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
Raleigh, S
Author Organization
Division of Health and Life Sciences, University of Northampton
Pubmed ID
19042922
Link

Author
Francis, P
Author Organization
Macular Degeneration Center, Casey Eye Institute, Oregon Health & Science University
Pubmed ID
19015224
Link

Author
Aulchenko, YS
Author Organization
Genetic Epidemiology Unit, Department of Epidemiology and Biostatistics and Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands
Pubmed ID
18997785
Link

Author
Staff
Author Organization
International Multiple Sclerosis Genetics Consortium
Pubmed ID
18987646
Link

Author
Cronin, S
Author Organization
Department of Clinical Neurological Sciences, Royal College of Surgeons in Ireland, Dublin 2, Ireland
Pubmed ID
18987618
Link

Author
Pankratz, N
Author Organization
Indiana University School of Medicine, Health Information and Translational Sciences Building, Indianapolis, IN
Pubmed ID
18985386
Link

Author
Prudente, S
Author Organization
CSS-Mendel Institute
Pubmed ID
18984671
Link

Author
Cooper, JD
Author Organization
Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK
Pubmed ID
18978792
Link

Author
Hoed, M
Author Organization
Department of Human Biology, Maastricht University
Pubmed ID
18957934
Link

Author
Zoledziewska, M
Author Organization
Dipartimento di Scienze Biomediche, University of Sassari, Sassari, Italy
Pubmed ID
18946483
Link

Author
Comabella, M
Author Organization
Unitat de Neuroimmunologia Clínica, CEM-Cat, Hospital Universitari Vall d'Hebron, Barcelona, Spain
Pubmed ID
18941528
Link

Author
DeVos, L
Author Organization
Eberly College of Science, Pennsylvania State University
Pubmed ID
18842806
Link

Author
McKay, G
Author Organization
Centre for Vision Sciences, Queen's University of Belfast
Pubmed ID
18806297
Link

Author
Suzuki, A
Author Organization
Laboratory for Autoimmune Diseases, Center for Genomic Medicine, RIKEN, Yokohama, Kanagawa 230-0045, Japan
Pubmed ID
18794858
Link

Author
Raychaudhuri, S
Author Organization
Program in Medical and Population Genetics, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, Massachusetts
Pubmed ID
18794853
Link

Author
Hivert, M
Author Organization
General Medicine Division, Massachusetts General Hospital
Pubmed ID
18776141
Link

Author
Yang, Z
Author Organization
Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu
Pubmed ID
18753640
Link

Author
Lemos da Luz, P
Author Organization
Universidade de Sao Paulo
Pubmed ID
18719750
Link



Author
Zervou, MI
Author Organization
Medical School, University of Crete, Heraklion, Greece
Pubmed ID
18703106
Link

Author
Orton, SM
Author Organization
Wellcome Trust Centre for Human Genetics and Department of Clinical Neurology, University of Oxford
Pubmed ID
18689381
Link

Author
Gaulton, K
Author Organization
Department of Genetics, University of North Carolina at Chapel Hill
Pubmed ID
18678618
Link


Author
Paffen, E
Author Organization
Leiden University Medical Center
Pubmed ID
18662263
Link

TitleAuthorAuthor OrganizationPubmed IDLink 
Variants within the MMP3 gene are associated with Achilles tendinopathy, possible interaction with the COL5A1 geneRaleigh, SDivision of Health and Life Sciences, University of Northampton19042922
Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual lossFrancis, PMacular Degeneration Center, Casey Eye Institute, Oregon Health & Science University19015224
Genetic Variation in the KIF1B Locus Influences Susceptibility to Multiple SclerosisAulchenko, YSGenetic Epidemiology Unit, Department of Epidemiology and Biostatistics and Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands18997785
The Expanding Genetic Overlap Between Multiple Sclerosis and Type I DiabetesStaffInternational Multiple Sclerosis Genetics Consortium18987646
Screening for replication of genome-wide SNP associations in sporadic ALS.Cronin, SDepartment of Clinical Neurological Sciences, Royal College of Surgeons in Ireland, Dublin 2, Ireland18987618
Genomewide association study for susceptibility genes contributing to familial Parkinson disease.Pankratz, NIndiana University School of Medicine, Health Information and Translational Sciences Building, Indianapolis, IN18985386
TheTRIB3Q84R Polymorphism and Risk of Early-Onset Type 2 DiabetesPrudente, SCSS-Mendel Institute18984671
Meta-analysis of Genome-Wide Association Study Data Identifies Additional Type 1 Diabetes Risk LociCooper, JDJuvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Addenbrooke's Hospital, Cambridge, UK18978792
SNP analyses of postprandial responses in(an)orexigenic hormones and feelings of hunger reveal long-term physiological adaptations to facilitate homeostasisHoed, MDepartment of Human Biology, Maastricht University18957934
Variation Within the CLEC16A Gene Shows Consistent Disease Association With Both Multiple Sclerosis and Type 1 Diabetes in SardiniaZoledziewska, MDipartimento di Scienze Biomediche, University of Sassari, Sassari, Italy18946483
Identification of a Novel Risk Locus for Multiple Sclerosis at 13q31.3 by a Pooled Genome-Wide Scan of 500,000 Single Nucleotide PolymorphismsComabella, MUnitat de Neuroimmunologia Clínica, CEM-Cat, Hospital Universitari Vall d'Hebron, Barcelona, Spain18941528
Associations between single nucleotide polymorphisms in folate uptake and metabolizing genes with blood folate, homocysteine, and DNA uracil concentrationsDeVos, LEberly College of Science, Pennsylvania State University18842806
Further Assessment of the Complement Component 2 and Factor B Region Associated with Age-Related Macular DegenerationMcKay, GCentre for Vision Sciences, Queen's University of Belfast18806297
Functional SNPs in CD244 Increase the Risk of Rheumatoid Arthritis in a Japanese PopulationSuzuki, ALaboratory for Autoimmune Diseases, Center for Genomic Medicine, RIKEN, Yokohama, Kanagawa 230-0045, Japan18794858
Common Variants at CD40 and Other Loci Confer Risk of Rheumatoid ArthritisRaychaudhuri, SProgram in Medical and Population Genetics, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, Massachusetts18794853
Common Variants in the Adiponectin Gene (ADIPOQ) Associated With Plasma Adiponectin Levels, Type 2 Diabetes, and Diabetes-Related Quantitative TraitsHivert, MGeneral Medicine Division, Massachusetts General Hospital18776141
Toll-Like Receptor-3 and Geographic Atrophy in Age-Related Macular DegenerationYang, ZSichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, Chengdu18753640
High Ratio of Triglycerides to HDL-Cholesterol Predicts Extensive Coronary DiseaseLemos da Luz, PUniversidade de Sao Paulo18719750
Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation studyLinsel-Nitschke, PUniversitat zu Lubeck18714375
Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease—A Mendelian Randomisation StudyLinsel-Nitschke, PUniversitat zu Lubeck18714375
STAT4, A Risk Factor for Type 1 Diabetes?Zervou, MIMedical School, University of Crete, Heraklion, Greece18703106
Evidence for genetic regulation of vitamin D status in twins with multiple sclerosisOrton, SMWellcome Trust Centre for Human Genetics and Department of Clinical Neurology, University of Oxford18689381
Comprehensive Association Study of Type 2 Diabetes and Related Quantitative Traits With 222 Candidate GenesGaulton, KDepartment of Genetics, University of North Carolina at Chapel Hill18678618
Human fasting plasma concentrations of vitamin E and carotenoids, and their association with genetic variants in apo C-III, cholesteryl ester transfer protein, hepatic lipase, intestinal fatty acid binding protein and microsomal triacylglycerol transfer proteinBorel, PNutriments Lipidiques et Prevention des Maladies Metaboliques18662427
The -589C>T polymorphism in the interleukin-4 gene (IL-4) is associated with a reduced risk of myocardial infarction in young individuals.Paffen, ELeiden University Medical Center18662263
Showing 551 through 575
These links are being provided as a convenience and for informational purposes only; they do not constitute an endorsement or an approval by AHS, Inc. of any of the products, services or opinions of the corporation or organization or individual. AHS Inc. bears no responsibility for the accuracy, legality or content of the external site or for that of subsequent links. Contact the external site for answers to questions regarding its content.
Click here to see your activities