Are Gamers Prone to eThrombosis during Long Gaming Sessions? von 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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Extraction of Cell-Free DNA: Evaluation of Efficiency, Quantity, and Quality von Terp, Simone K, Pedersen, Inge S, Stoico, Malene P

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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... von 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:... von 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 von 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 von 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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Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points‐based ACMG/AMP approach von Thomassen, Mads, Mesman, Romy L. S., Hansen, Thomas V. O., Menendez, Mireia, Rossing, Maria, Esteban‐Sánchez, Ada, Tudini, Emma, Törngren, Therese, Parsons, Michael T., Pedersen, Inge S., Teo, Soo H., Kruse, Torben A., Møller, Pål, Borg, Åke, Jensen, Uffe B., Christensen, Lise L., Singer, Christian F., Muhr, Daniela, Santamarina, Marta, Brandao, Rita, Andresen, Brage S., Feng, Bing‐Jian, Canson, Daffodil, Richardson, Marcy E., Karam, Rachid, Pesaran, Tina, LaDuca, Holly, Conner, Blair R., Abualkheir, Nelly, Hoang, Lily, Calléja, Fabienne M. G. R., Andrews, Lesley, James, Paul A., Bunyan, Dave, Hamblett, Amanda, Radice, Paolo, Goldgar, David E., Walker, Logan C., Engel, Christoph, Claes, Kathleen B. M., Macháčková, Eva, Baralle, Diana, Viel, Alessandra, Wappenschmidt, Barbara, Lazaro, Conxi, Vega, Ana, Vreeswijk, Maaike P. G., Hoya, Miguel, Spurdle, Amanda B.

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Cell-free DNA promoter hypermethylation as a diagnostic marker for pancreatic ductal adenocarcinoma – An external validation study von 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 von 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 von Bodker, Julie S., Sonderkaer, Mads, Vesteghem, Charles, Schmitz, Alexander, Brondum, 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., Dybkaer, Karen, Bogsted, Martin

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COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration von 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 von 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 von 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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Extraction of Cell-Free DNA von Terp, Simone K., Pedersen, Inge S., Stoico, Malene P.

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Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population von 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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Common polymorphisms in the microsomal epoxide hydrolase and N-acetyltransferase 2 genes in association with inflammatory bowel disease in the Danish population von Ernst, Anja, Andersen, Vibeke, Østergaard, Mette, Jacobsen, Bent A, Pedersen, Inge S, Drewes, Asbjørn M, Okkels, Henrik, Krarup, Henrik B

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Frequent loss of imprinting of PEG1/MEST in invasive breast cancer von 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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ENIGMA-Evidence-based network for the interpretation of germline mutant alleles: An international initiative to evaluate risk and clinical significance associated with sequence var... von Spurdle, Amanda B., Healey, Sue, Devereau, Andrew, Hogervorst, Frans B. L., Monteiro, Alvaro N. A., Nathanson, Katherine L., Radice, Paolo, Stoppa-Lyonnet, Dominique, Tavtigian, Sean, Wappenschmidt, Barbara, Couch, Fergus J., Goldgar, David E.

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Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status von 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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Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points‐based ACMG/AMP approach von Thomassen, Mads, Mesman, Romy L. S, Hansen, Thomas V. O, Menendez, Mireia, Rossing, Maria, Esteban Sánchez, Ada, Tudini, Emma, Törngren, Therese, Parsons, Michael T, Pedersen, Inge S, Teo, Soo H, Kruse, Torben A, Møller, Pål, Borg, Åke, Jensen, Uffe B, Christensen, Lise L, Singer, Christian F, Muhr, Daniela, Santamarina, Marta, Brandao, Rita, Andresen, Brage S, Feng, Bing Jian, Canson, Daffodil, Richardson, Marcy E, Karam, Rachid, Pesaran, Tina, Laduca, Holly, Conner, Blair R, Abualkheir, Nelly, Hoang, Lily, Calléja, Fabienne M. G. R, Andrews, Lesley, James, Paul A, Bunyan, Dave, Hamblett, Amanda, Radice, Paolo, Goldgar, David E, Walker, Logan C, Engel, Christoph, Claes, Kathleen B. M, Macháčková, Eva, Baralle, Diana, Viel, Alessandra, Wappenschmidt, Barbara, Lazaro, Conxi, Vega, Ana, Vreeswijk, Maaike P. G, Hoya, Miguel de la, Spurdle, Amanda B, Enigma Consortium

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