FGF23 and its role in X-linked hypophosphatemia-related morbidity von Beck-Nielsen, Signe Sparre, Mughal, Zulf, Haffner, Dieter, Nilsson, Ola, Levtchenko, Elena, Ariceta, Gema, de Lucas Collantes, Carmen, Schnabel, Dirk, Jandhyala, Ravi, Mäkitie, Outi

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New Insights Into Monogenic Causes of Osteoporosis von Mäkitie, Riikka E, Costantini, Alice, Kämpe, Anders, Alm, Jessica J, Mäkitie, Outi

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Altered MicroRNA Profile in Osteoporosis Caused by Impaired WNT Signaling von Mäkitie, Riikka E, Hackl, Matthias, Niinimäki, Riitta, Kakko, Sakari, Grillari, Johannes, Mäkitie, Outi

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Bisphosphonate treatment for skeletal complications in paediatric cancer—Experience from a single tertiary centre von Utriainen, Pauliina, Stenberg, Jalmari E. E., Vettenranta, Kim K., Mäkitie, Outi M.

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Early‐Onset Osteoporosis: Rare Monogenic Forms Elucidate the Complexity of Disease Pathogenesis Beyond Type I Collagen von Costantini, Alice, Mäkitie, Riikka E., Hartmann, Markus A., Fratzl‐Zelman, Nadja, Zillikens, M. Carola, Kornak, Uwe, Søe, Kent, Mäkitie, Outi

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Impaired WNT signaling and the spine—Heterozygous WNT1 mutation causes severe age-related spinal pathology von Mäkitie, Riikka E, Niinimäki, Tuukka, Nieminen, Miika T, Schalin-Jäntti, Camilla, Niinimäki, Jaakko, Mäkitie, Outi

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Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement von Mantovani, Giovanna, Bastepe, Murat, Monk, David, de Sanctis, Luisa, Thiele, Susanne, Usardi, Alessia, Ahmed, S. Faisal, Bufo, Roberto, Choplin, Timothée, De Filippo, Gianpaolo, Devernois, Guillemette, Eggermann, Thomas, Elli, Francesca M., Freson, Kathleen, García Ramirez, Aurora, Germain-Lee, Emily L., Groussin, Lionel, Hamdy, Neveen, Hanna, Patrick, Hiort, Olaf, Jüppner, Harald, Kamenický, Peter, Knight, Nina, Kottler, Marie-Laure, Le Norcy, Elvire, Lecumberri, Beatriz, Levine, Michael A., Mäkitie, Outi, Martin, Regina, Martos-Moreno, Gabriel Ángel, Minagawa, Masanori, Murray, Philip, Pereda, Arrate, Pignolo, Robert, Rejnmark, Lars, Rodado, Rebecca, Rothenbuhler, Anya, Saraff, Vrinda, Shoemaker, Ashley H., Shore, Eileen M., Silve, Caroline, Turan, Serap, Woods, Philip, Zillikens, M. Carola, Perez de Nanclares, Guiomar, Linglart, Agnès

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Decreasing incidence and changing pattern of childhood fractures: A population‐based study von Mäyränpää, Mervi K, Mäkitie, Outi, Kallio, Pentti E

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Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial von Bishop, Nick, Prof, Adami, Silvano, MD, Ahmed, S Faisal, MD, Antón, Jordi, MD, Arundel, Paul, MD, Burren, Christine P, MD, Devogelaer, Jean-Pierre, MD, Hangartner, Thomas, PhD, Hosszú, Eva, MD, Lane, Joseph M, MD, Lorenc, Roman, MD, Mäkitie, Outi, MD, Munns, Craig F, MD, Paredes, Ana, MD, Pavlov, Helene, MD, Plotkin, Horacio, MD, Raggio, Cathleen L, MD, Reyes, Maria Loreto, MD, Schoenau, Eckhard, MD, Semler, Oliver, MD, Sillence, David O, MD, Steiner, Robert D, MD

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SGMS2 in primary osteoporosis with facial nerve palsy von Pihlström, Sandra, Richardt, Sampo, Määttä, Kirsi, Pekkinen, Minna, Olkkonen, Vesa M., Mäkitie, Outi, Mäkitie, Riikka E.

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Mesenchymal Cell‐Derived Juxtacrine Wnt1 Signaling Regulates Osteoblast Activity and Osteoclast Differentiation von Wang, Fan, Tarkkonen, Kati, Nieminen‐Pihala, Vappu, Nagano, Kenichi, Majidi, Rana Al, Puolakkainen, Tero, Rummukainen, Petri, Lehto, Jemina, Roivainen, Anne, Zhang, Fu‐Ping, Mäkitie, Outi, Baron, Roland, Kiviranta, Riku

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Growth in achondroplasia: Development of height, weight, head circumference, and body mass index in a European cohort von Merker, Andrea, Neumeyer, Luitgard, Hertel, Niels Thomas, Grigelioniene, Giedre, Mäkitie, Outi, Mohnike, Klaus, Hagenäs, Lars

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Biomarkers in WNT1 and PLS3 Osteoporosis: Altered Concentrations of DKK1 and FGF23 von Mäkitie, Riikka E, Kämpe, Anders, Costantini, Alice, Alm, Jessica J, Magnusson, Per, Mäkitie, Outi

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Oral findings in patients with cartilage-hair hypoplasia - cross-sectional observational study von Arponen, Heidi, Vakkilainen, Svetlana, Rautava, Jaana, Mäkitie, Outi

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A 30-Year Prospective Follow-Up Study Reveals Risk Factors for Early Death in Cartilage-Hair Hypoplasia von Vakkilainen, Svetlana, Taskinen, Mervi, Klemetti, Paula, Pukkala, Eero, Mäkitie, Outi

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A novel link between chronic inflammation and humanin regulation in children von Zhao, Yunhan, Mäkitie, Outi, Laakso, Saila, Fedosova, Vera, Sävendahl, Lars, Zaman, Farasat

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Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathy von Ishaq, Tayyaba, Loid, Petra, Ishaq, Hafiza Abida, Seo, Go Hun, Mäkitie, Outi, Naz, Sadaf

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Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children von Kämpe, Anders, Enlund-Cerullo, Maria, Valkama, Saara, Holmlund-Suila, Elisa, Rosendahl, Jenni, Hauta-Alus, Helena, Pekkinen, Minna, Andersson, Sture, Mäkitie, Outi

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Lipocalin-2 is associated with FGF23 in WNT1 and PLS3 osteoporosis von Loid, Petra, Hauta-alus, Helena, Mäkitie, Outi, Magnusson, Per, Mäkitie, Riikka E.

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Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity von Loid, Petra, Mustila, Taina, Mäkitie, Riikka E, Viljakainen, Heli, Kämpe, Anders, Tossavainen, Päivi, Lipsanen-Nyman, Marita, Pekkinen, Minna, Mäkitie, Outi

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