FocalCall: An R Package for the Annotation of Focal Copy Number Aberrations

por Krijgsman, Oscar, Benner, Christian, Meijer, Gerrit A, van de Wiel, Mark A, Ylstra, Bauke
Publicado 2014

FINEMAP: efficient variable selection using summary data from genome-wide association studies

por Benner, Christian, Spencer, Chris C.A., Havulinna, Aki S., Salomaa, Veikko, Ripatti, Samuli, Pirinen, Matti
Publicado 2016

biMM: efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements

por Pirinen, Matti, Benner, Christian, Marttinen, Pekka, Järvelin, Marjo-Riitta, Rivas, Manuel A, Ripatti, Samuli
Publicado 2017

Genetic Loci Associated with Allergic Sensitization in Lithuanians

por Šaulienė, Ingrida, Greičiuvienė, Jūratė, Šukienė, Laura, Juškevičiūtė, Neringa, Benner, Christian, Zinkevičienė, Auksė, Ripatti, Samuli, Donner, Kati, Kainov, Denis
Publicado 2015

Genome-Wide Analysis of Evolutionary Markers of Human Influenza A(H1N1)pdm09 and A(H3N2) Viruses May Guide Selection of Vaccine Strain Candidates

por Belanov, Sergei S., Bychkov, Dmitrii, Benner, Christian, Ripatti, Samuli, Ojala, Teija, Kankainen, Matti, Kai Lee, Hong, Wei-Tze Tang, Julian, Kainov, Denis E.
Publicado 2015

Comparative Analysis of Whole-Genome Sequences of Influenza A(H1N1)pdm09 Viruses Isolated from Hospitalized and Nonhospitalized Patients Identifies Missense Mutations That Might Be...

por Mishel, Polina, Ojala, Teija, Benner, Christian, Lakspere, Triin, Bychkov, Dmitrii, Jalovaara, Petri, Kakkola, Laura, Kallio-Kokko, Hannimari, Kantele, Anu, Kankainen, Matti, Ikonen, Niina, Ripatti, Samuli, Julkunen, Ilkka, Kainov, Denis E.
Publicado 2015

Relevance of PTEN loss in brain metastasis formation in breast cancer patients

por Wikman, Harriet, Lamszus, Katrin, Detels, Niclas, Uslar, Liubov, Wrage, Michaela, Benner, Christian, Hohensee, Ina, Ylstra, Bauke, Eylmann, Kathrin, Zapatka, Marc, Sauter, Guido, Kemming, Dirk, Glatzel, Markus, Müller, Volkmar, Westphal, Manfred, Pantel, Klaus
Publicado 2012

Functionally-informed fine-mapping and polygenic localization of complex trait heritability

por Weissbrod, Omer, Hormozdiari, Farhad, Benner, Christian, Cui, Ran, Ulirsch, Jacob, Gazal, Steven, Schoech, Armin P., van de Geijn, Bryce, Reshef, Yakir, Márquez-Luna, Carla, O’Connor, Luke, Pirinen, Matti, Finucane, Hilary K., Price, Alkes L.
Publicado 2020

Reduced genomic tumor heterogeneity after neoadjuvant chemotherapy is related to favorable outcome in patients with esophageal adenocarcinoma

por Obulkasim, Askar, Ylstra, Bauke, van Essen, Hendrik F., Benner, Christian, Stenning, Sally, Langley, Ruth, Allum, William, Cunningham, David, Inam, Imran, Hewitt, Lindsay C., West, Nicolas P., Meijer, Gerrit A., van de Wiel, Mark A., Grabsch, Heike I.
Publicado 2016

Interrogation of human hematopoiesis at single-cell and single-variant resolution

por Ulirsch, Jacob C., Lareau, Caleb A., Bao, Erik L., Ludwig, Leif S., Guo, Michael H., Benner, Christian, Satpathy, Ansuman T., Kartha, Vinay K., Salem, Rany M., Hirschhorn, Joel N., Finucane, Hilary K., Aryee, Martin J., Buenrostro, Jason D., Sankaran, Vijay G.
Publicado 2019

Genome-Wide Meta-Analysis of Sciatica in Finnish Population

por Lemmelä, Susanna, Solovieva, Svetlana, Shiri, Rahman, Benner, Christian, Heliövaara, Markku, Kettunen, Johannes, Anttila, Verneri, Ripatti, Samuli, Perola, Markus, Seppälä, Ilkka, Juonala, Markus, Kähönen, Mika, Salomaa, Veikko, Viikari, Jorma, Raitakari, Olli T., Lehtimäki, Terho, Palotie, Aarno, Viikari-Juntura, Eira, Husgafvel-Pursiainen, Kirsti
Publicado 2016

Polygenic Hyperlipidemias and Coronary Artery Disease Risk

por Ripatti, Pietari, Rämö, Joel T., Mars, Nina J., Fu, Yu, Lin, Jake, Söderlund, Sanni, Benner, Christian, Surakka, Ida, Kiiskinen, Tuomo, Havulinna, Aki S., Palta, Priit, Freimer, Nelson B., Widén, Elisabeth, Salomaa, Veikko, Tukiainen, Taru, Pirinen, Matti, Palotie, Aarno, Taskinen, Marja-Riitta, Ripatti, Samuli
Publicado 2020

Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans

por Lemmelä, Susanna, Wigmore, Eleanor M, Benner, Christian, Havulinna, Aki S, Ong, Rachel MY, Kempf, Tibor, Wollert, Kai C, Blankenberg, Stefan, Zeller, Tanja, Peters, James E, Salomaa, Veikko, Fritsch, Maria, March, Ruth, Palotie, Aarno, Daly, Mark, Butterworth, Adam S, Kinnunen, Mervi, Paul, Dirk S, Matakidou, Athena
Publicado 2022

Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent

por Buchwald, Jadwiga, Chenoweth, Meghan J., Palviainen, Teemu, Zhu, Gu, Benner, Christian, Gordon, Scott, Korhonen, Tellervo, Ripatti, Samuli, Madden, Pamela A. F., Lehtimäki, Terho, Raitakari, Olli T., Salomaa, Veikko, Rose, Richard J., George, Tony P., Lerman, Caryn, Pirinen, Matti, Martin, Nicholas G., Kaprio, Jaakko, Loukola, Anu, Tyndale, Rachel F.
Publicado 2020

Genetics of 35 blood and urine biomarkers in the UK Biobank

por Armstrong, Nasa Sinnott-, Tanigawa, Yosuke, Amar, David, Mars, Nina, Benner, Christian, Aguirre, Matthew, Venkataraman, Guhan Ram, Wainberg, Michael, Ollila, Hanna M., Kiiskinen, Tuomo, Havulinna, Aki S., Pirruccello, James P., Qian, Junyang, Shcherbina, Anna, consortium, FinnGen, Rodriguez, Fatima, Assimes, Themistocles L., Agarwala, Vineeta, Tibshirani, Robert, Hastie, Trevor, Ripatti, Samuli, Pritchard, Jonathan K., Daly, Mark J., Rivas, Manuel A.
Publicado 2021

Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

por Praveen, Kavita, Dobbyn, Lee, Gurski, Lauren, Ayer, Ariane H., Staples, Jeffrey, Mishra, Shawn, Bai, Yu, Kaufman, Alexandra, Moscati, Arden, Benner, Christian, Chen, Esteban, Chen, Siying, Popov, Alexander, Smith, Janell, Melander, Olle, Jones, Marcus B., Marchini, Jonathan, Balasubramanian, Suganthi, Zambrowicz, Brian, Drummond, Meghan C., Baras, Aris, Abecasis, Goncalo R., Ferreira, Manuel A., Stahl, Eli A., Coppola, Giovanni
Publicado 2022

Exome sequencing and analysis of 454,787 UK Biobank participants

por Backman, Joshua D., Li, Alexander H., Marcketta, Anthony, Sun, Dylan, Mbatchou, Joelle, Kessler, Michael D., Benner, Christian, Liu, Daren, Locke, Adam E., Balasubramanian, Suganthi, Yadav, Ashish, Banerjee, Nilanjana, Gillies, Christopher E., Damask, Amy, Liu, Simon, Bai, Xiaodong, Hawes, Alicia, Maxwell, Evan, Gurski, Lauren, Watanabe, Kyoko, Kosmicki, Jack A., Rajagopal, Veera, Mighty, Jason, Jones, Marcus, Mitnaul, Lyndon, Stahl, Eli, Coppola, Giovanni, Jorgenson, Eric, Habegger, Lukas, Salerno, William J., Shuldiner, Alan R., Lotta, Luca A., Overton, John D., Cantor, Michael N., Reid, Jeffrey G., Yancopoulos, George, Kang, Hyun M., Marchini, Jonathan, Baras, Aris, Abecasis, Gonçalo R., Ferreira, Manuel A. R.
Publicado 2021

Plasma proteomic associations with genetics and health in the UK Biobank

por Sun, Benjamin B., Chiou, Joshua, Traylor, Matthew, Benner, Christian, Hsu, Yi-Hsiang, Richardson, Tom G., Surendran, Praveen, Mahajan, Anubha, Robins, Chloe, Vasquez-Grinnell, Steven G., Hou, Liping, Kvikstad, Erika M., Burren, Oliver S., Davitte, Jonathan, Ferber, Kyle L., Gillies, Christopher E., Hedman, Åsa K., Hu, Sile, Lin, Tinchi, Mikkilineni, Rajesh, Pendergrass, Rion K., Pickering, Corran, Prins, Bram, Baird, Denis, Chen, Chia-Yen, Ward, Lucas D., Deaton, Aimee M., Welsh, Samantha, Willis, Carissa M., Lehner, Nick, Arnold, Matthias, Wörheide, Maria A., Suhre, Karsten, Kastenmüller, Gabi, Sethi, Anurag, Cule, Madeleine, Raj, Anil, Burkitt-Gray, Lucy, Melamud, Eugene, Black, Mary Helen, Fauman, Eric B., Howson, Joanna M. M., Kang, Hyun Min, McCarthy, Mark I., Nioi, Paul, Petrovski, Slavé, Scott, Robert A., Smith, Erin N., Szalma, Sándor, Waterworth, Dawn M., Mitnaul, Lyndon J., Szustakowski, Joseph D., Gibson, Bradford W., Miller, Melissa R., Whelan, Christopher D.
Publicado 2023

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

por Hautakangas, Heidi, Winsvold, Bendik S., Ruotsalainen, Sanni E., Bjornsdottir, Gyda, Harder, Aster V. E., Kogelman, Lisette J. A., Thomas, Laurent F., Noordam, Raymond, Benner, Christian, Gormley, Padhraig, Artto, Ville, Banasik, Karina, Bjornsdottir, Anna, Boomsma, Dorret I., Brumpton, Ben M., Burgdorf, Kristoffer Sølvsten, Buring, Julie E., Chalmer, Mona Ameri, de Boer, Irene, Dichgans, Martin, Erikstrup, Christian, Färkkilä, Markus, Garbrielsen, Maiken Elvestad, Ghanbari, Mohsen, Hagen, Knut, Häppölä, Paavo, Hottenga, Jouke-Jan, Hrafnsdottir, Maria G., Hveem, Kristian, Johnsen, Marianne Bakke, Kähönen, Mika, Kristoffersen, Espen S., Kurth, Tobias, Lehtimäki, Terho, Lighart, Lannie, Magnusson, Sigurdur H., Malik, Rainer, Pedersen, Ole Birger, Pelzer, Nadine, Penninx, Brenda W. J. H., Ran, Caroline, Ridker, Paul M., Rosendaal, Frits R., Sigurdardottir, Gudrun R., Skogholt, Anne Heidi, Sveinsson, Olafur A., Thorgeirsson, Thorgeir E., Ullum, Henrik, Vijfhuizen, Lisanne S., Widén, Elisabeth, van Dijk, Ko Willems, Aromaa, Arpo, Belin, Andrea Carmine, Freilinger, Tobias, Ikram, M. Arfan, Järvelin, Marjo-Riitta, Raitakari, Olli T., Terwindt, Gisela M., Kallela, Mikko, Wessman, Maija, Olesen, Jes, Chasman, Daniel I., Nyholt, Dale R., Stefánsson, Hreinn, Stefansson, Kari, van den Maagdenberg, Arn M. J. M., Hansen, Thomas Folkmann, Ripatti, Samuli, Zwart, John-Anker, Palotie, Aarno, Pirinen, Matti
Publicado 2022