Profiling of Mitochondrial DNA Heteroplasmy in a Prospective Oral Squamous Cell Carcinoma Study von Fendt, Liane, Fazzini, Federica, Weissensteiner, Hansi, Bruckmoser, Emanuel, Schönherr, Sebastian, Schäfer, Georg, Losso, Jamie Lee, Streiter, Gertraud A, Lamina, Claudia, Rasse, Michael, Klocker, Helmut, Kofler, Barbara, Kloss-Brandstätter, Anita, Huck, Christian W, Kronenberg, Florian, Laimer, Johannes

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An in-depth analysis of the mitochondrial phylogenetic landscape of Cambodia von Kloss-Brandstätter, Anita, Summerer, Monika, Horst, David, Horst, Basil, Streiter, Gertraud, Raschenberger, Julia, Kronenberg, Florian, Sanguansermsri, Torpong, Horst, Jürgen, Weissensteiner, Hansi

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Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model von Di Maio, Silvia, Zöscher, Peter, Weissensteiner, Hansi, Forer, Lukas, Schachtl-Riess, Johanna F, Amstler, Stephan, Streiter, Gertraud, Pfurtscheller, Cathrin, Paulweber, Bernhard, Kronenberg, Florian, Coassin, Stefan, Schönherr, Sebastian

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The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat von Grüneis, Rebecca, Weissensteiner, Hansi, Lamina, Claudia, Schönherr, Sebastian, Forer, Lukas, Di Maio, Silvia, Streiter, Gertraud, Peters, Annette, Gieger, Christian, Kronenberg, Florian, Coassin, Stefan

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Lysis reagents, cell numbers, and calculation method influence high-throughput measurement of HDL-mediated cholesterol efflux capacity von Schachtl-Riess, Johanna F., Coassin, Stefan, Lamina, Claudia, Demetz, Egon, Streiter, Gertraud, Hilbe, Richard, Kronenberg, Florian

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Analyzing Low-Level mtDNA Heteroplasmy-Pitfalls and Challenges from Bench to Benchmarking von Fazzini, Federica, Fendt, Liane, Schönherr, Sebastian, Forer, Lukas, Schöpf, Bernd, Streiter, Gertraud, Losso, Jamie Lee, Kloss-Brandstätter, Anita, Kronenberg, Florian, Weissensteiner, Hansi

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Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR von Amstler, Stephan, Streiter, Gertraud, Pfurtscheller, Cathrin, Forer, Lukas, Di Maio, Silvia, Weissensteiner, Hansi, Paulweber, Bernhard, Schönherr, Sebastian, Kronenberg, Florian, Coassin, Stefan

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Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals von Di Maio, Silvia, Grüneis, Rebecca, Streiter, Gertraud, Lamina, Claudia, Maglione, Manuel, Schoenherr, Sebastian, üfner, Dietmar, Thorand, Barbara, Peters, Annette, Eckardt, Kai-Uwe, Köttgen, Anna, Kronenberg, Florian, Coassin, Stefan

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The effect of LPA Thr3888Pro on lipoprotein(a) and coronary artery disease is modified by the LPA KIV-2 variant 4925G>A von Grüneis, Rebecca, Lamina, Claudia, Di Maio, Silvia, Schönherr, Sebastian, Zoescher, Peter, Forer, Lukas, Streiter, Gertraud, Peters, Annette, Gieger, Christian, Köttgen, Anna, Kronenberg, Florian, Coassin, Stefan

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Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease von Schachtl-Riess, Johanna F, Kheirkhah, Azin, Grüneis, Rebecca, Di Maio, Silvia, Schoenherr, Sebastian, Streiter, Gertraud, Losso, Jamie Lee, Paulweber, Bernhard, Eckardt, Kai-Uwe, Köttgen, Anna, Lamina, Claudia, Kronenberg, Florian, Coassin, Stefan

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When the genome bluffs: a tandem duplication event during generation of a novel Agmo knockout mouse model fools routine genotyping von Sailer, Sabrina, Coassin, Stefan, Lackner, Katharina, Fischer, Caroline, McNeill, Eileen, Streiter, Gertraud, Kremser, Christian, Maglione, Manuel, Green, Catherine M, Moralli, Daniela, Moschen, Alexander R, Keller, Markus A, Golderer, Georg, Werner-Felmayer, Gabriele, Tegeder, Irmgard, Channon, Keith M, Davies, Benjamin, Werner, Ernst R, Watschinger, Katrin

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KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association study von Schachtl-Riess, Johanna F., Schönherr, Sebastian, Lamina, Claudia, Forer, Lukas, Coassin, Stefan, Streiter, Gertraud, Kheirkhah, Azin, Li, Yong, Meiselbach, Heike, Di Maio, Silvia, Eckardt, Kai-Uwe, Köttgen, Anna, Kronenberg, Florian

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The kringle IV type 2 domain variant 4925G>A causes the elusive association signal of the LPA pentanucleotide repeat von Grüneis, Rebecca, Weissensteiner, Hansi, Lamina, Claudia, Schönherr, Sebastian, Forer, Lukas, Di Maio, Silvia, Streiter, Gertraud, Peters, Annette, Gieger, Christian, Kronenberg, Florian, Coassin, Stefan

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Additional file 3 of Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR von Amstler, Stephan, Streiter, Gertraud, Pfurtscheller, Cathrin, Forer, Lukas, Di Maio, Silvia, Weissensteiner, Hansi, Paulweber, Bernhard, Schönherr, Sebastian, Kronenberg, Florian, Coassin, Stefan

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Additional file 2 of Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR von Amstler, Stephan, Streiter, Gertraud, Pfurtscheller, Cathrin, Forer, Lukas, Di Maio, Silvia, Weissensteiner, Hansi, Paulweber, Bernhard, Schönherr, Sebastian, Kronenberg, Florian, Coassin, Stefan

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Additional file 7 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model von Di Maio, Silvia, Zöscher, Peter, Weissensteiner, Hansi, Forer, Lukas, Schachtl-Riess, Johanna F., Amstler, Stephan, Streiter, Gertraud, Pfurtscheller, Cathrin, Paulweber, Bernhard, Kronenberg, Florian, Coassin, Stefan, Schönherr, Sebastian

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Additional file 1 of Resolving intra-repeat variation in medically relevant VNTRs from short-read sequencing data using the cardiovascular risk gene LPA as a model von Di Maio, Silvia, Zöscher, Peter, Weissensteiner, Hansi, Forer, Lukas, Schachtl-Riess, Johanna F., Amstler, Stephan, Streiter, Gertraud, Pfurtscheller, Cathrin, Paulweber, Bernhard, Kronenberg, Florian, Coassin, Stefan, Schönherr, Sebastian

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Additional file 2 of Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals von Di Maio, Silvia, Grüneis, Rebecca, Streiter, Gertraud, Lamina, Claudia, Maglione, Manuel, Schoenherr, Sebastian, Öfner, Dietmar, Thorand, Barbara, Peters, Annette, Eckardt, Kai-Uwe, Köttgen, Anna, Kronenberg, Florian, Coassin, Stefan

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Heteroplasmy Benchmark Dataset - mitochondrial DNA mixture model - MiSeq - U5-H1-M1-M2-M3-M4-M5 - FASTQ von Fazzini, Federica, Fendt, Liane, Forer, Lukas, Losso, Jamie Lee, Schönherr, Sebastian, Streiter, Gertraud, Schöpf, Bernd, Kloss-Brandstätter, Anita, Kronenberg, Florian, Weissensteiner, Hansi

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Heteroplasmy Benchmark Dataset - mitochondrial DNA mixture model - MiSeq - U5-H1-M1-M2-M3-M4-M5 - BAM von Fazzini, Federica, Fendt, Liane, Forer, Lukas, Schönherr, Sebastian, Losso, Jamie Lee, Streiter, Gertraud, Schöpf, Bernd, Kloss-Brandstätter, Anita, Kronenberg, Florian, Weissensteiner, Hansi

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