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

Meta-analysis of genome-wide association studies for cancer therapy-related cardiovascular dysfunction and functional mapping highlight an intergenic region close to TP63

对癌症治疗相关心血管功能障碍的全基因组关联研究进行荟萃分析和功能定位,突显了TP63基因附近的一个基因间区域。

Martínez-Campelo, L; Blanco-Verea, A; López-Fernández, T; Martínez-Monzonís, A; Buño, A; Mazón, P; Zamora, P; Norton, N; Reddy, J S; Velasco-Ruiz, A; González-Neira, A; Vulsteke, C; Alonso-Gordoa, T; Cruz, R; Diz-de Almeida, S; Carracedo, A; González-Juanatey, J R; López-Sendón, J; Brion, M

Effect of Age, Season, Body Condition, and Endocrine Status on Serum Free Cortisol Fraction and Insulin Concentration in Horses

年龄、季节、体况和内分泌状态对马血清游离皮质醇和胰岛素浓度的影响

Hart, K A; Wochele, D M; Norton, N A; McFarlane, D; Wooldridge, A A; Frank, N

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

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

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

强有力的遗传证据表明,GABAA受体对双相情感障碍表型的某个组成部分具有选择性影响

Craddock, N; Jones, L; Jones, I R; Kirov, G; Green, E K; Grozeva, D; Moskvina, V; Nikolov, I; Hamshere, M L; Vukcevic, D; Caesar, S; Gordon-Smith, K; Fraser, C; Russell, E; Norton, N; Breen, G; St Clair, D; Collier, D A; Young, A H; Ferrier, I N; Farmer, A; McGuffin, P; Holmans, P A; Donnelly, P; Owen, M J; O'Donovan, M C

Meta-analysis of 32 genome-wide linkage studies of schizophrenia

对32项精神分裂症全基因组连锁研究的荟萃分析

Ng, M Y M; Levinson, D F; Faraone, S V; Suarez, B K; DeLisi, L E; Arinami, T; Riley, B; Paunio, T; Pulver, A E; Irmansyah; Holmans, P A; Escamilla, M; Wildenauer, D B; Williams, N M; Laurent, C; Mowry, B J; Brzustowicz, L M; Maziade, M; Sklar, P; Garver, D L; Abecasis, G R; Lerer, B; Fallin, M D; Gurling, H M D; Gejman, P V; Lindholm, E; Moises, H W; Byerley, W; Wijsman, E M; Forabosco, P; Tsuang, M T; Hwu, H-G; Okazaki, Y; Kendler, K S; Wormley, B; Fanous, A; Walsh, D; O'Neill, F A; Peltonen, L; Nestadt, G; Lasseter, V K; Liang, K Y; Papadimitriou, G M; Dikeos, D G; Schwab, S G; Owen, M J; O'Donovan, M C; Norton, N; Hare, E; Raventos, H; Nicolini, H; Albus, M; Maier, W; Nimgaonkar, V L; Terenius, L; Mallet, J; Jay, M; Godard, S; Nertney, D; Alexander, M; Crowe, R R; Silverman, J M; Bassett, A S; Roy, M-A; Mérette, C; Pato, C N; Pato, M T; Roos, J Louw; Kohn, Y; Amann-Zalcenstein, D; Kalsi, G; McQuillin, A; Curtis, D; Brynjolfson, J; Sigmundsson, T; Petursson, H; Sanders, A R; Duan, J; Jazin, E; Myles-Worsley, M; Karayiorgou, M; Lewis, C M

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2

对 10 个独立样本的分析表明,精神分裂症与成纤维细胞生长因子受体 2 侧翼的 SNP 存在关联。

O'Donovan, M C; Norton, N; Williams, H; Peirce, T; Moskvina, V; Nikolov, I; Hamshere, M; Carroll, L; Georgieva, L; Dwyer, S; Holmans, P; Marchini, J L; Spencer, C C A; Howie, B; Leung, H-T; Giegling, I; Hartmann, A M; Möller, H-J; Morris, D W; Shi, Y; Feng, G; Hoffmann, P; Propping, P; Vasilescu, C; Maier, W; Rietschel, M; Zammit, S; Schumacher, J; Quinn, E M; Schulze, T G; Iwata, N; Ikeda, M; Darvasi, A; Shifman, S; He, L; Duan, J; Sanders, A R; Levinson, D F; Adolfsson, R; Osby, U; Terenius, L; Jönsson, E G; Cichon, S; Nöthen, M M; Gill, M; Corvin, A P; Rujescu, D; Gejman, P V; Kirov, G; Craddock, N; Williams, N M; Owen, M J

Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms

利用单核苷酸多态性对大型多中心家系样本进行精神分裂症的全基因组连锁扫描

Holmans, P A; Riley, B; Pulver, A E; Owen, M J; Wildenauer, D B; Gejman, P V; Mowry, B J; Laurent, C; Kendler, K S; Nestadt, G; Williams, N M; Schwab, S G; Sanders, A R; Nertney, D; Mallet, J; Wormley, B; Lasseter, V K; O'Donovan, M C; Duan, J; Albus, M; Alexander, M; Godard, S; Ribble, R; Liang, K Y; Norton, N; Maier, W; Papadimitriou, G; Walsh, D; Jay, M; O'Neill, A; Lerer, F B; Dikeos, D; Crowe, R R; Silverman, J M; Levinson, D F

Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene.

对 NRG1-ERBB4 信号传导的分子解析表明 PTPRZ1 可能是一种精神分裂症易感基因

Buxbaum J D, Georgieva L, Young J J, Plescia C, Kajiwara Y, Jiang Y, Moskvina V, Norton N, Peirce T, Williams H, Craddock N J, Carroll L, Corfas G, Davis K L, Owen M J, Harroch S, Sakurai T, O'Donovan M C

Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14

远端遗传性运动神经元病VII型(dHMN-VII)基因定位于2q14染色体

McEntagart, M; Norton, N; Williams, H; Teare, M D; Dunstan, M; Baker, P; Houlden, H; Reilly, M; Wood, N; Harper, P S; Futreal, P A; Williams, N; Rahman, N