Bone cell functions in PPIB knock-out mouse model for type IX osteogenesis imperfecta are distinct from classical dominant OI by Ying Liu, Theresa Hefferan, Nadja Fratzl-Zelman, Joan Marini

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Impact of Tenofovir Disoproxil‐Induced Fanconi Syndrome on Bone Material Quality: A Case Report by Benjamin Hadzimuratovic, Judith Haschka, Markus A Hartmann, Stéphane Blouin, Nadja Fratzl‐Zelman, Jochen Zwerina, Roland Kocijan

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Abnormal Bone Tissue Organization and Osteocyte Lacunocanalicular Network in Early‐Onset Osteoporosis Due to SGMS2 Mutations by Riikka E. Mäkitie, Stéphane Blouin, Ville‐Valtteri Välimäki, Sandra Pihlström, Kirsi Määttä, Minna Pekkinen, Nadja Fratzl‐Zelman, Outi Mäkitie, Markus A. Hartmann

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Cardiac, bone and growth plate manifestations in hypocalcemic infants: revealing the hidden body of the vitamin D deficiency iceberg by Suma Uday, Nadja Fratzl-Zelman, Paul Roschger, Klaus Klaushofer, Ashish Chikermane, Vrinda Saraff, Ted Tulchinsky, Tom D. Thacher, Tamas Marton, Wolfgang Högler

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Investigating the role of ASCC1 in the causation of bone fragility by Barbara Voraberger, Johannes A. Mayr, Nadja Fratzl-Zelman, Nadja Fratzl-Zelman, Stéphane Blouin, Stéphane Blouin, Suma Uday, Robert Kopajtich, Robert Kopajtich, Marijke Koedam, Helena Hödlmayr, Saskia B. Wortmann, Saskia B. Wortmann, Bernhard Csillag, Holger Prokisch, Holger Prokisch, Bram C. J. van der Eerden, Ahmed El-Gazzar, Wolfgang Högler

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Bone tissue in murine atypical type VI osteogenesis imperfecta has changes in vascular pores and matrix organization, plus classic OI hypermineralization by Ghazal Hedjazi, Gali Guterman-Ram, Stéphane Blouin, Paul Roschger, Victoria Schemenz, Wolfgang Wagermaier, Peter Fratzl, Jochen Zwerina, Nadja Fratzl-Zelman, Joan C. Marini

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A novel cryptic splice site mutation in COL1A2 as a cause of osteogenesis imperfecta by Ahmed El-Gazzar, Johannes A. Mayr, Barbara Voraberger, Karin Brugger, Stéphane Blouin, Katharina Tischlinger, Hans-Christoph Duba, Holger Prokisch, Nadja Fratzl-Zelman, Wolfgang Högler

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New Ifitm5 S42L mouse model for atypical type VI OI connects types V and VI Osteogenesis Imperfecta by Gali Guterman-Ram, Ghazal Hedjazi, Chris Stephan, Stéphane Blouin, Paul Roschger, Klaus Klaushofer, Jochen Zwerina, Kenneth M. Kozloff, Nadja Fratzl-Zelman, Joan C. Marini

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A neomorphic variant in SP7 alters sequence specificity and causes a high-turnover bone disorder by Julian C. Lui, Adalbert Raimann, Hironori Hojo, Lijin Dong, Paul Roschger, Bijal Kikani, Uwe Wintergerst, Nadja Fratzl-Zelman, Youn Hee Jee, Gabriele Haeusler, Jeffrey Baron

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Bone matrix mineralization increases with age and remains elevated after Teriparatide treatment in WNT1 or PLS3 mutation-related low-turnover osteoporosis: A transiliac bone biopsy... by Nadja Fratzl-Zelman, Katherine Wesseling-Perry, Riika E. Mäkitie, Paul Roschger, Jochen Zwerina, Ville-Valtteri Välimäki, Christine M. Laine, Matti J. Välimäki, Renata C. Pereira, Outi Mäkitie

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SMAD3 mutation in LDS3 causes bone fragility by impairing the TGF-β pathway and enhancing osteoclastogenesis by Ahmed El-Gazzar, Heeseog Kang, Nadja Fratzl-Zelman, Emma Webb, Aileen M. Barnes, Milena Jovanovic, Sarju G. Mehta, Vipan Datta, Vrinda Saraff, Ryan K. Dale, Frank Rauch, Joan C. Marini, Wolfgang Högler

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Somatic activating mutations in MAP2K1 cause melorheostosis by Heeseog Kang, Smita Jha, Zuoming Deng, Nadja Fratzl-Zelman, Wayne A. Cabral, Aleksandra Ivovic, Françoise Meylan, Eric P. Hanson, Eileen Lange, James Katz, Paul Roschger, Klaus Klaushofer, Edward W. Cowen, Richard M. Siegel, Joan C. Marini, Timothy Bhattacharyya

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Bi‐allelic mutation in SEC16B alters collagen trafficking and increases ER stress by Ahmed El‐Gazzar, Barbara Voraberger, Frank Rauch, Mario Mairhofer, Katy Schmidt, Brecht Guillemyn, Goran Mitulović, Veronika Reiterer, Margot Haun, Michaela M Mayr, Johannes A Mayr, Susanne Kimeswenger, Oliver Drews, Vrinda Saraff, Nick Shaw, Nadja Fratzl‐Zelman, Sofie Symoens, Hesso Farhan, Wolfgang Högler

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