Yiyuan Liu

发表

KLF4 binding during reprogramming is involved in 3D architectural rewiring and transcriptional regulation of enhancer hubs

A. Tsirigos, A. Kloetgen, D. C. Di Giammartino, 2018, bioRxiv.

Glycemic Exposure and Blood Pressure Influencing Progression and Remission of Diabetic Retinopathy

A. Morris, A. Doney, C. Palmer, 2013, Diabetes Care.

KLF4 binding is involved in the organization and regulation of 3D enhancer networks during acquisition and maintenance of pluripotency

Noah Dephoure, A. Tsirigos, A. Kloetgen, 2018 .

Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals

Lindsey J. Leach, Yiyuan Liu, Ning Jiang, 2014, BMC Genomics.

Addition of Capecitabine to Adjuvant Chemotherapy May be the Most Effective Strategy for Patients With Early-Stage Triple-Negative Breast Cancer: A Network Meta-Analysis of 9 Randomized Controlled Trials

Yiyuan Liu, Hai Lu, Jiehua Zheng, 2022, Frontiers in Endocrinology.

Bi‐allelic mutations in MCIDAS and CCNO cause human infertility associated with abnormal gamete transport

F. Tao, Yiyuan Liu, Yunxia Cao, 2021, Clinical genetics.

ELAVL4, splicing, and glutamatergic dysfunction precede neuron loss in MAPT mutation cerebral organoids

S. Haggarty, A. Goate, S. Goderie, 2021, Cell.

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

M. Daly, R. Klein, V. Gudnason, 2011, Investigative ophthalmology & visual science.

Integration of Alzheimer’s disease genetics and myeloid genomics identifies disease risk regulatory elements and genes

Anastasia G. Efthymiou, K. Hao, J. Björkegren, 2021, Nature Communications.

Promoter DNA hypermethylation – Implications for Alzheimer’s disease

Bin Zhang, A. Goate, Minghui Wang, 2019, Neuroscience Letters.

COMBAT: A Combined Association Test for Genes Using Summary Statistics

J. Potash, Shizhong Han, Minghui Wang, 2017, Genetics.

KLF4 is involved in the organization and regulation of pluripotency-associated three-dimensional enhancer networks

Aristotelis Tsirigos, Andreas Kloetgen, Alexander Polyzos, 2019, Nature Cell Biology.

Widespread Mitotic Bookmarking by Histone Marks and Transcription Factors in Pluripotent Stem Cells.

O. Elemento, P. Giannakakou, A. Doane, 2017, Cell reports.

Prognostic and Immune-Infiltrate Significance of miR-222-3p and Its Target Genes in Thyroid Cancer

Yiyuan Liu, Jiehua Zheng, Juan Zou, 2021, Frontiers in Genetics.

Clinical and genetic determinants of diabetic retinopathy

Yiyuan Liu, 2014 .

BHLHE40/41 regulate macrophage/microglia responses associated with Alzheimer’s disease and other disorders of lipid-rich tissues

A. Goate, C. Giannarelli, E. Marcora, 2023, bioRxiv.

APOE4 confers transcriptomic and functional alterations to primary mouse microglia

A. Goate, S. Neuner, E. Marcora, 2022, Neurobiology of Disease.

Nascent Induced Pluripotent Stem Cells Efficiently Generate Entirely iPSC-Derived Mice while Expressing Differentiation-Associated Genes.

A. Heguy, M. Stadtfeld, Yiyuan Liu, 2018, Cell reports.

Glutamatergic dysfunction precedes neuron loss in cerebral organoids with MAPT mutation

S. Haggarty, A. Goate, S. Goderie, 2021, bioRxiv.

Global Trends in Research of Androgen Receptor Associated With Breast Cancer From 2011 to 2020: A Scientometric Analysis

Yiyuan Liu, Jiehua Zheng, Yexi Chen, 2022, Frontiers in Endocrinology.

The Global, Regional, and National Burden and Trends of Breast Cancer From 1990 to 2019: Results From the Global Burden of Disease Study 2019

Yiyuan Liu, Jiehua Zheng, Yexi Chen, 2021, Frontiers in Oncology.

DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, Cell Death & Disease.

A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia

F. Tao, P. Zhou, Yiyuan Liu, 2021, Clinical genetics.

Mps one binder 2 gene upregulation in the stellation of astrocytes induced by cAMP‐dependent pathway

S. Tzeng, Yiyuan Liu, S. Fan, 2012, Journal of cellular biochemistry.

Successful treatment with crisaborole for facial lesions refractory to adalimumab in a man with psoriasis: A case report

Yiyuan Liu, Wei Li, 2022, Dermatologic therapy.

Crisaborole ointment as treatment for genital psoriasis

Yiyuan Liu, Wei Li, 2021, Journal of cosmetic dermatology.

Chemotherapy modulates CDK4/6 inhibitors resistance in metastatic breast cancer by Rb1 mutations: a case report and literature review

Yiyuan Liu, Xiaojia Wang, X. Shao, 2022, Annals of translational medicine.

Upregulated GIRK2 counteracts ethanol-induced changes in excitability & respiration in human neurons

B. Porjesz, D. Chorlian, H. Edenberg, 2023, bioRxiv.

Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations

Kuokuo Li, F. Tao, P. Zhou, 2022, Reproductive Biology and Endocrinology.

Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans

Kuokuo Li, Yiyuan Liu, Yunxia Cao, 2022, Human Genetics.

17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes

T. Raj, A. Goate, P. Heutink, 2019, bioRxiv.

Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia due to acrosomal hypoplasia and reduced progressive motility.

Kuokuo Li, P. Zhou, Yiyuan Liu, 2023, Human molecular genetics.

Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals

Lindsey J. Leach, Yiyuan Liu, Ning Jiang, 2014, BMC Genomics.

ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.

Kuokuo Li, Yiyuan Liu, Yunxia Cao, 2023, Human reproduction.

17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes

T. Raj, A. Goate, P. Heutink, 2022, Molecular Neurodegeneration.