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

A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing

通过光学基因组图谱和纳米孔测序检测到一种导致林奇综合征的39 kb结构变异。

Bjørnstad, Pål Marius; Aaløkken, Ragnhild; Åsheim, June; Sundaram, Arvind Y M; Felde, Caroline N; Østby, G Henriette; Dalland, Marianne; Sjursen, Wenche; Carrizosa, Christian; Vigeland, Magnus D; Sorte, Hanne S; Sheng, Ying; Ariansen, Sarah L; Grindedal, Eli Marie; Gilfillan, Gregor D

shinyseg: a web application for flexible cosegregation and sensitivity analysis

shinyseg:一个用于灵活共分离和敏感性分析的Web应用程序

Carrizosa, Christian; Undlien, Dag E; Vigeland, Magnus D

April, again

四月,又来了

Bjørnstad, Pål Marius; Aaløkken, Ragnhild; Åsheim, June; Sundaram, Arvind Y M; Felde, Caroline N; Østby, G Henriette; Dalland, Marianne; Sjursen, Wenche; Carrizosa, Christian; Vigeland, Magnus D; Sorte, Hanne S; Sheng, Ying; Ariansen, Sarah L; Grindedal, Eli Marie; Gilfillan, Gregor D; McNeill, Alisdair

Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study

对北欧裔烟雾病患者进行全外显子组测序,发现参与一氧化氮代谢的基因变异:一项初步研究

Wiedmann, Markus K H; Steinsvåg, Ingunn V; Dinh, Tovy; Vigeland, Magnus D; Larsson, Pål G; Hjorthaug, Hanne; Sheng, Ying; Mero, Inger-Lise; Selmer, Kaja K

QuickPed: an online tool for drawing pedigrees and analysing relatedness

QuickPed:一款用于绘制系谱图和分析亲缘关系的在线工具

Vigeland, Magnus D

Joint DNA-based disaster victim identification

联合DNA灾难遇难者身份识别

Vigeland, Magnus D; Egeland, Thore

Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7

TRAF7基因种系变异相关的表型谱和转录组特征

Castilla-Vallmanya, Laura; Selmer, Kaja K; Dimartino, Clémantine; Rabionet, Raquel; Blanco-Sánchez, Bernardo; Yang, Sandra; Reijnders, Margot R F; van Essen, Antonie J; Oufadem, Myriam; Vigeland, Magnus D; Stadheim, Barbro; Houge, Gunnar; Cox, Helen; Kingston, Helen; Clayton-Smith, Jill; Innis, Jeffrey W; Iascone, Maria; Cereda, Anna; Gabbiadini, Sara; Chung, Wendy K; Sanders, Victoria; Charrow, Joel; Bryant, Emily; Millichap, John; Vitobello, Antonio; Thauvin, Christel; Mau-Them, Frederic Tran; Faivre, Laurence; Lesca, Gaetan; Labalme, Audrey; Rougeot, Christelle; Chatron, Nicolas; Sanlaville, Damien; Christensen, Katherine M; Kirby, Amelia; Lewandowski, Raymond; Gannaway, Rachel; Aly, Maha; Lehman, Anna; Clarke, Lorne; Graul-Neumann, Luitgard; Zweier, Christiane; Lessel, Davor; Lozic, Bernarda; Aukrust, Ingvild; Peretz, Ryan; Stratton, Robert; Smol, Thomas; Dieux-Coëslier, Anne; Meira, Joanna; Wohler, Elizabeth; Sobreira, Nara; Beaver, Erin M; Heeley, Jennifer; Briere, Lauren C; High, Frances A; Sweetser, David A; Walker, Melissa A; Keegan, Catherine E; Jayakar, Parul; Shinawi, Marwan; Kerstjens-Frederikse, Wilhelmina S; Earl, Dawn L; Siu, Victoria M; Reesor, Emma; Yao, Tony; Hegele, Robert A; Vaske, Olena M; Rego, Shannon; Shapiro, Kevin A; Wong, Brian; Gambello, Michael J; McDonald, Marie; Karlowicz, Danielle; Colombo, Roberto; Serretti, Alessandro; Pais, Lynn; O'Donnell-Luria, Anne; Wray, Alison; Sadedin, Simon; Chong, Belinda; Tan, Tiong Y; Christodoulou, John; White, Susan M; Slavotinek, Anne; Barbouth, Deborah; Morel Swols, Dayna; Parisot, Mélanie; Bole-Feysot, Christine; Nitschké, Patrick; Pingault, Véronique; Munnich, Arnold; Cho, Megan T; Cormier-Daire, Valérie; Balcells, Susanna; Lyonnet, Stanislas; Grinberg, Daniel; Amiel, Jeanne; Urreizti, Roser; Gordon, Christopher T

Mitochondrial genome-wide association study of migraine - the HUNT Study

线粒体全基因组关联研究与偏头痛——HUNT 研究

Børte, Sigrid; Zwart, John-Anker; Skogholt, Anne Heidi; Gabrielsen, Maiken Elvestad; Thomas, Laurent F; Fritsche, Lars G; Surakka, Ida; Nielsen, Jonas B; Zhou, Wei; Wolford, Brooke N; Vigeland, Magnus D; Hagen, Knut; Kristoffersen, Espen Saxhaug; Nyholt, Dale R; Chasman, Daniel I; Brumpton, Ben M; Willer, Cristen J; Winsvold, Bendik S

Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease

自身免疫性艾迪生病患者中罕见 Toll 样受体 3 变异体的鉴定和表征

Aslaksen, Sigrid; Wolff, Anette B; Vigeland, Magnus D; Breivik, Lars; Sheng, Ying; Oftedal, Bergithe E; Artaza, Haydee; Skinningsrud, Beate; Undlien, Dag E; Selmer, Kaja K; Husebye, Eystein S; Bratland, Eirik

The Atlantic salmon genome provides insights into rediploidization.

大西洋鲑鱼基因组为二倍体重整化提供了见解

Lien Sigbjørn, Koop Ben F, Sandve Simen R, Miller Jason R, Kent Matthew P, Nome Torfinn, Hvidsten Torgeir R, Leong Jong S, Minkley David R, Zimin Aleksey, Grammes Fabian, Grove Harald, Gjuvsland Arne, Walenz Brian, Hermansen Russell A, von Schalburg Kris, Rondeau Eric B, Di Genova Alex, Samy Jeevan K A, Olav Vik Jon, Vigeland Magnus D, Caler Lis, Grimholt Unni, Jentoft Sissel, Våge Dag Inge, de Jong Pieter, Moen Thomas, Baranski Matthew, Palti Yniv, Smith Douglas R, Yorke James A, Nederbragt Alexander J, Tooming-Klunderud Ave, Jakobsen Kjetill S, Jiang Xuanting, Fan Dingding, Hu Yan, Liberles David A, Vidal Rodrigo, Iturra Patricia, Jones Steven J M, Jonassen Inge, Maass Alejandro, Omholt Stig W, Davidson William S