Frank Rutsch - Concepedia

Author

Frank Rutsch

Also Known As

Alberto Burlina, Dominique Roland, F Rutsch, F. Rutsch, Frank Rutsch, Julia Hannah Quitmann, Rutsch F, Rutsch, F., Rutsch, Frank

106

Publications

4.2K

Citations

H-Index

Concepts

All Affiliations

University Hospital Münster Heidelberg University University Medical Center Hamburg-Eppendorf Universität Hamburg Charité - Universitätsmedizin Berlin

About

Frank Rutsch is an author at University Hospital Münster specializing in medicine, inherited metabolic disease, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	19	2.4K
2	Health Sciences	6	6	395
3	Natural Sciences	2	2	390
4	Public Health	2	2	43
5	Social Sciences	2	2	121

Frank Rutsch

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
SAMHD1 restricts HIV-1 infection in resting CD4+ T cells Hanna-Mari Baldauf, Xiaoyu Pan, Elina Erikson, Nature Medicine Human RetrovirusImmunologyAntiviral ResponseHiv-1 InfectionChronic Viral Infection	2012	566
SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation Julien H. Park, Max Hogrebe, Marianne Grüneberg, The American Journal of Human Genetics Slc39a8 DeficiencyBiochemistryNatural SciencesMetalloproteinMolecular Biology	2015	303
PC-1 Nucleoside Triphosphate Pyrophosphohydrolase Deficiency in Idiopathic Infantile Arterial Calcification Frank Rutsch, Sucheta M. Vaingankar, Kristen Johnson, American Journal Of Pathology PhysiologyInherited Metabolic DiseasePediatricsMedicineAtherosclerosis	2001	299
SAMHD1-Deficient CD14+ Cells from Individuals with Aicardi-Goutières Syndrome Are Highly Susceptible to HIV-1 Infection André Berger, Andreas Sommer, Jenny Zwarg, PLoS Pathogens Primary ImmunodeficiencyAutoimmune DiseaseSamhd1 GeneHuman RetrovirusPathogenesis	2011	237
Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism David Coelho, Jaeseung Kim, Isabelle R. Miousse, Nature Genetics Vitamin NutritionGenetic DisorderGeneticsVitamin B12 MetabolismMolecular Biology	2012	233
A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome Frank Rutsch, Mary MacDougall, Changming Lu, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsDisease Gene Identification	2015	222
Congenital Glutamine Deficiency with Glutamine Synthetase Mutations Johannes Häberle, Boris Görg, Frank Rutsch, New England Journal of Medicine Developmental AnomalyDevelopmental BiologyMendelian DisorderBrain DevelopmentAcid-base Homeostasis	2005	207
Once-daily, subcutaneous vosoritide therapy in children with achondroplasia: a randomised, double-blind, phase 3, placebo-controlled, multicentre trial Ravi Savarirayan, Louise Tofts, Melita Irving, The Lancet Subcutaneous Vosoritide TherapyPediatricsMulticentre TrialMedicinePhase 3	2020	184
47 patients with FLNA associated periventricular nodular heterotopia Max Lange, Burkhard S. Kasper, Axel Bohring, Orphanet Journal of Rare Diseases	2015	105
Clinical burden of illness in patients with phenylketonuria (PKU) and associated comorbidities - a retrospective study of German health insurance claims data K. F. Trefz, Ania C. Muntau, KM Kohlscheen, Orphanet Journal of Rare Diseases	2019	89

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