نتایج جستجو برای: realized heritability

تعداد نتایج: 61070  

Journal: Iranian Economic Review 2020

F orecasting the volatility of a financial asset has wide implications in finance. Conditional variance extracted from the GARCH framework could be a suitable proxy of financial asset volatility. Option pricing, portfolio optimization, and risk management are examples of implications of conditional variance forecasting. One of the most recent methods of volatility forecasting is Real...

Journal: :Personality and Individual Differences 2023

Can heritability estimates provide causal information? This paper argues for an affirmative answer: since a non-nil estimate satisfies certain characteristic properties of causation (i.e., association, manipulability, and counterfactual dependence), it increases the probability that relation between genotypic variance phenotypic is (at least partly) causal. Contrary to earlier proposals in lite...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
David Golan Eric S Lander Saharon Rosset

Genome-wide association studies (GWASs), also called common variant association studies (CVASs), have uncovered thousands of genetic variants associated with hundreds of diseases. However, the variants that reach statistical significance typically explain only a small fraction of the heritability. One explanation for the "missing heritability" is that there are many additional disease-associate...

2013
Noah Zaitlen Peter Kraft Nick Patterson Bogdan Pasaniuc Gaurav Bhatia Samuela Pollack Alkes L. Price

Important knowledge about the determinants of complex human phenotypes can be obtained from the estimation of heritability, the fraction of phenotypic variation in a population that is determined by genetic factors. Here, we make use of extensive phenotype data in Iceland, long-range phased genotypes, and a population-wide genealogical database to examine the heritability of 11 quantitative and...

Journal: :Stroke 2013
William J Devan Guido J Falcone Christopher D Anderson Jeremiasz M Jagiella Helena Schmidt Björn M Hansen Jordi Jimenez-Conde Eva Giralt-Steinhauer Elisa Cuadrado-Godia Carolina Soriano Alison M Ayres Kristin Schwab Sylvia Baedorf Kassis Valerie Valant Joanna Pera Andrzej Urbanik Anand Viswanathan Natalia S Rost Joshua N Goldstein Paul Freudenberger Eva-Maria Stögerer Bo Norrving David L Tirschwell Magdy Selim Devin L Brown Scott L Silliman Bradford B Worrall James F Meschia Chelsea S Kidwell Joan Montaner Israel Fernandez-Cadenas Pilar Delgado Steven M Greenberg Jaume Roquer Arne Lindgren Agnieszka Slowik Reinhold Schmidt Daniel Woo Jonathan Rosand Alessandro Biffi

BACKGROUND AND PURPOSE Previous studies suggest that genetic variation plays a substantial role in occurrence and evolution of intracerebral hemorrhage (ICH). Genetic contribution to disease can be determined by calculating heritability using family-based data, but such an approach is impractical for ICH because of lack of large pedigree-based studies. However, a novel analytic tool based on ge...

2013
Lea K. Davis Dongmei Yu Clare L. Keenan Eric R. Gamazon Anuar I. Konkashbaev Eske M. Derks Benjamin M. Neale Jian Yang S. Hong Lee Patrick Evans Cathy L. Barr Laura Bellodi Fortu Benarroch Gabriel Bedoya Berrio Oscar J. Bienvenu Michael H. Bloch Rianne M. Blom Ruth D. Bruun Cathy L. Budman Beatriz Camarena Desmond Campbell Carolina Cappi Julio C. Cardona Silgado Danielle C. Cath Maria C. Cavallini Denise A. Chavira Sylvain Chouinard David V. Conti Edwin H. Cook Vladimir Coric Bernadette A. Cullen Dieter Deforce Richard Delorme Yves Dion Christopher K. Edlund Karin Egberts Peter Falkai Thomas V. Fernandez Patience J. Gallagher Helena Garrido Daniel Geller Simon L. Girard Hans J. Grabe Marco A. Grados Benjamin D. Greenberg Varda Gross-Tsur Stephen Haddad Gary A. Heiman Sian M. J. Hemmings Ana G. Hounie Cornelia Illmann Joseph Jankovic Michael A. Jenike James L. Kennedy Robert A. King Barbara Kremeyer Roger Kurlan Nuria Lanzagorta Marion Leboyer James F. Leckman Leonhard Lennertz Chunyu Liu Christine Lochner Thomas L. Lowe Fabio Macciardi James T. McCracken Lauren M. McGrath Sandra C. Mesa Restrepo Rainald Moessner Jubel Morgan Heike Muller Dennis L. Murphy Allan L. Naarden William Cornejo Ochoa Roel A. Ophoff Lisa Osiecki Andrew J. Pakstis Michele T. Pato Carlos N. Pato John Piacentini Christopher Pittenger Yehuda Pollak Scott L. Rauch Tobias J. Renner Victor I. Reus Margaret A. Richter Mark A. Riddle Mary M. Robertson Roxana Romero Maria C. Rosàrio David Rosenberg Guy A. Rouleau Stephan Ruhrmann Andres Ruiz-Linares Aline S. Sampaio Jack Samuels Paul Sandor Brooke Sheppard Harvey S. Singer Jan H. Smit Dan J. Stein E. Strengman Jay A. Tischfield Ana V. Valencia Duarte Homero Vallada Filip Van Nieuwerburgh Jeremy Veenstra-VanderWeele Susanne Walitza Ying Wang Jens R. Wendland Herman G. M. Westenberg Yin Yao Shugart Euripedes C. Miguel William McMahon Michael Wagner Humberto Nicolini Danielle Posthuma Gregory L. Hanna Peter Heutink Damiaan Denys Paul D. Arnold Ben A. Oostra Gerald Nestadt Nelson B. Freimer David L. Pauls Naomi R. Wray S. Evelyn Stewart Carol A. Mathews James A. Knowles Nancy J. Cox Jeremiah M. Scharf

The direct estimation of heritability from genome-wide common variant data as implemented in the program Genome-wide Complex Trait Analysis (GCTA) has provided a means to quantify heritability attributable to all interrogated variants. We have quantified the variance in liability to disease explained by all SNPs for two phenotypically-related neurobehavioral disorders, obsessive-compulsive diso...

Journal: :Fertility and Sterility 2015

Journal: :Archives of General Psychiatry 2009

Journal: :Journal of the European Economic Association 2009

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