverelli, ... Endocrine-Related Cancer 20 (5), 753-766, 2013 | 61 | 2013 |
| Aggressive pituitary adenomas occurring in young patients in a large Polynesian kindred with a germline R271W mutation in the AIP gene JE Jennings, M Georgitsi, I Holdaway, AF Daly, M Tichomirowa, ... European Journal of Endocrinology 161 (5), 799-804, 2009 | 61 | 2009 |
| The genetic etiology of Tourette syndrome: large-scale collaborative efforts on the precipice of discovery M Georgitsi, AJ Willsey, CA Mathews, M State, JM Scharf, P Paschou Frontiers in Neuroscience 10, 351, 2016 | 55 | 2016 |
| European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents A Schrag, D Martino, A Apter, J Ball, E Bartolini, N Benaroya-Milshtein, ... European child & adolescent psychiatry 28, 91-109, 2019 | 49 | 2019 |
| KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients J Borg, M Phylactides, M Bartsakoulia, C Tafrali, C Lederer, AE Felice, ... Pharmacogenomics 13 (13), 1487-1500, 2012 | 45 | 2012 |
| Meta-analysis of tourette syndrome and attention deficit hyperactivity disorder provides support for a shared genetic basis F Tsetsos, SS Padmanabhuni, J Alexander, I Karagiannidis, M Tsifintaris, ... Frontiers in neuroscience 10, 202929, 2016 | 40 | 2016 |
