Pei-Lung Chen

424 total citations
8 papers, 322 citations indexed

About

Pei-Lung Chen is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Pei-Lung Chen has authored 8 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Surgery. Recurrent topics in Pei-Lung Chen's work include Genetic Associations and Epidemiology (4 papers), Genetic Syndromes and Imprinting (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Pei-Lung Chen is often cited by papers focused on Genetic Associations and Epidemiology (4 papers), Genetic Syndromes and Imprinting (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Pei-Lung Chen collaborates with scholars based in United States and Taiwan. Pei-Lung Chen's co-authors include John A. McGrath, Paula Wolyniec, David Valle, Dimitrios Avramopoulos, Gerald Nestadt, Kung‐Yee Liang, Chris Merritt, Géraldine Seydoux, Kuppuswamy Subramaniam and Virginia K. Lasseter and has published in prestigious journals such as The American Journal of Human Genetics, Developmental Biology and Human Reproduction.

In The Last Decade

Pei-Lung Chen

7 papers receiving 318 citations

Peers

Countries citing papers authored by Pei-Lung Chen

Since Specialization

Citations

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

Fields of papers citing papers by Pei-Lung Chen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pei-Lung Chen. 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 Pei-Lung Chen. The network helps show where Pei-Lung Chen may publish in the future.

Co-authorship network of co-authors of Pei-Lung Chen

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Ocular Characteristics and Genotype-Oriented Disease Spectrum of Alström Syndrome in Taiwan 2025 ·Translational Vision Science & Technology ·(unknown), Chien‐Yu Lin, (unknown), Yu‐Shu Huang, (unknown), Chang‐Hao Yang, (unknown), Pei-Lung Chen, Ta‐Ching Chen	0
2	Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Kuster-Hauser syndrome 2015 ·Human Reproduction ·Mei‐Jou Chen, Shu‐Yi Wei, Wei‐Shiung Yang, Ting-Ting Wu, Hung‐Yuan Li, Hong‐Nerng Ho, Yu‐Shih Yang, Pei-Lung Chen	22
3	Functional Variants in DPYSL2 Sequence Increase Risk of Schizophrenia and Suggest a Link to mTOR Signaling 2014 ·G3 Genes Genomes Genetics ·Yaping Liu, (unknown), Lilei Zhang, Pei-Lung Chen, Grzegorz Burzynski, David McGaughey, Shan He, John A. McGrath, Paula Wolyniec, Margaret Daniele Fallin, (unknown), Andrew S. McCallion, Ann E. Pulver, Dimitrios Avramopoulos, David Valle	38
4	Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women 2010 ·Psychiatric Genetics ·Yaping Liu, Pei-Lung Chen, John A. McGrath, Paula Wolyniec, Daniele Fallin, Gerald Nestadt, Kung‐Yee Liang, Ann E. Pulver, David Valle, Dimitrios Avramopoulos	36
5	Linkage and association on 8p21.2-p21.1 in schizophrenia 2010 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·M. Daniele Fallin, Virginia K. Lasseter, Yaping Liu, Dimitrios Avramopoulos, John A. McGrath, Paula Wolyniec, Gerald Nestadt, Kung‐Yee Liang, Pei-Lung Chen, David Valle, Ann E. Pulver	25
6	Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia 2009 ·The American Journal of Human Genetics ·Pei-Lung Chen, Dimitrios Avramopoulos, Virginia K. Lasseter, John A. McGrath, M. Daniele Fallin, Kung‐Yee Liang, Gerald Nestadt, Ningping Feng, Gary Steel, Andrew S. Cutting, Paula Wolyniec, Ann E. Pulver, David Valle	67
7	Familiality of Novel Factorial Dimensions of Schizophrenia 2009 ·Archives of General Psychiatry ·John A. McGrath, Dimitrios Avramopoulos, Virginia K. Lasseter, Paula Wolyniec, M. Daniele Fallin, Kung‐Yee Liang, Gerald Nestadt, Mary H. Thornquist, James R. Luke, Pei-Lung Chen, David Valle, Ann E. Pulver	61
8	Translational repression restricts expression of the C. elegans Nanos homolog NOS-2 to the embryonic germline 2006 ·Developmental Biology ·(unknown), Chris Merritt, Pei-Lung Chen, Géraldine Seydoux, Kuppuswamy Subramaniam	73

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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