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H. Schmidt · SciRah

Researcher profile · Semantic Scholar

H. Schmidt

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H. Schmidt — researcher profile on SciRah

h-index: 24
Works: 63
Citations: 2,184

Most-cited papers

Germ-line mutations in nonsyndromic pheochromocytoma.
H. Neumann, B. Bausch, S. Mcwhinney, B. U. Bender +24 more
2002New England Journal of Medicine837 citations Open access
Semantic Scholar
Reduced final height outcome in congenital adrenal hyperplasia under prednisone treatment: deceleration of growth velocity during puberty.
W. Bonfig, S. Bechtold, H. Schmidt, D. Knorr +1 more
2007Journal of Clinical Endocrinology and Metabolism164 citations
Semantic Scholar
Hydrocortisone dosing during puberty in patients with classical congenital adrenal hyperplasia: an evidence-based recommendation.
W. Bonfig, S. B. Pozza, H. Schmidt, P. Pagel +2 more
2009Journal of Clinical Endocrinology and Metabolism122 citations
Semantic Scholar
Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes
Maximilian Witzel, Daniel Petersheim, Yanxin Fan, E. Bahrami +20 more
2017Nature Genetics97 citations Open access
Semantic Scholar
Testicular adrenal rest tumors develop independently of long-term disease control: a longitudinal analysis of 50 adult men with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency.
Nicole Reisch, M. Rottenkolber, A. Greifenstein, N. Krone +4 more
2013Journal of Clinical Endocrinology and Metabolism74 citations
Semantic Scholar
Children with classic congenital adrenal hyperplasia experience salt loss and hypoglycemia: evaluation of adrenal crises during the first 6 years of life.
B. Odenwald, U. Nennstiel-Ratzel, H. Dörr, H. Schmidt +2 more
2016European Journal of Endocrinology54 citations
Semantic Scholar
Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation
O. Fuchs, N. Pfarr, J. Pohlenz, H. Schmidt
2009Developmental Medicine & Child Neurology52 citations Open access
Semantic Scholar
Myb‐like, SWIRM, and MPN domains 1 (MYSM1) deficiency: Genotoxic stress‐associated bone marrow failure and developmental aberrations
E. Bahrami, Maximilian Witzel, T. Racek, Jaçek Puchalka +13 more
2017Journal of Allergy and Clinical Immunology50 citations
Semantic Scholar
Selenium Supplementation does not Decrease Thyroid Peroxidase Antibody Concentration in Children and Adolescents with Autoimmune Thyroiditis
W. Bonfig, R. Gaertner, H. Schmidt
2010TheScientificWorldJournal49 citations Open access
Semantic Scholar
Elevated 17-hydroxyprogesterone serum values in male patients with acne.
M. Placzek, B. Arnold, H. Schmidt, S. Gaube +3 more
2005Journal of American Academy of Dermatology46 citations
Semantic Scholar
A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck—a case report and review of the literature
W. Bonfig, H. Krude, H. Schmidt
2011European Journal of Pediatrics45 citations
Semantic Scholar
Effect of androgen excess and glucocorticoid exposure on metabolic risk profiles in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
L. Paizoni, M. Auer, H. Schmidt, A. Hübner +2 more
2019Journal of Steroid Biochemistry and Molecular Biology37 citations
Semantic Scholar
Successful Early Dietary Intervention Avoids Obesity in Patients with Prader-Willi Syndrome: A Ten-Year Follow-up
H. Schmidt, S. B. Pozza, W. Bonfig, H. Schwarz +1 more
2008Journal of Pediatric Endocrinology & Metabolism (JPEM)37 citations
Semantic Scholar
Cohen syndrome diagnosis using whole genome arrays
Núria Rivera-Brugués, B. Albrecht, D. Wieczorek, H. Schmidt +11 more
2010Journal of Medical Genetics35 citations Open access
Semantic Scholar
Familial polythelia over three generations with polymastia in the youngest girl
A. Galli-Tsinopoulou, Carsten Krohn, H. Schmidt
2001European Journal of Pediatrics35 citations
Semantic Scholar
Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT): case report of reversible coma and status epilepticus in an adolescent patient and review of the literature
J. Hilberath, H. Schmidt, G. Wolf
2014European Journal of Pediatrics34 citations
Semantic Scholar
Acne fulminans in late-onset congenital adrenal hyperplasia.
M. Placzek, K. Degitz, H. Schmidt, G. Plewig
1999The Lancet33 citations
Semantic Scholar
Hypercalcaemia after treatment with denosumab in children: bisphosphonates as an option for therapy and prevention?
Carmen Sydlik, H. Dürr, S. B. Pozza, C. Weißenbacher +2 more
2018World Journal of Pediatrics32 citations Open access
Semantic Scholar
Bone mass development and bone metabolism in juvenile idiopathic arthritis: treatment with growth hormone for 4 years.
S. Bechtold, P. Ripperger, W. Bonfig, H. Schmidt +3 more
2004Journal of Rheumatology32 citations
Semantic Scholar
Homozygous XYLT2 variants as a cause of spondyloocular syndrome
Muhammad Umair, G. Eckstein, G. Rudolph, T. Strom +7 more
2018Clinical Genetics29 citations
Semantic Scholar
Effects of androgen excess and glucocorticoid exposure on bone health in adult patients with 21-hydroxylase deficiency.
M. Auer, L. Paizoni, L. Hofbauer, M. Rauner +5 more
2020Journal of Steroid Biochemistry and Molecular Biology28 citations Open access
Semantic Scholar
Premature adrenarche, increased growth velocity and accelerated bone age in male patients with Prader-Labhart-Willi syndrome
H. Schmidt, H. Schwarz
2001European Journal of Pediatrics26 citations
Semantic Scholar
Central Precocious Puberty in a Girl with McCune-Albright Syndrome Responds to Treatment with GnRH Analogue
H. Schmidt, W. Kiess
1998Journal of Pediatric Endocrinology & Metabolism (JPEM)25 citations
Semantic Scholar
Levothyroxine Treatment of Euthyroid Children with Autoimmune Hashimoto Thyroiditis: Results of a Multicenter, Randomized, Controlled Trial
H. Dörr, M. Bettendorf, G. Binder, B. Karges +5 more
2015Hormone Research in Paediatrics24 citations Open access
Semantic Scholar
A Special, Strict, Fat-Reduced, and Carbohydrate-Modified Diet Leads to Marked Weight Reduction even in Overweight Adolescents with Prader-Willi Syndrome (PWS)
W. Bonfig, K. Dokoupil, H. Schmidt
2009TheScientificWorldJournal24 citations Open access
Semantic Scholar
Clinical, biochemical and molecular genetic data in five children with Gitelman's syndrome.
H. Schmidt, M. Kabesch, H. Schwarz, W. Kiess
2001Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme20 citations
Semantic Scholar
11-oxygenated androgens and their relation to hypothalamus-pituitary-gonadal-axis disturbances in adults with congenital adrenal hyperplasia.
M. Auer, L. Paizoni, M. Neuner, C. Lottspeich +5 more
2021Journal of Steroid Biochemistry and Molecular Biology17 citations Open access
Semantic Scholar
Spondylo-ocular syndrome: a new entity with crystalline lens malformation, cataract, retinal detachment, osteoporosis, and platyspondyly.
G. Rudolph, P. Kalpadakis, T. Bettecken, P. Lichtner +4 more
2003American journal of ophthalmology-glaucoma16 citations
Semantic Scholar
Pubertal Height Gain in Ullrich-Turner Syndrome
S. Bechtold, R. Pozza, H. Schmidt, W. Bonfig +1 more
2006Journal of Pediatric Endocrinology & Metabolism (JPEM)15 citations
Semantic Scholar
Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
H. Dörr, N. Schulze, M. Bettendorf, G. Binder +9 more
2020Molecular and Cellular Pediatrics13 citations Open access
Semantic Scholar
Effect of antiandrogen treatment on bone density and bone geometry in adolescents with polycystic ovary syndrome.
S. Bechtold, R. Dalla Pozza, S. Putzker, J. Roeb +3 more
2012Journal of Pediatric and Adolescent Gynecology13 citations
Semantic Scholar
Prader-Labhart-Willi syndrome: auxological response to a conventional dose of growth hormone in patients with classical growth hormone deficiency.
H. Schmidt, S. Bechtold, H. P. Schwarz
2000European Journal of Medical Research12 citations
Semantic Scholar
Multiple pheochromocytomas and paragangliomas in a young patient carrying a SDHD gene mutation
A. Novosel, A. Heger, P. Lohse, H. Schmidt
2004European Journal of Pediatrics11 citations
Semantic Scholar
Oral testosterone undecanoate for the induction of puberty in anorchid boys
H. Schmidt, D. Knorr, H. Schwarz
1998Archives of Disease in Childhood8 citations Open access
Semantic Scholar
Endochondral gigantism: A newly recognized skeletal dysplasia with pre‐ and postnatal overgrowth and endocrine abnormalities
H. Schmidt, B. Kammer, M. Grasser, A. Enders +2 more
2007American Journal of Medical Genetics. Part A7 citations
Semantic Scholar
Endosteal bone storage in young adults born small for gestational age – a study using peripheral quantitative computed tomography
S. Putzker, R. Pozza, H. P. Schwarz, H. Schmidt +1 more
2012Clinical Endocrinology5 citations
Semantic Scholar
Evaluation of Changes in Insulin Sensitivity in Prepubertal Small for Gestational Age Children Treated with Growth Hormone
Carmen Sydlik, C. Weißenbacher, J. Roeb, S. B. Pozza +1 more
2019Indian journal of endocrinology and metabolism4 citations Open access
Semantic Scholar
Sexual Difference in Bone Geometry of Adult Patients with Classical Congenital Adrenal Hyperplasia: Data Using Peripheral Quantitative Computed Tomography
S. Bechtold, Andreas Beyerlein, W. Bonfig, R. Dalla Pozza +4 more
2014Hormone Research in Paediatrics4 citations Open access
Semantic Scholar
SWI/SNF Protein SMARCD2 Orchestrates Transcriptional Networks Controlling Hematopoiesis and Neutrophil Granulocytes in Humans, Mice and Zebrafish
Maximilian Witzel, Daniel Petersheim, Yanxin Fan, E. Bahrami +20 more
20163 citations
Semantic Scholar
LINS1-associated neurodevelopmental disorder
C. Neuhofer, C. Catarino, H. Schmidt, K. Seelos +3 more
2020Neurology: Genetics2 citations Open access
Semantic Scholar
A Case of Ankyloblepharon-ectodermal Defects-cleft Lip/Palate-syndrome with Choanal Atresia and Skin Erosions: Phenotypic Variability of TP63-related Disorders.
L. Niculescu, M. Wagner, D. Westphal, M. Fischer +7 more
2019Acta Dermato-Venereologica2 citations Open access
Semantic Scholar
Medizinische Betreuung von jungen Frauen mit Ullrich-Turner-Syndrom in Deutschland Medical care of young women with Turner syndrome in Germany
H. Dörr, M. Bettendorf, G. Binder, J. Brämswig +7 more
20192 citations
Semantic Scholar
Lebenssituation von jungen Frauen mit Ullrich-Turner-Syndrom nach dem Ende der Wachstumshormontherapie: Ergebnisse einer Umfrage in Deutschland
H. Dörr, M. Bettendorf, G. Binder, J. Brämswig +7 more
2019Deutsche Medizinische Wochenschrift2 citations Open access
Semantic Scholar
Hormonelle Kontrolle des Wachstums
H. P. Schwarz, S. Bechtold, H. Schmidt
2004Monatsschrift Kinderheilkunde2 citations
Semantic Scholar
A Human Bone Marrow Failure Syndrome Caused By a Homozygous Mutation in MYSM1
E. Bahrami, T. Racek, Maximilian Witzel, Jaçek Puchalka +10 more
20151 citations Open access
Semantic Scholar
Dietary intervention in the first four years prevents abnormal weight gain but negatively affects height development in Prader-Willi syndrome.
H. Schmidt, H. Schwarz, A. Enders
2001Acta paediatrica1 citations
Semantic Scholar
Muscle density measurement in muscular dystrophy
S. Bechtold, A. Blaschek, W. Müller-Felber, J. Roeb +3 more
20170 citations
Semantic Scholar
Muscle Density Measurement in Duchenne Muscular Dystrophy
S. Bechtold, A. Blaschek, W. Müller-Felber, C. Weißenbacher +3 more
20170 citations
Semantic Scholar
Off-Label Use of the Aromatase Inhibitor Letrozole in Pubertal Boys to Improve Final Height: Laboratory, Auxological and Bone Age Data
H. Schmidt, C. Weißenbacher, Pozza Susanne Bechtold-Dalla, J. Roeb +1 more
20160 citations
Semantic Scholar
Evaluation of Prepubertal Patients with Suspected Neurosecretory Dysfunction of Growth Hormone Secretion: Diagnostic Steps and Treatment Response
Carmen Sydlik, C. Weißenbacher, J. Roeb, S. B. Pozza +1 more
2016Advances in Artificial Neural Systems0 citations Open access
Semantic Scholar

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