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Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data.
Published in:
2011
By:
- Sherva R;
- Baldwin CT;
- Inzelberg R;
- Vardarajan B;
- Cupples LA;
- Lunetta K;
- Bowirrat A;
- Naj A;
- Pericak-Vance M;
- Friedland RP;
- Farrer LA;
- Sherva, Richard;
- Baldwin, Clinton T;
- Inzelberg, Rivka;
- Vardarajan, Badri;
- Cupples, L Adrienne;
- Lunetta, Kathryn;
- Bowirrat, Abdalla;
- Naj, Adam;
- Pericak-Vance, Margaret
Publication type:
journal article
The Relationship Between Restrictive and Repetitive Behaviors in Individuals with Autism and Obsessive Compulsive Symptoms in Parents.
Published in:
Child Psychiatry & Human Development, 2005, v. 36, n. 2, p. 155, doi. 10.1007/s10578-005-2973-7
By:
- Abramson, R. K.;
- Ravan, S. A.;
- Wright, H. H.;
- Wieduwilt, K.;
- Wolpert, C. M.;
- Donnelly, S. A.;
- Pericak-Vance, M. A.;
- Cuccaro, M. L.
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
Morphological, Biochemical, and Genetic Support for an Apolipoprotein E Effect on Microtubular Metabolisma.
Published in:
Annals of the New York Academy of Sciences, 1996, v. 777, n. 1, p. 146, doi. 10.1111/j.1749-6632.1996.tb34413.x
By:
- ROSES, A. D.;
- EINSTEIN, G.;
- GILBERT, J.;
- GOEDERT, M.;
- HAN, S-H.;
- HUANG, D.;
- HULETTE, C.;
- MASLIAH, E.;
- PERICAK-VANCE, M. A.;
- SAUNDERS, A. M.;
- SCHMECHEL, D. E.;
- STRITTMATTTER, W. J.;
- WEISGRABER, K. H.;
- XI, P.-T.
Publication type:
Article
Genetic Heterogeneity in Tuberous Sclerosis. Study of a Large Collaborative Dataset<sup>a</sup>.
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
Linkage Studies in Tuberous Sclerosis.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 284, doi. 10.1111/j.1749-6632.1991.tb37770.x
By:
- KANDT, R. S.;
- PERICAK-VANCE, M. A.;
- HUNG, W.-Y.;
- GARDNER, R. J. M.;
- CROSSEN, P. E.;
- NELLIST, M. D.;
- SPEER, M. C.;
- ROSES, A. D.
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
Multiple rare SAPAP3 missense variants in trichotillomania and OCD.
Published in:
2009
By:
- Züchner, S.;
- Wendland, J. R.;
- Ashley-Koch, A. E.;
- Collins, A. L.;
- Tran-Viet, K. N.;
- Quinn, K.;
- Timpano, K. C.;
- Cuccaro, M. L.;
- Pericak-Vance, M. A.;
- Steffens, D. C.;
- Krishnan, K. R.;
- Feng, G.;
- Murphy, D. L.
Publication type:
Letter
Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotype.
Published in:
1989
By:
- McConkie-Rosell, Allyn;
- Chen, Yuan-Tsong;
- Harris, Denise;
- Speer, Marcy C.;
- Pericak-Vance, Margaret A.;
- Ding, Jia-Huan;
- Highsmith Jr., Edward;
- Knowles, Michael;
- Kahler, Stephen G.;
- McConkie-Rosell, A;
- Chen, Y T;
- Harris, D;
- Speer, M C;
- Pericak-Vance, M A;
- Ding, J H;
- Highsmith, W E Jr;
- Knowles, M;
- Kahler, S G
Publication type:
journal article
A Community’s Awareness and Perceptions of Genomic Medicine.
Published in:
Public Health Genomics, 2009, v. 13, n. 2, p. 63, doi. 10.1159/000218712
By:
- Hahn, S.;
- Letvak, S.;
- Powell, K.;
- Christianson, C.;
- Wallace, D.;
- Speer, M.;
- Lietz, P.;
- Blanton, S.;
- Vance, J.;
- Pericak-Vance, M.;
- Henrich, V. C.
Publication type:
Article
Absence of Mutation in the β- and γ-Synuclein Genes in Familial Autosomal Dominant Parkinson's Disease.
Published in:
DNA Research, 1998, v. 5, n. 6, p. 401, doi. 10.1093/dnares/5.6.401
By:
- Lavedan, C.;
- Buchholtz, S.;
- Auburger, G.;
- Albin, R. L.;
- Athanassiadou, A.;
- Blancato, J.;
- Burguera, J. A.;
- Ferrell, R. E.;
- Kostic, V.;
- Leroy, E.;
- Leube, B.;
- Mota-Vieira, L.;
- Papapetropoulos, T.;
- Pericak-Vance, M. A.;
- Pinkus, J.;
- Scott, W. K.;
- Ulm, G.;
- Vasconcelos, J.;
- Vilchez, J. J.;
- Nussbaum, R. L.
Publication type:
Article
Corrigendum: Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Published in:
2004
By:
- Züchner, S;
- Mersiyanova, I V;
- Muglia, M;
- Bissar-Tadmouri, N;
- Rochelle, J;
- Dadali, E L;
- Zappia, M;
- Nelis, E;
- Patitucci, A;
- Senderek, J;
- Parman, Y;
- Evgrafov, O;
- Jonghe, P De;
- Takahashi, Y;
- Tsuji, S;
- Pericak-Vance, M A;
- Quattrone, A;
- Battologlu, E;
- Polyakov, A V;
- Timmerman, V
Publication type:
Correction Notice
Erratum: The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
Published in:
2001
By:
- Yang, Y.;
- Hentati, A.;
- Deng, H.-X.;
- Dabbagh, O.;
- Sasaki, T.;
- Hirano, M.;
- Hung, W.-Y.;
- Ouahchi, K.;
- Yan, J.;
- Azim, A.C.;
- Cole, N.;
- Gascon, G.;
- Yagmour, A.;
- Ben-Hamida, M.;
- Pericak-Vance, M.;
- Hentati, F.;
- Siddique, T.
Publication type:
Erratum
Genetic analysis workshop IV: Huntington disease linkage analysis, data description.
Published in:
Genetic Epidemiology, 1986, v. 3, n. S1, p. 191, doi. 10.1002/gepi.1370030730
By:
- Pericak-Vance, M. A.;
- Meyers, D. A.;
- Gusella, J. F.;
- Folstein, S. E.;
- Conneally, P. M.
Publication type:
Article
Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms.
Published in:
1991
By:
- Laing, N. G.;
- Walker, A. P.;
- Akkari, P. A.;
- Chandler, D. C.;
- Layton, M. G.;
- Mears, M. E.;
- Yamada, T.;
- Bartlett, R. J.;
- Pericak-Vance, M. A.;
- Hung, W.-Y.;
- Wapenaar, M. C.;
- van Ommen, G.;
- Roses, A. D.;
- Kakulas, B. A.
Publication type:
journal 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
Genetic variation in nitric oxide synthase 2A (NOS2A) and risk for multiple sclerosis.
Published in:
Genes & Immunity, 2008, v. 9, n. 6, p. 493, doi. 10.1038/gene.2008.41
By:
- Barcellos, L. F.;
- Ramsay, P. P.;
- Caillier, S. J.;
- Sawcer, S.;
- Haines, J.;
- Schmidt, S.;
- Pericak-Vance, M.;
- Compston, D. A. S.;
- Gabatto, P.;
- Hauser, S. L.;
- Oksenberg, J. R.
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
Parkinson disease loci in the mid-western Amish.
Published in:
Human Genetics, 2013, v. 132, n. 11, p. 1213, doi. 10.1007/s00439-013-1316-1
By:
- Davis, M.;
- Cummings, A.;
- D'Aoust, L.;
- Jiang, L.;
- Velez Edwards, D.;
- Laux, R.;
- Reinhart-Mercer, L.;
- Fuzzell, D.;
- Scott, W.;
- Pericak-Vance, M.;
- Lee, S.;
- Haines, J.
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
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
An Analysis Paradigm for Investigating Multi-locus Effects in Complex Disease: Examination of Three GABA<sub>A</sub> Receptor Subunit Genes on 15q11-q13 as Risk Factors for Autistic Disorder.
Published in:
Annals of Human Genetics, 2006, v. 70, n. 3, p. 281, doi. 10.1111/j.1469-1809.2006.00253.x
By:
- Ashley-Koch, A. E.;
- Mei, H.;
- Jaworski, J.;
- Ma, D. Q.;
- Ritchie, M. D.;
- Menold, M. M.;
- Delong, G. R.;
- Abramson, R. K.;
- Wright, H. H.;
- Hussman, J. P.;
- Cuccaro, M. L.;
- Gilbert, J. R.;
- Martin, E. R.;
- Pericak-Vance, M. A.
Publication type:
Article
College students' attitudes regarding genetic testing.
Published in:
2007
By:
- Christianson C;
- Powell KP;
- Hahn S;
- Edwards T;
- Spoon D;
- Bartz D;
- Henrich V;
- Lietz P;
- Vance J;
- Pericak-Vance M
Publication type:
Journal Article
Web-Based Survey of Families With Autism: Reassessing the Need for Genetic Education.
Published in:
Journal of Genetic Counseling, 2002, v. 11, n. 6, p. 488
By:
- Rosen-Sheidley, B.;
- Wolpert, C.;
- Feigon-Schiffman, J.;
- Palmer, C.;
- Folstein, S.;
- Pericak-Vance, M.
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
Lewy body and Alzheimer pathology in a family with the amyloid-β precursor protein APP717 gene mutation.
Published in:
Acta Neuropathologica, 2000, v. 100, n. 2, p. 145, doi. 10.1007/s004019900155
By:
- Rosenberg, C. K.;
- Pericak-Vance, M. A.;
- Saunders, A. M.;
- Gilbert, J. R.;
- Gaskell, P. C.;
- Hulette, C. M.
Publication type:
Article
Apolipoprotein E E4 allele and risk of dementia.
Published in:
1995
By:
- Roses, A D;
- Saunders, A M;
- Alberts, M A;
- Strittmatter, W J;
- Schmechel, D;
- Gorder, E;
- Pericak-Vance, M A
Publication type:
commentary
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
SLITRK1 mutations in Trichotillomania.
Published in:
2006
By:
- Züchner, S.;
- Cuccaro, M. L.;
- Tran-Viet, K. N.;
- Cope, H.;
- Krishnan, R. R.;
- Pericak-Vance, M. A.;
- Wright, H. H.;
- Ashley-Koch, A.
Publication type:
Letter
SLITRK1 mutations in trichotillomania.
Published in:
Molecular Psychiatry, 2006, v. 11, n. 10, p. 887, doi. 10.1038/sj.mp.4001898
By:
- Züchner, S.;
- Cuccaro, M. L.;
- Tran-Viet, K. N.;
- Cope, H.;
- Krishnan, R. R.;
- Pericak-Vance, M. A.;
- Wright, H. H.;
- Ashley-Koch, 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
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
Examination of association of genes in the serotonin system to autism.
Published in:
Neurogenetics, 2009, v. 10, n. 3, p. 209, doi. 10.1007/s10048-009-0171-7
By:
- Anderson, B.;
- Schnetz-Boutaud, N.;
- Bartlett, J.;
- Wotawa, A.;
- Wright, H.;
- Abramson, R.;
- Cuccaro, M.;
- Gilbert, J.;
- Pericak-Vance, M.;
- Haines, J.
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).
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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
Carrier detection in Sanfilippo syndrome type B: report of six families.
Published in:
Clinical Genetics, 1981, v. 20, n. 2, p. 135, doi. 10.1111/j.1399-0004.1981.tb01818.x
By:
- Vance, J. M.;
- Conneally, P. M.;
- Wappner, R. S.;
- Yu, P. L.;
- Brandt, I. K.;
- Pericak-Vance, M. A.
Publication type:
Article

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