| Year |
Citation |
Score |
| 2024 |
Sampatakakis SN, Mourtzi N, Charisis S, Mamalaki E, Ntanasi E, Hatzimanolis A, Ramirez A, Lambert JC, Yannakoulia M, Kosmidis MH, Dardiotis E, Hadjigeorgiou G, Sakka P, Scarmeas N. Genetic Predisposition for White Matter Hyperintensities and Risk of Mild Cognitive Impairment and Alzheimer's Disease: Results from the HELIAD Study. Current Issues in Molecular Biology. 46: 934-947. PMID 38275674 DOI: 10.3390/cimb46010060 |
0.394 |
|
| 2023 |
Le Borgne J, Amouyel P, Andreassen O, Frikke-Schmidt R, Hiltunen M, Ingelsson M, Ramirez A, Rossi G, Ruiz A, Sanchez-Juan P, Sims R, Sleegers K, Tsolaki M, van der Lee SJ, Williams J, ... Lambert JC, et al. Association of MGMT and BIN1 genes with Alzheimer's disease risk across sex and APOE ε4 status. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 38041824 DOI: 10.1002/alz.13550 |
0.485 |
|
| 2023 |
Dalmasso MC, de Rojas I, Olivar N, Muchnik C, Angel B, Gloger S, Sanchez Abalos MS, Chacón MV, Aránguiz R, Orellana P, Cuesta C, Galeano P, Campanelli L, Novack GV, Martinez LE, ... ... Lambert JC, et al. The first genome-wide association study in the Argentinian and Chilean populations identifies shared genetics with Europeans in Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37985413 DOI: 10.1002/alz.13522 |
0.321 |
|
| 2023 |
Le Guen Y, Luo G, Ambati A, Damotte V, Jansen I, Yu E, Nicolas A, de Rojas I, Peixoto Leal T, Miyashita A, Bellenguez C, Lian MM, Parveen K, Morizono T, Park H, ... ... Lambert JC, et al. Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by subtypes. Proceedings of the National Academy of Sciences of the United States of America. 120: e2302720120. PMID 37643212 DOI: 10.1073/pnas.2302720120 |
0.71 |
|
| 2023 |
Luo J, Thomassen JQ, Bellenguez C, Grenier-Boley B, de Rojas I, Castillo A, Parveen K, Küçükali F, Nicolas A, Peters O, Schneider A, Dichgans M, Rujescu D, Scherbaum N, Jürgen D, ... ... Lambert JC, et al. Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease. Jama Network Open. 6: e2313734. PMID 37195665 DOI: 10.1001/jamanetworkopen.2023.13734 |
0.644 |
|
| 2023 |
Lambert JC, Ramirez A, Grenier-Boley B, Bellenguez C. Step by step: towards a better understanding of the genetic architecture of Alzheimer's disease. Molecular Psychiatry. PMID 37131074 DOI: 10.1038/s41380-023-02076-1 |
0.484 |
|
| 2023 |
Wittrahm R, Takalo M, Kuulasmaa T, Mäkinen PM, Mäkinen P, Končarević S, Fartzdinov V, Selzer S, Kokkola T, Antikainen L, Martiskainen H, Kemppainen S, Marttinen M, Jeskanen H, Rostalski H, ... ... Lambert JC, et al. Protective Alzheimer's disease-associated APP A673T variant predominantly decreases sAPPβ levels in cerebrospinal fluid and 2D/3D cell culture models. Neurobiology of Disease. 106140. PMID 37120095 DOI: 10.1016/j.nbd.2023.106140 |
0.386 |
|
| 2023 |
Mourtzi N, Charisis S, Tsapanou A, Ntanasi E, Hatzimanolis A, Ramirez A, Heilmann-Heimbach S, Grenier-Boley B, Lambert JC, Yannakoulia M, Kosmidis M, Dardiotis E, Hadjigeorgiou G, Sakka P, Georgakis M, et al. Genetic propensity for cerebral amyloidosis and risk of mild cognitive impairment and Alzheimer's disease within a cognitive reserve framework. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 36895094 DOI: 10.1002/alz.12980 |
0.361 |
|
| 2023 |
Xicota L, Lagarde J, Eysert F, Grenier-Boley B, Rivals I, Botté A, Forlani S, Landron S, Gautier C, Gabriel C, Bottlaender M, Lambert JC, Chami M, Sarazin M, Potier MC. Modifications of the endosomal compartment in fibroblasts from sporadic Alzheimer's disease patients are associated with cognitive impairment. Translational Psychiatry. 13: 54. PMID 36788216 DOI: 10.1038/s41398-023-02355-z |
0.415 |
|
| 2023 |
de Rojas I, Moreno-Grau S, Tesi N, Grenier-Boley B, Andrade V, Jansen IE, Pedersen NL, Stringa N, Zettergren A, Hernández I, Montrreal L, Antúnez C, Antonell A, Tankard RM, Bis JC, ... ... Lambert JC, et al. Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nature Communications. 14: 716. PMID 36759603 DOI: 10.1038/s41467-023-36192-x |
0.678 |
|
| 2022 |
Holstege H, Hulsman M, Charbonnier C, Grenier-Boley B, Quenez O, Grozeva D, van Rooij JGJ, Sims R, Ahmad S, Amin N, Norsworthy PJ, Dols-Icardo O, Hummerich H, Kawalia A, Amouyel P, ... ... Lambert JC, et al. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genetics. PMID 36411364 DOI: 10.1038/s41588-022-01208-7 |
0.601 |
|
| 2022 |
Jansen IE, van der Lee SJ, Gomez-Fonseca D, de Rojas I, Dalmasso MC, Grenier-Boley B, Zettergren A, Mishra A, Ali M, Andrade V, Bellenguez C, Kleineidam L, Küçükali F, Sung YJ, Tesí N, ... ... Lambert JC, et al. Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Acta Neuropathologica. PMID 36066633 DOI: 10.1007/s00401-022-02454-z |
0.47 |
|
| 2022 |
Hou J, Hess JL, Armstrong N, Bis JC, Grenier-Boley B, Karlsson IK, Leonenko G, Numbers K, O'Brien EK, Shadrin A, Thalamuthu A, Yang Q, Andreassen OA, Brodaty H, Gatz M, ... ... Lambert JC, et al. Polygenic resilience scores capture protective genetic effects for Alzheimer's disease. Translational Psychiatry. 12: 296. PMID 35879306 DOI: 10.1038/s41398-022-02055-0 |
0.335 |
|
| 2022 |
Le Guen Y, Belloy ME, Grenier-Boley B, de Rojas I, Castillo-Morales A, Jansen I, Nicolas A, Bellenguez C, Dalmasso C, Küçükali F, Eger SJ, Rasmussen KL, Thomassen JQ, Deleuze JF, He Z, ... ... Lambert JC, et al. Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease. Jama Neurology. PMID 35639372 DOI: 10.1001/jamaneurol.2022.1166 |
0.748 |
|
| 2022 |
Xicota L, Gyorgy B, Grenier-Boley B, Lecoeur A, Fontaine GL, Danjou F, Gonzalez JS, Colliot O, Amouyel P, Martin G, Levy M, Villain N, Habert MO, Dubois B, Lambert JC, et al. Association of APOE-Independent Alzheimer Disease Polygenic Risk Score With Brain Amyloid Deposition in Asymptomatic Older Adults. Neurology. PMID 35606148 DOI: 10.1212/WNL.0000000000200544 |
0.433 |
|
| 2022 |
Iohan LDCC, Lambert JC, Costa MR. Analysis of modular gene co-expression networks reveals molecular pathways underlying Alzheimer's disease and progressive supranuclear palsy. Plos One. 17: e0266405. PMID 35421130 DOI: 10.1371/journal.pone.0266405 |
0.45 |
|
| 2022 |
Sarnowski C, Ghanbari M, Bis JC, Logue M, Fornage M, Mishra A, Ahmad S, Beiser AS, Boerwinkle E, Bouteloup V, Chouraki V, Cupples LA, Damotte V, DeCarli CS, DeStefano AL, ... ... Lambert JC, et al. Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels. Communications Biology. 5: 336. PMID 35396452 DOI: 10.1038/s42003-022-03287-y |
0.384 |
|
| 2022 |
Bellenguez C, Küçükali F, Jansen IE, Kleineidam L, Moreno-Grau S, Amin N, Naj AC, Campos-Martin R, Grenier-Boley B, Andrade V, Holmans PA, Boland A, Damotte V, van der Lee SJ, Costa MR, ... ... Lambert JC, et al. New insights into the genetic etiology of Alzheimer's disease and related dementias. Nature Genetics. PMID 35379992 DOI: 10.1038/s41588-022-01024-z |
0.764 |
|
| 2022 |
Belloy ME, Eger SJ, Le Guen Y, Damotte V, Ahmad S, Ikram MA, Ramirez A, Tsolaki AC, Rossi G, Jansen IE, de Rojas I, Parveen K, Sleegers K, Ingelsson M, Hiltunen M, ... ... Lambert JC, et al. Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping. Alzheimer's Research & Therapy. 14: 22. PMID 35120553 DOI: 10.1186/s13195-022-00962-4 |
0.491 |
|
| 2022 |
Lambert E, Saha O, Soares Landeira B, Melo de Farias AR, Hermant X, Carrier A, Pelletier A, Gadaut J, Davoine L, Dupont C, Amouyel P, Bonnefond A, Lafont F, Abdelfettah F, Verstreken P, ... ... Lambert JC, et al. The Alzheimer susceptibility gene BIN1 induces isoform-dependent neurotoxicity through early endosome defects. Acta Neuropathologica Communications. 10: 4. PMID 34998435 DOI: 10.1186/s40478-021-01285-5 |
0.376 |
|
| 2021 |
de Rojas I, Moreno-Grau S, Tesi N, Grenier-Boley B, Andrade V, Jansen IE, Pedersen NL, Stringa N, Zettergren A, Hernández I, Montrreal L, Antúnez C, Antonell A, Tankard RM, Bis JC, ... ... Lambert JC, et al. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nature Communications. 12: 3417. PMID 34099642 DOI: 10.1038/s41467-021-22491-8 |
0.727 |
|
| 2021 |
Damotte V, van der Lee SJ, Chouraki V, Grenier-Boley B, Simino J, Adams H, Tosto G, White C, Terzikhan N, Cruchaga C, Knol MJ, Li S, Schraen S, Grove ML, Satizabal C, ... ... Lambert JC, et al. Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 34002480 DOI: 10.1002/alz.12333 |
0.323 |
|
| 2021 |
Madrid L, Moreno-Grau S, Ahmad S, González-Pérez A, de Rojas I, Xia R, Martino Adami PV, García-González P, Kleineidam L, Yang Q, Damotte V, Bis JC, Noguera-Perea F, Bellenguez C, Jian X, ... ... Lambert JC, et al. Multiomics integrative analysis identifies allele-specific blood biomarkers associated to Alzheimer's disease etiopathogenesis. Aging. 13: 9277-9329. PMID 33846280 DOI: 10.18632/aging.202950 |
0.504 |
|
| 2021 |
Marques-Coelho D, Iohan LDCC, Melo de Farias AR, Flaig A, Lambert JC, Costa MR. Differential transcript usage unravels gene expression alterations in Alzheimer's disease human brains. Npj Aging and Mechanisms of Disease. 7: 2. PMID 33398016 DOI: 10.1038/s41514-020-00052-5 |
0.406 |
|
| 2020 |
Kilinc D, Vreulx AC, Mendes T, Flaig A, Marques-Coelho D, Verschoore M, Demiautte F, Amouyel P, Eysert F, Dourlen P, Chapuis J, Costa MR, Malmanche N, Checler F, ... Lambert JC, et al. Pyk2 overexpression in postsynaptic neurons blocks amyloid β-induced synaptotoxicity in microfluidic co-cultures. Brain Communications. 2: fcaa139. PMID 33718872 DOI: 10.1093/braincomms/fcaa139 |
0.343 |
|
| 2020 |
Eysert F, Coulon A, Boscher E, Vreulx AC, Flaig A, Mendes T, Hughes S, Grenier-Boley B, Hanoulle X, Demiautte F, Bauer C, Marttinen M, Takalo M, Amouyel P, Desai S, ... ... Lambert JC, et al. Alzheimer's genetic risk factor FERMT2 (Kindlin-2) controls axonal growth and synaptic plasticity in an APP-dependent manner. Molecular Psychiatry. PMID 33144711 DOI: 10.1038/s41380-020-00926-w |
0.35 |
|
| 2020 |
Jones E, Hummerich H, Viré E, Uphill J, Dimitriadis A, Speedy H, Campbell T, Norsworthy P, Quinn L, Whitfield J, Linehan J, Jaunmuktane Z, Brandner S, Jat P, Nihat A, ... ... Lambert JC, et al. Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study. The Lancet. Neurology. 19: 840-848. PMID 32949544 DOI: 10.1016/S1474-4422(20)30273-8 |
0.344 |
|
| 2020 |
Kleineidam L, Chouraki V, Próchnicki T, van der Lee SJ, Madrid-Márquez L, Wagner-Thelen H, Karaca I, Weinhold L, Wolfsgruber S, Boland A, Martino Adami PV, Lewczuk P, Popp J, Brosseron F, Jansen IE, ... ... Lambert JC, et al. PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment. Acta Neuropathologica. PMID 32166339 DOI: 10.1007/S00401-020-02138-6 |
0.424 |
|
| 2020 |
Lambert E, Abdelfettah F, Barois N, Vandekerkhove D, Hermant X, Ayral A, Davoine L, Dupont C, Lafont F, Amouyel P, Chapuis J, Verstreken P, Dermaut B, Lambert J, Dourlen P. Isoform‐dependent neurotoxicity of the Alzheimer disease risk factor BIN1 Alzheimer's & Dementia. 16. DOI: 10.1002/alz.039402 |
0.386 |
|
| 2019 |
Bellenguez C, Grenier-Boley B, Lambert JC. Genetics of Alzheimer's disease: where we are, and where we are going. Current Opinion in Neurobiology. 61: 40-48. PMID 31863938 DOI: 10.1016/j.conb.2019.11.024 |
0.435 |
|
| 2019 |
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Lambert JC, et al. Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. PMID 31417202 DOI: 10.1038/s41588-019-0495-7 |
0.531 |
|
| 2019 |
Ma Y, Jun GR, Zhang X, Chung J, Naj AC, Chen Y, Bellenguez C, Hamilton-Nelson K, Martin ER, Kunkle BW, Bis JC, Debette S, DeStefano AL, Fornage M, Nicolas G, ... ... Lambert JC, et al. Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype. Jama Neurology. PMID 31180460 DOI: 10.1001/Jamaneurol.2019.1456 |
0.506 |
|
| 2019 |
Dourlen P, Kilinc D, Malmanche N, Chapuis J, Lambert JC. The new genetic landscape of Alzheimer's disease: from amyloid cascade to genetically driven synaptic failure hypothesis? Acta Neuropathologica. PMID 30982098 DOI: 10.1007/S00401-019-02004-0 |
0.41 |
|
| 2019 |
Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Lambert JC, et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. 51: 414-430. PMID 30820047 DOI: 10.1038/s41588-019-0358-2 |
0.564 |
|
| 2019 |
Dalmasso MC, Brusco LI, Olivar N, Muchnik C, Hanses C, Milz E, Becker J, Heilmann-Heimbach S, Hoffmann P, Prestia FA, Galeano P, Avalos MSS, Martinez LE, Carulla ME, Azurmendi PJ, ... ... Lambert JC, et al. Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease. Translational Psychiatry. 9: 55. PMID 30705288 DOI: 10.1038/S41398-019-0394-9 |
0.481 |
|
| 2019 |
Naj A, Sha J, Leonenko G, Chen Y, Chouraki V, Leber M, Sims R, Grenier-Boley B, Bis JC, Zhao Y, Kuzma AB, Kunkle BW, Karamujić-Čomić H, Lee SJVD, Bellenguez C, ... ... Lambert J, et al. O2‐10‐06: Genome‐Wide Meta‐Analysis Of Late‐Onset Alzheimer'S Disease Using Rare Variant Imputation In 64,859 Subjects Identifies Risk Loci With Roles In Innate Immunity And Cardiovascular Traits: The International Genomics Of Alzheimer'S Project (Igap) Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.4510 |
0.386 |
|
| 2018 |
Gusareva ES, Twizere JC, Sleegers K, Dourlen P, Abisambra JF, Meier S, Cloyd R, Weiss B, Dermaut B, Bessonov K, van der Lee SJ, Carrasquillo MM, Katsumata Y, Cherkaoui M, Asselbergh B, ... ... Lambert JC, et al. Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease. Neurobiology of Aging. PMID 30201328 DOI: 10.1016/J.Neurobiolaging.2018.08.001 |
0.472 |
|
| 2018 |
Dourlen P, Chapuis J, Lambert JC. Using High-Throughput Animal or Cell-Based Models to Functionally Characterize GWAS Signals. Current Genetic Medicine Reports. 6: 107-115. PMID 30147999 DOI: 10.1007/s40142-018-0141-1 |
0.452 |
|
| 2018 |
Bis JC, Jian X, Kunkle BW, Chen Y, Hamilton-Nelson KL, Bush WS, Salerno WJ, Lancour D, Ma Y, Renton AE, Marcora E, Farrell JJ, Zhao Y, Qu L, Ahmad S, ... ... Lambert JC, et al. Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry. PMID 30108311 DOI: 10.1038/S41380-018-0112-7 |
0.463 |
|
| 2017 |
Bellenguez C, Charbonnier C, Grenier-Boley B, Quenez O, Le Guennec K, Nicolas G, Chauhan G, Wallon D, Rousseau S, Richard AC, Boland A, Bourque G, Munter HM, Olaso R, Meyer V, ... ... Lambert JC, et al. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls. Neurobiology of Aging. PMID 28789839 DOI: 10.1016/J.Neurobiolaging.2017.07.001 |
0.496 |
|
| 2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Lambert JC, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.581 |
|
| 2017 |
Huang KL, Marcora E, Pimenova AA, Di Narzo AF, Kapoor M, Jin SC, Harari O, Bertelsen S, Fairfax BP, Czajkowski J, Chouraki V, Grenier-Boley B, Bellenguez C, Deming Y, McKenzie A, ... ... Lambert JC, et al. A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease. Nature Neuroscience. PMID 28628103 DOI: 10.1038/Nn.4587 |
0.489 |
|
| 2017 |
Bis JC, Jian X, Kunkle BW, Hamilton KL, Bush WS, Salerno W, Lancour D, Ma Y, Chen Y, Destefano AL, Dupuis J, Farrell J, Zhao Y, Qu L, Bellenguez C, ... Lambert J, et al. ALZHEIMER'S DISEASE SEQUENCING PROJECT: CASE-CONTROL ANALYSES Alzheimer's & Dementia. 13: P570-P571. DOI: 10.1016/j.jalz.2017.07.186 |
0.3 |
|
| 2017 |
Dourlen P, Abdelfettah F, Dupont C, Davoine L, Amouyel P, Lambert J, Dermaut B. [P3-099]: ISOFORM-DEPENDENT NEUROTOXICITY OF THE ALZHEIMER DISEASE RISK FACTOR BIN1 IN DROSOPHILA Alzheimer's & Dementia. 13: P972-P972. DOI: 10.1016/J.Jalz.2017.06.1309 |
0.371 |
|
| 2016 |
Gusareva ES, Carrasquillo MM, Bellenguez C, Cuyvers E, Colon S, Graff-Radford NR, Petersen RC, Dickson DW, Mahachie John JM, Bessonov K, Van Broeckhoven C, Ramirez A, Harold D, Williams J, ... ... Lambert JC, et al. Corrigendum to "Genome-wide association interaction analysis for Alzheimer's disease." [Neurobiol. Aging 35 (2014) 2436-2443]. Neurobiology of Aging. 37: 211. PMID 28757004 DOI: 10.1016/J.Neurobiolaging.2015.11.015 |
0.317 |
|
| 2016 |
Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard AC, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau MT, Olaso R, Boland A, ... ... Lambert JC, et al. 17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression. Molecular Psychiatry. PMID 27956742 DOI: 10.1038/Mp.2016.226 |
0.391 |
|
| 2016 |
Chapuis J, Flaig A, Grenier-Boley B, Eysert F, Pottiez V, Deloison G, Vandeputte A, Ayral AM, Mendes T, Desai S, Goate AM, Kauwe JS, Leroux F, Herledan A, Demiautte F, ... ... Lambert JC, et al. Genome-wide, high-content siRNA screening identifies the Alzheimer's genetic risk factor FERMT2 as a major modulator of APP metabolism. Acta Neuropathologica. PMID 27933404 DOI: 10.1007/S00401-016-1652-Z |
0.421 |
|
| 2016 |
Chouraki V, Reitz C, Maury F, Bis JC, Bellenguez C, Yu L, Jakobsdottir J, Mukherjee S, Adams HH, Choi SH, Larson EB, Fitzpatrick A, Uitterlinden AG, de Jager PL, Hofman A, ... ... Lambert JC, et al. Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. PMID 27340842 DOI: 10.3233/Jad-150749 |
0.422 |
|
| 2016 |
Letronne F, Laumet G, Ayral AM, Chapuis J, Demiautte F, Laga M, Vandenberghe ME, Malmanche N, Leroux F, Eysert F, Sottejeau Y, Chami L, Flaig A, Bauer C, Dourlen P, ... ... Lambert JC, et al. ADAM30 Downregulates APP-Linked Defects Through Cathepsin D Activation in Alzheimer's Disease. Ebiomedicine. PMID 27333034 DOI: 10.1016/J.Ebiom.2016.06.002 |
0.351 |
|
| 2016 |
Dumanski JP, Lambert JC, Rasi C, Giedraitis V, Davies H, Grenier-Boley B, Lindgren CM, Campion D, Dufouil C, Pasquier F, Amouyel P, Lannfelt L, Ingelsson M, Kilander L, et al. Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease. American Journal of Human Genetics. PMID 27231129 DOI: 10.1016/J.Ajhg.2016.05.014 |
0.432 |
|
| 2016 |
Delay C, Grenier-Boley B, Amouyel P, Dumont J, Lambert JC. miRNA-dependent target regulation: functional characterization of single-nucleotide polymorphisms identified in genome-wide association studies of Alzheimer's disease. Alzheimer's Research & Therapy. 8: 20. PMID 27215977 DOI: 10.1186/s13195-016-0186-x |
0.32 |
|
| 2016 |
Dourlen P, Fernandez-Gomez FJ, Dupont C, Grenier-Boley B, Bellenguez C, Obriot H, Caillierez R, Sottejeau Y, Chapuis J, Bretteville A, Abdelfettah F, Delay C, Malmanche N, Soininen H, Hiltunen M, ... ... Lambert JC, et al. Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology. Molecular Psychiatry. PMID 27113998 DOI: 10.1038/Mp.2016.59 |
0.392 |
|
| 2016 |
Le Guennec K, Nicolas G, Quenez O, Charbonnier C, Wallon D, Bellenguez C, Grenier-Boley B, Rousseau S, Richard AC, Rovelet-Lecrux A, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, ... ... Lambert JC, et al. ABCA7 rare variants and Alzheimer disease risk. Neurology. PMID 27037229 DOI: 10.1212/Wnl.0000000000002627 |
0.482 |
|
| 2016 |
Mohamad EH, Antoine P, Amouyel P, Lambert JC, Pasquier F, Kapogiannis D. Apolipoprotein E (APOE) ε4 and episodic memory decline in Alzheimer's disease: A review. Ageing Research Reviews. PMID 26876367 DOI: 10.1016/j.arr.2016.02.002 |
0.329 |
|
| 2016 |
Huang K, Jin SC, Harari O, Kapoor M, Bertelsen S, Czajkowski J, Lambert j, Chouraki V, Bellenguez C, Grenier-Boley B, Deming Y, McKenzie A, Renton AE, Budde J, Del-Aguila JL, et al. A Common Allele In Spi1 Lowers Risk And Delays Age At Onset For Alzheimer'S Disease Alzheimers & Dementia. 12: 253. DOI: 10.1016/J.Jalz.2016.06.453 |
0.44 |
|
| 2015 |
Escott-Price V, Sims R, Bannister C, Harold D, Vronskaya M, Majounie E, Badarinarayan N, Morgan K, Passmore P, Holmes C, Powell J, Brayne C, Gill M, ... ... Lambert JC, et al. Common polygenic variation enhances risk prediction for Alzheimer's disease. Brain : a Journal of Neurology. PMID 26490334 DOI: 10.1093/Brain/Awv268 |
0.543 |
|
| 2015 |
Sottejeau Y, Bretteville A, Cantrelle FX, Malmanche N, Demiaute F, Mendes T, Delay C, Alves Dos Alves H, Flaig A, Davies P, Dourlen P, Dermaut B, Laporte J, Amouyel P, Lippens G, ... ... Lambert JC, et al. Tau phosphorylation regulates the interaction between BIN1's SH3 domain and Tau's proline-rich domain. Acta Neuropathologica Communications. 3: 58. PMID 26395440 DOI: 10.1186/S40478-015-0237-8 |
0.357 |
|
| 2015 |
Nicolas G, Charbonnier C, Wallon D, Quenez O, Bellenguez C, Grenier-Boley B, Rousseau S, Richard AC, Rovelet-Lecrux A, Le Guennec K, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, ... ... Lambert JC, et al. SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease. Molecular Psychiatry. PMID 26303663 DOI: 10.1038/Mp.2015.121 |
0.403 |
|
| 2015 |
Lambert JC, Grenier-Boley B, Bellenguez C, Pasquier F, Campion D, Dartigues JF, Berr C, Tzourio C, Amouyel P. PLD3 and sporadic Alzheimer's disease risk. Nature. 520: E1. PMID 25832408 DOI: 10.1038/Nature14036 |
0.426 |
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| 2015 |
Nicolas G, Wallon D, Goupil C, Richard AC, Pottier C, Dorval V, Sarov-Rivière M, Riant F, Hervé D, Amouyel P, Guerchet M, Ndamba-Bandzouzi B, Mbelesso P, Dartigues JF, Lambert JC, et al. Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy. European Journal of Human Genetics : Ejhg. PMID 25828868 DOI: 10.1038/Ejhg.2015.61 |
0.306 |
|
| 2015 |
Jun G, Ibrahim-Verbaas CA, Vronskaya M, Lambert JC, Chung J, Naj AC, Kunkle BW, Wang LS, Bis JC, Bellenguez C, Harold D, Lunetta KL, Destefano AL, Grenier-Boley B, Sims R, et al. A novel Alzheimer disease locus located near the gene encoding tau protein. Molecular Psychiatry. PMID 25778476 DOI: 10.1038/Mp.2015.23 |
0.59 |
|
| 2015 |
Davies G, Armstrong N, Bis JC, Bressler J, Chouraki V, Giddaluru S, Hofer E, Ibrahim-Verbaas CA, Kirin M, Lahti J, van der Lee SJ, Le Hellard S, Liu T, Marioni RE, Oldmeadow C, ... ... Lambert JC, et al. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949). Molecular Psychiatry. 20: 183-92. PMID 25644384 DOI: 10.1038/Mp.2014.188 |
0.316 |
|
| 2015 |
Chouraki V, Beiser A, Younkin L, Preis SR, Weinstein G, Hansson O, Skoog I, Lambert JC, Au R, Launer L, Wolf PA, Younkin S, Seshadri S. Plasma amyloid-β and risk of Alzheimer's disease in the Framingham Heart Study. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 11: 249-57.e1. PMID 25217292 DOI: 10.1016/J.Jalz.2014.07.001 |
0.385 |
|
| 2015 |
Lambert JC. S2-02-02: Genetic risk factors of Alzheimer's disease and app metabolism Alzheimer's & Dementia. 11: P163-P163. DOI: 10.1016/j.jalz.2015.07.104 |
0.38 |
|
| 2014 |
Delay C, Dorval V, Fok A, Grenier-Boley B, Lambert JC, Hsiung GY, Hébert SS. MicroRNAs targeting Nicastrin regulate Aβ production and are affected by target site polymorphisms. Frontiers in Molecular Neuroscience. 7: 67. PMID 25100943 DOI: 10.3389/fnmol.2014.00067 |
0.31 |
|
| 2014 |
Gusareva ES, Carrasquillo MM, Bellenguez C, Cuyvers E, Colon S, Graff-Radford NR, Petersen RC, Dickson DW, Mahachie John JM, Bessonov K, Van Broeckhoven C, Harold D, Williams J, Amouyel P, ... ... Lambert JC, et al. Genome-wide association interaction analysis for Alzheimer's disease. Neurobiology of Aging. 35: 2436-43. PMID 24958192 DOI: 10.1016/J.Neurobiolaging.2014.05.014 |
0.398 |
|
| 2014 |
Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, et al. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Plos One. 9: e94661. PMID 24922517 DOI: 10.1371/Journal.Pone.0094661 |
0.556 |
|
| 2014 |
Benitez BA, Jin SC, Guerreiro R, Graham R, Lord J, Harold D, Sims R, Lambert JC, Gibbs JR, Bras J, Sassi C, Harari O, Bertelsen S, Lupton MK, Powell J, et al. Missense variant in TREML2 protects against Alzheimer's disease. Neurobiology of Aging. 35: 1510.e19-26. PMID 24439484 DOI: 10.1016/J.Neurobiolaging.2013.12.010 |
0.61 |
|
| 2014 |
Chouraki VA, DeStefano A, Bellenguez C, Reitz C, Duijn Cv, Bennett D, Maury F, Lambert J, Jakobsdottir J, Bis JC, Launer L, Crane P, Mayeux R, Choi SH, Seshadri S. Do The Variants Identified In Igap Improve Risk Prediction Of Alzheimer'S Disease? Alzheimers & Dementia. 10. DOI: 10.1016/J.Jalz.2014.04.377 |
0.406 |
|
| 2014 |
Dourlen P, Dermaut B, Grenier-Boley B, Bellenguez C, Dupont C, Abdelfettah F, Schellenberg GD, Lambert J, Williams J, Amouyel P, Seshadri S. Functional Validation Of Novel Alzheimer Genetic Risk Loci Using Drosophila Alzheimers & Dementia. 10: 246. DOI: 10.1016/J.Jalz.2014.04.376 |
0.329 |
|
| 2013 |
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-Wells TA, Jones N, Smith AV, Chouraki V, et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nature Genetics. 45: 1452-8. PMID 24162737 DOI: 10.1038/Ng.2802 |
0.579 |
|
| 2013 |
Greliche N, Germain M, Lambert JC, Cohen W, Bertrand M, Dupuis AM, Letenneur L, Lathrop M, Amouyel P, Morange PE, Trégouët DA. A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. Bmc Medical Genetics. 14: 36. PMID 23509962 DOI: 10.1186/1471-2350-14-36 |
0.355 |
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| 2013 |
Klebe S, Golmard JL, Nalls MA, Saad M, Singleton AB, Bras JM, Hardy J, Simon-Sanchez J, Heutink P, Kuhlenbäumer G, Charfi R, Klein C, Hagenah J, Gasser T, Wurster I, ... ... Lambert JC, et al. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. Journal of Neurology, Neurosurgery, and Psychiatry. 84: 666-73. PMID 23408064 DOI: 10.1136/Jnnp-2012-304475 |
0.456 |
|
| 2013 |
Chapuis J, Hansmannel F, Gistelinck M, Mounier A, Van Cauwenberghe C, Kolen KV, Geller F, Sottejeau Y, Harold D, Dourlen P, Grenier-Boley B, Kamatani Y, Delepine B, Demiautte F, Zelenika D, ... ... Lambert JC, et al. Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology. Molecular Psychiatry. 18: 1225-34. PMID 23399914 DOI: 10.1038/Mp.2013.1 |
0.478 |
|
| 2013 |
Guerreiro R, Wojtas A, Bras J, Carrasquillo M, Rogaeva E, Majounie E, Cruchaga C, Sassi C, Kauwe JS, Younkin S, Hazrati L, Collinge J, Pocock J, Lashley T, Williams J, ... Lambert JC, et al. TREM2 variants in Alzheimer's disease. The New England Journal of Medicine. 368: 117-27. PMID 23150934 DOI: 10.1056/Nejmoa1211851 |
0.625 |
|
| 2013 |
Gabelle A, Richard F, Gutierrez LA, Schraen S, Delva F, Rouaud O, Buée L, Dartigues JF, Touchon J, Lambert JC, Berr C. Plasma amyloid-β levels and prognosis in incident dementia cases of the 3-city study Journal of Alzheimer's Disease. 33: 381-391. PMID 22976074 DOI: 10.3233/Jad-2012-121147 |
0.311 |
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| 2013 |
Barberger-Gateau P, Lambert JC, Féart C, Pérès K, Ritchie K, Dartigues JF, Alpérovitch A. From genetics to dietetics: the contribution of epidemiology to understanding Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 33: S457-63. PMID 22683527 DOI: 10.3233/JAD-2012-129019 |
0.458 |
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| 2013 |
Lambert JC, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, et al. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Molecular Psychiatry. 18: 461-70. PMID 22430674 DOI: 10.1038/Mp.2012.14 |
0.505 |
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| 2013 |
Lambert JC, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, et al. Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease (Molecular Psychiatry (2013) 18 (521) DOI: 10.1038/mp.2012.75)) Molecular Psychiatry. 18. DOI: 10.1038/Mp.2012.75 |
0.426 |
|
| 2013 |
Lambert J. F1-01-01: Meta-analysis in more than 74,000 individuals identifies 11 new susceptibility loci for Alzheimer's disease Alzheimer's & Dementia. 9: P123-P123. DOI: 10.1016/j.jalz.2013.04.040 |
0.332 |
|
| 2012 |
Simon R, Girod M, Fonbonne C, Salvador A, Clément Y, Lantéri P, Amouyel P, Lambert JC, Lemoine J. Total ApoE and ApoE4 isoform assays in an Alzheimer's disease case-control study by targeted mass spectrometry (n=669): a pilot assay for methionine-containing proteotypic peptides. Molecular & Cellular Proteomics : McP. 11: 1389-403. PMID 22918225 DOI: 10.1074/mcp.M112.018861 |
0.385 |
|
| 2012 |
Ahmed I, Tamouza R, Delord M, Krishnamoorthy R, Tzourio C, Mulot C, Nacfer M, Lambert JC, Beaune P, Laurent-Puig P, Loriot MA, Charron D, Elbaz A. Association between Parkinson's disease and the HLA-DRB1 locus. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1104-10. PMID 22807207 DOI: 10.1002/mds.25035 |
0.309 |
|
| 2012 |
Gistelinck M, Lambert JC, Callaerts P, Dermaut B, Dourlen P. Drosophila models of tauopathies: what have we learned? International Journal of Alzheimer's Disease. 2012: 970980. PMID 22701808 DOI: 10.1155/2012/970980 |
0.353 |
|
| 2012 |
Bis JC, DeCarli C, Smith AV, van der Lijn F, Crivello F, Fornage M, Debette S, Shulman JM, Schmidt H, Srikanth V, Schuur M, Yu L, Choi SH, Sigurdsson S, Verhaaren BF, ... ... Lambert JC, et al. Common variants at 12q14 and 12q24 are associated with hippocampal volume. Nature Genetics. 44: 545-51. PMID 22504421 DOI: 10.1038/Ng.2237 |
0.315 |
|
| 2012 |
Hamilton G, Killick R, Lambert JC, Amouyel P, Carrasquillo MM, Pankratz VS, Graff-Radford NR, Dickson DW, Petersen RC, Younkin SG, Powell JF, Wade-Martins R. Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. Neurobiology of Aging. 33: 1848.e1-13. PMID 22405046 DOI: 10.1016/J.Neurobiolaging.2012.02.005 |
0.372 |
|
| 2012 |
Bettens K, Brouwers N, Engelborghs S, Lambert JC, Rogaeva E, Vandenberghe R, Le Bastard N, Pasquier F, Vermeulen S, Van Dongen J, Mattheijssens M, Peeters K, Mayeux R, St George-Hyslop P, Amouyel P, et al. Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk. Molecular Neurodegeneration. 7: 3. PMID 22248099 DOI: 10.1186/1750-1326-7-3 |
0.459 |
|
| 2012 |
Hong MG, Reynolds CA, Feldman AL, Kallin M, Lambert JC, Amouyel P, Ingelsson E, Pedersen NL, Prince JA. Genome-wide and gene-based association implicates FRMD6 in alzheimer disease Human Mutation. 33: 521-529. PMID 22190428 DOI: 10.1002/humu.22009 |
0.393 |
|
| 2012 |
Sanchez-Juan P, Bishop MT, Aulchenko YS, Brandel JP, Rivadeneira F, Struchalin M, Lambert JC, Amouyel P, Combarros O, Sainz J, Carracedo A, Uitterlinden AG, Hofman A, Zerr I, Kretzschmar HA, et al. Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk. Neurobiology of Aging. 33: 1487.e21-8. PMID 22137330 DOI: 10.1016/J.Neurobiolaging.2011.10.011 |
0.347 |
|
| 2012 |
Brouwers N, Van Cauwenberghe C, Engelborghs S, Lambert JC, Bettens K, Le Bastard N, Pasquier F, Montoya AG, Peeters K, Mattheijssens M, Vandenberghe R, Deyn PP, Cruts M, Amouyel P, Sleegers K, et al. Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites. Molecular Psychiatry. 17: 223-33. PMID 21403675 DOI: 10.1038/Mp.2011.24 |
0.391 |
|
| 2011 |
Féart C, Helmer C, Fleury H, Béjot Y, Ritchie K, Amouyel P, Schraen-Maschke S, Buée L, Lambert JC, Letenneur L, Dartigues JF. Association between IgM anti-herpes simplex virus and plasma amyloid-beta levels. Plos One. 6: e29480. PMID 22216291 DOI: 10.1371/Journal.Pone.0029480 |
0.321 |
|
| 2011 |
Lambert JC. [Genetics of Alzheimer's disease]. La Revue Du Praticien. 61: 922-3. PMID 22039726 |
0.397 |
|
| 2011 |
Germain M, Saut N, Greliche N, Dina C, Lambert JC, Perret C, Cohen W, Oudot-Mellakh T, Antoni G, Alessi MC, Zelenika D, Cambien F, Tiret L, Bertrand M, Dupuy AM, et al. Genetics of venous thrombosis: insights from a new genome wide association study. Plos One. 6: e25581. PMID 21980494 DOI: 10.1371/journal.pone.0025581 |
0.33 |
|
| 2011 |
Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, ... ... Lambert JC, et al. Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. Neurobiology of Aging. 32: 2108.e1-5. PMID 21782285 DOI: 10.1016/J.Neurobiolaging.2011.05.024 |
0.631 |
|
| 2011 |
Allanore Y, Saad M, Dieudé P, Avouac J, Distler JH, Amouyel P, Matucci-Cerinic M, Riemekasten G, Airo P, Melchers I, Hachulla E, Cusi D, Wichmann HE, Wipff J, Lambert JC, et al. Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. Plos Genetics. 7: e1002091. PMID 21750679 DOI: 10.1371/journal.pgen.1002091 |
0.323 |
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| 2011 |
Goumidi L, Dahlman-Wright K, Tapia-Paez I, Matsson H, Pasquier F, Amouyel P, Kere J, Lambert JC, Meirhaeghe A. Study of estrogen receptor-α and receptor-β gene polymorphisms on Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 26: 431-9. PMID 21673408 DOI: 10.3233/JAD-2011-110362 |
0.512 |
|
| 2011 |
Genin E, Hannequin D, Wallon D, Sleegers K, Hiltunen M, Combarros O, Bullido MJ, Engelborghs S, De Deyn P, Berr C, Pasquier F, Dubois B, Tognoni G, Fiévet N, Brouwers N, ... ... Lambert JC, et al. APOE and Alzheimer disease: a major gene with semi-dominant inheritance. Molecular Psychiatry. 16: 903-7. PMID 21556001 DOI: 10.1038/Mp.2011.52 |
0.457 |
|
| 2011 |
Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, et al. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature Genetics. 43: 429-35. PMID 21460840 DOI: 10.1038/Ng.803 |
0.453 |
|
| 2011 |
Elbaz A, Ross OA, Ioannidis JP, Soto-Ortolaza AI, Moisan F, Aasly J, Annesi G, Bozi M, Brighina L, Chartier-Harlin MC, Destée A, Ferrarese C, Ferraris A, Gibson JM, Gispert S, ... ... Lambert JC, et al. Independent and joint effects of the MAPT and SNCA genes in Parkinson disease. Annals of Neurology. 69: 778-92. PMID 21391235 DOI: 10.1002/Ana.22321 |
0.75 |
|
| 2011 |
Lambert JC, Amouyel P. Genetics of Alzheimer's disease: new evidences for an old hypothesis? Current Opinion in Genetics & Development. 21: 295-301. PMID 21371880 DOI: 10.1016/j.gde.2011.02.002 |
0.443 |
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| 2011 |
Schjeide BM, Schnack C, Lambert JC, Lill CM, Kirchheiner J, Tumani H, Otto M, Tanzi RE, Lehrach H, Amouyel P, von Arnim CA, Bertram L. The role of clusterin, complement receptor 1, and phosphatidylinositol binding clathrin assembly protein in Alzheimer disease risk and cerebrospinal fluid biomarker levels. Archives of General Psychiatry. 68: 207-13. PMID 21300948 DOI: 10.1001/Archgenpsychiatry.2010.196 |
0.367 |
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| 2011 |
Morange PE, Oudot-Mellakh T, Cohen W, Germain M, Saut N, Antoni G, Alessi MC, Bertrand M, Dupuy AM, Letenneur L, Lathrop M, Lopez LM, Lambert JC, Emmerich J, Amouyel P, et al. KNG1 Ile581Thr and susceptibility to venous thrombosis. Blood. 117: 3692-4. PMID 21270443 DOI: 10.1182/blood-2010-11-319053 |
0.337 |
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| 2011 |
Lambert JC, Zelenika D, Hiltunen M, Chouraki V, Combarros O, Bullido MJ, Tognoni G, Fiévet N, Boland A, Arosio B, Coto E, Del Zompo M, Mateo I, Frank-Garcia A, Helisalmi S, et al. Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations. Neurobiology of Aging. 32: 756.e11-5. PMID 21220176 DOI: 10.1016/J.Neurobiolaging.2010.11.022 |
0.486 |
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| 2011 |
Saad M, Lesage S, Saint-Pierre A, Corvol JC, Zelenika D, Lambert JC, Vidailhet M, Mellick GD, Lohmann E, Durif F, Pollak P, Damier P, Tison F, Silburn PA, Tzourio C, et al. Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. Human Molecular Genetics. 20: 615-27. PMID 21084426 DOI: 10.1093/Hmg/Ddq497 |
0.329 |
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| 2011 |
Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, ... ... Lambert JC, et al. A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease. Neurobiology of Aging. 32: 548.e9-18. PMID 20036034 DOI: 10.1016/J.Neurobiolaging.2009.11.021 |
0.347 |
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| 2011 |
Goumidi L, Flamant F, Lendon C, Galimberti D, Pasquier F, Scarpini E, Hannequin D, Campion D, Amouyel P, Lambert JC, Meirhaeghe A. Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease. Neurobiology of Aging. 32: 624-30. PMID 19427062 DOI: 10.1016/J.Neurobiolaging.2009.04.007 |
0.539 |
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| 2011 |
Richard F, Berr C, Dartigues J, Tzourio C, Goumidi L, Fievet N, Amouyel P, Lambert J. P1-257: Association of the APOE -219 Polymorphism with Alzheimer's Disease: The Prospective Three City Study Alzheimer's & Dementia. 7: S193-S193. DOI: 10.1016/j.jalz.2011.05.537 |
0.494 |
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| 2011 |
Hansmannel F, Mounier A, Gistelinck M, Grenier-Boley B, Maturski ME, Letronne F, Ayral A, Checler F, Buée L, Amouyel P, Dermaut B, Lambert J. Assessment of BIN1 involvement in the Alzheimer's Disease pathophysiological process Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.1117 |
0.343 |
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| 2010 |
Lambert JC. [Toward a better understanding of Alzheimer's disease]. Soins. Gerontologie. 40-1. PMID 21137496 |
0.392 |
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| 2010 |
Lambert JC, Sleegers K, González-Pérez A, Ingelsson M, Beecham GW, Hiltunen M, Combarros O, Bullido MJ, Brouwers N, Bettens K, Berr C, Pasquier F, Richard F, Dekosky ST, Hannequin D, et al. The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. Journal of Alzheimer's Disease : Jad. 22: 247-55. PMID 20847397 DOI: 10.3233/Jad-2010-100933 |
0.563 |
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| 2010 |
Hansmannel F, Sillaire A, Kamboh MI, Lendon C, Pasquier F, Hannequin D, Laumet G, Mounier A, Ayral AM, DeKosky ST, Hauw JJ, Berr C, Mann D, Amouyel P, Campion D, ... Lambert JC, et al. Is the urea cycle involved in Alzheimer's disease? Journal of Alzheimer's Disease : Jad. 21: 1013-21. PMID 20693631 DOI: 10.3233/Jad-2010-100630 |
0.478 |
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| 2010 |
Hong MG, Alexeyenko A, Lambert JC, Amouyel P, Prince JA. Genome-wide pathway analysis implicates intracellular transmembrane protein transport in Alzheimer disease. Journal of Human Genetics. 55: 707-9. PMID 20668461 DOI: 10.1038/jhg.2010.92 |
0.328 |
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| 2010 |
Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, Boada M, Bis JC, Smith AV, Carassquillo MM, Lambert JC, Harold D, Schrijvers EM, Ramirez-Lorca R, Debette S, Longstreth WT, et al. Genome-wide analysis of genetic loci associated with Alzheimer disease. Jama. 303: 1832-40. PMID 20460622 DOI: 10.1001/Jama.2010.574 |
0.484 |
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| 2010 |
Lambert JC, Grenier-Boley B, Chouraki V, Heath S, Zelenika D, Fievet N, Hannequin D, Pasquier F, Hanon O, Brice A, Epelbaum J, Berr C, Dartigues JF, Tzourio C, Campion D, et al. Implication of the immune system in Alzheimer's disease: evidence from genome-wide pathway analysis. Journal of Alzheimer's Disease : Jad. 20: 1107-18. PMID 20413860 DOI: 10.3233/Jad-2010-100018 |
0.511 |
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| 2010 |
Laumet G, Chouraki V, Grenier-Boley B, Legry V, Heath S, Zelenika D, Fievet N, Hannequin D, Delepine M, Pasquier F, Hanon O, Brice A, Epelbaum J, Berr C, Dartigues JF, ... ... Lambert JC, et al. Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study. Journal of Alzheimer's Disease : Jad. 20: 1181-8. PMID 20413850 DOI: 10.3233/JAD-2010-100126 |
0.518 |
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| 2010 |
Sleegers K, Lambert JC, Bertram L, Cruts M, Amouyel P, Van Broeckhoven C. The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects. Trends in Genetics : Tig. 26: 84-93. PMID 20080314 DOI: 10.1016/j.tig.2009.12.004 |
0.454 |
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| 2010 |
Laumet G, Petitprez V, Sillaire A, Ayral AM, Hansmannel F, Chapuis J, Hannequin D, Pasquier F, Scarpini E, Galimberti D, Lendon C, Campion D, Amouyel P, Lambert JC. A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease. Neuroscience Letters. 468: 1-2. PMID 19837132 DOI: 10.1016/J.Neulet.2009.10.040 |
0.537 |
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| 2010 |
Evangelou E, Maraganore DM, Annesi G, Brighina L, Brice A, Elbaz A, Ferrarese C, Hadjigeorgiou GM, Krueger R, Lambert JC, Lesage S, Markopoulou K, Mellick GD, Meeus B, Pedersen NL, et al. Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 220-8. PMID 19475631 DOI: 10.1002/Ajmg.B.30980 |
0.319 |
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| 2009 |
Lambert JC, Schraen-Maschke S, Richard F, Fievet N, Rouaud O, Berr C, Dartigues JF, Tzourio C, Alpérovitch A, Buée L, Amouyel P. Association of plasma amyloid β with risk of dementia The prospective Three-City Study Neurology. 73: 847-853. PMID 19752451 DOI: 10.1212/Wnl.0B013E3181B78448 |
0.326 |
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| 2009 |
Lambert JC, Heath S, Even G, Campion D, Sleegers K, Hiltunen M, Combarros O, Zelenika D, Bullido MJ, Tavernier B, Letenneur L, Bettens K, Berr C, Pasquier F, Fiévet N, et al. Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. Nature Genetics. 41: 1094-9. PMID 19734903 DOI: 10.1038/Ng.439 |
0.479 |
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| 2009 |
Chapuis J, Hot D, Hansmannel F, Kerdraon O, Ferreira S, Hubans C, Maurage CA, Huot L, Bensemain F, Laumet G, Ayral AM, Fievet N, Hauw JJ, DeKosky ST, Lemoine Y, ... ... Lambert JC, et al. Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease. Molecular Psychiatry. 14: 1004-16. PMID 19204726 DOI: 10.1038/Mp.2009.10 |
0.504 |
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| 2009 |
Lambert JC, Campagne F, Marambaud P. [CALHM1, a novel gene to blame in Alzheimer disease]. Medecine Sciences : M/S. 24: 923-4. PMID 19038093 DOI: 10.1051/medsci/20082411923 |
0.411 |
|
| 2009 |
Hansmannel F, Lendon C, Pasquier F, Dumont J, Hannequin D, Chapuis J, Laumet G, Ayral AM, Galimberti D, Scarpini E, Campion D, Amouyel P, Lambert JC. Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease? Neuroscience Letters. 449: 76-80. PMID 18983895 DOI: 10.1016/j.neulet.2008.10.081 |
0.564 |
|
| 2009 |
Bensemain F, Hot D, Ferreira S, Dumont J, Bombois S, Maurage CA, Huot L, Hermant X, Levillain E, Hubans C, Hansmannel F, Chapuis J, Hauw JJ, Schraen S, Lemoine Y, ... ... Lambert JC, et al. Evidence for induction of the ornithine transcarbamylase expression in Alzheimer's disease. Molecular Psychiatry. 14: 106-16. PMID 17893704 DOI: 10.1038/Sj.Mp.4002089 |
0.449 |
|
| 2009 |
Chapuis J, Boscher M, Bensemain F, Cottel D, Amouyel P, Lambert JC. Association study of the paraoxonase 1 gene with the risk of developing Alzheimer's disease. Neurobiology of Aging. 30: 152-6. PMID 17624629 DOI: 10.1016/j.neurobiolaging.2007.05.021 |
0.515 |
|
| 2009 |
Laumet G, Petitprez V, Ayral A, Hansmanel F, Chapuis J, Hannequin D, Pasquier F, Galimberti D, Scarpini E, Lendon C, Campion D, Amouyel P, Lambert J. Association study of the ADAM12 and SH3MD1 genes with the risk of developing Alzheimer's disease Alzheimers & Dementia. 5. DOI: 10.1016/J.Jalz.2009.04.775 |
0.463 |
|
| 2009 |
Hansmannel F, Mann D, Lendon C, Hauw JJ, Laumet G, Ayral AM, Chapuis J, Hannequin D, DeKosky S, Pasquier F, Berr C, Galimberti D, Scarpini E, Kamboh I, Campion D, ... ... Lambert JC, et al. Urea cycle and Alzheimer's disease Alzheimers & Dementia. 5: 461. DOI: 10.1016/J.Jalz.2009.04.769 |
0.369 |
|
| 2008 |
Dreses-Werringloer U, Lambert JC, Vingtdeux V, Zhao H, Vais H, Siebert A, Jain A, Koppel J, Rovelet-Lecrux A, Hannequin D, Pasquier F, Galimberti D, Scarpini E, Mann D, Lendon C, et al. A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk. Cell. 133: 1149-61. PMID 18585350 DOI: 10.1016/J.Cell.2008.05.048 |
0.417 |
|
| 2008 |
Chapuis J, Moisan F, Mellick G, Elbaz A, Silburn P, Pasquier F, Hannequin D, Lendon C, Campion D, Amouyel P, Lambert JC. Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease. Human Molecular Genetics. 17: 2863-7. PMID 18579580 DOI: 10.1093/Hmg/Ddn183 |
0.489 |
|
| 2008 |
Le Fur I, Laumet G, Richard F, Fievet N, Berr C, Rouaud O, Delcourt C, Amouyel P, Lambert JC. Association study of the CFH Y402H polymorphism with Alzheimer's disease. Neurobiology of Aging. 31: 165-6. PMID 18433936 DOI: 10.1016/j.neurobiolaging.2008.03.003 |
0.553 |
|
| 2008 |
Chapuis J, Hannequin D, Pasquier F, Bentham P, Brice A, Leber I, Frebourg T, Deleuze JF, Cousin E, Thaker U, Amouyel P, Mann D, Lendon C, Campion D, Lambert JC. Association study of the GAB2 gene with the risk of developing Alzheimer's disease. Neurobiology of Disease. 30: 103-6. PMID 18272374 DOI: 10.1016/J.Nbd.2007.12.006 |
0.57 |
|
| 2008 |
Marambaud P, Dreses-Werringloer U, Lambert J, Vingtdeux V, Zhao H, Koppel J, Pasquier F, Mann D, Lendon C, Amouyel P, Foskett JK, Campagne F, Davies P. O4-06-06: The calcium homeostasis modulator CALHM1 controls Abeta levels and Alzheimer's disease risk Alzheimer's & Dementia. 4: T197-T197. DOI: 10.1016/J.Jalz.2008.05.550 |
0.304 |
|
| 2008 |
Campagne F, Lambert JC, Dreses-Werringloer U, Vingtdeux V, Lendon C, Campion D, Amouyel P, Lee AT, Gregersen PK, Davies P, Marambaud P. Response: CALHM1 Association with Alzheimer's Disease Risk Cell. 135: 994-996. DOI: 10.1016/J.Cell.2008.11.031 |
0.426 |
|
| 2007 |
Lambert JC, Amouyel P. Genetic heterogeneity of Alzheimer's disease: complexity and advances. Psychoneuroendocrinology. S62-70. PMID 17659844 DOI: 10.1016/j.psyneuen.2007.05.015 |
0.506 |
|
| 2007 |
Lambert JC, Ferreira S, Gussekloo J, Christiansen L, Brysbaert G, Slagboom E, Cottel D, Petit T, Hauw JJ, DeKosky ST, Richard F, Berr C, Lendon C, Kamboh MI, Mann D, et al. Evidence for the association of the S100beta gene with low cognitive performance and dementia in the elderly. Molecular Psychiatry. 12: 870-80. PMID 17579612 DOI: 10.1038/Sj.Mp.4001974 |
0.437 |
|
| 2007 |
Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, Cousin E, Hannequin D, Raux G, Penet C, Ricard S, Macé S, Amouyel P, Deleuze JF, Frebourg T, Brice A, Lambert JC, Campion D. Variations in the APP gene promoter region and risk of Alzheimer disease. Neurology. 68: 684-7. PMID 17325276 DOI: 10.1212/01.Wnl.0000255938.33739.46 |
0.546 |
|
| 2007 |
Boddaert J, Kinugawa K, Lambert JC, Boukhtouche F, Zoll J, Merval R, Blanc-Brude O, Mann D, Berr C, Vilar J, Garabedian B, Journiac N, Charue D, Silvestre JS, Duyckaerts C, et al. Evidence of a role for lactadherin in Alzheimer's disease. The American Journal of Pathology. 170: 921-9. PMID 17322377 DOI: 10.2353/Ajpath.2007.060664 |
0.365 |
|
| 2006 |
Maraganore DM, de Andrade M, Elbaz A, Farrer MJ, Ioannidis JP, Krüger R, Rocca WA, Schneider NK, Lesnick TG, Lincoln SJ, Hulihan MM, Aasly JO, Ashizawa T, Chartier-Harlin MC, Checkoway H, ... ... Lambert JC, et al. Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. Jama. 296: 661-70. PMID 16896109 DOI: 10.1001/Jama.296.6.661 |
0.672 |
|
| 2006 |
Lambert JC, Bensemain F, Chapuis J, Cottel D, Amouyel P. Association study of the PIN1 gene with Alzheimer's disease. Neuroscience Letters. 402: 259-61. PMID 16701948 DOI: 10.1016/j.neulet.2006.04.010 |
0.565 |
|
| 2006 |
Bensemain F, Chapuis J, Tian J, Shi J, Thaker U, Lendon C, Iwatsubo T, Amouyel P, Mann D, Lambert JC. Association study of the Ubiquilin gene with Alzheimer's disease. Neurobiology of Disease. 22: 691-3. PMID 16504527 DOI: 10.1016/J.Nbd.2006.01.007 |
0.549 |
|
| 2006 |
Shi J, Tian J, Pritchard A, Lendon C, Lambert JC, Iwatsubo T, Mann DM. A 3'-UTR polymorphism in the oxidized LDL receptor 1 gene increases Abeta40 load as cerebral amyloid angiopathy in Alzheimer's disease. Acta Neuropathologica. 111: 15-20. PMID 16328515 DOI: 10.1007/S00401-005-1108-3 |
0.453 |
|
| 2006 |
Chapuis J, Tian J, Shi J, Bensemain F, Cottel D, Lendon C, Amouyel P, Mann D, Lambert JC. Association study of the vascular endothelial growth factor gene with the risk of developing Alzheimer's disease. Neurobiology of Aging. 27: 1212-5. PMID 16154235 DOI: 10.1016/J.Neurobiolaging.2005.07.013 |
0.436 |
|
| 2006 |
Richard F, Bruandet A, Sorel V, Dusart A, Chartier-Harlin M, Amouyel P, Lebert F, Pasquier F, Lambert J. P1-311: APOE locus and survival in a French cohort of demented cases Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.689 |
0.549 |
|
| 2006 |
Lambert J, Brysbaert G, George H, Bensemain F, Ferreira S, Mann D, Amouyel P. P1-289: Systematic screening for additional exons in brain-expressed genes: Clues for Alzheimer's disease? Alzheimer's & Dementia. 2: S181-S182. DOI: 10.1016/j.jalz.2006.05.666 |
0.342 |
|
| 2006 |
Chapuis J, Tian J, Shi J, Bensemain F, Cottel D, Lendon C, Amouyel P, Mann D, Lambert J. P1-271: Association study of the VEGF
and Meox2
genes with the risk of developing Alzheimer's disease Alzheimer's & Dementia. 2: S175-S176. DOI: 10.1016/j.jalz.2006.05.648 |
0.426 |
|
| 2006 |
Bensemain F, Hot D, Dumont J, Huot L, Ferreira S, Levillain E, Hubbans C, Chapuis J, Lemoine Y, Berr C, Mann D, Amouyel P, Lambert J. P1-269: Putative functional urea cycle in the brain of patients with Alzheimer’s disease and association of the ornithine transcarbamylase gene with the risk of developing Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.646 |
0.338 |
|
| 2006 |
Tian J, Shi J, Mann D, Lendon C, Green E, Lambert J, Araria-Goumidi L, Morgan K, Wang Y. P4-101: The influence of polymorphisms in interleukin -1 gene on amyloid and non-amyloid vascular pathologies in Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1840 |
0.417 |
|
| 2006 |
Tian J, Shi J, Mann D, Lendon C, Green E, Lambert J. P3-207: Association of the -491 but not -219 APOE promoter polymorphism with Aβ40
load as CAA in AD Alzheimer's & Dementia. 2: S436-S436. DOI: 10.1016/j.jalz.2006.05.1476 |
0.431 |
|
| 2005 |
Papassotiropoulos A, Lambert JC, Wavrant-De Vrièze F, Wollmer MA, von der Kammer H, Streffer JR, Maddalena A, Huynh KD, Wolleb S, Lutjohann D, Schneider B, Thal DR, Grimaldi LM, Tsolaki M, Kapaki E, et al. Cholesterol 25-hydroxylase on chromosome 10q is a susceptibility gene for sporadic Alzheimer's disease. Neuro-Degenerative Diseases. 2: 233-41. PMID 16909003 DOI: 10.1159/000090362 |
0.558 |
|
| 2005 |
Lambert JC, Mann D, Richard F, Tian J, Shi J, Thaker U, Merrot S, Harris J, Frigard B, Iwatsubo T, Lendon C, Amouyel P. Is there a relation between APOE expression and brain amyloid load in Alzheimer's disease? Journal of Neurology, Neurosurgery, and Psychiatry. 76: 928-33. PMID 15965197 DOI: 10.1136/jnnp.2004.048983 |
0.47 |
|
| 2005 |
Pritchard A, Harris J, Pritchard CW, St Clair D, Lemmon H, Lambert JC, Chartier-Harlin MC, Hayes A, Thaker U, Iwatsubo T, Mann DM, Lendon C. Association study and meta-analysis of low-density lipoprotein receptor related protein in Alzheimer's disease. Neuroscience Letters. 382: 221-6. PMID 15925094 DOI: 10.1016/J.Neulet.2005.03.016 |
0.727 |
|
| 2004 |
Hayes A, Green EK, Pritchard A, Harris JM, Zhang Y, Lambert JC, Chartier-Harlin MC, Pickering-Brown SM, Lendon CL, Mann DM. A polymorphic variation in the interleukin 1A gene increases brain microglial cell activity in Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 75: 1475-7. PMID 15377701 DOI: 10.1136/Jnnp.2003.030866 |
0.606 |
|
| 2004 |
Lambert JC, Berr C, Cottel D, Amouyel P, Helbecque N. APOE promoter polymorphisms and dementia in the elderly. Neuroscience Letters. 365: 116-9. PMID 15245790 DOI: 10.1016/j.neulet.2004.04.063 |
0.4 |
|
| 2004 |
Zhang Y, Hayes A, Pritchard A, Thaker U, Haque MS, Lemmon H, Harris J, Cumming A, Lambert JC, Chartier-Harlin MC, St Clair D, Iwatsubo T, Mann DM, Lendon CL. Interleukin-6 promoter polymorphism: risk and pathology of Alzheimer's disease. Neuroscience Letters. 362: 99-102. PMID 15193763 DOI: 10.1016/J.Neulet.2004.03.008 |
0.676 |
|
| 2004 |
Kabbara A, Payet N, Cottel D, Frigard B, Amouyel P, Lambert JC. Exclusion of CYP46 and APOM as candidate genes for Alzheimer's disease in a French population. Neuroscience Letters. 363: 139-43. PMID 15172102 DOI: 10.1016/j.neulet.2004.03.066 |
0.518 |
|
| 2004 |
Lambert JC, Mann D, Harris J, Araria-Goumidi L, Chartier-Harlin MC, Cottel D, Iwatsubo T, Amouyel P, Lendon C. Association study of Notch 4 polymorphisms with Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 75: 377-81. PMID 14966150 |
0.713 |
|
| 2004 |
Lambert JC, Coyle N, Lendon C. The allelic modulation of apolipoprotein E expression by oestrogen: potential relevance for Alzheimer's disease. Journal of Medical Genetics. 41: 104-12. PMID 14757857 DOI: 10.1136/jmg.2003.005033 |
0.48 |
|
| 2004 |
Tian J, Shi J, Bailey K, Harris JM, Pritchard A, Lambert JC, Chartier-Harlin MC, Pickering-Brown SM, Lendon CL, Mann DM. A polymorphism in the angiotensin 1-converting enzyme gene is associated with damage to cerebral cortical white matter in Alzheimer's disease. Neuroscience Letters. 354: 103-6. PMID 14698449 DOI: 10.1016/J.Neulet.2003.09.072 |
0.621 |
|
| 2004 |
Lambert J, Mann D, Richard F, Tian J, Shi J, Thaker U, Merrot S, Harris J, Chartier-Harlin M, Sazdovitch V, Mohr M, Frigard B, Hauw J, Lendon C, Iwatsubo T, et al. P4-083 Is there a relation between APOE expression and amyloid depositions in the brain of Alzheimer's disease cases? Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81641-5 |
0.649 |
|
| 2003 |
Lambert JC, Luedecking-Zimmer E, Merrot S, Hayes A, Thaker U, Desai P, Houzet A, Hermant X, Cottel D, Pritchard A, Iwatsubo T, Pasquier F, Frigard B, Conneally PM, Chartier-Harlin MC, et al. Association of 3'-UTR polymorphisms of the oxidised LDL receptor 1 (OLR1) gene with Alzheimer's disease. Journal of Medical Genetics. 40: 424-30. PMID 12807963 DOI: 10.1136/Jmg.40.6.424 |
0.723 |
|
| 2003 |
Araria-Goumidi L, Lambert JC, Cottel D, Amouyel P, Chartier-Harlin MC. No association of the HLA-A2 allele with Alzheimer's disease. Neuroscience Letters. 335: 75-8. PMID 12459502 DOI: 10.1016/S0304-3940(02)01057-1 |
0.688 |
|
| 2002 |
Lendon CL, Thaker U, Harris JM, McDonagh AM, Lambert JC, Chartier-Harlin MC, Iwatsubo T, Pickering-Brown SM, Mann DM. The angiotensin 1-converting enzyme insertion (I)/deletion (D) polymorphism does not influence the extent of amyloid or tau pathology in patients with sporadic Alzheimer's disease. Neuroscience Letters. 328: 314-8. PMID 12147333 DOI: 10.1016/S0304-3940(02)00553-0 |
0.436 |
|
| 2002 |
Araria-Goumidi L, Huguet JB, Lambert JC, Frigard B, Cottel D, Amouyel P, Chartier-Harlin MC. No association of the -48CT polymorphism of the presenilin 1 gene with Alzheimer disease in a late-onset sporadic population. Journal of Neural Transmission (Vienna, Austria : 1996). 109: 1023-7. PMID 12111439 DOI: 10.1007/s007020200085 |
0.719 |
|
| 2002 |
Lambert JC, Araria-Goumidi L, Myllykangas L, Ellis C, Wang JC, Bullido MJ, Harris JM, Artiga MJ, Hernandez D, Kwon JM, Frigard B, Petersen RC, Cumming AM, Pasquier F, Sastre I, et al. Contribution of APOE promoter polymorphisms to Alzheimer's disease risk. Neurology. 59: 59-66. PMID 12105308 DOI: 10.1212/Wnl.59.1.59 |
0.751 |
|
| 2002 |
Araria-Goumidi L, Lambert JC, Mann DM, Lendon C, Frigard B, Iwatsubo T, Cottel D, Amouyel P, Chartier-Harlin MC. Association study of three polymorphisms of TGF-beta1 gene with Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 73: 62-4. PMID 12082048 DOI: 10.1136/Jnnp.73.1.62 |
0.665 |
|
| 2002 |
Green EK, Harris JM, Lemmon H, Lambert JC, Chartier-Harlin MC, St Clair D, Mann DM, Iwatsubo T, Lendon CL. Are interleukin-1 gene polymorphisms risk factors or disease modifiers in AD? Neurology. 58: 1566-8. PMID 12034804 DOI: 10.1212/Wnl.58.10.1566 |
0.646 |
|
| 2002 |
Green EK, Thaker U, McDonagh AM, Iwatsubo T, Lambert JC, Chartier-Harlin MC, Harris JM, Pickering-Brown SM, Lendon CL, Mann DM. A polymorphism within intron 11 of the tau gene is not increased in frequency in patients with sporadic Alzheimer's disease, nor does it influence the extent of tau pathology in the brain. Neuroscience Letters. 324: 113-6. PMID 11988340 DOI: 10.1016/S0304-3940(02)00190-8 |
0.472 |
|
| 2001 |
Lambert JC, Mann D, Goumidi L, Harris J, Amouyel P, Iwatsubo T, Lendon C, Chartier-Harlin MC. Effect of the APOE promoter polymorphisms on cerebral amyloid peptide deposition in Alzheimer's disease. Lancet. 357: 608-9. PMID 11558492 DOI: 10.1016/S0140-6736(00)04063-0 |
0.703 |
|
| 2001 |
Lambert JC, Harris JM, Mann D, Lemmon H, Coates J, Cumming A, St-Clair D, Lendon C. Are the estrogen receptors involved in Alzheimer's disease? Neuroscience Letters. 306: 193-7. PMID 11406328 DOI: 10.1016/S0304-3940(01)01806-7 |
0.513 |
|
| 2001 |
Lambert JC, Mann DM, Harris JM, Chartier-Harlin MC, Cumming A, Coates J, Lemmon H, StClair D, Iwatsubo T, Lendon C. The -48 C/T polymorphism in the presenilin 1 promoter is associated with an increased risk of developing Alzheimer's disease and an increased Abeta load in brain. Journal of Medical Genetics. 38: 353-5. PMID 11389157 DOI: 10.1136/Jmg.38.6.353 |
0.726 |
|
| 2001 |
Berr C, Lambert JC, Sazdovitch V, Amouyel P, Chartier-Harlin MC, Mohr M, Heldt N, Kiesmann M, Hauw JJ. Neuropathological epidemiology of cerebral aging: a study of two genetic polymorphisms. Neurobiology of Aging. 22: 227-35. PMID 11182472 DOI: 10.1016/S0197-4580(00)00227-X |
0.339 |
|
| 2000 |
Lambert JC, Mann D, Goumidi L, Harris J, Pasquier F, Frigard B, Cottel D, Lendon C, Iwatsubo T, Amouyel P, Chartier-Harlin MC. A FE65 polymorphism associated with risk of developing sporadic late-onset alzheimer's disease but not with Abeta loading in brains. Neuroscience Letters. 293: 29-32. PMID 11065130 DOI: 10.1016/S0304-3940(00)01477-4 |
0.706 |
|
| 2000 |
Lambert JC, Goumidi L, Vrièze FW, Frigard B, Harris JM, Cummings A, Coates J, Pasquier F, Cottel D, Gaillac M, St Clair D, Mann DM, Hardy J, Lendon CL, Amouyel P, et al. The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease. Human Molecular Genetics. 9: 2275-80. PMID 11001930 DOI: 10.1093/Oxfordjournals.Hmg.A018918 |
0.744 |
|
| 2000 |
Lambert J, Brousseau T, Defosse V, Evans A, Arveiler D, Ruidavets J, Haas B, Cambou J, Luc G, Ducimetière P, Cambien F, Chartier-Harlin M, Amouyel P. Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations—the ECTIM Study Human Molecular Genetics. 9: 57-61. PMID 10587578 DOI: 10.1093/Hmg/9.1.57 |
0.705 |
|
| 2000 |
Lambert JC, Chartier-Harlin MC, Cottel D, Richard F, Neuman E, Guez D, Legrain S, Berr C, Amouyel P, Helbecque N. Is the LDL receptor-related protein involved in Alzheimer's disease? Neurogenetics. 2: 109-13. PMID 10369887 DOI: 10.1007/s100480050061 |
0.717 |
|
| 2000 |
Lambert J, Mann DM, Goumidi L, Harris JM, Amouyel P, Lendon CL, Iwatsubo T, Chatier-Harlin M. Impact of the APOE promoter polymorphisms on aβ loading in AD brains Neurobiology of Aging. 21: 205. DOI: 10.1016/S0197-4580(00)83249-2 |
0.394 |
|
| 2000 |
Chartier-Harlin M, Lambert J, Amouyel P. APOE polymorphisms in Alzheimer's disease Neurobiology of Aging. 21: 137. DOI: 10.1016/S0197-4580(00)82417-3 |
0.724 |
|
| 1999 |
Wavrant-DeVrièze F, Lambert JC, Stas L, Crook R, Cottel D, Pasquier F, Frigard B, Lambrechts M, Thiry E, Amouyel P, Tur JP, Chartier-Harlin MC, Hardy J, Van Leuven F. Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease. Human Genetics. 104: 432-4. PMID 10394937 DOI: 10.1007/S004390050980 |
0.628 |
|
| 1999 |
Sato N, Hori O, Yamaguchi A, Lambert JC, Chartier-Harlin MC, Robinson PA, Delacourte A, Schmidt AM, Furuyama T, Imaizumi K, Tohyama M, Takagi T. A novel presenilin-2 splice variant in human Alzheimer's disease brain tissue. Journal of Neurochemistry. 72: 2498-505. PMID 10349860 DOI: 10.1046/J.1471-4159.1999.0722498.X |
0.634 |
|
| 1999 |
Rudrasingham V, Wavrant-De Vrièze F, Lambert JC, Chakraverty S, Kehoe P, Crook R, Amouyel P, Wu W, Rice F, Pérez-Tur J, Frigard B, Morris JC, Carty S, Petersen R, Cottel D, et al. Alpha-2 macroglobulin gene and Alzheimer disease. Nature Genetics. 22: 17-9; author reply 2. PMID 10319854 DOI: 10.1038/8726 |
0.658 |
|
| 1999 |
Brique S, Destée A, Lambert JC, Mouroux V, Delacourte A, Amouyel P, Chartier-Harlin MC. A new GTP-cyclohydrolase I mutation in an unusual dopa-responsive dystonia, familial form. Neuroreport. 10: 487-91. PMID 10208576 DOI: 10.1097/00001756-199902250-00008 |
0.545 |
|
| 1999 |
Wavrant-DeVrièze F, Rudrasingham V, Lambert JC, Chakraverty S, Kehoe P, Crook R, Amouyel P, Wu W, Holmans P, Rice F, Pérez-Tur J, Frigard B, Morris JC, Carty S, Cottel D, et al. No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease. Neuroscience Letters. 262: 137-9. PMID 10203250 DOI: 10.1016/S0304-3940(99)00035-X |
0.739 |
|
| 1998 |
Lambert JC, Berr C, Pasquier F, Delacourte A, Frigard B, Cottel D, Pérez-Tur J, Mouroux V, Mohr M, Cécyre D, Galasko D, Lendon C, Poirier J, Hardy J, Mann D, et al. Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's disease. Human Molecular Genetics. 7: 1511-6. PMID 9700208 DOI: 10.1093/Hmg/7.9.1511 |
0.754 |
|
| 1998 |
Lambert J, Vrièze FW, Amouyel P, Chartier-Harlin M. Association at LRP gene locus with sporadic late-onset Alzheimer's disease The Lancet. 351: 1787-1788. PMID 9635959 DOI: 10.1016/S0140-6736(05)78749-3 |
0.703 |
|
| 1998 |
Lambert J, Pasquier F, Cottel D, Frigard B, Amouyel P, Chartier-Harlin M. A New Polymorphism in the Apoe Promoter Associated with Risk of Developing Alzheimer's Disease Human Molecular Genetics. 7: 533-540. PMID 9467014 DOI: 10.1093/Hmg/7.3.533 |
0.701 |
|
| 1997 |
Lambert JC, Pérez-Tur J, Dupire MJ, Galasko D, Mann D, Amouyel P, Hardy J, Delacourte A, Chartier-Harlin MC. Distortion of allelic expression of apolipoprotein E in Alzheimer's disease. Human Molecular Genetics. 6: 2151-4. PMID 9328480 DOI: 10.1093/Hmg/6.12.2151 |
0.736 |
|
| 1997 |
Wavrant-DeVrièze F, Pérez-Tur J, Lambert JC, Frigard B, Pasquier F, Delacourte A, Amouyel P, Hardy J, Chartier-Harlin MC. Association between the low density lipoprotein receptor-related protein (LRP) and Alzheimer's disease. Neuroscience Letters. 227: 68-70. PMID 9178861 DOI: 10.1016/S0304-3940(97)00304-2 |
0.773 |
|
| 1996 |
Lambert JC, Pérez-Tur J, Dupire MJ, Delacourte A, Frigard B, Chartier-Harlin MC. Analysis of the APOE alleles impact in Down's syndrome. Neuroscience Letters. 220: 57-60. PMID 8977148 DOI: 10.1016/S0304-3940(96)13244-4 |
0.698 |
|
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