Rini Pauly

583 total citations
31 papers, 335 citations indexed

About

Rini Pauly is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Rini Pauly has authored 31 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Rini Pauly's work include Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Rini Pauly is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Rini Pauly collaborates with scholars based in United States, Italy and Canada. Rini Pauly's co-authors include Luigi Boccuto, Sujata Srikanth, Roger E. Stevenson, Charles E. Schwartz, Cindy Skinner, Sriram Chandrasekaran, Robert M. Brucker, Seth R. Bordenstein, Kelly L. Jones and Jane H. Dean and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Journal of Clinical Oncology.

In The Last Decade

Rini Pauly

29 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rini Pauly United States 9 171 90 29 29 29 31 335
Rachita Yadav United States 12 192 1.1× 68 0.8× 12 0.4× 61 2.1× 14 0.5× 20 539
Marie Vincent France 16 422 2.5× 168 1.9× 32 1.1× 86 3.0× 21 0.7× 41 635
Elvira Khialeeva United States 8 141 0.8× 40 0.4× 15 0.5× 19 0.7× 75 2.6× 11 321
M. Cecilia Ljungberg United States 9 342 2.0× 155 1.7× 15 0.5× 24 0.8× 24 0.8× 17 601
Kristin Hartmann Germany 10 125 0.7× 58 0.6× 29 1.0× 18 0.6× 37 1.3× 17 330
Atsuhiko Sakai Japan 7 386 2.3× 97 1.1× 20 0.7× 22 0.8× 14 0.5× 10 505
Ivonne Jericó Spain 14 338 2.0× 43 0.5× 9 0.3× 30 1.0× 57 2.0× 35 632
Fangfang Zhu China 12 445 2.6× 75 0.8× 7 0.2× 27 0.9× 53 1.8× 29 735
Riina Žordania Estonia 12 182 1.1× 140 1.6× 15 0.5× 19 0.7× 24 0.8× 25 350
Justyna Augustyniak Poland 11 199 1.2× 37 0.4× 27 0.9× 17 0.6× 8 0.3× 19 317

Countries citing papers authored by Rini Pauly

Since Specialization
Citations

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

Fields of papers citing papers by Rini Pauly

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rini Pauly

This figure shows the co-authorship network connecting the top 25 collaborators of Rini Pauly. A scholar is included among the top collaborators of Rini Pauly 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 Rini Pauly. Rini Pauly 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
1.
Pauly, Rini & F. Alex Feltus. (2024). Simplified detection of genetic background admixture using artificial intelligence. Clinical Genetics. 106(3). 247–257. 1 indexed citations
2.
Konaté, Mariam M., Julia Krushkal, Li Chen, et al.. (2024). Insights into gemcitabine resistance in pancreatic cancer: association with metabolic reprogramming and TP53 pathogenicity in patient derived xenografts. Journal of Translational Medicine. 22(1). 733–733. 3 indexed citations
3.
Le, Bao T., Rini Pauly, Li Chen, et al.. (2024). Molecular profiling of plasma from matched NCI-MATCH gynecological cancers.. Journal of Clinical Oncology. 42(16_suppl). 5579–5579.
4.
Pauly, Rini, et al.. (2024). PhenoMetaboDiff: R Package for Analysis and Visualization of Phenotype Microarray Data. Genes. 15(11). 1362–1362.
5.
Oberman, Lindsay M., Sujata Srikanth, Kelly L. Jones, et al.. (2023). Sleep disturbances in Phelan‐McDermid syndrome: Clinical and metabolic profiling of 56 individuals. Clinical Genetics. 104(2). 198–209. 2 indexed citations
6.
Pauly, Rini, et al.. (2022). Discovery of eQTL Alleles Associated with Autism Spectrum Disorder: A Case–Control Study. Journal of Autism and Developmental Disorders. 53(9). 3595–3612. 4 indexed citations
7.
Pauly, Rini, et al.. (2022). Identification of condition-specific regulatory mechanisms in normal and cancerous human lung tissue. BMC Genomics. 23(1). 350–350. 1 indexed citations
8.
Bonner, Erin R., Robin A. Harrington, Miriam Bornhorst, et al.. (2022). Circulating tumor DNA sequencing provides comprehensive mutation profiling for pediatric central nervous system tumors. npj Precision Oncology. 6(1). 63–63. 7 indexed citations
9.
10.
Srikanth, Sujata, Cinthya Zepeda‐Mendoza, Kelly L. Jones, et al.. (2021). Position effects of 22q13 rearrangements on candidate genes in Phelan-McDermid syndrome. PLoS ONE. 16(7). e0253859–e0253859. 6 indexed citations
11.
Schenkel, Laila C., Erfan Aref‐Eshghi, Kathleen Rooney, et al.. (2021). DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome. Clinical Epigenetics. 13(1). 2–2. 21 indexed citations
12.
Pauly, Rini, et al.. (2020). New Strategies for Clinical Trials in Autism Spectrum Disorder. Reviews on Recent Clinical Trials. 16(2). 131–137. 2 indexed citations
13.
Pauly, Rini & Charles E. Schwartz. (2020). The Future of Clinical Diagnosis. Clinics in Laboratory Medicine. 40(2). 221–230. 1 indexed citations
14.
Pauly, Rini & Charles E. Schwartz. (2019). The Future of Clinical Diagnosis. 2(1). 13–19. 2 indexed citations
15.
16.
Li, Chong, Jennifer M. Brazill, Yi Zhu, et al.. (2017). Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome. Nature Communications. 8(1). 1257–1257. 65 indexed citations
17.
Kowalski, Jeanne, Bhakti Dwivedi, Scott Newman, et al.. (2016). Gene integrated set profile analysis: a context-based approach for inferring biological endpoints. Nucleic Acids Research. 44(7). e69–e69. 6 indexed citations
18.
Brucker, Robert M., et al.. (2012). Insect Innate Immunity Database (IIID): An Annotation Tool for Identifying Immune Genes in Insect Genomes. PLoS ONE. 7(9). e45125–e45125. 35 indexed citations
19.
Küerten, Stefanie, Rini Pauly, Stefan Blaschke, et al.. (2011). Die Relevanz einer B-Zell-abhängigen Immunpathologie für die Multiple Sklerose. Fortschritte der Neurologie · Psychiatrie. 79(2). 83–91. 6 indexed citations
20.
Ginzel, K. H., Gert S. Maritz, David F Marks, et al.. (2007). Nicotine for the Fetus, the Infant and the Adolescent?. 8 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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2026