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Quantitative Faunal Associates of the Serpulid Polychaete Hydroides dianthus
Published in:
Marine Biology, 1980, v. 56, n. 1, p. 43, doi. 10.1007/BF00390592
By:
- Haines, J. L.;
- Maurer, D.
Publication type:
Article
Further evidence linking late-onset Alzheimer disease with chromosome 12.
Published in:
1999
By:
- Scott, W K;
- Grubber, J M;
- Abou-Donia, S M;
- Church, T D;
- Saunders, A M;
- Roses, A D;
- Pericak-Vance, M A;
- Conneally, P M;
- Small, G W;
- Haines, J L
Publication type:
commentary
Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucoma.
Published in:
Clinical Genetics, 2013, v. 84, n. 2, p. 167, doi. 10.1111/cge.12176
By:
- Wiggs, J L;
- Howell, G R;
- Linkroum, K;
- Abdrabou, W;
- Hodges, E;
- Braine, C E;
- Pasquale, L R;
- Hannon, G J;
- Haines, J L;
- John, S W M
Publication type:
Article
Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataseta.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 256, doi. 10.1111/j.1749-6632.1991.tb37767.x
By:
- HAINES, J. L.;
- AMOS, J.;
- ATTWOOD, J.;
- BECH-HANSEN, N. T.;
- BURLEY, M.;
- CONNEALLY, P. M.;
- CONNOR, J. M.;
- FAHSOLD, R.;
- FLODMAN, P.;
- FRYER, A.;
- HALLEY, D. J. J.;
- JEWELL, A.;
- JANSSEN, L. A. J.;
- KANDT, R.;
- NORTHRUP, H.;
- OSBORNE, J.;
- PERICAK-VANCE, M.;
- POVEY, S.;
- SAMPSON, J.;
- SHORT, M. P.
Publication type:
Article
An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methodsa.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 298, doi. 10.1111/j.1749-6632.1991.tb37771.x
By:
- POVEY, S.;
- ATTWOOD, J.;
- JANSSEN, L. A. J.;
- BURLEY, M.;
- SMITH, M.;
- FLODMAN, P.;
- MORTON, N. E.;
- EDWARDS, J. H.;
- SAMPSON, J. R.;
- YATES, J. R. W.;
- HAINES, J. L.;
- AMOS, J.;
- SHORT, M. P.;
- SANDKUYL, L. A.;
- HALLEY, D. J. J.;
- FRYER, A. E.;
- BECH-HANSEN, T.;
- MUELLER, R.;
- AL-GHAZALI, L.;
- SUPER, M.
Publication type:
Article
A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22-23a.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 306, doi. 10.1111/j.1749-6632.1991.tb37772.x
By:
- JANSSEN, L. A. J.;
- POVEY, S.;
- ATTWOOD, J.;
- SANDKUYL, L. A.;
- LINDHOUT, D.;
- FLODMAN, P.;
- SMITH, M.;
- SAMPSON, J. R.;
- HAINES, J. L.;
- MERKENS, E. C.;
- FLEURY, P.;
- SHORT, P.;
- AMOS, J.;
- HALLEY, D. J. J.
Publication type:
Article
Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.
Published in:
Molecular Psychiatry, 2015, v. 20, n. 12, p. 1588, doi. 10.1038/mp.2015.6
By:
- Desikan, R S;
- Schork, A J;
- Wang, Y;
- Witoelar, A;
- Sharma, M;
- McEvoy, L K;
- Holland, D;
- Brewer, J B;
- Chen, C-H;
- Thompson, W K;
- Harold, D;
- Williams, J;
- Owen, M J;
- O'Donovan, M C;
- Pericak-Vance, M A;
- Mayeux, R;
- Haines, J L;
- Farrer, L A;
- Schellenberg, G D;
- Heutink, P
Publication type:
Article
Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6.
Published in:
Genetic Epidemiology, 1986, v. 3, n. 6, p. 399, doi. 10.1002/gepi.1370030604
By:
- Haines, J. L.;
- Trofatter, J. A.;
- Rao, D. C.
Publication type:
Article
Causes of death in huntington disease as reported on death certificates.
Published in:
Genetic Epidemiology, 1986, v. 3, n. 6, p. 417, doi. 10.1002/gepi.1370030606
By:
- Haines, J. L.;
- Conneally, P. M.;
- Rao, D. C.
Publication type:
Article
A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility.
Published in:
Genes & Immunity, 2011, v. 12, n. 5, p. 335, doi. 10.1038/gene.2011.3
By:
- Bush, W S;
- McCauley, J L;
- DeJager, P L;
- Dudek, S M;
- Hafler, D A;
- Gibson, R A;
- Matthews, P M;
- Kappos, L;
- Naegelin, Y;
- Polman, C H;
- Hauser, S L;
- Oksenberg, J;
- Haines, J L;
- Ritchie, M D
Publication type:
Article
Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.
Published in:
Genes & Immunity, 2009, v. 10, n. 7, p. 624, doi. 10.1038/gene.2009.53
By:
- McCauley, J. L.;
- Zuvich, R. L.;
- Bradford, Y.;
- Kenealy, S. J.;
- Schnetz-Boutaud, N.;
- Gregory, S. G.;
- Hauser, S. L.;
- Oksenberg, J. R.;
- Mortlock, D. P.;
- Pericak-Vance, M. A.;
- Haines, J. L.
Publication type:
Article
Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis.
Published in:
Genes & Immunity, 2006, v. 7, n. 5, p. 384, doi. 10.1038/sj.gene.6364311
By:
- Schmidt, S;
- Pericak-Vance, M A;
- Sawcer, S;
- Barcellos, L F;
- Hart, J;
- Sims, J;
- Prokop, A M;
- van der Walt, J;
- DeLoa, C;
- Lincoln, R R;
- Oksenberg, J R;
- Compston, A;
- Hauser, S L;
- Haines, J L;
- Gregory, S G
Publication type:
Article
Multifactor dimensionality reduction reveals gene–gene interactions associated with multiple sclerosis susceptibility in African Americans.
Published in:
Genes & Immunity, 2006, v. 7, n. 4, p. 310, doi. 10.1038/sj.gene.6364299
By:
- Brassat, D.;
- Motsinger, A. A.;
- Caillier, S. J.;
- Erlich, H. A.;
- Walker, K.;
- Steiner, L. L.;
- Cree, B. A. C.;
- Barcellos, L. F.;
- Pericak-Vance, M. A.;
- Schmidt, S.;
- Gregory, S.;
- Hauser, S. L.;
- Haines, J. L.;
- Oksenberg, J. R.;
- Ritchie, M. D.
Publication type:
Article
Examination of seven candidate regions for multiple sclerosis: strong evidence of linkage to chromosome 1q44.
Published in:
Genes & Immunity, 2006, v. 7, n. 1, p. 73, doi. 10.1038/sj.gene.6364275
By:
- Kenealy, S. J.;
- Herrel, L. A.;
- Bradford, Y.;
- Schnetz-Boutaud, N.;
- Oksenberg, J. R.;
- Hauser, S. L.;
- Barcellos, L. F.;
- Schmidt, S.;
- Gregory, S. G.;
- Pericak-Vance, M. A.;
- Haines, J. L.
Publication type:
Article
Osteopontin polymorphisms and disease course in multiple sclerosis.
Published in:
Genes & Immunity, 2003, v. 4, n. 4, p. 312
By:
- Caillier, S;
- Barcellos, L F;
- Baranzini, S E;
- Swerdlin, A;
- Lincoln, R R;
- Steinman, L;
- Martin, E;
- Haines, J L;
- Pericak-Vance, M;
- Hauser, S L;
- Oksenberg, J R
Publication type:
Article
Chromosome 17q22–q24 and multiple sclerosis genetic susceptibility.
Published in:
Genes & Immunity, 1999, v. 1, n. 2, p. 149
By:
- Fontaine, B;
- Cournu, I;
- Arnaud, I;
- Babron, M-C;
- Eichenbaum-Voline, S;
- Oksenberg, J R;
- Pericak-Vance, M A;
- Haines, J L;
- Semama, G;
- Liblau, R;
- Lyon-Caen, O;
- Clerget-Darpoux, F;
- Clanet, M;
- Hauser, S L
Publication type:
Article
Genetically meaningful phenotypic subgroups in autism spectrum disorders.
Published in:
Genes, Brain & Behavior, 2014, v. 13, n. 3, p. 276, doi. 10.1111/gbb.12117
By:
- Veatch, O. J.;
- Veenstra‐VanderWeele, J.;
- Potter, M.;
- Pericak‐Vance, M. A.;
- Haines, J. L.
Publication type:
Article
Examination of tetrahydrobiopterin pathway genes in autism.
Published in:
Genes, Brain & Behavior, 2009, v. 8, n. 8, p. 753, doi. 10.1111/j.1601-183X.2009.00521.x
By:
- Schnetz-Boutaud, N. C.;
- Anderson, B. M.;
- Brown, K. D.;
- Wright, H. H.;
- Abramson, R. K.;
- Cuccaro, M. L.;
- Gilbert, J. R.;
- Pericak-Vance, M. A.;
- Haines, J. L.
Publication type:
Article
Linkage and Association Study of Late-Onset Alzheimer Disease Families Linked to 9p21.3.
Published in:
Annals of Human Genetics, 2008, v. 72, n. 6, p. 725, doi. 10.1111/j.1469-1809.2008.00474.x
By:
- Züchner, S.;
- Gilbert, J. R.;
- Martin, E. R.;
- Leon-Guerrero, C. R.;
- Xu, P.-T.;
- Browning, C.;
- Bronson, P. G.;
- Whitehead, P.;
- Schmechel, D. E.;
- Haines, J. L.;
- Pericak-Vance, M. A.
Publication type:
Article
A Genome-wide Scan in an Amish Pedigree with Parkinsonism.
Published in:
Annals of Human Genetics, 2008, v. 72, n. 5, p. 621, doi. 10.1111/j.1469-1809.2008.00452.x
By:
- Lee, S. L.;
- Murdock, D. G.;
- McCauley, J. L.;
- Bradford, Y.;
- Crunk, A.;
- McFarland, L.;
- Jiang, L.;
- Wang, T.;
- Schnetz-Boutaud, N.;
- Haines, J. L.
Publication type:
Article
Polymorphisms of the Tumor Suppressor Gene LSAMP are Associated with Left Main Coronary Artery Disease.
Published in:
Annals of Human Genetics, 2008, v. 72, n. 4, p. 443, doi. 10.1111/j.1469-1809.2008.00433.x
By:
- Wang, L.;
- Hauser, E. R.;
- Shah, S. H.;
- Seo, D.;
- Sivashanmugam, P.;
- Exum, S. T.;
- Gregory, S. G.;
- Granger, C. B.;
- Haines, J. L.;
- Jones, C. J. H.;
- Crossman, D.;
- Haynes, C.;
- Kraus, W. E.;
- Freedman, N. J.;
- Pericak-Vance, M. A.;
- Goldschmidt-Clermont, P. J.;
- Vance, J. M.
Publication type:
Article
Serum Lipids in the GENECARD Study of Coronary Artery Disease Identify Quantitative Trait Loci and Phenotypic Subsets on Chromosomes 3q and 5q.
Published in:
Annals of Human Genetics, 2006, v. 70, n. 6, p. 738, doi. 10.1111/j.1469-1809.2006.00288.x
By:
- Shah, S. H.;
- Kraus, W. E.;
- Crossman, D. C.;
- Granger, C. B.;
- Haines, J. L.;
- Jones, C. J. H.;
- Mooser, V.;
- Huang, L.;
- Haynes, C.;
- Dowdy, E.;
- Vega, G. L.;
- Grundy, S. M.;
- Vance, J. M.;
- Hauser, E. R.
Publication type:
Article
Genetic basis for clinical expression in multiple sclerosis.
Published in:
2002
By:
- Barcellos, L F;
- Oksenberg, J R;
- Green, A J;
- Bucher, P;
- Rimmler, J B;
- Schmidt, S;
- Garcia, M E;
- Lincoln, R R;
- Pericak-Vance, M A;
- Haines, J L;
- Hauser, S L;
- Multiple Sclerosis Genetics Group
Publication type:
journal article
The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation.
Published in:
Bone Marrow Transplantation, 2005, v. 35, n. 12, p. 1155, doi. 10.1038/sj.bmt.1704943
By:
- Kallianpur, A. R.;
- Hall, L. D.;
- Yadav, M.;
- Byrne, D. W.;
- Speroff, T.;
- Dittus, R. S.;
- Haines, J. L.;
- Christman, B. W.;
- Summar, M. L.
Publication type:
Article
The apolipoprotein E E4 allele and sex-specific risk of Alzheimer's disease.
Published in:
1995
By:
- Corder, E H;
- Saunders, A M;
- Strittmatter, W J;
- Schmechel, D E;
- Gaskell, P C Jr;
- Roses, A D;
- Pericak-Vance, M A;
- Small, G W;
- Haines, J L
Publication type:
commentary
CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis.
Published in:
Immunogenetics, 2000, v. 51, n. 4/5, p. 281, doi. 10.1007/s002510050621
By:
- Barcellos, L. F.;
- Schito, A. M.;
- Rimmler, J. B.;
- Vittinghoff, E.;
- Shih, A.;
- Lincoln, R.;
- Callier, S.;
- Elkins, M. K.;
- Goodkin, D. E.;
- Haines, J. L.;
- Pericak-Vance, M. A.;
- Hauser, S. L.;
- Oksenberg, J. R.
Publication type:
Article
Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
Published in:
Molecular Psychiatry, 2007, v. 12, n. 4, p. 376, doi. 10.1038/sj.mp.4001927
By:
- Ma, D. Q.;
- Cuccaro, M. L.;
- Jaworski, J. M.;
- Haynes, C. S.;
- Stephan, D. A.;
- Parod, J.;
- Abramson, R. K.;
- Wright, H. H.;
- Gilbert, J. R.;
- Haines, J. L.;
- Pericak-Vance, M. A.
Publication type:
Article
Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus.
Published in:
Molecular Psychiatry, 2006, v. 11, n. 3, p. 280, doi. 10.1038/sj.mp.4001766
By:
- Liang, X.;
- Schnetz-Boutaud, N.;
- Kenealy, S. J.;
- Jiang, L.;
- Bartlett, J.;
- Lynch, B.;
- Gaskell, P. C.;
- Gwirtsman, H.;
- McFarland, L.;
- Bembe, M. L.;
- Bronson, P.;
- Gilbert, J. R.;
- Martin, E. R.;
- Pericak-Vance, M. A.;
- Haines, J. L.
Publication type:
Article
Analysis of the RELN gene as a genetic risk factor for autism.
Published in:
Molecular Psychiatry, 2005, v. 10, n. 6, p. 563, doi. 10.1038/sj.mp.4001614
By:
- Skaar, D. A.;
- Shao, Y.;
- Haines, J. L.;
- Stenger, J. E.;
- Jaworski, J.;
- Martin, E. R.;
- DeLong, G. R.;
- Moore, J. H.;
- McCauley, J. L.;
- Sutcliffe, J. S.;
- Ashley-Koch, A. E.;
- Cuccaro, M. L.;
- Folstein, S. E.;
- Gilbert, J. R.;
- Pericak-Vance, M. A.
Publication type:
Article
Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
Published in:
Molecular Psychiatry, 2003, v. 8, n. 6, p. 624, doi. 10.1038/sj.mp.4001283
By:
- Nurmi, E L;
- Amin, T;
- Olson, L M;
- Jacobs, M M;
- McCauley, J L;
- Lam, A Y;
- Organ, E L;
- Folstein, S E;
- Haines, J L;
- Sutcliffe, J S
Publication type:
Article
Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
Published in:
Molecular Psychiatry, 2003, v. 8, n. 6, p. 570, doi. 10.1038/sj.mp.4001361
By:
- Nurmi, E L;
- Amin, T;
- Olson, L M;
- Jacob, M M;
- McCauley, J L;
- Lam, A Y;
- Organ, E L;
- Folstein, S E;
- Haines, J L;
- Sutcliffe, J S
Publication type:
Article
Association between bleomycin hydrolase and Alzheimer's disease in caucasians.
Published in:
1998
By:
- Farrer, Lindsay A.;
- Abraham, Carmela R.;
- Haines, Jonathan L.;
- Rogaeva, Ekaterina A.;
- Song, Youqiang;
- McGraw, Walker T.;
- Brindle, Nicholas;
- Premkumar, Smita;
- Scott, William K.;
- Yamaoka, Larry H.;
- Saunders, Ann M.;
- Roses, Allen D.;
- Auerbach, Sanford A.;
- Sorbi, Sandro;
- Duara, Ranjan;
- Pericak-Vance, Margaret A.;
- St George-Hyslop, Peter H.;
- Farrer, L A;
- Abraham, C R;
- Haines, J L
Publication type:
journal article
Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease.
Published in:
1997
By:
- Scott, W K;
- Saunders, A M;
- Gaskell, P C;
- Locke, P A;
- Growdon, J H;
- Farrer, L A;
- Auerbach, S A;
- Roses, A D;
- Haines, J L;
- Pericak-Vance, M A
Publication type:
journal article
Apolipoprotein E ε2 does not increase risk of early-onset sporadic Alzheimer's disease.
Published in:
Annals of Neurology, 1997, v. 42, n. 3, p. 376, doi. 10.1002/ana.410420317
By:
- Scott, W. K.;
- Saunders, A. M.;
- Gaskell, P. C.;
- Locke, P. A.;
- Growdon, J. H.;
- Farrer, L. A.;
- Auerbach, S. A.;
- Roses, A. D.;
- Haines, J. L.;
- Pericak-Vance, M. A.
Publication type:
Article
Alzheimer's disease and apolipoprotein e-4 allele in an amish population.
Published in:
Annals of Neurology, 1996, v. 39, n. 6, p. 700, doi. 10.1002/ana.410390605
By:
- Pericak-Vance, M. A.;
- Johnson, C. C.;
- Rimmler, J. B.;
- Saunders, A. M.;
- Robinson, L. C.;
- D'Hondr, E. G.;
- Jackson, C. E.;
- Haines, J. L.
Publication type:
Article
A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's disease.
Published in:
1990
By:
- Grafton, Scott T.;
- Mazziotta, John C.;
- Pahl, Jorg J.;
- George-Hyslop, Peter St.;
- Haines, Jonathan L.;
- Gusella, James;
- Hoffman, John M.;
- Baxter, Lewis R.;
- Phelps, Michael E.;
- Grafton, S T;
- Mazziotta, J C;
- Pahl, J J;
- St George-Hyslop, P;
- Haines, J L;
- Gusella, J;
- Hoffman, J M;
- Baxter, L R;
- Phelps, M E
Publication type:
journal article
Apolipoprotein E4 allele and Alzheimer disease: Examination of Allelic association and effect on age at onset in both early-and late-onset cases.
Published in:
Genetic Epidemiology, 1995, v. 12, n. 1, p. 83, doi. 10.1002/gepi.1370120108
By:
- Locke, P. A.;
- Conneally, P. M.;
- Tanzi, R. E.;
- Gusella, J. F.;
- Haines, J. L.
Publication type:
Article
Linkage analysis in familial Alzheimer disease: Description of the Duke and Boston data sets.
Published in:
Genetic Epidemiology, 1993, v. 10, n. 6, p. 361, doi. 10.1002/gepi.1370100605
By:
- Pericak-Vance, M. A.;
- St. George-Hyslop, P. H.;
- Gaskell, P. C.;
- Growdon, J.;
- Crain, B. J.;
- Hulette, C.;
- Gusella, J. F.;
- Yamaoka, L.;
- Tanzi, R. E.;
- Roses, A. D.;
- Haines, J. L.
Publication type:
Article
Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP).
Published in:
Translational Psychiatry, 2013, v. 3, n. 5, p. 1, doi. 10.1038/tp.2013.13
By:
- Reitz, C.;
- Tosto, G.;
- Vardarajan, B.;
- Rogaeva, E.;
- Ghani, M.;
- Rogers, R. S.;
- Conrad, C.;
- Haines, J. L.;
- Pericak-Vance, M. A.;
- Fallin, M. D.;
- Foroud, T.;
- Farrer, L. A.;
- Schellenberg, G. D.;
- George-Hyslop, P. S.;
- Mayeux, R.
Publication type:
Article

Found: 39

Quantitative Faunal Associates of the Serpulid Polychaete Hydroides dianthus

Further evidence linking late-onset Alzheimer disease with chromosome 12.

Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucoma.

Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataset<sup>a</sup>.

An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two-Point Methods<sup>a</sup>.

A Comparative Study on Genetic Heterogeneity in Tuberous Sclerosis: Evidence for One Gene on 9q34 and a Second Gene on 11q22-23<sup>a</sup>.

Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus.

Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6.

Causes of death in huntington disease as reported on death certificates.

A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility.

Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.

Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis.

Multifactor dimensionality reduction reveals gene–gene interactions associated with multiple sclerosis susceptibility in African Americans.

Examination of seven candidate regions for multiple sclerosis: strong evidence of linkage to chromosome 1q44.

Osteopontin polymorphisms and disease course in multiple sclerosis.

Chromosome 17q22–q24 and multiple sclerosis genetic susceptibility.

Genetically meaningful phenotypic subgroups in autism spectrum disorders.

Examination of tetrahydrobiopterin pathway genes in autism.

Linkage and Association Study of Late-Onset Alzheimer Disease Families Linked to 9p21.3.

A Genome-wide Scan in an Amish Pedigree with Parkinsonism.

Polymorphisms of the Tumor Suppressor Gene LSAMP are Associated with Left Main Coronary Artery Disease.

Serum Lipids in the GENECARD Study of Coronary Artery Disease Identify Quantitative Trait Loci and Phenotypic Subsets on Chromosomes 3q and 5q.

Genetic basis for clinical expression in multiple sclerosis.

The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation.

The apolipoprotein E E4 allele and sex-specific risk of Alzheimer's disease.

CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.

Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus.

Analysis of the RELN gene as a genetic risk factor for autism.

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.

Association between bleomycin hydrolase and Alzheimer's disease in caucasians.

Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease.

Apolipoprotein E ε2 does not increase risk of early-onset sporadic Alzheimer's disease.

Alzheimer's disease and apolipoprotein e-4 allele in an amish population.

A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's disease.

Apolipoprotein E4 allele and Alzheimer disease: Examination of Allelic association and effect on age at onset in both early-and late-onset cases.

Linkage analysis in familial Alzheimer disease: Description of the Duke and Boston data sets.

Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP).