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

Cacao clones modulate pod tolerance to witches' broom and nutritional imbalances, enhancing cocoa production in the Amazon

可可克隆体能够调节可可豆荚对女巫扫帚病和营养失衡的耐受性,从而提高亚马逊地区的可可产量。

Traspadini, Edilaine Istéfani Franklin; de Mello Prado, Renato; Wadt, Paulo Guilherme Salvador; Gratão, Priscila Lupino; Ribeiro, Sylviane Beck; da Silva, Douglas Marcelo Pinheiro

Optimizing diagnostic resource use in suspected chronic coronary syndrome: pre-test probability and acoustic CAD rule-out in the FILTER-SCAD trial

优化疑似慢性冠状动脉综合征的诊断资源利用:FILTER-SCAD 试验中的预检概率和声学冠状动脉疾病排除

Bjerking, Louise Hougesen; Skak-Hansen, Kim Wadt; Heitmann, Merete; Hove, Jens Dahlgaard; Haahr-Pedersen, Sune Ammentorp; Engblom, Henrik; Erlinge, David; Räder, Sune Bernd Emil Werner; Brønnum-Schou, Jens; Biering-Sørensen, Tor; Kjærgaard, Camilla Lyngby; Strange, Søren; Prescott, Eva Irene Bossano; Galatius, Søren

Survey of bacteria associated with septic arthritis in beef feedlot cattle

对肉牛饲养场中与化脓性关节炎相关的细菌进行调查

Kos, Daniel; Warr, Brian; Suchan, Danae M; Wadt, Danilo; Russell, Jennifer N; Norfield, Mallory; Liang, Jenny; Jelinski, Murray; Cameron, Andrew D S; Ruzzini, Antonio

DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing data

DoBSeqWF:一种用于灵敏检测混合测序数据中个体遗传变异的框架

Cort Nielsen, Mads; Hagen, Christian Munch; Stoltze, Ulrik Kristoffer; Hansen, Thomas van Overeem; Nyegaard, Mette; Hjalgrim, Henrik; Bækvad-Hansen, Marie; Byrjalsen, Anna; Schmiegelow, Kjeld; Wadt, Karin; Bybjerg-Grauholm, Jonas; Rasmussen, Simon

Case report: Onychopapilloma in a patient with BAP1 tumor predisposition syndrome-a useful clinical marker?

病例报告:BAP1肿瘤易感综合征患者的甲乳头状瘤——一种有用的临床标志物?

Sjøstrøm, Emilie; Ahlborn, Lise Barlebo; Eliesen, Elisabeth Victoria; Wadt, Karin; Lei, Ulrikke; Byrjalsen, Anna

Re-evaluating hereditary breast and ovarian cancer risk: clinical impact of updated multigene panel sequencing and genetic counseling

重新评估遗传性乳腺癌和卵巢癌风险:更新的多基因panel测序和遗传咨询的临床影响

Gislinge, Julie Isabelle Plougmann; Byrjalsen, Anna; Naver, Klara Vinsand; Clausen, Helle Vibeke; Ravn, Pernille; Petersen, Kresten Rubeck; Wadt, Karin A W

Biallelic germline variants in the hematologic malignancy predisposition gene DDX41 cause retinal dystrophy through dysregulation of retinal homeostasis

血液系统恶性肿瘤易感基因DDX41的双等位基因种系变异通过扰乱视网膜稳态导致视网膜营养不良。

Mars, Zoéline; Zanetti, Andrea; Kaminska, Karolina; Miyagawa, Takero; Liu, Duanya; Antonio, Aline; Arno, Gavin; Audo, Isabelle; Ayuso, Carmen; Muhammad Jafar Hussain, Hafiz; Bao, Xuan; Barberán-Martínez, Pilar; Bocquet, Béatrice; Boguszewska-Chachulska, Anna; Condroyer, Christel; David, Pierre; Dollfus, Hélène; Fares-Taie, Lucas; Fernández-Caballero, Lidia; García-García, Gema; Michel, Victor; Guerrera, Chiara Ida; Jung, Vincent; Kessel, Line; Gioja, Louise; Lin, Siying; Matczynska, Ewa; Millán, Jose M; Moye, Abigail R; Martín-Gutiérrez, M Pilar; Quinodoz, Mathieu; Robert, Matthieu P; Roger, Jerome E; Sousa-Luis, Rui; Swafiri, Saoud Tahsin; Teper, Slawomir; Meunier, Isabelle; Patat, Olivier; Pennesi, Mark E; Wadt, Karin A W; Wang, Meng; Webster, Andrew R; Yang, Paul; Yumei, Li; Zeitz, Christina; Rieux-Laucat, Frederic; Giraudier, Stéphane; Chen, Rui; Fica, Sebastian M; Rivolta, Carlo; Sebert, Marie; Rozet, Jean-Michel; Perrault, Isabelle

CD19 exon 2 skipping is a potential prognostic correlate of anti-CD19 CAR-T therapy relapse

CD19 外显子 2 跳跃是抗 CD19 CAR-T 疗法复发的潜在预后相关因素

Dam, Søren Helweg; Moranzoni, Giorgia; Høie, Magnus Haraldson; Modvig, Signe; Wadt, Karin A W; Als-Nielsen, Bodil; Schmiegelow, Kjeld; Vitting-Seerup, Kristoffer; Barnkob, Mike Bogetofte; Olsen, Lars Rønn

Acoustic-based rule-out of stable coronary artery disease: the FILTER-SCAD trial

基于声学的稳定性冠状动脉疾病排除:FILTER-SCAD 试验

Louise Hougesen Bjerking, Kim Wadt Skak-Hansen, Merete Heitmann, Jens Dahlgaard Hove, Sune Ammentorp Haahr-Pedersen, Henrik Engblom, David Erlinge, Sune Bernd Emil Werner Räder, Jens Brønnum-Schou, Tor Biering-Sørensen, Camilla Lyngby Kjærgaard, Søren Strange, Søren Galatius, Eva Irene Bossano Presc

Data-driven discovery of gene expression markers distinguishing pediatric acute lymphoblastic leukemia subtypes

基于数据驱动的基因表达标记物发现,用于区分儿童急性淋巴细胞白血病亚型

Nourbakhsh, Mona; Tom, Nikola; Schrøder Lassen, Anna; Brasch Lind Petersen, Helene; Stoltze, Ulrik Kristoffer; Wadt, Karin; Schmiegelow, Kjeld; Tiberti, Matteo; Papaleo, Elena