|
🐜
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Association of AKT1 gene polymorphisms with risk of schizophrenia and with response to antipsychotics in the Chinese population.
10 auth.
Mingqing Xu,
Qinghe Xing,
Yonglan Zheng,
Sheng Li,
Jianjun Gao,
G. He,
...
T. Guo,
G. Feng,
Feng Xu,
Lin He
|
6 |
2007 |
6
🐜
|
|
🐜
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The relationship between the therapeutic response to risperidone and the dopamine D2 receptor polymorphism in Chinese schizophrenia patients.
13 auth.
Qinghe Xing,
X. Qian,
Hua-fang Li,
S.H. Wong,
Shengnan Wu,
G. Feng,
S. Duan,
Mingqing Xu,
Rui Gao,
W. Qin,
...
Jianjun Gao,
J. Meng,
Lin He
|
6 |
2007 |
6
🐜
|
|
🐜
|
A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.
11 auth.
Qinghe Xing,
Ming-tai Wang,
Xiangdong Chen,
G. Feng,
H. Ji,
Jian-dong Yang,
...
Jianjun Gao,
W. Qin,
X. Qian,
Sheng-nan Wu,
Lin He
|
5 |
2003 |
5
🐜
|
|
🐜
|
Long non-coding RNA HOTAIR promotes tumorigenesis and forecasts a poor prognosis in cholangiocarcinoma
9 auth.
W. Qin,
Peng-cheng Kang,
Yi Xu,
Kaiming Leng,
Zhenglong Li,
Lining Huang,
...
Jianjun Gao,
Yunfu Cui,
X. Zhong
|
5 |
2018 |
5
🐜
|
|
🐜
|
A family-based association study of PLP1 and schizophrenia
13 auth.
W. Qin,
Jianjun Gao,
Qinghe Xing,
Jian-dong Yang,
X. Qian,
Xing-wang Li,
Zhongmeng Guo,
Helong Chen,
Lijun Wang,
Xuanyin Huang,
...
N. Gu,
G. Feng,
Lin He
|
5 |
2005 |
5
🐜
|
|
🐜
|
No association between the promoter variants of tumor necrosis factor alpha (TNF-α) and schizophrenia in Chinese Han population
14 auth.
S. Duan,
Yifeng Xu,
Wuyan Chen,
Zhuang-jun Liu,
T. Guo,
Jianjun Gao,
L. Bian,
Yonglan Zhen,
Xiuxia Li,
Xiaoju Zhang,
...
Yuxi Pan,
N. Gu,
G. Feng,
Lin He
|
5 |
2004 |
5
🐜
|
|
🐜
|
Identification of a novel ADAR mutation in a Chinese family with dyschromatosis symmetrica hereditaria (DSH)
10 auth.
Qinghe Xing,
Ming-tai Wang,
Xiangdong Chen,
X. Qian,
W. Qin,
Jianjun Gao,
...
Shengnan Wu,
Rui Gao,
G. Feng,
Lin He
|
4 |
2005 |
4
🐜
|
|
🐜
|
Noncanonical and canonical splice sites: a novel mutation at the rare noncanonical splice-donor cut site (IVS4+1A>G) of SEDL causes variable splicing isoforms in X-linked spondyloepiphyseal dysplasia tarda
11 auth.
F. Xiong,
Jianjun Gao,
Jun Li,
Yun Liu,
G. Feng,
W. Fang,
...
Hongfen Chang,
Jiang Xie,
Haitao Zheng,
Tingyu Li,
Lin He
|
4 |
2009 |
4
🐜
|
