Human genome meeting 2016 : Houston, TX, USA. 28 February - 2 March 2016.
Srivastava AK, Wang Y, Huang R, Skinner C, Thompson T, Pollard L, Wood T, Luo F, Stevenson R, Polimanti R, Gelernter J, Lin X, Lim IY, Wu Y, Teh AL, Chen L, Aris IM, Soh SE, Tint MT, MacIsaac JL, Yap F, Kwek K, Saw SM, Kobor MS, Meaney MJ, Godfrey KM, Chong YS, Holbrook JD, Lee YS, Gluckman PD, Karnani N; GUSTO study group; Kapoor A, Lee D, Chakravarti A, Maercker C, Graf F, Boutros M, Stamoulis G, Santoni F, Makrythanasis P, Letourneau A, Guipponi M, Panousis N, Garieri M, Ribaux P, Falconnet E, Borel C, Antonarakis SE, Kumar S, Curran J, Blangero J, Chatterjee S, Kapoor A, Akiyama J, Auer D, Berrios C, Pennacchio L, Chakravarti A, Donti TR, Cappuccio G, Miller M, Atwal P, Kennedy A, Cardon A, Bacino C, Emrick L, Hertecant J, Baumer F, Porter B, Bainbridge M, Bonnen P, Graham B, Sutton R, Sun Q, Elsea S, Hu Z, Wang P, Zhu Y, Zhao J, Xiong M, Bennett DA, Hidalgo-Miranda A, Romero-Cordoba S, Rodriguez-Cuevas S, Rebollar-Vega R, Tagliabue E, Iorio M, D’Ippolito E, Baroni S, Kaczkowski B, Tanaka Y, Kawaji H, Sandelin A, Andersson R, Itoh M, Lassmann T; The FANTOM5 Consortium; Hayashizaki Y, Carninci P, Forrest ARR, Semple CA, Rosenthal EA, Shirts B, Amendola L, Gallego C, Horike-Pyne…
Hum Genomics. 2016 May 26;10 Suppl 1(Suppl 1):12. doi: 10.1186/s40246-016-0063-5.
Genetic correlation and causal relationships between cardio-metabolic traits and lung function impairment.
Wielscher M, Amaral AFS, van der Plaat D, Wain LV, Sebert S, Mosen-Ansorena D, Auvinen J, Herzig KH, Dehghan A, Jarvis DL, Jarvelin MR.
Genome Med. 2021 Jun 21;13(1):104. doi: 10.1186/s13073-021-00914-x.
The Identikit of Patient at Risk for Severe COVID-19 and Death: The Dysregulation of Renin-Angiotensin System as the Common Theme.
Sarzani R, Allevi M, Giulietti F, Di Pentima C, Re S, Giordano P, Spannella F.
J Clin Med. 2021 Dec 15;10(24):5883. doi: 10.3390/jcm10245883.
Disequilibrium between the classic renin-angiotensin system and its opposing arm in SARS-CoV-2-related lung injury.
Sarzani R, Giulietti F, Di Pentima C, Giordano P, Spannella F.
Am J Physiol Lung Cell Mol Physiol. 2020 Aug 1;319(2):L325-L336. doi: 10.1152/ajplung.00189.2020. Epub 2020 Jul 8.
African genetic diversity: implications for human demographic history, modern human origins, and complex disease mapping.
Campbell MC, Tishkoff SA.
Annu Rev Genomics Hum Genet. 2008;9:403-33. doi: 10.1146/annurev.genom.9.081307.164258.
Variations in CRHR1 are associated with persistent pulmonary hypertension of the newborn.
Byers HM, Dagle JM, Klein JM, Ryckman KK, McDonald EL, Murray JC, Borowski KS.
Pediatr Res. 2012 Feb;71(2):162-7. doi: 10.1038/pr.2011.24. Epub 2011 Dec 21.
Polymorphisms in lipid metabolism related miRNA binding sites and risk of metabolic syndrome.
Ye Q, Zhao X, Xu K, Li Q, Cheng J, Gao Y, Du J, Shi H, Zhou L.
Gene. 2013 Oct 10;528(2):132-8. doi: 10.1016/j.gene.2013.07.036. Epub 2013 Jul 31.
Epitope analysis of the collagen type V-specific T cell response in lung transplantation reveals an HLA-DRB1*15 bias in both recipient and donor.
Keller MR, Haynes LD, Jankowska-Gan E, Sullivan JA, Agashe VV, Burlingham SR, Burlingham WJ.
PLoS One. 2013 Nov 12;8(11):e79601. doi: 10.1371/journal.pone.0079601. eCollection 2013.
Association between functional polymorphisms in the nitric oxide synthase 3 gene and pediatric acute respiratory distress syndrome.
Wei L, An Y, Wang J.
Genet Mol Res. 2016 Sep 16;15(3). doi: 10.4238/gmr.15038401.
Haplotypes of the HRES-1 endogenous retrovirus are associated with development and disease manifestations of systemic lupus erythematosus.
Pullmann R Jr, Bonilla E, Phillips PE, Middleton FA, Perl A.
Arthritis Rheum. 2008 Feb;58(2):532-40. doi: 10.1002/art.23161.
