Prediction of Restraint Moments in Precast, Prestressed Structures Made Continuous by Kytölä Ulla, Laaksonen Anssi

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N-Glycomic Profiling of Microsatellite Unstable Colorectal Cancer by Iiris Ukkola, Pirjo Nummela, Annamari Heiskanen, Matilda Holm, Sadia Zafar, Mia Kero, Caj Haglund, Tero Satomaa, Soili Kytölä, Ari Ristimäki

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Chromosomal aberrations in benign and malignant Bilharzia-associated bladder lesions analyzed by comparative genomic hybridization by Ibrahim Muntaser, Elagib Atif, Mandahl Nils, Abdel-Hameed Mohamed, Leithy Mona EL, Kytola Soili, Fadl-Elmula Imad, Larsson Catharina, Heim Sverre

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Detection of KRAS mutations in liquid biopsies from metastatic colorectal cancer patients using droplet digital PCR, Idylla, and next generation sequencing. by Matilda Holm, Emma Andersson, Emerik Osterlund, Ali Ovissi, Leena-Maija Soveri, Anna-Kaisa Anttonen, Soili Kytölä, Kristiina Aittomäki, Pia Osterlund, Ari Ristimäki

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P626: Clinical utility of structural variant calling using breakpoint analysis method for targeted NGS gene panels by Lotta Koskinen, Margarita Andreevskaya, Mikko Muona, Tuuli Pietila, Janica Djupsjöbacka, Ville Kytölä, Kati Kämpjärvi, Samuel Myllykangas, Pertteli Salmenperä, Juha Koskenvuo, Miko Valori

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Targeting Apoptosis Pathways With BCL2 and MDM2 Inhibitors in Adult B-cell Acute Lymphoblastic Leukemia by Helena Hohtari, Matti Kankainen, Shady Adnan-Awad, Bhagwan Yadav, Swapnil Potdar, Aleksandr Ianevski, Olli Dufva, Caroline Heckman, Veronika Sexl, Soili Kytölä, Satu Mustjoki, Kimmo Porkka

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Epigenetic modifier gene mutations in chronic myeloid leukemia (CML) at diagnosis are associated with risk of relapse upon treatment discontinuation by Shady Adnan Awad, Oscar Brück, Naranie Shanmuganathan, Timo Jarvinen, Hanna Lähteenmäki, Jay Klievink, Hazem Ibrahim, Soili Kytölä, Perttu Koskenvesa, Timothy P. Hughes, Susan Branford, Matti Kankainen, Satu Mustjoki

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P409: BCL-2/BCL-XL INHIBITION INDUCES APOPTOSIS AND CIRCUMVENTS VENETOCLAX RESISTANCE IN TP53-MUTATED ACUTE MYELOID LEUKEMIA by Ida Vänttinen, Sari Kytölä, Olli Dufva, Monica Hellesøy, Stein-Erik Gullaksen, Tanja Ruokoranta, Oscar Brück, Sanna Siitonen, Pia Ettala, Marja Pyörälä, Johanna Rimpilainen, Timo Siitonen, Bjorn Tore Gjertsen, Caroline Heckman, Heikki Kuusanmäki, Mika Kontro

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P487: Genetic findings from multi-gene panel for primary ciliary dyskinesia by Victoria Howell, Johanna Huusko, Manuel Bernal, Allison Faber, Satu Valo, Kimberly Gall, Lotta Koskinen, Tiia Kangas-Kontio, Inka Saarinen, Ville Kytölä, Pauli Siivonen, Janica Djupsjöbacka, Massimiliano Gentile, Pertteli Salmenperä, Jussi Paananen, Samuel Myllykangas, Juha Koskenvuo

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Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients by Krista Heliö, Marcos Cicerchia, Julie Hathaway, Johanna Tommiska, Johanna Huusko, Inka Saarinen, Lotta Koskinen, Mikko Muona, Ville Kytölä, Janica Djupsjöbacka, Massimiliano Gentile, Pertteli Salmenperä, Tero-Pekka Alastalo, Christian Steinberg, Tiina Heliö, Jussi Paananen, Samuel Myllykangas, Juha Koskenvuo

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Whole-exome sequencing identifies novel protein-altering variants associated with serum apolipoprotein and lipid concentrations by Niina Sandholm, Ronja Hotakainen, Jani K. Haukka, Fanny Jansson Sigfrids, Emma H. Dahlström, Anni A. Antikainen, Erkka Valo, Anna Syreeni, Elina Kilpeläinen, Anastasia Kytölä, Aarno Palotie, Valma Harjutsalo, Carol Forsblom, Per-Henrik Groop, on behalf of the FinnDiane Study Group

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P562: CAPILLARY BLOOD SAMPLING ALLOWS FEASIBLE METHOD FOR VENETOCLAX CONCENTRATION MEASUREMENT IN AN ACADEMIC MULTICENTER CLINICAL TRIAL CONTEXT by Sari Kytölä, Ida Vänttinen, Heikki Kuusanmäki, Tanja Ruokoranta, Mika Kurkela, Johanna Kiiski, Annasofia Holopainen, Anu Partanen, Milla E.L. Kuusisto, Sirpa Koskela, Riikka Räty, Maija Itälä-Remes, Pia Ettala, Johanna Rimpiläinen, Timo Siitonen, Marja Pyörälä, Janne T. Backman, Mikko Niemi, Mika Kontro

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The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1) by Bassett, J, Pannett, A, Forbes, SA, Thakker, R, McCarthy, M, Read, A, Teh, B, Larsson, C, Kytola, S, Leisti, J, Salmela, P, Weber, G, Giraud, S, Zhang, C, Calender, A, Hoppener, J, vanAmstel, H, Lips, C, Kas, K, VandeVen, W, Gaudray, P

KRAS-G12C Mutation in One Real-Life and Three Population-Based Nordic Cohorts of Metastatic Colorectal Cancer by Emerik Osterlund, Ari Ristimäki, Ari Ristimäki, Soili Kytölä, Soili Kytölä, Teijo Kuopio, Teijo Kuopio, Eetu Heervä, Eetu Heervä, Timo Muhonen, Timo Muhonen, Päivi Halonen, Päivi Halonen, Raija Kallio, Raija Kallio, Leena-Maija Soveri, Leena-Maija Soveri, Jari Sundström, Jari Sundström, Mauri Keinänen, Annika Ålgars, Annika Ålgars, Raija Ristamäki, Raija Ristamäki, Halfdan Sorbye, Halfdan Sorbye, Per Pfeiffer, Per Pfeiffer, Luís Nunes, Tapio Salminen, Tapio Salminen, Annamarja Lamminmäki, Annamarja Lamminmäki, Markus J. Mäkinen, Markus J. Mäkinen, Tobias Sjöblom, Helena Isoniemi, Helena Isoniemi, Bengt Glimelius, Pia Osterlund, Pia Osterlund, Pia Osterlund, Pia Osterlund, Pia Osterlund, Pia Osterlund

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The European Consortium on MEN1. Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1). by Bassett, J, Pannett, A, Forbes, SA, Thakker, R, McCarthy, M, Read, A, Teh, B, Larsson, C, Kytölä, S, Leisti, J, Salmela, P, Weber, G, Giraud, S, Zhang, C, Calender, A, Höppener, J, Ploos van Amstel, H, Lips, C, Kas, K, Van de Yen, W, Gaudray, P

The search for the MEN1 gene. The European Consortium on MEN-1. by Lemmes, I, Van de Ven, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, Pugeat, M, Peix, J, Caldener, A, Parente, F, Quincey, D, Courseaux, A, Carle, G, Gaudray, P, De Wit, M, Lips, C, Hoppener, J, Khodaei, S, Grant, A, Weber, G, Teh, B, Farnebo, F, Kytola, S, Grimmond, S

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene by Lemmens, I, Merregaert, J, Van De Ven, W, Koen, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, De Witte, K, Salandre, J, Lenoir, G, Calender, A, Parente, F, Quincey, D, Courseaux, A, Carle, G, Gaudray, P, De Wit, M, Lips, C, Höppener, J, Khodaei, S, Grant, A, Weber, G, Kytölä, S, Teh, B

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1. by Lemmens, I, Merregaert, J, Van de Ven, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, De Witte, K, Salandre, J, Lenoir, G, Calender, A, Parente, F, Quincey, D, Courseaux, A, Carle, G, Gaudray, P, De Wit, M, Lips, C, Höppener, J, Khodaei, S, Grant, A, Weber, G, Kytölä, S, Thakker, R

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1. by Lemmens, I, Van de Ven, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, De Witte, K, Salandre, J, Lenoir, G, Pugeat, M, Calender, A, Parente, F, Quincey, D, Gaudray, P, De Wit, M, Lips, C, Höppener, J, Khodaei, S, Grant, A, Weber, G, Kytölä, S, Teh, B, Farnebo, F, Thakker, R

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene by Lemmens, I, VandeVen, W, Kas, K, Zhang, C, Giraud, S, Wautot, V, Buisson, N, DeWitte, K, Salandre, J, Lenoir, G, Pugeat, M, Calender, A, Parente, F, Quincey, D, Gaudray, P, DeWit, M, Lips, C, Hoppener, J, Khodaei, S, Grant, A, Weber, G, Kytola, S, Teh, B, Farnebo, F, Phelan, C