-
1
-
-
0024368549
-
The saga of cystatin C gene mutation causing amyloid angiopathy and brain hemorrhage – clinical genetics in Iceland
-
Jensson, O., Palsdottir, A., Thorsteinsson, L. and Arnason, A. (1989) The saga of cystatin C gene mutation causing amyloid angiopathy and brain hemorrhage – clinical genetics in Iceland. Clin. Genet. 47, 368–377.
-
(1989)
Clin. Genet.
, vol.47
, pp. 368-377
-
-
Jensson, O.1
Palsdottir, A.2
Thorsteinsson, L.3
Arnason, A.4
-
2
-
-
0014149954
-
Hereditary elliptocytosis in Iceland
-
Jensson, O., Jonasson, T. and Olafsson, O. (1967) Hereditary elliptocytosis in Iceland. Br. J. Haematol. 13, 844–854.
-
(1967)
Br. J. Haematol.
, vol.13
, pp. 844-854
-
-
Jensson, O.1
Jonasson, T.2
Olafsson, O.3
-
3
-
-
0017366878
-
Studies on herediatary spherocyto-sis in Iceland
-
Jensson, O., Jonasson, J. L. and Magnusson, S. (1977) Studies on herediatary spherocyto-sis in Iceland. Acta Med. Scand. 201, 187–195.
-
(1977)
Acta Med. Scand.
, vol.201
, pp. 187-195
-
-
Jensson, O.1
Jonasson, J.L.2
Magnusson, S.3
-
4
-
-
0017325536
-
Studies on the Pelger anomaly in Iceland
-
Jensson, O., Arnason, K., Johannesson G. M. and Ulfarsson J. (1977) Studies on the Pelger anomaly in Iceland. Acta Med. Scand. 201, 183–185.
-
(1977)
Acta Med. Scand.
, vol.201
, pp. 183-185
-
-
Jensson, O.1
Arnason, K.2
Johannesson, G.M.3
Ulfarsson, J.4
-
5
-
-
0014930946
-
Von Willebrand’s disease in an Icelandic family
-
Jensson, O. and Wallett, L. H. (1970) Von Willebrand’s disease in an Icelandic family. Acta Med. Scand. 187, 229–234.
-
(1970)
Acta Med. Scand.
, vol.187
, pp. 229-234
-
-
Jensson, O.1
Wallett, L.H.2
-
6
-
-
0019419771
-
Atrophia areata: A variant of peripapillary chorioretinal degernera-tion
-
Magnusson, L. (1981) Atrophia areata: a variant of peripapillary chorioretinal degernera-tion. Acta Ophthalmol. (Copenh) 59, 659–664.
-
(1981)
Acta Ophthalmol. (Copenh)
, vol.59
, pp. 659-664
-
-
Magnusson, L.1
-
7
-
-
85139117573
-
-
Sykes, B., Ogilvie, D., Wordsworth, P., Wallis, G., Mathes, C., Beighton, P., Nichols, A., Pope, M., Thomson, E., Tsipouras, P., Schwartz, R., Jensson, O., Arnason, A., Borresen, A. L., Heiberg, A., Frey, D. and Steinmann, B. (1990) Consistent linkage of dominantly inherited osteogenesis imperfecta to the two collagen 1 loci: COLIA1 and 47 COLIA2. Am. J. Hum. Genet. 47, 592–594.
-
600 V Power Device Technologies for Highly Efficient Power supplies,º in 2021 23Rd European Conference on Power Electronics and Applications
-
-
Siemieniec, R.1
Mente, R.2
-
8
-
-
85005097460
-
Huntington’s chorea in Iceland: Epidemiological study
-
Gudmundsson, G., Jensson, O., Arnason, A. and Stefansson, K. (1989) Huntington’s chorea in Iceland: epidemiological study. Clin. Genet. 35, 225.
-
(1989)
Clin. Genet.
, vol.35
, pp. 225
-
-
Gudmundsson, G.1
Jensson, O.2
Arnason, A.3
Stefansson, K.4
-
9
-
-
0020034028
-
Mode of inheritance of Hypertrophic cardiomyopathy in Iceland. Echographic study
-
Bjarnason, I., Jonsson, S. and Hardarson, Th. (1982). Mode of inheritance of Hypertrophic cardiomyopathy in Iceland. Echographic study. Br. Heart J. 47, 122–129.
-
(1982)
Br. Heart J
, vol.47
, pp. 122-129
-
-
Bjarnason, I.1
Jonsson, S.2
Hardarson, T.3
-
10
-
-
0023870488
-
Partly dominant transmission of Schizophrenia in Iceland
-
Karlsson, J. L. (1988). Partly dominant transmission of Schizophrenia in Iceland. Br. J. Psychiatry. 152, 324–329.
-
(1988)
Br. J. Psychiatry.
, vol.152
, pp. 324-329
-
-
Karlsson, J.L.1
-
11
-
-
0023716504
-
Localization of a susceptibility locus for schizophrenia on chromosome 5
-
Sherrington, T., Brynjolfsson, J., Petursson, H., Potter, M., Duleston, K., Barraclough, B., Wasmuth, J., Dobbs, M. and Gurling, H. (1988). Localization of a susceptibility locus for schizophrenia on chromosome 5. Nature 336, 164–167.
-
(1988)
Nature
, vol.336
, pp. 164-167
-
-
Sherrington, T.1
Brynjolfsson, J.2
Petursson, H.3
Potter, M.4
Duleston, K.5
Barraclough, B.6
Wasmuth, J.7
Dobbs, M.8
Gurling, H.9
-
12
-
-
85005182395
-
Deficiency of the second component (C2) in Iceland – a study of two cases
-
Arnason, A., Steinsson, K., Fossdal, R., Gunnarsdottir, H., Thorsteinsson, L., Palsdottir, A., Valdimarsson, H., Erlendsson, K. and Jensson, O. (1989). Deficiency of the second component (C2) in Iceland – a study of two cases. Clin. Genet. 35, 215.
-
(1989)
Clin. Genet.
, vol.35
, pp. 215
-
-
Arnason, A.1
Steinsson, K.2
Fossdal, R.3
Gunnarsdottir, H.4
Thorsteinsson, L.5
Palsdottir, A.6
Valdimarsson, H.7
Erlendsson, K.8
Jensson, O.9
-
13
-
-
85005113653
-
The first published cases of isovaleric acidaemia in Scandinavia are from Iceland
-
Gütller, F., Ludvigsson, P., Gregersen, N. and Gerdes, A. M. (1989). The first published cases of isovaleric acidaemia in Scandinavia are from Iceland. Clin. Genet. 35, 218.
-
(1989)
Clin. Genet.
, vol.35
, pp. 218
-
-
Gütller, F.1
Ludvigsson, P.2
Gregersen, N.3
Gerdes, A.M.4
-
14
-
-
85004981767
-
2.8-Dihydroxyadenine crystalluria in Iceland
-
Laxdal, Th. and Jonasson, T. A. (1989). 2.8-Dihydroxyadenine crystalluria in Iceland. Clin. Genet. 35, 219.
-
(1989)
Clin. Genet.
, vol.35
, pp. 219
-
-
Laxdal, T.1
Jonasson, T.A.2
-
15
-
-
0344567771
-
A new variant of biotin responsive holocarboxylase synthetase deficiency found in Iceland
-
Gütller, F., Laxdal, Th. and Sweetman, L. (1989). A new variant of biotin responsive holocarboxylase synthetase deficiency found in Iceland. Clin. Genet. 35, 220.
-
(1989)
Clin. Genet.
, vol.35
, pp. 220
-
-
Gütller, F.1
Laxdal, T.2
Sweetman, L.3
-
16
-
-
85004993053
-
Recessive osteopetrosis in Iceland
-
Jensson, O. and Arnason, A. (1989). Recessive osteopetrosis in Iceland. Clin Genet. 35, 223.
-
(1989)
Clin Genet
, vol.35
, pp. 223
-
-
Jensson, O.1
Arnason, A.2
-
17
-
-
85004937785
-
Autosomal recessive ichtyosis, lamellar type, in Iceland
-
Jensson, O., Baldursson, B. T. and Arnason, A. (1989) Autosomal recessive ichtyosis, lamellar type, in Iceland. Clin. Genet. 35, 224.
-
(1989)
Clin. Genet.
, vol.35
, pp. 224
-
-
Jensson, O.1
Baldursson, B.T.2
Arnason, A.3
-
18
-
-
85005121154
-
Homocystinuria (cystathionine beta-synthase deficiency) in Iceland
-
Jonsson, J. J., Jonasson, J. G., Sigurdsson, Th., Stefansdottir, A. and Halldorsson, S. (1989). Homocystinuria (cystathionine beta-synthase deficiency) in Iceland. Clin. Genet. 35, 224.
-
(1989)
Clin. Genet.
, vol.35
, pp. 224
-
-
Jonsson, J.J.1
Jonasson, J.G.2
Sigurdsson, T.3
Stefansdottir, A.4
Halldorsson, S.5
-
19
-
-
0016690813
-
Serum esterases of Icelanders I. A “silent” pseudocholinesterase gene in an Icelalndic family
-
Arnason, A., Jensson, O. and Gudmundsson, S. (1975) Serum esterases of Icelanders I. A “silent” pseudocholinesterase gene in an Icelalndic family. Clin. Genet. 7, 405–412.
-
(1975)
Clin. Genet.
, vol.7
, pp. 405-412
-
-
Arnason, A.1
Jensson, O.2
Gudmundsson, S.3
-
21
-
-
85005157637
-
Chromosome 6 markers and congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency in Iceland
-
Arnason, A., Gudmundsson, Th., Fossdal, R. and Jensson, O. (1989) Chromosome 6 markers and congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency in Iceland Clin. Genet. 5, 227.
-
(1989)
Clin. Genet.
, vol.5
, pp. 227
-
-
Arnason, A.1
Gudmundsson, T.2
Fossdal, R.3
Jensson, O.4
-
22
-
-
0023275513
-
Linkage of an X-chromosome cleft palate gene
-
Moore, G. E., Ivens, A., Chambers, J., Farrall, M., Williamson, R., Page, D. C., Björnsson, A., Arnason, A. and Jensson, O. (1987) Linkage of an X-chromosome cleft palate gene. Nature 326, 91–92.
-
(1987)
Nature
, vol.326
, pp. 91-92
-
-
Moore, G.E.1
Ivens, A.2
Chambers, J.3
Farrall, M.4
Williamson, R.5
Page, D.C.6
Björnsson, A.7
Arnason, A.8
Jensson, O.9
-
23
-
-
0023885799
-
X-linked cleft palate: The gene is localized between polymorphic DNA markers DXYS12 and DXS17
-
Ivens, A., Moore, G. E, Chambers J., Arnason A., Jensson, O., Björnsson, A. and Williamson, R. (1987) X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17. Hum. Genet. 78, 356–358.
-
(1987)
Hum. Genet.
, vol.78
, pp. 356-358
-
-
Ivens, A.1
Moore, G.E.2
Chambers, J.3
Arnason, A.4
Jensson, O.5
Björnsson, A.6
Williamson, R.7
-
24
-
-
0023687128
-
The application of molecular genetics to detection of craniofacial abnormality
-
Moore, G., Ivens, A., Chambers, J., Björnsson, A., Arnason, A., Jensson, O. and Williamson, R. (1988) The application of molecular genetics to detection of craniofacial abnormality. Development. 103, 233–239.
-
(1988)
Development
, vol.103
, pp. 233-239
-
-
Moore, G.1
Ivens, A.2
Chambers, J.3
Björnsson, A.4
Arnason, A.5
Jensson, O.6
Williamson, R.7
-
25
-
-
0023925265
-
A family showing apparent X linked inheritance of both anencephaly and spina bifida
-
Jensson, O., Arnason, A., Gunnarsdottir, I., Petursdottir, I., Fossdal, R. and Hreidarsson, S. (1988) A family showing apparent X linked inheritance of both anencephaly and spina bifida. J. Med. Genet. 25, 227–229.
-
(1988)
J. Med. Genet.
, vol.25
, pp. 227-229
-
-
Jensson, O.1
Arnason, A.2
Gunnarsdottir, I.3
Petursdottir, I.4
Fossdal, R.5
Hreidarsson, S.6
-
26
-
-
85005180294
-
Placental sulfatase deficiency
-
Hardardottir, H., Geirsson, R. T. and Hreidarsson, S. (1989) Placental sulfatase deficiency. Clin. Genet. 35, 224.
-
(1989)
Clin. Genet.
, vol.35
, pp. 224
-
-
Hardardottir, H.1
Geirsson, R.T.2
Hreidarsson, S.3
-
27
-
-
85004941918
-
Herreditary juvenile retionschisis in an Icelandic family
-
Thordarson, K. and Gislason, I. (1989). Herreditary juvenile retionschisis in an Icelandic family. Clin. Genet. 35, 225.
-
(1989)
Clin. Genet.
, vol.35
, pp. 225
-
-
Thordarson, K.1
Gislason, I.2
-
29
-
-
0021679977
-
Familial elevation of serum thyroxine binding globulin in an Icelandic Family
-
Sigurdsson, G. A., Arnason, A., Gudmundsson Th. V., Kjeld, M., Franzson, L. and Sigurdsson, G. (1984) Familial elevation of serum thyroxine binding globulin in an Icelandic Family. Acta Endocirnol. 107, 352–356.
-
(1984)
Acta Endocirnol
, vol.107
, pp. 352-356
-
-
Sigurdsson, G.A.1
Arnason, A.2
Gudmundsson Th, V.3
Kjeld, M.4
Franzson, L.5
Sigurdsson, G.6
-
30
-
-
85004931916
-
An Icelandic family with hypogammaglobulinemia, genetical and immunological study
-
Thorsteinsson, L., Ögmundsdottir, H., Sigfusson, A., Arnason, A., Eyjolfsson, G. and Jensson, O. (1989) An Icelandic family with hypogammaglobulinemia, genetical and immunological study. Clin. Genet. 35, 226.
-
(1989)
Clin. Genet.
, vol.35
, pp. 226
-
-
Thorsteinsson, L.1
Ögmundsdottir, H.2
Sigfusson, A.3
Arnason, A.4
Eyjolfsson, G.5
Jensson, O.6
-
31
-
-
0015503293
-
Familial acute myeloid leukaemia with acquired Pelger-Huët anomaly and aneuploidy of C group
-
Juginder, K., Catovsky, D., Valdimarsson, H., Jensson, O. and Spiers, A. S. D. (1972) Familial acute myeloid leukaemia with acquired Pelger-Huët anomaly and aneuploidy of C group.Br. Med. J. 4, 327–331.
-
(1972)
Br. Med. J.
, vol.4
, pp. 327-331
-
-
Juginder, K.1
Catovsky, D.2
Valdimarsson, H.3
Jensson, O.4
Spiers, A.S.D.5
-
32
-
-
0017838292
-
Macroglobulinaemia in an Icelandic Family
-
Björnsson, O. G., Arnason, A., Gudmundsson, S., Jensson, O, Olafsson, S. and Valdimarsson, H. (1978) Macroglobulinaemia in an Icelandic Family. Acta Med. Scand. 203, 283–288.
-
(1978)
Acta Med. Scand.
, vol.203
, pp. 283-288
-
-
Björnsson, O.G.1
Arnason, A.2
Gudmundsson, S.3
Jensson, O.4
Olafsson, S.5
Valdimarsson, H.6
-
33
-
-
0020025262
-
Serum amyloid p-component and C-reactive protein in serumof healthy Icelanders and members of an Icelandic family with macrog-logulinaemia
-
Jensson, O., Björnsson, O. G., Arnason, A., Birgisdottir, B. and Pepys, M. B. (1982) Serum amyloid p-component and C-reactive protein in serumof healthy Icelanders and members of an Icelandic family with macrog-logulinaemia. Acta Med. Scand. 211, 341–345.
-
(1982)
Acta Med. Scand.
, vol.211
, pp. 341-345
-
-
Jensson, O.1
Björnsson, O.G.2
Arnason, A.3
Birgisdottir, B.4
Pepys, M.B.5
-
34
-
-
0021856341
-
Rheumatic diseases in an Icelandic family
-
Teitsson, I., Thorsteinsson, J., Arnason, A. and Valdimarsson, H. (1985) Rheumatic diseases in an Icelandic family. Scand. J. Rheumatol. 14, 109–118.
-
(1985)
Scand. J. Rheumatol.
, vol.14
, pp. 109-118
-
-
Teitsson, I.1
Thorsteinsson, J.2
Arnason, A.3
Valdimarsson, H.4
-
35
-
-
0023196726
-
Gene organization of hap-lotypes expressing two different C4A allo-types
-
Palsdottir, A., Arnason, A., Fossdal, R. and Jensson, O. (1987) Gene organization of hap-lotypes expressing two different C4A allo-types. Hum. Genet. 76, 220–224.
-
(1987)
Hum. Genet.
, vol.76
, pp. 220-224
-
-
Palsdottir, A.1
Arnason, A.2
Fossdal, R.3
Jensson, O.4
-
36
-
-
0017884693
-
Ankylosing spondyli-tis, HLA-B27 and Bf
-
Arnason, A., Thorsteinsson, J. and Sigurbergsson, K. (1978) Ankylosing spondyli-tis, HLA-B27 and Bf. Lancet. 1, 339–340.
-
(1978)
Lancet
, vol.1
, pp. 339-340
-
-
Arnason, A.1
Thorsteinsson, J.2
Sigurbergsson, K.3
-
37
-
-
84931950047
-
HLA in insulin-dependent diabetes in Iceland
-
Arnason, A., Helgason, T. and Jensson, O. (1979) HLA in insulin-dependent diabetes in Iceland. Icelandic Med. J. 4, 189–190.
-
(1979)
Icelandic Med. J.
, vol.4
, pp. 189-190
-
-
Arnason, A.1
Helgason, T.2
Jensson, O.3
-
38
-
-
0020123682
-
HLA and retinopathy in type 1 (insulin-dependent) diabetic patients in Iceland
-
Danielsen, R., Helgason, T., Arnason, A. and Jonasson, F. (1982) HLA and retinopathy in type 1 (insulin-dependent) diabetic patients in Iceland. Diabetologia 22, 297–298.
-
(1982)
Diabetologia
, vol.22
, pp. 297-298
-
-
Danielsen, R.1
Helgason, T.2
Arnason, A.3
Jonasson, F.4
-
39
-
-
0002501396
-
HLA types, Gc protein and other genetic markers in multiple sclerosis and two other neurological diseases in Iceland
-
Arnason, A., Jensson, O., Skaftadottir, I., Birgisdottir, B., Gudmundsson, G. and Johanneson, G. (1980) HLA types, Gc protein and other genetic markers in multiple sclerosis and two other neurological diseases in Iceland. Acta Neurol. Scand. 62, 39–40.
-
(1980)
Acta Neurol. Scand.
, vol.62
, pp. 39-40
-
-
Arnason, A.1
Jensson, O.2
Skaftadottir, I.3
Birgisdottir, B.4
Gudmundsson, G.5
Johanneson, G.6
-
40
-
-
0019976012
-
Selective serum IgA deficiency in Icelanders: Frequency, family studies and IgA levels
-
Ulfarsson, J., Gudmundsson, S., Birgisdottir, B., Kjeld, M. J. and Jensson, O. (1982) Selective serum IgA deficiency in Icelanders: frequency, family studies and IgA levels. Acta Med. Scand. 211, 481–487.
-
(1982)
Acta Med. Scand.
, vol.211
, pp. 481-487
-
-
Ulfarsson, J.1
Gudmundsson, S.2
Birgisdottir, B.3
Kjeld, M.J.4
Jensson, O.5
-
41
-
-
85004991324
-
Genetical markers and leukaemia in Iceland – an association between homozygosity of HLA B7, HLA B40 and leukaemia
-
Arnason, A., Jonmundsson, G. K., Skaftadottir, I., Thorsteinsson, L., Johannesson, G. M., Eyjolfsson, G., Fossdal, R., Petursdottir, I. and Jensson, O. (1985) Genetical markers and leukaemia in Iceland – an association between homozygosity of HLA B7, HLA B40 and leukaemia. Scand. J. Immunol. 22, 441.
-
(1985)
Scand. J. Immunol.
, vol.22
, pp. 441
-
-
Arnason, A.1
Jonmundsson, G.K.2
Skaftadottir, I.3
Thorsteinsson, L.4
Johannesson, G.M.5
Eyjolfsson, G.6
Fossdal, R.7
Petursdottir, I.8
Jensson, O.9
-
42
-
-
0020050739
-
Familial breast cancer in Iceland
-
Tulinius, H., Day, N., Bjarnason, Ó., Geirsson, G., Jóhannesson, G., Conzales, M., Sigvaldason, H., Bjarnadóttir, G. and Grímsdóttir, K. (1982) Familial breast cancer in Iceland. Int. J. Cancer 29, 365–371.
-
(1982)
Int. J. Cancer
, vol.29
, pp. 365-371
-
-
Tulinius, H.1
Day, N.2
Bjarnason, Ó.3
Geirsson, G.4
Jóhannesson, G.5
Conzales, M.6
Sigvaldason, H.7
Bjarnadóttir, G.8
Grímsdóttir, K.9
-
43
-
-
85139137595
-
Familial Risk of Breast Cancer in Iceland
-
Müller, Weber (eds.), Karger, Basel
-
Tulinius, H. Familial Risk of Breast Cancer in Iceland. In: Müller, Weber (eds.). Familial Cancer. 1st Int. Res. Conf., Basel 1985, p. 25–26 (Karger, Basel 1985).
-
(1985)
Familial Cancer. 1St Int. Res. Conf., Basel 1985
, pp. 25-26
-
-
Tulinius, H.1
-
44
-
-
0342726363
-
Familial Cancer Registration in Iceland
-
Müller, Weber (eds.), Karger, Basel
-
Tulinius, H. Familial Cancer Registration in Iceland. In: Müller, Weber (eds.). Familial Cancer. 1st Int. Res. Conf., Basel 1985, p. 263–267 (Karger, Basel 1985).
-
(1985)
Familial Cancer. 1St Int. Res. Conf., Basel 1985
, pp. 263-267
-
-
Tulinius, H.1
-
45
-
-
0023723389
-
Familial and sporadic breast cancer cases in Iceland: A comparison with respect to ABO blood groups and the risk of bilateral cancer of the breast
-
Tryggvadóttir, L., Tulinius, H. and Robertson. J. M. (1988) Familial and sporadic breast cancer cases in Iceland: a comparison with respect to ABO blood groups and the risk of bilateral cancer of the breast. Int. J. Cancer 42, 499–501.
-
(1988)
Int. J. Cancer
, vol.42
, pp. 499-501
-
-
Tryggvadóttir, L.1
Tulinius, H.2
Robertson, J.M.3
-
46
-
-
85139092009
-
-
Tulinius, H., Egilsson, V., Olafsdottir, G. H. and Sigvaldason, H. (1992) Risque de cancer de la prostate, de l’ovaire et de l’endométre en cas d’antécédent familial de cancer du sein. le Journal International de Médecine 151, 25–28.
-
(1992)
Risque De Cancer De La Prostate, De l’ovaire Et De l’endométre En Cas d’antécédent Familial De Cancer Du Sein. Le Journal International De Médecine
, vol.151
, pp. 25-28
-
-
Tulinius, H.1
Egilsson, V.2
Olafsdottir, G.H.3
Sigvaldason, H.4
-
47
-
-
0028068230
-
Neoplastic diseases in families of breast cancer patients
-
Tulinius, H., Olafsdottir, G. H., Sigvaldason, H., Tryggvadottir, L. and Bjarnadottir, K. (1994) Neoplastic diseases in families of breast cancer patients. J. Med. Genet. 31, 618–621.
-
(1994)
J. Med. Genet.
, vol.31
, pp. 618-621
-
-
Tulinius, H.1
Olafsdottir, G.H.2
Sigvaldason, H.3
Tryggvadottir, L.4
Bjarnadottir, K.5
-
48
-
-
0029160005
-
Linkage to BRCA2 region in hereditary male breast cancer
-
Thorlacius, S., Tryggvadottir, L., Olafsdottir, G. H., Jonasson, J. G., Ogmundsdottir, H. M., Tulinius, H. and Eyfjord, J. E. (1995) Linkage to BRCA2 region in hereditary male breast cancer. Lancet 346, 544–545.
-
(1995)
Lancet
, vol.346
, pp. 544-545
-
-
Thorlacius, S.1
Tryggvadottir, L.2
Olafsdottir, G.H.3
Jonasson, J.G.4
Ogmundsdottir, H.M.5
Tulinius, H.6
Eyfjord, J.E.7
-
49
-
-
85139120569
-
Impact of genetics on cancer
-
Tulinius, H. (1995) Impact of genetics on cancer. In: Parr, E., Næss, A. and Rossland, T: Kreftepidemiologi. Oslo 1995, 56–59.
-
(1995)
Parr, E., Næss, A. and Rossland, T: Kreftepidemiologi. Oslo
, vol.1995
, pp. 56-59
-
-
Tulinius, H.1
-
50
-
-
0030140026
-
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
-
Thorlacius, S., Olafsdóttir, G. H., Tryggvadóttir, L., Neuhausen, S., Jónasson, J. G., Tavigian, S. V., Tulinius, H., Ögmundsdóttir, H. M. and Eyfjörð, J. E. (1996) A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Nat. Genet. 13, 117–119.
-
(1996)
Nat. Genet.
, vol.13
, pp. 117-119
-
-
Thorlacius, S.1
Olafsdóttir, G.H.2
Tryggvadóttir, L.3
Neuhausen, S.4
Jónasson, J.G.5
Tavigian, S.V.6
Tulinius, H.7
Ögmundsdóttir, H.M.8
Eyfjörð, J.E.9
-
51
-
-
0030956589
-
Study of a single BRCA2 mutation with high carrier frequency in a small population
-
Thorlacius, S., Sigurdsson, S., Bjarnadottir, H., Olafsdottir, G., Jonasson, J. G., Tryggvadottir, L., Tulinius, H. and Eyfjord, J. E. (1997) Study of a single BRCA2 mutation with high carrier frequency in a small population. Am. J. Hum. Genet. 60, 1079–1084.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1079-1084
-
-
Thorlacius, S.1
Sigurdsson, S.2
Bjarnadottir, H.3
Olafsdottir, G.4
Jonasson, J.G.5
Tryggvadottir, L.6
Tulinius, H.7
Eyfjord, J.E.8
-
52
-
-
18344410703
-
Population-based study of risk of breast cancer in carriers of BRCA2 mutation
-
Thorlacius, S., Struewing, J. P., Hartge, P., Ólafsdóttir, G. H., Sigvaldason, H., Tryggvadóttir, L., Wacholder, S., Tulinius, H. and Eyfjörð, J. E. (1998) Population-based study of risk of breast cancer in carriers of BRCA2 mutation. Lancet 352, 1337–1339.
-
(1998)
Lancet
, vol.352
, pp. 1337-1339
-
-
Thorlacius, S.1
Struewing, J.P.2
Hartge, P.3
Ólafsdóttir, G.H.4
Sigvaldason, H.5
Tryggvadóttir, L.6
Wacholder, S.7
Tulinius, H.8
Eyfjörð, J.E.9
-
53
-
-
85139087732
-
-
Tulinius, H., Sigvaldason, H., Ólafsdóttir, G., Tryggvadóttir, L. and Bjarnadóttir, K. (1999) Breast cancer incidence and familality in Iceland during 75 Years from 1921 to 1995. J. Med. Genet. 36, 103–107.
-
600 V Power Device Technologies for Highly Efficient Power supplies,º in 2021 23Rd European Conference on Power Electronics and Applications
-
-
Siemieniec, R.1
Mente, R.2
-
54
-
-
0033986316
-
Genetic epidemiology of breast cancer: Segregation analysis of 389 icelandic pedigrees
-
Baffoe-Bonnie A., Beaty, T. H., Bailey-Wilson, J. E., Kiemeney, L., Sigvaldason, H., Ólafsdóttir, G., Tryggvadóttir, L. and Tulinius, H. (2000) Genetic epidemiology of breast cancer: segregation analysis of 389 icelandic pedigrees. Genet. Epidemiol. 18, 81–94.
-
(2000)
Genet. Epidemiol.
, vol.18
, pp. 81-94
-
-
Baffoe-Bonnie, A.1
Beaty, T.H.2
Bailey-Wilson, J.E.3
Kiemeney, L.4
Sigvaldason, H.5
Ólafsdóttir, G.6
Tryggvadóttir, L.7
Tulinius, H.8
-
55
-
-
18444365255
-
The effect of a single BRCA2 mutation on cancer in Iceland
-
Tulinius, H., Olafsdottir, G. H., Sigvaldason, H., Arason, A., Barkardottir, R. B., Egilsson, V., Ogmundsdottir, H. M., Tryggvadottir, L., Gudlaugsdottir, S. and Eyfjord, J. E. (2002) The effect of a single BRCA2 mutation on cancer in Iceland. J. Med. Genet. 39, 457–452.
-
(2002)
J. Med. Genet.
, vol.39
, pp. 457-452
-
-
Tulinius, H.1
Olafsdottir, G.H.2
Sigvaldason, H.3
Arason, A.4
Barkardottir, R.B.5
Egilsson, V.6
Ogmundsdottir, H.M.7
Tryggvadottir, L.8
Gudlaugsdottir, S.9
Eyfjord, J.E.10
-
56
-
-
18744372430
-
Segregation analysis of 389 Icelandic pedigrees with breast and prostate cancer
-
Baffoe-Bonnie, A. B., Kiemeney, L. A. L. M., Beaty, T. H., Bailey-Wilson, J. E., Schnell, A. H., Sigvaldason, H., Ólafsdóttir, G., Tryggvadóttir, L. and Tulinius, H. (2002) Segregation analysis of 389 Icelandic pedigrees with breast and prostate cancer. Genet. Epidemiol. 23, 349–363.
-
(2002)
Genet. Epidemiol.
, vol.23
, pp. 349-363
-
-
Baffoe-Bonnie, A.B.1
Kiemeney, L.A.L.M.2
Beaty, T.H.3
Bailey-Wilson, J.E.4
Schnell, A.H.5
Sigvaldason, H.6
Ólafsdóttir, G.7
Tryggvadóttir, L.8
Tulinius, H.9
-
57
-
-
0038744296
-
Averge risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysing of 22 studies
-
Antoniou, A., Pharoah, P. D., Narod, S., Risch, H. A. et al. (2003) Averge risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysing of 22 studies. Am. J. Hum. Genet. 72, 5, 1117–1130.
-
(2003)
Am. J. Hum. Genet.
, vol.72
, Issue.5
, pp. 1117-1130
-
-
Antoniou, A.1
Pharoah, P.D.2
Narod, S.3
Risch, H.A.4
-
58
-
-
0141462835
-
BRCA2 mutation carriers, reproductive factors and breast cancer risk
-
Tryggvadottir, L., Olafsdottir, E. J., Gudlaugsdottir, S., Thorlacius, S., Jonasson, J. G., Tulinius, H. and Eyfjord, J. E. (2003) BRCA2 mutation carriers, reproductive factors and breast cancer risk. Breast Cancer Res. 5, 121–128. http://breast-cancer-research. com/content/5/5/R121
-
(2003)
Breast Cancer Res
, vol.5
, pp. 121-128
-
-
Tryggvadottir, L.1
Olafsdottir, E.J.2
Gudlaugsdottir, S.3
Thorlacius, S.4
Jonasson, J.G.5
Tulinius, H.6
Eyfjord, J.E.7
-
59
-
-
22244467729
-
Breast and ovarian cancer risks to carriers of the BRCA1 1382insC and 185delAG and VRCA2 6174delT mutations: A combined analysis of 22 population based studies
-
Antoniou, A. C., Pharoah, P. D., Narod, S., Risch, H. A. et al. (2005) Breast and ovarian cancer risks to carriers of the BRCA1 1382insC and 185delAG and VRCA2 6174delT mutations: a combined analysis of 22 population based studies. J. Med. Genet. 42, 602–603.
-
(2005)
J. Med. Genet.
, vol.42
, pp. 602-603
-
-
Antoniou, A.C.1
Pharoah, P.D.2
Narod, S.3
Risch, H.A.4
-
60
-
-
13244272305
-
Familiality of benign and malignant paraproteinemias. A population-based cancer-registry study of multiple myeloma families
-
Ögmundsdóttir, H., Haraldsdóttir, V., Jóhannesson, G. M., Ólafsdóttir, G., Bjarnadóttir, K., Sigvaldason, H. and Tulinius, H. (2005) Familiality of benign and malignant paraproteinemias. A population-based cancer-registry study of multiple myeloma families. Haematologica 90, 66–71.
-
(2005)
Haematologica
, vol.90
, pp. 66-71
-
-
Ögmundsdóttir, H.1
Haraldsdóttir, V.2
Jóhannesson, G.M.3
Ólafsdóttir, G.4
Bjarnadóttir, K.5
Sigvaldason, H.6
Tulinius, H.7
-
61
-
-
31544447725
-
Population-based study of changing breast cancer risk in Icelandic BRCA2 mutation carriers, 1920– 2000
-
Tryggvadottir, L., Sigvaldason, H., Olafsdottir, G. H., Jonasson, J. G., Jonsson, T., Tulinius, H. and Eyfjord, J. E. (2006) Population-based study of changing breast cancer risk in Icelandic BRCA2 mutation carriers, 1920– 2000. J. Natl. Cancer Inst. 98, 116–122.
-
(2006)
J. Natl. Cancer Inst.
, vol.98
, pp. 116-122
-
-
Tryggvadottir, L.1
Sigvaldason, H.2
Olafsdottir, G.H.3
Jonasson, J.G.4
Jonsson, T.5
Tulinius, H.6
Eyfjord, J.E.7
-
62
-
-
0024816270
-
Papillary thyroid carcinoma in Iceland. A study of the occurrence in families and the coexistence of other primary tumours
-
Hrafnkelsson, J., Tulinius, H., Jonasson, J. G., Ólafsdóttir, G. and Sigvaldason, H. (1989) Papillary thyroid carcinoma in Iceland. A study of the occurrence in families and the coexistence of other primary tumours. Acta Oncologica 28, 785–758.
-
(1989)
Acta Oncologica
, vol.28
, pp. 785-758
-
-
Hrafnkelsson, J.1
Tulinius, H.2
Jonasson, J.G.3
Ólafsdóttir, G.4
Sigvaldason, H.5
-
63
-
-
0036715339
-
Risk of cancer among relatives of patients with glioma
-
O´Neill, B. P., Blondal, H., Yang, P., Olafsdottir, G. H., Sigvaldason, H., Jenkins, R. B., Kimmel, D. W., Scheithauer, B. W., Rocca, W. A., Bjornsson, J. and Tulinius, H. (2002) Risk of cancer among relatives of patients with glioma. Cancer Epidemiol. Biomarkers Prev. 11, 921–924.
-
(2002)
Cancer Epidemiol. Biomarkers Prev.
, vol.11
, pp. 921-924
-
-
-
64
-
-
33646172092
-
A population-based study on the familial aggregation of cutaneous malignant melanoma in Iceland
-
Eldon, B. J., Thorlacius, S., Jonsson, T., Jonasson, J. G., Kjartansson, J., Bodvarsson, S., Steingrimsson, E. and Rafnar, T. (2006) A population-based study on the familial aggregation of cutaneous malignant melanoma in Iceland. Eur. J. Cancer. 42, 922–926.
-
(2006)
Eur. J. Cancer.
, vol.42
, pp. 922-926
-
-
Eldon, B.J.1
Thorlacius, S.2
Jonsson, T.3
Jonasson, J.G.4
Kjartansson, J.5
Bodvarsson, S.6
Steingrimsson, E.7
Rafnar, T.8
-
65
-
-
33745211695
-
Familial risk of colon and rectal cancer in Iceland: Evidence for different etiologic factors?
-
Stefansson, T., Moller, P. H., Sigurdsson, F., Steingrimsson, E. and Eldon B. J. (2006) Familial risk of colon and rectal cancer in Iceland: evidence for different etiologic factors? Int. J. Cancer. 119, 304–308.
-
(2006)
Int. J. Cancer.
, vol.119
, pp. 304-308
-
-
Stefansson, T.1
Moller, P.H.2
Sigurdsson, F.3
Steingrimsson, E.4
Eldon, B.J.5
-
66
-
-
9644257250
-
BRCA2, but not BRCA1, mutations account for familial ovarian cancer in Iceland: A population-based study
-
Rafnar, T., Benediktsdottir, K. R., Eldon, B. J., Gestsson, T., Saemundsson, H., Olafsson, K., Salvarsdottir, A., Steingrimsson, E. and Thorlacius, S. (2004) BRCA2, but not BRCA1, mutations account for familial ovarian cancer in Iceland: a population-based study. Eur. J. Cancer. 40, 2788–2793.
-
(2004)
Eur. J. Cancer.
, vol.40
, pp. 2788-2793
-
-
Rafnar, T.1
Benediktsdottir, K.R.2
Eldon, B.J.3
Gestsson, T.4
Saemundsson, H.5
Olafsson, K.6
Salvarsdottir, A.7
Steingrimsson, E.8
Thorlacius, S.9
-
67
-
-
0346119094
-
Familial risk of prostate cancer in Iceland
-
Eldon, B. J., Jonsson, E., Tomasson, J., Tryggvadottir, L. and Tulinius, H. (2003) Familial risk of prostate cancer in Iceland. BJU Int. 92, 915–919.
-
(2003)
BJU Int
, vol.92
, pp. 915-919
-
-
Eldon, B.J.1
Jonsson, E.2
Tomasson, J.3
Tryggvadottir, L.4
Tulinius, H.5
-
68
-
-
85139143222
-
-
Imsland, A. K., Eldon, B. J., Arinbjarnarson, S., Egilsson, V., Tulinius, H., Tryggvadottir, L., Arngrimsson, R. and Magnusson, J. (2002) Genetic epidemiologic aspects of gastric cancer in Iceland. J. Am. Coll. Surg. 195, 181–186; discussion: 186–187.
-
600 V Power Device Technologies for Highly Efficient Power supplies,º in 2021 23Rd European Conference on Power Electronics and Applications
-
-
Siemieniec, R.1
Mente, R.2
-
69
-
-
0036869426
-
Fifteen percent of myocardial infarctions and coronary revascularizations explained by family history unrelated to conventional risk factors
-
Andresdottir, M. B., Sigurdsson, G., Sigvaldason, H. and Gudnason, V. (2002) Fifteen percent of myocardial infarctions and coronary revascularizations explained by family history unrelated to conventional risk factors. Eur. Heart J. 23, 1655–1663.
-
(2002)
Eur. Heart J.
, vol.23
, pp. 1655-1663
-
-
Andresdottir, M.B.1
Sigurdsson, G.2
Sigvaldason, H.3
Gudnason, V.4
-
70
-
-
85139166844
-
-
Tryggvadóttir, L., Vidarsdóttir, L., Thorgeirsson, J. G., Olafsdóttir, E. J., Olafsdóttir, G. H., Rafnar, T., Thorlacius, S., Jonsson, E., Eyfjord, J. E. and Tulinius, H. J. (2007) Prostate cancer progression and survival in BRCA2 mutation carriers. Natl Cancer Inst. Jun 20; 99(12), 929–935.
-
600 V Power Device Technologies for Highly Efficient Power supplies,º in 2021 23Rd European Conference on Power Electronics and Applications
-
-
Siemieniec, R.1
Mente, R.2
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