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Items: 1 to 20 of 45

1.

Neural Plasticity in Obesity and Psychiatric Disorders.

Arcos-Burgos M, Acosta MT, Martinez AF, Muenke M, Enriori PJ, Mastronardi CA.

Neural Plast. 2016;2016:6053871. doi: 10.1155/2016/6053871. Epub 2016 Apr 7. No abstract available.

2.

A Mutation in DAOA Modifies the Age of Onset in PSEN1 E280A Alzheimer's Disease.

Vélez JI, Rivera D, Mastronardi CA, Patel HR, Tobón C, Villegas A, Cai Y, Easteal S, Lopera F, Arcos-Burgos M.

Neural Plast. 2016;2016:9760314. doi: 10.1155/2016/9760314. Epub 2016 Jan 5.

3.

Family-Based Association Study of Pulmonary Function in a Population in Northeast Asia.

Son HY, Sohn SW, Im SH, Kim HJ, Lee MK, Gombojav B, Kwon HS, Park DS, Kim HL, Min KU, Sung J, Seo JS, Kim JI.

PLoS One. 2015 Oct 2;10(10):e0139716. doi: 10.1371/journal.pone.0139716. eCollection 2015.

4.

The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.

Yan D, Kannan-Sundhari A, Vishwanath S, Qing J, Mittal R, Kameswaran M, Liu XZ.

Genet Test Mol Biomarkers. 2015 Sep;19(9):512-27. doi: 10.1089/gtmb.2015.0023. Epub 2015 Jul 17. Review.

5.

Ancestral association between HLA and HFE H63D and C282Y gene mutations from northwest Colombia.

Rodriguez LM, Giraldo MC, Velasquez LI, Alvarez CM, Garcia LF, Jimenez-Del-Rio M, Velez-Pardo C.

Genet Mol Biol. 2015 Mar;38(1):8-13. doi: 10.1590/S1415-475738120140080. Epub 2014 Mar 17.

6.

Genome-wide association study of susceptibility loci for breast cancer in Sardinian population.

Palomba G, Loi A, Porcu E, Cossu A, Zara I, Budroni M, Dei M, Lai S, Mulas A, Olmeo N, Ionta MT, Atzori F, Cuccuru G, Pitzalis M, Zoledziewska M, Olla N, Lovicu M, Pisano M, Abecasis GR, Uda M, Tanda F, Michailidou K, Easton DF, Chanock SJ, Hoover RN, Hunter DJ, Schlessinger D, Sanna S, Crisponi L, Palmieri G.

BMC Cancer. 2015 May 10;15:383. doi: 10.1186/s12885-015-1392-9.

7.

Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studies.

Peskin VA, Ordóñez A, Mackin RS, Delucchi K, Monge S, McGough JJ, Chavira DA, Berrocal M, Cheung E, Fournier E, Badner JA, Herrera LD, Mathews CA.

Am J Med Genet B Neuropsychiatr Genet. 2015 Jun;168B(4):247-57. doi: 10.1002/ajmg.b.32305. Epub 2015 Mar 31.

8.

Genetics and genomic medicine in Colombia.

De Castro M, Restrepo CM.

Mol Genet Genomic Med. 2015 Mar;3(2):84-91. doi: 10.1002/mgg3.139. No abstract available.

9.

Extensive genome-wide autozygosity in the population isolates of Daghestan.

Karafet TM, Bulayeva KB, Bulayev OA, Gurgenova F, Omarova J, Yepiskoposyan L, Savina OV, Veeramah KR, Hammer MF.

Eur J Hum Genet. 2015 Oct;23(10):1405-12. doi: 10.1038/ejhg.2014.299. Epub 2015 Jan 21.

10.

Genome-wide linkage disequilibrium in nine-spined stickleback populations.

Yang J, Shikano T, Li MH, Merilä J.

G3 (Bethesda). 2014 Aug 12;4(10):1919-29. doi: 10.1534/g3.114.013334.

11.

Using population isolates in genetic association studies.

Hatzikotoulas K, Gilly A, Zeggini E.

Brief Funct Genomics. 2014 Sep;13(5):371-7. doi: 10.1093/bfgp/elu022. Epub 2014 Jul 9. Review.

12.

Triple-negative breast cancer frequency and type of BRCA mutation: Clues from Sardinia.

Palomba G, Budroni M, Olmeo N, Atzori F, Ionta MT, Pisano M, Tanda F, Cossu A, Palmieri G.

Oncol Lett. 2014 Apr;7(4):948-952. Epub 2014 Jan 28.

13.

Random inbreeding, isonymy, and population isolates in Argentina.

Dipierri J, Rodríguez-Larralde A, Barrai I, Camelo JL, Redomero EG, Rodríguez CA, Ramallo V, Bronberg R, Alfaro E.

J Community Genet. 2014 Jul;5(3):241-8. doi: 10.1007/s12687-013-0181-x. Epub 2014 Feb 6.

14.

Heterogeneous distribution of BRAF/NRAS mutations among Italian patients with advanced melanoma.

Colombino M, Lissia A, Capone M, De Giorgi V, Massi D, Stanganelli I, Fonsatti E, Maio M, Botti G, Caracò C, Mozzillo N, Ascierto PA, Cossu A, Palmieri G.

J Transl Med. 2013 Aug 29;11:202. doi: 10.1186/1479-5876-11-202.

15.

Screening of Finnish RAD51C founder mutations in prostate and colorectal cancer patients.

Pelttari LM, Nurminen R, Gylfe A, Aaltonen LA, Schleutker J, Nevanlinna H.

BMC Cancer. 2012 Nov 23;12:552. doi: 10.1186/1471-2407-12-552.

16.

Comprehensive genomic analyses associate UGT8 variants with musical ability in a Mongolian population.

Park H, Lee S, Kim HJ, Ju YS, Shin JY, Hong D, von Grotthuss M, Lee DS, Park C, Kim JH, Kim B, Yoo YJ, Cho SI, Sung J, Lee C, Kim JI, Seo JS.

J Med Genet. 2012 Dec;49(12):747-52. doi: 10.1136/jmedgenet-2012-101209. Epub 2012 Nov 1.

17.

Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls.

Arcos-Burgos M, Londoño AC, Pineda DA, Lopera F, Palacio JD, Arbelaez A, Acosta MT, Vélez JI, Castellanos FX, Muenke M.

Atten Defic Hyperact Disord. 2012 Dec;4(4):205-12. doi: 10.1007/s12402-012-0088-0. Epub 2012 Jul 20.

18.

A population-based study of autosomal-recessive disease-causing mutations in a founder population.

Chong JX, Ouwenga R, Anderson RL, Waggoner DJ, Ober C.

Am J Hum Genet. 2012 Oct 5;91(4):608-20. doi: 10.1016/j.ajhg.2012.08.007. Epub 2012 Sep 13.

19.

Linkage and association of successful aging to the 6q25 region in large Amish kindreds.

Edwards DR, Gilbert JR, Hicks JE, Myers JL, Jiang L, Cummings AC, Guo S, Gallins PJ, Konidari I, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Laux R, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK.

Age (Dordr). 2013 Aug;35(4):1467-77. doi: 10.1007/s11357-012-9447-1. Epub 2012 Jul 7.

20.

GWAS reveals new recessive loci associated with non-syndromic facial clefting.

Camargo M, Rivera D, Moreno L, Lidral AC, Harper U, Jones M, Solomon BD, Roessler E, Vélez JI, Martinez AF, Chandrasekharappa SC, Arcos-Burgos M.

Eur J Med Genet. 2012 Oct;55(10):510-4. doi: 10.1016/j.ejmg.2012.06.005. Epub 2012 Jun 27.

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