books |
meeting abstracts |
book chapters
Rockefeller:
2007 |
2006 |
2005 |
2004 |
2003 |
2002 |
2001 |
2000 |
1999 |
1998 |
1997 |
1996
Columbia:
1995 |
1994 |
1993 |
1992 |
1991 |
1990 |
1989 |
1988
1987 |
1986 |
1985 |
1984 |
1983 |
1982 |
1981 |
1980 |
1979 |
1978 |
1977 |
1976 |
1975 |
1974
1999
-
Alkhateeb A, Al-Alami J, Leal SM, El-Shanti HE (1999),
"Fine mapping and further evidence of locus homogeneity for
Progressive Pseudorheumatoid Dysplasia",
Genetic Testing, 3:329-333.
-
Annunen S, Paassilta P, Lohiniva J, Perala M, Pihlajamaa T, Karppinen J,
Tervonen O, Kroger H, Lahde S, Vanharanta H, Ryhanen L, Goring HH, Ott J,
Prockop DJ, Ala-Kokko L (1999),
"An allele of COL9A2 associated with intervertebral disc
disease",
Science, 285(5426):409-412.
[ Medline entry]
-
Appukuttan B, Gillanders E, Juo SH, Freas-Lutz D, Ott S, Sood R, Van Auken
A, Bailey-Wilson J, Wang X, Patel R, Robbins CM, Chung M, Annett G,
Weinberg K, Borchert M, Trent JM, Brownstein MJ, Stout JT (1999),
"Localization of a Gene for Duane's Retraction Syndrome to Chromosome 2q31",
American Journal of Human Genetics, 65(6):1639-1646.
-
Barnes KC, Freidhoff LR, Nickel R, Chiu YF,
SH Juo , Hizawa N, Naidu RP, Ehrlich E, Duffy DL,
Schou C,Levett PN, Marsh DG, Beaty TH (1999),
"Dense mapping of chromosome 12q13.2-q23.3 and linkage to
Asthma and Atopy",
Journal of Allergy and Clinical Immunology, 104:485-491.
[ Medline entry]
-
A Bhat, SC Heath, J Ott (1999),
"Heterogeneity for multiple disease loci in linkage analysis",
Human Heredity, 49:229-231.
[ abstract]
[ Medline entry ]
-
A Bhat, PR Lucek, J Ott (1999),
"Analysis of complex traits using neural networks",
Genetic Epidemiology, 17, suppl 1: S503-S508.
-
DA Campbell, D Sundaramurthy, D Gordon,
AF Markham and LF Pieri (1999),
"Association between a marker in the UCP-2/UCP-3 gene
cluster and genetic susceptibility to anorexia nervosa",
Molecular Psychiatry, 4:68-70.
-
CH Chen, SJ Finch, NR Mendell, D Gordon (1999),
"Comparison of empirical strategies to maximize GENEHUNTER
LOD scores",
Genetic Epidemiology, 17, suppl 1: S103-S108.
-
Chung WK, Luke A, Rotini C, Vidal-Puig A, Rosenbaum M, Chua M,
Solanes G, Zheng M, Zhao L, LeDuc C, Eisberg A, Chu F, Murphy E, Schreier
M, Aronne L, Caprio S, Kahle B, Flier JS, D Gordon, Leal SM, Cooper RS,
Goldsmith R, Andreu AL, Brunno C, DiMauro S, Heo M, Lowe WL, Lowell BB,
Allison DB, Liebel RL (1999),
"Uncoupling protein 3 (UCP3): Mutation and linkage analysis
for possible role in adiposity of African Americans",
Diabetes, 48(9):1890-1895.
-
Chung WK, Luke A, Cooper RS, Rotini C, Vidal-Puig A, Rosenbaum M,
Gordon D, Leal SM, Caprio S, Goldsmith R, Andreu AL, Bruno C, DiMauro S,
Heo M, Lowe WL Jr., Lowell BB, Allison DB (1999)
"The long isoform uncoupling protein-2 (UCP3L) in human energy
homeostasis",
International Journal of Obesity, 23(Suppl 6):49-50.
-
Dansky HM, Charlton SA, Sikes JL, Heath SC, Simantov R, Levin LF,
Shu P, Moore KJ, Breslow JL, Smith JD (1999),
"Genetic background determines the extent of atherosclerosis in
ApoE-deficient mice",
Arterioscler Thromb Vasc Biol, 19(8):1960-1968.
[ Medline entry]
-
Daw EW, Heath SC, Wijsman EM (1999),
"Multipoint oligogenic analysis of age-at-onset data with applications to
Alzheimer disease pedigrees",
American Journal of Human Genetics, 64(3):839-851.
[ Medline entry]
-
Frank J, Pignata C, Panteleyev AA, Prowse DM, Baden H, Weiner L,
Gaetaniello L, Ahmad W, Pozzi N, Cserhalmi-Friedman PB, Aita VM,
Uyttendaele H, Gordon D, Ott J, Brissette JL, Christiano AM (1999),
"Exposing the human nude phenotype" (scientific correspondence),
Nature, 398(6727):473-474.
-
D Gordon, SC Heath, J Ott (1999),
"True pedigree errors more frequent than apparent
errors for single nucleotide polymorphisms",
Human Heredity,
49(2):65-70.
[ abstract]
[ Medline entry]
-
D Gordon, TC Matise, SC Heath, J Ott (1999),
"Power loss for multiallelic transmission disequilibrium test
when errors introduced: GAW11 simulated data",
Genetic Epidemiology, 17, suppl 1: S587-S592.
-
SH Juo, TH Beaty, D Duffy, J Coresh, PO Kwiterovich Jr (1999)
"No common major gene for Apolipoprotein A-I and HDL3-C levels: results
from bivariate segregation analysis",
Genetic Epidemiology, 16:54-68.
[ Medline entry]
-
SH Juo , Diego F. Wyszynski, Terri H. Beaty, Han-Yao
Huang, Joan E. Bailey-Wilson (1999),
"Mild association between the A/G polymorphism in the
promoter of the Apolipoprotein A-I gene and Apolipoprotein
A-I levels: a meta-analysis",
American Journal of Medical Genetics, 82:235-241.
[ Medline entry]
-
SH Juo , EW Pugh, A Baffoe-Bonnie, A Kingman,
AJM Sorant, A Klain, J O'Neill, R Mathias, AF Wilson, JE Bailey-Wilson
(1999),
"Possible linkage of alcoholism, monoamine oxidase (MAO) activity
and P300 amplitude to chromosome 12q24",
Genetic Epidemiology, 17, suppl 1:S193-S198.
-
Karayiorgou M, Sobin C, Blundell ML, Galke BL, Malinova L, Goldberg P,
Ott J, Gogos JA (1999),
"Family-based association studies support a sexually
dimorphic effect of COMT and MAOA on genetic
susceptibility to obsessive-compulsive disorder",
Biol Psychiatry, 45(9):1178-1189.
[ Medline entry]
-
SM Leal, SC Heath (1999),
"Searching for alcoholism susceptibility genes using MCMC
methods",
Genetic Epidemiology, 17, suppl 1: S217-S222.
-
Lewis CA, Batlle IR, Batlle KG, Banerjee P, Cideciyan AV, Huang J, Aleman
TS, Huang Y, Ott J, Gilliam TC, Knowles JA, Jacobson SG (1999)
"Tubby-like protein 1 homozygous splice-site mutation
causes early-onset severe retinal degeneration",
Invest Ophthalmol Vis Science,40(9):2106-2114.
[Medline entry]
-
W Li (1999),
"Statistical properties of open reading frames in complete
genome sequences",
Computer & Chemistry (informatics and the genome issue) , 23:283-301.
[ abstract]
[Medline entry]
[ full text (PDF) ]
-
W Li, F Haghighi, CT Falk (1999),
"Design of artificial neural network and its application
to the analysis of alcoholism data",
Genetic Epidemiology, 17, suppl 1: S223-S228.
-
M Marinov, TC Matise, GM Lathrop, DE Weeks (1999),
"A comparison of two algorithms, MultiMap and Gene Mapping System,
for automated construction of genetic linkage maps",
Genetic Epidemiology, 17, suppl 1: S649-S654.
-
ER de Oliveira e Silva, M Kong, Z Han, C Starr, EM Kass,
SH Juo, D Foster, HM Dansky, M Merkel, K Cundey, EA Brinton,
JL Breslow, JD Smith (1999),
"Metabolic and genetic determinants of HDL metabolism and
hepatic lipase activity in normolipidemic females",
Journal of Lipid Research, 40:1211-1221.
[ Medline entry]
-
J Ott (1999),
"Methods of analysis and resources available for genetic
trait mapping",
Journal of Heredity, 90(1):68-70.
[ Medline entry]
-
J Ott, P Lucek (1999),
"Complex traits on the map",
Recent Results Cancer Res, 154:285-291.
[ Medline entry]
-
J Ott, D Rabinowitz (1999),
"A principal-components approach based
on heritability for combining phenotype information",
Human Heredity,
49(2):106-111.
[abstract]
[ Medline entry]
-
Steen RG, Kwitek-Black AE, Glenn C, Gullings-Handley J, Van Etten W,
Atkinson OS, Appel D, Twigger S, Muir M, Mull T, Granados M, Kissebah M,
Russo K, Crane R, Popp M, Peden M, Matise T,
Brown DM, Lu J, Kingsmore S,
Tonellato PJ, Rozen S, Slonim D, Young P, Jacob HJ, et al (1999),
"A high-density integrated genetic linkage and radiation
hybrid map of the laboratory rat",
Genome Research (published online), 9(6):AP1-8, insert
[ html]
[Medline entry]
-
DA Stephan, E Gillanders, D Vanderveen, D Fraes-Lutz, G Wistow,
AD Baxevanis, CM Robbins, A Van Auken, MI Quesenberry, J Bailey-Wilson,
SH Juo , JM Trent, L Smith, MJ Brownstein (1999),
"Progressive juvenile-onset punctate cataracts caused by mutation
of the gD-crystallin gene",
Proceedings of National Academy of Sciences (USA), 96:1008-1012.
[ Medline entry]
[ full text (PDF) ]
-
Visscher PM, Haley CS, Heath SC, Muir WJ, Blackwood DH (1999),
"Detecting QTLs for uni- and bipolar disorder using a variance component
method",
Psychiatr Genetics, 9(2):75-84.
[ Medline entry]
-
Peter S White, Erik P Sulman, Christopher J Porter,
Tara C Matise (1999),
"A comprehensive view of human chromosome 1",
Genome Research, 9:978-988.
-
JD Winick, ML Blundell, BL Galke BL, AA Salam, SM Leal ,
Karayiorgou M (1999),
"Homozygosity mapping of the achromatopsia locus in the Pingelapese",
American Journal of Human Genetics , 64:1679-1685.
[ Medline entry]
[ full text (PDF) ]
