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

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy

RNU2-2基因的双等位基因变异会导致一种非常常见的发育性和癫痫性脑病。

Jackson, Adam; Blakes, Alexander J M; Alhaddad, Bader; Henry, Olivia J; Delgado-Vega, Angelica M; Wall, Elizabeth; Abdelhadi, Ola; Agrawal, Shakti; Bakur, Khadijah; Blair, Edward; Brady, Angela F; Brittain, Helen; Chandler, Kate E; Clarke, Natasha; Danelli, Miriana; Drinkall, Nicholas; Duba, Irene; Elmslie, Frances; Ellingford, Jamie; Ewans, Lisa J; Fennell, Andrew P; Gazdagh, Gabriella; Heller, Simon P; Hammarsjö, Anna; Karrman, Kristina; Kini, Usha; Lesko, Nicole; Lindstrand, Anna; Macintosh, Rebecca; Mansour, Sahar; Menzies, Lara; Metcalfe, Kay; Milhench, Alison; Nashef, Lina; O'Keefe, Raymond T; Pacheco, Nadja Pekkola; Palmer, Elizabeth E; Parida, Amitav; Prescott, Katrina; Redman, Melody; Renieri, Alessandra; Fallerini, Chiara; Rizzo, Caterina Lo; Sachdev, Rani; Simons, Cas; Sisodiya, Sanjay M; Stewart, Helen; Stödberg, Tommy; Banos-Pinero, Benito; Taylan, Fulya; Thomas, Huw B; Tinella, Flavia; Wiafe, Samuel; Wedell, Anna; Whiffin, Nicola; Walker, Susan; Rius, Rocio; Chae, Jong Hee; Nordgren, Ann; Alkuraya, Fowzan; Lord, Jenny; Banka, Siddharth

Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease

ZFHX3基因外显子三核苷酸重复序列扩增导致脊髓小脑性共济失调4型:一种聚甘氨酸病

Joel Wallenius,Efthymia Kafantari,Emma Jhaveri,Sorina Gorcenco,Adam Ameur,Christin Karremo,Sigurd Dobloug,Kristina Karrman,Tom de Koning,Andreea Ilinca,Maria Landqvist Waldö,Andreas Arvidsson,Staffan Persson,Elisabet Englund,Hans Ehrencrona,Andreas Puschmann

Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia

对一组被诊断为共济失调的瑞典患者进行临床和基因分析。

Gorcenco, Sorina; Kafantari, Efthymia; Wallenius, Joel; Karremo, Christin; Alinder, Erik; Dobloug, Sigurd; Landqvist Waldö, Maria; Englund, Elisabet; Ehrencrona, Hans; Wictorin, Klas; Karrman, Kristina; Puschmann, Andreas

Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A

对儿童T细胞急性淋巴细胞白血病进行深度测序和SNP芯片分析,发现少数亚克隆中存在NOTCH1突变,且CDKN2A单亲二体性发生率较高。

Karrman, Kristina; Castor, Anders; Behrendtz, Mikael; Forestier, Erik; Olsson, Linda; Ehinger, Mats; Biloglav, Andrea; Fioretos, Thoas; Paulsson, Kajsa; Johansson, Bertil

Promoter DNA methylation pattern identifies prognostic subgroups in childhood T-cell acute lymphoblastic leukemia

启动子 DNA 甲基化模式可识别儿童 T 细胞急性淋巴细胞白血病的预后亚群

Magnus Borssén, Lars Palmqvist, Kristina Karrman, Jonas Abrahamsson, Mikael Behrendtz, Jesper Heldrup, Erik Forestier, Göran Roos, Sofie Degerman

The t(X;7)(q22;q34) in paediatric T-cell acute lymphoblastic leukaemia results in overexpression of the insulin receptor substrate 4 gene through illegitimate recombination with the T-cell receptor beta locus

儿童急性淋巴细胞白血病中的 t(X;7)(q22;q34) 通过与 T 细胞受体 β 基因座的不正当重组导致胰岛素受体底物 4 基因过度表达

Kristina Karrman, Eigil Kjeldsen, Carin Lassen, Margareth Isaksson, Josef Davidsson, Anna Andersson, Henrik Hasle, Thoas Fioretos, Bertil Johansson