Farmer
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Last Posted: Sep 25, 2023
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry.
Ke Wang, et al. Cell genomics 2023 0 (9) 100377 - Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Munn-Chernoff Melissa A, et al. Addiction biology 2020 0 (1) e12880 - Response to Severe Acute Respiratory Syndrome Coronavirus 2 Initial Series and Additional Dose Vaccine in Patients With Predominant Antibody Deficiency.
Barmettler Sara, et al. The journal of allergy and clinical immunology. In practice 2022 0 (6) 1622-1634.e4 - Association of AGTR1 gene methylation and its genetic variant in Chinese farmer with hypertension: A case-control study.
Li Zhi-Yuan, et al. Medicine 2022 7 (29) e29712 - Genome-wide association study of suicidal behaviour severity in mood disorders.
Zai Clement C, et al. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2021 0 (9) 722-731 - Recommendations for designing genetic test reports to be understood by patients and non-specialists
GD Farmer et al, EJHG, February 5, 2020 - Adverse Events in Genetic Testing: The Fourth Case Series.
Farmer Meagan B et al. Cancer journal (Sudbury, Mass.) (4) 231-236 - Disease of the Week: Sickle Cell Disease
CDC,June 2019 - Vaccines: Life savers against infectious diseases
Wellcome Trust Sanger Blog, August 2, 2019 - CLINGEN Actionability Report for Li-Fraumeni Syndrome - TP53
ClinGen Actionability Working Group - NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.
Daly Mary B et al. Journal of the National Comprehensive Cancer Network : JNCCN 2017 Jan 15(1) 9-20 - Hypersensitivity Pneumonitis
From NHLBI health topic site - Systematic assessment of etiology in adults with a clinical diagnosis of young-onset type 2 diabetes is a successful strategy for identifying maturity-onset diabetes of the young.
Thanabalasingham Gaya, et al. Diabetes care 2012 6 (6) 1206-12 - Variation in GNB3 predicts response and adverse reactions to antidepressants.
Keers Robert, et al. Journal of psychopharmacology (Oxford, England) 2011 7 (7) 867-74 - Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.
Shatunov Aleksey, et al. The Lancet. Neurology 2010 10 (10) 986-94 - Meta-analysis and imputation refines the association of 15q25 with smoking quantity.
Liu Jason Z, et al. Nature genetics 2010 5 (5) 436-40 - Effects of G/A polymorphism, rs266882, in the androgen response element 1 of the PSA gene on prostate cancer risk, survival and circulating PSA levels.
Jesser C, et al. British journal of cancer 2008 11 (10) 1743-7 - PAH-DNA adducts in environmentally exposed population in relation to metabolic and DNA repair gene polymorphisms.
Binkova Blanka, et al. Mutation research 2007 7 (1-2) 49-61 - Monitoring low benzene exposure: comparative evaluation of urinary biomarkers, influence of cigarette smoking, and genetic polymorphisms.
Fustinoni Silvia, et al. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005 9 (9) 2237-44 - N-Acetyltransferase 2 gene polymorphism in a group of senile dementia patients in Shanghai suburb.
Guo Wei-Chao, et al. Acta pharmacologica Sinica 2004 9 (9) 1112-7
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About HLBS-PopOmics
HLBS-PopOmics is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to Heart and Vascular Diseases(H), Lung Diseases(L), Blood Diseases(B), and Sleep Disorders(S)...more
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Site Citation:
Mensah GA, Yu W, Barfield WL, Clyne M, Engelgau MM, Khoury MJ. HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders. Genet Med. 2018 Sep 10. doi: 10.1038/s41436-018-0118-1
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
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