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An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility.

• Authors : Wang L; Department of Molecular Genetics and Microbiology, School of Medicine, Duke University, 0049 CARL Building Box 3053, 213 Research Drive, Durham, NC, 27710, USA.; Balmat TJ

Subjects: Databases, Nucleic Acid* ; Genetic Predisposition to Disease* ; Linkage Disequilibrium*

• Source: Genome medicine [Genome Med] 2021 May 17; Vol. 13 (1), pp. 83. Date of Electronic Publication: 2021 May 17.Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X

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Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment.

• Authors : Wielscher M; Department of Epidemiology and Biostatistics, MRC-PHE Centre for Environment and Health, School of Public Health, Imperial College London, Norfolk Place, London, W2 1PG, UK.; Amaral AFS

Subjects: Cardiometabolic Risk Factors* ; Genetic Association Studies* ; Quantitative Trait Loci*

• Source: Genome medicine [Genome Med] 2021 Jun 21; Vol. 13 (1), pp. 104. Date of Electronic Publication: 2021 Jun 21.Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X

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A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer.

• Authors : López de Maturana E; PanGenEU Investigators; SBC/EPICURO Investigators;

Subjects: Genetic Predisposition to Disease* ; Genome-Wide Association Study*; Pancreatic Neoplasms/Pancreatic Neoplasms/Pancreatic Neoplasms/*genetics

• Source: Genome medicine [Genome Med] 2021 Feb 01; Vol. 13 (1), pp. 15. Date of Electronic Publication: 2021 Feb 01.Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X

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Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals.

• Authors : Di Maio S; Institute of Genetic Epidemiology, Department of Genetics and Pharmacology, Medical University of Innsbruck, Schöpfstrasse 41, A-6020, Innsbruck, Austria.; Grüneis R

Subjects: Alleles* ; Codon, Nonsense* ; Genetics, Population*/Genetics, Population*/Genetics, Population*/methods

• Source: Genome medicine [Genome Med] 2020 Aug 21; Vol. 12 (1), pp. 74. Date of Electronic Publication: 2020 Aug 21.Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X

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Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels.

• Authors : O'Brien TD; Vanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, TN, USA.; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.

Subjects: Gene Expression Regulation, Neoplastic* ; Genome-Wide Association Study*; Lung Neoplasms/Lung Neoplasms/Lung Neoplasms/*genetics

• Source: Genome medicine [Genome Med] 2018 Feb 27; Vol. 10 (1), pp. 16. Date of Electronic Publication: 2018 Feb 27.Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X

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Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels

• Authors : Zhongming Zhao; Peilin Jia; Neil E. Caporaso

Subjects: 0301 basic medicine; Linkage disequilibrium; Lung Neoplasms

• Source: Genome Medicine, Vol 10, Iss 1, Pp 1-14 (2018)Genome Medicine

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Complete re-sequencing of a 2Mb topological domain encompassing the FTO/IRXB genes identifies a novel obesity-associated region upstream of IRX5.

• Authors : Hunt LE; The Francis Crick Institute, Mill Hill Laboratory, The Ridgeway, Mill Hill, London, NW7 1AA, UK.; Noyvert B

Subjects: Genetic Loci*; Homeodomain Proteins/Homeodomain Proteins/Homeodomain Proteins/*genetics ; Obesity/Obesity/Obesity/*genetics

• Source: Genome medicine [Genome Med] 2015 Dec 07; Vol. 7, pp. 126. Date of Electronic Publication: 2015 Dec 07.Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X

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Complete re-sequencing of a 2Mb topological domain encompassing the FTO/IRXB genes identifies a novel obesity-associated region upstream of IRX5

• Authors : Greg Elgar; Niels Tommerup; Lilian Hunt

Subjects: Adult; Male; Linkage disequilibrium

• Source: Genome MedicineHunt, L E, Noyvert, B, Bhaw-Rosun, L, Sesay, A K, Paternoster, L, Nohr, E A, Davey Smith, G, Tommerup, N, Sørensen, T I A & Elgar, G 2015, '

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Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels.

• Authors : O’Brien, Timothy D.; Jia, Peilin; Caporaso, Neil E.

Subjects: LUNG cancer; SINGLE nucleotide polymorphisms; SMALL cell lung cancer

• Source: Genome Medicine; 2/27/2018, Vol. 10, p1-1, 1p

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Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer.

• Authors : Dong, Qian¹ (AUTHOR); Song, Nan^1,2 (AUTHOR); Qin, Na^1,3 (AUTHOR)

• Source: Genome Medicine. 3/22/2022, Vol. 14 Issue 1, p1-12. 12p.

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