Felipe Lorenzo

3.5k total citations · 1 hit paper
39 papers, 2.0k citations indexed

About

Felipe Lorenzo is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Felipe Lorenzo has authored 39 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 11 papers in Physiology. Recurrent topics in Felipe Lorenzo's work include Cancer, Hypoxia, and Metabolism (10 papers), Erythrocyte Function and Pathophysiology (9 papers) and High Altitude and Hypoxia (7 papers). Felipe Lorenzo is often cited by papers focused on Cancer, Hypoxia, and Metabolism (10 papers), Erythrocyte Function and Pathophysiology (9 papers) and High Altitude and Hypoxia (7 papers). Felipe Lorenzo collaborates with scholars based in United States, China and India. Felipe Lorenzo's co-authors include Josef T. Prchal, Tatum S. Simonson, Chad D. Huff, Lynn B. Jorde, Yingzhong Yang, Zhenzhong Bai, Ri-Li Ge, Jinchuan Xing, Haixia Yun and David J. Witherspoon and has published in prestigious journals such as Science, New England Journal of Medicine and Journal of Biological Chemistry.

In The Last Decade

Felipe Lorenzo

37 papers receiving 2.0k 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.

Genetic Evidence for High-Altitude Adaptation in Tibet

2010 862 citations Tatum S. Simonson, Yingzhong Yang et al. Science profile →

Peers

Felipe Lorenzo

GENET

PHYSI

SURGE

Martin Knöfler Austria

Alex Parker United States

Ricardo C. Ferreira United Kingdom

Almaz Aldashev Kyrgyzstan

Jonathan D. Wasserman Canada

Aleksandar Rajkovic United States

Thomas J. Musci United States

Xiayi Ke United Kingdom

Karen E. Heath Spain

Keisuke Nagasaki Japan

Martin Knöfler Austria

Felipe Lorenzo

811 ×0.8

GENET

735 ×1.1

3.0k ×5.8

181 ×0.5

PHYSI

810 ×2.4

SURGE

Citations per year, relative to Felipe Lorenzo Felipe Lorenzo (= 1×) peers Martin Knöfler

Countries citing papers authored by Felipe Lorenzo

Since Specialization

Citations

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

Fields of papers citing papers by Felipe Lorenzo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Felipe Lorenzo

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

20 of 20 papers shown

Wang, Zhan, Qingxia Zhao, Manal Zabalawi, et al.. (2023). Pyruvate dehydrogenase kinase supports macrophage NLRP3 inflammasome activation during acute inflammation. Cell Reports. 42(1). 111941–111941. 30 indexed citations

Gao, Yan, et al.. (2019). Iron down-regulates leptin by suppressing protein O-GlcNAc modification in adipocytes, resulting in decreased levels of O-glycosylated CREB. Journal of Biological Chemistry. 294(14). 5487–5495. 22 indexed citations

Tashi, Tsewang, N. Scott Reading, Xu Zhang, et al.. (2017). Gain-of-function EGLN1 prolyl hydroxylase (PHD2 D4E:C127S) in combination with EPAS1 (HIF-2α) polymorphism lowers hemoglobin concentration in Tibetan highlanders. Journal of Molecular Medicine. 95(6). 665–670. 58 indexed citations

Hu, Hao, Nayia Petousi, Gustavo Glusman, et al.. (2017). Evolutionary history of Tibetans inferred from whole-genome sequencing. PLoS Genetics. 13(4). e1006675–e1006675. 78 indexed citations

Downie, Jonathan M., Tsewang Tashi, Felipe Lorenzo, et al.. (2016). A Genome-Wide Search for Greek and Jewish Admixture in the Kashmiri Population. PLoS ONE. 11(8). e0160614–e0160614. 8 indexed citations

Pacák, Karel, Emily Y. Chew, Alberto S. Pappo, et al.. (2014). Ocular Manifestations of Hypoxia-Inducible Factor-2α Paraganglioma-Somatostatinoma-Polycythemia Syndrome. Ophthalmology. 121(11). 2291–2293. 23 indexed citations

Tashi, Tsewang, Parvaiz A Koul, Ricardo Amaru, et al.. (2014). High altitude genetic adaptation in Tibetans: No role of increased hemoglobin–oxygen affinity. Blood Cells Molecules and Diseases. 53(1-2). 27–29. 21 indexed citations

Lorenzo, Felipe, Chunzhang Yang, Mark Ng Tang Fui, et al.. (2012). A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paraganglioma. Journal of Molecular Medicine. 91(4). 507–512. 131 indexed citations

Zhuang, Zhengping, Chunzhang Yang, Felipe Lorenzo, et al.. (2012). SomaticHIF2AGain-of-Function Mutations in Paraganglioma with Polycythemia. New England Journal of Medicine. 367(10). 922–930. 278 indexed citations

10.

Lorenzo, Felipe, John D. Phillips, Roberto Nussenzveig, et al.. (2011). Molecular basis of two novel mutations found in type I methemoglobinemia. Blood Cells Molecules and Diseases. 46(4). 277–281. 16 indexed citations

11.

Simonson, Tatum S., Yingzhong Yang, Chad D. Huff, et al.. (2010). Genetic Evidence for High-Altitude Adaptation in Tibet. Science. 329(5987). 72–75. 862 indexed citations breakdown →

12.

Lorenzo, Felipe, Toshinori Tanaka, Hideyuki Takahashi, et al.. (2008). Mutational events during the primary propagation and consecutive passages of hepatitis E virus strain JE03-1760F in cell culture. Virus Research. 137(1). 86–96. 46 indexed citations

13.

Tsatsralt‐Od, Bira, Masaharu Takahashi, Kazunori Endo, et al.. (2007). Prevalence of hepatitis B, C, and delta virus infections among children in Mongolia: Progress in childhood immunization. Journal of Medical Virology. 79(8). 1064–1074. 18 indexed citations

14.

Lorenzo, Felipe, et al.. (2007). Analysis of the full‐length genome of hepatitis E virus isolates obtained from farm pigs in Mongolia. Journal of Medical Virology. 79(8). 1128–1137. 25 indexed citations

15.

Monma, Fumihiko, Kazuhiro Nishii, Shunji Yamamori, et al.. (2006). Molecular and phenotypic analysis of Philadelphia chromosome-positive bilineage leukemia: possibility of a lineage switch from T-lymphoid leukemic progenitor to myeloid cells. Cancer Genetics and Cytogenetics. 164(2). 118–121. 19 indexed citations

16.

Nishii, Kazuhiro, Naoyuki Katayama, Hideaki Maeda, et al.. (2001). Successful treatment with low‐dose splenic irradiation for massive splenomegaly in an elderly patient with hairy‐cell leukemia. European Journal Of Haematology. 67(4). 255–257. 11 indexed citations

17.

Kottler, Marie‐Laure, et al.. (1995). Subregional mapping of the human gonadotropin-releasing hormone receptor (GnRH-R) gene to 4q between the markers D4S392 and D4S409. Human Genetics. 96(4). 477–80. 19 indexed citations

18.

Lorenzo, Felipe, Nicole Dalla Venezia, Laurette Morlé, et al.. (1994). Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton.. Journal of Clinical Investigation. 94(4). 1651–1656. 29 indexed citations

19.

Lorenzo, Felipe, Antonella Monticelli, Sergio Cocozza, Benedetto Simone, & Paolo Rubba. (1994). Extracoronary atherosclerosis and genetic variants of apolipoprotein AI-CIII cluster in myocardial infarction survivors from southern Italy. Journal of Molecular Medicine. 72(6). 435–41. 5 indexed citations

20.

Lorenzo, Felipe, Emanuele Miraglia del Giudice, Nicole Alloisio, et al.. (1993). Severe poikilocytosis associated with a de novoα28 Arg→Cys mutation in spectrin. British Journal of Haematology. 83(1). 152–157. 15 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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