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Institution

University of Costa Rica

EducationSan José, Costa Rica
About: University of Costa Rica is a education organization based out in San José, Costa Rica. It is known for research contribution in the topics: Population & Venom. The organization has 9817 authors who have published 16781 publications receiving 238208 citations. The organization is also known as: UCR & Universidad de Costa Rica.


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Journal Article

626 citations

Journal ArticleDOI
10 Apr 2003-Nature
TL;DR: The anammox reaction is shown to be a globally significant sink for oceanic nitrogen in the anoxic waters of Golfo Dulce, a 200-m-deep coastal bay in Costa Rica, where it accounts for 19–35% of the total N2 formation in the water column.
Abstract: In oxygen-depleted zones of the open ocean, and in anoxic basins and fjords, denitrification (the bacterial reduction of nitrate to give N2) is recognized as the only significant process converting fixed nitrogen to gaseous N2. Primary production in the oceans is often limited by the availability of fixed nitrogen such as ammonium or nitrate1, and nitrogen-removal processes consequently affect both ecosystem function and global biogeochemical cycles. It was recently discovered that the anaerobic oxidation of ammonium with nitrite—the ‘anammox’ reaction, performed by bacteria—was responsible for a significant fraction of N2 production in some marine sediments2. Here we show that this reaction is also important in the anoxic waters of Golfo Dulce, a 200-m-deep coastal bay in Costa Rica, where it accounts for 19–35% of the total N2 formation in the water column. The water-column chemistry in Golfo Dulce is very similar to that in oxygen-depleted zones of the oceans—in which one-half to one-third of the global nitrogen removal is believed to occur3,4. We therefore expect the anammox reaction to be a globally significant sink for oceanic nitrogen.

623 citations

Journal ArticleDOI
TL;DR: The aim of this paper is to compile recent information on the functional properties of coffee, coffee beans and by-products in terms of the associated potential health benefits.

603 citations

Journal ArticleDOI
Ricardo Segurado1, Sevilla D. Detera-Wadleigh2, Douglas F. Levinson3, Cathryn M. Lewis4, Michael Gill, John I. Nurnberger5, Nicholas John Craddock6, J. Raymond DePaulo7, Miron Baron8, Elliot S. Gershon9, Jenny Ekholm10, Sven Cichon, Gustavo Turecki, Stephan Claes11, John R. Kelsoe12, Peter R. Schofield13, Renee F. Badenhop14, Renee F. Badenhop13, Jean Morissette15, Hilary Coon16, Douglas Blackwood17, L. Alison McInnes8, Tatiana Foroud5, Howard J. Edenberg5, Theodore Reich18, John P. Rice18, Alison Goate18, Melvin G. McInnis7, Francis J. McMahon2, Judith A. Badner9, Lynn R. Goldin2, Phil Bennett6, Virginia L. Willour7, Peter P. Zandi7, Jianjun Liu8, Conrad T. Gilliam8, S H Juo8, Wade H. Berrettini3, Takeo Yoshikawa, Leena Peltonen19, Leena Peltonen10, Jouko Lönnqvist, Markus M. Nöthen, Johannes Schumacher20, Christine Windemuth20, Marcella Rietschel, Peter Propping20, Wolfgang Maier20, Martin Alda21, Paul Grof22, Guy A. Rouleau23, Jurgen Del-Favero, Christine Van Broeckhoven, Julien Mendlewicz24, Rolf Adolfsson25, M. Anne Spence26, Hermann Luebbert, L. J. Adams13, Jennifer A. Donald27, Philip B. Mitchell14, Nicholas Barden15, Eric Shink15, William Byerley26, Walter J. Muir17, Peter M. Visscher17, Stuart MacGregor17, Hugh Gurling4, Gursharan Kalsi4, Andrew McQuillin4, Michael Escamilla28, Victor I. Reus29, Pedro León30, Nelson B. Freimer19, Henrik Ewald31, Torben A Kruse32, Ole Mors31, Uppala Radhakrishna33, Jean-Louis Blouin33, Stylianos E. Antonarakis33, Nurten A. Akarsu34 
TL;DR: The present results for the very narrow model are promising but suggest that more and larger data sets are needed to support linkage, as well as suggest that linkage might be detected in certain populations or subsets of pedigrees.
Abstract: Genome scans of bipolar disorder (BPD) have not produced consistent evidence for linkage. The rank-based genome scan meta-analysis (GSMA) method was applied to 18 BPD genome scan data sets in an effort to identify regions with significant support for linkage in the combined data. The two primary analyses considered available linkage data for "very narrow" (i.e., BP-I and schizoaffective disorder-BP) and "narrow" (i.e., adding BP-II disorder) disease models, with the ranks weighted for sample size. A "broad" model (i.e., adding recurrent major depression) and unweighted analyses were also performed. No region achieved genomewide statistical significance by several simulation-based criteria. The most significant P values (<.01) were observed on chromosomes 9p22.3-21.1 (very narrow), 10q11.21-22.1 (very narrow), and 14q24.1-32.12 (narrow). Nominally significant P values were observed in adjacent bins on chromosomes 9p and 18p-q, across all three disease models on chromosomes 14q and 18p-q, and across two models on chromosome 8q. Relatively few BPD pedigrees have been studied under narrow disease models relative to the schizophrenia GSMA data set, which produced more significant results. There was no overlap of the highest-ranked regions for the two disorders. The present results for the very narrow model are promising but suggest that more and larger data sets are needed. Alternatively, linkage might be detected in certain populations or subsets of pedigrees. The narrow and broad data sets had considerable power, according to simulation studies, but did not produce more highly significant evidence for linkage. We note that meta-analysis can sometimes provide support for linkage but cannot disprove linkage in any candidate region.

585 citations

Journal ArticleDOI
TL;DR: Evidence is observed of a higher level of diversity and lower level of population structure in western South America compared to eastern South America, a relative lack of differentiation between Mesoamerican and Andean populations, and a partial agreement on a local scale between genetic similarity and the linguistic classification of populations.
Abstract: We examined genetic diversity and population structure in the American landmass using 678 autosomal microsatellite markers genotyped in 422 individuals representing 24 Native American populations sampled from North, Central, and South America. These data were analyzed jointly with similar data available in 54 other indigenous populations worldwide, including an additional five Native American groups. The Native American populations have lower genetic diversity and greater differentiation than populations from other continental regions. We observe gradients both of decreasing genetic diversity as a function of geographic distance from the Bering Strait and of decreasing genetic similarity to Siberians—signals of the southward dispersal of human populations from the northwestern tip of the Americas. We also observe evidence of: (1) a higher level of diversity and lower level of population structure in western South America compared to eastern South America, (2) a relative lack of differentiation between Mesoamerican and Andean populations, (3) a scenario in which coastal routes were easier for migrating peoples to traverse in comparison with inland routes, and (4) a partial agreement on a local scale between genetic similarity and the linguistic classification of populations. These findings offer new insights into the process of population dispersal and differentiation during the peopling of the Americas.

542 citations


Authors

Showing all 9922 results

NameH-indexPapersCitations
Alberto Ascherio13646269578
Gervasio Gomez133184499695
Myron M. Levine12378960865
Hong-Cai Zhou11448966320
Edward O. Wilson10140689994
Mary Claire King10033647454
Olga Martín-Belloso8638423428
José María Gutiérrez8460726779
Cesare Montecucco8438227738
Rodolphe Clérac7850622604
Kim R. Dunbar7447020262
Paul J. Hanson7025119504
Hannia Campos6921015164
Jean-Pierre Gorvel6723115005
F. Albert Cotton66102327647
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202325
2022155
2021865
20201,009
2019894
2018834