Lin Li • UCSF Profiles

Lin Li, MD, PhD

Title(s)	Postdoctoral Scholar, Ob/Gyn, Reproductive Sciences
School	School of Medicine
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Bibliographic

Publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.

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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.

COVID-19 mRNA Vaccination in Lactation: Assessment of Adverse Events and Vaccine Related Antibodies in Mother-Infant Dyads. Front Immunol. 2021; 12:777103. Golan Y, Prahl M, Cassidy AG, Gay C, Wu AHB, Jigmeddagva U, Lin CY, Gonzalez VJ, Basilio E, Chidboy MA, Warrier L, Buarpung S, Li L, Murtha AP, Asiodu IV, Ahituv N, Flaherman VJ, Gaw SL. PMID: 34804068; PMCID: PMC8595828.

View in: PubMed Mentions: 11 Fields:
All Allergy and Immunology
Translation:Humans Cells CTClinical Trials
Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies. Ultrasound Obstet Gynecol. 2020 04; 55(4):502-509. Li L, He Z, Huang X, Lin S, Wu J, Huang L, Wan Y, Fang Q. PMID: 30977228.

View in: PubMed Mentions: 1 Fields:
Dia Diagnostic Imaging Gyn Gynecology Obs Obstetrics
Translation:Humans
miRNA-210-3p regulates trophoblast proliferation and invasiveness through fibroblast growth factor 1 in selective intrauterine growth restriction. J Cell Mol Med. 2019 06; 23(6):4422-4433. Li L, Huang X, He Z, Xiong Y, Fang Q. PMID: 30993882; PMCID: PMC6533475.

View in: PubMed Mentions: 13 Fields:
Cel Cell Biology Mol Molecular Biology
Translation:Humans Cells
Prenatal diagnosis of Pallister-Killian syndrome in one twin. Clin Case Rep. 2018 Aug; 6(8):1470-1473. Li L, Huang L, Huang X, Lin S, He Z, Fang Q. PMID: 30147884; PMCID: PMC6099054.

View in: PubMed Mentions: 1
Chromosomal aberrations and CNVs in twin fetuses with cardiovascular anomalies: Comparison between monochorionic diamniotic and dichorionic diamniotic twins. Prenat Diagn. 2018 04; 38(5):318-327. Zhang Y, Huang L, Huang X, He Z, Lin S, Wang Y, Li L, Luo Y, Fang Q. PMID: 29460287.

View in: PubMed Mentions: 2 Fields:
Obs Obstetrics
Translation:Humans
Fetal Aneuploidy: A Comparison of Dichorionic Twins and Monochorionic Twins. Fetal Diagn Ther. 2018; 44(2):124-128. Shi X, Li L, Huang X, Chen B, Zhou Y, Fang Q. PMID: 28869935.

View in: PubMed Mentions: 1 Fields:
Dia Diagnostic Imaging Obs Obstetrics Per Perinatology
Translation:Humans
Successful management of a hydropic fetus with severe anemia and thrombocytopenia caused by anti-CD36 antibody. Int J Hematol. 2018 Feb; 107(2):251-256. Xu X, Li L, Xia W, Ding H, Chen D, Liu J, Deng J, Chen Y, He Z, Wang J, Shao Y, Santoso S, Ye X, Fang Q. PMID: 28815406.

View in: PubMed Mentions: 1 Fields:
Hem Hematology
Translation:Humans
Prenatal treatment of severe fetal hemolytic disease due to anti-M alloimmunization by serial intrauterine transfusions. Taiwan J Obstet Gynecol. 2017 Jun; 56(3):379-381. Li L, Huang L, Luo G, Luo Y, Fang Q. PMID: 28600054.

View in: PubMed Mentions: Fields:
Gyn Gynecology Obs Obstetrics
Translation:Humans
Discordant phenotypes in monozygotic twins with 16p11.2 microdeletions including the SH2B1 gene. Am J Med Genet A. 2017 Aug; 173(8):2284-2288. Li L, Huang L, Lin S, Luo Y, Fang Q. PMID: 28544142.

View in: PubMed Mentions: 5 Fields:
Gen Genetics
Translation:Humans Cells
Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis. Mol Syndromol. 2016 Feb; 6(6):268-75. Li L, Huang L, Luo Y, Huang X, Lin S, Fang Q. PMID: 27022327; PMCID: PMC4802981.

View in: PubMed Mentions: 6