Christoph J. Mache - Concepedia

Author

Christoph J. Mache

Also Known As

C J Mache, C Mache, C. J. Mache, C. MACHE, C. Mache, C.J Mache, C.J. Mache, Christoph J Mache, Christoph J. Mache, Christoph Johannes Mache

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Medical University of Graz University of Graz Graz University Hospital Heidelberg University Inserm

About

Christoph J. Mache is an author at Medical University of Graz specializing in medicine, pathology, and nephrology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	19	972
2	Public Health	2	2	59
3	Health Sciences	1	1	19
4	Cell Biology	1	1	23
5	Cellular Physiology	1	1	137

Christoph J. Mache

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Transforming Growth Factor-β Receptor Mutations and Pulmonary Arterial Hypertension in Childhood Rachel E. Harrison, Rolf M.F. Berger, Sheila G. Haworth, Circulation	2005	230
Polyhydramnios, Transient Antenatal Bartter’s Syndrome, and<i>MAGED2</i>Mutations Kamel Laghmani, Bodo B. Beck, Sung-Sen Yang, New England Journal of Medicine	2016	181
Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome Franz Schaefer, Gianluigi Ardissino, Gema Ariceta, Kidney International HemodialysisGenetic DisorderMedicineKidney FailureGenetic Epidemiology	2018	169
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor Asif Ali, P. T. Christie, I. V. Grigorieva, Human Molecular Genetics Developmental BiologyDna BindingGata3 MutationsSplice Site MutationMedicine	2006	149
Complement Inhibitor Eculizumab in Atypical Hemolytic Uremic Syndrome Christoph J. Mache, Birgit Acham‐Roschitz, Véronique Frémeaux‐Bacchi, Clinical Journal of the American Society of Nephrology	2009	149
Combined <scp>NGS</scp> Approaches Identify Mutations in the Intraflagellar Transport Gene <i>IFT140</i> in Skeletal Ciliopathies with Early Progressive Kidney Disease Miriam Schmidts, Valeska Frank, Tobias Eisenberger, Human Mutation Skeletal CiliopathiesGeneticsPathologyMolecular GeneticsDisease Gene Identification	2013	137
Successful Treatment of Chronic Recurrent Multifocal Osteomyelitis With Tumor Necrosis Factor-α Blockage Andrea Deutschmann, Christoph J. Mache, Koppany Bodó, PEDIATRICS	2005	132
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function Mathilda Bedin, Olivia Boyer, Aude Servais, Journal of Clinical Investigation	2019	97
Eculizumab Use for Kidney Transplantation in Patients With a Diagnosis of Atypical Hemolytic Uremic Syndrome Andrew M. Siedlecki, Nicole M. Isbel, Johan Vande Walle, Kidney International Reports	2018	82
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies Bodo B. Beck, Anne Baasner, Anja Buescher, European Journal of Human Genetics Novel FindingsRenal FunctionMedicinePathologyLaboratory Medicine	2012	81

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