日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

inMOTIFin: a lightweight end-to-end simulation software for regulatory sequences

inMOTIFin:一款用于调控序列的轻量级端到端模拟软件

Ferenc, Katalin; Martini, Lorenzo; Rauluseviciute, Ieva; Sandve, Geir Kjetil Ferkingstad; Mathelier, Anthony

Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations

作者更正:通过遗传学和疾病关联进行大规模血浆蛋白质组学比较

Eldjarn, Grimur Hjorleifsson; Ferkingstad, Egil; Lund, Sigrun H; Helgason, Hannes; Magnusson, Olafur Th; Gunnarsdottir, Kristbjorg; Olafsdottir, Thorunn A; Halldorsson, Bjarni V; Olason, Pall I; Zink, Florian; Gudjonsson, Sigurjon A; Sveinbjornsson, Gardar; Magnusson, Magnus I; Helgason, Agnar; Oddsson, Asmundur; Halldorsson, Gisli H; Magnusson, Magnus K; Saevarsdottir, Saedis; Eiriksdottir, Thjodbjorg; Masson, Gisli; Stefansson, Hreinn; Jonsdottir, Ingileif; Holm, Hilma; Rafnar, Thorunn; Melsted, Pall; Saemundsdottir, Jona; Norddahl, Gudmundur L; Thorleifsson, Gudmar; Ulfarsson, Magnus O; Gudbjartsson, Daniel F; Thorsteinsdottir, Unnur; Sulem, Patrick; Stefansson, Kari

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

整合常见和罕见变异分析有助于深入了解肝硬化的遗传结构。

Ghouse, Jonas; Sveinbjörnsson, Gardar; Vujkovic, Marijana; Seidelin, Anne-Sofie; Gellert-Kristensen, Helene; Ahlberg, Gustav; Tragante, Vinicius; Rand, Søren A; Brancale, Joseph; Vilarinho, Silvia; Lundegaard, Pia Rengtved; Sørensen, Erik; Erikstrup, Christian; Bruun, Mie Topholm; Jensen, Bitten Aagaard; Brunak, Søren; Banasik, Karina; Ullum, Henrik; Verweij, Niek; Lotta, Luca; Baras, Aris; Mirshahi, Tooraj; Carey, David J; Kaplan, David E; Lynch, Julie; Morgan, Timothy; Schwantes-An, Tae-Hwi; Dochtermann, Daniel R; Pyarajan, Saiju; Tsao, Philip S; Laisk, Triin; Mägi, Reedik; Kozlitina, Julia; Tybjærg-Hansen, Anne; Jones, David; Knowlton, Kirk U; Nadauld, Lincoln; Ferkingstad, Egil; Björnsson, Einar S; Ulfarsson, Magnus O; Sturluson, Árni; Sulem, Patrick; Pedersen, Ole B; Ostrowski, Sisse R; Gudbjartsson, Daniel F; Stefansson, Kari; Olesen, Morten Salling; Chang, Kyong-Mi; Holm, Hilma; Bundgaard, Henning; Stender, Stefan

Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease

LAG3基因起始密码子变异与LAG-3表达降低和自身免疫性甲状腺疾病风险增加相关。

Saedis Saevarsdottir ,Kristbjörg Bjarnadottir ,Thorsteinn Markusson ,Jonas Berglund ,Thorunn A Olafsdottir ,Gisli H Halldorsson ,Gudrun Rutsdottir ,Kristbjorg Gunnarsdottir ,Asgeir Orn Arnthorsson ,Sigrun H Lund ,Lilja Stefansdottir ,Julius Gudmundsson ,Ari J Johannesson ,Arni Sturluson ,Asmundur Oddsson ,Bjarni Halldorsson ,Björn R Ludviksson ,Egil Ferkingstad ,Erna V Ivarsdottir ,Gardar Sveinbjornsson ,Gerdur Grondal ,Gisli Masson ,Grimur Hjorleifsson Eldjarn ,Gudmundur A Thorisson ,Katla Kristjansdottir ,Kirk U Knowlton ,Kristjan H S Moore ,Sigurjon A Gudjonsson ,Solvi Rognvaldsson ,Stacey Knight ,Lincoln D Nadauld ,Hilma Holm ,Olafur T Magnusson ,Patrick Sulem ,Daniel F Gudbjartsson ,Thorunn Rafnar ,Gudmar Thorleifsson ,Pall Melsted ,Gudmundur L Norddahl ,Ingileif Jonsdottir ,Kari Stefansson

Genome-Wide Association Study of Accessory Atrioventricular Pathways

全基因组关联研究发现房室旁路

Aegisdottir, Hildur M; Andreasen, Laura; Thorolfsdottir, Rosa B; Sveinbjornsson, Gardar; Jonsdottir, Andrea B; Stefansdottir, Lilja; Thorleifsson, Gudmar; Sigurdsson, Asgeir; Halldorsson, Gisli H; Barc, Julien; Simonet, Floriane; Tragante, Vinicius; Oddsson, Asmundur; Ferkingstad, Egil; Svendsen, Jesper Hastrup; Ghouse, Jonas; Ahlberg, Gustav; Paludan-Müller, Christian; Hadji-Turdeghal, Katra; Bustamante, Mariana; Ulfarsson, Magnus O; Helgadottir, Anna; Gretarsdottir, Solveig; Saevarsdottir, Saedis; Jonsdottir, Ingileif; Erikstrup, Christian; Ullum, Henrik; Sørensen, Erik; Brunak, Søren; Jøns, Christian; Zheng, Chaoqun; Bezzina, Connie R; Knowlton, Kirk U; Nadauld, Lincoln D; Sulem, Patrick; Ostrowski, Sisse R; Pedersen, Ole B; Arnar, David O; Gudbjartsson, Daniel F; Olesen, Morten S; Bundgaard, Henning; Holm, Hilma; Stefansson, Kari

Novel loci and biomedical consequences of iron homoeostasis variation

铁稳态变异的新位点及其生物医学后果

Allara, Elias; Bell, Steven; Smith, Rebecca; Keene, Spencer J; Gill, Dipender; Gaziano, Liam; Morselli Gysi, Deisy; Wang, Feiyi; Tragante, Vinicius; Mason, Amy; Karthikeyan, Savita; Lumbers, R Thomas; Bonglack, Emmanuela; Ouwehand, Willem; Roberts, David J; Dowsett, Joseph; Ostrowski, Sisse Rye; Larsen, Margit Hørup; Ullum, Henrik; Pedersen, Ole Birger; Brunak, Søren; Banasik, Karina; Erikstrup, Christian; Mitchell, Jonathan; Fuchsberger, Christian; Pattaro, Cristian; Pramstaller, Peter P; Girelli, Domenico; Arvas, Mikko; Toivonen, Jarkko; Molnos, Sophie; Peters, Annette; Polasek, Ozren; Rudan, Igor; Hayward, Caroline; McDonnell, Ciara; Pirastu, Nicola; Wilson, James F; van den Hurk, Katja; Quee, Franke; Ferrucci, Luigi; Bandinelli, Stefania; Tanaka, Toshiko; Girotto, Giorgia; Concas, Maria Pina; Pecori, Alessandro; Verweij, Niek; van der Harst, Pim; van de Vegte, Yordi J; Kiemeney, Lambertus A; Sweep, Fred C; Galesloot, Tessel E; Sulem, Patrick; Gudbjartsson, Daniel; Ferkingstad, Egil; Djousse, Luc; Cho, Kelly; Inouye, Michael; Burgess, Stephen; Benyamin, Beben; Oexle, Konrad; Swinkels, Dorine; Stefansson, Kari; Magnusson, Magnus; Ganna, Andrea; Gaziano, Michael; Ivey, Kerry; Danesh, John; Pereira, Alexandre; Wood, Angela M; Butterworth, Adam S; Di Angelantonio, Emanuele

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

具有重大影响的罕见变异为有先兆和无先兆的偏头痛亚型的病理学提供了功能性见解

Gyda Bjornsdottir #, Mona A Chalmer #, Lilja Stefansdottir, Astros Th Skuladottir, Gudmundur Einarsson, Margret Andresdottir, Doruk Beyter, Egil Ferkingstad, Solveig Gretarsdottir, Bjarni V Halldorsson, Gisli H Halldorsson, Anna Helgadottir, Hannes Helgason, Grimur Hjorleifsson Eldjarn, Adalbjorg Jo

Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

出版商更正:152万个体中纯合性缺失以及隐性致死的遗传原因

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

Sequence variants affecting voice pitch in humans

影响人类音调的序列变异

Gisladottir, Rosa S; Helgason, Agnar; Halldorsson, Bjarni V; Helgason, Hannes; Borsky, Michal; Chien, Yu-Ren; Gudnason, Jon; Gudjonsson, Sigurjon A; Moisik, Scott; Dediu, Dan; Thorleifsson, Gudmar; Tragante, Vinicius; Bustamante, Mariana; Jonsdottir, Gudrun A; Stefansdottir, Lilja; Rutsdottir, Gudrun; Magnusson, Sigurdur H; Hardarson, Marteinn; Ferkingstad, Egil; Halldorsson, Gisli H; Rognvaldsson, Solvi; Skuladottir, Astros; Ivarsdottir, Erna V; Norddahl, Gudmundur; Thorgeirsson, Gudmundur; Jonsdottir, Ingileif; Ulfarsson, Magnus O; Holm, Hilma; Stefansson, Hreinn; Thorsteinsdottir, Unnur; Gudbjartsson, Daniel F; Sulem, Patrick; Stefansson, Kari

Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor

丛集性头痛全基因组关联研究和荟萃分析确定了八个基因位点,并指出吸烟是其致病风险因素。

Winsvold, Bendik S; Harder, Aster V E; Ran, Caroline; Chalmer, Mona A; Dalmasso, Maria Carolina; Ferkingstad, Egil; Tripathi, Kumar Parijat; Bacchelli, Elena; Børte, Sigrid; Fourier, Carmen; Petersen, Anja S; Vijfhuizen, Lisanne S; Magnusson, Sigurdur H; O'Connor, Emer; Bjornsdottir, Gyda; Häppölä, Paavo; Wang, Yen-Feng; Callesen, Ida; Kelderman, Tim; Gallardo, Victor J; de Boer, Irene; Olofsgård, Felicia Jennysdotter; Heinze, Katja; Lund, Nunu; Thomas, Laurent F; Hsu, Chia-Lin; Pirinen, Matti; Hautakangas, Heidi; Ribasés, Marta; Guerzoni, Simona; Sivakumar, Prasanth; Yip, Janice; Heinze, Axel; Küçükali, Fahri; Ostrowski, Sisse R; Pedersen, Ole B; Kristoffersen, Espen S; Martinsen, Amy E; Artigas, María S; Lagrata, Susie; Cainazzo, Maria Michela; Adebimpe, Joycee; Quinn, Olivia; Göbel, Carl; Cirkel, Anna; Volk, Alexander E; Heilmann-Heimbach, Stefanie; Skogholt, Anne Heidi; Gabrielsen, Maiken E; Wilbrink, Leopoldine A; Danno, Daisuke; Mehta, Dwij; Guðbjartsson, Daníel F; Rosendaal, Frits R; Willems van Dijk, Ko; Fronczek, Rolf; Wagner, Michael; Scherer, Martin; Göbel, Hartmut; Sleegers, Kristel; Sveinsson, Olafur A; Pani, Luca; Zoli, Michele; Ramos-Quiroga, Josep A; Dardiotis, Efthimios; Steinberg, Anna; Riedel-Heller, Steffi; Sjöstrand, Christina; Thorgeirsson, Thorgeir E; Stefansson, Hreinn; Southgate, Laura; Trembath, Richard C; Vandrovcova, Jana; Noordam, Raymond; Paemeleire, Koen; Stefansson, Kari; Fann, Cathy Shen-Jang; Waldenlind, Elisabet; Tronvik, Erling; Jensen, Rigmor H; Chen, Shih-Pin; Houlden, Henry; Terwindt, Gisela M; Kubisch, Christian; Maestrini, Elena; Vikelis, Michail; Pozo-Rosich, Patricia; Belin, Andrea C; Matharu, Manjit; van den Maagdenberg, Arn M J M; Hansen, Thomas F; Ramirez, Alfredo; Zwart, John-Anker