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 601 through 625
Author
Oishi, T
Author Organization
Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University of Tokyo, 4-6-1 Shirokanedai, Minato, Department of Medicine, Kidney Center, Tokyo Women's Medical University, Tokyo
Pubmed ID
18219441
Link

Author
Nair, RP
Author Organization
Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan 
Pubmed ID
18219280
Link

Author
Beckly, JB
Author Organization
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
Pubmed ID
18200509
Link

Author
Kathiresan, S
Author Organization
Massachusetts General Hospital
Pubmed ID
18193044
Link

Author
Willer, C, J
Author Organization
University of Michigan
Pubmed ID
18193043
Link


Author
Judd, S
Author Organization
Emory University School of Medicine
Pubmed ID
18180395
Link

Author
Omori, S
Author Organization
Laboratory for Diabetic Nephropathy, SNP Research Center
Pubmed ID
18162508
Link

Author
Kilpelainen, T
Author Organization
Institute of Biomedicine, Physiology, University of Kuopio
Pubmed ID
18091023
Link

Author
Huber, AK
Author Organization
Division of Endocrinology, The Vontz Center, ML 0547, University of Cincinnati College of Medicine, Cincinnati, Ohio
Pubmed ID
18073300
Link

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

TitleAuthorAuthor OrganizationPubmed IDLink 
A Functional SNP in the NKX2.5-binding Site of ITPR3 Promoter Is Associated With Susceptibility to Systemic Lupus Erythematosus in Japanese PopulationOishi, TLaboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University of Tokyo, 4-6-1 Shirokanedai, Minato, Department of Medicine, Kidney Center, Tokyo Women's Medical University, Tokyo18219441
Polymorphisms of the IL12B and IL23R Genes Are Associated With PsoriasisNair, RPDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan 18219280
Two-stage Candidate Gene Study of Chromosome 3p Demonstrates an Association Between Nonsynonymous Variants in the MST1R Gene and Crohn's DiseaseBeckly, JBWellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK18200509
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humansKathiresan, SMassachusetts General Hospital18193044
Newly identified loci that influence lipid concentrations and risk of coronary artery diseaseWiller, C, JUniversity of Michigan18193043
Association of variants in the sterol regulatory element-binding factor 1 (SREBF1) gene with type 2 diabetes, glycemia, and insulin resistanceGrarup, NSteno Diabetes Center, Copenhagen18192539
Vitamin D Deficiency and Risk for Cardiovascular DiseaseJudd, SEmory University School of Medicine18180395
Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 With Susceptibility to Type 2 Diabetes in a Japanese PopulationOmori, SLaboratory for Diabetic Nephropathy, SNP Research Center18162508
SNPs in PPARG associate with type 2 diabetes and interact with physical activity.Kilpelainen, TInstitute of Biomedicine, Physiology, University of Kuopio18091023
Interleukin (IL)-23 Receptor Is a Major Susceptibility Gene for Graves' Ophthalmopathy, The IL-23/T-helper 17 Axis Extends to Thyroid AutoimmunityHuber, AKDivision of Endocrinology, The Vontz Center, ML 0547, University of Cincinnati College of Medicine, Cincinnati, Ohio18073300
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
Showing 601 through 625
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