Tian D - Search Results

1

Clinical and genetic identification of a large chinese family with autosomal dominant retinitis pigmentosa.

Yang Y, Tian D, Lee J, Zeng J, Zhang H, Chen S, Guo H, Xiong Z, Xia K, Hu Z, Luo J. Yang Y, et al. Among authors: tian d. Ophthalmic Genet. 2015 Mar;36(1):64-9. doi: 10.3109/13816810.2013.809458. Epub 2013 Jul 8. Ophthalmic Genet. 2015. PMID: 23834559

2

AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis.

Li W, Li Y, Zhang L, Guo H, Tian D, Li Y, Peng Y, Zheng Y, Dai Y, Xia K, Lan X, Wang B, Hu Z. Li W, et al. Among authors: tian d. J Med Genet. 2016 Jul;53(7):488-93. doi: 10.1136/jmedgenet-2015-103684. Epub 2016 Mar 17. J Med Genet. 2016. PMID: 26989089 Free PMC article.

3

Common genetic variants on 1p13.2 associate with risk of autism.

Xia K, Guo H, Hu Z, Xun G, Zuo L, Peng Y, Wang K, He Y, Xiong Z, Sun L, Pan Q, Long Z, Zou X, Li X, Li W, Xu X, Lu L, Liu Y, Hu Y, Tian D, Long L, Ou J, Liu Y, Li X, Zhang L, Pan Y, Chen J, Peng H, Liu Q, Luo X, Su W, Wu L, Liang D, Dai H, Yan X, Feng Y, Tang B, Li J, Miedzybrodzka Z, Xia J, Zhang Z, Luo X, Zhang X, St Clair D, Zhao J, Zhang F. Xia K, et al. Among authors: tian d. Mol Psychiatry. 2014 Nov;19(11):1212-9. doi: 10.1038/mp.2013.146. Epub 2013 Nov 5. Mol Psychiatry. 2014. PMID: 24189344

4

Novel mutations in mevalonate kinase cause disseminated superficial actinic porokeratosis.

Zhu T, Tian D, Zhang L, Xu X, Xia K, Hu Z, Xiong Z, Tan J. Zhu T, et al. Among authors: tian d. Br J Dermatol. 2019 Aug;181(2):304-313. doi: 10.1111/bjd.17596. Epub 2019 Mar 18. Br J Dermatol. 2019. PMID: 30597534

5

AMPD1 functional variants associated with autism in Han Chinese population.

Zhang L, Ou J, Xu X, Peng Y, Guo H, Pan Y, Chen J, Wang T, Peng H, Liu Q, Tian D, Pan Q, Zou X, Zhao J, Hu Z, Xia K. Zhang L, et al. Among authors: tian d. Eur Arch Psychiatry Clin Neurosci. 2015 Sep;265(6):511-7. doi: 10.1007/s00406-014-0524-6. Epub 2014 Aug 26. Eur Arch Psychiatry Clin Neurosci. 2015. PMID: 25155876

6

Common and rare variants of the THBS1 gene associated with the risk for autism.

Lu L, Guo H, Peng Y, Xun G, Liu Y, Xiong Z, Tian D, Liu Y, Li W, Xu X, Zhao J, Hu Z, Xia K. Lu L, et al. Among authors: tian d. Psychiatr Genet. 2014 Dec;24(6):235-40. doi: 10.1097/YPG.0000000000000054. Psychiatr Genet. 2014. PMID: 25304225

7

Single-cell analysis of nonhuman primate preimplantation development in comparison to humans and mice.

Hu Y, Huang K, Zeng Q, Feng Y, Ke Q, An Q, Qin LJ, Cui Y, Guo Y, Zhao D, Peng Y, Tian D, Xia K, Chen Y, Ni B, Wang J, Zhu X, Wei L, Liu Y, Xiang P, Liu JY, Xue Z, Fan G. Hu Y, et al. Among authors: tian d. Dev Dyn. 2021 Jul;250(7):974-985. doi: 10.1002/dvdy.295. Epub 2021 Feb 4. Dev Dyn. 2021. PMID: 33449399 Free article.

8

[Revelations of the origin of Chinese nation from clustering analysis and frequency distribution of HLA polymorphism in major minority nationalities in mainland China].

Chen R, Ye G, Geng Z, Wang Z, Kong F, Tian D, Bao P, Liu R, Liu J, Song F, et al. Chen R, et al. Among authors: tian d. Yi Chuan Xue Bao. 1993;20(5):389-98. Yi Chuan Xue Bao. 1993. PMID: 8161470 Chinese.

9

[Hereditary gingival fibromatosis: a three-generation case report].

He XF, Xu CJ, Tian D, Wang MM, Zhang WR, Guo YT. He XF, et al. Among authors: tian d. Hua Xi Kou Qiang Yi Xue Za Zhi. 2020 Feb 1;38(1):104-107. doi: 10.7518/hxkq.2020.01.019. Hua Xi Kou Qiang Yi Xue Za Zhi. 2020. PMID: 32037776 Free PMC article. Chinese.

10

Biallelic pathogenic variants in TBCD-related neurodevelopment disease with mild clinical features.

Tian D, Rizwan K, Liu Y, Kang L, Yang Y, Mao X, Shu L. Tian D, et al. Neurol Sci. 2019 Nov;40(11):2325-2331. doi: 10.1007/s10072-019-03979-0. Epub 2019 Jun 25. Neurol Sci. 2019. PMID: 31240573

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