Ina Knerr - Concepedia

Author

Ina Knerr

Friedrich-Alexander-Universität Erlangen-Nürnberg ORCID

Also Known As

I Knerr, I. Knerr, I. M. Knerr, Ina Knerr

209

Publications

4.7K

Citations

H-Index

106

Concepts

All Affiliations

Friedrich-Alexander-Universität Erlangen-Nürnberg Temple Street Children's University Hospital Universitätsklinikum Erlangen University College Dublin Mater Misericordiae University Hospital

About

Ina Knerr is an author at Friedrich-Alexander-Universität Erlangen-Nürnberg specializing in medicine, diabetes, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	32	1.5K
2	Public Health	9	9	446
3	Health Sciences	6	6	353
4	Biochemistry	5	5	293
5	Natural Sciences	3	3	240

Ina Knerr

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
Treatment recommendations in long‐chain fatty acid oxidation defects: consensus from a workshop Ute Spiekerkoetter, Martin Lindner, René Santer, Journal of Inherited Metabolic Disease	2009	219
Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients Sarah C. Grünert, S. Müllerleile, Linda De Silva, Orphanet Journal of Rare Diseases	2013	185
The ‘accelerator hypothesis’: relationship between weight, height, body mass index and age at diagnosis in a large cohort of 9,248 German and Austrian children with type 1 diabetes mellitus Ina Knerr, Johannes Wolf, Thomas Reinehr, Diabetologia ObesityMetabolic SyndromeType 1Childhood ObesityBody Composition	2005	177
Management and outcome in 75 individuals with long‐chain fatty acid oxidation defects: results from a workshop Ute Spiekerkoetter, Martin Lindner, René Santer, Journal of Inherited Metabolic Disease	2009	173
Syncytin, a novel human endogenous retroviral gene in human placenta: Evidence for its dysregulation in preeclampsia and HELLP syndrome Ina Knerr, Ernst Beinder, Wolfgang Rascher American Journal of Obstetrics and Gynecology Human PlacentaGeneticsGynecologyMaternal HealthPlacental Disease	2002	151
Stimulation of GCMa and syncytin via cAMP mediated PKA signaling in human trophoblastic cells under normoxic and hypoxic conditions Ina Knerr, Steffen Schubert, Christina Wich, FEBS Letters Molecular RegulationHuman Trophoblastic CellsCellular PhysiologyTarget GeneOxidative Stress	2005	144
The natural history of classic galactosemia: lessons from the GalNet registry M. Estela Rubio‐Gozalbo, Minela Haskovic, Annet M. Bosch, Orphanet Journal of Rare Diseases	2019	141
Classical Galactosaemia in Ireland: incidence, complications and outcomes of treatment Karen P. Coss, Peter Doran, C. Owoeye, Journal of Inherited Metabolic Disease	2012	99
Propionic acidemia: neonatal versus selective metabolic screening Sarah C. Grünert, S. Müllerleile, L. de Silva, Journal of Inherited Metabolic Disease	2011	90
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity ofMCCA andMCCB mutations and impact on risk assessment Sonja C. Stadler, Roman Polanetz, Esther M. Maier, Human Mutation	2006	89

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