Thiselton相关文献与解析，生知库 | 链接生命科学的每一步

Developing community-based health education strategies with family history: Assessing the association between community resident family history and interest in health education

结合家族史制定社区健康教育策略：评估社区居民家族史与健康教育兴趣之间的关联

doi:10.1016/j.socscimed.2019.02.011

Prom-Wormley, Elizabeth C; Clifford, James S; Bourdon, Jessica L; Barr, Peter; Blondino, Courtney; Ball, Kevin M; Montgomery, Joshua; Davis, Jonathan K; Real, Joseph E; Edwards, Alexis C; Thiselton, Dawn L; Creighton, Gwen Corley; Wilson, De'Nisha; Newbille, Cynthia

发表日期：2021

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Serum α-hydroxybutyrate (α-HB) predicts elevated 1 h glucose levels and early-phase β-cell dysfunction during OGTT

血清α-羟基丁酸（α-HB）水平可预测口服葡萄糖耐量试验（OGTT）中1小时血糖升高和早期β细胞功能障碍。

期刊:Bmj Open Diabetes Research & Care

影响因子:4.1

doi:10.1136/bmjdrc-2014-000038

Varvel, Stephen A; Pottala, James V; Thiselton, Dawn L; Caffrey, Rebecca; Dall, Tara; Sasinowski, Maciek; McConnell, Joseph P; Warnick, G Russell; Voros, Szilard; Graham, Timothy E

细胞生物学

发表日期：2014

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Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis

利用多领域循证优先排序算法和神经发育假说筛选出167个精神分裂症候选基因，并对其进行关联研究。

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0067776

Zhao, Zhongming; Webb, Bradley T; Jia, Peilin; Bigdeli, T Bernard; Maher, Brion S; van den Oord, Edwin; Bergen, Sarah E; Amdur, Richard L; O'Neill, Francis A; Walsh, Dermot; Thiselton, Dawn L; Chen, Xiangning; Pato, Carlos N; Riley, Brien P; Kendler, Kenneth S; Fanous, Ayman H

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

通过靶向基因组下一代测序发现 OFD1 基因的深内含子突变会导致严重的 X 连锁视网膜色素变性 (RP23)。

期刊:Human Molecular Genetics

影响因子:3.2

doi:10.1093/hmg/dds194

Webb, Tom R; Parfitt, David A; Gardner, Jessica C; Martinez, Ariadna; Bevilacqua, Dalila; Davidson, Alice E; Zito, Ilaria; Thiselton, Dawn L; Ressa, Jacob H C; Apergi, Marina; Schwarz, Nele; Kanuga, Naheed; Michaelides, Michel; Cheetham, Michael E; Gorin, Michael B; Hardcastle, Alison J

发表日期：2012

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Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

ZNF804A的精细定位及其与精神分裂症和双相情感障碍相关的全基因组显著证据

期刊:Molecular Psychiatry

影响因子:10.1

doi:10.1038/mp.2010.36

Williams, H J; Norton, N; Dwyer, S; Moskvina, V; Nikolov, I; Carroll, L; Georgieva, L; Williams, N M; Morris, D W; Quinn, E M; Giegling, I; Ikeda, M; Wood, J; Lencz, T; Hultman, C; Lichtenstein, P; Thiselton, D; Maher, B S; Malhotra, A K; Riley, B; Kendler, K S; Gill, M; Sullivan, P; Sklar, P; Purcell, S; Nimgaonkar, V L; Kirov, G; Holmans, P; Corvin, A; Rujescu, D; Craddock, N; Owen, M J; O'Donovan, M C

The AVPR1A gene and substance use disorders: association, replication, and functional evidence

AVPR1A基因与物质使用障碍：关联性、重复性和功能性证据

期刊:Biological Psychiatry

影响因子:9

doi:10.1016/j.biopsych.2011.02.023

Maher, Brion S; Vladimirov, Vladimir I; Latendresse, Shawn J; Thiselton, Dawn L; McNamee, Rebecca; Kang, Moonsu; Bigdeli, Tim B; Chen, Xiangning; Riley, Brien P; Hettema, John M; Chilcoat, Howard; Heidbreder, Christian; Muglia, Pierandrea; Murrelle, E Lenn; Dick, Danielle M; Aliev, Fazil; Agrawal, Arpana; Edenberg, Howard J; Kramer, John; Nurnberger, John; Tischfield, Jay A; Devlin, Bernie; Ferrell, Robert E; Kirillova, Galina P; Tarter, Ralph E; Kendler, Kenneth S; Vanyukov, Michael M

发表日期：2011

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Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness

一项基于基因的综合性关联研究，针对20号染色体连锁区域，揭示了与精神病患者抑郁症状相关的新风险位点。

期刊:PLoS One

影响因子:2.6

doi:10.1371/journal.pone.0021440

Bigdeli, T Bernard; Maher, Brion S; Zhao, Zhongming; Oord, Edwin J C G van den; Thiselton, Dawn L; Sun, Jingchun; Webb, Bradley T; Amdur, Richard L; Wormley, Brandon; O'Neill, Francis A; Walsh, Dermot; Riley, Brien P; Kendler, Kenneth S; Fanous, Ayman H

Correction: Parameterisation and Prediction of Intra-canal Cochlear Structures

校正：耳蜗内结构参数化和预测

Can a Cochlear Implant Be Used as an Electrical Impedance Tomography Device?

人工耳蜗可以用作电阻抗断层扫描设备吗？

Parameterisation and Prediction of Intra-canal Cochlear Structures

耳蜗管内结构的参数化和预测

Developing community-based health education strategies with family history: Assessing the association between community resident family history and interest in health education

结合家族史制定社区健康教育策略：评估社区居民家族史与健康教育兴趣之间的关联

Serum α-hydroxybutyrate (α-HB) predicts elevated 1 h glucose levels and early-phase β-cell dysfunction during OGTT

血清α-羟基丁酸（α-HB）水平可预测口服葡萄糖耐量试验（OGTT）中1小时血糖升高和早期β细胞功能障碍。

Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis

利用多领域循证优先排序算法和神经发育假说筛选出167个精神分裂症候选基因，并对其进行关联研究。

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

通过靶向基因组下一代测序发现 OFD1 基因的深内含子突变会导致严重的 X 连锁视网膜色素变性 (RP23)。

Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

ZNF804A的精细定位及其与精神分裂症和双相情感障碍相关的全基因组显著证据

The AVPR1A gene and substance use disorders: association, replication, and functional evidence

AVPR1A基因与物质使用障碍：关联性、重复性和功能性证据

Comprehensive gene-based association study of a chromosome 20 linked region implicates novel risk loci for depressive symptoms in psychotic illness

一项基于基因的综合性关联研究，针对20号染色体连锁区域，揭示了与精神病患者抑郁症状相关的新风险位点。