Bibliography

Wild Avocado strives to bring cutting-edge scientific research and data analytics together in our services.

Comprehensive

Our research process is backed by hundreds of articles from top-tier organizations published in reputable, peer-reviewed journals.

Accessible 

We strive to make your data easy to understand and to help you utilize our scientific research to achieve your health goals.

Validated

Our research analysis goes through extensive internal peer review and assessment by physicians, health coaches, and certified genetic counselors.View our bibliography to explore where we obtained the powerful research information that fuels our science. 
Showing 551 through 575
Author
Shen, G, Q
Author Organization
Cleveland Clinic
Pubmed ID
18066490
Link

Author
Winkelmann, J
Author Organization
GSF - Research Center for Environment and Health
Pubmed ID
18058820
Link

Author
Cronin, S
Author Organization
Department of Clinical Neurological Sciences, Royal College of Surgeons in Ireland, Dublin 2, Ireland
Pubmed ID
18057069
Link


Author
Weersma, RK
Author Organization
Department of Gastroenterology and Hepatology, University Medical Center Groningen, The Netherlands
Pubmed ID
18047540
Link

Author
Nagai, T
Author Organization
Ehime University Graduate School of Medicine
Pubmed ID
18037749
Link

Author
Kato, N
Author Organization
International Medical Center of Japan
Pubmed ID
18003638
Link

Author
Fernando, MMA
Author Organization
Section of Molecular Genetics and Rheumatology, Imperial College London, London, United Kingdom
Pubmed ID
17997607
Link

Author
Vaxillaire, M
Author Organization
UMR8090 and Institute of Biology, Lille 2 University, CNRS and Pasteur Institute
Pubmed ID
17977958
Link

Author
Furukawa, Y
Author Organization
The First Department of Medicine, Wakayama Medical University
Pubmed ID
17971426
Link

Author
Bennet, AM
Author Organization
Department of Public Health and Primary Care, University of Cambridge, Cambridge, England
Pubmed ID
17878422
Link

Author
Remmers, EF
Author Organization
National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD
Pubmed ID
17804842
Link

Author
Plenge, RM
Author Organization
Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA
Pubmed ID
17804836
Link

Author
Maller, J
Author Organization
Center for Human Genetic Research, Massachusetts General Hospital
Pubmed ID
17767156
Link

Author
Huang, Q, Y
Author Organization
Department of Medicine, The University of Hong Kong, Hong Kong, Hong Kong.
Pubmed ID
17687619
Link

Author
Franke, A
Author Organization
Institute for Clinical Molecular Biology, Christian-Albrechts University Kiel, Kiel, Germany
Pubmed ID
17684544
Link

Author
Jin, Y
Author Organization
Human Medical Genetics Program, School of Medicine, University of Colorado, Aurora, CO
Pubmed ID
17637824
Link

Author
Winkelmann, J
Author Organization
GSF - Research Center for Environment and Health
Pubmed ID
17637780
Link

Author
Samani, N, J
Author Organization
University of Leicester
Pubmed ID
17634449
Link

Author
Stefansson, H
Author Organization
deCODE Genetics, Reykjavik, Iceland
Pubmed ID
17634447
Link

Author
Avena, N, M
Author Organization
Princeton University
Pubmed ID
17617461
Link

Author
Jacq, L
Author Organization
Evry-Paris VII Universities, 91057 Evry-Genopole cedex, France
Pubmed ID
17615072
Link

Author
van Heel, DA
Author Organization
Centre for Gastroenterology, Institute of Cell and Molecular Science, Queen Mary University of London, London E1 2AT, UK
Pubmed ID
17558408
Link

Author
Staff
Author Organization
Wellcome Trust Case Control Consortium
Pubmed ID
17554300
Link

Author
Burton, P, R
Author Organization
Wellcome Trust Case Control Consortium
Pubmed ID
17554300
Link

TitleAuthorAuthor OrganizationPubmed IDLink 
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian populationShen, G, QCleveland Clinic18066490
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome.Winkelmann, JGSF - Research Center for Environment and Health18058820
A genome-wide association study of sporadic ALS in a homogenous Irish population.Cronin, SDepartment of Clinical Neurological Sciences, Royal College of Surgeons in Ireland, Dublin 2, Ireland18057069
Four SNPs on Chromosome 9p21 in a South Korean Population Implicate a Genetic Locus That Confers High Cross-Race Risk for Development of Coronary Artery DiseaseShen, G, QLerner Research Institute, Cleveland Clinic18048766
ATG16L1 and IL23R Are Associated With Inflammatory Bowel Diseases but Not With Celiac Disease in the NetherlandsWeersma, RKDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, The Netherlands18047540
A985G polymorphism of the endothelin-2 gene and atrial fibrillation in patients with hypertrophic cardiomyopathy.Nagai, TEhime University Graduate School of Medicine18037749
High-density association study and nomination of susceptibility genes for hypertension in the Japanese National ProjectKato, NInternational Medical Center of Japan18003638
Identification of Two Independent Risk Factors for Lupus Within the MHC in United Kingdom FamiliesFernando, MMASection of Molecular Genetics and Rheumatology, Imperial College London, London, United Kingdom17997607
Impact of common type 2 diabetes risk polymorphisms in the DESIR prospective study.Vaxillaire, MUMR8090 and Institute of Biology, Lille 2 University, CNRS and Pasteur Institute17977958
Polymorphisms in the IDE-KIF11-HHEX gene locus are reproducibly associated with type 2 diabetes in a Japanese population.Furukawa, YThe First Department of Medicine, Wakayama Medical University17971426
Association of apolipoprotein E genotypes with lipid levels and coronary riskBennet, AMDepartment of Public Health and Primary Care, University of Cambridge, Cambridge, England17878422
STAT4 and the Risk of Rheumatoid Arthritis and Systemic Lupus ErythematosusRemmers, EFNational Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD17804842
TRAF1-C5 as a Risk Locus for Rheumatoid Arthritis--A Genomewide StudyPlenge, RMBroad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA17804836
Variation in complement factor 3 is associated with risk of age-related macular degenerationMaller, JCenter for Human Genetic Research, Massachusetts General Hospital17767156
The association of common polymorphisms in the QPCT gene with bone mineral density in the Chinese population.Huang, Q, YDepartment of Medicine, The University of Hong Kong, Hong Kong, Hong Kong.17687619
Systematic Association Mapping Identifies NELL1 as a Novel IBD Disease GeneFranke, AInstitute for Clinical Molecular Biology, Christian-Albrechts University Kiel, Kiel, Germany17684544
Genetic Variations in NALP1 Are Associated With Generalized Vitiligo in a Romanian PopulationJin, YHuman Medical Genetics Program, School of Medicine, University of Colorado, Aurora, CO17637824
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.Winkelmann, JGSF - Research Center for Environment and Health17637780
Genomewide Association Analysis of Coronary Artery DiseaseSamani, N, JUniversity of Leicester17634449
A genetic risk factor for periodic limb movements in sleep.Stefansson, HdeCODE Genetics, Reykjavik, Iceland17634447
Evidence for sugar addiction: Behavioral and neurochemical effects of intermittent, excessive sugar intakeAvena, N, MPrinceton University17617461
The ITGAV rs3738919-C Allele Is Associated With Rheumatoid Arthritis in the European Caucasian Population, A Family-Based StudyJacq, LEvry-Paris VII Universities, 91057 Evry-Genopole cedex, France17615072
A Genome-Wide Association Study for Celiac Disease Identifies Risk Variants in the Region Harboring IL2 and IL21van Heel, DACentre for Gastroenterology, Institute of Cell and Molecular Science, Queen Mary University of London, London E1 2AT, UK17558408
Genome-wide Association Study of 14,000 Cases of Seven Common Diseases and 3,000 Shared ControlsStaffWellcome Trust Case Control Consortium17554300
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsBurton, P, RWellcome Trust Case Control Consortium17554300
Showing 551 through 575
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