Qin Q - Search Results

1

Amplitude of low-frequency fluctuation may be an early predictor of delayed motor development due to neonatal hyperbilirubinemia: a fMRI study.

Yan K, Xiao F, Jiang Y, Lu C, Zhang Y, Kong Y, Zhou J, Wang J, Lin C, Yang H, Zhang D, Cheng G, Qiao Z, Wang L, Qin Q, Zhou W. Yan K, et al. Among authors: qin q. Transl Pediatr. 2021 May;10(5):1271-1284. doi: 10.21037/tp-20-447. Transl Pediatr. 2021. PMID: 34189085 Free PMC article.

2

Early-onset infant epileptic encephalopathy associated with a de novo PPP3CA gene mutation.

Qian Y, Wu B, Lu Y, Dong X, Qin Q, Zhou W, Wang H. Qian Y, et al. Among authors: qin q. Cold Spring Harb Mol Case Stud. 2018 Dec 17;4(6):a002949. doi: 10.1101/mcs.a002949. Print 2018 Dec. Cold Spring Harb Mol Case Stud. 2018. PMID: 30455226 Free PMC article.

3

Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.

Chen X, Yan K, Gao Y, Wang H, Chen G, Wu B, Qin Q, Yang L, Zhou W. Chen X, et al. Among authors: qin q. BMC Med Genet. 2019 May 30;20(1):93. doi: 10.1186/s12881-019-0813-z. BMC Med Genet. 2019. PMID: 31146700 Free PMC article.

4

Relationship between phenotype and genotype of 102 Chinese newborns with Prader-Willi syndrome.

Ge MM, Gao YY, Wu BB, Yan K, Qin Q, Wang H, Zhou W, Yang L. Ge MM, et al. Among authors: qin q. Mol Biol Rep. 2019 Oct;46(5):4717-4724. doi: 10.1007/s11033-019-04916-2. Epub 2019 Jul 3. Mol Biol Rep. 2019. PMID: 31270759

5

Survival Motor Neuron Gene Copy Number Analysis by Exome Sequencing: Assisting Spinal Muscular Atrophy Diagnosis and Carrier Screening.

Liu B, Lu Y, Wu B, Yang L, Liu R, Wang H, Dong X, Li G, Qin Q, Zhou W. Liu B, et al. Among authors: qin q. J Mol Diagn. 2020 May;22(5):619-628. doi: 10.1016/j.jmoldx.2020.01.015. Epub 2020 Feb 21. J Mol Diagn. 2020. PMID: 32092542 Free article.

6

Clinical utility of 24-h rapid trio-exome sequencing for critically ill infants.

Wang H, Qian Y, Lu Y, Qin Q, Lu G, Cheng G, Zhang P, Yang L, Wu B, Zhou W. Wang H, et al. Among authors: qin q. NPJ Genom Med. 2020 May 5;5:20. doi: 10.1038/s41525-020-0129-0. eCollection 2020. NPJ Genom Med. 2020. PMID: 32411386 Free PMC article.

7

[No title available]

[No authors listed] [No authors listed] PMID: 33579960

8

Genetic background of idiopathic neurodevelopmental delay patients with significant brain deviation volume.

Chen X, Chen Y, Yan K, Chen H, Qin Q, Yang L, Liu B, Cheng G, Cao Y, Wu B, Dong X, Qiao Z, Zhou W. Chen X, et al. Among authors: qin q. Chin Med J (Engl). 2023 Apr 5;136(7):807-814. doi: 10.1097/CM9.0000000000002297. Chin Med J (Engl). 2023. PMID: 36806579 Free PMC article.

9

Ligand-binding assays validated for quantitative bioanalysis of a novel antibody-drug conjugate in monkey serum and related application in a nonclinical study.

Hou Y, Miao J, Sun Y, Shi L, Ouyang L, Chen X, Li Z, Liu T, Qin G, Qin Q, Gong L. Hou Y, et al. Among authors: qin q. J Pharmacol Toxicol Methods. 2024 Dec 30:107580. doi: 10.1016/j.vascn.2024.107580. Online ahead of print. J Pharmacol Toxicol Methods. 2024. PMID: 39743180

10

Long-Stay Nursing Home Residents With Dementia: Telemedicine Mental Health Use During the COVID-19 Pandemic.

Qin Q, Temkin-Greener H, Simning A, Yousefi-Nooraie R, Cai S. Qin Q, et al. J Am Med Dir Assoc. 2024 Dec 28:105438. doi: 10.1016/j.jamda.2024.105438. Online ahead of print. J Am Med Dir Assoc. 2024. PMID: 39740765

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