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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 5
2022
Grüneis, Rebecca 
ORCID: https://orcid.org/0000-0001-7154-9736; Weissensteiner, Hansi ORCID: https://orcid.org/0000-0002-2871-8669; Lamina, Claudia; Schönherr, Sebastian; Forer, Lukas ORCID: https://orcid.org/0000-0003-2139-7329; Di Maio, Silvia; Streiter, Gertraud ORCID: https://orcid.org/0000-0002-4810-2984; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Gieger, Christian; Kronenberg, Florian ORCID: https://orcid.org/0000-0003-2229-1120 und Coassin, Stefan ORCID: https://orcid.org/0000-0001-5677-8979
(2022):
The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat.
In: Journal of Lipid Research, Bd. 63, Nr. 12, 100306
[PDF, 1MB]
ORCID: https://orcid.org/0000-0001-7154-9736; Weissensteiner, Hansi ORCID: https://orcid.org/0000-0002-2871-8669; Lamina, Claudia; Schönherr, Sebastian; Forer, Lukas ORCID: https://orcid.org/0000-0003-2139-7329; Di Maio, Silvia; Streiter, Gertraud ORCID: https://orcid.org/0000-0002-4810-2984; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Gieger, Christian; Kronenberg, Florian ORCID: https://orcid.org/0000-0003-2229-1120 und Coassin, Stefan ORCID: https://orcid.org/0000-0001-5677-8979
(2022):
The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat.
In: Journal of Lipid Research, Bd. 63, Nr. 12, 100306
[PDF, 1MB]
2021
Aboulmaouahib, Brahim; Kastenmüller, Gabi; Suhre, Karsten; Zöllner, Sebastian; Weissensteiner, Hansi; Prehn, Cornelia; Adamski, Jerzy; Gieger, Christian; Wang-Sattler, Rui; Lichtner, Peter; Strauch, Konstantin und Flaquer, Antònia
(2021):
First mitochondrial genome wide association study with metabolomics. Konstantin Strauch,.
In: Human Molecular Genetics
[PDF, 746kB]
2019
Fazzini, Federica; Lamina, Claudia; Fendt, Liane; Schultheiss, Ulla T.; Kotsis, Fruzsina; Hicks, Andrew A.; Meiselbach, Heike; Weissensteiner, Hansi; Forer, Lukas; Krane, Vera; Eckardt, Kai-Uwe; Koettgen, Anna; Kronenberg, Florian; Schneider, Markus; Dienemann, Thomas; Prokosch, Hans-Ulrich; Barthlein, Barbara; Beck, Andreas; Ganslandt, Thomas; Reis, Andre; Ekici, Arif B.; Avendano, Susanne; Becker-Grosspitsch, Dinah; Alberth-Schmidt, Ulrike; Hausknecht, Birgit; Zitzmann, Rita; Weigel, Anke; Walz, Gerd; Schultheiss, Ulla; Kotsis, Fruzsina; Meder, Simone; Mitsch, Erna; Reinhard, Ursula; Floege, Jurgen; Schlieper, Georg; Saritas, Turgay; Ernst, Sabine; Beaujean, Nicole; Schaeffner, Elke; Baid-Agrawal, Seema; Theisen, Kerstin; Haller, Hermann; Menne, Jan; Zeier, Martin; Sommerer, Claudia; Woitke, Rebecca; Wolf, Gunter; Busch, Martin; Fuss, Rainer; Sitter, Thomas; Blank, Claudia; Wanner, Christoph; Krane, Vera; Borner-Klein, Antje; Bauer, Britta; Raschenberger, Julia; Kollerits, Barbara; Forer, Lukas; Schonherr, Sebastian; Weissensteiner, Hansi; Oefner, Peter; Gronwald, Wolfram; Zacharias, Helena; Schmid, Matthias und Nadal, Jennifer
(2019):
Mitochondrial DNA copy number is associated with mortality and infections in a large cohort of patients with chronic kidney disease.
In: Kidney International, Bd. 96, Nr. 2: S. 480-488
2017
Coassin, Stefan; Erhart, Gertraud; Weissensteiner, Hansi; Guimaraes de Araujo, Mariana Eca; Lamina, Claudia; Schönherr, Sebastian; Forer, Lukas; Haun, Margot; Losso, Jamie Lee; Köttgen, Anna; Schmidt, Konrad; Utermann, Gerd; Peters, Annette; Gieger, Christian; Strauch, Konstantin; Finkenstedt, Armin; Bale, Reto; Zoller, Heinz; Paulweber, Bernhard; Eckardt, Kai-Uwe; Hüttenhofer, Alexander; Huber, Lukas A. und Kronenberg, Florian
(2017):
A novel but frequent variant in LPA KIV-2 is associated with a pronounced Lp(a) and cardiovascular risk reduction.
In: European Heart Journal, Bd. 38, Nr. 23: S. 1823-1831
[PDF, 754kB]
2010
Forer, Lukas; Schoenherr, Sebastian; Weissensteiner, Hansi; Haider, Florian; Kluckner, Thomas; Gieger, Christian; Wichmann, Heinz-Erich; Specht, Guenther; Kronenberg, Florian und Kloss-Brandstaetter, Anita
(2010):
CONAN: copy number variation analysis software for genome-wide association studies.
In: BMC Bioinformatics
11:318
[PDF, 1MB]