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

Quantum interference in heterogeneous superconducting-photonic circuits on a silicon chip

硅芯片上异质超导-光子电路中的量子干涉

Schuck, C; Guo, X; Fan, L; Ma, X; Poot, M; Tang, H X

Common variant at 16p11.2 conferring risk of psychosis

16p11.2 上的常见变异会增加患精神病的风险

Steinberg, S; de Jong, S; Mattheisen, M; Costas, J; Demontis, D; Jamain, S; Pietiläinen, O P H; Lin, K; Papiol, S; Huttenlocher, J; Sigurdsson, E; Vassos, E; Giegling, I; Breuer, R; Fraser, G; Walker, N; Melle, I; Djurovic, S; Agartz, I; Tuulio-Henriksson, A; Suvisaari, J; Lönnqvist, J; Paunio, T; Olsen, L; Hansen, T; Ingason, A; Pirinen, M; Strengman, E; Hougaard, D M; Orntoft, T; Didriksen, M; Hollegaard, M V; Nordentoft, M; Abramova, L; Kaleda, V; Arrojo, M; Sanjuán, J; Arango, C; Etain, B; Bellivier, F; Méary, A; Schürhoff, F; Szoke, A; Ribolsi, M; Magni, V; Siracusano, A; Sperling, S; Rossner, M; Christiansen, C; Kiemeney, L A; Franke, B; van den Berg, L H; Veldink, J; Curran, S; Bolton, P; Poot, M; Staal, W; Rehnstrom, K; Kilpinen, H; Freitag, C M; Meyer, J; Magnusson, P; Saemundsen, E; Martsenkovsky, I; Bikshaieva, I; Martsenkovska, I; Vashchenko, O; Raleva, M; Paketchieva, K; Stefanovski, B; Durmishi, N; Pejovic Milovancevic, M; Lecic Tosevski, D; Silagadze, T; Naneishvili, N; Mikeladze, N; Surguladze, S; Vincent, J B; Farmer, A; Mitchell, P B; Wright, A; Schofield, P R; Fullerton, J M; Montgomery, G W; Martin, N G; Rubino, I A; van Winkel, R; Kenis, G; De Hert, M; Réthelyi, J M; Bitter, I; Terenius, L; Jönsson, E G; Bakker, S; van Os, J; Jablensky, A; Leboyer, M; Bramon, E; Powell, J; Murray, R; Corvin, A; Gill, M; Morris, D; O'Neill, F A; Kendler, K; Riley, B; Craddock, N; Owen, M J; O'Donovan, M C; Thorsteinsdottir, U; Kong, A; Ehrenreich, H; Carracedo, A; Golimbet, V; Andreassen, O A; Børglum, A D; Mors, O; Mortensen, P B; Werge, T; Ophoff, R A; Nöthen, M M; Rietschel, M; Cichon, S; Ruggeri, M; Tosato, S; Palotie, A; St Clair, D; Rujescu, D; Collier, D A; Stefansson, H; Stefansson, K

Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss

非综合征性听力损失男孩的平衡易位导致ATE1和SLC12A1基因发生破坏

Vona, B; Neuner, C; El Hajj, N; Schneider, E; Farcas, R; Beyer, V; Zechner, U; Keilmann, A; Poot, M; Bartsch, O; Nanda, I; Haaf, T

Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes

一名肥胖男性患有智力障碍、先天性心脏缺陷和多个超数环状染色体,其FAM123B和ARHGEF9基因获得

Hochstenbach, R; van Gijn, M E; Krijtenburg, P-J; Raemakers, R; van 't Slot, R; Renkens, I; Eleveld, M J; van der Smagt, J J; Poot, M

Towards identification of individual etiologies by resolving genomic and biological conundrums in patients with autism spectrum disorders

通过解决自闭症谱系障碍患者的基因组和生物学难题,探寻个体病因

Poot, M

Beware of Hemizygous Deletions That May Unmask Deleterious Variants

警惕可能揭示有害变异的半合子缺失

Poot, M

Chromothripsis Challenges the Germline

染色体碎裂病对种系构成挑战

Poot, M

Don't Mess with RUNX1

别招惹 RUNX1

Poot, M

Congenital diaphragmatic hernia associated with duplication of 11q23-qter

先天性膈疝伴11q23-qter重复

Klaassens, M; Scott, D A; van Dooren, M; Hochstenbach, R; Eussen, H J; Cai, W W; Galjaard, R J; Wouters, C; Poot, M; Laudy, J; Lee, B; Tibboel, D; de Klein, A

Disruption of redox homeostasis in tumor necrosis factor-induced apoptosis in a murine hepatocyte cell line.

肿瘤坏死因子诱导小鼠肝细胞系凋亡过程中氧化还原稳态的破坏

Pierce R H, Campbell J S, Stephenson A B, Franklin C C, Chaisson M, Poot M, Kavanagh T J, Rabinovitch P S, Fausto N