-
1
-
-
0004959009
-
-
-
-
-
4
-
-
0032554222
-
The new genetics of clinical practice
-
(1998)
BMJ
, vol.316
, pp. 618-620
-
-
Bell, J.1
-
5
-
-
0033168459
-
Shattuck lecture - Medical and societal consequences of the Human Genome Project
-
(1999)
N. Engl. J. Med.
, vol.341
, Issue.1
, pp. 28-37
-
-
Collins, F.S.1
-
7
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer - Analysis of cohorts of twins from Sweden, Denmark, and Finland
-
(2000)
N. Engl. J. Med.
, vol.343
, Issue.2
, pp. 78-85
-
-
Lichtenstein, P.1
-
10
-
-
0033671717
-
Dominant modifier DFNM1 suppresses recessive deafness DFNB26
-
(2000)
Nat. Genet.
, vol.26
, Issue.4
, pp. 431-434
-
-
Riazuddin, S.1
-
11
-
-
0034724857
-
Gene therapy of human severe combined immunodeficiency (SCID) disease
-
(2000)
Science
, vol.288
, pp. 669-672
-
-
Cavazzana-Calvo, M.1
-
12
-
-
0033517343
-
A population-based study of the clinical expression of the hemochromatosis gene
-
(1999)
N. Engl. J. Med.
, vol.341
, Issue.10
, pp. 718-724
-
-
Olynyk, J.K.1
-
14
-
-
0031012805
-
Cancer risk associated with germline DNA mismatch repair gene mutations
-
(1997)
Hum. Mol. Genet.
, vol.6
, Issue.1
, pp. 105-110
-
-
Dunlop, M.G.1
-
15
-
-
0033516265
-
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
-
(1999)
J. Natl. Cancer Inst.
, vol.91
, Issue.11
, pp. 943-949
-
-
Peto, J.1
-
16
-
-
0032555020
-
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
-
(1998)
N. Engl. J. Med.
, vol.338
, Issue.21
, pp. 1481-1487
-
-
Aaltonen, L.A.1
-
17
-
-
0030910022
-
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
-
(1997)
N. Engl. J. Med.
, vol.336
, Issue.20
, pp. 1401-1408
-
-
Struewing, J.P.1
-
18
-
-
0032231617
-
Frequency and carrier risk associated with common BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer patients
-
(1998)
Am. J. Hum. Genet.
, vol.63
, Issue.1
, pp. 45-51
-
-
Fodor, F.H.1
-
21
-
-
0033803952
-
Synergistic heterozygosity: Disease resulting from multiple partial defects in one or more metabolic pathways
-
(2000)
Mol. Genet. Metab.
, vol.71
, Issue.1-2
, pp. 10-18
-
-
Vockley, J.1
-
22
-
-
0032543748
-
High risk of cerebral-vein thrombosis in carriers of a prothrombingene mutation and in users of oral contraceptives
-
(1998)
N. Engl. J. Med.
, vol.338
, Issue.25
, pp. 1793-1797
-
-
Martinelli, I.1
-
23
-
-
17044452367
-
HIV-1 resistance phenotype conferred by combination of two separate inherited mutations of CCR5 gene
-
(1998)
Lancet
, vol.351
, pp. 14-18
-
-
Quillent, C.1
-
24
-
-
0004959010
-
Breast and ovarian cancer risks among women with BRCA1 and BRCA2 mutations in the New York Breast Cancer Study (NYBCS)
-
follows p. 291
-
Am. J. Hum. Genet.
, vol.68
, pp. 2001
-
-
-
27
-
-
0030614816
-
Apolipoprotein E epsilon4 and incidence of Alzheimer disease in a community population of older persons
-
(1997)
JAMA
, vol.277
, Issue.10
, pp. 822-824
-
-
Evans, D.A.1
-
32
-
-
0004974348
-
The RAD51-135 SNP modifies breast and ovarian cancer risk in BRCA2 carriers, but not in BRCA1 carriers
-
(2000)
Am. J. Hum. Genet.
, vol.67
, Issue.SUPPL. 2
, pp. 59
-
-
Levy-Lahad, E.1
-
34
-
-
0033909667
-
Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype
-
(2000)
Am. J. Hum. Genet.
, vol.66
, Issue.1
, pp. 205-215
-
-
Friddle, C.1
-
36
-
-
0033772073
-
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
-
(2000)
Nat. Genet.
, vol.26
, Issue.2
, pp. 163-175
-
-
Horikawa, Y.1
-
39
-
-
0034684425
-
Proteomics: New perspectives, new biomedical opportunities
-
(2000)
Lancet
, vol.356
, Issue.9243
, pp. 1749-1756
-
-
Banks, R.E.1
-
40
-
-
0027320812
-
Associations of disease with genetic markers: Deja vu all over again
-
(1993)
Am. J. Med. Genet.
, vol.48
, Issue.2
, pp. 71-73
-
-
Kidd, K.K.1
-
41
-
-
0032217019
-
Eugenics and individual phenotypic variation: To what extent is biology a predictive science?
-
(1998)
Science in Context
, vol.11
, pp. 331-356
-
-
Balaban, E.1
-
43
-
-
0034638766
-
Pharmacogenetics and adverse drug reactions
-
(2000)
Lancet
, vol.356
, Issue.9242
, pp. 1667-1671
-
-
Meyer, U.A.1
-
44
-
-
0034162075
-
Serotonin receptor 2A, 2C, 1A genes and response to lithium prophylaxis in mood disorders
-
(2000)
J. Psychiatr. Res.
, vol.34
, Issue.2
, pp. 89-98
-
-
Serretti, A.1
-
45
-
-
0028124367
-
Offering cystic fibrosis carrier screening to an HMO population: Factors associated with utilization
-
(1994)
Am. J. Hum. Genet.
, vol.55
, pp. 626-637
-
-
Tambor, E.S.1
|