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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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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Targeted Exome Sequencing of Genes Involved in Rare CNVs in Early-Onset Severe Obesity von Loid, Petra, Pekkinen, Minna, Mustila, Taina, Tossavainen, Päivi, Viljakainen, Heli, Lindstrand, Anna, Mäkitie, Outi

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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, Makitie, Riikka E., Viljakainen, Heli, Kampe, Anders, Tossavainen, Paivi, Lipsanen-Nyman, Marita, Pekkinen, Minna, Makitie, Outi

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A clinical and molecular characterization of a Pakistani family with multicentric osteolysis, nodulosis and arthropathy (MONA) syndrome von Ahmad, Safeer, Muurinen, Mari, Loid, Petra, Ali, Muhammad Zeeshan, Muzammal, Muhammad, Fatima, Sana, Khan, Jabbar, Khan, Muzammil Ahmad, Mäkitie, Outi

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Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome von Loid, Petra, Lipsanen-Nyman, Marita, Ala-Mello, Sirpa, Hannula-Jouppi, Katariina, Kere, Juha, Mäkitie, Outi, Muurinen, Mari

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GNAS, PDE4D, and PRKAR1A Mutations and GNAS Methylation Changes Are Not a Common Cause of Isolated Early-Onset Severe Obesity Among Finnish Children von Loid, Petra, Pekkinen, Minna, Reyes, Monica, Mustila, Taina, Viljakainen, Heli, Juppner, Harald, Makitie, Outi

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SLC26A2-Associated Diastrophic Dysplasia and rMED-Clinical Features in Affected Finnish Children and Review of the Literature von Harkonen, Helmi, Loid, Petra, Makitie, Outi

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Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways von Pettersson, Maria, Viljakainen, Heli, Loid, Petra, Mustila, Taina, Pekkinen, Minna, Armenio, Miriam, Andersson-Assarsson, Johanna C, Mäkitie, Outi, Lindstrand, Anna

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A novel MYT1L mutation in a patient with severe early‐onset obesity and intellectual disability von Loid, Petra, Mäkitie, Riikka, Costantini, Alice, Viljakainen, Heli, Pekkinen, Minna, Mäkitie, Outi

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Germline mutations in a G protein identify signaling cross-talk in T cells von Ham, Hyoungjun, Jing, Huie, Lamborn, Ian T, Kober, Megan M, Koval, Alexey, Berchiche, Yamina A, Anderson, D Eric, Druey, Kirk M, Mandl, Judith N, Isidor, Bertrand, Ferreira, Carlos R, Freeman, Alexandra F, Ganesan, Sundar, Karsak, Meliha, Mustillo, Peter J, Teo, Juliana, Zolkipli-Cunningham, Zarazuela, Chatron, Nicolas, Lecoquierre, François, Oler, Andrew J, Schmid, Jana Pachlopnik, Kuhns, Douglas B, Xu, Xuehua, Hauck, Fabian, Al-Herz, Waleed, Wagner, Matias, Terhal, Paulien A, Muurinen, Mari, Barlogis, Vincent, Cruz, Phillip, Danielson, Jeffrey, Stewart, Helen, Loid, Petra, Rading, Sebastian, Keren, Boris, Pfundt, Rolph, Zarember, Kol A, Vill, Katharina, Potocki, Lorraine, Olivier, Kenneth N, Lesca, Gaetan, Faivre, Laurence, Wong, Melanie, Puel, Anne, Chou, Janet, Tusseau, Maud, Moutsopoulos, Niki M, Matthews, Helen F, Simons, Cas, Taft, Ryan J, Soldatos, Ariane, Masle-Farquhar, Etienne, Pittaluga, Stefania, Brink, Robert, Fink, Danielle L, Kong, Heidi H, Kabat, Juraj, Kim, Woo Sung, Bierhals, Tatjana, Meguro, Kazuyuki, Hsu, Amy P, Gu, Jingwen, Stoddard, Jennifer, Banos-Pinero, Benito, Slack, Maria, Trivellin, Giampaolo, Mazel, Benoît, Soomann, Maarja, Li, Samuel, Watts, Val J, Stratakis, Constantine A, Rodriguez-Quevedo, Maria F, Bruel, Ange-Line, Lipsanen-Nyman, Marita, Saultier, Paul, Jain, Rashmi, Lehalle, Daphne, Torres, Daniel, Sullivan, Kathleen E, Barbarot, Sébastien, Neu, Axel, Duffourd, Yannis, Similuk, Morgan, McWalter, Kirsty, Blanc, Pierre, Bézieau, Stéphane, Jin, Tian, Geha, Raif S, Casanova, Jean-Laurent, Makitie, Outi M, Kubisch, Christian, Edery, Patrick, Christodoulou, John, Germain, Ronald N, Goodnow, Christopher C, Sakmar, Thomas P, Billadeau, Daniel D, Küry, Sébastien, Katanaev, Vladimir L, Zhang, Yu

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Identification of IGLI1/I and IKIAA0825/I Variants in Two Families with Postaxial Polydactyly von Ahmad, Safeer, Ali, Muhammad Zeeshan, Muzammal, Muhammad, Khan, Amjad Ullah, Ikram, Muhammad, Muurinen, Mari, Hussain, Shabir, Loid, Petra, Khan, Muzammil Ahmad, Mäkitie, Outi

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Antibiotics in the first week of life is a risk factor for allergic rhinitis at school age von Alm, Bernt, Goksör, Emma, Pettersson, Rolf, Möllborg, Per, Erdes, Laslo, Loid, Petra, Åberg, Nils, Wennergren, Göran

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The allergic march comprises the coexistence of related patterns of allergic disease not just the progressive development of one disease von Goksör, Emma, Loid, Petra, Alm, Bernt, Åberg, Nils, Wennergren, Göran

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Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly von Ahmad, Safeer, Ali, Muhammad Zeeshan, Muzammal, Muhammad, Khan, Amjad Ullah, Ikram, Muhammad, Muurinen, Mari, Hussain, Shabir, Loid, Petra, Khan, Muzammil Ahmad, Mäkitie, Outi

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Prothrombotic state in young females with severe early-onset obesity von Loid, Petra, Långström, Satu, Viljakainen, Heli, Mäkipernaa, Anne, Heikinheimo, Markku, Mäkitie, Outi

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A persistently high body mass index increases the risk of atopic asthma at school age von Loid, Petra, Goksör, Emma, Alm, Bernt, Pettersson, Rolf, Möllborg, Per, Erdes, Laslo, Åberg, Nils, Wennergren, Göran

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PD05 ‐ Asthma and allergy from infancy into school age – the allergic march revisited von Goksör, Emma, Alm, Bernt, Pettersson, Rolf, Möllborg, Per, Erdes, Laslo, Loid, Petra, Åberg, Nils, Wennergren, Göran

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Case report: A novel de novo IGF2 missense variant in a Finnish patient with Silver-Russell syndrome von Loid, Petra, Lipsanen-Nyman, Marita, Ala-Mello, Sirpa, Hannula-Jouppi, Katariina, Kere, Juha, Mäkitie, Outi, Muurinen, Mari

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