-
2
-
-
0031760712
-
Familial leukoencephalopathy in bipolar disorder
-
(1998)
Am J Psychiatry
, vol.155
, pp. 1605-1607
-
-
Ahearn, E.P.1
Steffens, D.C.2
Cassidy, F.3
Van Meter, S.A.4
Provenzale, J.M.5
Seldin, M.F.6
Weisler, R.H.7
Krishnan, K.R.8
-
6
-
-
0029403019
-
Inferring microstructural features and the physiological state of tissues from diffusion-weighted images
-
(1995)
NMR Biomed
, vol.8
, pp. 333-344
-
-
Basser, P.J.1
-
10
-
-
15144347946
-
A linkage study of bipolar illness
-
(1997)
Arch Gen Psychiatry
, vol.54
, pp. 27-35
-
-
Berrettini, W.H.1
Ferraro, T.N.2
Goldin, L.R.3
Detera-Wadleigh, S.D.4
Choi, H.5
Muniec, D.6
Guroff, J.J.7
Kazuba, D.M.8
Nurnberger J.I., Jr.9
Hsieh, W.T.10
Hoehe, M.R.11
Gershon, E.S.12
-
14
-
-
0030574075
-
Accuracy and reproducibility of brain and tissue volumes using a magnetic resonance segmentation method
-
(1996)
Psychiatry Res
, vol.67
, pp. 215-234
-
-
Byrum, C.E.1
MacFall, J.R.2
Charles, H.C.3
Chitilla, V.R.4
Boyko, O.B.5
Upchurch, L.6
Smith, J.S.7
Rajagopalan, P.8
Passe, T.9
Kim, D.10
Xanthakos, S.11
Krishnan, R.12
-
16
-
-
0029089247
-
Clinical spectrum of CADASIL: A study of 7 families
-
(1995)
Lancet
, vol.346
, pp. 934-939
-
-
Chabriat, H.1
Vahedi, K.2
Iba-Zizen, M.T.3
Joutel, A.4
Nibbio, A.5
Nagy, T.G.6
Krebs, M.O.7
Julien, J.8
Dubois, B.9
Ducrocq, X.10
Levasseur, M.11
Homeyer, P.12
Mas, J.L.13
Lyon-Caen, O.14
Tournier Lasserve, E.15
Bousser, M.G.16
-
20
-
-
0027194791
-
Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families
-
(1993)
Science
, vol.261
, pp. 921-923
-
-
Corder, E.H.1
Saunders, A.M.2
Strittmatter, W.J.3
Schmechel, D.E.4
Gaskell, P.C.5
Small, G.W.6
Roses, A.D.7
Haines, J.L.8
Pericak-Vance, M.A.9
-
23
-
-
0027933734
-
A genome-wide search for human type 1 diabetes susceptibility genes
-
(1994)
Nature
, vol.371
, pp. 130-136
-
-
Davies, J.L.1
Kawaguchi, Y.2
Bennett, S.T.3
Copeman, J.B.4
Cordell, H.J.5
Pritchard, L.E.6
Reed, P.W.7
Gough, S.C.L.8
Jenkins, S.C.9
Palmer, S.M.10
Balfour, K.M.11
Rowe, B.R.12
Farral, M.13
Barnett, A.H.14
Bain, S.C.15
Todd, J.A.16
-
26
-
-
0029885038
-
Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q
-
(1996)
Am J Hum Gen
, vol.58
, pp. 1279-1285
-
-
Detera-Wadleigh, S.D.1
Badner, J.A.2
Goldin, L.R.3
Berrettini, W.H.4
Sanders, A.R.5
Rollins, D.Y.6
Turner, G.7
Moses, T.8
Haerian, H.9
Muniec, D.10
Nurnberger J.I., Jr.11
Gershon, E.S.12
-
27
-
-
13044281675
-
A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2
-
(1999)
Genetics
, vol.96
, pp. 5604-5609
-
-
Detera-Wadleigh, S.D.1
Badner, J.A.2
Berrettini, W.H.3
Yoshikawa, T.4
Goldin, L.R.5
Turner, G.6
Rollins, D.Y.7
Moses, T.8
-
28
-
-
0031738054
-
The phenotypic spectrum of CADASIL: Clinical findings in 102 cases
-
(1998)
Ann Neurol
, vol.44
, pp. 731-739
-
-
Dichgans, M.1
Mayer, M.2
Uttner, D.P.3
Bruning, R.4
Muller-Hocker, J.5
Rungger, G.6
Ebke, M.7
Klockgether, T.8
Gasser, T.9
-
29
-
-
0031470730
-
Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity
-
(1997)
Ann Neurol
, vol.42
, pp. 885-890
-
-
Ducros, A.1
Joutel, A.2
Vahedi, K.3
Cecillon, M.4
Ferreira, A.5
Bernard, E.6
Verier, A.7
Echenne, B.8
Demunain, A.L.9
Bousser, M.G.10
Tournier-Lasserve, E.11
-
33
-
-
0028997998
-
Genetic heterogeneity in attention-deficit hyperactivity disorder (ADHD): Gender, psychiatric comorbidity, and maternal ADHD
-
(1995)
J Abnorm Psychol
, vol.104
, pp. 334-345
-
-
Faraone, S.V.1
Biederman, J.2
Chen, W.J.3
Milberger, S.4
Warburton, R.5
Tsuang, M.T.6
-
35
-
-
0027460755
-
Hyperkalemic periodic paralysis: Rapid molecular diagnosis and relationship of genotype to phenotype in 12 families
-
(1993)
Neurology
, vol.43
, pp. 668-673
-
-
Feero, W.G.1
Wang, J.2
Barany, F.3
Zhou, J.4
Todorovic, S.M.5
Conwit, R.6
Galloway, G.7
Hausmanowa-Petrusewicz, I.8
Fidzianska, A.9
Arahata, K.10
Wessel, H.B.11
Wadelius, C.12
Marks, H.G.13
Hartlage, P.14
Hayakawa, H.15
Hoffman, E.P.16
-
37
-
-
13344269025
-
Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23
-
(1996)
Nat Genet
, vol.12
, pp. 436-441
-
-
Freimer, N.B.1
Reus, V.I.2
Escamilla, M.A.3
McInnes, L.A.4
Spesny, M.5
Leon, P.6
Service, S.K.7
Smith, L.B.8
Silva, S.9
Rojas, E.10
Gallegos, A.11
Meza, L.12
Fournier, E.13
Baharloo, S.14
Blankenship, K.15
Tyler, D.J.16
Batki, S.17
Vinogradov, S.18
Weissenbach, J.19
Barondes, S.H.20
Sandkuijl, L.A.21
more..
-
38
-
-
0033909667
-
Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype
-
(2000)
Am J Hum Gen
, vol.66
, pp. 205-215
-
-
Friddle, C.1
Koskela, R.2
Ranada, K.3
Hebert, J.4
Cargill, M.5
Clark, C.D.6
McInnis, M.7
Simpson, S.8
McMahon, F.9
Stine, O.S.10
Meyers, D.11
Xu, J.12
MacKinnon, D.13
Swift Scanlan, T.14
Jamison, K.15
Folstein, S.16
Daly, M.17
Kruglyak, L.18
Marr, T.19
DePaulo, J.R.20
Botstein, D.21
more..
-
40
-
-
0019975573
-
A family study of schizoaffective, bipolar I, bipolar II, unipolar, and normal control probands
-
(1982)
Arch Gen Psychiatry
, vol.39
, pp. 1157-1167
-
-
Gershon, E.S.1
Hamovit, J.2
Guroff, J.J.3
Dibble, E.4
Leckman, J.F.5
Sceery, W.6
Targum, S.D.7
Nurnberger J.I., Jr.8
Goldin, L.R.9
Bunney W.E., Jr.10
-
41
-
-
0026088977
-
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
-
(1991)
Nature
, vol.349
, pp. 704-706
-
-
Goate, A.1
Chartier-Harlin, M.C.2
Mullan, M.3
Brown, J.4
Crawford, F.5
Fidani, L.6
Giuffra, L.7
Haynes, A.8
Irving, N.9
James, L.10
Mant, R.11
Newton, P.12
Rooke, K.13
Roques, P.14
Talbot, C.15
Pericak-Vance, M.A.16
Roses, A.17
Williamson, R.18
Rossor, M.19
Owen, M.20
Hardy, J.21
more..
-
50
-
-
0034284682
-
Myotilin is mutated in limb girdle muscular dystrophy 1A
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2141-2147
-
-
Hauser, M.A.1
Horrigan, S.K.2
Salmikangas, P.3
Viles, K.D.4
Tim, R.W.5
Torian, U.M.6
Taivainen, U.7
Bartoloni, L.8
Dancel, R.9
Gilchrist, J.M.10
Stajich, J.M.11
Gaskell, P.C.12
Gilbert, J.R.13
Vance, J.M.14
Pericak-Vance, M.A.15
Carpen, O.16
Westbrook, C.A.17
Speer, M.C.18
-
53
-
-
0026709919
-
Do bilineal pedigrees represent a problem for linkage analysis? Basic principles and simulation results for single-gene diseases with no heterogeneity
-
(1992)
Genet Epidemiol
, vol.9
, pp. 191-206
-
-
Hodge, S.E.1
-
56
-
-
16044362074
-
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
(1996)
Nature
, vol.383
, pp. 707-710
-
-
Joutel, A.1
Corpechot, C.2
Ducros, A.3
Vahedi, K.4
Chabriat, H.5
Mouton, P.6
Alamowitch, S.7
Domenga, V.8
Cecillion, M.9
Marechal, E.10
Maciazek, J.11
Vayssiere, C.12
Cruaud, C.13
Cabanis, E.14
Ruchoux, M.M.15
Weissenbach, J.16
Bach, J.F.17
Bousser, M.G.18
Tournier-Lasserve, E.19
-
57
-
-
0031590602
-
Strong clustering and stereotyped nature of Notch 3 mutations in CADASIL patients
-
(1997)
Lancet
, vol.350
, pp. 1511-1515
-
-
Joutel, A.1
Vahedi, K.2
Corpechot, C.3
Troesch, A.4
Chabriat, H.5
Vayssiere, C.6
Craud, C.7
Macìazek, J.8
Weissenbach, J.9
Bousser, M.G.10
Bach, J.F.11
Tournier Lasserue, E.12
-
58
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Hattori, N.3
Matsumine, H.4
Yamamura, Y.5
Minoshima, S.6
Yokochi, M.7
Mizuno, Y.8
Shimizu, N.9
-
59
-
-
17344368986
-
No evidence for significant linkage between bipolar affective disorder and chromosome 18 pericentromeric markers in a large series of multiplex extended pedigrees
-
(1998)
Am J Hum Gen
, vol.62
, pp. 916-924
-
-
Knowles, J.A.1
Rao, P.A.2
Cox-Matise, T.3
Loth, J.E.4
De Jesus, G.M.5
Levine, L.6
Das, K.7
Penchaszadeh, G.K.8
Alexander, J.R.9
Lerer, B.10
Endicott, J.11
Ott, J.12
Gilliam, T.C.13
Baron, M.14
-
60
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
-
(1995)
Science
, vol.269
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
Romano, D.M.4
Oshima, J.5
Pettingell, W.H.6
Yu, C.E.7
Jondro, P.D.8
Schmidt, S.D.9
Wang, K.10
Crowley, A.C.11
Fu, Y.H.12
Guenette, S.Y.13
Galas, D.14
Nemens, E.15
Wijsman, E.M.16
Bird, T.D.17
Schellenberg, G.D.18
Tanzi, R.E.19
-
63
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
(1995)
Nat Genet
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
64
-
-
7144255542
-
Missense mutation in a von Willebrand factor type A domain of the a3 (VI) collagen gene (COL6A3) in a family with Bethlem myopathy
-
(1998)
Hum Mol Genet
, vol.7
, pp. 807-812
-
-
Pan, T.C.1
Zhang, R.Z.2
Pericak-Vance, M.A.3
Tandan, R.4
Fries, T.5
Stajich, J.6
Viles, K.7
Vance, J.M.8
Chu, M.L.9
Speer, M.C.10
-
65
-
-
0025735884
-
Linkage studies in familial Alzheimer's disease: Evidence for chromosome 19 linkage
-
(1991)
Am J Hum Gen
, vol.48
, pp. 1034-1050
-
-
Pericak-Vance, M.A.1
Bebout, J.L.2
Gaskell, P.C.3
Yamaoka, L.H.4
Hung, W.Y.5
Alberts, M.J.6
Walker, A.P.7
Bartlett, R.J.8
Haynes, C.S.9
Welsh, K.A.10
Earl, N.L.11
Heyman, A.12
Clark, C.M.13
Roses, A.D.14
-
66
-
-
0030770726
-
Complete genomic screen in late-onset familial Alzheimer disease: Evidence for a new locus on chromosome 12
-
(1997)
JAMA
, vol.278
, pp. 1237-1241
-
-
Pericak-Vance, M.A.1
Bass, M.P.2
Yamaoka, L.H.3
Gaskell, P.C.4
Scott, W.K.5
Terwedow, H.A.6
Menold, M.M.7
Conneally, P.M.8
Small, G.W.9
Vance, J.M.10
Saunders, A.M.11
Roses, A.D.12
Haines, J.L.13
-
68
-
-
0025008677
-
Linkage strategies for genetically complex traits. II. The power of affected relative pairs
-
(1990)
Am J Hum Gen
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
69
-
-
0027337858
-
Apolipoprotein E ε4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases
-
(1993)
Lancet
, vol.342
, pp. 710-711
-
-
Saunders, A.M.1
Schmader, K.E.2
Breitner, J.C.3
Benson, M.D.4
Brown, W.T.5
Goldfarb, L.6
Goldgaber, D.7
Manwaring, M.G.8
Szymanski, M.H.9
McCown, N.10
Dole, K.C.11
Schmechel, D.E.12
Strittmatter, W.J.13
Pericak-Vance, M.A.14
Roses, A.D.15
-
71
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Lin, C.8
Li, G.9
Holman, K.10
Tsuda, T.11
Mar, L.12
Foncin, J.F.13
Bruni, A.C.14
Montesi, M.P.15
Sorbi, S.16
Rainero, I.17
Pinessi, L.18
Nee, L.19
Chumakov, I.20
Pollen, D.A.21
Brookes, A.22
Sanseau, P.23
Polinsky, R.J.24
Wasco, W.25
Da Silva, H.A.R.26
Haines, J.L.27
Pericak-Vance, M.A.28
Tanzi, R.E.29
Roses, A.D.30
Fraser, P.E.31
Rommens, J.M.32
St George-Hyslop, P.H.33
more..
-
72
-
-
0033073978
-
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7
-
(1999)
Am J Hum Gen
, vol.64
, pp. 556-562
-
-
Speer, M.C.1
Vance, J.M.2
Grubber, J.M.3
Graham, F.L.4
Stajich, J.M.5
Viles, K.D.6
Rogala, A.7
McMichael, R.8
Chutkow, J.9
Goldsmith, C.10
Tim, R.W.11
Pericak-Vance, M.A.12
-
74
-
-
0028875316
-
Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect
-
(1995)
Am J Hum Gen
, vol.57
, pp. 1384-1394
-
-
Stine, O.C.1
Xu, J.2
Koskela, R.3
McMahon, F.J.4
Gschwend, M.5
Friddle, C.6
Clark, C.D.7
McInnis, M.G.8
Simpson, S.G.9
Breschel, T.S.10
Vishio, E.11
Riskin, K.12
Feilotter, H.13
Chen, E.14
Shen, S.15
Folstein, S.16
Meyers, D.A.17
Botstein, D.18
Marr, T.G.19
DePaulo, J.R.20
more..
-
75
-
-
0027987228
-
A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3
-
(1994)
Nat Genet
, vol.8
, pp. 291-296
-
-
Straub, R.E.1
Lehner, T.2
Luo, Y.3
Loth, J.E.4
Shao, W.5
Sharpe, L.6
Alexander, J.R.7
Das, K.8
Simon, R.9
Fieve, R.R.10
Lerer, B.11
Endicott, J.12
Ott, J.13
Gilliam, T.C.14
Baron, M.15
-
78
-
-
0027479304
-
Cerebral sutosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
-
(1993)
Nat Genet
, vol.3
, pp. 256-259
-
-
Tournier-Lasserve, E.1
Joutel, A.2
Melki, J.3
Weissenbach, J.4
Lathrop, G.M.5
Chabriat, H.6
Mas, J.7
Cabanis, E.8
Baudrimont, M.9
Maciazek, J.10
Bach, M.11
Bousser, M.12
-
80
-
-
0024510662
-
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17
-
(1989)
Exp Neurol
, vol.104
, pp. 186-189
-
-
Vance, J.M.1
Nicholson, G.A.2
Yamaoka, L.H.3
Stajich, J.4
Stewart, C.S.5
Speer, M.C.6
Hung, W.Y.7
Roses, A.D.8
Barker, D.9
Pericak-Vance, M.A.10
|