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

The Effects of Light Therapy on Cognitive Function and Stress in Women With Breast Cancer Before Systemic Treatment

光疗对乳腺癌女性全身治疗前认知功能和压力的影响

Aspelund, Snaefridur Gudmundsdottir; Halldorsdottir, Thorhildur; Agustsson, Gudjon; Tobin, Hannah Ros Sigurdardottir; Wu, Lisa M; Amidi, Ali; Johannsdottir, Kamilla R; Lutgendorf, Susan K; Telles, Rachel; Daly, Huldis Franksdottir; Sigurdardottir, Kristin; Figueiro, Mariana G; Redd, William H; Valdimarsdottir, Heiddis B; Baldursdottir, Birna

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

CCDC201基因中终止密码子突变的纯合子会导致原发性卵巢功能不全。

Oddsson, Asmundur; Steinthorsdottir, Valgerdur; Oskarsson, Gudjon R; Styrkarsdottir, Unnur; Moore, Kristjan H S; Isberg, Salvor; Halldorsson, Gisli H; Sveinbjornsson, Gardar; Westergaard, David; Nielsen, Henriette Svarre; Fridriksdottir, Run; Jensson, Brynjar O; Arnadottir, Gudny A; Jonsson, Hakon; Sturluson, Arni; Snaebjarnarson, Audunn S; Andreassen, Ole A; Walters, G Bragi; Nyegaard, Mette; Erikstrup, Christian; Steingrimsdottir, Thora; Lie, Rolv T; Melsted, Pall; Jonsdottir, Ingileif; Halldorsson, Bjarni V; Thorleifsson, Gudmar; Saemundsdottir, Jona; Magnusson, Olafur Th; Banasik, Karina; Sorensen, Erik; Masson, Gisli; Pedersen, Ole Birger; Tryggvadottir, Laufey; Haavik, Jan; Ostrowski, Sisse Rye; Stefansson, Hreinn; Holm, Hilma; Rafnar, Thorunn; Gudbjartsson, Daniel F; Sulem, Patrick; Stefansson, Kari

Current status of pre- and retropectoral breast reconstructions worldwide: a narrative review

全球胸大肌前和胸大肌后乳房重建的现状:叙述性综述

Gunnarsson, Gudjon Leifur; Salzberg, C Andrew

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

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

152 万个体的纯合性缺陷和隐性致死的遗传原因

Asmundur Oddsson #, Patrick Sulem #, Gardar Sveinbjornsson, Gudny A Arnadottir, Valgerdur Steinthorsdottir, Gisli H Halldorsson, Bjarni A Atlason, Gudjon R Oskarsson, Hannes Helgason, Henriette Svarre Nielsen, David Westergaard, Juha M Karjalainen, Hildigunnur Katrinardottir, Run Fridriksdottir, Bry

Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria

序列变异影响 GCSAML 剪接、肥大细胞特异性蛋白和荨麻疹风险

Ragnar P Kristjansson #, Gudjon R Oskarsson #, Astros Skuladottir, Asmundur Oddsson, Solvi Rognvaldsson, Gardar Sveinbjornsson, Sigrun H Lund, Brynjar O Jensson, Edda L Styrmisdottir, Gisli H Halldorsson, Egil Ferkingstad, Grimur Hjorleifsson Eldjarn, Doruk Beyter, Snædis Kristmundsdottir, Kristinn

NeuroWRAP: integrating, validating, and sharing neurodata analysis workflows

NeuroWRAP:整合、验证和共享神经数据分析工作流程

Bowen, Zac; Magnusson, Gudjon; Diep, Madeline; Ayyangar, Ujjwal; Smirnov, Aleksandr; Kanold, Patrick O; Losert, Wolfgang

Breast reconstruction with donor tissue from the back-an evolution towards customized reconstructive solutions guided by innovative surgery and patient wishes

利用背部供体组织进行乳房重建——在创新手术和患者意愿的指导下,向个性化重建方案演进

Gunnarsson, Gudjon L; Lilja, Caroline; Thomsen, Jørn Bo

Multiomics study of nonalcoholic fatty liver disease

非酒精性脂肪肝疾病的多组学研究

Sveinbjornsson, Gardar; Ulfarsson, Magnus O; Thorolfsdottir, Rosa B; Jonsson, Benedikt A; Einarsson, Eythor; Gunnlaugsson, Gylfi; Rognvaldsson, Solvi; Arnar, David O; Baldvinsson, Magnus; Bjarnason, Ragnar G; Eiriksdottir, Thjodbjorg; Erikstrup, Christian; Ferkingstad, Egil; Halldorsson, Gisli H; Helgason, Hannes; Helgadottir, Anna; Hindhede, Lotte; Hjorleifsson, Grimur; Jones, David; Knowlton, Kirk U; Lund, Sigrun H; Melsted, Pall; Norland, Kristjan; Olafsson, Isleifur; Olafsson, Sigurdur; Oskarsson, Gudjon R; Ostrowski, Sisse Rye; Pedersen, Ole Birger; Snaebjarnarson, Auðunn S; Sigurdsson, Emil; Steinthorsdottir, Valgerdur; Schwinn, Michael; Thorgeirsson, Gudmundur; Thorleifsson, Gudmar; Jonsdottir, Ingileif; Bundgaard, Henning; Nadauld, Lincoln; Bjornsson, Einar S; Rulifson, Ingrid C; Rafnar, Thorunn; Norddahl, Gudmundur L; Thorsteinsdottir, Unnur; Sulem, Patrick; Gudbjartsson, Daniel F; Holm, Hilma; Stefansson, Kari

Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene

人群水平的纯合性缺陷揭示了 CPSF3 是一种智力障碍综合征基因

Gudny A Arnadottir, Asmundur Oddsson, Brynjar O Jensson, Svanborg Gisladottir, Mariella T Simon, Asgeir O Arnthorsson, Hildigunnur Katrinardottir, Run Fridriksdottir, Erna V Ivarsdottir, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Rebekah Barrick, Jona Saemundsdottir, Louise le Roux, Gudjon R Oskarss