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Results: 1-25 | 26-48 |
Results: 26-48/48
CC-chemokine receptor 5 polymorphism and age of onset in familial multiplesclerosis
Authors: Barcellos, LF Schito, AM Rimmler, JB Vittinghoff, E Shih, A Lincoln, R Callier, S Elkins, MK Goodkin, DE Haines, JL Pericak-Vance, MA Hauser, SL Oksenberg, JR
Citation: Lf. Barcellos et al., CC-chemokine receptor 5 polymorphism and age of onset in familial multiplesclerosis, IMMUNOGENET, 51(4-5), 2000, pp. 281-288
Patterns of brain activation in people at risk for Alzheimer's disease
Authors: Bookheimer, SY Strojwas, MH Cohen, MS Saunders, AM Pericak-Vance, MA Mazziotta, JC Small, GW
Citation: Sy. Bookheimer et al., Patterns of brain activation in people at risk for Alzheimer's disease, N ENG J MED, 343(7), 2000, pp. 450-456
Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer's disease
Authors: Small, GW Ercoli, LM Silverman, DHS Huang, SC Komo, S Bookheimer, SY Lavretsky, H Miller, K Siddarth, P Rasgon, NL Mazziotta, JC Saxena, S Wu, HM Mega, MS Cummings, JL Saunders, AM Pericak-Vance, MA Roses, AD Barrio, JR Phelps, ME
Citation: Gw. Small et al., Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer's disease, P NAS US, 97(11), 2000, pp. 6037-6042
SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease
Authors: Martin, ER Lai, EH Gilbert, JR Rogala, AR Afshari, AJ Riley, L Finch, KL Stevens, F Livak, KJ Slotterbeck, BD Slifer, SH Warren, LL Conneally, PM Schmechel, DE Purvis, I Pericak-Vance, MA Roses, AD Vance, JM
Citation: Er. Martin et al., SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease, AM J HU GEN, 67(2), 2000, pp. 383-394
Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: Potential genetic and phenotypic heterogeneity
Authors: Scott, WK Grubber, JM Conneally, PM Small, GW Hulette, CM Rosenberg, CK Saunders, AM Roses, AD Haines, JL Pericak-Vance, MA
Citation: Wk. Scott et al., Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: Potential genetic and phenotypic heterogeneity, AM J HU GEN, 66(3), 2000, pp. 922-932
Genetic analysis for common complex disease
Authors: Hauser, ER Pericak-Vance, MA
Citation: Er. Hauser et Ma. Pericak-vance, Genetic analysis for common complex disease, AM HEART J, 140(4), 2000, pp. S36-S44
Lewy body and Alzheimer pathology in a family with the amyloid-beta precursor protein APP717 gene mutation
Authors: Rosenberg, CK Pericak-Vance, MA Saunders, AM Gilbert, JR Gaskell, PC Hulette, CM
Citation: Ck. Rosenberg et al., Lewy body and Alzheimer pathology in a family with the amyloid-beta precursor protein APP717 gene mutation, ACT NEUROP, 100(2), 2000, pp. 145-152
Physical and cDNA mapping in the DBH region of human chromosome 9q34
Authors: Gilbert, JR Kumar, A Newey, S Rao, N Ioannou, P Qiu, H Lin, D Xu, P Pettenati, MJ Pericak-Vance, MA
Citation: Jr. Gilbert et al., Physical and cDNA mapping in the DBH region of human chromosome 9q34, HUMAN HERED, 50(3), 2000, pp. 151-157
Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing
Authors: Messiaen, LM Callens, T Roux, KJ Mortier, GR De Paepe, A Abramowicz, M Pericak-Vance, MA Vance, JM Wallace, MR
Citation: Lm. Messiaen et al., Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing, GENET MED, 1(6), 1999, pp. 248-253
An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease
Authors: Rogaeva, EA Premkumar, S Grubber, J Serneels, L Scott, WK Kawarai, T Song, YQ Hill, DM Abou-Donia, SM Martin, ER Vance, JJ Yu, G Orlacchio, A Pei, Y Nishimura, M Supala, A Roberge, B Saunders, AM Roses, AD Schmechel, D Crane-Gatherum, A Sorbi, S Bruni, A Small, GW Conneally, PM Haines, JL Van Leuven, F St George-Hyslop, PH Farrer, LA Pericak-Vance, MA
Citation: Ea. Rogaeva et al., An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease, NAT GENET, 22(1), 1999, pp. 19-21
Autistic disorder and chromosome 15q11-q13: Construction and analysis of aBAC/PAC contig
Authors: Maddox, LO Menold, MM Bass, MP Rogala, AR Pericak-Vance, MA Vance, JM Gilbert, JR
Citation: Lo. Maddox et al., Autistic disorder and chromosome 15q11-q13: Construction and analysis of aBAC/PAC contig, GENOMICS, 62(3), 1999, pp. 325-331
Genetic studies of autistic disorder and chromosome 7
Authors: Ashley-Koch, A Wolpert, CM Menold, MM Zaeem, L Basu, S Donnelly, SL Ravan, SA Powell, CM Qumsiyeh, MB Aylsworth, AS Vance, JM Gilbert, JR Wright, HH Abramson, RK DeLong, GR Cuccaro, ML Pericak-Vance, MA
Citation: A. Ashley-koch et al., Genetic studies of autistic disorder and chromosome 7, GENOMICS, 61(3), 1999, pp. 227-236
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity
Authors: Winn, MP Conlon, PJ Lynn, KL Howell, DN Slotterbeck, BD Smith, AH Graham, FL Bembe, M Quarles, LD Pericak-Vance, MA Vance, JM
Citation: Mp. Winn et al., Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity, GENOMICS, 58(2), 1999, pp. 113-120
Complete genomic screen for disease susceptibility loci in nuclear families
Authors: Anderson, JL Hauser, ER Martin, ER Scott, WK Ashley-Koch, A Kim, KJ Monks, SA Haynes, CS Speer, MC Pericak-Vance, MA
Citation: Jl. Anderson et al., Complete genomic screen for disease susceptibility loci in nuclear families, GENET EPID, 17, 1999, pp. S473-S478
Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K)
Authors: Grubber, JM Saunders, AM Crane-Gatherum, AR Scott, WK Martin, ER Haynes, CS Conneally, PM Small, GW Roses, AD Haines, JL Pericak-Vance, MA
Citation: Jm. Grubber et al., Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K), NEUROSCI L, 269(2), 1999, pp. 115-119
Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration
Authors: De La Paz, MA Guy, VK Abou-Donia, S Heinis, R Bracken, B Vance, JM Gilbert, JR Gass, JDM Haines, JL Pericak-Vance, MA
Citation: Ma. De La Paz et al., Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration, OPHTHALMOL, 106(8), 1999, pp. 1531-1536
Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22
Authors: Anderson, JL Khan, M David, WS Mahdavi, Z Nuttall, FQ Krech, E West, SG Vance, JM Pericak-Vance, MA Nance, MA
Citation: Jl. Anderson et al., Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22, AM J MED G, 82(2), 1999, pp. 161-165
Further evidence linking late-onset Alzheimer disease with chromosome 12
Authors: Scott, WK Grubber, JM Abou-Donia, SM Church, TD Saunders, AM Roses, AD Pericak-Vance, MA Conneally, PM Small, GW Haines, JL
Citation: Wk. Scott et al., Further evidence linking late-onset Alzheimer disease with chromosome 12, J AM MED A, 281(6), 1999, pp. 513-514
Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis
Authors: Winn, MP Conlon, PJ Lynn, KL Howell, DN Gross, DA Rogala, AR Smith, AH Graham, FL Bembe, M Quarles, LD Pericak-Vance, MA Vance, JM
Citation: Mp. Winn et al., Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis, KIDNEY INT, 55(4), 1999, pp. 1241-1246
Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke family 1684
Authors: Hulette, CM Pericak-Vance, MA Roses, AD Schmechel, DE Yamaoka, LH Gaskell, PC Welsh-Bohmer, KA Crowther, RA Spillantini, MG
Citation: Cm. Hulette et al., Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke family 1684, J NE EXP NE, 58(8), 1999, pp. 859-866
Memory self-appraisal in middle-aged and older adults with the apolipoprotein e-4 allele
Authors: Small, GW Chen, ST Komo, S Ercoli, L Bookheimer, S Miller, K Lavretsky, H Saxena, S Kaplan, A Dorsey, D Scott, WK Saunders, AM Haines, JL Roses, AD Pericak-Vance, MA
Citation: Gw. Small et al., Memory self-appraisal in middle-aged and older adults with the apolipoprotein e-4 allele, AM J PSYCHI, 156(7), 1999, pp. 1035-1038
Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7
Authors: Speer, MC Vance, JM Grubber, JM Graham, FL Stajich, JM Viles, KD Rogala, A McMichael, R Chutkow, J Goldsmith, C Tim, RW Pericak-Vance, MA
Citation: Mc. Speer et al., Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7, AM J HU GEN, 64(2), 1999, pp. 556-562
Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31
Authors: Bartoloni, L Horrigan, SK Viles, KD Gilchrist, JM Stajich, JM Vance, JM Yamaoka, LH Pericak-Vance, MA Westbrook, CA Speer, MC
Citation: L. Bartoloni et al., Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31, GENOMICS, 54(2), 1998, pp. 250-255
Risultati: 1-25 | 26-48 |