Yi‐Ning Su

1.4k total citations
45 papers, 991 citations indexed

About

Yi‐Ning Su is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Yi‐Ning Su has authored 45 papers receiving a total of 991 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 25 papers in Pediatrics, Perinatology and Child Health and 17 papers in Molecular Biology. Recurrent topics in Yi‐Ning Su's work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (20 papers) and Chromosomal and Genetic Variations (8 papers). Yi‐Ning Su is often cited by papers focused on Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (20 papers) and Chromosomal and Genetic Variations (8 papers). Yi‐Ning Su collaborates with scholars based in Taiwan, United States and France. Yi‐Ning Su's co-authors include Wu‐Shiun Hsieh, Pau‐Chung Chen, Mei-Huei Chen, Chih‐Ping Chen, Wayseen Wang, Eun‐Hee Ha, C. Chen, Schu‐Rern Chern, Fuu‐Jen Tsai and Hua-Fang Liao and has published in prestigious journals such as PLoS ONE, American Journal of Respiratory and Critical Care Medicine and Analytical Biochemistry.

In The Last Decade

Yi‐Ning Su

45 papers receiving 974 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Yi‐Ning Su Taiwan	16	372	287	274	225	218	45	991
Maya Kappil United States	18	218 0.6×	183 0.6×	155 0.6×	55 0.2×	646 3.0×	27	1.1k
Linn Salto Mamsen Denmark	20	278 0.7×	220 0.8×	323 1.2×	318 1.4×	382 1.8×	64	1.5k
Rondi A. Butler United States	19	160 0.4×	175 0.6×	236 0.9×	81 0.4×	964 4.4×	38	1.4k
Susan R. Panny United States	22	406 1.1×	674 2.3×	265 1.0×	40 0.2×	527 2.4×	34	1.7k
Sara E. Pinney United States	15	318 0.9×	198 0.7×	120 0.4×	39 0.2×	426 2.0×	24	1.1k
Y. Sumiyoshi Japan	12	195 0.5×	62 0.2×	320 1.2×	83 0.4×	65 0.3×	16	851
Gregory D. Bennett United States	21	598 1.6×	142 0.5×	104 0.4×	62 0.3×	462 2.1×	46	1.3k
Hui‐Ju Wen Taiwan	21	89 0.2×	50 0.2×	393 1.4×	87 0.4×	209 1.0×	63	1.1k
Muraly Puttabyatappa United States	23	430 1.2×	128 0.4×	245 0.9×	34 0.2×	214 1.0×	51	1.2k
Shigeki Uehara Japan	19	297 0.8×	282 1.0×	289 1.1×	42 0.2×	184 0.8×	59	1.1k

Countries citing papers authored by Yi‐Ning Su

Since Specialization

Citations

This map shows the geographic impact of Yi‐Ning Su'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‐Ning Su with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yi‐Ning Su more than expected).

Fields of papers citing papers by Yi‐Ning Su

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yi‐Ning Su. 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‐Ning Su. The network helps show where Yi‐Ning Su may publish in the future.

Co-authorship network of co-authors of Yi‐Ning Su

This figure shows the co-authorship network connecting the top 25 collaborators of Yi‐Ning Su. A scholar is included among the top collaborators of Yi‐Ning Su 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‐Ning Su. Yi‐Ning Su is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Jou, Shiann‐Tarng, Chien‐Yu Lin, Kai‐Hsin Lin, et al.. (2020). MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia. Scientific Reports. 10(1). 11501–11501. 14 indexed citations

Chen, Mei-Huei, Eun‐Hee Ha, Hua-Fang Liao, et al.. (2013). Perfluorinated Compound Levels in Cord Blood and Neurodevelopment at 2 Years of Age. Epidemiology. 24(6). 800–808. 93 indexed citations

Lin, Ching‐Chun, Feng‐Chiao Su, Chien-Mu Lin, et al.. (2013). In utero exposure to environmental lead and manganese and neurodevelopment at 2 years of age. Environmental Research. 123. 52–57. 134 indexed citations

Chen, Chih‐Ping, Yi‐Ning Su, Shun-Long Weng, et al.. (2012). Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester. Taiwanese Journal of Obstetrics and Gynecology. 51(3). 481–484. 9 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, Tsang‐Ming Ko, Yi‐Ning Su, et al.. (2012). Prenatal diagnosis of mosaic tetrasomy 18p. Taiwanese Journal of Obstetrics and Gynecology. 51(4). 625–629. 15 indexed citations

Wang, Shih‐Hao, Chen‐Chi Wu, Yingchang Lu, et al.. (2012). Mutation screening of the EYA1, SIX1, and SIX5 genes in an east asian cohort with branchio‐oto‐renal syndrome. The Laryngoscope. 122(5). 1130–1136. 25 indexed citations

Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2011). Inv dup del(9p): Prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. Taiwanese Journal of Obstetrics and Gynecology. 50(1). 67–73. 13 indexed citations

Chen, Chih‐Ping, Pei‐Ying Ling, Yi‐Ning Su, et al.. (2011). A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings. Taiwanese Journal of Obstetrics and Gynecology. 50(4). 492–498. 5 indexed citations

10.

Chen, Chih‐Ping, Ming Chen, Yi‐Ning Su, et al.. (2011). Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4. Taiwanese Journal of Obstetrics and Gynecology. 50(2). 188–195. 7 indexed citations

11.

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

12.

Chen, Chih‐Ping, C.-C. Chiang, Yi‐Ning Su, et al.. (2011). Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis. Taiwanese Journal of Obstetrics and Gynecology. 50(2). 245–248. 7 indexed citations

13.

Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2010). Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses. Taiwanese Journal of Obstetrics and Gynecology. 49(3). 341–350. 49 indexed citations

14.

Chen, Chih‐Ping, Ming Chen, Yi‐Ning Su, et al.. (2010). Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings. Taiwanese Journal of Obstetrics and Gynecology. 49(4). 473–480. 7 indexed citations

15.

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

16.

Chen, Chih‐Ping, Yi‐Ning Su, Fuu‐Jen Tsai, et al.. (2010). Partial Trisomy 16p (16p12.2→pter) and Partial Monosomy 22q (22q13.31 →qter) Presenting With Fetal Ascites and Ventriculomegaly: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization. Taiwanese Journal of Obstetrics and Gynecology. 49(4). 506–512. 2 indexed citations

17.

Hwa, Hsiao‐Lin, et al.. (2010). Seventeen Y-chromosomal short tandem repeat haplotypes in seven groups of population living in Taiwan. International Journal of Legal Medicine. 124(4). 295–300. 12 indexed citations

18.

Chen, Chih‐Ping, Yi‐Ning Su, Schu‐Rern Chern, et al.. (2010). Ellis-Van Creveld Syndrome: Prenatal Diagnosis, Molecular Analysis and Genetic Counseling. Taiwanese Journal of Obstetrics and Gynecology. 49(4). 481–486. 13 indexed citations

19.

Wu, Kang‐Hsi, et al.. (2009). Treatment with Deferiprone for Iron Overload Alleviates Bone Marrow Failure in a Fanconi Anemia Patient. Hemoglobin. 33(5). 346–351. 12 indexed citations

20.

Tsao, Po‐Nien, Yi‐Ning Su, Hung Li, et al.. (2003). Overexpression of Placenta Growth Factor Contributes to the Pathogenesis of Pulmonary Emphysema. American Journal of Respiratory and Critical Care Medicine. 169(4). 505–511. 72 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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