Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects von Machado, Rajiv D., Southgate, Laura, Eichstaedt, Christina A., Aldred, Micheala A., Austin, Eric D., Best, D. Hunter, Chung, Wendy K., Benjamin, Nicola, Elliott, C. Gregory, Eyries, Mélanie, Fischer, Christine, Gräf, Stefan, Hinderhofer, Katrin, Humbert, Marc, Keiles, Steven B., Loyd, James E., Morrell, Nicholas W., Newman, John H., Soubrier, Florent, Trembath, Richard C., Viales, Rebecca Rodríguez, Grünig, Ekkehard

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Regulation of Bone Morphogenetic Protein Receptor Type II Expression by FMR1 /Fragile X Mental Retardation Protein in Human Granulosa Cells in the Context of Poor Ovarian Response von Nguyen, Xuan Phuoc, Vilkaite, Adriana, Bender, Ulrike, Dietrich, Jens E, Hinderhofer, Katrin, Strowitzki, Thomas, Rehnitz, Julia

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Activation of AKT/mammalian target of rapamycin signaling in the peripheral blood of women with premature ovarian insufficiency and its correlation with FMR1 expression von Rehnitz, Julia, Messmer, Birgitta, Bender, Ulrike, Nguyen, Xuan Phuoc, Germeyer, Ariane, Hinderhofer, Katrin, Strowitzki, Thomas, Capp, Edison

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Marker chromosomes can arise from chromothripsis and predict adverse prognosis in acute myeloid leukemia von Bochtler, Tilmann, Granzow, Martin, Stölzel, Friedrich, Kunz, Christina, Mohr, Brigitte, Kartal-Kaess, Mutlu, Hinderhofer, Katrin, Heilig, Christoph E., Kramer, Michael, Thiede, Christian, Endris, Volker, Kirchner, Martina, Stenzinger, Albrecht, Benner, Axel, Bornhäuser, Martin, Ehninger, Gerhard, Ho, Anthony D., Jauch, Anna, Krämer, Alwin

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Gene panel diagnostics reveals new pathogenic variants in pulmonary arterial hypertension von Eichstaedt, Christina A, Saßmannshausen, Zoe, Shaukat, Memoona, Cao, Ding, Xanthouli, Panagiota, Gall, Henning, Sommer, Natascha, Ghofrani, Hossein-Ardeschir, Seyfarth, Hans-Jürgen, Lerche, Marianne, Halank, Michael, Kleymann, Janina, Benjamin, Nicola, Harutyunova, Satenik, Egenlauf, Benjamin, Milger, Katrin, Rosenkranz, Stephan, Ewert, Ralf, Klose, Hans, Hoeper, Marius M, Olsson, Karen M, Lankeit, Mareike, Lange, Tobias J, Hinderhofer, Katrin, Grünig, Ekkehard

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Identification of a transcription factor specifically expressed at the onset of leaf senescence von Hinderhofer, Katrin, Zentgraf, Ulrike

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Myeloproliferative Diseases as Possible Risk Factor for Development of Chronic Thromboembolic Pulmonary Hypertension-A Genetic Study von Eichstaedt, Christina A, Verweyen, Jeremias, Halank, Michael, Benjamin, Nicola, Fischer, Christine, Mayer, Eckhard, Guth, Stefan, Wiedenroth, Christoph B, Egenlauf, Benjamin, Harutyunova, Satenik, Xanthouli, Panagiota, Marra, Alberto M, Wilkens, Heinrike, Ewert, Ralf, Hinderhofer, Katrin, Grünig, Ekkehard

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FMR1 expression in human granulosa cells increases with exon 1 CGG repeat length depending on ovarian reserve von Rehnitz, Julia, Alcoba, Diego D, Brum, Ilma S, Dietrich, Jens E, Youness, Berthe, Hinderhofer, Katrin, Messmer, Birgitta, Freis, Alexander, Strowitzki, Thomas, Germeyer, Ariane

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Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wi... von Granzow, Martin, Hegenbart, Ute, Hinderhofer, Katrin, Hose, Dirk, Seckinger, Anja, Bochtler, Tilmann, Hemminki, Kari, Goldschmidt, Hartmut, Schönland, Stefan O, Jauch, Anna

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Noninvasive Risk Stratification of Patients With Transthyretin Amyloidosis von Kristen, Arnt V., MD, Scherer, Katrin, MS, Buss, Sebastian, MD, aus dem Siepen, Fabian, MS, Haufe, Sabine, MD, Bauer, Ralf, MD, Hinderhofer, Katrin, PhD, Giannitsis, Evangelos, MD, Hardt, Stefan, MD, Haberkorn, Uwe, MD, Katus, Hugo A., MD, Steen, Henning, MD

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Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: urinary organic acid profiles and expanded spectrum of mutations von Pitt, James J., Peters, Heidi, Boneh, Avihu, Yaplito-Lee, Joy, Wieser, Stefanie, Hinderhofer, Katrin, Johnson, David, Zschocke, Johannes

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Identification of a new intronic BMPR2-mutation and early diagnosis of heritable pulmonary arterial hypertension in a large family with mean clinical follow-up of 12 years von Hinderhofer, Katrin, Fischer, Christine, Pfarr, Nicole, Szamalek-Hoegel, Justyna, Lichtblau, Mona, Nagel, Christian, Egenlauf, Benjamin, Ehlken, Nicola, Grünig, Ekkehard

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Mutation in BMPR2 Promoter: A 'Second Hit' for Manifestation of Pulmonary Arterial Hypertension? von Viales, Rebecca Rodríguez, Eichstaedt, Christina A, Ehlken, Nicola, Fischer, Christine, Lichtblau, Mona, Grünig, Ekkehard, Hinderhofer, Katrin

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The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1 von Ott, Tim, Kaufmann, Lilian, Granzow, Martin, Hinderhofer, Katrin, Bartram, Claus R, Theiß, Susanne, Seitz, Angelika, Paramasivam, Nagarajan, Schulz, Angela, Moog, Ute, Blum, Martin, Evers, Christina M

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Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary Genes von Weiss, Birgit, Eberle, Birgit, Roeth, Ralph, de Bruin, Christiaan, Lui, Julian C, Paramasivam, Nagarajan, Hinderhofer, Katrin, van Duyvenvoorde, Hermine A, Baron, Jeffrey, Wit, Jan M, Rappold, Gudrun A

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Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension von Pfarr, Nicole, Fischer, Christine, Ehlken, Nicola, Becker-Grünig, Tabea, López-González, Vanesa, Gorenflo, Matthias, Hager, Alfred, Hinderhofer, Katrin, Miera, Oliver, Nagel, Christian, Schranz, Dietmar, Grünig, Ekkehard

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Mutually reinforcing effects of genetic variants and interferon-β 1a therapy for pulmonary arterial hypertension development in multiple sclerosis patients von Lerche, Marianne, Eichstaedt, Christina A., Hinderhofer, Katrin, Grünig, Ekkehard, Tausche, Kristin, Ziemssen, Tjalf, Halank, Michael, Wirtz, Hubert, Seyfarth, Hans-Jürgen

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Clinical Research in Vulnerable Populations: Variability and Focus of Institutional Review Boards' Responses von Kästner, Bärbel, Behre, Simone, Lutz, Nadine, Bürger, Friederike, Luntz, Steffen, Hinderhofer, Katrin, Bendszus, Martin, Hoffmann, Georg F, Ries, Markus

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Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations von Pfarr, Nicole, Szamalek-Hoegel, Justyna, Fischer, Christine, Hinderhofer, Katrin, Nagel, Christian, Ehlken, Nicola, Tiede, Henning, Olschewski, Horst, Reichenberger, Frank, Ghofrani, Ardeschir H A, Seeger, Werner, Grünig, Ekkehard

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Is iron deficiency caused by BMPR2 mutations or dysfunction in pulmonary arterial hypertension patients? von Theobald, Vivienne, Grünig, Ekkehard, Benjamin, Nicola, Seyfarth, Hans‐Jürgen, Halank, Michael, Schneider, Marc A., Richtmann, Sarah, Kazdal, Daniel, Hinderhofer, Katrin, Xanthouli, Panagiota, Egenlauf, Benjamin, Harutyunova, Satenik, Hoeper, Marius M., Jonigk, Danny, Sparla, Richard, Muckenthaler, Martina U., Eichstaedt, Christina A.

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