文献库，生知库 | 链接生命科学的每一步

日期影响因子

A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives

一项针对瑞典结直肠癌患者及其亲属中患有胃癌和前列腺癌患者的全基因组关联研究

期刊:Hereditary Cancer in Clinical Practice

影响因子:2.4

doi:10.1186/s13053-024-00299-z

Samola Winnberg, Johanna; Vermani, Litika; Liu, Wen; Soller, Veronika; Thutkawkorapin, Jessada; Lindblad, Mats; Lindblom, Annika

发表日期：2024

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A Swedish Familial Genome-Wide Haplotype Analysis Identified Five Novel Breast Cancer Susceptibility Loci on 9p24.3, 11q22.3, 15q11.2, 16q24.1 and Xq21.31

瑞典一项家族全基因组单倍型分析发现了五个新的乳腺癌易感基因位点，分别位于 9p24.3、11q22.3、15q11.2、16q24.1 和 Xq21.31。

期刊:International Journal of Molecular Sciences

影响因子:4.9

doi:10.3390/ijms24054468

Barnekow, Elin; Hasslow, Johan; Liu, Wen; Bryant, Patrick; Thutkawkorapin, Jessada; Wendt, Camilla; Czene, Kamila; Hall, Per; Margolin, Sara; Lindblom, Annika

发表日期：2023

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A Swedish Genome-Wide Haplotype Association Analysis Identifies a Novel Breast Cancer Susceptibility Locus in 8p21.2 and Characterizes Three Loci on Chromosomes 10, 11 and 16

瑞典一项全基因组单倍型关联分析在8p21.2区域发现了一个新的乳腺癌易感基因位点，并对10号、11号和16号染色体上的三个位点进行了表征。

影响因子:4.4

doi:10.3390/cancers14051206

Barnekow, Elin; Liu, Wen; Helgadottir, Hafdis T; Michailidou, Kyriaki; Dennis, Joe; Bryant, Patrick; Thutkawkorapin, Jessada; Wendt, Camilla; Czene, Kamila; Hall, Per; Margolin, Sara; Lindblom, Annika

发表日期：2022

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Sequencing for germline mutations in Swedish breast cancer families reveals novel breast cancer risk genes

对瑞典乳腺癌家族的种系突变进行测序，揭示了新的乳腺癌风险基因

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-021-94316-z

Helgadottir, Hafdis T; Thutkawkorapin, Jessada; Lagerstedt-Robinson, Kristina; Lindblom, Annika

发表日期：2021

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A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients

寻找CHEK2:c.1100delC乳腺癌患者的修饰基因因素

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-021-93926-x

Wendt, Camilla; Muranen, Taru A; Mielikäinen, Lotta; Thutkawkorapin, Jessada; Blomqvist, Carl; Jiao, Xiang; Ehrencrona, Hans; Tham, Emma; Arver, Brita; Melin, Beatrice; Kuchinskaya, Ekaterina; Stenmark Askmalm, Marie; Paulsson-Karlsson, Ylva; Einbeigi, Zakaria; von Wachenfeldt Väppling, Anna; Kalso, Eija; Tasmuth, Tiina; Kallioniemi, Anne; Aittomäki, Kristiina; Nevanlinna, Heli; Borg, Åke; Lindblom, Annika

发表日期：2021

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Massive parallel sequencing in a family with rectal cancer

对一个直肠癌家族进行大规模平行测序

期刊:Hereditary Cancer in Clinical Practice

影响因子:2.4

doi:10.1186/s13053-021-00181-2

Wallander, Karin; Thutkawkorapin, Jessada; Sahlin, Ellika; Lindblom, Annika; Lagerstedt-Robinson, Kristina

发表日期：2021

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pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencing

pyCancerSig：利用全基因组测序数据，通过全面的单核苷酸、结构和微卫星突变特征解析，对人类癌症进行亚分类

期刊:BMC Bioinformatics

影响因子:3.3

doi:10.1186/s12859-020-3451-8

Thutkawkorapin, Jessada; Eisfeldt, Jesper; Tham, Emma; Nilsson, Daniel

发表日期：2020

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Genetic analyses supporting colorectal, gastric, and prostate cancer syndromes

支持结直肠癌、胃癌和前列腺癌综合征的基因分析

期刊:Genes Chromosomes & Cancer

影响因子:2.8

doi:10.1002/gcc.22786

Wallander, Karin; Liu, Wen; von Holst, Susanna; Thutkawkorapin, Jessada; Kontham, Vinaykumar; Forsberg, Anna; Lindblom, Annika; Lagerstedt-Robinson, Kristina

发表日期：2019

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Exome sequencing in 51 early onset non-familial CRC cases

对 51 例早发性非家族性结直肠癌病例进行外显子组测序

期刊:Molecular Genetics & Genomic Medicine

影响因子:1.6

doi:10.1002/mgg3.605

Thutkawkorapin, Jessada; Lindblom, Annika; Tham, Emma

发表日期：2019

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Two novel colorectal cancer risk loci in the region on chromosome 9q22.32

9q22.32 染色体区域内的两个新的结直肠癌风险位点

期刊:Oncotarget

doi:10.18632/oncotarget.24340

Thutkawkorapin, Jessada; Mahdessian, Hovsep; Barber, Tom; Picelli, Simone; von Holst, Susanna; Lundin, Johanna; Valle, Laura; Kontham, Vinaykumar; Liu, Tao; Nilsson, Daniel; Jiao, Xiang; Lindblom, Annika

发表日期：2018

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