Klaus Mohnike

Families USA — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

37h-index5.6kcitations264works1.92yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Connective tissue disorders research(57), Hyperglycemia and glycemic control in critically ill and hospitalized patients(53), Sexual Differentiation and Disorders(29), Growth Hormone and Insulin-like Growth Factors(23), Diabetes Management and Research(21)

Publications263 total

Automated Segmentation and Length Measurement of Metacarpal and Phalangeal Bones for Hand Radiograph Evaluation
2025Open Access
EndoCompass Project: Research Roadmap for Diabetes, Obesity, and Metabolism
Hormone Research in Paediatrics·2025Open Access
Practice patterns and treatment outcomes of growth-promoting therapies in CAH: insights from real-world data
Endocrine Abstracts·2025
EndoCompass project: research roadmap for diabetes, obesity, and metabolism
European Journal of Endocrinology·2025Open Access
A markerless gait analysis in a child with achondroplasia. A case study
Gait & Posture·2025
Artificial intelligence for diagnosing rare bone diseases: a global survey of healthcare professionals
Orphanet Journal of Rare Diseases·2025Open Access
Differences in gait parameters between children with achondroplasia and an age-matched control group of typically developed children in the age range of 6 to 12 years
PLoS ONE·2025· 1 citedOpen Access
Coping and quality of life of parents of children with achondroplasia—a narrative review
Frontiers in Medicine·2025Open Access
Perspectives on the Current and Future State of Artificial Intelligence in Medical Genetics
American Journal of Medical Genetics Part A·2025· 3 citedOpen Access
Management of sleep-disordered breathing in achondroplasia: guiding principles of the European Achondroplasia Forum
Orphanet Journal of Rare Diseases·2025· 2 citedOpen Access
"Variable phenotypic expression of NR5A1 mutation in a family: sex development abnormalities and management challenges"
Endocrine Abstracts·2025
Deeplasia: a novel tool for the assessment of bone age in skeletal dysplasia
Endocrine Abstracts·2025
Growth-promoting therapy in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Real-world data from the I-CAH registry
Endocrine Abstracts·2025
Onset of puberty in achondroplasia
Endocrine Abstracts·2025
Design of a randomized, multicentre, phase 2 study of vosoritide in children with turner syndrome, noonan syndrome, or short stature homeobox-containing gene (SHOX) deficiency
Endocrine Abstracts·2025
Global, multi-center, repeat-dose, phase 2 study of RZ358 (ersodetug), an insulin receptor antibody, for congenital hyperinsulinism
Med·2025· 2 citedOpen Access
Limb lengthening in individuals with achondroplasia: Analysis of an international survey
Bone·2025· 2 cited
Recommendations for management of infants and young children with achondroplasia: Does clinical practice align?
Orphanet Journal of Rare Diseases·2025· 1 citedOpen Access
Non-coding cis-regulatory variants in HK1 cause congenital hyperinsulinism with variable disease severity
Genome Medicine·2025· 7 citedOpen Access
Considerations for Anthropometry Specific to People with Disproportionate Short Stature
Advances in Therapy·2025· 8 citedOpen Access
page 1 of 14Next →

Frequent Co-authors

Ravi Savarirayan(7), Melita Irving(7), Julie Hoover‐Fong(7), Lars Hagenäs(7), Oliver Blankenstein(7), Keiichi Ozono(6), Walter Bonfig(5), Susann Empting(5), William R. Wilcox(4), Michael B. Bober(4), Klane K. White(4), Antonio Leiva‐Gea(4), Markus Bettendorf(4), Peter Wieacker(4), Valérie Cormier‐Daire(4), Thomas Meißner(4), Wolfgang Mohnike(4), Niels Thomas Hertel(4), Reinhard W. Holl(4), Peter Rowe(3)