Growth of patients with 21-hydroxylase deficiency: an analysis of the factors influencing adult height J Jääskeläinen, R Voutilainen Pediatric research 41 (1), 30-33, 1997 | 181 | 1997 |
Premature adrenarche: etiology, clinical findings, and consequences R Voutilainen, J Jääskeläinen The Journal of steroid biochemistry and molecular biology 145, 226-236, 2015 | 148 | 2015 |
Premature adrenarche-a common condition with variable presentation P Utriainen, S Laakso, J Liimatta, J Jääskeläinen, R Voutilainen Hormone research in paediatrics 83 (4), 221-231, 2015 | 144 | 2015 |
Assessment of body composition by dual‐energy X‐ray absorptiometry, bioimpedance analysis and anthropometrics in children: the P hysical A ctivity and N utrition in C hildren study TT Tompuri, TA Lakka, M Hakulinen, V Lindi, DE Laaksonen, ... Clinical physiology and functional imaging 35 (1), 21-33, 2015 | 125 | 2015 |
Bone mineral density in relation to glucocorticoid substitution therapy in adult patients with 21‐hydroxylase deficiency J Jääskeläinen, R Voutilainen Clinical endocrinology 45 (6), 707-713, 1996 | 110 | 1996 |
Long‐term outcome of classical 21‐hydroxylase deficiency: diagnosis, complications and quality of life J Jääskeläinen, R Voutilainen Acta paediatrica 89 (2), 183-187, 2000 | 103 | 2000 |
Molecular biology of androgen insensitivity J Jääskeläinen Molecular and cellular endocrinology 352 (1-2), 4-12, 2012 | 102 | 2012 |
Child rate, pregnancy outcome and ovarian function in females with classical 21‐hydroxylase deficiency J JÄÄSKELÄINEN, M HIPPELÄINEN, O KIEKARA, R VOUTILAINEN Acta Obstetricia et Gynecologica Scandinavica: ORIGINAL ARTICLE 79 (8), 687-692, 2000 | 91 | 2000 |
Androgen receptor gene CAG length polymorphism in women with polycystic ovary syndrome J Jääskeläinen, S Korhonen, R Voutilainen, M Hippeläinen, S Heinonen Fertility and Sterility 83 (6), 1724-1728, 2005 | 90 | 2005 |
Pituitary gonadal axis and child rate in males with classical 21-hydroxylase deficiency J Jääskeläinen, O Kiekara, M Hippeläinen, R Voutilainen Journal of endocrinological investigation 23, 23-27, 2000 | 90 | 2000 |
Birth size as a determinant of cardiometabolic risk factors in children H Nordman, J Jääskeläinen, R Voutilainen Hormone Research in Paediatrics 93 (3), 144-153, 2020 | 82 | 2020 |
Detection of novel gene variants associated with congenital hypothyroidism in a Finnish patient cohort C Löf, K Patyra, T Kuulasmaa, J Vangipurapu, H Undeutsch, H Jaeschke, ... Thyroid 26 (9), 1215-1224, 2016 | 78 | 2016 |
Analysis by LC–MS/MS of endogenous steroids from human serum, plasma, endometrium and endometriotic tissue MR Häkkinen, T Heinosalo, N Saarinen, T Linnanen, R Voutilainen, ... Journal of Pharmaceutical and Biomedical Analysis 152, 165-172, 2018 | 73 | 2018 |
Girls with premature adrenarche have accelerated early childhood growth P Utriainen, R Voutilainen, J Jääskeläinen The Journal of pediatrics 154 (6), 882-887, 2009 | 71 | 2009 |
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly KA Bear, BD Solomon, S Antonini, IJP Arnhold, MM França, EH Gerkes, ... Journal of medical genetics 51 (6), 413-418, 2014 | 69 | 2014 |
The presentation of adrenarche is sexually dimorphic and modified by body adiposity A Mäntyselkä, J Jääskeläinen, V Lindi, A Viitasalo, T Tompuri, ... The Journal of Clinical Endocrinology & Metabolism 99 (10), 3889-3894, 2014 | 66 | 2014 |
Post‐prandial insulin lispro vs. human regular insulin in prepubertal children with Type 1 diabetes mellitus S Tupola, J Komulainen, J Jääskeläinen, I Sipilä Diabetic medicine 18 (8), 654-658, 2001 | 66 | 2001 |
Interleukins 1α and 1β as regulators of steroidogenesis in human NCI-H295R adrenocortical cells IV Tkachenko, T Jääskeläinen, J Jääskeläinen, JJ Palvimo, R Voutilainen Steroids 76 (10-11), 1103-1115, 2011 | 62 | 2011 |
Simultaneous analysis by LC–MS/MS of 22 ketosteroids with hydroxylamine derivatization and underivatized estradiol from human plasma, serum and prostate tissue MR Häkkinen, T Murtola, R Voutilainen, M Poutanen, T Linnanen, ... Journal of pharmaceutical and biomedical analysis 164, 642-652, 2019 | 58 | 2019 |
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism H Cangul, XH Liao, E Schoenmakers, J Kero, S Barone, P Srichomkwun, ... JCI insight 3 (20), 2018 | 58 | 2018 |