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

The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation

卡罗林斯卡基因组医学中心关于罕见病基因组测序的十年报告及分阶段临床实施策略

Lindstrand, Anna; Lagerstedt-Robinson, Kristina; Jemt, Anders; Kvarnung, Malin; Ygberg, Sofia; Vonlanthen, Sofie; Oscarson, Mikael; Nilsson, Daniel; Lesko, Nicole; Mantero, Angelo Salazar; Anderlid, Britt-Marie; Arnell, Henrik; Arthur, Cecilia; Bajalica-Lagercrantz, Svetlana; Barbaro, Michela; Bergman, Peter; Björck, Erik; Picard, Oda Blomqvist; Bruhn, Helene; Carlsten, Jonas; Correia, Sandrina P; De Geer, Karl; Delgado Vega, Angelica M; Ehn, Emma; Eisfeldt, Jesper; Ek, Marlene; Elvers, Ingegerd; Engvall, Martin; Freyer, Christoph; Frisk, Sofia; Graff, Caroline; Grigelioniené, Giedré; Gustafsson, Peter; Hammarsjö, Anna; Helgadottir, Hafdis T; Hellström Pigg, Maritta; Henry, Olivia J; Hägglund, Moa; Iwarsson, Erik; Janvid, Vincent; Soller, Maria Johansson; Sundin, Leif; Kuchinskaya, Ekaterina; Kämpe, Anders; Leinfelt, Anna; Liedén, Agne; Lindelöf, Hillevi; Lyander, Anna; Malmgren, Helena; Mannila, Maria; Marits, Per; Naess, Karin; Neethiraj, Ramprasad; Nyren, Karl; Pappas, Christoforos; Paucar, Martin; Pekkola Pacheco, Nadja; Peña Perez, Lucia; Pettersson, Maria; Pruisscher, Peter; Rasi, Chiara; Renevey, Annick; Rössner, Sophia; Sahlin, Ellika; Stenund, Erik; Stödberg, Tommy; Sundin, Mikael; Svärd, Karl; Tesi, Bianca; Tham, Emma; Thonberg, Håkan; Töhönen, Virpi; Ueberschär, Malin; Wallander, Karin; Westenius, Eini; Winberg, Johanna; Winblad, Nerges; Wincent, Josephine; Winerdal, Malin; Wredenberg, Anna; Zetterlund, Anna; Zetterström, Rolf H; Öfverholm, Ingegerd; Nordgren, Ann; Stranneheim, Henrik; Wirta, Valtteri; Wedell, Anna

Surgical Outcomes After Risk-Reducing Mastectomy Among BRCA1 and BRCA2 Carriers

BRCA1和BRCA2基因携带者接受风险降低性乳房切除术后的手术结果

Wiberg, Rebecca; Hägglund, Signe; Numan Hellquist, Barbro; Rosén, Anna; Idahl, Annika; Mani, Maria; Bajalica-Lagercrantz, Svetlana; Ehrencrona, Hans; Karlsson, Per; Loman, Niklas; Sund, Malin

Implementing mainstream germline genetic testing in breast cancer across Europe

在欧洲范围内推广乳腺癌主流生殖系基因检测

Pérez-Ballestero, Eduard; Shire, Sagal Ahmed; Krajc, Mateja; Irmejs, Arvīds; Foretová, Lenka; Frank, Sophie; Kahre, Tiina; van Overeem Hansen, Thomas; Koppert, Linetta; Burgemeister, Anna Lena; Tischkowitz, Marc; Balmaña, Judith; Bajalica-Lagercrantz, Svetlana

Characterisation of heritable TP53-related cancer syndrome in Sweden-a nationwide study of genotype-phenotype correlations in 90 families

瑞典遗传性TP53相关癌症综合征的特征分析——一项针对90个家族的全国性基因型-表型相关性研究

Omran, Meis; Liu, Yaxuan; Sun Zhang, Alexander; Poluha, Anna; Stenmark-Askmalm, Marie; Persson, Fredrik; Hallbeck, Anna-Lotta; Rosén, Anna; Helgadottir, Hafdis T; Tham, Emma; Bajalica-Lagercrantz, Svetlana

Challenges of Transitional Care for Young Allergy and Asthma Patients From Healthcare Professionals' Perspectives

从医疗专业人员的角度看年轻过敏和哮喘患者过渡期护理面临的挑战

Ödling, Maria; Lagercrantz, Birgitta; Lundin, Susanne; Sandelowsky, Hanna; Janson, Christer; Kull, Inger

TP53 p.R181H is enriched in the Swedish cohort (SWEP53) and associated with a distinct breast and prostate phenotype

TP53 p.R181H 在瑞典人群队列 (SWEP53) 中富集,并与独特的乳腺癌和前列腺癌表型相关。

Sun Zhang, Alexander; Omran, Meis; Arthur, Cecilia; Malmgren, Helena; Barbosa-Matos, Rita; Seixas, Susana; Oliveira, Carla; Tham, Emma; Bajalica-Lagercrantz, Svetlana

The Awakening of the Newborn Human Infant and the Emergence of Consciousness

新生儿的觉醒与意识的出现

Lagercrantz, Hugo

Investigation of Genetic Alterations Associated With Interval Breast Cancer

对与间隔期乳腺癌相关的基因改变进行研究

Rodriguez, Juan; Grassmann, Felix; Xiao, Qingyang; Eriksson, Mikael; Mao, Xinhe; Bajalica-Lagercrantz, Svetlana; Hall, Per; Czene, Kamila

Comprehensive genomic analysis of adrenocortical carcinoma reveals genetic profiles associated with patient survival

对肾上腺皮质癌进行全面的基因组分析揭示了与患者生存相关的遗传特征

Sun-Zhang, A; Juhlin, C C; Carling, T; Scholl, U; Schott, M; Larsson, C; Bajalica-Lagercrantz, S

Public attitudes challenge clinical practice on genetic risk disclosure in favour of healthcare-provided direct dissemination to relatives

公众态度对临床实践中关于基因风险披露的做法提出了挑战,倾向于由医疗机构直接向亲属告知相关信息。

Rosén, Anna; Krajc, Mateja; Ehrencrona, Hans; Bajalica-Lagercrantz, Svetlana