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ArticlesPeer ReviewedFull Text
Urine albumin‐to‐creatinine ratio within the normal range and risk of hypertension in the general population: A meta‐analysis
Author / Creator:Ren, Fei ; Li, Mingzhu ; Xu, Hua ; Qin, Xiaowei ; Teng, Yanling
Publisher:United States: John Wiley & Sons, Inc
Journal title:The journal of clinical hypertension (Greenwich, Conn.), 2021-07, Vol.23 (7), p.1284-1290
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ArticlesPeer ReviewedFull Text
Oligogenic effect is associated with the clinical heterogeneity of autosomal dominant deafness-15
Author / Creator:Pan, Jianyan ; Teng, Hua ; Liu, Fang ; Chen, Siyi ; Liu, Yaning ; Teng, Yanling ; Liang, Desheng ; Li, Zhuo ; Wu, Lingqian
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2025-01, Vol.15 (1), p.1981-11, Article 1981
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ArticlesPeer ReviewedFull Text
Diagnostic accuracy of different ECG-based algorithms in wide QRS complex tachycardia: a systematic review and meta-analysis
Author / Creator:Sun, Xingxing ; Teng, Yanling ; Mu, Shengnan ; Wang, Yilian ; Chen, Hongwu
Publisher:England: British Medical Journal Publishing Group
Journal title:BMJ open, 2023-07, Vol.13 (7), p.e069273-e069273
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ArticlesPeer ReviewedFull Text
PIGK defects induce apoptosis in Purkinje cells and acceleration of neuroectodermal differentiation
Author / Creator:Chen, Siyi ; You, Jiali ; Zhou, Xiaowei ; Li, Yan ; Liu, Fang ; Teng, Yanling ; Teng, Hua ; Li, Yunlong ; Liang, Desheng ; Li, Zhuo ; Wu, Lingqian
Publisher:London: Nature Publishing Group UK
Journal title:Cell death & disease, 2024-11, Vol.15 (11), p.808-11, Article 808
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ArticlesPeer ReviewedFull Text
Comprehensive analysis of NGS-based expanded carrier screening and follow-up in southern and southwestern China: results from 3024 Chinese individuals
Author / Creator:Huang, Qinlin ; Wen, Juan ; Zhang, Hongyun ; Teng, Yanling ; Zhang, Wen ; Zhu, Huimin ; Liang, Desheng ; Wu, Lingqian ; Li, Zhuo
Publisher:England: BioMed Central
Journal title:Human genomics, 2024-10, Vol.18 (1), p.111-12, Article 111
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ArticlesPeer ReviewedFull Text
Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosis
Author / Creator:Chen, Xin ; Yin, Wu ; Chen, Siyi ; Zhang, Wenyu ; Li, Hongyan ; Kuang, Hanzhe ; Zhou, Miaojin ; Teng, Yanling ; Zhang, Junlong ; Shen, Guodong ; Liang, Desheng ; Li, Zhuo ; Hu, Bing ; Wu, Lingqian
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2021-05, Vol.140 (5), p.791-803
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ArticlesPeer ReviewedFull Text
The Caenorhabditis elegans Gene mfap-1 Encodes a Nuclear Protein That Affects Alternative Splicing
Author / Creator:Ma, Long ; Gao, Xiaoyang ; Luo, Jintao ; Huang, Liange ; Teng, Yanling ; Horvitz, H. Robert
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2012-07, Vol.8 (7), p.e1002827-e1002827
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ArticlesPeer ReviewedFull Text
Prenatal case of Simpson–Golabi–Behmel syndrome with a de novo 370Kb‐sized microdeletion of Xq26.2 compassing partial GPC3 gene and review
Author / Creator:Liu, Jing ; Liu, Qin ; Yang, Shuting ; Ma, Na ; Pang, Jialun ; Peng, Ying ; Xi, Hui ; Jia, Zhengjun ; Luo, Yingchun ; Jiang, Meiping ; Teng, Yanling ; Yu, Wenxian ; Li, Zhuo ; Wang, Hua
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2021-08, Vol.9 (8), p.e1750-n/a
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ArticlesPeer ReviewedFull Text
A novel GJB1 mutation associated with X‐linked Charcot–Marie–Tooth disease in a large Chinese family pedigree
Author / Creator:Liu, Yingdi ; Xue, Jinjie ; Li, Zhuo ; Linpeng, Siyuan ; Tan, Hu ; Teng, Yanling ; Liang, Desheng ; Wu, Lingqian
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2020-03, Vol.8 (3), p.e1127-n/a
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ArticlesPeer ReviewedFull Text
O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells
Author / Creator:Teng, Hua ; Chen, Siyi ; Liu, Fang ; Teng, Yanling ; Li, Yunlong ; Liang, Desheng ; Wu, Lingqian ; Li, Zhuo
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-07, Vol.25 (14), p.7889
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ArticlesPeer ReviewedFull Text
Diagnosis of Joubert Syndrome 10 in a Fetus with Suspected Dandy-Walker Variant by WES: A Novel Splicing Mutation in OFD1
Author / Creator:Wu, Lingqian ; Liang, Desheng ; Teng, Yanling ; Cao, Yingxi ; Pan, Jianyan ; Liu, Jing ; Linpeng, Siyuan ; Li, Zhuo
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:BioMed research international, 2018-01, Vol.2018 (2018), p.1-7
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ArticlesPeer ReviewedFull Text
Cover
Author / Creator:Liu, Yingdi ; Xue, Jinjie ; Li, Zhuo ; Linpeng, Siyuan ; Tan, Hu ; Teng, Yanling ; Liang, Desheng ; Wu, Lingqian
Publisher:Hoboken: John Wiley and Sons Inc
Journal title:Molecular genetics & genomic medicine, 2020-03, Vol.8 (3)
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ArticlesPeer ReviewedFull Text
Cover
Author / Creator:Liu, Yingdi ; Xue, Jinjie ; Li, Zhuo ; Linpeng, Siyuan ; Tan, Hu ; Teng, Yanling ; Liang, Desheng ; Wu, Lingqian
Journal title:Molecular genetics & genomic medicine, 2020-03, Vol.8 (3)
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Urine albumin‐to‐creatinine ratio within the normal range and risk of hypertension in the general population: A meta‐analysis

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Oligogenic effect is associated with the clinical heterogeneity of autosomal dominant deafness-15

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Diagnostic accuracy of different ECG-based algorithms in wide QRS complex tachycardia: a systematic review and meta-analysis

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PIGK defects induce apoptosis in Purkinje cells and acceleration of neuroectodermal differentiation

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Comprehensive analysis of NGS-based expanded carrier screening and follow-up in southern and southwestern China: results from 3024 Chinese individuals

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Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosis

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The Caenorhabditis elegans Gene mfap-1 Encodes a Nuclear Protein That Affects Alternative Splicing

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Prenatal case of Simpson–Golabi–Behmel syndrome with a de novo 370Kb‐sized microdeletion of Xq26.2 compassing partial GPC3 gene and review

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A novel GJB1 mutation associated with X‐linked Charcot–Marie–Tooth disease in a large Chinese family pedigree

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O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells

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Diagnosis of Joubert Syndrome 10 in a Fetus with Suspected Dandy-Walker Variant by WES: A Novel Splicing Mutation in OFD1

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