-
2
-
-
0017640298
-
Linkage between an X-chromosome marker (deutan color blindness) and bipolar affective illness
-
Baron, M. 1977. Linkage between an X-chromosome marker (deutan color blindness) and bipolar affective illness. Arch. Gen. Psychiatry 34: 721-725.
-
(1977)
Arch. Gen. Psychiatry
, vol.34
, pp. 721-725
-
-
Baron, M.1
-
3
-
-
0023146964
-
Genetic linkage between X-chromosome markers and bipolar affective illness
-
Baron, M., N. Risch, R. Hamburger, B. Mandel, M. Kushner, M. Newman, D. Drumer, and R.H. Belmaker. 1987. Genetic linkage between X-chromosome markers and bipolar affective illness. Nature 326: 289-292.
-
(1987)
Nature
, vol.326
, pp. 289-292
-
-
Baron, M.1
Risch, N.2
Hamburger, R.3
Mandel, B.4
Kushner, M.5
Newman, M.6
Drumer, D.7
Belmaker, R.H.8
-
4
-
-
0027509066
-
Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees
-
Baron, M., N.F. Freimer, N. Risch, B. Lerer, J.R. Alexander, R.E. Straub, S. Asokan, K. Das, A. Peterson, J. Amos, J. Endicott, J. Ott, and T.C. Gilliam. 1993. Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees. Nature Genet. 3: 49-55.
-
(1993)
Nature Genet.
, vol.3
, pp. 49-55
-
-
Baron, M.1
Freimer, N.F.2
Risch, N.3
Lerer, B.4
Alexander, J.R.5
Straub, R.E.6
Asokan, S.7
Das, K.8
Peterson, A.9
Amos, J.10
Endicott, J.11
Ott, J.12
Gilliam, T.C.13
-
5
-
-
0025309725
-
X-chromosome markers and manic-depressive illness. Rejection of linkage to Xq28 in nine bipolar pedigrees
-
Berrettini, W.H., L.R. Goldin, J. Gelernter, P.V. Gejman, E.S. Gershon, and S. Detera-Wadleigh. 1990. X-chromosome markers and manic-depressive illness. Rejection of linkage to Xq28 in nine bipolar pedigrees. Arch. Gen. Psychiatry 47: 366-373.
-
(1990)
Arch. Gen. Psychiatry
, vol.47
, pp. 366-373
-
-
Berrettini, W.H.1
Goldin, L.R.2
Gelernter, J.3
Gejman, P.V.4
Gershon, E.S.5
Detera-Wadleigh, S.6
-
6
-
-
0027234013
-
Bipolar disorder in an extended pedigree with a segregation pattern compatible with X-linked transmission: Exclusion of the previously reported linkage to F9
-
Bredbacka, P.-E., P. Pekkarinen, L. Peltonen, and J. Lönnqvist. 1993. Bipolar disorder in an extended pedigree with a segregation pattern compatible with X-linked transmission: Exclusion of the previously reported linkage to F9. Psychiatr. Genet. 3: 79-87.
-
(1993)
Psychiatr. Genet.
, vol.3
, pp. 79-87
-
-
Bredbacka, P.-E.1
Pekkarinen, P.2
Peltonen, L.3
Lönnqvist, J.4
-
7
-
-
0018639079
-
Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
-
Chirgwin, J.M., A.E. Przybyla, R.J. MacDonald, and W.J. Rutter. 1979. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18: 5294-5299.
-
(1979)
Biochemistry
, vol.18
, pp. 5294-5299
-
-
Chirgwin, J.M.1
Przybyla, A.E.2
MacDonald, R.J.3
Rutter, W.J.4
-
9
-
-
0026551370
-
Christmas disease and major affective disorder
-
Craddock, N. and M. Owen. 1992. Christmas disease and major affective disorder. Br. J. Psychiatry 160: 715.
-
(1992)
Br. J. Psychiatry
, vol.160
, pp. 715
-
-
Craddock, N.1
Owen, M.2
-
10
-
-
0028673724
-
Linkage analysis of bipolar illness with X-chromosome DNA markers: A susceptibility gene in Xq27-q28 cannot be excluded
-
De bruyn, A., P. Raeymaekers, K. Mendelbaum, L.A. Sandkuijl, G. Raes, V. Delvenne, D. Hirsch, L. Staner, J. Mendlewicz, and C. Van Broeckhoven. 1994. Linkage analysis of bipolar illness with X-chromosome DNA markers: A susceptibility gene in Xq27-q28 cannot be excluded. Am. J. Med. Genet. 54: 411-419.
-
(1994)
Am. J. Med. Genet.
, vol.54
, pp. 411-419
-
-
De Bruyn, A.1
Raeymaekers, P.2
Mendelbaum, K.3
Sandkuijl, L.A.4
Raes, G.5
Delvenne, V.6
Hirsch, D.7
Staner, L.8
Mendlewicz, J.9
Van Broeckhoven, C.10
-
11
-
-
0027507885
-
Disease gene mapping in isolated human populations: The example of Finland
-
de la Chapelle, A. 1993. Disease gene mapping in isolated human populations: The example of Finland. J. Med. Genet. 30: 857-865.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 857-865
-
-
De La Chapelle, A.1
-
12
-
-
0021179097
-
Linkage between X-chromosome markers and manic-depressive illness: Two Sardinian pedigrees
-
Del Zompo, M., A. Bocchetta, L.R. Goldin, and G.U. Corsini. 1984. Linkage between X-chromosome markers and manic-depressive illness: Two Sardinian pedigrees. Acta Psychiatr. Scand. 70: 282-287.
-
(1984)
Acta Psychiatr. Scand.
, vol.70
, pp. 282-287
-
-
Del Zompo, M.1
Bocchetta, A.2
Goldin, L.R.3
Corsini, G.U.4
-
13
-
-
0028264926
-
A linkage map of microsatellite markers on the human X chromosome
-
Donnelly, A., H. Kozman, A.K. Gedeon, S. Webb, M. Lynch, G.R. Sutherland, R.I. Richards, and J.C. Mulley. 1994. A linkage map of microsatellite markers on the human X chromosome. Genomics 20: 363-370.
-
(1994)
Genomics
, vol.20
, pp. 363-370
-
-
Donnelly, A.1
Kozman, H.2
Gedeon, A.K.3
Webb, S.4
Lynch, M.5
Sutherland, G.R.6
Richards, R.I.7
Mulley, J.C.8
-
14
-
-
0018119373
-
A diagnostic interview: The schedule for affective disorders and schizophrenia
-
Endicott, J. and R.L. Spitzer. 1978. A diagnostic interview: The schedule for affective disorders and schizophrenia. Arch. Gen. Psychiat. 35: 837- 844.
-
(1978)
Arch. Gen. Psychiat.
, vol.35
, pp. 837-844
-
-
Endicott, J.1
Spitzer, R.L.2
-
15
-
-
0025678560
-
Manic depressive illness not linked to factor IX region in an independent series of pedigrees
-
Gejman, P.V., S. Detera-Wadleigh, M.M. Martinez, W.H. Berrettini, L.R. Goldin, J. Gelernter, W.-T. Hsieh, and E.S. Gershon. 1990. Manic depressive illness not linked to factor IX region in an independent series of pedigrees. Genomics 8: 648-655.
-
(1990)
Genomics
, vol.8
, pp. 648-655
-
-
Gejman, P.V.1
Detera-Wadleigh, S.2
Martinez, M.M.3
Berrettini, W.H.4
Goldin, L.R.5
Gelernter, J.6
Hsieh, W.-T.7
Gershon, E.S.8
-
16
-
-
0017742233
-
X-linkage: Ascertainment through doubly ill probands
-
Gershon, E.S. and S. Matthysse. 1977. X-linkage: Ascertainment through doubly ill probands. J. Psychiatr. Res. 13: 161-168.
-
(1977)
J. Psychiatr. Res.
, vol.13
, pp. 161-168
-
-
Gershon, E.S.1
Matthysse, S.2
-
17
-
-
0018576999
-
Color blindness not closely linked to bipolar illness
-
Gershon, E.S., S.D. Targum, S. Matthysse, and W.E. Bunney, Jr. 1979. Color blindness not closely linked to bipolar illness. Arch. Gen. Psychiatr. 36: 1423-1431.
-
(1979)
Arch. Gen. Psychiatr.
, vol.36
, pp. 1423-1431
-
-
Gershon, E.S.1
Targum, S.D.2
Matthysse, S.3
Bunney Jr., W.E.4
-
18
-
-
0018888604
-
A collaborative study of genetic linkage of bipolar manic-depressive illness and red/green colorblindness
-
Gershon, E.S., J. Mendlewicx, M. Gastpar, P. Bech, L.R. Goldin, P. Kielholz, O.J. Rafaelsen, F. Vartanian, and W.E. Bunney Jr. 1980. A collaborative study of genetic linkage of bipolar manic-depressive illness and red/green colorblindness. Acta Psychiatr. Scand. 61: 319-338.
-
(1980)
Acta Psychiatr. Scand.
, vol.61
, pp. 319-338
-
-
Gershon, E.S.1
Mendlewicx, J.2
Gastpar, M.3
Bech, P.4
Goldin, L.R.5
Kielholz, P.6
Rafaelsen, O.J.7
Vartanian, F.8
Bunney Jr., W.E.9
-
19
-
-
0026527197
-
Cosegregation of Christmas disease and major affective disorder in a pedigree
-
Gill, M., D. Castle, and C. Duggan. 1992. Cosegregation of Christmas disease and major affective disorder in a pedigree. Br. J. Psychiatry 160: 112-114.
-
(1992)
Br. J. Psychiatry
, vol.160
, pp. 112-114
-
-
Gill, M.1
Castle, D.2
Duggan, C.3
-
21
-
-
0028231090
-
The 1993-94 Genethon human genetic linkage map
-
Gyapay, G., J. Morissette, A. Vignal, C. Dib, C. Fizames, P. Millasseau, S. Marc, G. Bernardi, M. Lathrop, and J. Weissenbach. 1994. The 1993-94 Genethon human genetic linkage map. Nature Genet. 7: 246-339.
-
(1994)
Nature Genet.
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
22
-
-
0026584305
-
A critical appraisal of X-linked bipolar illness
-
Hebebrand, J. 1992. A critical appraisal of X-linked bipolar illness. Br. J. Psychiatry 160: 7-11.
-
(1992)
Br. J. Psychiatry
, vol.160
, pp. 7-11
-
-
Hebebrand, J.1
-
23
-
-
0027480146
-
Bipolar spectrum disorder and fragile X syndrome: A family study
-
Jeffries, F.M., A.L. Reiss, W.T. Brown, D.A. Meyers, A.C. Glicksman, and S. Bandyopadhyay. 1993. Bipolar spectrum disorder and fragile X syndrome: A family study. Biol. Psychiatry 33: 213-216.
-
(1993)
Biol. Psychiatry
, vol.33
, pp. 213-216
-
-
Jeffries, F.M.1
Reiss, A.L.2
Brown, W.T.3
Meyers, D.A.4
Glicksman, A.C.5
Bandyopadhyay, S.6
-
24
-
-
0020652713
-
Isolation and characterization of a full-length expressible cDNA for human hypoxanthine phosphoribosyltransferase
-
Jolly, D.J., H. Okayama, P. Berg, A.C. Esty, D. Filpula, P. Bohlen, G.G. Johnson, J.E. Shively, T. Hunkapillar, and T. Friedmann. 1983. Isolation and characterization of a full-length expressible cDNA for human hypoxanthine phosphoribosyltransferase. Proc. Natl. Acad. Sci. 80:447-481.
-
(1983)
Proc. Natl. Acad. Sci.
, vol.80
, pp. 447-481
-
-
Jolly, D.J.1
Okayama, H.2
Berg, P.3
Esty, A.C.4
Filpula, D.5
Bohlen, P.6
Johnson, G.G.7
Shively, J.E.8
Hunkapillar, T.9
Friedmann, T.10
-
25
-
-
0342499587
-
Strategies for multilocus linkage analysis in humans
-
Lathrop, G.M., J.-M. Lalouel, C.A. Julier, and J. Ott. 1984. Strategies for multilocus linkage analysis in humans. Proc. Natl. Acad. Sci. 81: 3443-3446.
-
(1984)
Proc. Natl. Acad. Sci.
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Lalouel, J.-M.2
Julier, C.A.3
Ott, J.4
-
26
-
-
0026673533
-
Manic depressive illness is linked to factor IX in a French pedigree
-
Lucotte, G., A. Landoulsi, S. Berriche, F. David, and M.C. Babron. 1992. Manic depressive illness is linked to factor IX in a French pedigree. Ann. Genet. 35: 93-95.
-
(1992)
Ann. Genet.
, vol.35
, pp. 93-95
-
-
Lucotte, G.1
Landoulsi, A.2
Berriche, S.3
David, F.4
Babron, M.C.5
-
27
-
-
0016329602
-
Linkage studies with X-chromosome markers in bipolar (manic-depressive) and unipolar (depressive) illnesses
-
Mendlewicz, J. and J.L. Fleiss. 1974. Linkage studies with X-chromosome markers in bipolar (manic-depressive) and unipolar (depressive) illnesses. Biol. Psychiatry 9: 261-294.
-
(1974)
Biol. Psychiatry
, vol.9
, pp. 261-294
-
-
Mendlewicz, J.1
Fleiss, J.L.2
-
28
-
-
0015524236
-
Evidence for X-linkage in the transmission of manic-depressive illness
-
Mendlewicz, J., J.L. Fleiss, and R.R. Fieve. 1972. Evidence for X-linkage in the transmission of manic-depressive illness. J. Am. Med. Assoc. 222: 1624-1627.
-
(1972)
J. Am. Med. Assoc.
, vol.222
, pp. 1624-1627
-
-
Mendlewicz, J.1
Fleiss, J.L.2
Fieve, R.R.3
-
29
-
-
0018604858
-
Colour blindness linkage to bipolar manic depressive illness: New evidence
-
Mendlewicz, J., P. Linowski, J.J. Guroff, and H.M. Van Praag. 1979. Colour blindness linkage to bipolar manic depressive illness: New evidence. Arch. Gen. Psychiatry 36: 1442-1447.
-
(1979)
Arch. Gen. Psychiatry
, vol.36
, pp. 1442-1447
-
-
Mendlewicz, J.1
Linowski, P.2
Guroff, J.J.3
Van Praag, H.M.4
-
30
-
-
0019142381
-
Linkage between glucose-6-phosphate-dehydrogenase deficiency and manic-depressive psychosis
-
Mendlewicz, J., P. Linkowski, and J. Wilmotte. 1980. Linkage between glucose-6-phosphate-dehydrogenase deficiency and manic-depressive psychosis. Br. J. Psychiatry 137: 337-342.
-
(1980)
Br. J. Psychiatry
, vol.137
, pp. 337-342
-
-
Mendlewicz, J.1
Linkowski, P.2
Wilmotte, J.3
-
31
-
-
0023668035
-
Polymorphic DNA marker on X-chromosome and manic depression
-
Mendlewicz, J., P. Simon, S. Sevy, F. Charon, H. Brocas, S. Legros, and G. Vassart. 1987. Polymorphic DNA marker on X-chromosome and manic depression. Lancet 1: 1230-1232.
-
(1987)
Lancet
, vol.1
, pp. 1230-1232
-
-
Mendlewicz, J.1
Simon, P.2
Sevy, S.3
Charon, F.4
Brocas, H.5
Legros, S.6
Vassart, G.7
-
32
-
-
0028363434
-
X-chromosome inactivation: Molecular mechanisms and genetic consequences
-
Migeon, B. 1994. X-chromosome inactivation: Molecular mechanisms and genetic consequences. Trends Genet. 10: 230-235.
-
(1994)
Trends Genet.
, vol.10
, pp. 230-235
-
-
Migeon, B.1
-
33
-
-
0015858194
-
Hereditary diseases in Finland; rare flora in rare soil. Ann
-
Norio, R., H.R. Nevanlinna, and J. Perheentupa. 1973. Hereditary diseases in Finland; rare flora in rare soil. Ann. Clin. Res. 5: 109-141.
-
(1973)
Clin. Res.
, vol.5
, pp. 109-141
-
-
Norio, R.1
Nevanlinna, H.R.2
Perheentupa, J.3
-
34
-
-
0002380820
-
Genetics
-
(ed. E.S. Paykel), 2nd ed., Churchill Livingstone, Edinburgh, UK
-
Nurnberger, J.I. and E.S. Gershon. 1992. Genetics. In Handbook of affective disorders (ed. E.S. Paykel), 2nd ed., pp. 131-148. Churchill Livingstone, Edinburgh, UK.
-
(1992)
Handbook of Affective Disorders
, pp. 131-148
-
-
Nurnberger, J.I.1
Gershon, E.S.2
-
35
-
-
0026763262
-
Advances and retreats in the molecular genetics of major mental illness
-
O'Donovan, M.C. and M.J. Owen. 1992. Advances and retreats in the molecular genetics of major mental illness. Ann. Med. 24: 167-173.
-
(1992)
Ann. Med.
, vol.24
, pp. 167-173
-
-
O'Donovan, M.C.1
Owen, M.J.2
-
36
-
-
0039513062
-
Computer-simulation methods in human linkage analysis
-
Ott, J. 1989. Computer-simulation methods in human linkage analysis. Proc. Natl. Acad. Sci. 86: 4175-4178.
-
(1989)
Proc. Natl. Acad. Sci.
, vol.86
, pp. 4175-4178
-
-
Ott, J.1
-
37
-
-
0003408936
-
-
The Johns Hopkins University Press, Baltimore, MD and London, UK
-
_. 1991. Analysis of human genetic linkage, revised ed. The Johns Hopkins University Press, Baltimore, MD and London, UK.
-
(1991)
Analysis of Human Genetic Linkage, Revised Ed.
-
-
-
38
-
-
0014497720
-
Family history studies: V. The genetics of mania
-
Reich, T., P.J. Clayton, and G. Winokur. 1969. Family history studies: V. The genetics of mania. Am. J. Psychiatry 125: 1358-1369.
-
(1969)
Am. J. Psychiatry
, vol.125
, pp. 1358-1369
-
-
Reich, T.1
Clayton, P.J.2
Winokur, G.3
-
39
-
-
0002980254
-
Hypoxanthine phosphoribosyltransferase deficiency: The Lesch-Nyhan syndrome and gouty arthritis
-
(ed. C.R. Scriver, A.L. Beaudet, W.S. Sly, and D. Valle), McGraw-Hill. Inc., New York
-
Stout, T.J. and T.C. Caskey. 1989. Hypoxanthine phosphoribosyltransferase deficiency: The Lesch-Nyhan syndrome and gouty arthritis. In The metabolic basis of inherited disease (ed. C.R. Scriver, A.L. Beaudet, W.S. Sly, and D. Valle), pp. 1007-1028. McGraw-Hill. Inc., New York.
-
(1989)
The Metabolic Basis of Inherited Disease
, pp. 1007-1028
-
-
Stout, T.J.1
Caskey, T.C.2
-
40
-
-
0024437865
-
Direct sequencing of affinity-captured amplified human DNA: Application to the detection of apolipoprotein E polymorphism
-
Syvänen, A.-C., K. Aalto-Setälä, K. Kontula, and H. Söderlund. 1989. Direct sequencing of affinity-captured amplified human DNA: Application to the detection of apolipoprotein E polymorphism. FEB 258: 71-74.
-
(1989)
FEB
, vol.258
, pp. 71-74
-
-
Syvänen, A.-C.1
Aalto-Setälä, K.2
Kontula, K.3
Söderlund, H.4
-
41
-
-
0027730113
-
A novel polylocus method for linkage analyses using the lod-score or affected sib-pair method
-
Terwilliger, J.D. and J. Ott. 1993. A novel polylocus method for linkage analyses using the lod-score or affected sib-pair method. Genet. Epidemiol. 10: 477-482.
-
(1993)
Genet. Epidemiol.
, vol.10
, pp. 477-482
-
-
Terwilliger, J.D.1
Ott, J.2
-
42
-
-
0021180032
-
Blot hybridisation analysis of genomic DNA
-
Vandenplas, S., I. Wiid, A. Grobler-Rabie, K. Brebner, M. Ricketts, G. Wallis, A. Bester, C. Boyd, and C. Mathew. 1984. Blot hybridisation analysis of genomic DNA. J. Med. Genet. 21: 164-172.
-
(1984)
J. Med. Genet.
, vol.21
, pp. 164-172
-
-
Vandenplas, S.1
Wiid, I.2
Grobler-Rabie, A.3
Brebner, K.4
Ricketts, M.5
Wallis, G.6
Bester, A.7
Boyd, C.8
Mathew, C.9
-
43
-
-
0027932287
-
Integration of gene maps: Chromosome X
-
Wang, L.H., A. Collins, S. Lawrence, B.J. Keats, and N.E. Morton. 1994. Integration of gene maps: Chromosome X. Genomics 22: 590-604.
-
(1994)
Genomics
, vol.22
, pp. 590-604
-
-
Wang, L.H.1
Collins, A.2
Lawrence, S.3
Keats, B.J.4
Morton, N.E.5
-
45
-
-
0021329916
-
Psychiatric disorders in the relatives of probands with affective disorders
-
Weissman, M.M., E.S. Gershon, K.K. Kidd, B.A. Prusoff, J.F. Leckman, E. Dibble, J. Hamovit, W.D. Thompson, D.L. Pauls, and J.J. Guroff. 1984. Psychiatric disorders in the relatives of probands with affective disorders. Arch. Gen. Psychiatry 41: 13-21.
-
(1984)
Arch. Gen. Psychiatry
, vol.41
, pp. 13-21
-
-
Weissman, M.M.1
Gershon, E.S.2
Kidd, K.K.3
Prusoff, B.A.4
Leckman, J.F.5
Dibble, E.6
Hamovit, J.7
Thompson, W.D.8
Pauls, D.L.9
Guroff, J.J.10
-
46
-
-
0027936475
-
Report of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27 1994
-
Willard, H.F., F. Cremers, J.L. Mandel, A.P. Monaco, D.L. Nelson, and D. Schlessinger. 1994. Report of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27 1994. Cytogenet. Cell Genet. 67: 295-358.
-
(1994)
Cytogenet. Cell Genet.
, vol.67
, pp. 295-358
-
-
Willard, H.F.1
Cremers, F.2
Mandel, J.L.3
Monaco, A.P.4
Nelson, D.L.5
Schlessinger, D.6
-
47
-
-
0029071390
-
A family study of manic-depressive (bipolar I) disease. Is it a distinct illness separable from primary unipolar depression?
-
Winokur, G., W. Coryell, M. Keller, J. Endicott, and A. Leon. 1995. A family study of manic-depressive (bipolar I) disease. Is it a distinct illness separable from primary unipolar depression? Arch. Gen. Psychiatry 52: 367-373.
-
(1995)
Arch. Gen. Psychiatry
, vol.52
, pp. 367-373
-
-
Winokur, G.1
Coryell, W.2
Keller, M.3
Endicott, J.4
Leon, A.5
|