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

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

全基因组线粒体DNA拷贝数分析揭示了与核苷酸代谢、血小板活化和巨核细胞增殖相关的基因位点

Longchamps, R J; Yang, S Y; Castellani, C A; Shi, W; Lane, J; Grove, M L; Bartz, T M; Sarnowski, C; Liu, C; Burrows, K; Guyatt, A L; Gaunt, T R; Kacprowski, T; Yang, J; De Jager, P L; Yu, L; Bergman, A; Xia, R; Fornage, M; Feitosa, M F; Wojczynski, M K; Kraja, A T; Province, M A; Amin, N; Rivadeneira, F; Tiemeier, H; Uitterlinden, A G; Broer, L; Van Meurs, J B J; Van Duijn, C M; Raffield, L M; Lange, L; Rich, S S; Lemaitre, R N; Goodarzi, M O; Sitlani, C M; Mak, A C Y; Bennett, D A; Rodriguez, S; Murabito, J M; Lunetta, K L; Sotoodehnia, N; Atzmon, G; Ye, K; Barzilai, N; Brody, J A; Psaty, B M; Taylor, K D; Rotter, J I; Boerwinkle, E; Pankratz, N; Arking, D E

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

原钙黏蛋白17基因影响认知、人格、杏仁核结构和功能、突触发育以及罹患严重情绪障碍的风险。

Chang, H; Hoshina, N; Zhang, C; Ma, Y; Cao, H; Wang, Y; Wu, D-D; Bergen, S E; Landén, M; Hultman, C M; Preisig, M; Kutalik, Z; Castelao, E; Grigoroiu-Serbanescu, M; Forstner, A J; Strohmaier, J; Hecker, J; Schulze, T G; Müller-Myhsok, B; Reif, A; Mitchell, P B; Martin, N G; Schofield, P R; Cichon, S; Nöthen, M M; Walter, H; Erk, S; Heinz, A; Amin, N; van Duijn, C M; Meyer-Lindenberg, A; Tost, H; Xiao, X; Yamamoto, T; Rietschel, M; Li, M

A rare missense variant in RCL1 segregates with depression in extended families.

RCL1基因中的一种罕见错义变异与大家族中的抑郁症共分离

Amin N, de Vrij F M S, Baghdadi M, Brouwer R W W, van Rooij J G J, Jovanova O, Uitterlinden A G, Hofman A, Janssen H L A, Darwish Murad S, Kraaij R, Stedehouder J, van den Hout M C G N, Kros J M, van IJcken W F J, Tiemeier H, Kushner S A, van Duijn C M

Short telomere length is associated with impaired cognitive performance in European ancestry cohorts

端粒长度较短与欧洲血统人群认知能力受损有关。

Hägg, S; Zhan, Y; Karlsson, R; Gerritsen, L; Ploner, A; van der Lee, S J; Broer, L; Deelen, J; Marioni, R E; Wong, A; Lundquist, A; Zhu, G; Hansell, N K; Sillanpää, E; Fedko, I O; Amin, N A; Beekman, M; de Craen, A J M; Degerman, S; Harris, S E; Kan, K-J; Martin-Ruiz, C M; Montgomery, G W; Adolfsson, A N; Reynolds, C A; Samani, N J; Suchiman, H E D; Viljanen, A; von Zglinicki, T; Wright, M J; Hottenga, J-J; Boomsma, D I; Rantanen, T; Kaprio, J A; Nyholt, D R; Martin, N G; Nyberg, L; Adolfsson, R; Kuh, D; Starr, J M; Deary, I J; Slagboom, P E; van Duijn, C M; Codd, V; Pedersen, N L

The Alzheimer's Disease Sequencing Project: Study design and sample selection

阿尔茨海默病基因测序项目:研究设计和样本选择

Beecham, Gary W; Bis, J C; Martin, E R; Choi, S-H; DeStefano, A L; van Duijn, C M; Fornage, M; Gabriel, S B; Koboldt, D C; Larson, D E; Naj, A C; Psaty, B M; Salerno, W; Bush, W S; Foroud, T M; Wijsman, E; Farrer, L A; Goate, A; Haines, J L; Pericak-Vance, Margaret A; Boerwinkle, E; Mayeux, R; Seshadri, S; Schellenberg, G

Rare, low frequency and common coding variants in CHRNA5 and their contribution to nicotine dependence in European and African Americans

CHRNA5基因中罕见、低频和常见编码变异及其对欧洲裔和非裔美国人尼古丁依赖的影响

Olfson, E; Saccone, N L; Johnson, E O; Chen, L-S; Culverhouse, R; Doheny, K; Foltz, S M; Fox, L; Gogarten, S M; Hartz, S; Hetrick, K; Laurie, C C; Marosy, B; Amin, N; Arnett, D; Barr, R G; Bartz, T M; Bertelsen, S; Borecki, I B; Brown, M R; Chasman, D I; van Duijn, C M; Feitosa, M F; Fox, E R; Franceschini, N; Franco, O H; Grove, M L; Guo, X; Hofman, A; Kardia, S L R; Morrison, A C; Musani, S K; Psaty, B M; Rao, D C; Reiner, A P; Rice, K; Ridker, P M; Rose, L M; Schick, U M; Schwander, K; Uitterlinden, A G; Vojinovic, D; Wang, J-C; Ware, E B; Wilson, G; Yao, J; Zhao, W; Breslau, N; Hatsukami, D; Stitzel, J A; Rice, J; Goate, A; Bierut, L J

A novel Alzheimer disease locus located near the gene encoding tau protein

一种位于编码tau蛋白基因附近的新型阿尔茨海默病基因位点

Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M; Lambert, J-C; Chung, J; Naj, A C; Kunkle, B W; Wang, L-S; Bis, J C; Bellenguez, C; Harold, D; Lunetta, K L; Destefano, A L; Grenier-Boley, B; Sims, R; Beecham, G W; Smith, A V; Chouraki, V; Hamilton-Nelson, K L; Ikram, M A; Fievet, N; Denning, N; Martin, E R; Schmidt, H; Kamatani, Y; Dunstan, M L; Valladares, O; Laza, A R; Zelenika, D; Ramirez, A; Foroud, T M; Choi, S-H; Boland, A; Becker, T; Kukull, W A; van der Lee, S J; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, A L; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, D A; Amin, N; Berr, C; Tsolaki, Magda; Buxbaum, J D; Lopez, O L; Deramecourt, V; Fox, N C; Cantwell, L B; Tárraga, L; Dufouil, C; Hardy, J; Crane, P K; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, T H Jr; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, J-F; Hampel, H; Kamboh, M I; de Bruijn, R F A G; Tzourio, C; Pastor, P; Larson, E B; Rotter, J I; O'Donovan, M C; Montine, T J; Nalls, M A; Mead, S; Reiman, E M; Jonsson, P V; Holmes, C; St George-Hyslop, P H; Boada, M; Passmore, P; Wendland, J R; Schmidt, R; Morgan, K; Winslow, A R; Powell, J F; Carasquillo, M; Younkin, S G; Jakobsdóttir, J; Kauwe, J S K; Wilhelmsen, K C; Rujescu, D; Nöthen, M M; Hofman, A; Jones, L; Haines, J L; Psaty, B M; Van Broeckhoven, C; Holmans, P; Launer, L J; Mayeux, R; Lathrop, M; Goate, A M; Escott-Price, V; Seshadri, S; Pericak-Vance, M A; Amouyel, P; Williams, J; van Duijn, C M; Schellenberg, G D; Farrer, L A

GWAS for executive function and processing speed suggests involvement of the CADM2 gene

针对执行功能和处理速度的全基因组关联研究(GWAS)表明,CADM2基因参与其中。

Ibrahim-Verbaas, C A; Bressler, J; Debette, S; Schuur, M; Smith, A V; Bis, J C; Davies, G; Trompet, S; Smith, J A; Wolf, C; Chibnik, L B; Liu, Y; Vitart, V; Kirin, M; Petrovic, K; Polasek, O; Zgaga, L; Fawns-Ritchie, C; Hoffmann, P; Karjalainen, J; Lahti, J; Llewellyn, D J; Schmidt, C O; Mather, K A; Chouraki, V; Sun, Q; Resnick, S M; Rose, L M; Oldmeadow, C; Stewart, M; Smith, B H; Gudnason, V; Yang, Q; Mirza, S S; Jukema, J W; deJager, P L; Harris, T B; Liewald, D C; Amin, N; Coker, L H; Stegle, O; Lopez, O L; Schmidt, R; Teumer, A; Ford, I; Karbalai, N; Becker, J T; Jonsdottir, M K; Au, R; Fehrmann, Rsn; Herms, S; Nalls, M; Zhao, W; Turner, S T; Yaffe, K; Lohman, K; van Swieten, J C; Kardia, Slr; Knopman, D S; Meeks, W M; Heiss, G; Holliday, E G; Schofield, P W; Tanaka, T; Stott, D J; Wang, J; Ridker, P; Gow, A J; Pattie, A; Starr, J M; Hocking, L J; Armstrong, N J; McLachlan, S; Shulman, J M; Pilling, L C; Eiriksdottir, G; Scott, R J; Kochan, N A; Palotie, A; Hsieh, Y-C; Eriksson, J G; Penman, A; Gottesman, R F; Oostra, B A; Yu, L; DeStefano, A L; Beiser, A; Garcia, M; Rotter, J I; Nöthen, M M; Hofman, A; Slagboom, P E; Westendorp, Rgj; Buckley, B M; Wolf, P A; Uitterlinden, A G; Psaty, B M; Grabe, H J; Bandinelli, S; Chasman, D I; Grodstein, F; Räikkönen, K; Lambert, J-C; Porteous, D J; Price, J F; Sachdev, P S; Ferrucci, L; Attia, J R; Rudan, I; Hayward, C; Wright, A F; Wilson, J F; Cichon, S; Franke, L; Schmidt, H; Ding, J; de Craen, Ajm; Fornage, M; Bennett, D A; Deary, I J; Ikram, M A; Launer, L J; Fitzpatrick, A L; Seshadri, S; van Duijn, C M; Mosley, T H

Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies

流行病学研究中心抑郁量表(CES-D)的躯体、阳性和阴性维度:全基因组关联研究的荟萃分析

Demirkan, A; Lahti, J; Direk, N; Viktorin, A; Lunetta, K L; Terracciano, A; Nalls, M A; Tanaka, T; Hek, K; Fornage, M; Wellmann, J; Cornelis, M C; Ollila, H M; Yu, L; Smith, J A; Pilling, L C; Isaacs, A; Palotie, A; Zhuang, W V; Zonderman, A; Faul, J D; Sutin, A; Meirelles, O; Mulas, A; Hofman, A; Uitterlinden, A; Rivadeneira, F; Perola, M; Zhao, W; Salomaa, V; Yaffe, K; Luik, A I; Liu, Y; Ding, J; Lichtenstein, P; Landén, M; Widen, E; Weir, D R; Llewellyn, D J; Murray, A; Kardia, S L R; Eriksson, J G; Koenen, K; Magnusson, P K E; Ferrucci, L; Mosley, T H; Cucca, F; Oostra, B A; Bennett, D A; Paunio, T; Berger, K; Harris, T B; Pedersen, N L; Murabito, J M; Tiemeier, H; van Duijn, C M; Räikkönen, K

ATP5H/KCTD2 locus is associated with Alzheimer's disease risk

ATP5H/KCTD2基因座与阿尔茨海默病风险相关

Boada, M; Antúnez, C; Ramírez-Lorca, R; DeStefano, A L; González-Pérez, A; Gayán, J; López-Arrieta, J; Ikram, M A; Hernández, I; Marín, J; Galán, J J; Bis, J C; Mauleón, A; Rosende-Roca, M; Moreno-Rey, C; Gudnasson, V; Morón, F J; Velasco, J; Carrasco, J M; Alegret, M; Espinosa, A; Vinyes, G; Lafuente, A; Vargas, L; Fitzpatrick, A L; Launer, L J; Sáez, M E; Vázquez, E; Becker, J T; López, O L; Serrano-Ríos, M; Tárraga, L; van Duijn, C M; Real, L M; Seshadri, S; Ruiz, A