
Runz, Heiko Dr. med.Universität HeidelbergHeidelberg
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Co-Autoren (Uni Heidelberg)
- Stampfer, Miriam (2)
- Thormälen, Aenne Solvejg (2)
- Pepperkok, Rainer (2)
- Weiss, Karl Heinz (2)
- Schuberth, Christian (2)
- Stremmel, Wolfgang (2)
- Grimm, Dirk (1)
- Schirmacher, Peter (1)
- Nawroth, Peter Paul (1)
- Schemmer, Peter (1)
- Kölker, Stefan (1)
- Akhavanpoor, Mohammadreza (1)
- Steinbeisser, Herbert (1958-2014) (1)
- ̇Iskar, Murat (1)
- Erfle, Holger (1)
- Sauer, Sven (1)
- Wahlster, Lara (1)
- Bierhaus, Angelika (1962-2012) (1)
- Sauer, Peter (1)
- Bertsch, Thomas (1)
- Ebinger, Friedrich (1)
- Linden, Fabian (1)
- Domschke, Gabriele (1)
- Maas, Bianca (1)
- Hartmann, Tobias (1)
- Katus, Hugo (1)
- Gavin, Anne-Claude (1)
- Werenbeck-Ueding, Jennifer (1)
- Weber, Dominik (1)
- Arnold, Bernd (1)
- Assmann, Birgit (1)
- Hoffmann, Georg F. (1)
- Kühl, Sandra (1)
- (weitere Einträge vorhanden...)
Co-Autoren (extern)
- Teufel, Andreas (2)
- Rust, Christian (2)
- Weersma, Rinse K. (2)
- Grziwa, Beate (1)
- Schwarz, Heinz (1)
- Schilde, Jessica (1)
- Rauschenberger, Katharina (1)
- Weber, Christian (1)
- Benes, Vladimir (1)
- Folseraas, Trine (1)
- Herzog, Andreas (1)
- Schwerd, Tobias (1)
- Haberlandt, Edda (1)
- Connemann, Bernhard J. (1)
- Mengel, Eugen (1)
- Ferenci, Peter (1)
- Frühmesser, Anne (1)
- Kotzot, Dieter (1)
- Fauth, Christine (1)
- Nothnagel, Michael (1)
- Hampe, Jochen (1)
- Zhang, Jessie (1)
- Praggastis, Maria (1)
- Bartz, Fabian (1)
- Baying, Bianka (1)
- Jiang, Xuntian (1)
- Zhang, Xiaokui (1)
- Sidhu, Rohini (1)
- Scherrer, David E. (1)
- Schaffer, Jean E. (1)
- Reunert, Janice (1)
- Raeder, Benjamin (1)
- Porter, Forbes D. (1)
- (weitere Einträge vorhanden...)
Publikationen in heiBIB 
- Domschke, Gabriele: Systematic RNA-interference in primary human monocyte-derived macrophages : A high-throughput platform to study foam cell formation / Gabriele Domschke, Fabian Linden, Lukas Pawig, Anna Hafner, Mohammadreza Akhavanpoor, Jürgen Reymann… , 12 July 2018. - 11 S.
In: Scientific reports, ISSN 2045-2322. 8(2018), Artikel-ID 10516, Seite 1-11
DOI: 10.1038/s41598-018-28790-3
- Thormälen, Aenne Solvejg: Systematic cell-based phenotyping of missense alleles / Aenne S. Thormählen, Heiko Runz. - 14 S.
In: Cell Viability Assays. (2017), S. 215-228
DOI: 10.1007/978-1-4939-6960-9_17
- Jiang, Xuntian: Development of a bile acid-based newborn screen for Niemann-Pick disease type C / Xuntian Jiang, Rohini Sidhu, Laurel Mydock-McGrane, Fong-Fu Hsu, Douglas F. Covey, David E. Scherrer… , 4 May 2016. - 10 S. : Diagramme
In: Science translational medicine, ISSN 1946-6242. 8(2016,337) Artikel-Nummer 337ra63, 10 Seiten
DOI: 10.1126/scitranslmed.aaf2326
- Ebrahimi-Fakhari, Darius: Reduction of TMEM97 increases NPC1 protein levels and restores cholesterol trafficking in Niemann-pick type C1 disease cells / Darius Ebrahimi-Fakhari, Lara Wahlster, Fabian Bartz, Jennifer Werenbeck-Ueding, Maria Praggastis, J… , 4 July 2016. - 12 S.
In: Human molecular genetics, ISSN 1460-2083. 25(2016), 16, Seite 3588-3599
DOI: 10.1093/hmg/ddw204
- Schwerd, Tobias: Impaired antibacterial autophagy links granulomatous intestinal inflammation in Niemann-Pick disease type C1 and XIAP deficiency with NOD2 variants in Crohn's disease / Tobias Schwerd, Sumeet Pandey, Huei-Ting Yang, Katrin Bagola, Elisabeth Jameson, Jonathan Jung, Robi… . - 14 S.
In: Gut, ISSN 1468-3288. 66(2017), 6, S. 1060-1073
DOI: 10.1136/gutjnl-2015-310382
- Thormälen, Aenne Solvejg: Systematic cell-based phenotyping of missense alleles empowers rare variant association studies : a case for LDLR and myocardial infarction / Aenne S. Thormaehlen, Christian Schuberth, Hong-Hee Won, Peter Blattmann, Brigitte Joggerst-Thomalla… , February 3, 2015. - 23 S.
In: PLoS Genetics, ISSN 1553-7404. 11(2015,2) Artikel-Nummer e1004855, 23 Seiten
DOI: 10.1371/journal.pgen.1004855
- Medina, Marisa W.: Transmembrane protein 55B is a novel regulator of cellular cholesterol metabolism / Marisa W. Medina, Frederick Bauzon, Devesh Naidoo, Elizabeth Theusch, Kristen Stevens, Jessica Schil… , [September 2014]. - 7 S. : Diagramme
In: Arteriosclerosis, thrombosis, and vascular biology, ISSN 1524-4636. 34(2014), 9, Seite 1917-1923
DOI: 10.1161/ATVBAHA.113.302806
- Ebrahimi-Fakhari, Darius: Disruption of SOX6 is associated with a rapid-onset dopa-responsive movement disorder, delayed development, and dysmorphic features : clinical observations / Darius Ebrahimi-Fakhari, Bianca Maas, Christian Haneke, Tim Niehues, Katrin Hinderhofer, Birgit E. A… . - 4 S.
In: Pediatric neurology, ISSN 1873-5150. 52(2015), 1, S. 115-118
DOI: 10.1016/j.pediatrneurol.2014.08.021
- Stampfer, Miriam: Niemann-Pick disease type C clinical database : cognitive and coordination deficits are early disease indicators / Miriam Stampfer, Susanne Theiss, Yasmina Amraoui, Xuntian Jiang, Sigrid Keller, Daniel S. Ory, Eugen… , 2013. - 11 S.
In: Orphanet journal of rare diseases, ISSN 1750-1172. 8(2013), Artikel-ID 35, Seite 1-11
DOI: 10.1186/1750-1172-8-35
- Runz, Heiko: Lipids : new biology and therapeutic targets revealed through human genetics / Heiko Runz, 2013. - 5 S.
In: Clinical lipidology, ISSN 1758-4302. 8(2013), 3, Seite 295-298
DOI: 10.2217/clp.13.22
- Sürmeli Onay, Özge: Prenatal-onset Niemann-Pick type C disease with nonimmune hydrops fetalis / Ozge Surmeli-Onay, Selin Yakarisik, Ayse Korkmaz, Zuhal Akcoren, Aysel Yuce, Heiko Runz, Miriam Stam… , 11 March 2013. - 4 S.
In: Pediatrics and neonatology, ISSN 2212-1692. 54(2013), 5, Seite 344-347
DOI: 10.1016/j.pedneo.2013.01.015
- Frühmesser, Anne: Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation / Anne Frühmesser, Jonathon Blake, Edda Haberlandt, Bianka Baying, Benjamin Raeder, Heiko Runz, Ana Sp… , 20 February 2013. - 4 S.
In: European journal of human genetics, ISSN 1476-5438. 21(2013), 10, Seite 1177-1180
DOI: 10.1038/ejhg.2013.18
- Friedrich, Kilian: A frequent PNPLA3 variant is a sex specific disease modifier in PSC patients with bile duct stenosis / Kilian Friedrich, Christian Rupp, Johannes Roksund Hov, Niels Steinebrunner, Karl-Heinz Weiss, Adolf… , March 7, 2013. - 7 S.
In: PLOS ONE, ISSN 1932-6203. 8(2013), 3, Artikel-ID e58734, Seite 1-7
DOI: 10.1371/journal.pone.0058734
- ̇Iskar, Murat: Characterization of drug-induced transcriptional modules : towards drug repositioning and functional understanding / Murat Iskar, Georg Zeller, Peter Blattmann, Monica Campillos, Michael Kuhn, Katarzyna H Kaminska, He… , 30 April 2013. - 13 S.
In: Molecular systems biology, ISSN 1744-4292. 9(2013), Artikel-ID 662, Seite 1-13
DOI: 10.1038/msb.2013.20
- Blattmann, Peter Nils: RNAi-based functional profiling of loci from blood lipid genome-wide association studies identifies genes with cholesterol-regulatory function / Peter Blattmann, Christian Schuberth, Rainer Pepperkok, Heiko Runz, February 28, 2020
In: PLoS Genetics, ISSN 1553-7404. (2020,2) Artikel-Nummer e1003338, 13 Seiten
DOI: 10.1371/journal.pgen.1003338
- Ellinghaus, David: Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4 / David Ellinghaus, Trine Folseraas, Kristian Holm, Eva Ellinghaus, Espen Melum, Tobias Balschun, Jon … , 2013. - 10 S.
In: Hepatology, ISSN 1527-3350. 58(2013), 3, Seite 1074-1083
DOI: 10.1002/hep.25977
- Mengel, Eugen: Morbus Niemann-Pick Typ C : Klinik, Diagnostik und Therapie / E. Mengel, M. Beck, A.M. Das, F. Ebinger, S. Koch, H.H. Klünemann, M. Rohrbach, H. Runz, F. Rutsch, … , January 2012. - 8 S.
In: Monatsschrift Kinderheilkunde, ISSN 1433-0474. 160(2012), 1, Seite 47-54
DOI: 10.1007/s00112-011-2532-1
- Connemann, Bernhard J.: Low ceruloplasmin in a patient with Niemann-Pick Type C disease / Bernhard J. Connemann, Maximilian Gahr, Markus Schmid, Heiko Runz, Roland W. Freudenmann, April 2012. - 2 S.
In: Journal of clinical neuroscience, ISSN 1532-2653. 19(2012), 4, Seite 620-621
DOI: 10.1016/j.jocn.2011.05.038
- Herzog, Andreas: A cross-sectional single-centre study on the spectrum of Pompe disease, German patients : molecular analysis of the GAA gene, manifestation and genotype-phenotype correlations / Andreas Herzog, Ralf Hartung, Arnold J.J. Reuser, Pia Hermanns, Heiko Runz, Nesrin Karabul, Seyfulla…
In: Orphanet journal of rare diseases, ISSN 1750-1172. 7(2012), Artikelnummer 35, 14 Seiten
DOI: 10.1186/1750-1172-7-35
- Runz, Heiko: Integrated approaches to functionally characterize novel factors in lipoprotein metabolism / Heiko Runz, April 2012. - 7 S.
In: Current opinion in lipidology, ISSN 1473-6535. 23(2012), 2, Seite 104-110
DOI: 10.1097/MOL.0b013e328350fc3d
- Folseraas, Trine: Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci / Trine Folseraas, Espen Melum, Philipp Rausch, Brian D. Juran, Eva Ellinghaus, Alexey Shiryaev, Jon K… . - 10 S.
In: Journal of hepatology, ISSN 1600-0641. 57(2012), 2, S. 366-375
DOI: 10.1016/j.jhep.2012.03.031
- Tängemo, Carolina: Niemann-Pick Type C disease : characterizing lipid levels in patients with variant lysosomal cholesterol storage / Carolina Tängemo, Dominik Weber, Susanne Theiss, Eugen Mengel, and Heiko Runz, 17 January 2011. - 13 S.
In: Journal of lipid research, ISSN 1539-7262. 52(2011), 4 vom: Apr., Seite 813-825
DOI: 10.1194/jlr.P013524
- Runz, Heiko: Identifizierung und Charakterisierung molekularer Mechanismen zur Regulation des zellulären Cholesterinhaushalts / vorgelegt von Heiko Runz, 2011. - Getr. Zählung : Ill., graph. Darst.
- Weiss, Karl Heinz: Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease / Karl Heinz Weiss, Heiko Runz, Barbara Noe, Daniel Nils Gotthardt, Uta Merle, Peter Ferenci, Wolfgang… , 2 June 2010. - 8 S. : Diagramme
In: Journal of inherited metabolic disease, ISSN 1573-2665. 33(2010), S3 vom: Dez., Seite 233-240
DOI: 10.1007/s10545-010-9123-5
- Strauss, Katrin: Exosome secretion ameliorates lysosomal storage of cholesterol in Niemann-Pick type C disease / Katrin Strauss, Cornelia Goebel, Heiko Runz, Wiebke Möbius, Sievert Weiss, Ivo Feussner, Mikael Simo… , 16 June 2010. - 10 S.
In: The journal of biological chemistry, ISSN 1083-351X. 285(2010), 34, Seite 26279-26288
DOI: 10.1074/jbc.M110.134775
- Runz, Heiko: Einführung zum Schwerpunktthema Datenbanken / H. Runz, Ch. Fischer, 2010-06-12. - 4 S.
In: Medizinische Genetik, ISSN 1863-5490. 22(2010), 2, Seite 209-212
DOI: 10.1007/s11825-010-0224-1
- Rauschenberger, Katharina: A non-enzymatic function of 17β-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival / Katharina Rauschenberger, Katja Schöler, Jörn Oliver Sass, Sven Sauer, Zdenka Djuric, Cordula Rumig,… , 4 February 2010. - 12 S.
In: EMBO molecular medicine, ISSN 1757-4684. 2(2010), 2 vom: Feb., Seite 51-62
DOI: 10.1002/emmm.200900055
- Hov, Johannes R.: Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis / Johannes R. Hov, Verena Keitel, Jon K. Laerdahl, Lina Spomer, Eva Ellinghaus, Abdou ElSharawy, Espen… , [August 2010]. - 13 S. : Illustrationen
In: PLOS ONE, ISSN 1932-6203. 5(2010), 8 vom: Aug., Artikel-ID 12403, Seite 1-13
DOI: 10.1371/journal.pone.0012403
- Karlsen, Tom H.: Genome-wide association analysis in primary sclerosing cholangitis / Tom H. Karlsen, Andre Franke, Espen Melum, Arthur Kaser, Johannes Roksund Hov, Tobias Balschun, Bene… , 2010. - 10 S.
In: Gastroenterology, ISSN 1528-0012. 138(2010), 3 vom: März, Seite 1102-1111
DOI: 10.1053/j.gastro.2009.11.046
- Runz, Heiko: Einfluss der subzellulären Verteilung von Cholesterin auf die Prozessierung des Alzheimer Amyloid-Vorläuferproteins / vorgelegt von Heiko Runz, 2004 [ersch.] 2005. - Getr. Zählung : Ill., graph. Darst.
- Faßbender, Klaus: Simvastatin strongly reduces levels of Alzheimer's disease β-amyloid peptides Aβ42 and Aβ40 in vitro and in vivo / K. Fassbender, M. Simons, C. Bergmann, M. Stroick, D. Lütjohann, P. Keller, H. Runz, S. Kühl, T. Ber… , [May 8, 2001]. - 6 S.
In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 1091-6490. 98(2001), 10 vom: Mai, Seite 5856-5861
DOI: 10.1073/pnas.081620098
