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 1990
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M Baron, J Endicott, J Ott (1990)
"Genetic linkage in mental illness Limitations and prospects",
Brit J Psychiatry, 157: 645-655
[ abstract]
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M Baron, R Hamburger, LA Sandkuyl, N Risch,
B Mandel, J Endicott, RH Belmaker, J Ott (1990)
"The impact of phenotypic variation on genetic linkage analysis:
application to X-linkage in manic-depressive illness",
Acta Psychiatr Scand, 82:196-203
[ abstract]
[ Medline entry]
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LM Brzustowicz, T Lehner, LH Castilla,
GK Penchaszadeh, KC Wilhelmsen, R Daniels,
KE Davies, M Leppert, F Ziter, D Wood, V
Dubowitz, K Zerres, I Hausmanova-Petrusewicz,
J Ott, TL Munsat, TC Gilliam (1990)
"Genetic mapping of chronic childhood-onset
spinal muscular atrophy to chromosome 5q112-133",
Nature, 344, 540-541
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TC Gilliam, LM Brzustowicz, LH Castilla,
T Lehner, GK Penchaszadeh, RJ Daniels,
BC Byth, J Knowles, JE Hislop, Y Shapira, V
Dubowitz, TL Munsat, J Ott, KE Davies (1990)
Genetic homogeneity between acute and chronic forms of spinal
muscular atrophy ,
Nature, 345, 823-825
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E Ikonen, J Palo, J Ott, J Gusella,
H Somer, L Karila, A Palotie, L Peltonen (1990)
"Huntington disease in Finland: Linkage disequilibrium of chromosome 4
RFLP haplotypes and exclusion of a tight linkage between the disease
and D4S43 locus",
American Journal of Human Genetics, 46:5-11.
[abstract]
[ Medline entry]
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BJB Keats, SL Sherman, J Ott (1990)
"Human Gene Mapping 105 - Report of the committee on linkage and gene
order",
Cytogenetics and Cell Genetics,
55, 387-94
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S-P Kwan, J Terwilliger, R Parmley,
G Raghu, LA Sandkuyl, J Ott, H Ochs,
R Wedgwood, F Rosen (1990)
"Identification of a closely linked DNA marker, DXS178, to further
refine the X-linked agammaglobulinemia locus",
Genomics, 6:238-242
[abstract]
[ Medline entry]
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MA Musarella, L Anson-Cartwright, SM Leal,
LD Gilbert, RG Worton, GA Fishman, J Ott (1990)
"Multipoint linkage analysis and heterogeneity testing in 20 X-linked
retinitis pigmentosa families",
Genomics,
8:286-296.
[ abstract]
[ Medline entry]
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J Ott (1990)
"Genetic linkage and complex diseases: A comment",
Genetic Epidemiology, 7, 35-36
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J Ott (1990)
"Invited editorial: Cutting a Gordian knot in
the linkage analysis of complex human traits",
American Journal of Human Genetics, 46, 219-221
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J Ott, S Bhattacharya, JD Chen, MJ Denton,
J Donald, C Dubay, GJ Farrar, GA Fishman, D Frey, A Gal,
P Humphries, B Jay, M Jay, M Litt, M Machler M Musarella,
M Neugebauer, RL Nussbaum, JD Terwilliger,
GG Weleber, B Wirth, F Wong, RG Worton, AF Wright (1990)
"Localizing multiple X chromosome-linked retinitis pigmentosa
loci using multilocus homogeneity tests",
Proceedings of National Academy of Sciences, 87: 701-704
[ abstract]
[ Medline entry]
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J Ott, J Caesar, M Machler, A Schinzel, W Schmid
(1990)
Presymptomatic exclusion of myotonic dystrophy in a one-generation
pedigree of half-sibs ,
Human Heredity,
40, 305-307
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Y Shiloh, G Litvak, Y Ziv, T Lehner, L Sandkuyl,
M Hildesheimer, V Buchris, FPM Cremers, P Szabo,
BN White, JJA Holden, J Ott (1990)
Genetic mapping of X-linked albinism-deafness syndrome
(ADFN) to Xq263-q271 ,
American Journal of Human Genetics, 47, 20-27
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A Superti-Furga, B Steinmann, B Lee, F Ramirez,
T Lehner, J Ott, A Gaucher, P Morreau, G Werhya
(1990)
"Autosomal dominant spondyloarthropathy: No linkage to
the type II collagen gene", (correspondence),
New England Journal of Medicine, 322, 552-553
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DE Weeks, L Brzustowicz, E Squires-Wheeler, B Cornblatt,
T Lehner, M Stefanovich, A Bassett, TC Gilliam,
J Ott, L Erlenmeyer-Kimling (1990)
"Report of a workshop on genetic linkage studies in schizophrenia"
(Meeting Report),
Schizophrenia Bulletin,16:673-86.
[ abstract]
[ Medline entry]
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DE Weeks, T Lehner, E Squires-Wheeler,
C Kaufmann, J Ott (1990)
"Measuring the inflation of the lod score due to its
maximization over model parameter values in human linkage analysis",
Genetic Epidemiology, 7:237-243.
[ abstract]
[ Medline entry]
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DE Weeks, J Ott (1990)
"Reply to Dr Carothers: Support intervals for genetic risks",
American Journal of Human Genetics, 47, 166
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