Impaired vascular function after exposure to diesel exhaust generated at urban transient running conditions

by Barath, Stefan, Mills, Nicholas L, Lundbäck, Magnus, Törnqvist, Håkan, Lucking, Andrew J, Langrish, Jeremy P, Söderberg, Stefan, Boman, Christoffer, Westerholm, Roger, Löndahl, Jakob, Donaldson, Ken, Mudway, Ian S, Sandström, Thomas, Newby, David E, Blomberg, Anders
Published in Particle and fibre toxicology

Reduced Proliferative Capacity of Hematopoietic Stem Cells Deficient in Hoxb3 and Hoxb4

by Björnsson, Jon Mar, Larsson, Nina, Brun, Ann C M, Magnusson, Mattias, Andersson, Elisabet, Lundström, Patrik, Larsson, Jonas, Repetowska, Ewa, Ehinger, Mats, Humphries, R Keith, Karlsson, Stefan
Published in Blood

Education in Medical Genetics for Non-Genetic Health Care Providers in Sweden

by Henriksson, Karin, Kristoffersson, Ulf
Published in Community genetics

The impact of demographic, clinical, genetic, and imaging variables on tau PET status

by Ossenkoppele, Rik, Leuzy, Antoine, Cho, Hanna, Sudre, Carole H., Strandberg, Olof, Smith, Ruben, Palmqvist, Sebastian, Mattsson-Carlgren, Niklas, Olsson, Tomas, Jögi, Jonas, Stormrud, Erik, Ryu, Young Hoon, Choi, Jae Yong, Boxer, Adam L., Gorno-Tempini, Maria L., Miller, Bruce L., Soleimani-Meigooni, David, Iaccarino, Leonardo, La Joie, Renaud, Borroni, Edilio, Klein, Gregory, Pontecorvo, Michael J., Devous, Michael D., Villeneuve, Sylvia, Lyoo, Chul Hyoung, Rabinovici, Gil D., Hansson, Oskar
Published in European journal of nuclear medicine and molecular imaging

Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness

by Severin, Franziska, Borry, Pascal, Cornel, Martina C, Daniels, Norman, Fellmann, Florence, Victoria Hodgson, Shirley, Howard, Heidi C, John, Jürgen, Kääriäinen, Helena, Kayserili, Hülya, Kent, Alastair, Koerber, Florian, Kristoffersson, Ulf, Kroese, Mark, Lewis, Celine, Marckmann, Georg, Meyer, Peter, Pfeufer, Arne, Schmidtke, Jörg, Skirton, Heather, Tranebjærg, Lisbeth, Rogowski, Wolf H
Published in European journal of human genetics : EJHG

Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer

by Nilsson, Martin P., Winter, Christof, Kristoffersson, Ulf, Rehn, Martin, Larsson, Christer, Saal, Lao H., Loman, Niklas
Published in Familial cancer

SHANK1 Deletions in Males with Autism Spectrum Disorder

by Sato, Daisuke, Lionel, Anath C., Leblond, Claire S., Prasad, Aparna, Pinto, Dalila, Walker, Susan, O'Connor, Irene, Russell, Carolyn, Drmic, Irene E., Hamdan, Fadi F., Michaud, Jacques L., Endris, Volker, Roeth, Ralph, Delorme, Richard, Huguet, Guillaume, Leboyer, Marion, Rastam, Maria, Gillberg, Christopher, Lathrop, Mark, Stavropoulos, Dimitri J., Anagnostou, Evdokia, Weksberg, Rosanna, Fombonne, Eric, Zwaigenbaum, Lonnie, Fernandez, Bridget A., Roberts, Wendy, Rappold, Gudrun A., Marshall, Christian R., Bourgeron, Thomas, Szatmari, Peter, Scherer, Stephen W.
Published in American journal of human genetics

Genetic anticipation in Swedish Lynch syndrome families

by von Salomé, Jenny, Boonstra, Philip S, Karimi, Masoud, Silander, Gustav, Stenmark-Askmalm, Marie, Gebre-Medhin, Samuel, Aravidis, Christos, Nilbert, Mef, Lindblom, Annika, Lagerstedt-Robinson, Kristina
Published in PLoS genetics

Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia

by Gorcenco, Sorina, Kafantari, Efthymia, Wallenius, Joel, Karremo, Christin, Alinder, Erik, Dobloug, Sigurd, Landqvist Waldö, Maria, Englund, Elisabet, Ehrencrona, Hans, Wictorin, Klas, Karrman, Kristina, Puschmann, Andreas
Published in Journal of neurology

When a Synonymous Variant Is Nonsynonymous

by Vihinen, Mauno
Published in Genes

Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke

by Ilinca, Andreea, Martinez-Majander, Nicolas, Samuelsson, Sofie, Piccinelli, Paul, Truvé, Katarina, Cole, John, Kittner, Steven, Soller, Maria, Kristoffersson, Ulf, Tatlisumak, Turgut, Puschmann, Andreas, Putaala, Jukka, Lindgren, Arne
Published in Stroke (1970)

Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma

by MICCI, Francesca, PANAGOPOULOS, Ioannis, BJERKEHAGEN, Bodil, HEIM, Sverre
Published in Cancer research (Chicago, Ill.)

Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome

by Chen, Yin-Huai, Grigelioniene, Giedre, Newton, Phillip T, Gullander, Jacob, Elfving, Maria, Hammarsjö, Anna, Batkovskyte, Dominyka, Alsaif, Hessa S, Kurdi, Wesam I Y, Abdulwahab, Firdous, Shanmugasundaram, Veerabahu, Devey, Luke, Bacrot, Séverine, Brodszki, Jana, Huber, Celine, Hamel, Ben, Gisselsson, David, Papadogiannakis, Nikos, Jedrycha, Katarina, Gürtl-Lackner, Barbara, Chagin, Andrei S, Nishimura, Gen, Aschenbrenner, Dominik, Alkuraya, Fowzan S, Laurence, Arian, Cormier-Daire, Valérie, Uhlig, Holm H
Published in The Journal of experimental medicine

Rare and low-frequency coding variants alter human adult height

by Marouli, Eirini, Lo, Ken Sin, Kjaer, Troels R, Rüeger, Sina, Young, Kristin L, Esko, Tõnu, Karaderi, Tugce, Aben, Katja K, Adair, Linda S, Alam, Dewan S, Albrecht, Eva, Auer, Paul L, Bonnycastle, Lori L, Bots, Michiel L, Brandslund, Ivan, Butterworth, Adam S, Chambers, John C, Chen, Yii-Der Ida, Chowdhury, Rajiv, Christensen, Cramer, Chu, Audrey Y, Cook, James P, Cox, Amanda J, Demerath, Ellen W, Drenos, Fotios, Ebeling, Tapani, Ferrario, Marco M, Fornage, Myriam, Galesloot, Tessel E, Gasparini, Paolo, Giri, Ayush, Hayward, Caroline, Hocking, Lynne J, Ikram, M Arfan, Jensen, Gorm B, Jiang, Xuejuan, Kee, Frank, Kitajima, Hidetoshi, Komulainen, Pirjo, Kontto, Jukka, Kuivaniemi, Helena, Laakso, Markku, Lange, Leslie A, Lewis, Cora E, Lind, Lars, Liu, Yeheng, Luan, Jian'an, Lubitz, Steven A, Männistö, Satu, Marten, Jonathan, Mitchell, Paul, Nauck, Matthias, Neville, Matt, Nielsen, Sune F, Nordestgaard, Børge G, Ntalla, Ioanna, Owen, Katharine R, Padmanabhan, Sandosh, Palmer, Colin N A, Patel, Aniruddh P, Perry, James A, Perry, John R B, Polasek, Ozren, Reiner, Alex P, Renström, Frida, Rioux, John D, Rudan, Igor, Sapkota, Yadav, Schreiner, Pamela J, Scott, Robert A, Shah, Svati, Sim, Xueling, Smith, Albert Vernon, Southam, Lorraine, Spector, Timothy D, Thorsteinsdottir, Unnur, Tuomilehto, Jaakko, Tybjaerg-Hansen, Anne, Uitterlinden, André G, Ulivi, Sheila, van Schoor, Natasja M, van Setten, Jessica, Vermeulen, Sita H, Vestergaard, Henrik, Vogt, Thomas F, Vozzi, Diego, Wang, Carol A, Wang, Shuai, Wang, Yiqin, Wareham, Nicholas J, Wu, Ying, Zhan, Xiaowei, Zheng, He, Zhou, Wei, Boehnke, Michael, Borecki, Ingrid B, Kutalik, Zoltán, Frayling, Timothy M, Hirschhorn, Joel N, Deloukas, Panos
Published in Nature (London)

Core Circadian Clock Genes Regulate Leukemia Stem Cells in AML

by Puram, Rishi V., Kowalczyk, Monika S., de Boer, Carl G., Schneider, Rebekka K., Miller, Peter G., McConkey, Marie, Tothova, Zuzana, Tejero, Héctor, Heckl, Dirk, Järås, Marcus, Chen, Michelle C., Li, Hubo, Tamayo, Alfred, Cowley, Glenn S., Rozenblatt-Rosen, Orit, Al-Shahrour, Fatima, Regev, Aviv, Ebert, Benjamin L.
Published in Cell

Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines

by HEIDENBLAD, Markus, SCHOENMAKERS, Eric F. P. M, JONSON, Tord, GORUNOVA, Ludmila, VELTMAN, Joris A, VAN KESSEL, Ad Geurts, HÖGLUND, Mattias
Published in Cancer research (Chicago, Ill.)

Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13)

by BEVERLOO, H. Berna, PANAGOPOULOS, Loannis, ISAKSSON, Magareth, VAN WERING, Elisabeth, VAN DRUNEN, Ellen, DE KLEIN, Annelies, JOHANSSON, Bertil, SLATER, Rosalyn
Published in Cancer research (Chicago, Ill.)

Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer

by Bolton, Kelly L, Chenevix- Trench, Georgia, Goh, Cindy, Sadetzki, Siegal, Ramus, Susan J, Karlan, Beth Y, Lambrechts, Diether, Despierre, Evelyn, Barrowdale, Daniel, McGuffog, Lesley, Healey, Sue, Easton, Douglas F, Sinilnikova, Olga, Benítez, Javier, García, María J, Neuhausen, Susan, Gail, Mitchell H, Hartge, Patricia, Peock, Susan, Frost, Debra, Evans, D. Gareth, Eeles, Rosalind, Godwin, Andrew K, Daly, Mary B, Kwong, Ava, Ma, Edmond S. K, Lázaro, Conxi, Blanco, Ignacio, Montagna, Marco, D'Andrea, Emma, Nicoletto, Maria Ornella, Johnatty, Sharon E, Kjær, Susanne Krüger, Jensen, Allan, Høgdall, Estrid, Goode, Ellen L, Fridley, Brooke L, Loud, Jennifer T, Greene, Mark H, Mai, Phuong L, Chetrit, Angela, Lubin, Flora, Hirsh-Yechezkel, Galit, Glendon, Gord, Andrulis, Irene L, Toland, Amanda E, Senter, Leigha, Gore, Martin E, Gourley, Charlie, Michie, Caroline O, Song, Honglin, Tyrer, Jonathan, Whittemore, Alice S, McGuire, Valerie, Sieh, Weiva, Kristoffersson, Ulf, Olsson, Håkan, Borg, Åke, Levine, Douglas A, Steele, Linda, Beattie, Mary S, Chan, Salina, Nussbaum, Robert L, Moysich, Kirsten B, Gross, Jenny, Cass, Ilana, Walsh, Christine, Li, Andrew J, Leuchter, Ronald, Gordon, Ora, Garcia-Closas, Montserrat, Gayther, Simon A, Chanock, Stephen J, Antoniou, Antonis C, Pharoah, Paul D. P, EMBRACE, kConFab Investigators, and The Cancer Genome Atlas Research Network, for the
Published in JAMA : the journal of the American Medical Association

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

by Fachal, Laura, Aschard, Hugues, Beesley, Jonathan, Barnes, Daniel R, Allen, Jamie, Kristensen, Vessela N, Kar, Siddhartha, Pooley, Karen A, Dennis, Joe, Michailidou, Kyriaki
Published in Nature genetics

Activation of endogenous retroviruses during brain development causes an inflammatory response

by Jönsson, Marie E, Garza, Raquel, Sharma, Yogita, Petri, Rebecca, Södersten, Erik, Johansson, Jenny G, Johansson, Pia A, Atacho, Diahann AM, Pircs, Karolina, Madsen, Sofia, Yudovich, David, Ramakrishnan, Ramprasad, Holmberg, Johan, Larsson, Jonas, Jern, Patric, Jakobsson, Johan
Published in The EMBO journal