Are Gamers Prone to eThrombosis during Long Gaming Sessions? by Krarup, Kasper B, Krarup, Henrik B, Mørk, Morten, Lundbye-Christensen, Søren, Handberg, Aase, Nguyen, Hien T T, Pedersen, Inge S, Kristensen, Søren R

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Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) s... by Herlin, Morten K, Le, Vang Q, Højland, Allan T, Ernst, Anja, Okkels, Henrik, Petersen, Astrid C, Petersen, Michael B, Pedersen, Inge S

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Patients' choices and opinions on chorionic villous sampling and non‐invasive alternatives for prenatal testing following preimplantation genetic testing for hereditary disorders:... by Toft, Christian L. F., Diemer, Tue, Ingerslev, Hans J., Pedersen, Inge S., Adrian, Stine W., Kesmodel, Ulrik S.

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Epigenetic Regulation of Ferroportin in Primary Cultures of the Rat Blood-Brain Barrier by Helgudottir, Steinunn Sara, Routhe, Lisa J., Burkhart, Annette, Jønsson, Katrine, Pedersen, Inge S., Lichota, Jacek, Moos, Torben

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Promoter hypermethylation of SFRP1 as a prognostic and potentially predictive blood-based biomarker in patients with stage III or IV pancreatic ductal adenocarcinoma by Stubbe, Benjamin E., Madsen, Poul H., Larsen, Anders C., Krarup, Henrik B., Pedersen, Inge S., Hansen, Carsten P., Johansen, Julia S., Henriksen, Stine D., Thorlacius-Ussing, Ole

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Cell-free DNA promoter hypermethylation as a diagnostic marker for pancreatic ductal adenocarcinoma – An external validation study by Henriksen, Stine D., Stubbe, Benjamin E., Madsen, Poul H., Johansen, Julia S., Jensen, Benny V., Hansen, Carsten P., Johansen, Martin N., Pedersen, Inge S., Krarup, Henrik, Thorlacius-Ussing, Ole

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Characterization of BRCA1 and BRCA2 splicing variants: a collaborative report by ENIGMA consortium members by Thomassen, Mads, Blanco, Ana, Montagna, Marco, Hansen, Thomas V. O., Pedersen, Inge S., Gutiérrez-Enríquez, Sara, Menéndez, Mireia, Fachal, Laura, Santamariña, Marta, Steffensen, Ane Y., Jønson, Lars, Agata, Simona, Whiley, Phillip, Tognazzo, Silvia, Tornero, Eva, Jensen, Uffe B., Balmaña, Judith, Kruse, Torben A., Goldgar, David E., Lázaro, Conxi, Diez, Orland, Spurdle, Amanda B., Vega, Ana

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Development of a Precision Medicine Workflow in Hematological Cancers, Aalborg University Hospital, Denmark by Bødker, Julie S, Sønderkær, Mads, Vesteghem, Charles, Schmitz, Alexander, Brøndum, Rasmus F, Sommer, Mia, Rytter, Anne S, Nielsen, Marlene M, Madsen, Jakob, Jensen, Paw, Pedersen, Inge S, Grubach, Lykke, Severinsen, Marianne T, Roug, Anne S, El-Galaly, Tarec C, Dybkær, Karen, Bøgsted, Martin

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COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration by Southey, Melissa C, Park, Daniel J, Nguyen-Dumont, Tu, Campbell, Ian, Thompson, Ella, Trainer, Alison H, Chenevix-Trench, Georgia, Simard, Jacques, Dumont, Martine, Soucy, Penny, Thomassen, Mads, Jønson, Lars, Pedersen, Inge S, Hansen, Thomas Vo, Nevanlinna, Heli, Khan, Sofia, Sinilnikova, Olga, Mazoyer, Sylvie, Lesueur, Fabienne, Damiola, Francesca, Schmutzler, Rita, Meindl, Alfons, Hahnen, Eric, Dufault, Michael R, Chris Chan, Tl, Kwong, Ava, Barkardóttir, Rosa, Radice, Paolo, Peterlongo, Paolo, Devilee, Peter, Hilbers, Florentine, Benitez, Javier, Kvist, Anders, Törngren, Therese, Easton, Douglas, Hunter, David, Lindstrom, Sara, Kraft, Peter, Zheng, Wei, Gao, Yu-Tang, Long, Jirong, Ramus, Susan, Feng, Bing-Jian, Weitzel, Jeffrey N, Nathanson, Katherine, Offit, Kenneth, Joseph, Vijai, Robson, Mark, Schrader, Kasmintan, Wang, San, Kim, Yeong C, Lynch, Henry, Snyder, Carrie, Tavtigian, Sean, Neuhausen, Susan, Couch, Fergus J, Goldgar, David E

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De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome by Lundsgaard, Malene, Le, Vang Q., Ernst, Anja, Laugaard-Jacobsen, Hans C., Rasmussen, Kirsten, Pedersen, Inge S., Petersen, Michael B.

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The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys by Ernst, Anja, Le, Vang Q., Højland, Allan T., Pedersen, Inge S., Sørensen, Tine H., Bjerregaard, Lise L., Lyngbye, Troels J.B., Gammelager, Ninna M., Krarup, Henrik, Petersen, Michael B.

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Genetic variants of glutathione S-transferases μ, θ, and π display no susceptibility to inflammatory bowel disease in the Danish population by Ernst, Anja, Andersen, Vibeke, Østergaard, Mette, Jacobsen, Bent A., Dagiliene, Enrika, Pedersen, Inge S., Drewes, Asbjørn M., Okkels, Henrik, Krarup, Henrik B.

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Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population by Ernst, Anja, Jacobsen, Bent, Østergaard, Mette, Okkels, Henrik, Andersen, Vibeke, Dagiliene, Enrika, Pedersen, Inge S., Thorsgaard, Niels, Drewes, Asbjørn M., Krarup, Henrik B.

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Frequent loss of imprinting of PEG1/MEST in invasive breast cancer by PEDERSEN, I. S, DERVAN, P. A, TOBIN, B, GOREY, T, MCCANN, A, BRODERICK, D, HARRISON, M, MILLER, N, DELANY, E, O'SHEA, D, COSTELLO, P, MCGOLDRICK, A, KEATING, G

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Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status by Pasaniuc, Bogdan, Wu, Lang, Long, Jirong, Andrulis, Irene L., Anton‐Culver, Hoda, Antoniou, Antonis C., Aronson, Kristan J., Auer, Paul L., Barnes, Daniel R., Benitez, Javier, Bermisheva, Marina, Blanco, Ana, Boeckx, Bram, Bolla, Manjeet K., Bonanni, Bernardo, Borg, Ake, Brenner, Hermann, Brüning, Thomas, Cai, Qiuyin, Campbell, Ian, Canisius, Sander, Chang‐Claude, Jenny, Couch, Fergus J., Cox, Angela, Czene, Kamila, Hoya, Miguel, Devilee, Peter, Diez, Orland, Domchek, Susan M., Dörk, Thilo, Eccles, Diana M., Ellberg, Carolina, Engel, Christoph, Friedman, Eitan, Gabrielson, Marike, García‐Closas, Montserrat, García‐Sáenz, José A., Glendon, Gord, Godwin, Andrew K., Goldberg, Mark S., González‐Neira, Anna, Gronwald, Jacek, Haiman, Christopher A., He, Wei, Heyworth, Jane, Hopper, John L., Humphreys, Keith, Jakimovska, Milena, Jakubowska, Anna, James, Paul, Janavicius, Ramunas, John, Esther M., Jung, Audrey, Karlan, Beth Y., Khusnutdinova, Elza, Kristensen, Vessela N., Laitman, Yael, Lindström, Sara, Lubiński, Jan, Mannermaa, Arto, Manoukian, Siranoush, Martens, John W.M., Martinez, Maria E., Matricardi, Laura, Maurer, Tabea, Meindl, Alfons, Menon, Usha, Miller, Austin, Moreno, Fernando, Moserle, Lidia, Offit, Kenneth, Olopade, Olufunmilayo I., Olsson, Håkan, Papp, Janos, Park‐Simon, Tjoung‐Won, Peixoto, Ana, Peterlongo, Paolo, Phillips, Kelly‐Anne, Poppe, Bruce, Radice, Paolo, Rantala, Johanna, Romero, Atocha, Sandler, Dale P., Schmutzler, Rita K., Schoemaker, Minouk J., Soucy, Penny, Stone, Jennifer, Tapper, William J., Thull, Darcy L., Tischkowitz, Marc, Torres, Diana, Truong, Thérèse, Tung, Nadine, Asperen, Christi J., Wappenschmidt, Barbara, Weitzel, Jeffrey N., Yannoukakos, Drakoulis, Ziogas, Argyrios, Easton, Douglas F., Zheng, Wei

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Abstract B047: Promoter hypermethylation of SFRP1 as a prognostic and predictive blood-based biomarker in patients with stage IV pancreatic ductal adenocarcinoma by Stubbe, Benjamin E., Henriksen, Stine D., Madsen, Poul H., Larsen, Anders C., Krarup, Henrik B., Pedersen, Inge S., Johansen, Julia S., Hansen, Carsten P., Thorlacius-Ussing, Ole

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High recovery of cell-free methylated DNA based on a rapid bisulfite-treatment protocol by Pedersen, Inge Søkilde, Krarup, Henrik Bygum, Thorlacius-Ussing, Ole, Madsen, Poul Henning

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The PHF6 Mutation c.1A>G; pM1V Causes Brjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys by Ernst, Anja, Le, Vang Q, Hjland, Allan T, Pedersen, Inge S, Srensen, Tine H, Bjerregaard, Lise L, Lyngbye, Troels JB, Gammelager, Ninna M, Krarup, Henrik, Petersen, Michael B

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Serological and molecular evidence of Rickettsia helvetica in Denmark by Nielsen, Henrik, Fournier, Pierre-Edouard, Pedersen, Inge S., Krarup, Henrik, Ejlertsen, Tove, Raoult, Didier

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Mutations in CARD 15 and smoking confer susceptibility to Crohn's disease in the Danish population by ERNST, Anja, JACOBSEN, Bent, OSTERGAARD, Mette, OKKELS, Henrik, ANDERSEN, Vibeke, DAGILIENE, Enrika, PEDERSEN, Inge S, THORSGAARD, Niels, DREWES, Asbjørn M, KRARUP, Henrik B

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