Lars Feuk相关文献与解析，生知库 | 链接生命科学的每一步

Mariya Lysenkova Wiklander, Gustav Arvidsson, Ignas Bunikis, Anders Lundmark, Amanda Raine, Yanara Marincevic-Zuniga, Henrik Gezelius, Anna Bremer, Lars Feuk, Adam Ameur, Jessica Nordlund

肿瘤

白血病

其它细胞

发表日期：2024

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Long-read whole-genome analysis of human single cells

人类单细胞长读全基因组分析

期刊:Nature Communications

影响因子:14.7

doi:10.1038/s41467-023-40898-3

Joanna Hård, Jeff E Mold, Jesper Eisfeldt, Christian Tellgren-Roth, Susana Häggqvist, Ignas Bunikis, Orlando Contreras-Lopez, Chen-Shan Chin, Jessica Nordlund, Carl-Johan Rubin, Lars Feuk, Jakob Michaëlsson, Adam Ameur3

CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations

CRISPR-Cas9 在体内靶位点和非靶位点诱导产生大的结构变异，这些变异会跨代遗传。

期刊:

影响因子:14.7

doi:10.1038/s41467-022-28244-5.

Ida Höijer,Anastasia Emmanouilidou,Rebecka Östlund,Robin van Schendel,Selma Bozorgpana,Marcel Tijsterman,Lars Feuk,Ulf Gyllensten,Marcel den Hoed #,Adam Ameur #

CAS9

发表日期：2022

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Transcriptome Analysis of Post-Mortem Brain Tissue Reveals Up-Regulation of the Complement Cascade in a Subgroup of Schizophrenia Patients

死后脑组织的转录组分析揭示了精神分裂症患者亚群中补体级联的上调

期刊:Genes

影响因子:

doi:10.3390/genes12081242

Eva Lindholm Carlström, Adnan Niazi, Mitra Etemadikhah, Jonatan Halvardson, Stefan Enroth, Craig A Stockmeier, Grazyna Rajkowska, Bo Nilsson, Lars Feuk

Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

无扩增长读测序揭示了不可预见的 CRISPR-Cas9 脱靶活性

期刊:Genome Biology

影响因子:10.1

doi:10.1186/s13059-020-02206-w

Ida Höijer, Josefin Johansson, Sanna Gudmundsson, Chen-Shan Chin, Ignas Bunikis, Susana Häggqvist, Anastasia Emmanouilidou, Maria Wilbe, Marcel den Hoed, Marie-Louise Bondeson, Lars Feuk, Ulf Gyllensten, Adam Ameur

信号转导

发表日期：2020

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Exploring autoantibody signatures in brain tissue from patients with severe mental illness

探索严重精神疾病患者脑组织中的自身抗体特征

期刊:Translational Psychiatry

影响因子:5.8

doi:10.1038/s41398-020-01079-8

David Just, Anna Månberg, Nicholas Mitsios, Craig A Stockmeier, Grazyna Rajkowska, Mathias Uhlén, Jan Mulder, Lars Feuk, Janet L Cunningham, Peter Nilsson, Eva Lindholm Carlström

Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorder

导致智力障碍的 tRNA 摆动肌苷缺乏症的识别和挽救

期刊:RNA

影响因子:4.2

doi:10.1261/rna.076380.120

Jillian Ramos, Melissa Proven, Jonatan Halvardson, Felix Hagelskamp, Ekaterina Kuchinskaya, Benjamin Phelan, Ryan Bell, Stefanie M Kellner, Lars Feuk, Ann-Charlotte Thuresson, Dragony Fu

Copy number determination of the gene for the human pancreatic polypeptide receptor NPY4R using read depth analysis and droplet digital PCR

使用读取深度分析和液滴数字 PCR 确定人类胰腺多肽受体 NPY4R 基因的拷贝数

期刊:BMC Biotechnology

影响因子:3.5

doi:10.1186/s12896-019-0523-9

Kateryna Shebanits, Torsten Günther, Anna C V Johansson, Khurram Maqbool, Lars Feuk, Mattias Jakobsson, Dan Larhammar

Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family

连锁和外显子组分析表明瑞典一个大家族中存在多个基因导致无综合征智力障碍

期刊:BMC Medical Genomics

影响因子:2.1

doi:10.1186/s12920-019-0606-4

Eva Lindholm Carlström, Jonatan Halvardson, Mitra Etemadikhah, Lennart Wetterberg, Karl-Henrik Gustavson, Lars Feuk

信号转导

发表日期：2019

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Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing

使用靶向无扩增长读测序对人类血液中的 HTT 重复元素进行详细分析

期刊:Human Mutation

影响因子:3.3

doi:10.1002/humu.23580

Ida Höijer, Yu-Chih Tsai, Tyson A Clark, Paul Kotturi, Niklas Dahl, Eva-Lena Stattin, Marie-Louise Bondeson, Lars Feuk, Ulf Gyllensten, Adam Ameur

发表日期：2018

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A multiomic characterization of the leukemia cell line REH using short- and long-read sequencing

使用短读和长读测序对白血病细胞系 REH 进行多组学表征

Long-read whole-genome analysis of human single cells

人类单细胞长读全基因组分析

CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations

CRISPR-Cas9 在体内靶位点和非靶位点诱导产生大的结构变异，这些变异会跨代遗传。

Transcriptome Analysis of Post-Mortem Brain Tissue Reveals Up-Regulation of the Complement Cascade in a Subgroup of Schizophrenia Patients

死后脑组织的转录组分析揭示了精神分裂症患者亚群中补体级联的上调

Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

无扩增长读测序揭示了不可预见的 CRISPR-Cas9 脱靶活性

Exploring autoantibody signatures in brain tissue from patients with severe mental illness

探索严重精神疾病患者脑组织中的自身抗体特征

Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorder

导致智力障碍的 tRNA 摆动肌苷缺乏症的识别和挽救

Copy number determination of the gene for the human pancreatic polypeptide receptor NPY4R using read depth analysis and droplet digital PCR

使用读取深度分析和液滴数字 PCR 确定人类胰腺多肽受体 NPY4R 基因的拷贝数

Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family

连锁和外显子组分析表明瑞典一个大家族中存在多个基因导致无综合征智力障碍

Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing

使用靶向无扩增长读测序对人类血液中的 HTT 重复元素进行详细分析