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.

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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 426 through 450
Author
Edwards, TL
Author Organization
John P. Hussman Institute for Human Genomics, University of Miami, FL
Pubmed ID
20070850
Link

Author
Csongei, V
Author Organization
Department of Medical Genetics, University of Pecs, Pecs 7624, Hungary
Pubmed ID
20066736
Link

Author
Liu, Y
Author Organization
Chinese Academy of Sciences
Pubmed ID
20057365
Link

Author
Cluett, C
Author Organization
Peninsula Medical School
Pubmed ID
20031606
Link


Author
Gómez-Gallego, F
Author Organization
Universidad Europea de Madrid
Pubmed ID
20029521
Link

Author
Staff
Author Organization
International Multiple Sclerosis Genetics Consortium
Pubmed ID
20007504
Link

Author
Epstein, L, J
Author Organization
Sleep HealthCenters, Brighton, MA 02135, USA.
Pubmed ID
19960649
Link

Author
Carr, E, J
Author Organization
Cambridge Institute for Medical Research
Pubmed ID
19951419
Link

Author
Simón-Sanchez, J
Author Organization
Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland
Pubmed ID
19915575
Link

Author
Li, D
Author Organization
Kaiser Foundation Research Institute
Pubmed ID
19906654
Link

Author
Tanaka, T
Author Organization
MedStar Research Institute
Pubmed ID
19880490
Link

Author
Ganesh, S
Author Organization
National Human Genome Research Institute
Pubmed ID
19862010
Link

Author
Hong, X
Author Organization
Northwestern University Feinberg School of Medicine
Pubmed ID
19851108
Link

Author
Tanofsky-Kraff, M
Author Organization
Unit on Growth and Obesity, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services
Pubmed ID
19828706
Link

Author
Soranzo, N
Author Organization
Wellcome Trust Sanger Institute
Pubmed ID
19820697
Link

Author
Niu, W
Author Organization
Ruijin Hospital, Shanghai Jiaotong University School of Medicine, China
Pubmed ID
19816504
Link


Author
Rivadeneira, F
Author Organization
Department of Internal Medicine, Erasmus MC, Rotterdam
Pubmed ID
19801982
Link

Author
Hoed, M
Author Organization
Department of Human Biology, Maastricht University
Pubmed ID
19793853
Link

Author
Kiecolt-Glaser, JK
Author Organization
Department of Psychiatry and The Ohio State Institute for Behavioral Medicine Research, The Ohio State University College of Medicine, Columbus, Ohio
Pubmed ID
19751761
Link

Author
Hazra, A
Author Organization
Program in Molecular and Genetic Epidemiology, Department of Epidemiology, Harvard School of Public Health
Pubmed ID
19744961
Link

Author
Harold, D
Author Organization
Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Cardiff, UK
Pubmed ID
19734902
Link

Author
Gómez-Gallego, F
Author Organization
Universidad Europea de Madrid
Pubmed ID
19701646
Link

Author
Amundsen, SS
Author Organization
Centre for Immune Regulation, Institute of Immunology, University of Oslo and Rikshospitalet University Hospital, Oslo, Norway
Pubmed ID
19693089
Link

TitleAuthorAuthor OrganizationPubmed IDLink 
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.Edwards, TLJohn P. Hussman Institute for Human Genomics, University of Miami, FL20070850
Interaction of the Major Inflammatory Bowel Disease Susceptibility Alleles in Crohn's Disease PatientsCsongei, VDepartment of Medical Genetics, University of Pecs, Pecs 7624, Hungary20066736
Meta-analysis added power to identify variants in FTO associated with type 2 diabetes and obesity in the Asian population.Liu, YChinese Academy of Sciences20057365
The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people.Cluett, CPeninsula Medical School20031606
Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction: Genomewide Analysis among 18,245 Initially Healthy Women from the Women’s Genome Health StudyRidker, P, MBrigham and Women's Hospital20031564
The C allele of the AGT Met235Thr polymorphism is associated with power sports performance.Gómez-Gallego, FUniversidad Europea de Madrid20029521
Comprehensive Follow-Up of the First Genome-Wide Association Study of Multiple Sclerosis Identifies KIF21B and TMEM39A as Susceptibility LociStaffInternational Multiple Sclerosis Genetics Consortium20007504
Clinical Guidance for the Evaluation, Management and Long-term Care of Obstructive Sleep Apnea in AdultsEpstein, L, JSleep HealthCenters, Brighton, MA 02135, USA.19960649
Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitisCarr, E, JCambridge Institute for Medical Research19951419
Genome-wide association study reveals genetic risk underlying Parkinson's disease.Simón-Sanchez, JLaboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland19915575
Occupational exposure to bisphenol-A (BPA) and the risk of self-reported male sexual dysfunctionLi, DKaiser Foundation Research Institute19906654
A genome-wide association analysis of serum iron concentrationsTanaka, TMedStar Research Institute19880490
Multiple loci influence erythrocyte phenotypes in the CHARGE ConsortiumGanesh, SNational Human Genome Research Institute19862010
Genetics of Food allergyHong, XNorthwestern University Feinberg School of Medicine19851108
The FTO gene rs9939609 obesity-risk allele and loss of control over eatingTanofsky-Kraff, MUnit on Growth and Obesity, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services19828706
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortiumSoranzo, NWellcome Trust Sanger Institute19820697
The relationship between apolipoprotein E epsilon2/epsilon3/epsilon4 polymorphisms and hypertension, a meta-analysis of six studies comprising 1812 cases and 1762 controlsNiu, WRuijin Hospital, Shanghai Jiaotong University School of Medicine, China19816504
Genetic loci associated with plasma concentration of LDL-C, HDL-C, triglycerides, ApoA1, and ApoB among 6382 Caucasian women in genome-wide analysis with replicationChasman, D, IBrigham and Women's Hospital19802338
Twenty bone mineral density loci identified by large-scale meta-analysis of genome-wide association studiesRivadeneira, FDepartment of Internal Medicine, Erasmus MC, Rotterdam19801982
Postprandial Responses in Hunger and Satiety Are Associated With the rs9939609 Single Nucleotide Polymorphism in FTOHoed, MDepartment of Human Biology, Maastricht University19793853
Close relationships, inflammation and healthKiecolt-Glaser, JKDepartment of Psychiatry and The Ohio State Institute for Behavioral Medicine Research, The Ohio State University College of Medicine, Columbus, Ohio19751761
Genome-wide significant predictors of metabolites in the one-carbon metabolism pathwayHazra, AProgram in Molecular and Genetic Epidemiology, Department of Epidemiology, Harvard School of Public Health19744961
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.Harold, DMedical Research Council Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Cardiff, UK19734902
The -786 T/C polymorphism of the NOS3 gene is associated with elite performance in power sports.Gómez-Gallego, FUniversidad Europea de Madrid19701646
Four Novel Coeliac Disease Regions Replicated in an Association Study of a Swedish-Norwegian Family CohortAmundsen, SSCentre for Immune Regulation, Institute of Immunology, University of Oslo and Rikshospitalet University Hospital, Oslo, Norway19693089
Showing 426 through 450
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