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Olaf Hiort
Olaf Hiort
University of Luebeck
Verified email at uksh.de - Homepage
Title
Cited by
Cited by
Year
Epidemiology and initial management of ambiguous genitalia at birth in Germany
U Thyen, K Lanz, PM Holterhus, O Hiort
Hormone research in paediatrics 66 (4), 195-203, 2006
2982006
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement
G Mantovani, M Bastepe, D Monk, L De Sanctis, S Thiele, A Usardi, ...
Nature Reviews Endocrinology 14 (8), 476-500, 2018
2672018
Phenotypic classification of male pseudohermaphroditism due to steroid 5α‐reductase 2 deficiency
GHG Sinnecker, O Hiort, L Dibbelt, N Albers, HG Dörr, H Hauß, U Heinrich, ...
American journal of medical genetics 63 (1), 223-230, 1996
2371996
Significance of mutations in the androgen receptor gene in males with idiopathic infertility
O Hiort, PM Holterhus, T Horter, W Schulze, B Kremke, M Bals-Pratsch, ...
The Journal of Clinical Endocrinology & Metabolism 85 (8), 2810-2815, 2000
2042000
A novel ultrapressure liquid chromatography tandem mass spectrometry method for the simultaneous determination of androstenedione, testosterone, and dihydrotestosterone in …
AE Kulle, FG Riepe, D Melchior, O Hiort, PM Holterhus
The Journal of Clinical Endocrinology & Metabolism 95 (5), 2399-2409, 2010
1902010
Satisfaction with genital surgery and sexual life of adults with XY disorders of sex development: results from the German clinical evaluation study
B Köhler, E Kleinemeier, A Lux, O Hiort, A Grüters, U Thyen, ...
The Journal of Clinical Endocrinology & Metabolism 97 (2), 577-588, 2012
1752012
Management of disorders of sex development
O Hiort, W Birnbaum, L Marshall, L Wünsch, R Werner, T Schröder, ...
Nature Reviews Endocrinology 10 (9), 520-529, 2014
1732014
Epigenetic Defects of GNAS in Patients with Pseudohypoparathyroidism and Mild Features of Albright’s Hereditary Osteodystrophy
GP De Nanclares, E Fernández-Rebollo, I Santin, B García-Cuartero, ...
The Journal of Clinical Endocrinology & Metabolism 92 (6), 2370-2373, 2007
1662007
Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas
EK Kunz, X Matias‐Guiu, O Hiort, G Christiansen, A Colomer, J Roth, ...
Cancer 76 (3), 479-489, 1995
1661995
Basal inhibin B and the testosterone response to human chorionic gonadotropin correlate in prepubertal boys
K Kubini, M Zachmann, N Albers, O Hiort, M Bettendorf, J Wölfle, ...
The Journal of Clinical Endocrinology & Metabolism 85 (1), 134-138, 2000
1502000
Functional assessment and clinical classification of androgen sensitivity in patients with mutations of the androgen receptor gene
GHG Sinnecker, O Hiort, EM Nitsche, PM Holterhus, K Kruse, GCIS Group
European journal of pediatrics 156, 7-14, 1996
1461996
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network
S Thiele, G Mantovani, A Barlier, V Boldrin, P Bordogna, L De Sanctis, ...
European Journal of Endocrinology 175 (6), P1-P17, 2016
1432016
Deletion and point mutations of PTHLH cause brachydactyly type E
E Klopocki, BP Hennig, K Dathe, R Koll, T de Ravel, E Baten, E Blom, ...
The American Journal of Human Genetics 86 (3), 434-439, 2010
1422010
Genetics in endocrinology: approaches to molecular genetic diagnosis in the management of differences/disorders of sex development (DSD): position paper of EU COST Action BM …
L Audi, SF Ahmed, N Krone, M Cools, K McElreavey, PM Holterhus, ...
European Journal of Endocrinology 179 (4), R197-R206, 2018
1412018
The molecular basis of male sexual differentiation
O Hiort, PM Holterhus
European journal of endocrinology 142 (2), 101-110, 2000
1402000
The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males …
B Köhler, L Lin, I Mazen, C Cetindag, H Biebermann, I Akkurt, R Rossi, ...
European Journal of Endocrinology 161 (2), 237-242, 2009
1322009
Changes over time in sex assignment for disorders of sex development
Z Kolesinska, SF Ahmed, M Niedziela, J Bryce, M Molinska-Glura, ...
Pediatrics 134 (3), e710-e715, 2014
1302014
Homozygous Disruption of P450 Side-Chain Cleavage (CYP11A1) Is Associated with Prematurity, Complete 46,XY Sex Reversal, and Severe Adrenal Failure
O Hiort, PM Holterhus, R Werner, C Marschke, U Hoppe, CJ Partsch, ...
The Journal of Clinical Endocrinology & Metabolism 90 (1), 538-541, 2005
1302005
Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci
S Ledig, O Hiort, G Scherer, M Hoffmann, G Wolff, S Morlot, A Kuechler, ...
Human reproduction 25 (10), 2637-2646, 2010
1282010
Gender role behavior in children with XY karyotype and disorders of sex development
M Jürgensen, O Hiort, PM Holterhus, U Thyen
Hormones and behavior 51 (3), 443-453, 2007
1282007
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