Bai‐Lin Wu

3.3k citations

41 papers · 1.7k indexed · 1 hit paper · h-index 20

Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 7
Genetics top 2%
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 3
Reproductive Medicine top 5%
Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics 3
Molecular Biology top 10%
- RNA modifications and cancer 5
- Congenital heart defects research 4
- Epigenetics and DNA Methylation 3
Plant Science
- Chromosomal and Genetic Variations 6

Co-authors: Va Lip Gerald F. Cox Bernhard Horsthemke Joachim Bürger Karl Sperling Ulrike Mau Yiping Shen Rong Liao
Cited by: Pediatrics, Perinatology and Child Health Genetics Reproductive Medicine
Partner nations: United States China Germany

In The Last Decade

Bai‐Lin Wu

40 papers receiving 1.7k citations

Hit Papers

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Peers

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

The 25 scholars most cited alongside Bai‐Lin Wu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bai‐Lin Wu Line = papers co-authored together Bai‐Lin Wu links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Cardiac regeneration: Unraveling the complex network of intercellular crosstalk Bai‐Lin Wu,Florian Constanty,Arica Beisaw	2025	0
2	Border-zone cardiomyocytes and macrophages regulate extracellular matrix remodeling to promote cardiomyocyte protrusion during cardiac regeneration Florian Constanty,Bai‐Lin Wu,Ke-Hsuan Wei,I-Ting Lin,Julia Dallmann,Stefan Günther,Till Lautenschlaeger,Rashmi Priya,Shih-Lei Lai,Didier Y. R. Stainier,Arica Beisaw	2025	2
3	Single-cell transcriptomic landscapes of the otic neuronal lineage at multiple early embryonic ages Yuwei Sun,Luyue Wang,Tong Zhu,Bai‐Lin Wu,Guangqin Wang,Zhengnan Luo,Chao Li,Wu Wei,Zhiyong Liu	2022	25
4	LHCGR and ALMS1 defects likely cooperate in the development of polycystic ovary syndrome indicated by double-mutant mice Li Yu,Lina Wang,Wufan Tao,Wenxiang Zhang,Shuanghao Yang,Jian Wang,Jia Fei,Rui Peng,Yiming Wu,Xiumei Zhen,Hong Shao,Weiyue Gu,Rong Li,Bai‐Lin Wu,Hongyan Wang	2021	7
5	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 Weiqiang Liu,Jieliang Li,Jian Wang,Wenyin He,Va Lip,Xiaoming Sheng,Bai‐Lin Wu,Xiaofang Sun	2015	2
6	Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure Yuqin Ye,Xiaoping Lan,Jin Cong,Na Li,Yiming Wu,Min Zhang,Jiayin Liu,Yugui Cui,Bai‐Lin Wu,Yu An,Jie Wu	2014	12
7	Molecular Diagnostic of Pediatrics Rare Disease in Children��s Hospital of Fudan University Huijun Wang,Bingbing Wu,Yu An,Yi Yang,Bai‐Lin Wu,Wenhao Zhou	2013	1
8	Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy Annapurna Poduri,Sameer S. Chopra,Edward Neilan,Princess C. Elhosary,Manju A. Kurian,Esther Meyer,Brenda J. Barry,Omar Khwaja,Mustafa A. Salih,Tommy Stödberg,Ingrid E. Scheffer,Eamonn R. Maher,Mustafa Şahin,Bai‐Lin Wu,Gerard T. Berry,Christopher A. Walsh,Jonathan Picker,Sanjeev V. Kothare	2012	68
9	A Genome-Wide Search for Signals of High-Altitude Adaptation in Tibetans Shuhua Xu,S. Li,H. J. Yang,Jianxin Tan,Hua Jane Lou,Wenfei Jin,Li Yang,Xinwei Pan,Jian Wang,Yan Shen,Bai‐Lin Wu,Hongguang Wang,Jin Li	2010	247
10	Familial Dilated Cardiomyopathy Secondary to Dystrophin Splice Site Mutation Dita Obler,Bai‐Lin Wu,Va Lip,Elicia Estrella,Sally Keck,C. Haggan,Marc J. Semigran,Leslie Smoot	2010	13
11	Large-Scale Medical Resequencing for X-Linked Mental Retardation Yiping Shen,Bai‐Lin Wu,James F. Gusella	2009	2
12	[GJB6 gene mutation analysis in Chinese nonsyndromic deaf population]. Yongyi Yuan,Deliang Huang,Pu Dai,Qingwen Zhu,Xin Liu,Guojian Wang,Qi Li,Bai‐Lin Wu	2007	3
13	Atypical cases of Angelman syndrome Amy Lawson‐Yuen,Bai‐Lin Wu,Va Lip,Trilochan Sahoo,Virginia Kimonis	2006	19
14	High Intensity ras Signaling Induces Premature Senescence by Activating p38 Pathway in Primary Human Fibroblasts Qingdong Deng,Rong Liao,Bai‐Lin Wu,Peiqing Sun	2004	140
15	Comparison of PCR-RFLP with Allele-Specific PCR in Genetic Testing for Spinal Muscular Atrophy Ruliang Xu,Shuji Ogino,Va Lip,Hong Fang,Bai‐Lin Wu	2003	13
16	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 Bai‐Lin Wu,Margaret A. Kenna,Va Lip,Mira Irons,Orah S. Platt	2003	29
17	Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defectsbreakdown → Gerald F. Cox,Joachim Bürger,Va Lip,Ulrike Mau,Karl Sperling,Bai‐Lin Wu,Bernhard Horsthemke	2002	519
18	Distal 8p deletion (8)(p23.1): An easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation Bai‐Lin Wu,Gretchen Schneider,Denise E. Sabatino,Ljiljana Z. Bozovic,Benning Cao,Bruce R. Korf	1996	52
19	High-Resolution Mapping of Probes near the X-Linked Lymphoproliferative Disease (XLP) Locus Bai‐Lin Wu,Aubrey Milunsky,David Lee Nelson,Barbara J. Schmeckpeper,Giovanni Porta,David Schlessinger,James Skare	1993	10
20	In Situ Hybridization applied to Waardenburg Syndrome Bai‐Lin Wu,Aubrey Milunsky,HE Wyandt,Christopher F. Hoth,Clinton T. Baldwin,James Skare	1993	14

About Bai‐Lin Wu

Bai‐Lin Wu is a scholar working on Sensory Systems, Genetics and Pediatrics, Perinatology and Child Health, having authored 41 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (7 papers), Chromosomal and Genetic Variations (6 papers), RNA modifications and cancer (5 papers), Congenital heart defects research (4 papers), Genomics and Rare Diseases (3 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Epigenetics and DNA Methylation (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (543 citations), Genetics (764 citations) and Reproductive Medicine (172 citations). Bai‐Lin Wu has collaborated with scholars based in United States, China and Germany. Frequent 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.

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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