Bai-Lin Wu

1.8k total citations
7 papers, 228 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 7 papers receiving a total of 228 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bai-Lin Wu's work include Genetics and Neurodevelopmental Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Bai-Lin Wu is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Bai-Lin Wu collaborates with scholars based in United States and China. Bai-Lin Wu's co-authors include Bruce R. Korf, Yiping Shen, John B. Mulliken, Catherine E. Keegan, Joan H.M. Knoll, Lisa White, Robert D. Nicholls, Peter K. Rogan, Yueying Wang and Peining Li and has published in prestigious journals such as The American Journal of Human Genetics, Human Mutation and Genetics in Medicine.

In The Last Decade

Bai-Lin Wu

7 papers receiving 217 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bai-Lin Wu United States	6	163	142	51	20	15	7	228
Alaa K. Kamel Egypt	9	180 1.1×	138 1.0×	61 1.2×	25 1.3×	21 1.4×	34	227
Ariella Weinberg‐Shukron Israel	9	173 1.1×	229 1.6×	55 1.1×	15 0.8×	16 1.1×	15	377
Chiara Castronovo Italy	9	183 1.1×	122 0.9×	51 1.0×	49 2.5×	13 0.9×	16	275
Carla S. D’Angelo Brazil	10	229 1.4×	156 1.1×	42 0.8×	27 1.4×	30 2.0×	15	302
Fernando Santos Spain	9	228 1.4×	193 1.4×	84 1.6×	21 1.1×	23 1.5×	13	325
U Theile Germany	9	147 0.9×	144 1.0×	36 0.7×	17 0.8×	12 0.8×	23	242
Norio Niikawa Japan	8	192 1.2×	214 1.5×	75 1.5×	20 1.0×	14 0.9×	10	268
M.L. Martínez‐Fernández Spain	9	154 0.9×	78 0.5×	48 0.9×	58 2.9×	9 0.6×	20	196
Yoko Hiraki Japan	10	131 0.8×	97 0.7×	22 0.4×	18 0.9×	21 1.4×	17	219
A. Saad Tunisia	9	130 0.8×	97 0.7×	42 0.8×	16 0.8×	9 0.6×	24	255

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

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Yan, Shi, Yi Ding, Yunping Lei, et al.. (2012). Identification of novel rare mutations of DACT1 in human neural tube defects. Human Mutation. 33(10). 1450–1455. 34 indexed citations

2.

Dauber, Andrew, Yongguo Yu, Michael C. Turchin, et al.. (2011). Genome-wide Association of Copy-Number Variation Reveals an Association between Short Stature and the Presence of Low-Frequency Genomic Deletions. The American Journal of Human Genetics. 89(6). 751–759. 56 indexed citations

3.

Kluk, Michael, Yu An, Philip James, et al.. (2011). Avoiding Pitfalls in Molecular Genetic Testing. Journal of Molecular Diagnostics. 13(3). 363–367. 5 indexed citations

4.

Xiang, Bixia, Hongbo Zhu, Yiping Shen, et al.. (2010). Genome-Wide Oligonucleotide Array Comparative Genomic Hybridization for Etiological Diagnosis of Mental Retardation. Journal of Molecular Diagnostics. 12(2). 204–212. 58 indexed citations

5.

Neilan, Edward, et al.. (2008). Response of Motor Complications in Cockayne Syndrome to Carbidopa-Levodopa. Archives of Neurology. 65(8). 1117–21. 16 indexed citations

6.

Keegan, Catherine E., John B. Mulliken, Bai-Lin Wu, & Bruce R. Korf. (2001). Townes-Brocks syndrome versus expanded spectrum hemifacial microsomia: Review of eight patients and further evidence of a “hot spot” for mutation in the SALL1 gene. Genetics in Medicine. 3(4). 310–313. 26 indexed citations

7.

White, Lisa, Peter K. Rogan, Robert D. Nicholls, et al.. (1996). Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.. PubMed. 59(2). 423–30. 33 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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