Publications by authors named "Yaping Qian"

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PDS5B positively regulates PTEN by binding to YTHDC1 to inhibit the malignant progression of endometrial carcinoma.
Hanyi Wang, Yaping Qian, Jie Li, Qianyun Gao

Discov Oncol· July 2025

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Germline de novo alterations of RUNX1T1 in individuals with neurodevelopmental and congenital anomalies.
Erfan Aref-Eshghi, Katherine J Anderson, Lauren Boulay, Kathleen Brown, Jessica Duis, Yaping Qian

HGG Adv· January 2025

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Predicting ventilator-associated pneumonia in elderly patients requiring mechanical ventilation through the detection in tracheal aspirates.
Dan Wang, Peng Zhao, Yan-Xin Liu, Peng Wang, Mei-Liang Gong, Ya-Ping Qian

Postgrad Med· November 2023

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Development of a machine learning-based signature utilizing inflammatory response genes for predicting prognosis and immune microenvironment in ovarian cancer.
Li Dong, Ya-Ping Qian, Shu-Xiu Li, Hao Pan

Open Med (Wars)· June 2023

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Hereditary cancer testing challenges: assembling the analytical pieces to solve the patient clinical puzzle.
Karla R Bowles, Debora Mancini-DiNardo, Bradford Coffee, Hannah C Cox, Yaping Qian

Future Oncol· January 2019

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Identification of pathogenic retrotransposon insertions in cancer predisposition genes.
Yaping Qian, Debora Mancini-DiNardo, Thaddeus Judkins, Hannah C Cox, Krystal Brown

Cancer Genet· October 2017

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Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism.
C Alexander Valencia, Xinjian Wang, Jin Wang, Anna Peters, Julia R Simmons, Yaping Qian

PLoS One· August 2017

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Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience.
C Alexander Valencia, Ammar Husami, Jennifer Holle, Judith A Johnson, Yaping Qian

Front Pediatr· August 2015

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Combined immune deficiency in a patient with a novel NFKB2 mutation.
Andrew W Lindsley, Yaping Qian, C Alexander Valencia, Kara Shah, Kejian Zhang

J Clin Immunol· November 2014

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The 253-kb inversion and deep intronic mutations in UNC13D are present in North American patients with familial hemophagocytic lymphohistiocytosis 3.
Yaping Qian, Judith A Johnson, Jessica A Connor, C Alexander Valencia, Nathaniel Barasa

Pediatr Blood Cancer· June 2014

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The struggle to find reliable results in exome sequencing data: filtering out Mendelian errors.
Zubin H Patel, Leah C Kottyan, Sara Lazaro, Marc S Williams, David H Ledbetter, Yaping Qian

Front Genet· February 2014

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Calpains mediate axonal cytoskeleton disintegration during Wallerian degeneration.
Marek Ma, Toby A Ferguson, Kathleen M Schoch, Jian Li, Yaping Qian

Neurobiol Dis· August 2013

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Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families.
Xiangtian Zhou, Yaping Qian, Juanjuan Zhang, Yi Tong, Pingping Jiang

Invest Ophthalmol Vis Sci· July 2012

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The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation.
Yaping Qian, Xiangtian Zhou, Min Liang, Jia Qu, Min-Xin Guan

Mitochondrion· November 2011

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Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family.
Hao Sun, Wataru Satake, Changjun Zhang, Yoshitaka Nagai, Youyong Tian, Yaping Qian, Yuan Qian

J Hum Genet· April 2011

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Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family.
Shiwen Wang, Ronghua Li, Andrea Fettermann, Zongbin Li, Yaping Qian

Circ Res· April 2011

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Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
Xiangtian Zhou, Hongxing Zhang, Fuxin Zhao, Yanchun Ji, Yi Tong, Yaping Qian

Mol Genet Metab· August 2010

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Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.
Jianxin Lu, Yaping Qian, Zhiyuan Li, Aifen Yang, Yi Zhu

Mitochondrion· January 2010

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[Screening of anti-Cry1Ac scFv from A phage display antibody library.].
Yun Wang, Yuan Liu, Xiang Wang, Ya-Ping Qian, Xian-Jin Liu

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi· December 2009

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Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation.
Yaping Qian, Min-Xin Guan

Antimicrob Agents Chemother· November 2009

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Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.
Xinjian Wang, Jianxin Lu, Yi Zhu, Aifen Yang, Li Yang, Yaping Qian

Pharmacogenet Genomics· December 2008

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Low dose naltrexone administration in morphine dependent rats attenuates withdrawal-induced norepinephrine efflux in forebrain.
Elisabeth J Van Bockstaele, Yaping Qian, Robert C Sterling, Michelle E Page

Prog Neuropsychopharmacol Biol Psychiatry· May 2008

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Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family.
Jia Qu, Ronghua Li, Xiangtian Zhou, Yi Tong, Li Yang, Yaping Qian

Mitochondrion· July 2007

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The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.
Dongyi Han, Pu Dai, Qingwen Zhu, Xin Liu, Deliang Huang, Yaping Qian

Biochem Biophys Res Commun· June 2007

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Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
Xiaowen Tang, Li Yang, Yi Zhu, Zhisu Liao, Jindan Wang, Yaping Qian

Gene· May 2007

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