Paul C. Lott

2.8k total citations · 1 hit paper
23 papers, 1.7k citations indexed

About

Paul C. Lott is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Paul C. Lott has authored 23 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Pathology and Forensic Medicine and 6 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Paul C. Lott's work include Genetic factors in colorectal cancer (6 papers), Epigenetics and DNA Methylation (5 papers) and Thyroid Cancer Diagnosis and Treatment (4 papers). Paul C. Lott is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), Epigenetics and DNA Methylation (5 papers) and Thyroid Cancer Diagnosis and Treatment (4 papers). Paul C. Lott collaborates with scholars based in United States, Colombia and United Kingdom. Paul C. Lott's co-authors include Ian Korf, Frédéric Chédin, Paul A. Ginno, Yoong Wearn Lim, Luis G. Carvajal‐Carmona, Janine M. LaSalle, Diane I. Schroeder, Cheryl K. Walker, John D. Blair and Wendy P. Robinson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Molecular Cell and Bioinformatics.

In The Last Decade

Paul C. Lott

22 papers receiving 1.6k 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.

R-Loop Formation Is a Distinctive Characteristic of Unmethylated Human CpG Island Promoters

2012 641 citations Paul A. Ginno, Paul C. Lott et al. Molecular Cell profile →

Peers

Paul C. Lott

GENET

PPCH

Florencia Pauli United States

Małgorzata J.M. Nowaczyk Canada

Xiaoji Wu United States

Marcel W. Coolen Netherlands

Lorena Pantano United States

Sam Buckberry Australia

Omkaram Gangisetty United States

Pavlo Lutsik Germany

Laura Crisponi Italy

Lawrence C. Layman United States

Florencia Pauli United States

Paul C. Lott

1.8k ×1.3

589 ×2.0

GENET

269 ×1.7

120 ×0.9

PPCH

158 ×1.4

Citations per year, relative to Paul C. Lott Paul C. Lott (= 1×) peers Florencia Pauli

Countries citing papers authored by Paul C. Lott

Since Specialization

Citations

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

Fields of papers citing papers by Paul C. Lott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul C. Lott. 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 Paul C. Lott. The network helps show where Paul C. Lott may publish in the future.

Co-authorship network of co-authors of Paul C. Lott

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

All Works

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20 of 20 papers shown

Lott, Paul C., et al.. (2024). Development and Application of Genetic Ancestry Reconstruction Methods to Study Diversity of Patient-Derived Models in the NCI PDXNet Consortium. Cancer Research Communications. 4(8). 2147–2152. 1 indexed citations

Toal, Ted, Ana P. Estrada-Florez, Guadalupe Polanco‐Echeverry, et al.. (2022). Multiregional Sequencing Analysis Reveals Extensive Genetic Heterogeneity in Gastric Tumors from Latinos. Cancer Research Communications. 2(11). 1487–1496. 7 indexed citations

Cardoso, Marta, Sofia Maia, Andreia Brandão, et al.. (2022). Exome sequencing of affected duos and trios uncovers PRUNE2 as a novel prostate cancer predisposition gene. British Journal of Cancer. 128(6). 1077–1085. 6 indexed citations

Filshtein, Teresa, Brittany N. Dugger, Lee‐Way Jin, et al.. (2019). Neuropathological Diagnoses of Demented Hispanic, Black, and Non-Hispanic White Decedents Seen at an Alzheimer’s Disease Center. Journal of Alzheimer s Disease. 68(1). 145–158. 65 indexed citations

Lott, Paul C. & Luis G. Carvajal‐Carmona. (2018). Resolving gastric cancer aetiology: an update in genetic predisposition. The Lancet. Gastroenterology & hepatology. 3(12). 874–883. 63 indexed citations

Dunaway, Keith W., Mohammad Saharul Islam, Rochelle L. Coulson, et al.. (2016). Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes. Cell Reports. 17(11). 3035–3048. 55 indexed citations

Estrada-Florez, Ana P., Mábel Bohórquez, Ruta Sahasrabudhe, et al.. (2016). Clinical features of Hispanic thyroid cancer cases and the role of known genetic variants on disease risk. Medicine. 95(32). e4148–e4148. 12 indexed citations

Bohórquez, Mábel, Ana P. Estrada-Florez, Jacob Stultz, et al.. (2016). The HABP2 G534E polymorphism does not increase nonmedullary thyroid cancer risk in Hispanics. Endocrine Connections. 5(3). 123–127. 12 indexed citations

Sahasrabudhe, Ruta, Ana P. Estrada-Florez, Paul C. Lott, et al.. (2015). The 8q24 rs6983267G variant is associated with increased thyroid cancer risk. Endocrine Related Cancer. 22(5). 841–849. 15 indexed citations

10.

Sahasrabudhe, Ruta, Paul C. Lott, John B. Williamson, et al.. (2014). Abstract 42: Development of low-cost high-throughput screening methods for detecting germline mutations in multiple cancer genes. Cancer Research. 74(23_Supplement). 42–42. 1 indexed citations

11.

Ginno, Paul A., Yoong Wearn Lim, Paul C. Lott, Ian Korf, & Frédéric Chédin. (2013). GC skew at the 5′ and 3′ ends of human genes links R-loop formation to epigenetic regulation and transcription termination. Genome Research. 23(10). 1590–1600. 275 indexed citations

12.

Schroeder, Diane I., John D. Blair, Paul C. Lott, et al.. (2013). The human placenta methylome. Proceedings of the National Academy of Sciences. 110(15). 6037–6042. 221 indexed citations

13.

Ginno, Paul A., et al.. (2012). R-Loop Formation Is a Distinctive Characteristic of Unmethylated Human CpG Island Promoters. Molecular Cell. 45(6). 814–825. 641 indexed citations breakdown →

14.

Schroeder, Diane I., Paul C. Lott, Ian Korf, & Janine M. LaSalle. (2011). Large-scale methylation domains mark a functional subset of neuronally expressed genes. Genome Research. 21(10). 1583–1591. 67 indexed citations

15.

Yamagami, Takashi, Qini Gan, Yongping Wang, et al.. (2011). Canonical Wnt signaling promotes the proliferation and neurogenesis of peripheral olfactory stem cells during postnatal development and adult regeneration. Journal of Cell Science. 124(9). 1553–1563. 52 indexed citations

16.

Gociman, Barbu, Andreas Rohrwasser, Elaine Hillas, et al.. (2008). Response to genetic manipulations of liver angiotensinogen in the physiological range. Journal of Human Genetics. 53(9). 775–788. 4 indexed citations

17.

Rohrwasser, Andreas, Paul C. Lott, Robert B. Weiss, & Jean‐Marc Lalouel. (2008). From Genetics to Mechanism of Disease Liability. Advances in genetics. 60. 701–726. 6 indexed citations

18.

Amiott, Elizabeth, Paul C. Lott, Jamie Soto, et al.. (2008). Mitochondrial fusion and function in Charcot–Marie–Tooth type 2A patient fibroblasts with mitofusin 2 mutations. Experimental Neurology. 211(1). 115–127. 84 indexed citations

19.

Gociman, Barbu, Andreas Rohrwasser, Pierre Lantelme, et al.. (2004). Expression of angiotensinogen in proximal tubule as a function of glomerular filtration rate. Kidney International. 65(6). 2153–2160. 26 indexed citations

20.

Driel, Mieke van, et al.. (1998). 303. Response to flumazenil in women with premenstrual dysphoric disorder. Biological Psychiatry. 43(8). S91–S91. 4 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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