D. Tian

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D Tian, Di Tian
Publication record
17 papers · 905 citations · H-index 12

PAPERS

Single‐cell analysis of nonhuman primate preimplantation development in comparison to humans and mice
202112 citationsauthor #12
De novo mutation of cancer-related genes associates with particular neurodevelopmental disorders
202011 citationsauthor #3
Biallelic pathogenic variants in TBCD-related neurodevelopment disease with mild clinical features
20197 citationsauthor #1
Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency
201927 citationsauthor #5
Novel mutations in mevalonate kinase cause disseminated superficial actinic porokeratosis
201916 citationsauthor #2
Altered sleep architecture, rapid eye movement sleep, and neural oscillation in a mouse model of human chromosome 16p11.2 microdeletion
201820 citationsauthor #5
Altered synaptic transmission and maturation of hippocampal CA1 neurons in a mouse model of human chr16p11.2 microdeletion.
201819 citationsauthor #3
AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis
201635 citationsauthor #5
AKAP 2 identi fi ed as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis
20161 citationsauthor #5
AMPD1 functional variants associated with autism in Han Chinese population
20158 citationsauthor #11
Contribution of mGluR5 to hippocampal pathophysiology in a mouse model of human chromosome 16p11.2 microdeletion
201564 citationsauthor #1
Clinical and Genetic Identification of a Large Chinese Family with Autosomal Dominant Retinitis Pigmentosa
201512 citationsauthor #2
Contribution of mGluR5 to pathophysiology in a mouse model of human chromosome 16p11.2 microdeletion
201545 citationsauthor #1
Contribution of mGluR 5 to hippocampal pathophysiology in a mouse model of human chromosome 16 p 11 . 2 microdeletion
20153 citationsauthor #1
Common and rare variants of the THBS1 gene associated with the risk for autism
201421 citationsauthor #7
Common genetic variants on 1p13.2 associate with risk of autism
2014101 citationsauthor #20
The long noncoding RNA, Jpx, is a molecular switch for X chromosome inactivation.
2010504 citationsauthor #1

TIMELINE

2010 504 citations

2014 122 citations

2015 132 citations

2016 36 citations

2018 39 citations

2019 50 citations

2020 11 citations

2021 12 citations

D. Tian

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