Annie Pao

3.2k total citations · 1 hit paper
29 papers, 2.3k citations indexed

About

Annie Pao is a scholar working on Molecular Biology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Annie Pao has authored 29 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 14 papers in Genetics and 10 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Annie Pao's work include Down syndrome and intellectual disability research (10 papers), DNA Repair Mechanisms (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Annie Pao is often cited by papers focused on Down syndrome and intellectual disability research (10 papers), DNA Repair Mechanisms (9 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Annie Pao collaborates with scholars based in United States, Canada and China. Annie Pao's co-authors include Moon‐shong Tang, Gerd P. Pfeifer, Mikhail F. Denissenko, Yichao Yu, Zhongyou Li, Tao Yu, Masae Morishima, William C. Mobley, Chunhong Liu and Jeffrey M. Conroy and has published in prestigious journals such as Science, Journal of Biological Chemistry and Molecular and Cellular Biology.

In The Last Decade

Annie Pao

29 papers receiving 2.2k citations

Hit Papers

Preferential Formation of Benzo[ a ]pyrene Adducts at Lun... 1996 2026 2006 2016 1996 400 800 1.2k
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.

  1. Preferential Formation of Benzo[ a ]pyrene Adducts at Lung Cancer Mutational Hotspots in P53
    1996 1.3k citations Mikhail F. Denissenko, Annie Pao et al. profile →

Peers

Annie Pao
Kathleen T. Shiverick United States
Francesco Marchetti United States
Sumedha Gunewardena United States
Kiminobu Goto Japan
Christa E. Flück Switzerland
Erika Ginsburg United States
Vincent L. Wilson United States
Hongmei Nan United States
Patricia Ruíz Germany
Nicholas P. Illsley United States
Kathleen T. Shiverick United States
Annie Pao
Citations per year, relative to Annie Pao Annie Pao (= 1×) peers Kathleen T. Shiverick

Countries citing papers authored by Annie Pao

Since Specialization
Citations

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

Fields of papers citing papers by Annie Pao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annie Pao

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

All Works

20 of 20 papers shown
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2.
Yu, Yichao, Zhuo Xing, Catherine Do, et al.. (2020). Genetic and epigenetic pathways in Down syndrome: Insights to the brain and immune system from humans and mouse models. Progress in brain research. 251. 1–28. 22 indexed citations
3.
Xing, Zhuo, Lei Wei, Xiaoling Jiang, et al.. (2018). Analysis of mutations in primary and metastatic synovial sarcoma. Oncotarget. 9(96). 36878–36888. 13 indexed citations
4.
Xing, Zhuo, Yichen Li, Annie Pao, et al.. (2016). Mouse-based genetic modeling and analysis of Down syndrome. British Medical Bulletin. 120(1). 111–122. 18 indexed citations
5.
Jiang, Xiaoling, Chunhong Liu, Tao Yu, et al.. (2015). Genetic dissection of the Down syndrome critical region. Human Molecular Genetics. 24(22). 6540–6551. 58 indexed citations
6.
Zhang, Lijun, Kai Meng, Xiaoling Jiang, et al.. (2013). Human chromosome 21 orthologous region on mouse chromosome 17 is a major determinant of Down syndrome-related developmental cognitive deficits. Human Molecular Genetics. 23(3). 578–589. 33 indexed citations
7.
Liu, Chunhong, Masae Morishima, Xiaoling Jiang, et al.. (2013). Engineered chromosome-based genetic mapping establishes a 3.7 Mb critical genomic region for Down syndrome-associated heart defects in mice. Human Genetics. 133(6). 743–753. 25 indexed citations
8.
Zhang, Li, Da‐Wei Fu, Pavel V. Belichenko, et al.. (2012). Genetic analysis of Down syndrome facilitated by mouse chromosome engineering. Bioengineered. 3(1). 8–12. 10 indexed citations
9.
Liu, Chunhong, Masae Morishima, Tao Yu, et al.. (2011). Genetic analysis of Down syndrome-associated heart defects in mice. Human Genetics. 130(5). 623–632. 37 indexed citations
10.
Wen, Lei, Jeane Silva, Zhongyou Li, et al.. (2010). Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability. Human Molecular Genetics. 19(9). 1702–1711. 92 indexed citations
11.
Yu, Tao, Chunhong Liu, Pavel V. Belichenko, et al.. (2010). Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice. Brain Research. 1366. 162–171. 89 indexed citations
12.
Yu, Tao, Steven J. Clapcote, Zhongyou Li, et al.. (2010). Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice. Mammalian Genome. 21(5-6). 258–267. 23 indexed citations
13.
Li, Zhongyou, Tao Yu, Masae Morishima, et al.. (2007). Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities. Human Molecular Genetics. 16(11). 1359–1366. 144 indexed citations
14.
Li, Zhongyou, Paul F. Szurek, Annie Pao, et al.. (2005). Neuronal differentiation of NTE-deficient embryonic stem cells. Biochemical and Biophysical Research Communications. 330(4). 1103–1109. 12 indexed citations
15.
Tang, Moon‐shong, Gerd P. Pfeifer, Mikhail F. Denissenko, et al.. (2002). Mapping polycyclic aromatic hydrocarbon and aromatic amine-induced DNA damage in cancer-related genes at the sequence level. International Journal of Hygiene and Environmental Health. 205(1-2). 103–113. 9 indexed citations
16.
Feng, Zhaohui, Wenwei Hu, Elena V. Komissarova, et al.. (2002). Transcription-coupled DNA Repair Is Genomic Context-dependent. Journal of Biological Chemistry. 277(15). 12777–12783. 21 indexed citations
17.
Zheng, Yi, Annie Pao, Gerald M. Adair, & Moon‐shong Tang. (2001). Cyclobutane Pyrimidine Dimers and Bulky Chemical DNA Adducts Are Efficiently Repaired in Both Strands of Either a Transcriptionally Active or Promoter-deleted APRT Gene. Journal of Biological Chemistry. 276(20). 16786–16796. 20 indexed citations
18.
Wang, Shao‐Chun, Keisuke Makino, Li-Kuo Su, et al.. (2001). Ultraviolet irradiation induces BRCA2 protein depletion through a p53-independent and protein synthesis-dependent pathway.. PubMed. 61(7). 2838–42. 11 indexed citations
19.
20.
Doermann, A. H. & Annie Pao. (1987). Genetic control of capsid length in bacteriophage T4: phenotypes displayed by ptg mutants. Journal of Virology. 61(9). 2835–2842. 9 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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