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Genetic risk score AND (genetic OR genomic) AND review - PubMed - NCBI

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Genetic risk score AND (genetic OR genomic) AND review - PubMed - NCBI

Genetic risk score AND (genetic OR genomic) AND review - PubMed - NCBI

Genetic Risk Score



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Genetics of nonsyndromic obesity.Lee YS et al. Curr Opin Pediatr. (2013)

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1.
Hypertrophic Cardiomyopathy Genotype Prediction Models in a Pediatric Population.
Newman R, Jefferies JL, Chin C, He H, Shikany A, Miller EM, Parrott A.
Pediatr Cardiol. 2018 Jan 24. doi: 10.1007/s00246-018-1810-2. [Epub ahead of print]

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Genetic risk factors in thrombotic primary antiphospholipid syndrome: A systematic review with bioinformatic analyses.
Islam MA, Khandker SS, Alam F, Kamal MA, Gan SH.
Autoimmun Rev. 2018 Jan 19. pii: S1568-9972(18)30006-5. doi: 10.1016/j.autrev.2017.10.014. [Epub ahead of print] Review.

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Opportunities of next-generation sequencing in non-muscle invasive bladder cancer outcome prediction.
Pang KH, Esperto F, Noon AP; EAU Young Academic Urologists-Urothelial Cancer Working party.
Transl Androl Urol. 2017 Dec;6(6):1043-1048. doi: 10.21037/tau.2017.10.04. Review.

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4.
Genetics in the prevention and management of coronary artery disease.
Roberts R.
Curr Opin Cardiol. 2018 Jan 9. doi: 10.1097/HCO.0000000000000501. [Epub ahead of print]

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Polygenic influences on dyslipidemias.
Dron JS, Hegele RA.
Curr Opin Lipidol. 2018 Jan 2. doi: 10.1097/MOL.0000000000000482. [Epub ahead of print]

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Systemic pharmacological treatments for chronic plaque psoriasis: a network meta-analysis.
Sbidian E, Chaimani A, Garcia-Doval I, Do G, Hua C, Mazaud C, Droitcourt C, Hughes C, Ingram JR, Naldi L, Chosidow O, Le Cleach L.
Cochrane Database Syst Rev. 2017 Dec 22;12:CD011535. doi: 10.1002/14651858.CD011535.pub2. Review.

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7.
Advances in predicting venous thromboembolism risk in children.
Rühle F, Stoll M.
Br J Haematol. 2017 Dec 19. doi: 10.1111/bjh.15060. [Epub ahead of print] Review.

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8.
Diabetes in China: Epidemiology and Genetic Risk Factors and Their Clinical Utility in Personalized Medication.
Hu C, Jia W.
Diabetes. 2018 Jan;67(1):3-11. doi: 10.2337/dbi17-0013. Review.

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9.
Prader-Willi Syndrome.
Driscoll DJ, Miller JL, Schwartz S, Cassidy SB.
In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
1998 Oct 6 [updated 2017 Dec 14].

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10.
Chronic obstructive pulmonary disease and lung cancer: inter-relationships.
Biswas A, Mehta HJ, Folch EE.
Curr Opin Pulm Med. 2018 Mar;24(2):152-160. doi: 10.1097/MCP.0000000000000451.

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11.
Pooling-analysis on hMLH1 polymorphisms and cancer risk: evidence based on 31,484 cancer cases and 45,494 cancer-free controls.
Li S, Zheng Y, Tian T, Wang M, Liu X, Liu K, Zhai Y, Dai C, Deng Y, Li S, Dai Z, Lu J.
Oncotarget. 2017 Oct 10;8(54):93063-93078. doi: 10.18632/oncotarget.21810. eCollection 2017 Nov 3.

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12.
Current Perspectives on Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis.
Lerch M, Mainetti C, Terziroli Beretta-Piccoli B, Harr T.
Clin Rev Allergy Immunol. 2017 Nov 29. doi: 10.1007/s12016-017-8654-z. [Epub ahead of print] Review.

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13.
Genes to predict VO<sub>2max</sub> trainability: a systematic review.
Williams CJ, Williams MG, Eynon N, Ashton KJ, Little JP, Wisloff U, Coombes JS.
BMC Genomics. 2017 Nov 14;18(Suppl 8):831. doi: 10.1186/s12864-017-4192-6. Review.

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14.
New Histopathological &amp; Genetic Features to Improve Active Surveillance Selection for Low-Risk Prostate Cancer.
Wong LM, Chu K, Corcoran N, Norden S.
Anticancer Agents Med Chem. 2017 Nov 13. doi: 10.2174/1871520617666171114105846. [Epub ahead of print]

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15.
The use of polygenic risk scores to identify phenotypes associated with genetic risk of schizophrenia: Systematic review.
Mistry S, Harrison JR, Smith DJ, Escott-Price V, Zammit S.
Schizophr Res. 2017 Nov 9. pii: S0920-9964(17)30665-5. doi: 10.1016/j.schres.2017.10.037. [Epub ahead of print] Review.

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16.
Genomic Markers in Prostate Cancer Decision Making.
Cucchiara V, Cooperberg MR, Dall'Era M, Lin DW, Montorsi F, Schalken JA, Evans CP.
Eur Urol. 2017 Nov 9. pii: S0302-2838(17)30975-2. doi: 10.1016/j.eururo.2017.10.036. [Epub ahead of print] Review.

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17.
Recent development of risk-prediction models for incident hypertension: An updated systematic review.
Sun D, Liu J, Xiao L, Liu Y, Wang Z, Li C, Jin Y, Zhao Q, Wen S.
PLoS One. 2017 Oct 30;12(10):e0187240. doi: 10.1371/journal.pone.0187240. eCollection 2017. Review.

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18.
Genetic Risk Scores for Type 1 Diabetes Prediction and Diagnosis.
Redondo MJ, Oram RA, Steck AK.
Curr Diab Rep. 2017 Oct 28;17(12):129. doi: 10.1007/s11892-017-0961-5. Review.

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19.
Marfan Syndrome.
Dietz H.
In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2001 Apr 18 [updated 2017 Oct 12].

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20.
Bypassing agent prophylaxis in people with hemophilia A or B with inhibitors.
Chai-Adisaksopha C, Nevitt SJ, Simpson ML, Janbain M, Konkle BA.
Cochrane Database Syst Rev. 2017 Sep 25;9:CD011441. doi: 10.1002/14651858.CD011441.pub2. Review.

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