Ma J - Search Results

1

A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.

Li J, Xie M, Wang F, Ma J, Li J, Chen C, Li Z, Wang J, Zhang Y, Li Y. Li J, et al. Among authors: ma j. Mol Genet Genomic Med. 2020 Aug;8(8):e1279. doi: 10.1002/mgg3.1279. Epub 2020 May 28. Mol Genet Genomic Med. 2020. PMID: 32463164 Free PMC article.

2

Case Report: Prenatal and Postnatal Management for Fetal Bronchogenic Cysts During the COVID-19 Pandemic.

Cheng L, Duan J, Wang M, Lu D, Li H, Ma J, Liu J, Wang C, Zhang Y. Cheng L, et al. Among authors: ma j. Front Pediatr. 2021 Jul 7;9:675883. doi: 10.3389/fped.2021.675883. eCollection 2021. Front Pediatr. 2021. PMID: 34307253 Free PMC article.

3

Identification of Novel Compound Heterozygous Variants of MMP9 in Fetus With Metaphyseal Anadysplasia Type 2.

Cheng L, Yang F, Chen X, Kang J, Li J, Zhang Y, Liu J, Li J, Ma J, Duan J. Cheng L, et al. Among authors: ma j. Front Genet. 2022 Aug 12;13:938457. doi: 10.3389/fgene.2022.938457. eCollection 2022. Front Genet. 2022. PMID: 36035187 Free PMC article.

4

Identification of Gravida Serum Biomarkers for Noninvasive Prenatal Diagnosis Fetal Congenital Heart Disease.

Xia Y, Cheng L, Duan J, Ma J, Zhang Y. Xia Y, et al. Among authors: ma j. J Cardiovasc Transl Res. 2023 Feb;16(1):255-266. doi: 10.1007/s12265-022-10301-5. Epub 2022 Sep 30. J Cardiovasc Transl Res. 2023. PMID: 36178661

5

Association of low birthweight and small for gestational age with maternal ferritin levels: A retrospective cohort study in China.

Tao Y, Kang J, Liu J, Duan J, Wang F, Shi Y, Li Y, Wang C, Xu D, Qu X, Guo J, Ma J, Zhang Y. Tao Y, et al. Among authors: ma j. Front Nutr. 2022 Oct 10;9:1002702. doi: 10.3389/fnut.2022.1002702. eCollection 2022. Front Nutr. 2022. PMID: 36299991 Free PMC article.

6

Genetic characteristics of suspected retinitis pigmentosa in a cohort of Chinese patients.

Jin B, Li J, Yang Q, Tang X, Wang C, Zhao Y, Zheng F, Zhang Y, Ma J, Yan M. Jin B, et al. Among authors: ma j. Gene. 2023 Feb 15;853:147087. doi: 10.1016/j.gene.2022.147087. Epub 2022 Dec 2. Gene. 2023. PMID: 36464167

7

Construction of an aging-related risk signature in high-grade serous ovarian cancer for predicting survival outcome and immunogenicity.

Liu S, Liu Y, Ma J, Lv R, Wang F. Liu S, et al. Among authors: ma j. Medicine (Baltimore). 2023 Sep 1;102(35):e34851. doi: 10.1097/MD.0000000000034851. Medicine (Baltimore). 2023. PMID: 37657028 Free PMC article.

8

The comprehensive study on the role of POSTN in fetal congenital heart disease and clinical applications.

Xia Y, Chen L, Lu J, Ma J, Zhang Y. Xia Y, et al. Among authors: ma j. J Transl Med. 2023 Dec 11;21(1):901. doi: 10.1186/s12967-023-04529-1. J Transl Med. 2023. PMID: 38082393 Free PMC article.

9

Identification of chromosomal abnormalities in miscarriages by CNV-Seq.

Shao Y, Yang S, Cheng L, Duan J, Li J, Kang J, Wang F, Liu J, Zheng F, Ma J, Zhang Y. Shao Y, et al. Among authors: ma j. Mol Cytogenet. 2024 Feb 18;17(1):4. doi: 10.1186/s13039-024-00671-7. Mol Cytogenet. 2024. PMID: 38369498 Free PMC article.

10

Compound heterozygous mutation of the SNX14 gene causes autosomal recessive spinocerebellar ataxia 20.

Shao Y, Yang S, Li J, Cheng L, Kang J, Liu J, Ma J, Duan J, Zhang Y. Shao Y, et al. Among authors: ma j. Front Genet. 2024 Apr 9;15:1379366. doi: 10.3389/fgene.2024.1379366. eCollection 2024. Front Genet. 2024. PMID: 38655056 Free PMC article.

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