Detalhe da pesquisa
1.
High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.
Circulation
; 125(18): 2232-42, 2012 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-22499950
2.
Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children.
Am J Respir Crit Care Med
; 186(2): 140-6, 2012 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22652028
3.
African ancestry and lung function in Puerto Rican children.
J Allergy Clin Immunol
; 129(6): 1484-90.e6, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22560959
4.
Type of pain, pain-associated complications, quality of life, disability and resource utilisation in chronic pancreatitis: a prospective cohort study.
Gut
; 60(1): 77-84, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21148579
5.
A novel locus for familial migraine on Xp22.
Headache
; 50(6): 955-62, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20412323
6.
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.
Eur J Hum Genet
; 14(10): 1097-105, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16773128
7.
The IBD international genetics consortium provides further evidence for linkage to IBD4 and shows gene-environment interaction.
Inflamm Bowel Dis
; 11(1): 1-7, 2005 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-15674107
8.
Rarity of the Alzheimer disease-protective APP A673T variant in the United States.
JAMA Neurol
; 72(2): 209-16, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25531812
9.
The functional angiotensin converting enzyme gene I/D polymorphism does not alter susceptibility to chronic pancreatitis.
JOP
; 5(6): 457-63, 2004 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-15536282
10.
Identifying genetic interactions associated with late-onset Alzheimer's disease.
BioData Min
; 7(1): 35, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25649863
11.
Genome-wide association study of antiphospholipid antibodies.
Autoimmune Dis
; 2013: 761046, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23509613
12.
Biogenetic mechanisms predisposing to complex phenotypes in parents may function differently in their children.
J Gerontol A Biol Sci Med Sci
; 68(7): 760-8, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23213029
13.
Genetic variants within the MHC region are associated with immune responsiveness to childhood vaccinations.
Vaccine
; 31(46): 5381-91, 2013 Nov 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-24075919
14.
Beta-amyloid toxicity modifier genes and the risk of Alzheimer's disease.
Am J Neurodegener Dis
; 1(2): 191-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22984654
15.
Novel late-onset Alzheimer disease loci variants associate with brain gene expression.
Neurology
; 79(3): 221-8, 2012 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22722634
16.
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Nat Genet
; 43(5): 436-41, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21460841
17.
An efficient bayesian method for predicting clinical outcomes from genome-wide data.
AMIA Annu Symp Proc
; 2010: 127-31, 2010 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21346954
18.
"Predicting" parental longevity from offspring endophenotypes: data from the Long Life Family Study (LLFS).
Mech Ageing Dev
; 131(3): 215-22, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20184914
19.
Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.
J Am Soc Nephrol
; 14(7): 1794-803, 2003 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12819239
20.
African American hypertensive nephropathy maps to a new locus on chromosome 9q31-q32.
Am J Hum Genet
; 73(2): 420-9, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12840782