Bai‐Lin Wu

3.3k total citations · 1 hit paper
41 papers, 1.7k citations indexed

About

Bai‐Lin Wu is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bai‐Lin Wu has authored 41 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 16 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bai‐Lin Wu's work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (6 papers). Bai‐Lin Wu is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (7 papers) and Chromosomal and Genetic Variations (6 papers). Bai‐Lin Wu collaborates with scholars based in United States, China and Germany. Bai‐Lin Wu's co-authors include Va Lip, Gerald F. Cox, Bernhard Horsthemke, Joachim Bürger, Karl Sperling, Ulrike Mau, Yiping Shen, Rong Liao, Qingdong Deng and Peiqing Sun and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and International Journal of Molecular Sciences.

In The Last Decade

Bai‐Lin Wu

40 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects

2002 519 citations Gerald F. Cox, Joachim Bürger et al. The American Journal of Human Genetics profile →

Peers

Bai‐Lin Wu

GENET

PPCH

PHEOH

Cédric Le Caignec France

Oliver Bartsch Germany

Julie Désir Belgium

Ana Cristina Victorino Krepischi Brazil

Lisbeth S. Laursen Denmark

Palma Finelli Italy

R. J. M. Gardner New Zealand

Michael J. Friez United States

Ayala Frumkin Israel

Uppala Radhakrishna United States

Cédric Le Caignec France

Bai‐Lin Wu

1.7k ×2.2

1.5k ×1.9

GENET

770 ×1.4

PPCH

237 ×1.1

PHEOH

94 ×0.5

Citations per year, relative to Bai‐Lin Wu Bai‐Lin Wu (= 1×) peers Cédric Le Caignec

Countries citing papers authored by Bai‐Lin Wu

Since Specialization

Citations

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

Fields of papers citing papers by Bai‐Lin Wu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bai‐Lin Wu. 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 Bai‐Lin Wu. The network helps show where Bai‐Lin Wu may publish in the future.

Co-authorship network of co-authors of Bai‐Lin Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Bai‐Lin Wu. A scholar is included among the top collaborators of Bai‐Lin Wu 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 Bai‐Lin Wu. Bai‐Lin Wu 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

Wu, Bai‐Lin, et al.. (2025). Cardiac regeneration: Unraveling the complex network of intercellular crosstalk. Seminars in Cell and Developmental Biology. 171. 103619–103619.

Wu, Bai‐Lin, I-Ting Lin, Stefan Günther, et al.. (2025). Border-zone cardiomyocytes and macrophages regulate extracellular matrix remodeling to promote cardiomyocyte protrusion during cardiac regeneration. Nature Communications. 16(1). 3823–3823. 2 indexed citations

Sun, Yuwei, Tong Zhu, Bai‐Lin Wu, et al.. (2022). Single-cell transcriptomic landscapes of the otic neuronal lineage at multiple early embryonic ages. Cell Reports. 38(12). 110542–110542. 25 indexed citations

Wang, Lina, Wufan Tao, Wenxiang Zhang, et al.. (2021). LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant mice. Journal of genetics and genomics. 48(5). 384–395. 7 indexed citations

Liu, Weiqiang, Jieliang Li, Jian Wang, et al.. (2015). Genetic Evaluation of Copy Number Variations, Loss of Heterozygosity, and Single-Nucleotide Variant Levels in Human Embryonic Stem Cells With or Without Skewed X Chromosome Inactivation. Stem Cells and Development. 24(15). 1779–1792. 2 indexed citations

Ye, Yuqin, Na Li, Yiming Wu, et al.. (2014). Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure. Reproductive BioMedicine Online. 29(3). 382–387. 12 indexed citations

Wang, Huijun, Bingbing Wu, Yu An, et al.. (2013). Molecular Diagnostic of Pediatrics Rare Disease in Children��s Hospital of Fudan University. North American Journal of Medicine and Science. 6(4). 219–219. 1 indexed citations

Poduri, Annapurna, Edward Neilan, Princess C. Elhosary, et al.. (2012). Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy. Epilepsia. 53(8). e146–50. 68 indexed citations

Xu, Shuhua, S. Li, H. J. Yang, et al.. (2010). A Genome-Wide Search for Signals of High-Altitude Adaptation in Tibetans. Molecular Biology and Evolution. 28(2). 1003–1011. 247 indexed citations

10.

Wu, Bai‐Lin, Va Lip, Elicia Estrella, et al.. (2010). Familial Dilated Cardiomyopathy Secondary to Dystrophin Splice Site Mutation. Journal of Cardiac Failure. 16(3). 194–199. 13 indexed citations

11.

Shen, Yiping, Bai‐Lin Wu, & James F. Gusella. (2009). Large-Scale Medical Resequencing for X-Linked Mental Retardation. Clinical Chemistry. 56(3). 339–341. 2 indexed citations

12.

Yuan, Yongyi, Deliang Huang, Pu Dai, et al.. (2007). [GJB6 gene mutation analysis in Chinese nonsyndromic deaf population].. PubMed. 21(1). 3–6. 3 indexed citations

13.

Lawson‐Yuen, Amy, Bai‐Lin Wu, Va Lip, Trilochan Sahoo, & Virginia Kimonis. (2006). Atypical cases of Angelman syndrome. American Journal of Medical Genetics Part A. 140A(21). 2361–2364. 19 indexed citations

14.

Deng, Qingdong, Rong Liao, Bai‐Lin Wu, & Peiqing Sun. (2004). High Intensity ras Signaling Induces Premature Senescence by Activating p38 Pathway in Primary Human Fibroblasts. Journal of Biological Chemistry. 279(2). 1050–1059. 140 indexed citations

15.

Xu, Ruliang, Shuji Ogino, Va Lip, Hong Fang, & Bai‐Lin Wu. (2003). Comparison of PCR-RFLP with Allele-Specific PCR in Genetic Testing for Spinal Muscular Atrophy. Genetic Testing. 7(4). 277–281. 13 indexed citations

16.

Wu, Bai‐Lin, Margaret A. Kenna, Va Lip, Mira Irons, & Orah S. Platt. (2003). Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness. American Journal of Medical Genetics Part A. 121A(2). 102–108. 29 indexed citations

17.

Cox, Gerald F., Joachim Bürger, Va Lip, et al.. (2002). Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects. The American Journal of Human Genetics. 71(1). 162–164. 519 indexed citations breakdown →

18.

Wu, Bai‐Lin, et al.. (1996). Distal 8p deletion (8)(p23.1): An easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation. American Journal of Medical Genetics. 62(1). 77–83. 52 indexed citations

19.

Wu, Bai‐Lin, Aubrey Milunsky, David Lee Nelson, et al.. (1993). High-Resolution Mapping of Probes near the X-Linked Lymphoproliferative Disease (XLP) Locus. Genomics. 17(1). 163–170. 10 indexed citations

20.

Wu, Bai‐Lin, et al.. (1993). In Situ Hybridization applied to Waardenburg Syndrome. Cytogenetic and Genome Research. 63(1). 29–32. 14 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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