نتایج جستجو برای: polygenic dyslipidemia

تعداد نتایج: 16254  

Journal: :international journal of pediatrics 0
roya kelishadi 1professor, pediatrics department, child growth and development research center, research institute for primordial prevention of non-communicable disease, isfahan university of medical sciences, isfahan, iran. marjan mansourian assistant professor, department of biostatitics, faculty of health, isfahan university of medical sciences, isfahan, iran. mustafa ghanadian assistant professor, pharmacognosy department, isfahan pharmaceutical sciences research center, faculty of pharmacy, isfahan university of medical sciences, isfahan, iran. ehsan ataei child growth and development research center, research institute for primordial prevention of non-communicable disease, isfahan university of medical sciences, isfahan, iran. parisa mirmoghtadaee research assistant, specialist in community medicine, isfahan university of medical sciences, isfahan, iran.

background dyslipidemia is a major risk for cardiovascular diseases. the aim of this study is to review the effects of nutraceuticals to modify lipid disorders in children. materials and methods the literature research was conducted in embase, medline, pubmed, scopus, isi web of science, and cochrane library from 2002 until january 2015. the following keywords were used: dyslipidemia, hyperlipi...

2014
Joanna Martin Marian L. Hamshere Evangelia Stergiakouli Michael C. O’Donovan Anita Thapar

BACKGROUND Attention-deficit/hyperactivity disorder (ADHD) can be viewed as the extreme end of traits in the general population. Epidemiological and twin studies suggest that ADHD frequently co-occurs with and shares genetic susceptibility with autism spectrum disorder (ASD) and ASD-related traits. The aims of this study were to determine whether a composite of common molecular genetic variants...

2013
Marian L. Hamshere Kate Langley Joanna Martin Sharifah Shameem Agha Evangelia Stergiakouli Richard J.L. Anney Jan Buitelaar Stephen V. Faraone Klaus-Peter Lesch Benjamin M. Neale Barbara Franke Edmund Sonuga-Barke Philip Asherson Andrew Merwood Jonna Kuntsi Sarah E. Medland Stephan Ripke Hans-Christoph Steinhausen Christine Freitag Andreas Reif Tobias J. Renner Marcel Romanos Jasmin Romanos Andreas Warnke Jobst Meyer Haukur Palmason Alejandro Arias Vasquez Nanda Lambregts-Rommelse Herbert Roeyers Joseph Biederman Alysa E. Doyle Hakon Hakonarson Aribert Rothenberger Tobias Banaschewski Robert D. Oades James J. McGough Lindsey Kent Nigel Williams Michael J. Owen Peter Holmans Michael C. O’Donovan Anita Thapar

OBJECTIVE Although attention deficit hyperactivity disorder (ADHD) is highly heritable, genome-wide association studies (GWAS) have not yet identified any common genetic variants that contribute to risk. There is evidence that aggression or conduct disorder in children with ADHD indexes higher genetic loading and clinical severity. The authors examine whether common genetic variants considered ...

Journal: :The American journal of psychiatry 2015
Dongmei Yu Carol A Mathews Jeremiah M Scharf Benjamin M Neale Lea K Davis Eric R Gamazon Eske M Derks Patrick Evans Christopher K Edlund Jacquelyn Crane Jesen A Fagerness Lisa Osiecki Patience Gallagher Gloria Gerber Stephen Haddad Cornelia Illmann Lauren M McGrath Catherine Mayerfeld Sampath Arepalli Cristina Barlassina Cathy L Barr Laura Bellodi Fortu Benarroch Gabriel Bedoya Berrió O Joseph Bienvenu Donald W Black Michael H Bloch Helena Brentani Ruth D Bruun Cathy L Budman Beatriz Camarena Desmond D Campbell Carolina Cappi Julio C Cardona Silgado Maria C Cavallini Denise A Chavira Sylvain Chouinard Edwin H Cook M R Cookson Vladimir Coric Bernadette Cullen Daniele Cusi Richard Delorme Damiaan Denys Yves Dion Valsama Eapen Karin Egberts Peter Falkai Thomas Fernandez Eduardo Fournier Helena Garrido Daniel Geller Donald L Gilbert Simon L Girard Hans J Grabe Marco A Grados Benjamin D Greenberg Varda Gross-Tsur Edna Grünblatt John Hardy Gary A Heiman Sian M J Hemmings Luis D Herrera Dianne M Hezel Pieter J Hoekstra Joseph Jankovic James L Kennedy Robert A King Anuar I Konkashbaev Barbara Kremeyer Roger Kurlan Nuria Lanzagorta Marion Leboyer James F Leckman Leonhard Lennertz Chunyu Liu Christine Lochner Thomas L Lowe Sara Lupoli Fabio Macciardi Wolfgang Maier Paolo Manunta Maurizio Marconi James T McCracken Sandra C Mesa Restrepo Rainald Moessner Priya Moorjani Jubel Morgan Heike Muller Dennis L Murphy Allan L Naarden Erika Nurmi William Cornejo Ochoa Roel A Ophoff Andrew J Pakstis Michele T Pato Carlos N Pato John Piacentini Christopher Pittenger Yehuda Pollak Scott L Rauch Tobias Renner Victor I Reus Margaret A Richter Mark A Riddle Mary M Robertson Roxana Romero Maria C Rosário David Rosenberg Stephan Ruhrmann Chiara Sabatti Erika Salvi Aline S Sampaio Jack Samuels Paul Sandor Susan K Service Brooke Sheppard Harvey S Singer Jan H Smit Dan J Stein Eric Strengman Jay A Tischfield Maurizio Turiel Ana V Valencia Duarte Homero Vallada Jeremy Veenstra-VanderWeele Susanne Walitza Ying Wang Mike Weale Robert Weiss Jens R Wendland Herman G M Westenberg Yin Yao Shugart Ana G Hounie Euripedes C Miguel Humberto Nicolini Michael Wagner Andres Ruiz-Linares Danielle C Cath William McMahon Danielle Posthuma Ben A Oostra Gerald Nestadt Guy A Rouleau Shaun Purcell Michael A Jenike Peter Heutink Gregory L Hanna David V Conti Paul D Arnold Nelson B Freimer S Evelyn Stewart James A Knowles Nancy J Cox David L Pauls

OBJECTIVE Obsessive-compulsive disorder (OCD) and Tourette's syndrome are highly heritable neurodevelopmental disorders that are thought to share genetic risk factors. However, the identification of definitive susceptibility genes for these etiologically complex disorders remains elusive. The authors report a combined genome-wide association study (GWAS) of Tourette's syndrome and OCD. METHOD...

2013
Jung Sub Lim

Cardiovascular disease (CVD) is a leading cause of death worldwide including Korea. The risk factors of CVD are known as positive family history of early CVD, obesity, hypertension, diabetes, and dyslipidemia. Among those, dyslipidemia is one of modifiable risk factors. Dyslipidemia starts in childhood and progress to adulthood. Furthermore, dyslipidemia cause atherosclerosis and is closely rel...

Background: The risk of disease with 1 risk factor is increased by the presence of additional risk factors. The goal of this study was to assess the prevalence of multiple coronary artery disease (CAD) risk factors among adults in Kerman, Iran, to identify the population groups most at risk.Methods: The present study included 5900 adults aged between 15 and 75 years in 2011 in Kerman, Iran. The...

Journal: :Neurology Genetics 2019

Journal: :Obesity Facts 2008

Journal: :Proceedings of the National Academy of Sciences 1970

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