Lisette Nevarez

1.3k total citations
13 papers, 542 citations indexed

About

Lisette Nevarez is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Lisette Nevarez has authored 13 papers receiving a total of 542 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Immunology. Recurrent topics in Lisette Nevarez's work include Connective tissue disorders research (6 papers), Cell Adhesion Molecules Research (3 papers) and Inflammation biomarkers and pathways (2 papers). Lisette Nevarez is often cited by papers focused on Connective tissue disorders research (6 papers), Cell Adhesion Molecules Research (3 papers) and Inflammation biomarkers and pathways (2 papers). Lisette Nevarez collaborates with scholars based in United States, Saudi Arabia and Spain. Lisette Nevarez's co-authors include Daniel H. Cohn, Deborah Krakow, Clifford A. Lowell, Steven S. Branda, Catherine Branda, William E. Seaman, Elsa-Noah N’Diaye, Marco Colonna, Jessica A. Hamerman and Ralph S. Lachman and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Experimental Medicine and The Journal of Cell Biology.

In The Last Decade

Lisette Nevarez

13 papers receiving 537 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lisette Nevarez United States	9	264	242	176	128	52	13	542
Neal D. Heuss United States	18	222 0.8×	53 0.2×	293 1.7×	178 1.4×	31 0.6×	28	666
Robert Feakes United Kingdom	8	197 0.7×	164 0.7×	331 1.9×	26 0.2×	111 2.1×	9	702
Elizabeth Kropf United States	11	196 0.7×	96 0.4×	175 1.0×	32 0.3×	11 0.2×	14	510
Ken Flanagan United States	9	185 0.7×	38 0.2×	250 1.4×	170 1.3×	23 0.4×	12	565
Mariam Al‐Mureikhi Qatar	12	334 1.3×	280 1.2×	33 0.2×	37 0.3×	24 0.5×	18	591
Wouter Steyaert Belgium	14	392 1.5×	318 1.3×	29 0.2×	29 0.2×	86 1.7×	27	639
Petra Vogelsang Norway	15	186 0.7×	107 0.4×	179 1.0×	20 0.2×	100 1.9×	20	603
Cecily Q. Bernales Canada	12	147 0.6×	47 0.2×	136 0.8×	28 0.2×	37 0.7×	23	381
Wenyi Wu China	13	352 1.3×	77 0.3×	48 0.3×	20 0.2×	21 0.4×	38	537
Michela Manni United States	15	148 0.6×	37 0.2×	366 2.1×	37 0.3×	114 2.2×	19	607

Countries citing papers authored by Lisette Nevarez

Since Specialization

Citations

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

Fields of papers citing papers by Lisette Nevarez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lisette Nevarez

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

All Works

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13 of 13 papers shown

Zieba, Jennifer, et al.. (2023). Altered Sox9 and FGF signaling gene expression in Aga2 OI mice negatively affects linear growth. JCI Insight. 8(21). 4 indexed citations

Zhang, Wenjuan, S. Paige Taylor, Iván Durán, et al.. (2017). Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies. Human Mutation. 39(1). 152–166. 83 indexed citations

Bae, Yangjin, Ming-Ming Jiang, David S. Liu, et al.. (2017). Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasia. Journal of Clinical Investigation. 127(4). 1475–1484. 53 indexed citations

Li, Bing, Deborah Krakow, Lisette Nevarez, et al.. (2017). MED resulting from recessively inherited mutations in the gene encoding calcium‐activated nucleotidase CANT1. American Journal of Medical Genetics Part A. 173(9). 2415–2421. 21 indexed citations

Zhang, Wenjuan, S. Paige Taylor, Lisette Nevarez, et al.. (2016). IFT52mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome. Human Molecular Genetics. 25(18). 4012–4020. 34 indexed citations

Durán, Iván, Jorge Martı́n, Lisette Nevarez, et al.. (2016). Correction: Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis. PLoS Genetics. 12(12). e1006502–e1006502. 3 indexed citations

Lee, Hane, Lisette Nevarez, Ralph S. Lachman, et al.. (2015). A second locus for schneckenbecken dysplasia identified by a mutation in the gene encoding inositol polyphosphate phosphatase‐like 1 (INPPL1). American Journal of Medical Genetics Part A. 167(10). 2470–2473. 8 indexed citations

Durán, Iván, Lisette Nevarez, Pavel Krejčı́, et al.. (2014). HSP47 and FKBP65 cooperate in the synthesis of type I procollagen. Human Molecular Genetics. 24(7). 1918–1928. 45 indexed citations

Tompson, Stuart W., Eissa Faqeih, Leena Ala‐Kokko, et al.. (2012). Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2. American Journal of Medical Genetics Part A. 158A(2). 309–314. 13 indexed citations

10.

Tompson, Stuart W., Carlos A. Bacino, Nicole P. Safina, et al.. (2010). Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene. The American Journal of Human Genetics. 87(5). 708–712. 54 indexed citations

11.

Funari, Vincent, Deborah Krakow, Lisette Nevarez, et al.. (2010). BMPER Mutation in Diaphanospondylodysostosis Identified by Ancestral Autozygosity Mapping and Targeted High-Throughput Sequencing. The American Journal of Human Genetics. 87(4). 532–537. 26 indexed citations

12.

N’Diaye, Elsa-Noah, Catherine Branda, Steven S. Branda, et al.. (2009). TREM-2 (triggering receptor expressed on myeloid cells 2) is a phagocytic receptor for bacteria. The Journal of Experimental Medicine. 206(2). i3–i3. 3 indexed citations

13.

N’Diaye, Elsa-Noah, Catherine Branda, Steven S. Branda, et al.. (2009). TREM-2 (triggering receptor expressed on myeloid cells 2) is a phagocytic receptor for bacteria. The Journal of Cell Biology. 184(2). 215–223. 195 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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