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

Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.

人类肾脏和泌尿道先天性异常中茶衫锌指同源框 3 (TSHZ3) 基因的杂合变异

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-024-01710-y
Kesdiren Esra, Martens Helge, Brand Frank, Werfel Lina, Wedekind Lukas, Trowe Mark-Oliver, Schmitz Jessica, Hennies Imke, Geffers Robert, Gucev Zoran, Seeman Tomáš, Schmidt Sonja, Tasic Velibor, Fasano Laurent, Bräsen Jan H, Kispert Andreas, Christians Anne, Haffner Dieter, Weber Ruthild G
其它
Human
发表日期：2025
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SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia

肌萎缩侧索硬化症中的SPG7基因突变：与遗传性痉挛性截瘫的遗传联系

期刊:Journal of Neurology
影响因子:4.6
doi:10.1007/s00415-020-09861-w
Osmanovic, Alma; Widjaja, Maylin; Förster, Alisa; Weder, Julia; Wattjes, Mike P; Lange, Inken; Sarikidi, Anastasia; Auber, Bernd; Raab, Peter; Christians, Anne; Preller, Matthias; Petri, Susanne; Weber, Ruthild G
发表日期：2020
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Rare heterozygous GDF6 variants in patients with renal anomalies.

肾脏畸形患者中罕见的杂合 GDF6 变异

期刊:European Journal of Human Genetics
影响因子:4.6
doi:10.1038/s41431-020-0678-9
Martens Helge, Hennies Imke, Getwan Maike, Christians Anne, Weiss Anna-Carina, Brand Frank, Gjerstad Ann Christin, Christians Arne, Gucev Zoran, Geffers Robert, Seeman Tomáš, Kispert Andreas, Tasic Velibor, Bjerre Anna, Lienkamp Soeren S, Haffner Dieter, Weber Ruthild G
其它
发表日期：2020
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