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

Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients

Abelson辅助整合位点1单倍型和外周血表达与双相情感障碍患者的锂反应和免疫调节相关

Sakrajda, Kosma; Bilska, Karolina; Czerski, Piotr M; Narożna, Beata; Dmitrzak-Węglarz, Monika; Heilmann-Heimbach, Stefanie; Brockschmidt, Felix F; Herms, Stefan; Nöthen, Markus M; Cichon, Sven; Więckowska, Barbara; Rybakowski, Janusz K; Pawlak, Joanna; Szczepankiewicz, Aleksandra

Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancrofti.

血管生成和淋巴管生成途径中的单核苷酸多态性与班氏丝虫引起的淋巴水肿有关

Debrah Linda Batsa, Albers Anna, Debrah Alexander Yaw, Brockschmidt Felix F, Becker Tim, Herold Christine, Hofmann Andrea, Osei-Mensah Jubin, Mubarik Yusif, Fröhlich Holger, Hoerauf Achim, Pfarr Kenneth

Population Pharmacokinetics and Target Attainment of Meropenem in Plasma and Tissue of Morbidly Obese Patients after Laparoscopic Intraperitoneal Surgery

腹腔镜腹腔手术后病态肥胖患者血浆和组织中美罗培南的群体药代动力学和靶浓度达标情况

Wittau, Mathias; Scheele, Jan; Kurlbaum, Max; Brockschmidt, Claas; Wolf, Anna M; Hemper, Evelyn; Henne-Bruns, Doris; Bulitta, Jürgen B

Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder

全基因组关联研究和鼠类表达数据表明,WNT3 和 WNT9b 之间高度保守的 32 kb 基因间区可能是孤立性经典膀胱外翻的易感基因位点。

Reutter, Heiko; Draaken, Markus; Pennimpede, Tracie; Wittler, Lars; Brockschmidt, Felix F; Ebert, Anne-Karolin; Bartels, Enrika; Rösch, Wolfgang; Boemers, Thomas M; Hirsch, Karin; Schmiedeke, Eberhard; Meesters, Christian; Becker, Tim; Stein, Raimund; Utsch, Boris; Mangold, Elisabeth; Nordenskjöld, Agneta; Barker, Gillian; Kockum, Christina Clementsson; Zwink, Nadine; Holmdahl, Gundula; Läckgren, Göran; Jenetzky, Ekkehart; Feitz, Wouter F J; Marcelis, Carlo; Wijers, Charlotte H W; Van Rooij, Iris A L M; Gearhart, John P; Herrmann, Bernhard G; Ludwig, Michael; Boyadjiev, Simeon A; Nöthen, Markus M; Mattheisen, Manuel

Microdeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies

三名智力障碍女性患者存在包括FMR1在内的微缺失——进一步阐明表型和表达研究

Zink, A M; Wohlleber, E; Engels, H; Rødningen, O K; Ravn, K; Heilmann, S; Rehnitz, J; Katzorke, N; Kraus, C; Blichfeldt, S; Hoffmann, P; Reutter, H; Brockschmidt, F F; Kreiß-Nachtsheim, M; Vogt, P H; Prescott, T E; Tümer, Z; Lee, J A

Laparoscopic intraperitoneal mesh fixation with fibrin sealant of a Spigelian hernia

腹腔镜下腹膜内网片固定联合纤维蛋白密封剂治疗斯皮格尔疝

Huber, Nadine; Paschke, Stephan; Henne-Bruns, Doris; Brockschmidt, Claas

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

全基因组混合分析方法鉴定出SPATA5是斑秃的一个新的易感基因位点

Forstbauer, Lina M; Brockschmidt, Felix F; Moskvina, Valentina; Herold, Christine; Redler, Silke; Herzog, Alexandra; Hillmer, Axel M; Meesters, Christian; Heilmann, Stefanie; Albert, Florian; Alblas, Margrieta; Hanneken, Sandra; Eigelshoven, Sibylle; Giehl, Kathrin A; Jagielska, Dagny; Blume-Peytavi, Ulrike; Garcia Bartels, Natalie; Kuhn, Jennifer; Hennies, Hans Christian; Goebeler, Matthias; Jung, Andreas; Peitsch, Wiebke K; Kortüm, Anne-Katrin; Moll, Ingrid; Kruse, Roland; Lutz, Gerhard; Wolff, Hans; Blaumeiser, Bettina; Böhm, Markus; Kirov, George; Becker, Tim; Nöthen, Markus M; Betz, Regina C

CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT)

CHD1L:肾脏和泌尿道先天性异常(CAKUT)的新候选基因

Antje Brockschmidt, Boidinh Chung, Stefanie Weber, Dagmar-Christiane Fischer, Maria Kolatsi-Joannou, Laura Christ, André Heimbach, Diamant Shtiza, Günter Klaus, Giacomo D Simonetti, Martin Konrad, Paul Winyard, Dieter Haffner, Franz Schaefer, Ruthild G Weber

Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature

衔接蛋白复合物4缺乏症会导致严重的常染色体隐性遗传性智力障碍、进行性痉挛性截瘫、性格内向和身材矮小。

Abou Jamra, Rami; Philippe, Orianne; Raas-Rothschild, Annick; Eck, Sebastian H; Graf, Elisabeth; Buchert, Rebecca; Borck, Guntram; Ekici, Arif; Brockschmidt, Felix F; Nöthen, Markus M; Munnich, Arnold; Strom, Tim M; Reis, Andre; Colleaux, Laurence

Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26

全基因组扫描和精细定位连锁分析揭示了雄激素性脱发的致病基因位点位于3q26染色体上

Hillmer, Axel M; Flaquer, Antonia; Hanneken, Sandra; Eigelshoven, Sibylle; Kortüm, Anne-Katrin; Brockschmidt, Felix F; Golla, Astrid; Metzen, Christine; Thiele, Holger; Kolberg, Susanne; Reinartz, Roman; Betz, Regina C; Ruzicka, Thomas; Hennies, Hans Christian; Kruse, Roland; Nöthen, Markus M