Detalhe da pesquisa
1.
Neutrophil-to-lymphocyte ratio (NLR) variations in relationship with childhood maltreatment in patients with anorexia nervosa: a retrospective cohort study.
Eat Weight Disord
; 27(6): 2201-2212, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35128621
2.
Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study.
Mol Psychiatry
; 22(9): 1359-1367, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28485404
3.
Risk factors of suicide re-attempt: A two-year prospective study.
J Affect Disord
; 356: 535-544, 2024 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38657762
4.
Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7.
Nat Genet
; 10(2): 240-2, 1995 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-7663523
5.
Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees.
Nat Genet
; 3(1): 49-55, 1993 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8490654
6.
Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q.
Nat Genet
; 5(4): 386-91, 1993 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-8298648
7.
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis.
Nat Genet
; 11(3): 325-7, 1995 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-7581458
8.
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population.
Nat Genet
; 9(2): 152-9, 1995 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-7719342
9.
Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes.
Nat Genet
; 27(4): 435-8, 2001 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11279528
10.
Localization of a gene for partial epilepsy to chromosome 10q.
Nat Genet
; 10(1): 56-60, 1995 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-7647791
11.
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.
Nat Genet
; 16(2): 202-5, 1997 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-9171836
12.
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease.
Nat Genet
; 7(2): 180-4, 1994 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-7920638
13.
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus.
Nat Genet
; 19(3): 292-6, 1998 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-9662408
14.
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.
Nat Genet
; 17(1): 40-8, 1997 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-9288096
15.
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.
Nat Genet
; 13(4): 399-408, 1996 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-8696333
16.
A full genome search in multiple sclerosis.
Nat Genet
; 13(4): 472-6, 1996 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-8696345
17.
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.
Nat Genet
; 13(2): 161-6, 1996 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-8640221
18.
Cystic fibrosis mutations for p.F508del compound heterozygotes predict sweat chloride levels and pancreatic sufficiency.
Clin Genet
; 82(6): 546-51, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22035343
19.
A brief note on the resemblance between relatives in the presence of population stratification.
Heredity (Edinb)
; 108(5): 563-8, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22234249
20.
An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus.
Proc Natl Acad Sci U S A
; 104(52): 20896-901, 2007 Dec 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-18087043