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 476 through 500
Author
Zhang, X
Author Organization
Department of Respiratory Medicine, The First Affiliated Hospital, Medical College of Soochow University
Pubmed ID
19288024
Link

Author
Kemlink, D
Author Organization
Helmholtz Zentrum Munich, National Research Center of Environment and Health, Institute of Human Genetics, Munich, Germany
Pubmed ID
19279021
Link

Author
Bergeron-Sawitzke, J
Author Organization
SAIC-Frederick, Basic Science Program, Human Genetics Section
Pubmed ID
19259132
Link

Author
Ahn, J
Author Organization
Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
Pubmed ID
19255064
Link

Author
Tong, Y
Author Organization
Open laboratory, West China Second University Hospital, Sichuan University
Pubmed ID
19228405
Link

Author
Erdmann, J
Author Organization
Universitat zu Lubeck
Pubmed ID
19198612
Link

Author
Gudbjartsson, D, F
Author Organization
deCODE Genetics
Pubmed ID
19198610
Link


Author
Ferrucci, L
Author Organization
National Institute on Aging, National Institutes of Health
Pubmed ID
19185284
Link

Author
Zhang, X
Author Organization
Institute of Dermatology and Department of Dermatology at No.1 Hospital, Anhui Medical University, Hefei, Anhui 230022, China
Pubmed ID
19169255
Link

Author
Nair, RP
Author Organization
Department of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan 
Pubmed ID
19169254
Link

Author
de Cid, R
Author Organization
Genes and Disease Programme, Centre for Genomic Regulation (CRG) and Public Health and Epidemiology Network Biomedical Research Center (CIBERESP), 08003 Barcelona, Spain
Pubmed ID
19169253
Link

Author
Kripke, D
Author Organization
Department of Psychiatry 0939, University of California
Pubmed ID
19166596
Link

Author
Samani, N, J
Author Organization
Coronary Artery Disease Consortium
Pubmed ID
19164808
Link

Author
Kaab, S
Author Organization
University Hospital Grosshadern
Pubmed ID
19141561
Link

Author
Leung, W
Author Organization
Human Nutrition Research Centre, Newcastle University
Pubmed ID
19103647
Link

Author
Smyth, DJ
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, United Kingdom
Pubmed ID
19073967
Link

Author
Anderson, CA
Author Organization
Genetic and Genomic Epidemiology Unit, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, UK
Pubmed ID
19068216
Link

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

TitleAuthorAuthor OrganizationPubmed IDLink 
Genetic variants in interleukin-6 modified risk of obstructive sleep apnea syndromeZhang, XDepartment of Respiratory Medicine, The First Affiliated Hospital, Medical College of Soochow University19288024
Replication of restless legs syndrome loci in three European populationsKemlink, DHelmholtz Zentrum Munich, National Research Center of Environment and Health, Institute of Human Genetics, Munich, Germany19279021
Multilocus analysis of age-related macular degenerationBergeron-Sawitzke, JSAIC-Frederick, Basic Science Program, Human Genetics Section19259132
Vitamin D-related genes, serum vitamin D concentrations and prostate cancer riskAhn, JDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health19255064
Association between TCF7L2 gene polymorphisms and susceptibility to type 2 diabetes mellitus, a large Human Genome Epidemiology (HuGE) review and meta-analysis.Tong, YOpen laboratory, West China Second University Hospital, Sichuan University19228405
New susceptibility locus for coronary artery disease on chromosome 3q22.3Erdmann, JUniversitat zu Lubeck19198612
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionGudbjartsson, D, FdeCODE Genetics19198610
Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variantsKathiresan, SMyocardial Infarction Genetics Consortium19198609
Common Variation in theb-Carotene15,150-Monooxygenase 1 Gene Affects Circulating Levels of Carotenoids, A Genome-wide Association StudyFerrucci, LNational Institute on Aging, National Institutes of Health19185284
Psoriasis Genome-Wide Association Study Identifies Susceptibility Variants Within LCE Gene Cluster at 1q21Zhang, XInstitute of Dermatology and Department of Dermatology at No.1 Hospital, Anhui Medical University, Hefei, Anhui 230022, China19169255
Genome-wide Scan Reveals Association of Psoriasis With IL-23 and NF-kappaB PathwaysNair, RPDepartment of Dermatology, University of Michigan Medical School, Ann Arbor, Michigan 19169254
Deletion of the Late Cornified Envelope LCE3B and LCE3C Genes as a Susceptibility Factor for Psoriasisde Cid, RGenes and Disease Programme, Centre for Genomic Regulation (CRG) and Public Health and Epidemiology Network Biomedical Research Center (CIBERESP), 08003 Barcelona, Spain19169253
Circadian polymorphisms associated with affective disordersKripke, DDepartment of Psychiatry 0939, University of California19166596
Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery DiseaseSamani, N, JCoronary Artery Disease Consortium19164808
Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillationKaab, SUniversity Hospital Grosshadern19141561
Two common single nucleotide polymorphisms in the gene encoding beta-carotene 15,15'-monoxygenase alter beta-carotene metabolism in female volunteers.Leung, WHuman Nutrition Research Centre, Newcastle University19103647
Shared and Distinct Genetic Variants in Type 1 Diabetes and Celiac DiseaseSmyth, DJJuvenile 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, United Kingdom19073967
Investigation of Crohn's Disease Risk Loci in Ulcerative Colitis Further Defines Their Molecular RelationshipAnderson, CAGenetic and Genomic Epidemiology Unit, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford, UK19068216
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
Showing 476 through 500
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