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Institution

University of Lausanne

EducationLausanne, Switzerland
About: University of Lausanne is a education organization based out in Lausanne, Switzerland. It is known for research contribution in the topics: Population & Medicine. The organization has 20508 authors who have published 46458 publications receiving 1996655 citations. The organization is also known as: Université de Lausanne & UNIL.


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Journal ArticleDOI
TL;DR: This work redefined the traditional concept of assembly rules in a more general framework where the co‐occurrence of species is a product of chance, historical patterns of speciation and migration, dispersal, abiotic environmental factors, and biotic interactions, with none of these processes being mutually exclusive.
Abstract: Understanding how communities of living organisms assemble has been a central question in ecology since the early days of the discipline. Disentangling the different processes involved in community assembly is not only interesting in itself but also crucial for an understanding of how communities will behave under future environmental scenarios. The traditional concept of assembly rules reflects the notion that species do not co-occur randomly but are restricted in their co-occurrence by interspecific competition. This concept can be redefined in a more general framework where the co-occurrence of species is a product of chance, historical patterns of speciation and migration, dispersal, abiotic environmental factors, and biotic interactions, with none of these processes being mutually exclusive. Here we present a survey and meta-analyses of 59 papers that compare observed patterns in plant communities with null models simulating random patterns of species assembly. According to the type of data under study and the different methods that are applied to detect community assembly, we distinguish four main types of approach in the published literature: species co-occurrence, niche limitation, guild proportionality and limiting similarity. Results from our meta-analyses suggest that non-random co-occurrence of plant species is not a widespread phenomenon. However, whether this finding reflects the individualistic nature of plant communities or is caused by methodological shortcomings associated with the studies considered cannot be discerned from the available metadata. We advocate that more thorough surveys be conducted using a set of standardized methods to test for the existence of assembly rules in data sets spanning larger biological and geographical scales than have been considered until now. We underpin this general advice with guidelines that should be considered in future assembly rules research. This will enable us to draw more accurate and general conclusions about the non-random aspect of assembly in plant communities.

719 citations

Journal ArticleDOI
TL;DR: The members of the extended GLUT family exhibit a surprisingly diverse substrate specificity, and the definition of sequence elements determining this substrate specificity will require a full functional characterization of all members.
Abstract: During the last 2 years, several novel genes that encode glucose transporter-like proteins have been identified and characterized. Because of their sequence similarity with GLUT1, these genes appear to belong to the family of solute carriers 2A ( SLC2A, protein symbol GLUT). Sequence comparisons of all 13 family members allow the definition of characteristic sugar/polyol transporter signatures: (1) the presence of 12 membrane-spanning helices, (2) seven conserved glycine residues in the helices, (3) several basic and acidic residues at the intracellular surface of the proteins, (4) two conserved tryptophan residues, and (5) two conserved tyrosine residues. On the basis of sequence similarities and characteristic elements, the extended GLUTfamily can be divided intothree subfamilies, namely class I (the previously known glucose transporters GLUT1-4), class II (the previously known fructose transporter GLUT5, the GLUT7, GLUT9 and GLUT11), and class III (GLUT6, 8, 10, 12, and the myoinositol transporter HMIT...

716 citations

Journal ArticleDOI
Inga Prokopenko1, Claudia Langenberg2, Jose C. Florez3, Jose C. Florez4, Richa Saxena4, Richa Saxena3, Nicole Soranzo5, Nicole Soranzo6, Gudmar Thorleifsson7, Ruth J. F. Loos2, Alisa K. Manning8, Anne U. Jackson9, Yurii S. Aulchenko10, Simon C. Potter5, Michael R. Erdos11, Serena Sanna, Jouke-Jan Hottenga12, Eleanor Wheeler5, Marika Kaakinen13, Valeriya Lyssenko14, Wei-Min Chen15, Kourosh R. Ahmadi6, Jacques S. Beckmann16, Jacques S. Beckmann17, Richard N. Bergman18, Murielle Bochud17, Lori L. Bonnycastle11, Thomas A. Buchanan18, Antonio Cao, Alessandra C. L. Cervino6, Lachlan J. M. Coin19, Francis S. Collins11, Laura Crisponi, Eco J. C. de Geus12, Abbas Dehghan10, Panos Deloukas5, Alex S. F. Doney20, Paul Elliott19, Nelson B. Freimer21, Vesela Gateva9, Christian Herder22, Albert Hofman10, Thomas Edward Hughes23, Sarah E. Hunt5, Thomas Illig, Michael Inouye5, Bo Isomaa, Toby Johnson24, Toby Johnson17, Toby Johnson16, Augustine Kong7, Maria Krestyaninova25, Johanna Kuusisto26, Markku Laakso26, Noha Lim27, Ulf Lindblad14, Cecilia M. Lindgren1, O. T. McCann5, Karen L. Mohlke28, Andrew D. Morris20, Silvia Naitza, Marco Orru, Colin N. A. Palmer20, Anneli Pouta29, Joshua C. Randall1, Wolfgang Rathmann22, Jouko Saramies, Paul Scheet9, Laura J. Scott9, Angelo Scuteri11, Stephen J. Sharp2, Eric J.G. Sijbrands10, Jan H. Smit30, Kijoung Song27, Valgerdur Steinthorsdottir7, Heather M. Stringham9, Tiinamaija Tuomi31, Jaakko Tuomilehto, André G. Uitterlinden10, Benjamin F. Voight3, Benjamin F. Voight4, Dawn M. Waterworth27, H-Erich Wichmann32, Gonneke Willemsen12, Jacqueline C.M. Witteman10, Xin Yuan27, Jing Hua Zhao2, Eleftheria Zeggini1, David Schlessinger11, Manjinder S. Sandhu33, Manjinder S. Sandhu2, Dorret I. Boomsma12, Manuela Uda, Tim D. Spector6, Brenda W.J.H. Penninx33, Brenda W.J.H. Penninx34, Brenda W.J.H. Penninx35, David Altshuler3, David Altshuler4, Peter Vollenweider17, Marjo-Riitta Järvelin19, Marjo-Riitta Järvelin13, Edward G. Lakatta11, Gérard Waeber17, Caroline S. Fox11, Caroline S. Fox36, Leena Peltonen5, Leena Peltonen37, Leif Groop14, Vincent Mooser27, L. Adrienne Cupples8, Unnur Thorsteinsdottir7, Unnur Thorsteinsdottir38, Michael Boehnke9, Inês Barroso5, Cornelia M. van Duijn10, Josée Dupuis8, Richard M. Watanabe18, Kari Stefansson7, Kari Stefansson38, Mark I. McCarthy1, Mark I. McCarthy39, Nicholas J. Wareham2, James B. Meigs4, Gonçalo R. Abecasis9 
TL;DR: Variants in the gene encoding melatonin receptor 1B (MTNR1B) were consistently associated with fasting glucose across all ten genome-wide association scans, and previous associations of fasting glucose with variants at the G6PC2 and GCK loci are confirmed.
Abstract: To identify previously unknown genetic loci associated with fasting glucose concentrations, we examined the leading association signals in ten genome-wide association scans involving a total of 36,610 individuals of European descent. Variants in the gene encoding melatonin receptor 1B (MTNR1B) were consistently associated with fasting glucose across all ten studies. The strongest signal was observed at rs10830963, where each G allele (frequency 0.30 in HapMap CEU) was associated with an increase of 0.07 (95% CI = 0.06-0.08) mmol/l in fasting glucose levels (P = 3.2 x 10(-50)) and reduced beta-cell function as measured by homeostasis model assessment (HOMA-B, P = 1.1 x 10(-15)). The same allele was associated with an increased risk of type 2 diabetes (odds ratio = 1.09 (1.05-1.12), per G allele P = 3.3 x 10(-7)) in a meta-analysis of 13 case-control studies totaling 18,236 cases and 64,453 controls. Our analyses also confirm previous associations of fasting glucose with variants at the G6PC2 (rs560887, P = 1.1 x 10(-57)) and GCK (rs4607517, P = 1.0 x 10(-25)) loci.

716 citations

Journal ArticleDOI
TL;DR: The various epistatic effects observed here for common, distinct KIR3DL1 and HLA-B Bw4 combinations are unprecedented with regard to any pair of genetic loci in human disease, and indicate that NK cells may have a critical role in the natural history of HIV infection.
Abstract: Allotypes of the natural killer (NK) cell receptor KIR3DL1 vary in both NK cell expression patterns and inhibitory capacity upon binding to their ligands, HLA-B Bw4 molecules, present on target cells. Using a sample size of over 1,500 human immunodeficiency virus (HIV)+ individuals, we show that various distinct allelic combinations of the KIR3DL1 and HLA-B loci significantly and strongly influence both AIDS progression and plasma HIV RNA abundance in a consistent manner. These genetic data correlate very well with previously defined functional differences that distinguish KIR3DL1 allotypes. The various epistatic effects observed here for common, distinct KIR3DL1 and HLA-B Bw4 combinations are unprecedented with regard to any pair of genetic loci in human disease, and indicate that NK cells may have a critical role in the natural history of HIV infection.

712 citations

Journal ArticleDOI
TL;DR: It is predicted that darker wild vertebrates are more aggressive, sexually active and resistant to stress than lighter individuals, and pleiotropic effects of the melanocortins might account for the widespread covariance between melanin-based coloration and other phenotypic traits in vertebrates.
Abstract: In vertebrates, melanin-based coloration is often associated with variation in physiological and behavioural traits. We propose that this association stems from pleiotropic effects of the genes regulating the synthesis of brown to black eumelanin. The most important regulators are the melanocortin 1 receptor and its ligands, the melanocortin agonists and the agouti-signalling protein antagonist. On the basis of the physiological and behavioural functions of the melanocortins, we predict five categories of traits correlated with melanin-based coloration. A review of the literature indeed reveals that, as predicted, darker wild vertebrates are more aggressive, sexually active and resistant to stress than lighter individuals. Pleiotropic effects of the melanocortins might thus account for the widespread covariance between melanin-based coloration and other phenotypic traits in vertebrates.

709 citations


Authors

Showing all 20911 results

NameH-indexPapersCitations
Peer Bork206697245427
Aaron R. Folsom1811118134044
Kari Alitalo174817114231
Ralph A. DeFronzo160759132993
Johan Auwerx15865395779
Silvia Franceschi1551340112504
Matthias Egger152901184176
Bart Staels15282486638
Fernando Rivadeneira14662886582
Christopher George Tully1421843111669
Richard S. J. Frackowiak142309100726
Peter Timothy Cox140126795584
Jürg Tschopp14032886900
Stylianos E. Antonarakis13874693605
Michael Weller134110591874
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023249
2022635
20213,970
20203,508
20193,091
20182,776