Publications by authors named "Bai-Lin Wu"

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Cardiac computer tomography-derived radiomics in assessing myocardial characteristics at the connection between the left atrial appendage and the left atrium in atrial fibrillation patients.
Xiao-Xuan Wei, Cai-Ying Li, Hai-Qing Yang, Peng Song, Bai-Lin Wu

Front Cardiovasc Med· January 2025

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The initial clinical application of standard PCNL combined with visual needle nephroscope in the treatment of complex renal calculi by holmium YAG laser: a retrospective case series study.
Engo Ovone Yanne, Bai Lin Wu, Cong Li, Jiaqiao Zhang, Xiao Yu

BMC Urol· December 2024

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Three-Tesla magnetic resonance imaging of left ventricular volume and function in comparison with computed tomography and echocardiography.
Fu-Qian Guo, Bai-Lin Wu, Xiao-Wei Liu, Tong Pan, Bu-Lang Gao

Medicine (Baltimore)· April 2023

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Majority of transferred mosaic embryos developed healthy live births revealed by a preclinical study using embryonic morphology assessment and noninvasive PGT-A on cell-free DNA in blastocoel fluid.
Lingbo Cai, Qiao Zeng, Chao Gao, Wei Wu, Jiandong Shen, Bai-Lin Wu, Dao Wu Wang

J Assist Reprod Genet· November 2022

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GABA Signaling Pathway-associated Gene PLCL1 Rare Variants May be Associated with Autism Spectrum Disorders.
Fengyun Zheng, Guoyuan Liu, Ting Dang, Qiaowen Chen, Yu An, Meng Wu, Bai-Lin Wu

Neurosci Bull· August 2021

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LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant mice.
Li Yu, Lina Wang, Wufan Tao, Wenxiang Zhang, Shuanghao Yang, Yiming Wu, Bai-Lin Wu

J Genet Genomics· May 2021

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A recurrent mutation in TBPL2 causes diminished ovarian reserve and female infertility.
Wen-Bin He, Ya-Xin Zhang, Chen Tan, Lan-Lan Meng, Gang Liu, Bai-Lin Wu

J Genet Genomics· December 2020

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Developing a one-step triplet-repeat primed PCR assay for diagnosing myotonic dystrophy.
Xiaoping Lan, Na Li, Hongling Wan, Lintong Luo, Yiming Wu, Bai-Lin Wu

J Genet Genomics· October 2018

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Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation.
Xiaoli Chen, Yu An, Yonghui Gao, Liu Guo, Lei Rui, Bai-Lin Wu

Hum Mutat· April 2017

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Association analysis between HFM1 variations and idiopathic azoospermia or severe oligozoospermia in Chinese Men.
Wenxiang Zhang, Xiaomin Song, Feng Ni, Jinbao Cheng, Bai-Lin Wu

Sci China Life Sci· March 2017

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Quantitative evaluation of left ventricular volume and function in middle-aged healthy chinese people with 3 Tesla MRI.
Cai-Ying Li, Bu-Lang Gao, Fu-Qian Guo, Xue-Jing Zhang, Qiong-Ying Fan, Bai-Lin Wu

J Magn Reson Imaging· November 2016

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Extracellular Cl(-) regulates human SO4 (2-)/anion exchanger SLC26A1 by altering pH sensitivity of anion transport.
Meng Wu, John F Heneghan, David H Vandorpe, Laura I Escobar, Bai-Lin Wu

Pflugers Arch· August 2016

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Parenting stress and affective symptoms in parents of autistic children.
Yun Gong, YaSong Du, HuiLin Li, XiYan Zhang, Yu An, Bai-Lin Wu

Sci China Life Sci· October 2015

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Genetic architecture, epigenetic influence and environment exposure in the pathogenesis of Autism.
Li Yu, YiMing Wu, Bai-Lin Wu

Sci China Life Sci· October 2015

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Genetic Evaluation of Copy Number Variations, Loss of Heterozygosity, and Single-Nucleotide Variant Levels in Human Embryonic Stem Cells With or Without Skewed X Chromosome Inactivation.
Wei-Qiang Liu, Jie-Liang Li, Jian Wang, Wen-Yin He, Lip Va, Bai-Lin Wu

Stem Cells Dev· August 2015

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Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393W.
Fabian R Reimold, Savithri Balasubramanian, David B Doroquez, Boris E Shmukler, Zsuzsanna K Zsengeller, Bai-Lin Wu

Front Physiol· July 2015

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Autistic children exhibit decreased levels of essential Fatty acids in red blood cells.
Sarah A Brigandi, Hong Shao, Steven Y Qian, Yiping Shen, Bai-Lin Wu

Int J Mol Sci· May 2015

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Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure.
Yuqin Ye, Xiaoping Lan, Jin Cong, Na Li, Yiming Wu, Bai-Lin Wu, Jie Wu

Reprod Biomed Online· September 2014

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Somatic mutations in cerebral cortical malformations.
Saumya S Jamuar, Anh-Thu N Lam, Martin Kircher, Alissa M D'Gama, Jian Wang, Bai Lin Wu

N Engl J Med· August 2014

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Copy number variation plays an important role in clinical epilepsy.
Heather Olson, Yiping Shen, Jennifer Avallone, Beth R Sheidley, Rebecca Pinsky, Bai-Lin Wu

Ann Neurol· June 2014

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Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
Anath C Lionel, Kristiina Tammimies, Andrea K Vaags, Jill A Rosenfeld, Joo Wook Ahn, Bai-Lin Wu

Hum Mol Genet· May 2014

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Mutations in HFM1 in recessive primary ovarian insufficiency.
Jian Wang, Wenxiang Zhang, Hong Jiang, Bai-Lin Wu,

N Engl J Med· March 2014

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SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay.
Yu An, Sami S Amr, Alcy Torres, Laura Weissman, Peter Raffalli, Bai-Lin Wu

Am J Med Genet B Neuropsychiatr Genet· December 2013

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Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities.
Heather Mason-Suares, Wayne Kim, Leslie Grimmett, Eli S Williams, Vanessa L Horner, Bai-Lin Wu

Genet Med· September 2013

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Reply to Dr. Jeffrey Brent.
Bai-Lin Wu, Bo Song

Neurotoxicology· July 2013

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