Daily interpersonal conflicts and daily exposure to bullying behaviors at work: The moderating roles of trait anger and trait anxiety von Zahlquist, Lena, Hetland, Jørn, Einarsen, Ståle V., Bakker, Arnold B., Hoprekstad, Øystein L., Espevik, Roar, Olsen, Olav K.

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QT prolongation predicts short-term mortality independent of comorbidity von Gibbs, Charlotte, Thalamus, Jacob, Kristoffersen, Doris Tove, Svendsen, Martin Veel, Holla, Øystein L, Heldal, Kristian, Haugaa, Kristina H, Hysing, Jan

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Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing von Skjelbred, Camilla F., Russell, Michael B., Høyer, Helle, Strand, Linda, Hilmarsen, Hilde T., Svendsen, Marit, Braathen, Geir J., Busk, Øyvind L., Holla, Øystein L.

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De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders von Dulovic-Mahlow, Marija, Trinh, Joanne, Kandaswamy, Krishna Kumar, Braathen, Geir Julius, Di Donato, Nataliya, Rahikkala, Elisa, Beblo, Skadi, Werber, Martin, Krajka, Victor, Busk, Øyvind L., Baumann, Hauke, Al-Sannaa, Nouriya Abbas, Hinrichs, Frauke, Affan, Rabea, Navot, Nir, Al Balwi, Mohammed A., Oprea, Gabriela, Holla, Øystein L., Weiss, Maximilian E.R., Jamra, Rami A., Kahlert, Anne-Karin, Kishore, Shivendra, Tveten, Kristian, Vos, Melissa, Rolfs, Arndt, Lohmann, Katja

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An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP von Mah-Som, Annelise Y., Daw, Jil, Huynh, Diana, Wu, Mengcheng, Creekmore, Benjamin C., Burns, William, Skinner, Steven A., Holla, Øystein L., Smeland, Marie F., Planes, Marc, Uguen, Kevin, Redon, Sylvia, Bierhals, Tatjana, Scholz, Tasja, Denecke, Jonas, Mensah, Martin A., Sczakiel, Henrike L., Tichy, Heidelis, Verheyen, Sarah, Blatterer, Jasmin, Schreiner, Elisabeth, Thies, Jenny, Lam, Christina, Spaeth, Christine G., Pena, Loren, Ramsey, Keri, Narayanan, Vinodh, Seaver, Laurie H., Rodriguez, Diana, Afenjar, Alexandra, Burglen, Lydie, Lee, Edward B., Chou, Tsui-Fen, Weihl, Conrad C., Shinawi, Marwan S.

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Next-generation sequencing of the monogenic obesity genes LEP, LEPR, MC4R, PCSK1 and POMC in a Norwegian cohort of patients with morbid obesity and normal weight controls von Nordang, Gry B.N., Busk, Øyvind L., Tveten, Kristian, Hanevik, Hans Ivar, Fell, Anne Kristin M., Hjelmesæth, Jøran, Holla, Øystein L., Hertel, Jens K.

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A Nationwide Study of GATA2 Deficiency in Norway—the Majority of Patients Have Undergone Allo-HSCT von Jørgensen, Silje F., Buechner, Jochen, Myhre, Anders E., Galteland, Eivind, Spetalen, Signe, Kulseth, Mari Ann, Sorte, Hanne S., Holla, Øystein L., Lundman, Emma, Alme, Charlotte, Heier, Ingvild, Flægstad, Trond, Fløisand, Yngvar, Benneche, Andreas, Fevang, Børre, Aukrust, Pål, Stray-Pedersen, Asbjørg, Gedde-Dahl, Tobias, Nordøy, Ingvild

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Role of the C-terminal domain of PCSK9 in degradation of the LDL receptors von Holla, Øystein L., Cameron, Jamie, Tveten, Kristian, Str⊘m, Thea Bismo, Berge, Knut Erik, Laerdahl, Jon K., Leren, Trond P.

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Pre-breakdown phenomena in hydrocarbon liquids in a point-plane gap under step voltage. Part 2: behaviour under negative polarity and comparison with positive polarity von Lundgaard, Lars, Linhjell, Dag, Hestad, Øystein L, Unge, Mikael, Hjortstam, Olof

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Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy von Voisin, Norine, Schnur, Rhonda E., Douzgou, Sofia, Hiatt, Susan M., Rustad, Cecilie F., Brown, Natasha J., Earl, Dawn L., Keren, Boris, Levchenko, Olga, Geuer, Sinje, Verheyen, Sarah, Johnson, Diana, Zarate, Yuri A., Hančárová, Miroslava, Amor, David J., Bebin, E. Martina, Blatterer, Jasmin, Brusco, Alfredo, Cappuccio, Gerarda, Charrow, Joel, Chatron, Nicolas, Cooper, Gregory M., Courtin, Thomas, Dadali, Elena, Delafontaine, Julien, Del Giudice, Ennio, Doco, Martine, Douglas, Ganka, Eisenkölbl, Astrid, Funari, Tara, Giannuzzi, Giuliana, Gruber-Sedlmayr, Ursula, Guex, Nicolas, Heron, Delphine, Holla, Øystein L., Hurst, Anna C.E., Juusola, Jane, Kronn, David, Lavrov, Alexander, Lee, Crystle, Lorrain, Séverine, Merckoll, Else, Mikhaleva, Anna, Norman, Jennifer, Pradervand, Sylvain, Prchalová, Darina, Rhodes, Lindsay, Sanders, Victoria R., Sedláček, Zdeněk, Seebacher, Heidelis A., Sellars, Elizabeth A., Sirchia, Fabio, Takenouchi, Toshiki, Tanaka, Akemi J., Taska-Tench, Heidi, Tønne, Elin, Tveten, Kristian, Vitiello, Giuseppina, Vlčková, Markéta, Uehara, Tomoko, Nava, Caroline, Yalcin, Binnaz, Kosaki, Kenjiro, Donnai, Dian, Mundlos, Stefan, Brunetti-Pierri, Nicola, Chung, Wendy K., Reymond, Alexandre

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Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobi... von Lippe, Charlotte, Tveten, Kristian, Prescott, Trine E., Holla, Øystein L., Busk, Øyvind L., Burke, Katherine B., Sansbury, Francis H., Baptista, Júlia, Fry, Andrew E., Lim, Derek, Jolles, Stephen, Evans, Jennifer, Osio, Deborah, Macmillan, Carol, Bruno, Irene, Faletra, Flavio, Climent, Salvador, Urreitzi, Roser, Hoenicka, Janet, Palau, Francesc, Cohen, Ana S. A., Engleman, Kendra, Zhou, Dihong, Amudhavalli, Shivarajan M., Jeanne, Médéric, Bonnet‐Brilhault, Frédérique, Lévy, Jonathan, Drunat, Séverine, Derive, Nicolas, Haug, Marte G., Thorstensen, Wenche M.

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A monoallelic UXS1 variant associated with short‐limbed short stature von Rustad, Cecilie F., Backe, Paul Hoff, Jin, Chunsheng, Merckoll, Else, Tveten, Kristian, Maciej‐Hulme, Marissa Lucy, Karlsson, Niclas, Prescott, Trine, Sand, Elise Sandås, Woldseth, Berit, Elgstøen, Katja Benedikte Prestø, Holla, Øystein L.

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Interaction between the ligand-binding domain of the LDL receptor and the C-terminal domain of PCSK9 is required for PCSK9 to remain bound to the LDL receptor during endosomal acid... von TVETEN, Kristian, HOLLA, Øystein L, CAMERON, Jamie, BISMO STRØM, Thea, ERIK BERGE, Knut, LAERDAHL, Jon K, LEREN, Trond P

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Genetic and Phenotypic Characterization of Community Hospital Patients With QT Prolongation von Gibbs, Charlotte, Thalamus, Jacob, Tveten, Kristian, Busk, Øyvind L, Hysing, Jan, Haugaa, Kristina H, Holla, Øystein L

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Effect of mutations in the PCSK9 gene on the cell surface LDL receptors von Cameron, Jamie, Holla, Øystein L., Ranheim, Trine, Kulseth, Mari Ann, Berge, Knut Erik, Leren, Trond P.

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Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia von Barish, Scott, Lin, Sheng-Jia, Maroofian, Reza, Gezdirici, Alper, Alhebby, Hamoud, Trimouille, Aurélien, Biderman Waberski, Marta, Mitani, Tadahiro, Huber, Ilka, Tveten, Kristian, Holla, Øystein L., Busk, Øyvind L., Houlden, Henry, Ghayoor Karimiani, Ehsan, Beiraghi Toosi, Mehran, Shervin Badv, Reza, Najarzadeh Torbati, Paria, Eghbal, Fatemeh, Akhondian, Javad, Al Safar, Ayat, Alswaid, Abdulrahman, Zifarelli, Giovanni, Bauer, Peter, Marafi, Dana, Fatih, Jawid M., Huang, Kevin, Petree, Cassidy, Calame, Daniel G., von der Lippe, Charlotte, Alkuraya, Fowzan S., Wali, Sami, Lupski, James R., Varshney, Gaurav K., Posey, Jennifer E., Pehlivan, Davut

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Genome-wide expression analysis of cells expressing gain of function mutant D374Y-PCSK9 von Ranheim, Trine, Mattingsdal, Morten, Lindvall, Jessica M., Holla, Øystein L., Berge, Knut Erik, Kulseth, Mari Ann, Leren, Trond P.

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Removal of acidic residues of the prodomain of PCSK9 increases its activity towards the LDL receptor von Holla, Øystein L., Laerdahl, Jon K., Strøm, Thea Bismo, Tveten, Kristian, Cameron, Jamie, Berge, Knut Erik, Leren, Trond P.

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Venture capital funds: Do they meet the expectations of portfolio firms? von Berg-Utby, Terje, Sørheim, Roger, Widding, L. Øystein

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4‐Phenylbutyrate restores the functionality of a misfolded mutant low‐density lipoprotein receptor von Tveten, Kristian, Holla, Øystein L., Ranheim, Trine, Berge, Knut E., Leren, Trond P., Kulseth, Mari A.

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