Search Results - "Moore, Kristjan H.S."

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    HaploGrouper: a generalized approach to haplogroup classification by Jagadeesan, Anuradha, Ebenesersdóttir, S Sunna, Guðmundsdóttir, Valdis B, Thordardottir, Elisabet Linda, Moore, Kristjan H S, Helgason, Agnar

    Published in Bioinformatics (01-05-2021)
    “…Abstract Motivation We introduce HaploGrouper, a versatile software to classify haplotypes into haplogroups on the basis of a known phylogenetic tree. A…”
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    The Anglo-Saxon migration and the formation of the early English gene pool by Gretzinger, Joscha, Sayer, Duncan, Justeau, Pierre, Altena, Eveline, Pala, Maria, Dulias, Katharina, Edwards, Ceiridwen J., Jodoin, Susanne, Lacher, Laura, Sabin, Susanna, Vågene, Åshild J., Haak, Wolfgang, Ebenesersdóttir, S. Sunna, Moore, Kristjan H. S., Radzeviciute, Rita, Schmidt, Kara, Brace, Selina, Bager, Martina Abenhus, Patterson, Nick, Papac, Luka, Broomandkhoshbacht, Nasreen, Callan, Kimberly, Harney, Éadaoin, Iliev, Lora, Lawson, Ann Marie, Michel, Megan, Stewardson, Kristin, Zalzala, Fatma, Rohland, Nadin, Kappelhoff-Beckmann, Stefanie, Both, Frank, Winger, Daniel, Neumann, Daniel, Saalow, Lars, Krabath, Stefan, Beckett, Sophie, Van Twest, Melanie, Faulkner, Neil, Read, Chris, Barton, Tabatha, Caruth, Joanna, Hines, John, Krause-Kyora, Ben, Warnke, Ursula, Schuenemann, Verena J., Barnes, Ian, Dahlström, Hanna, Clausen, Jane Jark, Richardson, Andrew, Popescu, Elizabeth, Dodwell, Natasha, Ladd, Stuart, Phillips, Tom, Mortimer, Richard, Sayer, Faye, Swales, Diana, Stewart, Allison, Powlesland, Dominic, Kenyon, Robert, Ladle, Lilian, Peek, Christina, Grefen-Peters, Silke, Ponce, Paola, Daniels, Robin, Spall, Cecily, Woolcock, Jennifer, Jones, Andy M., Roberts, Amy V., Symmons, Robert, Rawden, Anooshka C., Cooper, Alan, Bos, Kirsten I., Booth, Tom, Schroeder, Hannes, Thomas, Mark G., Helgason, Agnar, Richards, Martin B., Reich, David, Krause, Johannes, Schiffels, Stephan

    Published in Nature (London) (06-10-2022)
    “…The history of the British Isles and Ireland is characterized by multiple periods of major cultural change, including the influential transformation after the…”
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    Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura by Bjornsdottir, Gyda, Chalmer, Mona A., Stefansdottir, Lilja, Skuladottir, Astros Th, Einarsson, Gudmundur, Andresdottir, Margret, Beyter, Doruk, Ferkingstad, Egil, Gretarsdottir, Solveig, Halldorsson, Bjarni V., Halldorsson, Gisli H., Helgadottir, Anna, Helgason, Hannes, Hjorleifsson Eldjarn, Grimur, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Jonsdottir, Ingileif, Knowlton, Kirk U., Nadauld, Lincoln D., Lund, Sigrun H., Magnusson, Olafur Th, Melsted, Pall, Moore, Kristjan H. S., Oddsson, Asmundur, Olason, Pall I., Sigurdsson, Asgeir, Stefansson, Olafur A., Saemundsdottir, Jona, Sveinbjornsson, Gardar, Tragante, Vinicius, Unnsteinsdottir, Unnur, Walters, G. Bragi, Zink, Florian, Rødevand, Linn, Andreassen, Ole A., Igland, Jannicke, Lie, Rolv T., Haavik, Jan, Banasik, Karina, Brunak, Søren, Didriksen, Maria, T. Bruun, Mie, Erikstrup, Christian, Kogelman, Lisette J. A., Nielsen, Kaspar R., Sørensen, Erik, Pedersen, Ole B., Ullum, Henrik, Masson, Gisli, Thorsteinsdottir, Unnur, Olesen, Jes, Ludvigsson, Petur, Thorarensen, Olafur, Bjornsdottir, Anna, Sigurdardottir, Gudrun R., Sveinsson, Olafur A., Ostrowski, Sisse R., Holm, Hilma, Gudbjartsson, Daniel F., Thorleifsson, Gudmar, Sulem, Patrick, Stefansson, Hreinn, Thorgeirsson, Thorgeir E., Hansen, Thomas F., Stefansson, Kari

    Published in Nature genetics (01-11-2023)
    “…Migraine is a complex neurovascular disease with a range of severity and symptoms, yet mostly studied as one phenotype in genome-wide association studies…”
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    Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality by Oddsson, Asmundur, Sulem, Patrick, Sveinbjornsson, Gardar, Arnadottir, Gudny A., Steinthorsdottir, Valgerdur, Halldorsson, Gisli H., Atlason, Bjarni A., Oskarsson, Gudjon R., Helgason, Hannes, Nielsen, Henriette Svarre, Westergaard, David, Karjalainen, Juha M., Katrinardottir, Hildigunnur, Fridriksdottir, Run, Jensson, Brynjar O., Tragante, Vinicius, Ferkingstad, Egil, Jonsson, Hakon, Gudjonsson, Sigurjon A., Beyter, Doruk, Moore, Kristjan H. S., Thordardottir, Helga B., Kristmundsdottir, Snaedis, Stefansson, Olafur A., Rantapää-Dahlqvist, Solbritt, Sonderby, Ida Elken, Didriksen, Maria, Stridh, Pernilla, Haavik, Jan, Tryggvadottir, Laufey, Frei, Oleksandr, Walters, G. Bragi, Kockum, Ingrid, Hjalgrim, Henrik, Olafsdottir, Thorunn A., Selbaek, Geir, Nyegaard, Mette, Erikstrup, Christian, Brodersen, Thorsten, Saevarsdottir, Saedis, Olsson, Tomas, Nielsen, Kaspar Rene, Haraldsson, Asgeir, Bruun, Mie Topholm, Hansen, Thomas Folkmann, Steingrimsdottir, Thora, Jacobsen, Rikke Louise, Lie, Rolv T., Djurovic, Srdjan, Alfredsson, Lars, Lopez de Lapuente Portilla, Aitzkoa, Brunak, Soren, Melsted, Pall, Halldorsson, Bjarni V., Saemundsdottir, Jona, Magnusson, Olafur Th, Padyukov, Leonid, Banasik, Karina, Rafnar, Thorunn, Askling, Johan, Klareskog, Lars, Pedersen, Ole Birger, Masson, Gisli, Havdahl, Alexandra, Nilsson, Bjorn, Andreassen, Ole A., Daly, Mark, Ostrowski, Sisse Rye, Jonsdottir, Ingileif, Stefansson, Hreinn, Holm, Hilma, Helgason, Agnar, Thorsteinsdottir, Unnur, Stefansson, Kari, Gudbjartsson, Daniel F.

    Published in Nature communications (10-06-2023)
    “…Genotypes causing pregnancy loss and perinatal mortality are depleted among living individuals and are therefore difficult to find. To explore genetic causes…”
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    The genetic structure of Norway by Mattingsdal, Morten, Ebenesersdóttir, S Sunna, Moore, Kristjan H S, Andreassen, Ole A, Hansen, Thomas F, Werge, Thomas, Kockum, Ingrid, Olsson, Tomas, Alfredsson, Lars, Helgason, Agnar, Stefánsson, Kári, Hovig, Eivind

    Published in European journal of human genetics : EJHG (01-11-2021)
    “…The aim of the present study was to describe the genetic structure of the Norwegian population using genotypes from 6369 unrelated individuals with detailed…”
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    The rate and nature of mitochondrial DNA mutations in human pedigrees by Árnadóttir, Erla R, Moore, Kristján H S, Guðmundsdóttir, Valdís B, Ebenesersdóttir, S Sunna, Guity, Kamran, Jónsson, Hákon, Stefánsson, Kári, Helgason, Agnar

    Published in Cell (25-07-2024)
    “…We examined the rate and nature of mitochondrial DNA (mtDNA) mutations in humans using sequence data from 64,806 contemporary Icelanders from 2,548 matrilines…”
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