Yi-Hui Lin

480 total citations
14 papers, 245 citations indexed

About

Yi-Hui Lin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Yi-Hui Lin has authored 14 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Yi-Hui Lin's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). Yi-Hui Lin is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). Yi-Hui Lin collaborates with scholars based in Taiwan, Canada and Germany. Yi-Hui Lin's co-authors include Chii‐Ruey Tzeng, Chun-Sen Hsu, Ming‐I Hsu, Wan‐Chun Chiu, Chien-Hua Wu, Chih‐Ping Chen, Wayseen Wang, Schu‐Rern Chern, Yi‐Ning Su and Purvi M. Kakadia and has published in prestigious journals such as Blood, Fertility and Sterility and European Journal of Obstetrics & Gynecology and Reproductive Biology.

In The Last Decade

Yi-Hui Lin

14 papers receiving 239 citations

Peers

Yi-Hui Lin

PHEOH

PPCH

GENET

Maria João Pinho Portugal

R Sudik Germany

Kristjan Pomm Estonia

Gail Fullerton United Kingdom

Schill Wb Germany

Beate Lemcke Germany

Vladimir Vihljajev Estonia

Federica Finocchi Italy

Jolanda C. Boxmeer Netherlands

Judith Gianotten Netherlands

Maria João Pinho Portugal

Yi-Hui Lin

131 ×1.3

98 ×1.0

PHEOH

155 ×1.8

87 ×1.3

PPCH

115 ×2.0

GENET

Citations per year, relative to Yi-Hui Lin Yi-Hui Lin (= 1×) peers Maria João Pinho

Countries citing papers authored by Yi-Hui Lin

Since Specialization

Citations

This map shows the geographic impact of Yi-Hui Lin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Yi-Hui Lin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yi-Hui Lin more than expected).

Fields of papers citing papers by Yi-Hui Lin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yi-Hui Lin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Yi-Hui Lin. The network helps show where Yi-Hui Lin may publish in the future.

Co-authorship network of co-authors of Yi-Hui Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Yi-Hui Lin. A scholar is included among the top collaborators of Yi-Hui Lin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Yi-Hui Lin. Yi-Hui Lin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Chen, Chih‐Ping, et al.. (2020). Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 59(1). 146–149. 12 indexed citations

Chen, Chi‐Huang, et al.. (2019). Adjusted mitochondrial DNA quantification in human embryos may not be applicable as a biomarker of implantation potential. Journal of Assisted Reproduction and Genetics. 36(9). 1855–1865. 15 indexed citations

Chen, Chien‐Wen, et al.. (2017). Prediction of a rare chromosomal aberration simultaneously with next generation sequencing-based comprehensive chromosome screening in human preimplantation embryos for recurrent pregnancy loss. Journal of Assisted Reproduction and Genetics. 35(1). 171–176. 1 indexed citations

Chen, Chih‐Ping, et al.. (2016). Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities. Taiwanese Journal of Obstetrics and Gynecology. 55(6). 852–855. 3 indexed citations

Lin, Yi-Hui, Shih‐Yi Huang, Ming-I Hsu, et al.. (2013). Hyperhomocysteinaemia is associated with biochemical hyperandrogenaemia in women with reproductive age. European Journal of Obstetrics & Gynecology and Reproductive Biology. 171(2). 314–318. 11 indexed citations

Chen, Chih‐Ping, Yi-Hui Lin, Yi‐Ning Su, et al.. (2012). Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1–q21.2 and 5-Mb deletion of 21q22.3. Taiwanese Journal of Obstetrics and Gynecology. 51(1). 71–76. 15 indexed citations

Chen, Chih‐Ping, Ming Chen, Gwo‐Chin Ma, et al.. (2012). Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosomes. Journal of the Chinese Medical Association. 76(1). 53–56. 5 indexed citations

Lin, Yi-Hui, et al.. (2011). Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction. Taiwanese Journal of Obstetrics and Gynecology. 50(4). 528–530. 1 indexed citations

Chen, Chih‐Ping, Yi-Hui Lin, Heng‐Kien Au, et al.. (2011). Chromosome 15q overgrowth syndrome: Prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3). Taiwanese Journal of Obstetrics and Gynecology. 50(3). 359–365. 9 indexed citations

10.

Lin, Yi-Hui, Wan‐Chun Chiu, Chien-Hua Wu, et al.. (2011). Antimüllerian hormone and polycystic ovary syndrome. Fertility and Sterility. 96(1). 230–235. 96 indexed citations

11.

Chen, Chih‐Ping, Yung‐Ting Kuo, Shuan-Pei Lin, et al.. (2010). Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic Hybridization. Taiwanese Journal of Obstetrics and Gynecology. 49(3). 327–332. 16 indexed citations

12.

Lin, Yi-Hui, Purvi M. Kakadia, Ying Chen, et al.. (2009). Global reduction of the epigenetic H3K79 methylation mark and increased chromosomal instability in CALM-AF10–positive leukemias. Blood. 114(3). 651–658. 49 indexed citations

13.

Hsu, Chun-Sen, et al.. (2006). Malignant Fibrous Histiocytoma During Pregnancy: a Case Report. Taiwanese Journal of Obstetrics and Gynecology. 45(1). 86–88. 3 indexed citations

14.

Chen, Chih‐Ping, Schu‐Rern Chern, Fuu‐Jen Tsai, et al.. (2005). A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error. Prenatal Diagnosis. 25(4). 327–330. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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