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Results:
1-16
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Results: 16
Authors:
Glatt, CE
DeYoung, JA
Delgado, S
Service, SK
Giacomini, KM
Edwards, RH
Risch, N
Freimer, NB
Citation: Ce. Glatt et al., Screening a large reference sample to identify very low frequency sequencevariants: comparisons between two genes, NAT GENET, 27(4), 2001, pp. 435-438
Authors:
Service, SK
Ophoff, RA
Freimer, NB
Citation: Sk. Service et al., The genome-wide distribution of background linkage disequilibrium in a population isolate, HUM MOL GEN, 10(5), 2001, pp. 545-551
Authors:
Faham, M
Baharloo, S
Tomitaka, S
DeYoung, J
Freimer, NB
Citation: M. Faham et al., Mismatch repair detection (MRD): high-throughput scanning for DNA variations, HUM MOL GEN, 10(16), 2001, pp. 1657-1664
Authors:
Mathews, CA
Amighetti, LDH
Lowe, TL
van de Wetering, BJM
Freimer, NB
Reus, VI
Citation: Ca. Mathews et al., Cultural influences on diagnosis and perception of Tourette syndrome in Costa Rica, J AM A CHIL, 40(4), 2001, pp. 456-463
Authors:
Escamilla, MA
McInnes, LA
Service, SK
Spesny, M
Reus, VI
Molina, J
Gallegos, A
Fournier, E
Batki, S
Neylan, T
Matthews, C
Vinogradov, S
Roche, E
Tyler, DJ
Shimayoshi, N
Mendez, R
Ramirez, R
Ramirez, M
Araya, C
Araya, X
Leon, PE
Sandkuijl, LA
Freimer, NB
Citation: Ma. Escamilla et al., Genome screening for linkage disequilibrium in a Costa Rican sample of patients with bipolar-I disorder: A follow-up study on chromosome 18, AM J MED G, 105(2), 2001, pp. 207-213
Authors:
McInnes, LA
Service, SK
Reus, VI
Barnes, G
Charlat, O
Jawahar, S
Lewitzky, S
Yang, Q
Duong, QY
Spesny, M
Araya, C
Araya, X
Gallegos, A
Meza, L
Molina, J
Ramirez, R
Mendez, R
Silva, S
Fournier, E
Batki, SL
Mathews, CA
Neylan, T
Glatt, CE
Escamilla, MA
Luo, D
Gajiwala, P
Song, T
Crook, S
Nguyen, JB
Roche, E
Meyer, JM
Leon, P
Sandkuijl, LA
Freimer, NB
Chen, H
Citation: La. Mcinnes et al., Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population, P NAS US, 98(20), 2001, pp. 11485-11490
Authors:
Ophoff, RA
DeYoung, J
Service, SK
Joose, M
Caffo, NA
Sandkuijl, LA
Terwindt, GM
Haan, J
van den Maagdenberg, AMJM
Jen, J
Baloh, RW
Barilla-LaBarca, ML
Saccone, NL
Atkinson, JP
Ferrari, MD
Freimer, NB
Frants, RR
Citation: Ra. Ophoff et al., Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3, AM J HU GEN, 69(2), 2001, pp. 447-453
Authors:
Garner, C
McInnes, LA
Service, SK
Spesny, M
Fournier, E
Leon, P
Freimer, NB
Citation: C. Garner et al., Linkage analysis of a complex pedigree with severe bipolar disorder, usinga Markov chain Monte Carlo method, AM J HU GEN, 68(4), 2001, pp. 1061-1064
Authors:
Bull, LN
Roche, E
Song, EJ
Pedersen, J
Knisely, AS
van der Hagen, CB
Eiklid, K
Aagenaes, O
Freimer, NB
Citation: Ln. Bull et al., Mapping of the locus for cholestasis-lymphedema syndrome (Aagenaes syndrome) to a 6.6-cM interval on chromosome 15q, AM J HU GEN, 67(4), 2000, pp. 994-999
Authors:
Baharloo, S
Service, SK
Risch, N
Gitschier, J
Freimer, NB
Citation: S. Baharloo et al., Familial aggregation absolute pitch, AM J HU GEN, 67(3), 2000, pp. 755-758
Authors:
Escamilla, MA
DeMille, MC
Benavides, E
Roche, E
Almasy, L
Pittman, S
Hauser, J
Lew, DF
Freimer, NB
Whittle, MR
Citation: Ma. Escamilla et al., A minimalist approach to gene mapping: Locating the gene for acheiropodia,by homozygosity analysis, AM J HU GEN, 66(6), 2000, pp. 1995-2000
Authors:
Bull, LN
Pabon-Pena, CR
Freimer, NB
Citation: Ln. Bull et al., Compound microsatellite repeats: Practical and theoretical features, GENOME RES, 9(9), 1999, pp. 830-838
Authors:
Bull, LN
Juijn, JA
Liao, M
van Eijk, MJT
Sinke, RJ
Stricker, NL
DeYoung, JA
Carlton, VEH
Baharloo, S
Klomp, LWJ
Abukawa, D
Barton, DE
Bass, NM
Bourke, B
Drumm, B
Jankowska, I
Lovisetto, P
McQuaid, S
Pawlowska, J
Tazawa, Y
Villa, E
Tygstrup, N
Berger, R
Knisely, AS
Houwen, RHJ
Freimer, NB
Citation: Ln. Bull et al., Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC (vol 104, pg 241, 1999), HUM GENET, 104(6), 1999, pp. 528-528
Authors:
Bull, LN
Juijn, JA
Liao, M
van Eijk, MJT
Sinke, RJ
Stricker, NL
DeYoung, JA
Carlton, VEH
Baharloo, S
Klomp, LWJ
Abukawa, D
Barton, DE
Bass, NM
Bourke, B
Drumm, B
Jankowska, I
Lovisetto, P
McQuaid, S
Pawlowska, J
Tazawa, Y
Villa, E
Tygstrup, N
Berger, R
Knisely, AS
Houwen, RHJ
Freimer, NB
Citation: Ln. Bull et al., Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC, HUM GENET, 104(3), 1999, pp. 241-248
Authors:
Escamilla, MA
McInnes, LA
Spesny, M
Reus, VI
Service, SK
Shimayoshi, N
Tyler, DJ
Silva, S
Molina, J
Gallegos, A
Meza, L
Cruz, ML
Batki, S
Vinogradov, S
Neylan, T
Nguyen, JB
Fournier, E
Araya, C
Barondes, SH
Leon, P
Sandkuijl, LA
Freimer, NB
Citation: Ma. Escamilla et al., Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: An initial screen for bipolar disorder loci on chromosome 18, AM J HU GEN, 64(6), 1999, pp. 1670-1678
Authors:
Service, SK
Lang, DWT
Freimer, NB
Sandkuijl, LA
Citation: Sk. Service et al., Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations, AM J HU GEN, 64(6), 1999, pp. 1728-1738
Risultati:
1-16
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