Va Lip

1.5k total citations · 1 hit paper
17 papers, 883 citations indexed

About

Va Lip is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Va Lip has authored 17 papers receiving a total of 883 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Va Lip's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and Muscle Physiology and Disorders (3 papers). Va Lip is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (4 papers) and Muscle Physiology and Disorders (3 papers). Va Lip collaborates with scholars based in United States, Canada and China. Va Lip's co-authors include Bai‐Lin Wu, Gerald F. Cox, Joachim Bürger, Bernhard Horsthemke, Karl Sperling, Ulrike Mau, Orah S. Platt, Mira Irons, Margaret A. Kenna and Yiping Shen and has published in prestigious journals such as PLoS ONE, Neurology and Scientific Reports.

In The Last Decade

Va Lip

17 papers receiving 828 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

Va Lip

PPCH

GENET

PHEOH

Sophie Brisset France

Sylvie Jaillard France

Brigitte Benzacken France

Vanna Pecile Italy

Ada Rosenmann Israel

Thomas A. Maher United States

Amanda H. Mortensen United States

Hayk Barseghyan United States

Michèle Mathieu France

Maria Tereza Matias Baptista Brazil

Sophie Brisset France

Va Lip

194 ×0.4

183 ×0.4

PPCH

378 ×1.0

GENET

27 ×0.2

PHEOH

89 ×0.6

Citations per year, relative to Va Lip Va Lip (= 1×) peers Sophie Brisset

Countries citing papers authored by Va Lip

Since Specialization

Citations

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

Fields of papers citing papers by Va Lip

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Va Lip. 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 Va Lip. The network helps show where Va Lip may publish in the future.

Co-authorship network of co-authors of Va Lip

This figure shows the co-authorship network connecting the top 25 collaborators of Va Lip. A scholar is included among the top collaborators of Va Lip 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 Va Lip. Va Lip 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:

17 of 17 papers shown

Al‐Ibraheemi, Alyaa, Juan Putra, Harrison Tsai, et al.. (2021). Assessment of BCOR Internal Tandem Duplications in Pediatric Cancers by Targeted RNA Sequencing. Journal of Molecular Diagnostics. 23(10). 1269–1278. 7 indexed citations

Xia, Daniel, Chen Zhang, Va Lip, Marian H. Harris, & Yiping Shen. (2018). Trio-R: a script for assessing maternity and paternity in trio studies performed on Agilent chromosomal microarrays. BMC Medical Informatics and Decision Making. 18(1). 91–91. 1 indexed citations

Brownstein, Catherine A., Robin J. Kleiman, Elizabeth C. Engle, et al.. (2016). Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports. American Journal of Medical Genetics Part A. 170(5). 1165–1173. 14 indexed citations

Chennagiri, Niru, Eric J. White, Daniel S. Lieber, et al.. (2016). Orthogonal NGS for High Throughput Clinical Diagnostics. Scientific Reports. 6(1). 24650–24650. 11 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

Chen, Xiaoli, Yiping Shen, Yonghui Gao, et al.. (2013). Detection of Copy Number Variants Reveals Association of Cilia Genes with Neural Tube Defects. PLoS ONE. 8(1). e54492–e54492. 31 indexed citations

An, Yu, Sami S. Amr, Alcy Torres, et al.. (2013). SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(8). 832–840. 28 indexed citations

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

Smoot, Leslie, et al.. (2009). Clinical features of pulmonary arterial hypertension in young people with an ALK1 mutation and hereditary haemorrhagic telangiectasia. Archives of Disease in Childhood. 94(7). 506–511. 18 indexed citations

10.

Bennett, Richard Rodney, Hal E. Schneider, Elicia Estrella, et al.. (2009). Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes. BMC Genetics. 10(1). 66–66. 8 indexed citations

11.

Shen, Yiping, David T. Miller, Sau Wai Cheung, et al.. (2007). Development of a Focused Oligonucleotide-Array Comparative Genomic Hybridization Chip for Clinical Diagnosis of Genomic Imbalance. Clinical Chemistry. 53(12). 2051–2059. 43 indexed citations

12.

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

13.

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

14.

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

15.

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 →

16.

Wu, Bai-Lin, Neal I. Lindeman, Va Lip, et al.. (2002). Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testing. Genetics in Medicine. 4(4). 279–288. 57 indexed citations

17.

Wattanasirichaigoon, Duangrurdee, Kathryn J. Swoboda, Fumio Takada, et al.. (2002). Mutations of the slow muscle α-tropomyosin gene, TPM3 , are a rare cause of nemaline myopathy. Neurology. 59(4). 613–617. 70 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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