Olaf Rittinger - Concepedia

Author

Olaf Rittinger

Paracelsus Medical University

Also Known As

O Rittinger, O. Rittinger, Olaf Rittinger

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Paracelsus Medical University Salzburger Landeskliniken Innsbruck Medical University Ludwig-Maximilians-Universität München Unfallkrankenhaus Salzburg

About

Olaf Rittinger is an author at Paracelsus Medical University specializing in medicine, genetics, and epigenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	463
2	Molecular Genetics	4	4	117
3	Cell Biology	2	2	94
4	Health Sciences	1	1	20
5	Molecular Biology	1	1	11

Olaf Rittinger

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability Katrina Tatton‐Brown, Chey Loveday, Shawn Yost, The American Journal of Human Genetics	2017	208
Clinical and Mutational Spectrum of Mowat–Wilson Syndrome Christiane Zweier, Christian T. Thiel, Andreas Dufke, European Journal of Medical Genetics Genetic DisorderGeneticsPathologyDisease Gene IdentificationMedicine	2005	135
Ocular manifestations of keratitis– ichthyosis–deafness (KID) syndrome Elisabeth M. Messmer, Kenneth R. Kenyon, Olaf Rittinger, Ophthalmology Pediatric OphthalmologyOcular PathologyOphthalmologyOcular Manifestations	2005	100
<i>GJB2</i> mutations in keratitis‐ichthyosis‐deafness syndrome including its fatal form Andreas Janecke, Hans Christian Hennies, Barbara Günther, American Journal of Medical Genetics Part A	2005	92
Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes Ilaria Parenti, Maria Esperanza Teresa‐Rodrigo, Jelena Pozojevic, Human Genetics ChromatinGenome InstabilityMendelian DisorderChromatin RemodelingGenetic Disorder	2017	81
Polytopic anomalies with agenesis of the lower vertebral column Axel Bohring, Susan O. Lewin, James F. Reynolds, American Journal of Medical Genetics	1999	62
Common and recurrent HPGD mutations in Caucasian individuals with primary hypertrophic osteoarthropathy Christine P. Diggle, Ian Carr, Emanuel Zitt, Lara D. Veeken	2010	55
Bainbridge–Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition Alma Kuechler, Johanna Christina Czeschik, Elisabeth Graf, European Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyLoss-of-function Variants	2016	49
Malignant Glioma as a Secondary Malignant Neoplasm after Radiation Therapy for Craniopharyngioma. Report of a Case and Review of Reported Cases M. Kranzinger, Nathaniel S. Jones, Olaf Rittinger, Oncology Research and Treatment	2001	48
Histology and synchrotron radiation‐based microtomography of the inner ear in a molecularly confirmed case of CHARGE syndrome Rudolf Glueckert, Helge Rask‐Andersen, Consolato Sergi, American Journal of Medical Genetics Part A OtorhinolaryngologyPathologyNeurotologyEmbryologyCharge Syndrome	2010	42

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