Are Gamers Prone to eThrombosis during Long Gaming Sessions?
Krarup, Kasper B, Krarup, Henrik B, Mørk, Morten, Lundbye-Christensen, Søren, Handberg, Aase, Nguyen, Hien T T, Pedersen, Inge S, Kristensen, Søren R
Published in Life (Basel, Switzerland) (01.04.2024)
Published in Life (Basel, Switzerland) (01.04.2024)
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Development of a Precision Medicine Workflow in Hematological Cancers, Aalborg University Hospital, Denmark
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
Published in Cancers (29.01.2020)
Published in Cancers (29.01.2020)
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Extraction of Cell-Free DNA: Evaluation of Efficiency, Quantity, and Quality
Terp, Simone K, Pedersen, Inge S, Stoico, Malene P
Published in The Journal of molecular diagnostics : JMD (01.04.2024)
Published in The Journal of molecular diagnostics : JMD (01.04.2024)
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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) syndrome. A case report
Herlin, Morten K, Le, Vang Q, Højland, Allan T, Ernst, Anja, Okkels, Henrik, Petersen, Astrid C, Petersen, Michael B, Pedersen, Inge S
Published in Human reproduction (Oxford) (29.09.2019)
Published in Human reproduction (Oxford) (29.09.2019)
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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: A cross‐sectional questionnaire study
Toft, Christian L. F., Diemer, Tue, Ingerslev, Hans J., Pedersen, Inge S., Adrian, Stine W., Kesmodel, Ulrik S.
Published in Prenatal diagnosis (01.02.2022)
Published in Prenatal diagnosis (01.02.2022)
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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
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
Published in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] (01.08.2023)
Published in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] (01.08.2023)
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Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points‐based ACMG/AMP approach
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.
Published in Human mutation (01.12.2022)
Published in Human mutation (01.12.2022)
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Cell-free DNA promoter hypermethylation as a diagnostic marker for pancreatic ductal adenocarcinoma – An external validation study
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
Published in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] (01.09.2021)
Published in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] (01.09.2021)
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Characterization of BRCA1 and BRCA2 splicing variants: a collaborative report by ENIGMA consortium members
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
Published in Breast cancer research and treatment (01.04.2012)
Published in Breast cancer research and treatment (01.04.2012)
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COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
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
Published in Breast cancer research : BCR (21.06.2013)
Published in Breast cancer research : BCR (21.06.2013)
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De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome
Lundsgaard, Malene, Le, Vang Q., Ernst, Anja, Laugaard-Jacobsen, Hans C., Rasmussen, Kirsten, Pedersen, Inge S., Petersen, Michael B.
Published in Molecular syndromology (01.01.2017)
Published in Molecular syndromology (01.01.2017)
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Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group
Nielsen, Sarah M, Eccles, Diana M, Romero, Iris L, Al-Mulla, Fahd, Balmaña, Judith, Biancolella, Michela, Bslok, Rien, Caligo, Maria Adelaide, Calvello, Mariarosaria, Capone, Gabriele Lorenzo, Cavalli, Pietro, Chan, T L Chris, Claes, Kathleen B M, Cortesi, Laura, Couch, Fergus J, de la Hoya, Miguel, De Toffol, Simona, Diez, Orland, Domchek, Susan M, Eeles, Ros, Efremidis, Anna, Fostira, Florentia, Goldgar, David, Hadjisavvas, Andreas, Hansen, Thomas V O, Hirasawa, Akira, Houdayer, Claude, Kleiblova, Petra, Krieger, Sophie, Lázaro, Conxi, Loizidou, Maria, Manoukian, Siranoush, Mensenkamp, Arjen R, Moghadasi, Setareh, Monteiro, Alvaro N, Mori, Luigi, Morrow, April, Naldi, Nadia, Nielsen, Henriette R, Olopade, Olufunmilayo I, Pachter, Nicholas S, Palmero, Edenir I, Pedersen, Inge S, Piane, Maria, Puzzo, Marianna, Robson, Mark, Rossing, Maria, Sini, Maria Christina, Solano, Angela, Soukupova, Jana, Tedaldi, Gianluca, Teixeira, Manuel, Thomassen, Mads, Tibiletti, Maria Grazia, Toland, Amanda, Törngren, Therese, Vaccari, Erica, Varesco, Liliana, Vega, Ana, Wallis, Yvonne, Wappenschmidt, Barbara, Weitzel, Jeffrey, Spurdle, Amanda B, De Nicolo, Arcangela, Gómez-García, Encarna B
Published in JCO precision oncology (2018)
Published in JCO precision oncology (2018)
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The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys
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.
Published in Molecular syndromology (01.10.2015)
Published in Molecular syndromology (01.10.2015)
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Genetic variants of glutathione S-transferases mu, theta, and pi display no susceptibility to inflammatory bowel disease in the Danish population
Ernst, Anja, Andersen, Vibeke, Østergaard, Mette, Jacobsen, Bent A, Dagiliene, Enrika, Pedersen, Inge S, Drewes, Asbjørn M, Okkels, Henrik, Krarup, Henrik B
Published in Scandinavian journal of gastroenterology (01.09.2010)
Published in Scandinavian journal of gastroenterology (01.09.2010)
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Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population
Ernst, Anja, Jacobsen, Bent, Østergaard, Mette, Okkels, Henrik, Andersen, Vibeke, Dagiliene, Enrika, Pedersen, Inge S, Thorsgaard, Niels, Drewes, Asbjørn M, Krarup, Henrik B
Published in Scandinavian journal of gastroenterology (01.01.2007)
Published in Scandinavian journal of gastroenterology (01.01.2007)
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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
Ernst, Anja, Andersen, Vibeke, Ostergaard, Mette, Jacobsen, Bent A, Pedersen, Inge S, Drewes, Asbjørn M, Okkels, Henrik, Krarup, Henrik B
Published in European journal of gastroenterology & hepatology (01.03.2011)
Published in European journal of gastroenterology & hepatology (01.03.2011)
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Frequent loss of imprinting of PEG1/MEST in invasive breast cancer
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
Published in Cancer research (Chicago, Ill.) (01.11.1999)
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Published in Cancer research (Chicago, Ill.) (01.11.1999)
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Extraction of Cell-Free DNA
Terp, Simone K., Pedersen, Inge S., Stoico, Malene P.
Published in The Journal of molecular diagnostics : JMD (01.04.2024)
Published in The Journal of molecular diagnostics : JMD (01.04.2024)
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Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status
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
Published in Genetic epidemiology (01.07.2020)
Published in Genetic epidemiology (01.07.2020)
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