 Lin Li, MD, PhD
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| Title(s) | Postdoctoral Scholar, Ob/Gyn, Reproductive Sciences |
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| School | School of Medicine |
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| Address | 550 16th Street
San Francisco CA 94158
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| Phone | -- |
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| vCard | Download vCard |
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 Bibliographic
Altmetrics Details
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.
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Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies. Ultrasound Obstet Gynecol. 2020 Apr; 55(4):502-509.
Li L, He Z, Huang X, Lin S, Wu J, Huang L, Wan Y, Fang Q. PMID: 30977228.
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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.
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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.
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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.
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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.
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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.
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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.
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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:
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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.
View in: PubMed Mentions:
This graph shows the total number of publications by year. To see the data as text, click here.
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| Year | Publications |
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| 2016 | 1 | | 2017 | 4 | | 2018 | 2 | | 2019 | 1 | | 2020 | 1 |
This graph shows the number and percent of publications by field.
Fields are based on how the National Library of Medicine (NLM) classifies the publications' journals and might not represent the specific topics of the publications.
Note that an individual publication can be assigned to more than one field. As a result, the publication counts in this graph might add up to more than the number of publications the person has written.
To see the data as text, click here.
This graph shows the number and percent of publications by field.
Fields are based on how the National Library of Medicine (NLM) classifies the publications' journals and might not represent the specific topics of the publications.
Note that an individual publication can be assigned to more than one field. As a result, the publication counts in this graph might add up to more than the number of publications the person has written.
To see the data as text, click here.
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