Alpha 1-antichymotrypsin regulates Alzheimer beta-amyloid peptide fibril formation.

Por Eriksson, S, Janciauskiene, S, Lannfelt, L
Publicado em 1995

Genetic counseling in a Swedish Alzheimer family with amyloid precursor protein mutation.

Por Lannfelt, L, Axelman, K, Lilius, L, Basun, H
Publicado em 1995

Amyloid-ß-directed immunotherapy for Alzheimer's disease

Por Lannfelt, L, Relkin, N R, Siemers, E R
Publicado no J Intern Med (2014)

Human beta-2 adrenoceptor gene polymorphisms are highly frequent in obesity and associate with altered adipocyte beta-2 adrenoceptor function.

Por Large, V, Hellström, L, Reynisdottir, S, Lönnqvist, F, Eriksson, P, Lannfelt, L, Arner, P
Publicado em 1997

Apolipoprotein E ε4 allele decreases functional connectivity in Alzheimer's disease as measured by EEG coherence

Por Jelic, V., Julin, P., Shigeta, M., Nordberg, A., Lannfelt, L., Winblad, B., Wahlund, L.
Publicado em 1997

New Alzheimer's disease locus on chromosome 8

Por Giedraitis, V, Hedlund, M, Skoglund, L, Blom, E, Ingvast, S, Brundin, R, Lannfelt, L, Glaser, A
Publicado em 2006

Re-Evaluation of Clinical Dementia Diagnoses with Pittsburgh Compound B Positron Emission Tomography

Por Degerman Gunnarsson, M., Lindau, M., Santillo, A.F., Wall, A., Engler, H., Lannfelt, L., Basun, H., Kilander, L.
Publicado em 2013

Quantification of Alzheimer amyloid beta peptides ending at residues 40 and 42 by novel ELISA systems.

Por Jensen, M., Hartmann, T., Engvall, B., Wang, R., Uljon, S. N., Sennvik, K., Näslund, J., Muehlhauser, F., Nordstedt, C., Beyreuther, K., Lannfelt, L.
Publicado em 2000

Relative abundance of Alzheimer A beta amyloid peptide variants in Alzheimer disease and normal aging.

Por Näslund, J, Schierhorn, A, Hellman, U, Lannfelt, L, Roses, A D, Tjernberg, L O, Silberring, J, Gandy, S E, Winblad, B, Greengard, P
Publicado em 1994

Association between schizophrenia and homozygosity at the dopamine D3 receptor gene.

Por Crocq, M A, Mant, R, Asherson, P, Williams, J, Hode, Y, Mayerova, A, Collier, D, Lannfelt, L, Sokoloff, P, Schwartz, J C
Publicado em 1992

Excessive production of amyloid beta-protein by peripheral cells of symptomatic and presymptomatic patients carrying the Swedish familial Alzheimer disease mutation.

Por Citron, M, Vigo-Pelfrey, C, Teplow, D B, Miller, C, Schenk, D, Johnston, J, Winblad, B, Venizelos, N, Lannfelt, L, Selkoe, D J
Publicado em 1994

Predominant deposition of amyloid-beta 42(43) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor prote...

Por Mann, D. M., Iwatsubo, T., Ihara, Y., Cairns, N. J., Lantos, P. L., Bogdanovic, N., Lannfelt, L., Winblad, B., Maat-Schieman, M. L., Rossor, M. N.
Publicado em 1996

Genetic variants near the MGAT1 gene are associated with body weight, BMI and fatty acid metabolism among adults and children

Por Jacobsson, J A, Rask-Andersen, M, Risérus, U, Moschonis, G, Koumpitski, A, Chrousos, G P, Lannfelt, L, Marcus, C, Gyllensten, U, Schiöth, H B, Fredriksson, R
Publicado em 2012

Serum cystatin C and the risk of Alzheimer disease in elderly men

Por Sundelöf, J, Ärnlöv, J, Ingelsson, E, Sundström, J, Basu, S, Zethelius, B, Larsson, A, Irizarry, M C., Giedraitis, V, Rönnemaa, E, Degerman-Gunnarsson, M, Hyman, B T., Basun, H, Kilander, L, Lannfelt, L
Publicado em 2008

Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locus

Por Chase, A, Leung, W, Tapper, W, Jones, A V, Knoops, L, Rasi, C, Forsberg, L A, Guglielmelli, P, Zoi, K, Hall, V, Chiecchio, L, Eder-Azanza, L, Bryant, C, Lannfelt, L, Docherty, L, White, H E, Score, J, Mackay, D J G, Vannucchi, A M, Dumanski, J P, Cross, N C P
Publicado no Leukemia (2015)

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

Por Lambert, J-C, Grenier-Boley, B, Harold, D, Zelenika, D, Chouraki, V, Kamatani, Y, Sleegers, K, Ikram, M A, Hiltunen, M, Reitz, C, Mateo, I, Feulner, T, Bullido, M, Galimberti, D, Concari, L, Alvarez, V, Sims, R, Gerrish, A, Chapman, J, Deniz-Naranjo, C, Solfrizzi, V, Sorbi, S, Arosio, B, Spalletta, G, Siciliano, G, Epelbaum, J, Hannequin, D, Dartigues, J-F, Tzourio, C, Berr, C, Schrijvers, E M C, Rogers, R, Tosto, G, Pasquier, F, Bettens, K, Van Cauwenberghe, C, Fratiglioni, L, Graff, C, Delepine, M, Ferri, R, Reynolds, C A, Lannfelt, L, Ingelsson, M, Prince, J A, Chillotti, C, Pilotto, A, Seripa, D, Boland, A, Mancuso, M, Bossù, P, Annoni, G, Nacmias, B, Bosco, P, Panza, F, Sanchez-Garcia, F, Del Zompo, M, Coto, E, Owen, M, O'Donovan, M, Valdivieso, F, Caffara, P, Scarpini, E, Combarros, O, Buée, L, Campion, D, Soininen, H, Breteler, M, Riemenschneider, M, Van Broeckhoven, C, Alpérovitch, A, Lathrop, M, Trégouët, D-A, Williams, J, Amouyel, P
Publicado em 2013

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

Por Lambert, J-C, Grenier-Boley, B, Harold, D, Zelenika, D, Chouraki, V, Kamatani, Y, Sleegers, K, Ikram, M A, Hiltunen, M, Reitz, C, Mateo, I, Feulner, T, Bullido, M, Galimberti, D, Concari, L, Alvarez, V, Sims, R, Gerrish, A, Chapman, J, Deniz-Naranjo, C, Solfrizzi, V, Sorbi, S, Arosio, B, Spalletta, G, Siciliano, G, Epelbaum, J, Hannequin, D, Dartigues, J-F, Tzourio, C, Berr, C, Schrijvers, E M C, Rogers, R, Tosto, G, Pasquier, F, Bettens, K, Van Cauwenberghe, C, Fratiglioni, L, Graff, C, Delepine, M, Ferri, R, Reynolds, C A, Lannfelt, L, Ingelsson, M, Prince, J A, Chillotti, C, Pilotto, A, Seripa, D, Boland, A, Mancuso, M, Bossù, P, Annoni, G, Nacmias, B, Bosco, P, Panza, F, Sanchez-Garcia, F, Zompo, M Del, Coto, E, Owen, M, O'Donovan, M, Valdivieso, F, Caffara, P, Scarpini, E, Combarros, O, Buée, L, Campion, D, Soininen, H, Breteler, M, Riemenschneider, M, Van Broeckhoven, C, Alpérovitch, A, Lathrop, M, Trégouët, D-A, Williams, J, Amouyel, P
Publicado em 2013