Carolina Muchnik

2.6k total citations
6 papers, 45 citations indexed

About

Carolina Muchnik is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Carolina Muchnik has authored 6 papers receiving a total of 45 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Psychiatry and Mental health. Recurrent topics in Carolina Muchnik's work include Hedgehog Signaling Pathway Studies (3 papers), Dementia and Cognitive Impairment Research (2 papers) and Genetic and rare skin diseases. (2 papers). Carolina Muchnik is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Dementia and Cognitive Impairment Research (2 papers) and Genetic and rare skin diseases. (2 papers). Carolina Muchnik collaborates with scholars based in Argentina, Germany and United States. Carolina Muchnik's co-authors include Pablo Javier Azurmendi, Fernando Stengel, Luis Daniel Mazzuoccolo, Alfredo P. Martínez, Luis Ignacio Brusco, Elvira Arrizurieta, Laura Morelli, Rodolfo S. Martín, Cecilia Forcato and Patricia Solís and has published in prestigious journals such as PLoS ONE, Neurobiology of Aging and Cells.

In The Last Decade

Carolina Muchnik

6 papers receiving 44 citations

Peers

Carolina Muchnik

MB

GENET

DERMA

NEPHR

EPIDE

Belén Gil-Fournier Spain

Keta Joshipura United States

Naomi Yachelevich United States

Mike A. Nalls United States

Henrik Åhlman Sweden

Rui Kishimoto Japan

Xiuqing Guo United States

Lal D V Nair India

Kisung Nam South Korea

Kimberly Nugent United States

Belén Gil-Fournier Spain

Carolina Muchnik

16 ×0.6

MB

10 ×0.7

GENET

2 ×0.3

DERMA

3 ×0.5

NEPHR

1 ×0.2

EPIDE

Citations per year, relative to Carolina Muchnik Carolina Muchnik (= 1×) peers Belén Gil-Fournier

Countries citing papers authored by Carolina Muchnik

Since Specialization

Citations

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

Fields of papers citing papers by Carolina Muchnik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carolina Muchnik

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

All Works

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6 of 6 papers shown

1.

Muchnik, Carolina, Patricia Solís, Nancy Medel, et al.. (2020). Memory reconsolidation as a tool to endure encoding deficits in elderly. PLoS ONE. 15(8). e0237361–e0237361. 7 indexed citations

2.

Martínez, Alfredo P., et al.. (2019). Nevoid Basal Cell Carcinoma Syndrome: PTCH1 Mutation Profile and Expression of Genes Involved in the Hedgehog Pathway in Argentinian Patients. Cells. 8(2). 144–144. 17 indexed citations

3.

Mazzuoccolo, Luis Daniel, et al.. (2018). Co-Inheritance of Autosomal Dominant Polycystic Kidney Disease and Naevoid Basal Cell Carcinoma Syndrome: Effects on Renal Progression. The Nephron journals/Nephron journals. 140(4). 282–288. 2 indexed citations

4.

Muchnik, Carolina, Natividad Olivar, Carolina Dalmasso, et al.. (2015). Identification of PSEN2 mutation p.N141I in Argentine pedigrees with early-onset familial Alzheimer's disease. Neurobiology of Aging. 36(10). 2674–2677.e1. 7 indexed citations

5.

Mazzuoccolo, Luis Daniel, et al.. (2014). [Nevoid basal cell carcinoma syndrome with corpus callosum agenesis, PTCH1 mutation and absence of basal cell carcinoma].. PubMed. 74(4). 307–10. 3 indexed citations

6.

Azurmendi, Pablo Javier, et al.. (2004). [Progression of autosomic dominant polycystic kidney disease. Influence of endothelial NO synthase (ecNOS) and renin angiotensin system gene polymorphisms].. PubMed. 64(2). 139–42. 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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